Dr Peter Visscher Email
Telephone: +61 7 3362 0166
Facsimile: +61 7 3362 0101
Email: Peter.Visscher@qimrberghofer.edu.au

Peter Visscher is a Senior Principal Research Fellow (SPRF) at QIMR, and holds an honorary professorship with the Institute for Molecular Bioscience at UQ. He was born in Holland from Dutch and English parents. His children are first backcrosses. After obtaining a BSc in Animal Science he worked for a couple of years in the Department of Agriculture in Holland before moving to Edinburgh for a Masters and PhD in animal breeding and genetics (supervised by Bill Hill FRS and Robin Thompson FRSE), working on the estimation of genetic parameters in large dairy cattle pedigrees. A productive postdoc with Mike Goddard (Melbourne) was followed by a return to Edinburgh, where he worked with Chris Haley (Roslin Institute) on marker-assisted-selection and QTL mapping methodology. In 1995 he moved to a faculty position at the University of Edinburgh, working on QTL mapping methods, software tools and practical applications. Since ~1998 his main interest and research focus has been in genetic epidemiology, statistical genetics and human quantitative & population genetics. He joined the Queensland Institute of Medical Research in January 2005.


Publications
2014
 Benyamin B, Pourcain B, Davis OS, Davies G, Hansell NK, Brion MJ, Kirkpatrick RM, Cents RA, Franic S, Miller MB, Haworth CM, Meaburn E, Price TS, Evans DM, Timpson N, Kemp J, Ring S, McArdle W, Medland SE, Yang J, Harris SE, Liewald DC, Scheet P, Xiao X, Hudziak JJ, de Geus EJ, Wellcome Trust Case Control Consortium 2 (WTCCC2), Jaddoe VW, Starr JM, Verhulst FC, Pennell C, Tiemeier H, Iacono WG, Palmer LJ, Montgomery GW, Martin NG, Boomsma DI, Posthuma D, McGue M, Wright MJ, Davey Smith G, Deary IJ, Plomin R, Visscher PM: Childhood intelligence is heritable, highly polygenic and associated with FNBP1L. Molecular Psychiatry 19(2):253-258, 2014 [PDF unavailable] [PubMed] [More...]
 Parnell GP, Gatt PN, McKay FC, Schibeci S, Krupa M, Powell JE, Visscher PM, Montgomery GW, Lechner-Scott J, Broadley S, Liddle C, Slee M, Vucic S, Stewart GJ, Booth DR: Ribosomal protein S6 mRNA is a biomarker upregulated in multiple sclerosis, downregulated by interferon treatment, and affected by season. Multiple sclerosis (Houndmills, Basingstoke, England) 20:675-685, 2014 [PDF unavailable] [PubMed] [More...]
 Hemani G, Shakhbazov K, Westra HJ, Esko T, Henders AK, McRae AF, Yang J, Gibson G, Martin NG, Metspalu A, Franke L, Montgomery GW, Visscher PM, Powell JE: Detection and replication of epistasis influencing transcription in humans. Nature 508(7495):249-253, 2014 [PDF unavailable] [PubMed] [More...]
 Chen GB, Lee SH, Brion MJ, Montgomery GW, Wray NR, Radford-Smith GL, Visscher PM, the International IBD Genetics Consortium: Estimation and partitioning of (co)heritability of inflammatory bowel disease from GWAS and immunochip data. Human Molecular Genetics 2014 [PDF unavailable] [PubMed] [More...]
2013
 Lee SH, Harold D, Nyholt DR, ANZGene Consortium, ENDOGENE Consortium, the Genetic and Environmental Risk for Alzheimer's disease (GERAD1) Consortium, Goddard ME, Zondervan KT, Williams J, Montgomery GW, Wray NR, Visscher PM: Estimation and partitioning of polygenic variation captured by common SNPs for Alzheimer's disease, multiple sclerosis and endometriosis. Human Molecular Genetics 22:832-841, 2013 [PDF unavailable] [PubMed] [More...]
 Berndt SI, Gustafsson S, Magi R, Ganna A, Wheeler E, Feitosa MF, Justice AE, Monda KL, Croteau-Chonka DC, Day FR, Esko T, Fall T, Ferreira T, Gentilini D, Jackson AU, Luan J, Randall JC, Vedantam S, Willer CJ, Winkler TW, Wood AR, Workalemahu T, Hu YJ, Lee SH, Liang L, Lin DY, Min JL, Neale BM, Thorleifsson G, Yang J, Albrecht E, Amin N, Bragg-Gresham JL, Cadby G, den Heijer M, Eklund N, Fischer K, Goel A, Hottenga JJ, Huffman JE, Jarick I, Johansson A, Johnson T, Kanoni S, Kleber ME, Konig IR, Kristiansson K, Kutalik Z, Lamina C, Lecoeur C, Li G, Mangino M, McArdle WL, Medina-Gomez C, Muller-Nurasyid M, Ngwa JS, Nolte IM, Paternoster L, Pechlivanis S, Perola M, Peters MJ, Preuss M, Rose LM, Shi J, Shungin D, Smith AV, Strawbridge RJ, Surakka I, Teumer A, Trip MD, Tyrer J, van Vliet-Ostaptchouk JV, Vandenput L, Waite LL, Zhao JH, Absher D, Asselbergs FW, Atalay M, Attwood AP, Balmforth AJ, Basart H, Beilby J, Bonnycastle LL, Brambilla P, Bruinenberg M, Campbell H, Chasman DI, Chines PS, Collins FS, Connell JM, Cookson WO, de Faire U, de Vegt F, Dei M, Dimitriou M, Edkins S, Estrada K, Evans DM, Farrall M, Ferrario MM, Ferrieres J, Franke L, Frau F, Gejman PV, Grallert H, Gronberg H, Gudnason V, Hall AS, Hall P, Hartikainen AL, Hayward C, Heard-Costa NL, Heath AC, Hebebrand J, Homuth G, Hu FB, Hunt SE, Hypponen E, Iribarren C, Jacobs KB, Jansson JO, Jula A, Kahonen M, Kathiresan S, Kee F, Khaw KT, Kivimaki M, Koenig W, Kraja AT, Kumari M, Kuulasmaa K, Kuusisto J, Laitinen JH, Lakka TA, Langenberg C, Launer LJ, Lind L, Lindstrom J, Liu J, Liuzzi A, Lokki ML, Lorentzon M, Madden PA, Magnusson PK, Manunta P, Marek D, Marz W, Leach IM, McKnight B, Medland SE, Mihailov E, Milani L, Montgomery GW, Mooser V, Muhleisen TW, Munroe PB, Musk AW, Narisu N, Navis G, Nicholson G, Nohr EA, Ong KK, Oostra BA, Palmer CN, Palotie A, Peden JF, Pedersen N, Peters A, Polasek O, Pouta A, Pramstaller PP, Prokopenko I, Putter C, Radhakrishnan A, Raitakari O, Rendon A, Rivadeneira F, Rudan I, Saaristo TE, Sambrook JG, Sanders AR, Sanna S, Saramies J, Schipf S, Schreiber S, Schunkert H, Shin SY, Signorini S, Sinisalo J, Skrobek B, Soranzo N, Stancakova A, Stark K, Stephens JC, Stirrups K, Stolk RP, Stumvoll M, Swift AJ, Theodoraki EV, Thorand B, Tregouet DA, Tremoli E, Van der Klauw MM, van Meurs JB, Vermeulen SH, Viikari J, Virtamo J, Vitart V, Waeber G, Wang Z, Widen E, Wild SH, Willemsen G, Winkelmann BR, Witteman JC, Wolffenbuttel BH, Wong A, Wright AF, Zillikens MC, Amouyel P, Boehm BO, Boerwinkle E, Boomsma DI, Caulfield MJ, Chanock SJ, Cupples LA, Cusi D, Dedoussis GV, Erdmann J, Eriksson JG, Franks PW, Froguel P, Gieger C, Gyllensten U, Hamsten A, Harris TB, Hengstenberg C, Hicks AA, Hingorani A, Hinney A, Hofman A, Hovingh KG, Hveem K, Illig T, Jarvelin MR, Jockel KH, Keinanen-Kiukaanniemi SM, Kiemeney LA, Kuh D, Laakso M, Lehtimaki T, Levinson DF, Martin NG, Metspalu A, Morris AD, Nieminen MS, Njolstad I, Ohlsson C, Oldehinkel AJ, Ouwehand WH, Palmer LJ, Penninx B, Power C, Province MA, Psaty BM, Qi L, Rauramaa R, Ridker PM, Ripatti S, Salomaa V, Samani NJ, Snieder H, Sorensen TI, Spector TD, Stefansson K, Tonjes A, Tuomilehto J, Uitterlinden AG, Uusitupa M, van der Harst P, Vollenweider P, Wallaschofski H, Wareham NJ, Watkins H, Wichmann HE, Wilson JF, Abecasis GR, Assimes TL, Barroso I, Boehnke M, Borecki IB, Deloukas P, Fox CS, Frayling T, Groop LC, Haritunian T, Heid IM, Hunter D, Kaplan RC, Karpe F, Moffatt MF, Mohlke KL, O'Connell JR, Pawitan Y, Schadt EE, Schlessinger D, Steinthorsdottir V, Strachan DP, Thorsteinsdottir U, van Duijn CM, Visscher PM, Di Blasio AM, Hirschhorn JN, Lindgren CM, Morris AP, Meyre D, Scherag A, McCarthy MI, Speliotes EK, North KE, Loos RJ, Ingelsson E: Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture. Nature Genetics 45(5):501-512, 2013 [PDF unavailable] [PubMed] [More...]
 den Hoed M, Eijgelsheim M, Esko T, Brundel BJ, Peal DS, Evans DM, Nolte IM, Segre AV, Holm H, Handsaker RE, Westra HJ, Johnson T, Isaacs A, Yang J, Lundby A, Zhao JH, Kim YJ, Go MJ, Almgren P, Bochud M, Boucher G, Cornelis MC, Gudbjartsson D, Hadley D, van der Harst P, Hayward C, den Heijer M, Igl W, Jackson AU, Kutalik Z, Luan J, Kemp JP, Kristiansson K, Ladenvall C, Lorentzon M, Montasser ME, Njajou OT, O'Reilly PF, Padmanabhan S, St Pourcain B, Rankinen T, Salo P, Tanaka T, Timpson NJ, Vitart V, Waite L, Wheeler W, Zhang W, Draisma HH, Feitosa MF, Kerr KF, Lind PA, Mihailov E, Onland-Moret NC, Song C, Weedon MN, Xie W, Yengo L, Absher D, Albert CM, Alonso A, Arking DE, de Bakker PI, Balkau B, Barlassina C, Benaglio P, Bis JC, Bouatia-Naji N, Brage S, Chanock SJ, Chines PS, Chung M, Darbar D, Dina C, Dorr M, Elliott P, Felix SB, Fischer K, Fuchsberger C, de Geus EJ, Goyette P, Gudnason V, Harris TB, Hartikainen AL, Havulinna AS, Heckbert SR, Hicks AA, Hofman A, Holewijn S, Hoogstra-Berends F, Hottenga JJ, Jensen MK, Johansson A, Junttila J, Kaab S, Kanon B, Ketkar S, Khaw KT, Knowles JW, Kooner AS, Kors JA, Kumari M, Milani L, Laiho P, Lakatta EG, Langenberg C, Leusink M, Liu Y, Luben RN, Lunetta KL, Lynch SN, Markus MR, Marques-Vidal P, Leach IM, McArdle WL, McCarroll SA, Medland SE, Miller KA, Montgomery GW, Morrison AC, M Vuml Ller-Nurasyid M, Navarro P, Nelis M, O'Connell JR, O'Donnell CJ, Ong KK, Newman AB, Peters A, Polasek O, Pouta A, Pramstaller PP, Psaty BM, Rao DC, Ring SM, Rossin EJ, Rudan D, Sanna S, Scott RA, Sehmi JS, Sharp S, Shin JT, Singleton AB, Smith AV, Soranzo N, Spector TD, Stewart C, Stringham HM, Tarasov KV, Uitterlinden AG, Vandenput L, Hwang SJ, Whitfield JB, Wijmenga C, Wild SH, Willemsen G, Wilson JF, Witteman JC, Wong A, Wong Q, Jamshidi Y, Zitting P, Boer JM, Boomsma DI, Borecki IB, van Duijn CM, Ekelund U, Forouhi NG, Froguel P, Hingorani A, Ingelsson E, Kivimaki M, Kronmal RA, Kuh D, Lind L, Martin NG, Oostra BA, Pedersen NL, Quertermous T, Rotter JI, van der Schouw YT, Verschuren WM, Walker M, Albanes D, Arnar DO, Assimes TL, Bandinelli S, Boehnke M, de Boer RA, Bouchard C, Caulfield WL, Chambers JC, Curhan G, Cusi D, Eriksson J, Ferrucci L, van Gilst WH, Glorioso N, de Graaf J, Groop L, Gyllensten U, Hsueh WC, Hu FB, Huikuri HV, Hunter DJ, Iribarren C, Isomaa B, Jarvelin MR, Jula A, Kahonen M, Kiemeney LA, Van der Klauw MM, Kooner JS, Kraft P, Iacoviello L, Lehtimaki T, Lokki ML, Mitchell BD, Navis G, Nieminen MS, Ohlsson C, Poulter NR, Qi L, Raitakari OT, Rimm EB, Rioux JD, Rizzi F, Rudan I, Salomaa V, Sever PS, Shields DC, Shuldiner AR, Sinisalo J, Stanton AV, Stolk RP, Strachan DP, Tardif JC, Thorsteinsdottir U, Tuomilehto J, van Veldhuisen DJ, Virtamo J, Viikari J, Vollenweider P, Waeber G, Widen E, Cho YS, Olsen JV, Visscher PM, Willer C, Franke L, Global BPgen Consortium, CARDIoGRAM Consortium, Erdmann J, Thompson JR, PR GWAS Consortium, Pfeufer A, QRS GWAS Consortium, Sotoodehnia N, QT-IGC Consortium, Newton-Cheh C, CHARGE-AF Consortium, Ellinor PT, Stricker BH, Metspalu A, Perola M, Beckmann JS, Smith GD, Stefansson K, Wareham NJ, Munroe PB, Sibon OC, Milan DJ, Snieder H, Samani NJ, Loos RJ: Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders. Nature Genetics 45(6):621-631, 2013 [PDF unavailable] [PubMed] [More...]
 Rietveld CA, Medland SE, Derringer J, Yang J, Esko T, Martin NW, Westra HJ, Shakhbazov K, Abdellaoui A, Agrawal A, Albrecht E, Alizadeh BZ, Amin N, Barnard J, Baumeister SE, Benke KS, Bielak LF, Boatman JA, Boyle PA, Davies G, de Leeuw C, Eklund N, Evans DS, Ferhmann R, Fischer K, Gieger C, Gjessing HK, Hagg S, Harris JR, Hayward C, Holzapfel C, Ibrahim-Verbaas CA, Ingelsson E, Jacobsson B, Joshi PK, Jugessur A, Kaakinen M, Kanoni S, Karjalainen J, Kolcic I, Kristiansson K, Kutalik Z, Lahti J, Lee SH, Lin P, Lind PA, Liu Y, Lohman K, Loitfelder M, McMahon G, Vidal PM, Meirelles O, Milani L, Myhre R, Nuotio ML, Oldmeadow CJ, Petrovic KE, Peyrot WJ, Polasek O, Quaye L, Reinmaa E, Rice JP, Rizzi TS, Schmidt H, Schmidt R, Smith AV, Smith JA, Tanaka T, Terracciano A, van der Loos MJ, Vitart V, Volzke H, Wellmann J, Yu L, Zhao W, Allik J, Attia JR, Bandinelli S, Bastardot F, Beauchamp J, Bennett DA, Berger K, Bierut LJ, Boomsma DI, Bultmann U, Campbell H, Chabris CF, Cherkas L, Chung MK, Cucca F, de Andrade M, De Jager PL, De Neve JE, Deary IJ, Dedoussis GV, Deloukas P, Dimitriou M, Eiriksdottir G, Elderson MF, Eriksson JG, Evans DM, Faul JD, Ferrucci L, Garcia ME, Gronberg H, Gudnason V, Hall P, Harris JM, Harris TB, Hastie ND, Heath AC, Hernandez DG, Hoffmann W, Hofman A, Holle R, Holliday EG, Hottenga JJ, Iacono WG, Illig T, Jarvelin MR, Kahonen M, Kaprio J, Kirkpatrick RM, Kowgier M, Latvala A, Launer LJ, Lawlor DA, Lehtimaki T, Li J, Lichtenstein P, Lichtner P, Liewald DC, Madden PA, Magnusson PK, Makinen TE, Masala M, McGue M, Metspalu A, Mielck A, Miller MB, Montgomery GW, Mukherjee S, Nyholt DR, Oostra BA, Palmer LJ, Palotie A, Penninx B, Perola M, Peyser PA, Preisig M, Raikkonen K, Raitakari OT, Realo A, Ring SM, Ripatti S, Rivadeneira F, Rudan I, Rustichini A, Salomaa V, Sarin AP, Schlessinger D, Scott RJ, Snieder H, St Pourcain B, Starr JM, Sul JH, Surakka I, Svento R, Teumer A, The LifeLines Cohort Study, Tiemeier H, van Rooij FJ, Van Wagoner DR, Vartiainen E, Viikari J, Vollenweider P, Vonk JM, Waeber G, Weir DR, Wichmann HE, Widen E, Willemsen G, Wilson JF, Wright AF, Conley D, Davey-Smith G, Franke L, Groenen PJ, Hofman A, Johannesson M, Kardia SL, Krueger RF, Laibson D, Martin NG, Meyer MN, Posthuma D, Thurik AR, Timpson NJ, Uitterlinden AG, van Duijn CM, Visscher PM, Benjamin DJ, Cesarini D, Koellinger PD: GWAS of 126,559 Individuals Identifies Genetic Variants Associated with Educational Attainment. Science (New York, N.Y.) 340:1467-1471, 2013 [PDF unavailable] [PubMed] [More...]
 Powell JE, Henders AK, McRae AF, Kim J, Hemani G, Martin NG, Dermitzakis ET, Gibson G, Montgomery GW, Visscher PM: Congruence of additive and non-additive effects on gene expression estimated from pedigree and SNP data. PLoS Genetics 9(5):e1003502, 2013 [PDF unavailable] [PubMed] [More...]
 Revez JA, Bain L, Chapman B, Powell JE, Jansen R, Duffy DL, Tung JY, AAGC Collaborators, Matheson MC, Marks GB, Hui J, Le Souef P, Danoy P, Baltic S, Nyholt DR, Jenkins M, Hayden C, Beilby J, Cheah F, Madden PA, Heath AC, Hopper JL, Musk B, Leeder SR, Walters EH, James A, Jones G, Abramson MJ, Robertson CF, Dharmage SC, Brown MA, Thompson PJ, Penninx BW, Visscher PM, de Geus EJ, Boomsma DI, Hinds DA, Martin NG, Montgomery GW, Ferreira MA: A new regulatory variant in the interleukin-6 receptor gene associates with asthma risk. Genes and Immunity 14(7):441-446, 2013 [PDF unavailable] [PubMed] [More...]
 Cross-Disorder Group of the Psychiatric Genomics Consortium, Lee SH, Ripke S, Neale BM, Faraone SV, Purcell SM, Perlis RH, Mowry BJ, Thapar A, Goddard ME, Witte JS, Absher D, Agartz I, Akil H, Amin F, Andreassen OA, Anjorin A, Anney R, Anttila V, Arking DE, Asherson P, Azevedo MH, Backlund L, Badner JA, Bailey AJ, Banaschewski T, Barchas JD, Barnes MR, Barrett TB, Bass N, Battaglia A, Bauer M, Bayes M, Bellivier F, Bergen SE, Berrettini W, Betancur C, Bettecken T, Biederman J, Binder EB, Black DW, Blackwood DH, Bloss CS, Boehnke M, Boomsma DI, Breen G, Breuer R, Bruggeman R, Cormican P, Buccola NG, Buitelaar JK, Bunney WE, Buxbaum JD, Byerley WF, Byrne EM, Caesar S, Cahn W, Cantor RM, Casas M, Chakravarti A, Chambert K, Choudhury K, Cichon S, Cloninger CR, Collier DA, Cook EH, Coon H, Cormand B, Corvin A, Coryell WH, Craig DW, Craig IW, Crosbie J, Cuccaro ML, Curtis D, Czamara D, Datta S, Dawson G, Day R, de Geus EJ, Degenhardt F, Djurovic S, Donohoe GJ, Doyle AE, Duan J, Dudbridge F, Duketis E, Ebstein RP, Edenberg HJ, Elia J, Ennis S, Etain B, Fanous A, Farmer AE, Ferrier IN, Flickinger M, Fombonne E, Foroud T, Frank J, Franke B, Fraser C, Freedman R, Freimer NB, Freitag CM, Friedl M, Frisen L, Gallagher L, Gejman PV, Georgieva L, Gershon ES, Geschwind DH, Giegling I, Gill M, Gordon SD, Gordon-Smith K, Green EK, Greenwood TA, Grice DE, Gross M, Grozeva D, Guan W, Gurling H, de Haan L, Haines JL, Hakonarson H, Hallmayer J, Hamilton SP, Hamshere ML, Hansen TF, Hartmann AM, Hautzinger M, Heath AC, Henders AK, Herms S, Hickie IB, Hipolito M, Hoefels S, Holmans PA, Holsboer F, Hoogendijk WJ, Hottenga JJ, Hultman CM, Hus V, Ingason A, Ising M, Jamain S, Jones EG, Jones I, Jones L, Tzeng JY, Kahler AK, Kahn RS, Kandaswamy R, Keller MC, Kennedy JL, Kenny E, Kent L, Kim Y, Kirov GK, Klauck SM, Klei L, Knowles JA, Kohli MA, Koller DL, Konte B, Korszun A, Krabbendam L, Krasucki R, Kuntsi J, Kwan P, Landen M, Langstrom N, Lathrop M, Lawrence J, Lawson WB, Leboyer M, Ledbetter DH, Lee PH, Lencz T, Lesch KP, Levinson DF, Lewis CM, Li J, Lichtenstein P, Lieberman JA, Lin DY, Linszen DH, Liu C, Lohoff FW, Loo SK, Lord C, Lowe JK, Lucae S, Macintyre DJ, Madden PA, Maestrini E, Magnusson PK, Mahon PB, Maier W, Malhotra AK, Mane SM, Martin CL, Martin NG, Mattheisen M, Matthews K, Mattingsdal M, McCarroll SA, McGhee KA, McGough JJ, McGrath PJ, McGuffin P, McInnis MG, McIntosh A, McKinney R, McLean AW, McMahon FJ, McMahon WM, McQuillin A, Medeiros H, Medland SE, Meier S, Melle I, Meng F, Meyer J, Middeldorp CM, Middleton L, Milanova V, Miranda A, Monaco AP, Montgomery GW, Moran JL, Moreno-De-Luca D, Morken G, Morris DW, Morrow EM, Moskvina V, Muglia P, Muhleisen TW, Muir WJ, Muller-Myhsok B, Murtha M, Myers RM, Myin-Germeys I, Neale MC, Nelson SF, Nievergelt CM, Nikolov I, Nimgaonkar V, Nolen WA, Nothen MM, Nurnberger JI, Nwulia EA, Nyholt DR, O'Dushlaine C, Oades RD, Olincy A, Oliveira G, Olsen L, Ophoff RA, Osby U, Owen MJ, Palotie A, Parr JR, Paterson AD, Pato CN, Pato MT, Penninx BW, Pergadia ML, Pericak-Vance MA, Pickard BS, Pimm J, Piven J, Posthuma D, Potash JB, Poustka F, Propping P, Puri V, Quested DJ, Quinn EM, Ramos-Quiroga JA, Rasmussen HB, Raychaudhuri S, Rehnstrom K, Reif A, Ribases M, Rice JP, Rietschel M, Roeder K, Roeyers H, Rossin L, Rothenberger A, Rouleau G, Ruderfer D, Rujescu D, Sanders AR, Sanders SJ, Santangelo SL, Sergeant JA, Schachar R, Schalling M, Schatzberg AF, Scheftner WA, Schellenberg GD, Scherer SW, Schork NJ, Schulze TG, Schumacher J, Schwarz M, Scolnick E, Scott LJ, Shi J, Shilling PD, Shyn SI, Silverman JM, Slager SL, Smalley SL, Smit JH, Smith EN, Sonuga-Barke EJ, St Clair D, State M, Steffens M, Steinhausen HC, Strauss JS, Strohmaier J, Stroup TS, Sutcliffe JS, Szatmari P, Szelinger S, Thirumalai S, Thompson RC, Todorov AA, Tozzi F, Treutlein J, Uhr M, van den Oord EJ, Van Grootheest G, van Os J, Vicente AM, Vieland VJ, Vincent JB, Visscher PM, Walsh CA, Wassink TH, Watson SJ, Weissman MM, Werge T, Wienker TF, Wijsman EM, Willemsen G, Williams N, Willsey AJ, Witt SH, Xu W, Young AH, Yu TW, Zammit S, Zandi PP, Zhang P, Zitman FG, Zollner S, International Inflammatory Bowel Disease Genetics Consortium (IIBDGC), Devlin B, Kelsoe JR, Sklar P, Daly MJ, O'Donovan MC, Craddock N, Sullivan PF, Smoller JW, Kendler KS, Wray NR: Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. Nature Genetics 45(9):984-994, 2013 [PDF unavailable] [PubMed] [More...]
 Goldinger A, Henders AK, McRae AF, Martin NG, Gibson G, Montgomery GW, Visscher PM, Powell JE: Genetic and Non-Genetic Variation Revealed for the Principal Components of Human Gene Expression. Genetics 195(3):1117-1128, 2013 [PDF unavailable] [PubMed] [More...]
 Westra HJ, Peters MJ, Esko T, Yaghootkar H, Schurmann C, Kettunen J, Christiansen MW, Fairfax BP, Schramm K, Powell JE, Zhernakova A, Zhernakova DV, Veldink JH, van den Berg LH, Karjalainen J, Withoff S, Uitterlinden AG, Hofman A, Rivadeneira F, 't Hoen PA, Reinmaa E, Fischer K, Nelis M, Milani L, Melzer D, Ferrucci L, Singleton AB, Hernandez DG, Nalls MA, Homuth G, Nauck M, Radke D, Volker U, Perola M, Salomaa V, Brody J, Suchy-Dicey A, Gharib SA, Enquobahrie DA, Lumley T, Montgomery GW, Makino S, Prokisch H, Herder C, Roden M, Grallert H, Meitinger T, Strauch K, Li Y, Jansen RC, Visscher PM, Knight JC, Psaty BM, Ripatti S, Teumer A, Frayling TM, Metspalu A, van Meurs JB, Franke L: Systematic identification of trans eQTLs as putative drivers of known disease associations. Nature Genetics 45(10):1238-1243, 2013 [PDF unavailable] [PubMed] [More...]
 Hemani G, Yang J, Vinkhuyzen A, Powell JE, Willemsen G, Hottenga JJ, Abdellaoui A, Mangino M, Valdes AM, Medland SE, Madden PA, Heath AC, Henders AK, Nyholt DR, de Geus EJ, Magnusson PK, Ingelsson E, Montgomery GW, Spector TD, Boomsma DI, Pedersen NL, Martin NG, Visscher PM: Inference of the Genetic Architecture Underlying BMI and Height with the Use of 20,240 Sibling Pairs. American Journal of Human Genetics 93(5):865-875, 2013 [PDF unavailable] [PubMed] [More...]
 Robinson EB, Howrigan D, Yang J, Ripke S, Anttila V, Duncan LE, Jostins L, Barrett JC, Medland SE, Macarthur DG, Breen G, O'Donovan MC, Wray NR, Devlin B, Daly MJ, Visscher PM, Sullivan PF, Neale BM: Response to 'Predicting the diagnosis of autism spectrum disorder using gene pathway analysis'. Molecular Psychiatry 2013 [PDF unavailable] [PubMed] [More...]
2012
 Powell JE, Henders AK, McRae AF, Wright MJ, Martin NG, Dermitzakis ET, Montgomery GW, Visscher PM: Genetic control of gene expression in whole blood and lymphoblastoid cell lines is largely independent. Genome Research 22(3):456-466, 2012 [PDF unavailable] [PubMed] [More...]
 Stolk L, Perry JR, Chasman DI, He C, Mangino M, Sulem P, Barbalic M, Broer L, Byrne EM, Ernst F, Esko T, Franceschini N, Gudbjartsson DF, Hottenga JJ, Kraft P, McArdle PF, Porcu E, Shin SY, Smith AV, van Wingerden S, Zhai G, Zhuang WV, Albrecht E, Alizadeh BZ, Aspelund T, Bandinelli S, Lauc LB, Beckmann JS, Boban M, Boerwinkle E, Broekmans FJ, Burri A, Campbell H, Chanock SJ, Chen C, Cornelis MC, Corre T, Coviello AD, d'Adamo P, Davies G, de Faire U, de Geus EJ, Deary IJ, Dedoussis GV, Deloukas P, Ebrahim S, Eiriksdottir G, Emilsson V, Eriksson JG, Fauser BC, Ferreli L, Ferrucci L, Fischer K, Folsom AR, Garcia ME, Gasparini P, Gieger C, Glazer N, Grobbee DE, Hall P, Haller T, Hankinson SE, Hass M, Hayward C, Heath AC, Hofman A, Ingelsson E, Janssens AC, Johnson AD, Karasik D, Kardia SL, Keyzer J, Kiel DP, Kolcic I, Kutalik Z, Lahti J, Lai S, Laisk T, Laven JS, Lawlor DA, Liu J, Lopez LM, Louwers YV, Magnusson PK, Marongiu M, Martin NG, Klaric IM, Masciullo C, McKnight B, Medland SE, Melzer D, Mooser V, Navarro P, Newman AB, Nyholt DR, Onland-Moret NC, Palotie A, Pare G, Parker AN, Pedersen NL, Peeters PH, Pistis G, Plump AS, Polasek O, Pop VJ, Psaty BM, Raikkonen K, Rehnberg E, Rotter JI, Rudan I, Sala C, Salumets A, Scuteri A, Singleton A, Smith JA, Snieder H, Soranzo N, Stacey SN, Starr JM, Stathopoulou MG, Stirrups K, Stolk RP, Styrkarsdottir U, Sun YV, Tenesa A, Thorand B, Toniolo D, Tryggvadottir L, Tsui K, Ulivi S, van Dam RM, van der Schouw YT, van Gils CH, van Nierop P, Vink JM, Visscher PM, Voorhuis M, Waeber G, Wallaschofski H, Wichmann HE, Widen E, Wijnands-van Gent CJ, Willemsen G, Wilson JF, Wolffenbuttel BH, Wright AF, Yerges-Armstrong LM, Zemunik T, Zgaga L, Zillikens MC, Zygmunt M, Study TL, Arnold AM, Boomsma DI, Buring JE, Crisponi L, Demerath EW, Gudnason V, Harris TB, Hu FB, Hunter DJ, Launer LJ, Metspalu A, Montgomery GW, Oostra BA, Ridker PM, Sanna S, Schlessinger D, Spector TD, Stefansson K, Streeten EA, Thorsteinsdottir U, Uda M, Uitterlinden AG, van Duijn CM, Volzke H, Murray A, Murabito JM, Visser JA, Lunetta KL: Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways. Nature Genetics 44(3):260-268, 2012 [PDF unavailable] [PubMed] [More...]
 Yang J, Ferreira T, Morris AP, Medland SE, Genetic Investigation of Anthropometric Traits (GIANT) Consortium, DIAbetes Genetics Replication And Meta-analysis (DIAGRAM) Consortium, Madden PA, Heath AC, Martin NG, Montgomery GW, Weedon MN, Loos RJ, Frayling TM, McCarthy MI, Hirschhorn JN, Goddard ME, Visscher PM: Conditional and joint multiple-SNP analysis of GWAS summary statistics identifies additional variants influencing complex traits. Nature Genetics 44(4):369-375, 2012 [PDF unavailable] [PubMed] [More...]
 Powell JE, Henders AK, McRae AF, Caracella A, Smith S, Wright MJ, Whitfield JB, Dermitzakis ET, Martin NG, Visscher PM, Montgomery GW: The Brisbane Systems Genetics Study: Genetical genomics meets complex trait genetics. PLoS ONE 7(4):e35430, 2012 [PDF unavailable] [PubMed] [More...]
 Vinkhuyzen AA, Pedersen NL, Yang J, Lee SH, Magnusson PKE, Iacono WG, McGue M, Madden PAF, Heath AC, Luciano M, Payton A, Horan M, Ollier W, Pendleton N, Deary IJ, Montgomery GW, Martin NG, Visscher PM, Wray NR: Common SNPs explain some of the variation in the personality dimensions of neuroticism and extraversion. Translational Psychiatry 2:e102, 2012 [PDF unavailable]
 McQuillan R, Eklund N, Pirastu N, Kuningas M, McEvoy BP, Esko T, Corre T, Davies G, Kaakinen M, Lyytikainen LP, Kristiansson K, Havulinna AS, Gogele M, Vitart V, Tenesa A, Aulchenko Y, Hayward C, Johansson A, Boban M, Ulivi S, Robino A, Boraska V, Igl W, Wild SH, Zgaga L, Amin N, Theodoratou E, Polasek O, Girotto G, Lopez LM, Sala C, Lahti J, Laatikainen T, Prokopenko I, Kals M, Viikari J, Yang J, Pouta A, Estrada K, Hofman A, Freimer N, Martin NG, Kahonen M, Milani L, Heliovaara M, Vartiainen E, Raikkonen K, Masciullo C, Starr JM, Hicks AA, Esposito L, Kolcic I, Farrington SM, Oostra B, Zemunik T, Campbell H, Kirin M, Pehlic M, Faletra F, Porteous D, Pistis G, Widen E, Salomaa V, Koskinen S, Fischer K, Lehtimaki T, Heath A, McCarthy MI, Rivadeneira F, Montgomery GW, Tiemeier H, Hartikainen AL, Madden PA, d'Adamo P, Hastie ND, Gyllensten U, Wright AF, van Duijn CM, Dunlop M, Rudan I, Gasparini P, Pramstaller PP, Deary IJ, Toniolo D, Eriksson JG, Jula A, Raitakari OT, Metspalu A, Perola M, Jarvelin MR, Uitterlinden A, Visscher PM, Wilson JF, on behalf of the ROHgen Consortium: Evidence of Inbreeding Depression on Human Height. PLoS Genetics 8(7):e1002655, 2012 [PDF unavailable] [PubMed] [More...]
 Vinkhuyzen AA, Pedersen NL, Yang J, Lee SH, Magnusson PK, Iacono WG, McGue M, Madden PA, Heath AC, Luciano M, Payton A, Horan M, Ollier W, Pendleton N, Deary IJ, Montgomery GW, Martin NG, Visscher PM, Wray NR: Common SNPs explain some of the variation in the personality dimensions of neuroticism and extraversion. Translational Psychiatry 2:e102, 2012 [PDF unavailable] [PubMed] [More...]
 Yang J, Loos RJ, Powell JE, Medland SE, Speliotes EK, Chasman DI, Rose LM, Thorleifsson G, Steinthorsdottir V, Magi R, Waite L, Vernon Smith A, Yerges-Armstrong LM, Monda KL, Hadley D, Mahajan A, Li G, Kapur K, Vitart V, Huffman JE, Wang SR, Palmer C, Esko T, Fischer K, Hua Zhao J, Demirkan A, Isaacs A, Feitosa MF, Luan J, Heard-Costa NL, White C, Jackson AU, Preuss M, Ziegler A, Eriksson J, Kutalik Z, Frau F, Nolte IM, van Vliet-Ostaptchouk JV, Hottenga JJ, Jacobs KB, Verweij N, Goel A, Medina-Gomez C, Estrada K, Lynn Bragg-Gresham J, Sanna S, Sidore C, Tyrer J, Teumer A, Prokopenko I, Mangino M, Lindgren CM, Assimes TL, Shuldiner AR, Hui J, Beilby JP, McArdle WL, Hall P, Haritunians T, Zgaga L, Kolcic I, Polasek O, Zemunik T, Oostra BA, Juhani Junttila M, Gronberg H, Schreiber S, Peters A, Hicks AA, Stephens J, Foad NS, Laitinen J, Pouta A, Kaakinen M, Willemsen G, Vink JM, Wild SH, Navis G, Asselbergs FW, Homuth G, John U, Iribarren C, Harris T, Launer L, Gudnason V, O'Connell JR, Boerwinkle E, Cadby G, Palmer LJ, James AL, Musk AW, Ingelsson E, Psaty BM, Beckmann JS, Waeber G, Vollenweider P, Hayward C, Wright AF, Rudan I, Groop LC, Metspalu A, Tee Khaw K, van Duijn CM, Borecki IB, Province MA, Wareham NJ, Tardif JC, Huikuri HV, Adrienne Cupples L, Atwood LD, Fox CS, Boehnke M, Collins FS, Mohlke KL, Erdmann J, Schunkert H, Hengstenberg C, Stark K, Lorentzon M, Ohlsson C, Cusi D, Staessen JA, Van der Klauw MM, Pramstaller PP, Kathiresan S, Jolley JD, Ripatti S, Jarvelin MR, de Geus EJ, Boomsma DI, Penninx B, Wilson JF, Campbell H, Chanock SJ, van der Harst P, Hamsten A, Watkins H, Hofman A, Witteman JC, Carola Zillikens M, Uitterlinden AG, Rivadeneira F, Carola Zillikens M, Kiemeney LA, Vermeulen SH, Abecasis GR, Schlessinger D, Schipf S, Stumvoll M, Tonjes A, Spector TD, North KE, Lettre G, McCarthy MI, Berndt SI, Heath AC, Madden PA, Nyholt DR, Montgomery GW, Martin NG, McKnight B, Strachan DP, Hill WG, Snieder H, Ridker PM, Thorsteinsdottir U, Stefansson K, Frayling TM, Hirschhorn JN, Goddard ME, Visscher PM: FTO genotype is associated with phenotypic variability of body mass index. Nature 490:267-272, 2012 [PDF unavailable] [PubMed] [More...]
 Surakka I, Whitfield JB, Perola M, Visscher PM, Montgomery GW, Falchi M, Willemsen G, de Geus EJ, Magnusson PK, Christensen K, Sorensen TI, Pietilainen KH, Rantanen T, Silander K, Widen E, Muilu J, Rahman I, Liljedahl U, Syvanen AC, Palotie A, Kaprio J, Kyvik KO, Pedersen NL, Boomsma DI, Spector T, Martin NG, Ripatti S, Peltonen L: A Genome-Wide Association Study of Monozygotic Twin-Pairs Suggests a Locus Related to Variability of Serum High-Density Lipoprotein Cholesterol. Twin Research and Human Genetics 15(6):691-699, 2012 [PDF unavailable] [N/OSI] [PubMed] [More...]
 Verweij KJ, Yang J, Lahti J, Veijola J, Hintsanen M, Pulkki-Raback L, Heinonen K, Pouta A, Pesonen AK, Widen E, Taanila A, Isohanni M, Miettunen J, Palotie A, Penke L, Service SK, Heath AC, Montgomery GW, Raitakari O, Kahonen M, Viikari J, Raikkonen K, Eriksson JG, Keltikangas-Jarvinen L, Lehtimaki T, Martin NG, Jarvelin MR, Visscher PM, Keller MC, Zietsch BP: MAINTENANCE OF GENETIC VARIATION IN HUMAN PERSONALITY: TESTING EVOLUTIONARY MODELS BY ESTIMATING HERITABILITY DUE TO COMMON CAUSAL VARIANTS AND INVESTIGATING THE EFFECT OF DISTANT INBREEDING. Evolution 66(10):3238-3251, 2012 [PDF unavailable] [PubMed] [More...]
 Witte JS, Visscher PM: Reclassify controls at your own risk. Epidemiology (Cambridge, Mass.) 23(6):910-911, 2012 [PDF unavailable] [PubMed] [More...]
 Kemper KE, Daetwyler HD, Visscher PM, Goddard ME: Comparing linkage and association analyses in sheep points to a better way of doing GWAS. Genetics research 94(4):191-203, 2012 [PDF unavailable] [PubMed] [More...]
 van der Harst P, Zhang W, Mateo Leach I, Rendon A, Verweij N, Sehmi J, Paul DS, Elling U, Allayee H, Li X, Radhakrishnan A, Tan ST, Voss K, Weichenberger CX, Albers CA, Al-Hussani A, Asselbergs FW, Ciullo M, Danjou F, Dina C, Esko T, Evans DM, Franke L, Gogele M, Hartiala J, Hersch M, Holm H, Hottenga JJ, Kanoni S, Kleber ME, Lagou V, Langenberg C, Lopez LM, Lyytikainen LP, Melander O, Murgia F, Nolte IM, O'Reilly PF, Padmanabhan S, Parsa A, Pirastu N, Porcu E, Portas L, Prokopenko I, Ried JS, Shin SY, Tang CS, Teumer A, Traglia M, Ulivi S, Westra HJ, Yang J, Hua Zhao J, Anni F, Abdellaoui A, Attwood A, Balkau B, Bandinelli S, Bastardot F, Benyamin B, Boehm BO, Cookson WO, Das D, de Bakker PI, de Boer RA, de Geus EJ, de Moor MH, Dimitriou M, Domingues FS, Doring A, Engstrom G, Ingi Eyjolfsson G, Ferrucci L, Fischer K, Galanello R, Garner SF, Genser B, Gibson QD, Girotto G, Fannar Gudbjartsson D, Harris SE, Hartikainen AL, Hastie CE, Hedblad B, Illig T, Jolley J, Kahonen M, Kema IP, Kemp JP, Liang L, Lloyd-Jones H, Loos RJ, Meacham S, Medland SE, Meisinger C, Memari Y, Mihailov E, Miller K, Moffatt MF, Nauck M, Novatchkova M, Nutile T, Olafsson I, Onundarson PT, Parracciani D, Penninx BW, Perseu L, Piga A, Pistis G, Pouta A, Puc U, Raitakari O, Ring SM, Robino A, Ruggiero D, Ruokonen A, Saint-Pierre A, Sala C, Salumets A, Sambrook J, Schepers H, Oliver Schmidt C, Sillje HH, Sladek R, Smit JH, Starr JM, Stephens J, Sulem P, Tanaka T, Thorsteinsdottir U, Tragante V, van Gilst WH, Joost van Pelt L, van Veldhuisen DJ, Volker U, Whitfield JB, Willemsen G, Winkelmann BR, Wirnsberger G, Algra A, Cucca F, d'Adamo AP, Danesh J, Deary IJ, Dominiczak AF, Elliott P, Fortina P, Froguel P, Gasparini P, Greinacher A, Hazen SL, Jarvelin MR, Tee Khaw K, Lehtimaki T, Maerz W, Martin NG, Metspalu A, Mitchell BD, Montgomery GW, Moore C, Navis G, Pirastu M, Pramstaller PP, Ramirez-Solis R, Schadt E, Scott J, Shuldiner AR, Davey Smith G, Gustav Smith J, Snieder H, Sorice R, Spector TD, Stefansson K, Stumvoll M, Wilson Tang WH, Toniolo D, Tonjes A, Visscher PM, Vollenweider P, Wareham NJ, Wolffenbuttel BH, Boomsma DI, Beckmann JS, Dedoussis GV, Deloukas P, Ferreira MA, Sanna S, Uda M, Hicks AA, Martin Penninger J, Gieger C, Kooner JS, Ouwehand WH, Soranzo N, Chambers JC: Seventy-five genetic loci influencing the human red blood cell. Nature 492(7429):369-375, 2012 [PDF unavailable] [PubMed] [More...]
2011
 Davidson SI, Liu Y, Danoy PA, Wu X, Thomas GP, Jiang L, Sun L, Wang N, Han J, Han H, Australo-Anglo-American Spondyloarthritis Consortium, Visscher PM, Brown MA, Xu H: Association of STAT3 and TNFRSF1A with ankylosing spondylitis in Han Chinese. Annals of the Rheumatic Diseases 70:289-292, 2011 [PDF unavailable] [PubMed] [More...]
 Painter JN, Anderson CA, Nyholt DR, Macgregor S, Lin J, Lee SH, Lambert A, Zhao ZZ, Roseman F, Guo Q, Gordon SD, Wallace L, Henders AK, Visscher PM, Kraft P, Martin NG, Morris AP, Treloar SA, Kennedy SH, Missmer SA, Montgomery GW, Zondervan KT: Genome-wide association study identifies a locus at 7p15.2 associated with endometriosis. Nature Genetics 43(1):51-54, 2011 [PDF unavailable] [PubMed] [More...]
 Ferreira MA, McRae AF, Medland SE, Nyholt DR, Gordon SD, Wright MJ, Henders AK, Madden PA, Visscher PM, Wray NR, Heath AC, Montgomery GW, Duffy DL, Martin NG: Association between ORMDL3, IL1RL1 and a deletion on chromosome 17q21 with asthma risk in Australia. European Journal of Human Genetics 19:458-464, 2011 [PDF unavailable] [PubMed] [More...]
 Yang J, Lee SH, Goddard ME, Visscher PM: GCTA: A Tool for Genome-wide Complex Trait Analysis. American Journal of Human Genetics 88(1):76-82, 2011 [PDF unavailable] [PubMed] [More...]
 Wray NR, Purcell SM, Visscher PM: Synthetic Associations Created by Rare Variants Do Not Explain Most GWAS Results. PLoS biology 9(1):e1000579, 2011 [PDF unavailable] [PubMed] [More...]
 Webbink D, Martin NG, Visscher PM: Does teenage childbearing reduce investment in human capital? . Journal of Population Economics 24:701-730, 2011 [PDF unavailable]
 Richards AL, Jones L, Moskvina V, Kirov G, Gejman PV, Levinson DF, Sanders AR, Molecular Genetics of Schizophrenia Collaboration (MGS), International Schizophrenia Consortium (ISC), Purcell S, Visscher PM, Craddock N, Owen MJ, Holmans P, O'Donovan MC: Schizophrenia susceptibility alleles are enriched for alleles that affect gene expression in adult human brain. Molecular Psychiatry 2011 [PDF unavailable] [PubMed] [More...]
 Lee SH, Wray NR, Goddard ME, Visscher PM: Estimating Missing Heritability for Disease from Genome-wide Association Studies. American Journal of Human Genetics 88(3):294-305, 2011 [PDF unavailable] [PubMed] [More...]
 Yang J, Weedon MN, Purcell S, Lettre G, Estrada K, Willer CJ, Smith AV, Ingelsson E, O'Connell JR, Mangino M, Magi R, Madden PA, Heath AC, Nyholt DR, Martin NG, Montgomery GW, Frayling TM, Hirschhorn JN, McCarthy MI, Goddard ME, Visscher PM, GIANT Consortium: Genomic inflation factors under polygenic inheritance. European Journal of Human Genetics 19:807-812, 2011 [PDF unavailable] [PubMed] [More...]
 Demirkan A, Amin N, Isaacs A, Jarvelin MR, Whitfield JB, Wichmann HE, Kyvik KO, Rudan I, Gieger C, Hicks AA, Johansson A, Hottenga JJ, Smith JJ, Wild SH, Pedersen NL, Willemsen G, Mangino M, Hayward C, Uitterlinden AG, Hofman A, Witteman J, Montgomery GW, Pietilainen KH, Rantanen T, Kaprio J, Doring A, Pramstaller PP, Gyllensten U, de Geus EJ, Penninx BW, Wilson JF, Rivadeneria F, Magnusson PK, Boomsma DI, Spector T, Campbell H, Hoehne B, Martin NG, Oostra BA, McCarthy M, Peltonen-Palotie L, Aulchenko Y, Visscher PM, Ripatti S, Janssens AC, van Duijn CM, ENGAGE Consortium: Genetic architecture of circulating lipid levels. European Journal of Human Genetics 19:813-819, 2011 [PDF unavailable] [PubMed] [More...]
 Visscher PM, Goddard ME: Cattle gain stature. Nature Genetics 43(5):397-398, 2011 [PDF unavailable] [PubMed] [More...]
 Smith NL, Huffman JE, Strachan DP, Huang J, Dehghan A, Trompet S, Lopez LM, Shin SY, Baumert J, Vitart V, Bis JC, Wild SH, Rumley A, Yang Q, Uitterlinden AG, Stott DJ, Davies G, Carter AM, Thorand B, Polasek O, McKnight B, Campbell H, Rudnicka AR, Chen MH, Buckley BM, Harris SE, Peters A, Pulanic D, Lumley T, de Craen AJ, Liewald DC, Gieger C, Campbell S, Ford I, Gow AJ, Luciano M, Porteous DJ, Guo X, Sattar N, Tenesa A, Cushman M, Slagboom PE, Visscher PM, Spector TD, Illig T, Rudan I, Bovill EG, Wright AF, McArdle WL, Tofler G, Hofman A, Westendorp RG, Starr JM, Grant PJ, Karakas M, Hastie ND, Psaty BM, Wilson JF, Lowe GD, O'Donnell CJ, Witteman JC, Jukema JW, Deary IJ, Soranzo N, Koenig W, Hayward C: Genetic predictors of fibrin d-dimer levels in healthy adults. Circulation 123(17):1864-1872, 2011 [PDF unavailable] [PubMed] [More...]
 McEvoy BP, Powell JE, Goddard ME, Visscher PM: Human population dispersal "Out of Africa" estimated from linkage disequilibrium and allele frequencies of SNPs. Genome Research 21:821-829, 2011 [PDF unavailable] [PubMed] [More...]
 Maugeri N, Powell JE, 't Hoen PA, de Geus EJ, Willemsen G, Kattenberg M, Henders AK, Wallace L, Penninx B, Hottenga JJ, Medland SE, Saviouk V, Martin NG, Visscher PM, van Ommen GJ, Frazer IH, Boomsma DI, Montgomery GW, Ferreira MA: LPAR1 and ITGA4 regulate peripheral blood monocyte counts. Human Mutation 32:873-876, 2011 [PDF unavailable] [PubMed] [More...]
 Frank RA, McRae AF, Pocklington AJ, van de Lagemaat LN, Navarro P, Croning MD, Komiyama NH, Bradley SJ, Challiss RA, Armstrong JD, Finn RD, Malloy MP, MacLean AW, Harris SE, Starr JM, Bhaskar SS, Howard EK, Hunt SE, Coffey AJ, Ranganath V, Deloukas P, Rogers J, Muir WJ, Deary IJ, Blackwood DH, Visscher PM, Grant SG: Clustered coding variants in the glutamate receptor complexes of individuals with schizophrenia and bipolar disorder. PLoS ONE 6(4):e19011, 2011 [PDF unavailable] [PubMed] [More...]
 Yang J, Manolio TA, Pasquale LR, Boerwinkle E, Caporaso N, Cunningham JM, de Andrade M, Feenstra B, Feingold E, Hayes MG, Hill WG, Landi MT, Alonso A, Lettre G, Lin P, Ling H, Lowe W, Mathias RA, Melbye M, Pugh E, Cornelis MC, Weir BS, Goddard ME, Visscher PM: Genome partitioning of genetic variation for complex traits using common SNPs. Nature Genetics 43(6):519-525, 2011 [PDF unavailable] [PubMed] [More...]
 Keller MC, Visscher PM, Goddard ME: Quantification of inbreeding due to distant ancestors and its detection using dense single nucleotide polymorphism data. Genetics 189:237-249, 2011 [PDF unavailable] [PubMed] [More...]
 Visscher PM, Goddard ME, Derks EM, Wray NR: Evidence-based psychiatric genetics, AKA the false dichotomy between common and rare variant hypotheses. Molecular Psychiatry 2011 [PDF unavailable] [PubMed] [More...]
 Danoy P, Wei M, Johanna H, Jiang L, He D, Sun L, Zeng X, Visscher PM, Brown MA, Xu H: Association of variants in MMEL1 and CTLA4 with rheumatoid arthritis in the Han Chinese population. Annals of the Rheumatic Diseases 70:1793-1797, 2011 [PDF unavailable] [PubMed] [More...]
 Goddard ME, Lee SH, Yang J, Wray NR, Visscher PM: Response to browning and browning. American Journal of Human Genetics 89(1):193-195, 2011 [PDF unavailable] [PubMed] [More...]
 Benyamin B, Middelberg RPS, Lind PA, Valle AM, Gordon S, Nyholt DR, Medland SE, Henders AK, Heath AC, Madden PA, Visscher PM, O'Connor DT, Montgomery GW, Martin NG, Whitfield JB: GWAS of butyrylcholinesterase activity identifies four novel loci, independent effects within BCHE and secondary associations with metabolic risk factors. Human Molecular Genetics 20:4504-4514, 2011 [PDF unavailable] [PubMed] [More...]
 Davies G, Tenesa A, Payton A, Yang J, Harris SE, Liewald D, Ke X, Le Hellard S, Christoforou A, Luciano M, McGhee K, Lopez L, Gow AJ, Corley J, Redmond P, Fox HC, Haggarty P, Whalley LJ, McNeill G, Goddard ME, Espeseth T, Lundervold AJ, Reinvang I, Pickles A, Steen VM, Ollier W, Porteous DJ, Horan M, Starr JM, Pendleton N, Visscher PM, Deary IJ: Genome-wide association studies establish that human intelligence is highly heritable and polygenic. Molecular Psychiatry 16(10):996-1005, 2011 [PDF unavailable] [PubMed] [More...]
 Lips ES, Cornelisse LN, Toonen RF, Min JL, Hultman CM, the International Schizophrenia Consortium, Holmans PA, O'Donovan MC, Purcell SM, Smit AB, Verhage M, Sullivan PF, Visscher PM, Posthuma D: Functional gene group analysis identifies synaptic gene groups as risk factor for schizophrenia. Molecular Psychiatry 2011 [PDF unavailable] [PubMed] [More...]
 The Schizophrenia Psychiatric Genome-Wide Association Study (GWAS) Consortium, Ripke S, Sanders AR, Kendler KS, Levinson DF, Sklar P, Holmans PA, Lin DY, Duan J, Ophoff RA, Andreassen OA, Scolnick E, Cichon S, St Clair D, Corvin A, Gurling H, Werge T, Rujescu D, Blackwood DH, Pato CN, Malhotra AK, Purcell S, Dudbridge F, Neale BM, Rossin L, Visscher PM, Posthuma D, Ruderfer DM, Fanous A, Stefansson H, Steinberg S, Mowry BJ, Golimbet V, De Hert M, Jonsson EG, Bitter I, Pietilainen OP, Collier DA, Tosato S, Agartz I, Albus M, Alexander M, Amdur RL, Amin F, Bass N, Bergen SE, Black DW, Borglum AD, Brown MA, Bruggeman R, Buccola NG, Byerley WF, Cahn W, Cantor RM, Carr VJ, Catts SV, Choudhury K, Cloninger CR, Cormican P, Craddock N, Danoy PA, Datta S, de Haan L, Demontis D, Dikeos D, Djurovic S, Donnelly P, Donohoe G, Duong L, Dwyer S, Fink-Jensen A, Freedman R, Freimer NB, Friedl M, Georgieva L, Giegling I, Gill M, Glenthoj B, Godard S, Hamshere M, Hansen M, Hansen T, Hartmann AM, Henskens FA, Hougaard DM, Hultman CM, Ingason A, Jablensky AV, Jakobsen KD, Jay M, Jurgens G, Kahn RS, Keller MC, Kenis G, Kenny E, Kim Y, Kirov GK, Konnerth H, Konte B, Krabbendam L, Krasucki R, Lasseter VK, Laurent C, Lawrence J, Lencz T, Lerer FB, Liang KY, Lichtenstein P, Lieberman JA, Linszen DH, Lonnqvist J, Loughland CM, MacLean AW, Maher BS, Maier W, Mallet J, Malloy P, Mattheisen M, Mattingsdal M, McGhee KA, McGrath JJ, McIntosh A, McLean DE, McQuillin A, Melle I, Michie PT, Milanova V, Morris DW, Mors O, Mortensen PB, Moskvina V, Muglia P, Myin-Germeys I, Nertney DA, Nestadt G, Nielsen J, Nikolov I, Nordentoft M, Norton N, Nothen MM, O'Dushlaine CT, Olincy A, Olsen L, O'Neill FA, Orntoft TF, Owen MJ, Pantelis C, Papadimitriou G, Pato MT, Peltonen L, Petursson H, Pickard B, Pimm J, Pulver AE, Puri V, Quested D, Quinn EM, Rasmussen HB, Rethelyi JM, Ribble R, Rietschel M, Riley BP, Ruggeri M, Schall U, Schulze TG, Schwab SG, Scott RJ, Shi J, Sigurdsson E, Silverman JM, Spencer CC, Stefansson K, Strange A, Strengman E, Stroup TS, Suvisaari J, Terenius L, Thirumalai S, Thygesen JH, Timm S, Toncheva D, van den Oord E, van Os J, van Winkel R, Veldink J, Walsh D, Wang AG, Wiersma D, Wildenauer DB, Williams HJ, Williams NM, Wormley B, Zammit S, Sullivan PF, O'Donovan MC, Daly MJ, Gejman PV: Genome-wide association study identifies five new schizophrenia loci. Nature Genetics 43:969-976, 2011 [PDF unavailable] [PubMed] [More...]
 Ferreira MA, Matheson MC, Duffy DL, Marks GB, Hui J, Le Souef P, Danoy P, Baltic S, Nyholt DR, Jenkins M, Hayden C, Willemsen G, Ang W, Kuokkanen M, Beilby J, Cheah F, de Geus EJ, Ramasamy A, Vedantam S, Salomaa V, Madden PA, Heath AC, Hopper JL, Visscher PM, Musk B, Leeder SR, Jarvelin MR, Pennell C, Boomsma DI, Hirschhorn JN, Walters H, Martin NG, James A, Jones G, Abramson MJ, Robertson CF, Dharmage SC, Brown MA, Montgomery GW, Thompson PJ, Australian Asthma Genetics Consortium: Identification of IL6R and chromosome 11q13.5 as risk loci for asthma. Lancet 378(9795):1006-1014, 2011 [PDF unavailable] [PubMed] [More...]
 Heid IM, Jackson AU, Randall JC, Winkler TW, Qi L, Steinthorsdottir V, Thorleifsson G, Zillikens MC, Speliotes EK, Magi R, Workalemahu T, White CC, Bouatia-Naji N, Harris TB, Berndt SI, Ingelsson E, Willer CJ, Weedon MN, Luan J, Vedantam S, Esko T, Kilpelainen TO, Kutalik Z, Li S, Monda KL, Dixon AL, Holmes CC, Kaplan LM, Liang L, Min JL, Moffatt MF, Molony C, Nicholson G, Schadt EE, Zondervan KT, Feitosa MF, Ferreira T, Allen HL, Weyant RJ, Wheeler E, Wood AR, Estrada K, Goddard ME, Lettre G, Mangino M, Nyholt DR, Purcell S, Vernon Smith A, Visscher PM, Yang J, McCarroll SA, Nemesh J, Voight BF, Absher D, Amin N, Aspelund T, Coin L, Glazer NL, Hayward C, Heard-Costa NL, Hottenga JJ, Johansson A, Johnson T, Kaakinen M, Kapur K, Ketkar S, Knowles JW, Kraft P, Kraja AT, Lamina C, Leitzmann MF, McKnight B, Morris AP, Ong KK, Perry JR, Peters MJ, Polasek O, Prokopenko I, Rayner NW, Ripatti S, Rivadeneira F, Robertson NR, Sanna S, Sovio U, Surakka I, Teumer A, van Wingerden S, Vitart V, Zhao JH, Cavalcanti-Proenca C, Chines PS, Fisher E, Kulzer JR, Lecoeur C, Narisu N, Sandholt C, Scott LJ, Silander K, Stark K, Tammesoo ML, Teslovich TM, Timpson NJ, Watanabe RM, Welch R, Chasman DI, Cooper MN, Jansson JO, Kettunen J, Lawrence RW, Pellikka N, Perola M, Vandenput L, Alavere H, Almgren P, Atwood LD, Bennett AJ, Biffar R, Bonnycastle LL, Bornstein SR, Buchanan TA, Campbell H, Day IN, Dei M, Dorr M, Elliott P, Erdos MR, Eriksson JG, Freimer NB, Fu M, Gaget S, Geus EJ, Gjesing AP, Grallert H, Grassler J, Groves CJ, Guiducci C, Hartikainen AL, Hassanali N, Havulinna AS, Herzig KH, Hicks AA, Hui J, Igl W, Jousilahti P, Jula A, Kajantie E, Kinnunen L, Kolcic I, Koskinen S, Kovacs P, Kroemer HK, Krzelj V, Kuusisto J, Kvaloy K, Laitinen J, Lantieri O, Lathrop GM, Lokki ML, Luben RN, Ludwig B, McArdle WL, McCarthy A, Morken MA, Nelis M, Neville MJ, Pare G, Parker AN, Peden JF, Pichler I, Pietilainen KH, Platou CG, Pouta A, Ridderstrale M, Samani NJ, Saramies J, Sinisalo J, Smit JH, Strawbridge RJ, Stringham HM, Swift AJ, Teder-Laving M, Thomson B, Usala G, van Meurs JB, van Ommen GJ, Vatin V, Volpato CB, Wallaschofski H, Walters GB, Widen E, Wild SH, Willemsen G, Witte DR, Zgaga L, Zitting P, Beilby JP, James AL, Kahonen M, Lehtimaki T, Nieminen MS, Ohlsson C, Palmer LJ, Raitakari O, Ridker PM, Stumvoll M, Tonjes A, Viikari J, Balkau B, Ben-Shlomo Y, Bergman RN, Boeing H, Smith GD, Ebrahim S, Froguel P, Hansen T, Hengstenberg C, Hveem K, Isomaa B, Jorgensen T, Karpe F, Khaw KT, Laakso M, Lawlor DA, Marre M, Meitinger T, Metspalu A, Midthjell K, Pedersen O, Salomaa V, Schwarz PE, Tuomi T, Tuomilehto J, Valle TT, Wareham NJ, Arnold AM, Beckmann JS, Bergmann S, Boerwinkle E, Boomsma DI, Caulfield MJ, Collins FS, Eiriksdottir G, Gudnason V, Gyllensten U, Hamsten A, Hattersley AT, Hofman A, Hu FB, Illig T, Iribarren C, Jarvelin MR, Kao WH, Kaprio J, Launer LJ, Munroe PB, Oostra B, Penninx BW, Pramstaller PP, Psaty BM, Quertermous T, Rissanen A, Rudan I, Shuldiner AR, Soranzo N, Spector TD, Syvanen AC, Uda M, Uitterlinden A, Volzke H, Vollenweider P, Wilson JF, Witteman JC, Wright AF, Abecasis GR, Boehnke M, Borecki IB, Deloukas P, Frayling TM, Groop LC, Haritunians T, Hunter DJ, Kaplan RC, North KE, O'Connell JR, Peltonen L, Schlessinger D, Strachan DP, Hirschhorn JN, Assimes TL, Wichmann HE, Thorsteinsdottir U, van Duijn CM, Stefansson K, Cupples LA, Loos RJ, Barroso I, McCarthy MI, Fox CS, Mohlke KL, Lindgren CM: Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. Nature Genetics 43(11):1164-1164, 2011 [PDF unavailable] [PubMed] [More...]
 Gieger C, Radhakrishnan A, Cvejic A, Tang W, Porcu E, Pistis G, Serbanovic-Canic J, Elling U, Goodall AH, Labrune Y, Lopez LM, Magi R, Meacham S, Okada Y, Pirastu N, Sorice R, Teumer A, Voss K, Zhang W, Ramirez-Solis R, Bis JC, Ellinghaus D, Gogele M, Hottenga JJ, Langenberg C, Kovacs P, O'Reilly PF, Shin SY, Esko T, Hartiala J, Kanoni S, Murgia F, Parsa A, Stephens J, van der Harst P, Ellen van der Schoot C, Allayee H, Attwood A, Balkau B, Bastardot F, Basu S, Baumeister SE, Biino G, Bomba L, Bonnefond A, Cambien F, Chambers JC, Cucca F, d'Adamo P, Davies G, de Boer RA, de Geus EJ, Doring A, Elliott P, Erdmann J, Evans DM, Falchi M, Feng W, Folsom AR, Frazer IH, Gibson QD, Glazer NL, Hammond C, Hartikainen AL, Heckbert SR, Hengstenberg C, Hersch M, Illig T, Loos RJ, Jolley J, Tee Khaw K, Kuhnel B, Kyrtsonis MC, Lagou V, Lloyd-Jones H, Lumley T, Mangino M, Maschio A, Mateo Leach I, McKnight B, Memari Y, Mitchell BD, Montgomery GW, Nakamura Y, Nauck M, Navis G, Nothlings U, Nolte IM, Porteous DJ, Pouta A, Pramstaller PP, Pullat J, Ring SM, Rotter JI, Ruggiero D, Ruokonen A, Sala C, Samani NJ, Sambrook J, Schlessinger D, Schreiber S, Schunkert H, Scott J, Smith NL, Snieder H, Starr JM, Stumvoll M, Takahashi A, Tang WH, Taylor K, Tenesa A, Lay Thein S, Tonjes A, Uda M, Ulivi S, van Veldhuisen DJ, Visscher PM, Volker U, Wichmann HE, Wiggins KL, Willemsen G, Yang TP, Hua Zhao J, Zitting P, Bradley JR, Dedoussis GV, Gasparini P, Hazen SL, Metspalu A, Pirastu M, Shuldiner AR, Joost van Pelt L, Zwaginga JJ, Boomsma DI, Deary IJ, Franke A, Froguel P, Ganesh SK, Jarvelin MR, Martin NG, Meisinger C, Psaty BM, Spector TD, Wareham NJ, Akkerman JW, Ciullo M, Deloukas P, Greinacher A, Jupe S, Kamatani N, Khadake J, Kooner JS, Penninger J, Prokopenko I, Stemple D, Toniolo D, Wernisch L, Sanna S, Hicks AA, Rendon A, Ferreira MA, Ouwehand WH, Soranzo N: New gene functions in megakaryopoiesis and platelet formation. Nature 480(7376):201-208, 2011 [PDF unavailable] [PubMed] [More...]
2010
 Macgregor S, Bellis C, Lea RA, Cox H, Dyer T, Blangero J, Visscher PM, Griffiths LR: Legacy of mutiny on the Bounty: founder effect and admixture on Norfolk Island. European Journal of Human Genetics 18:67-72, 2010 [PDF unavailable] [PubMed] [More...]
 Yang J, Visscher PM, Wray NR: Sporadic cases are the norm for complex disease. European Journal of Human Genetics 18:1039-1043, 2010 [PDF unavailable] [PubMed] [More...]
 Yang J, Wray NR, Visscher PM: Comparing apples and oranges: equating the power of case-control and quantitative trait association studies. Genetic Epidemiology 34(3):254-257, 2010 [PDF unavailable] [PubMed] [More...]
 Idaghdour Y, Czika W, Shianna KV, Lee SH, Visscher PM, Martin HC, Miclaus K, Jadallah SJ, Goldstein DB, Wolfinger RD, Gibson G: Geographical genomics of human leukocyte gene expression variation in southern Morocco. Nature Genetics 42(1):62-67, 2010 [PDF unavailable] [PubMed] [More...]
 Wray NR, Visscher PM: Narrowing the boundaries of the genetic architecture of schizophrenia. Schizophrenia bulletin 36(1):14-23, 2010 [PDF unavailable] [PubMed] [More...]
 McEvoy BP, Zhao ZZ, Macgregor S, Bellis C, Lea RA, Cox H, Montgomery GW, Griffiths LR, Visscher PM: European and Polynesian admixture in the Norfolk Island population. Heredity 105:229-234, 2010 [PDF unavailable] [PubMed] [More...]
 Webbink D, Martin NG, Visscher PM: Does education reduce the probability of being overweight? Journal of Health Economics 29:29-38, 2010 [PDF unavailable] [PubMed] [More...]
 Wray NR, Yang J, Goddard ME, Visscher PM: The genetic interpretation of area under the ROC curve in genomic profiling. PLoS Genetics 6(2):e1000864, 2010 [PDF unavailable] [PubMed] [More...]
 Houlihan LM, Davies G, Tenesa A, Harris SE, Luciano M, Gow AJ, McGhee KA, Liewald DC, Porteous DJ, Starr JM, Lowe GD, Visscher PM, Deary IJ: Common Variants of Large Effect in F12, KNG1, and HRG Are Associated with Activated Partial Thromboplastin Time. American Journal of Human Genetics 86:626-631, 2010 [PDF unavailable] [PubMed] [More...]
 Visscher PM, Posthuma D: Statistical Power to Detect Genetic Loci Affecting Environmental Sensitivity. Behavior Genetics 40:728-733, 2010 [PDF unavailable] [PubMed] [More...]
 Gratten J, Wilson AJ, McRae AF, Beraldi D, Visscher PM, Pemberton JM, Slate J: No evidence for warming climate theory of coat colour change in Soay sheep: a comment on Maloney et al. Biology Letters 6:678-679, 2010 [PDF unavailable] [PubMed] [More...]
 Yang J, Benyamin B, McEvoy BP, Gordon S, Henders AK, Nyholt DR, Madden PA, Heath AC, Martin NG, Montgomery GW, Goddard ME, Visscher PM: Common SNPs explain a large proportion of the heritability for human height. Nature Genetics 42(7):565-569, 2010 [PDF unavailable] [PubMed] [More...]
 Lee SH, Goddard ME, Visscher PM, van der Werf JH: Using the realized relationship matrix to disentangle confounding factors for the estimation of genetic variance components of complex traits. Genetics, selection, evolution 42(1):22-22, 2010 [PDF unavailable] [PubMed] [More...]
 Liu JZ, McRae AF, Nyholt DR, Medland SE, Wray NR, Brown KM, AMFS Investigators, Hayward NK, Montgomery GW, Visscher PM, Martin NG, Macgregor S: A versatile gene-based test for genome-wide association studies. American Journal of Human Genetics 87(1):139-145, 2010 [PDF unavailable] [PubMed] [More...]
 McEvoy BP, Lind JM, Wang ET, Moyzis RK, Visscher PM, van Holst Pellekaan SM, Wilton AN: Whole-Genome Genetic Diversity in a Sample of Australians with Deep Aboriginal Ancestry. American Journal of Human Genetics 87(2):297-305, 2010 [PDF unavailable] [PubMed] [More...]
 Powell JE, Visscher PM, Goddard ME: Reconciling the analysis of IBD and IBS in complex trait studies. Nature reviews. Genetics 11:800-805, 2010 [PDF unavailable] [PubMed] [More...]
 Visscher PM, Goddard ME: Systems genetics: the added value of gene expression. HFSP journal 4(1):6-10, 2010 [PDF unavailable] [PubMed] [More...]
 Lango Allen H, Estrada K, Lettre G, Berndt SI, Weedon MN, Rivadeneira F, Willer CJ, Jackson AU, Vedantam S, Raychaudhuri S, Ferreira T, Wood AR, Weyant RJ, Segre AV, Speliotes EK, Wheeler E, Soranzo N, Park JH, Yang J, Gudbjartsson D, Heard-Costa NL, Randall JC, Qi L, Vernon Smith A, Magi R, Pastinen T, Liang L, Heid IM, Luan J, Thorleifsson G, Winkler TW, Goddard ME, Sin Lo K, Palmer C, Workalemahu T, Aulchenko YS, Johansson A, Carola Zillikens M, Feitosa MF, Esko T, Johnson T, Ketkar S, Kraft P, Mangino M, Prokopenko I, Absher D, Albrecht E, Ernst F, Glazer NL, Hayward C, Hottenga JJ, Jacobs KB, Knowles JW, Kutalik Z, Monda KL, Polasek O, Preuss M, Rayner NW, Robertson NR, Steinthorsdottir V, Tyrer JP, Voight BF, Wiklund F, Xu J, Hua Zhao J, Nyholt DR, Pellikka N, Perola M, Perry JR, Surakka I, Tammesoo ML, Altmaier EL, Amin N, Aspelund T, Bhangale T, Boucher G, Chasman DI, Chen C, Coin L, Cooper MN, Dixon AL, Gibson Q, Grundberg E, Hao K, Juhani Junttila M, Kaplan LM, Kettunen J, Konig IR, Kwan T, Lawrence RW, Levinson DF, Lorentzon M, McKnight B, Morris AP, Muller M, Suh Ngwa J, Purcell S, Rafelt S, Salem RM, Salvi E, Sanna S, Shi J, Sovio U, Thompson JR, Turchin MC, Vandenput L, Verlaan DJ, Vitart V, White CC, Ziegler A, Almgren P, Balmforth AJ, Campbell H, Citterio L, De Grandi A, Dominiczak A, Duan J, Elliott P, Elosua R, Eriksson JG, Freimer NB, Geus EJ, Glorioso N, Haiqing S, Hartikainen AL, Havulinna AS, Hicks AA, Hui J, Igl W, Illig T, Jula A, Kajantie E, Kilpelainen TO, Koiranen M, Kolcic I, Koskinen S, Kovacs P, Laitinen J, Liu J, Lokki ML, Marusic A, Maschio A, Meitinger T, Mulas A, Pare G, Parker AN, Peden JF, Petersmann A, Pichler I, Pietilainen KH, Pouta A, Ridderstrale M, Rotter JI, Sambrook JG, Sanders AR, Oliver Schmidt C, Sinisalo J, Smit JH, Stringham HM, Bragi Walters G, Widen E, Wild SH, Willemsen G, Zagato L, Zgaga L, Zitting P, Alavere H, Farrall M, McArdle WL, Nelis M, Peters MJ, Ripatti S, van Meurs JB, Aben KK, Ardlie KG, Beckmann JS, Beilby JP, Bergman RN, Bergmann S, Collins FS, Cusi D, den Heijer M, Eiriksdottir G, Gejman PV, Hall AS, Hamsten A, Huikuri HV, Iribarren C, Kahonen M, Kaprio J, Kathiresan S, Kiemeney L, Kocher T, Launer LJ, Lehtimaki T, Melander O, Mosley TH Jr, Musk AW, Nieminen MS, O'Donnell CJ, Ohlsson C, Oostra B, Palmer LJ, Raitakari O, Ridker PM, Rioux JD, Rissanen A, Rivolta C, Schunkert H, Shuldiner AR, Siscovick DS, Stumvoll M, Tonjes A, Tuomilehto J, van Ommen GJ, Viikari J, Heath AC, Martin NG, Montgomery GW, Province MA, Kayser M, Arnold AM, Atwood LD, Boerwinkle E, Chanock SJ, Deloukas P, Gieger C, Gronberg H, Hall P, Hattersley AT, Hengstenberg C, Hoffman W, Mark Lathrop G, Salomaa V, Schreiber S, Uda M, Waterworth D, Wright AF, Assimes TL, Barroso I, Hofman A, Mohlke KL, Boomsma DI, Caulfield MJ, Adrienne Cupples L, Erdmann J, Fox CS, Gudnason V, Gyllensten U, Harris TB, Hayes RB, Jarvelin MR, Mooser V, Munroe PB, Ouwehand WH, Penninx BW, Pramstaller PP, Quertermous T, Rudan I, Samani NJ, Spector TD, Volzke H, Watkins H, Wilson JF, Groop LC, Haritunians T, Hu FB, Kaplan RC, Metspalu A, North KE, Schlessinger D, Wareham NJ, Hunter DJ, O'Connell JR, Strachan DP, Wichmann HE, Borecki IB, van Duijn CM, Schadt EE, Thorsteinsdottir U, Peltonen L, Uitterlinden AG, Visscher PM, Chatterjee N, Loos RJ, Boehnke M, McCarthy MI, Ingelsson E, Lindgren CM, Abecasis GR, Stefansson K, Frayling TM, Hirschhorn JN: Hundreds of variants clustered in genomic loci and biological pathways affect human height. Nature 467(7317):832-838, 2010 [PDF unavailable] [PubMed] [More...]
 Heid IM, Jackson AU, Randall JC, Winkler TW, Qi L, Steinthorsdottir V, Thorleifsson G, Zillikens MC, Speliotes EK, Magi R, Workalemahu T, White CC, Bouatia-Naji N, Harris TB, Berndt SI, Ingelsson E, Willer CJ, Weedon MN, Luan J, Vedantam S, Esko T, Kilpelainen TO, Kutalik Z, Li S, Monda KL, Dixon AL, Holmes CC, Kaplan LM, Liang L, Min JL, Moffatt MF, Molony C, Nicholson G, Schadt EE, Zondervan KT, Feitosa MF, Ferreira T, Allen HL, Weyant RJ, Wheeler E, Wood AR, MAGIC, Estrada K, Goddard ME, Lettre G, Mangino M, Nyholt DR, Purcell S, Smith AV, Visscher PM, Yang J, McCarroll SA, Nemesh J, Voight BF, Absher D, Amin N, Aspelund T, Coin L, Glazer NL, Hayward C, Heard-Costa NL, Hottenga JJ, Johansson A, Johnson T, Kaakinen M, Kapur K, Ketkar S, Knowles JW, Kraft P, Kraja AT, Lamina C, Leitzmann MF, McKnight B, Morris AP, Ong KK, Perry JR, Peters MJ, Polasek O, Prokopenko I, Rayner NW, Ripatti S, Rivadeneira F, Robertson NR, Sanna S, Sovio U, Surakka I, Teumer A, van Wingerden S, Vitart V, Zhao JH, Cavalcanti-Proenca C, Chines PS, Fisher E, Kulzer JR, Lecoeur C, Narisu N, Sandholt C, Scott LJ, Silander K, Stark K, Tammesoo ML, Teslovich TM, Timpson NJ, Watanabe RM, Welch R, Chasman DI, Cooper MN, Jansson JO, Kettunen J, Lawrence RW, Pellikka N, Perola M, Vandenput L, Alavere H, Almgren P, Atwood LD, Bennett AJ, Biffar R, Bonnycastle LL, Bornstein SR, Buchanan TA, Campbell H, Day IN, Dei M, Dorr M, Elliott P, Erdos MR, Eriksson JG, Freimer NB, Fu M, Gaget S, Geus EJ, Gjesing AP, Grallert H, Grassler J, Groves CJ, Guiducci C, Hartikainen AL, Hassanali N, Havulinna AS, Herzig KH, Hicks AA, Hui J, Igl W, Jousilahti P, Jula A, Kajantie E, Kinnunen L, Kolcic I, Koskinen S, Kovacs P, Kroemer HK, Krzelj V, Kuusisto J, Kvaloy K, Laitinen J, Lantieri O, Lathrop GM, Lokki ML, Luben RN, Ludwig B, McArdle WL, McCarthy A, Morken MA, Nelis M, Neville MJ, Pare G, Parker AN, Peden JF, Pichler I, Pietilainen KH, Platou CG, Pouta A, Ridderstrale M, Samani NJ, Saramies J, Sinisalo J, Smit JH, Strawbridge RJ, Stringham HM, Swift AJ, Teder-Laving M, Thomson B, Usala G, van Meurs JB, van Ommen GJ, Vatin V, Volpato CB, Wallaschofski H, Walters GB, Widen E, Wild SH, Willemsen G, Witte DR, Zgaga L, Zitting P, Beilby JP, James AL, Kahonen M, Lehtimaki T, Nieminen MS, Ohlsson C, Palmer LJ, Raitakari O, Ridker PM, Stumvoll M, Tonjes A, Viikari J, Balkau B, Ben-Shlomo Y, Bergman RN, Boeing H, Smith GD, Ebrahim S, Froguel P, Hansen T, Hengstenberg C, Hveem K, Isomaa B, Jorgensen T, Karpe F, Khaw KT, Laakso M, Lawlor DA, Marre M, Meitinger T, Metspalu A, Midthjell K, Pedersen O, Salomaa V, Schwarz PE, Tuomi T, Tuomilehto J, Valle TT, Wareham NJ, Arnold AM, Beckmann JS, Bergmann S, Boerwinkle E, Boomsma DI, Caulfield MJ, Collins FS, Eiriksdottir G, Gudnason V, Gyllensten U, Hamsten A, Hattersley AT, Hofman A, Hu FB, Illig T, Iribarren C, Jarvelin MR, Kao WH, Kaprio J, Launer LJ, Munroe PB, Oostra B, Penninx BW, Pramstaller PP, Psaty BM, Quertermous T, Rissanen A, Rudan I, Shuldiner AR, Soranzo N, Spector TD, Syvanen AC, Uda M, Uitterlinden A, Volzke H, Vollenweider P, Wilson JF, Witteman JC, Wright AF, Abecasis GR, Boehnke M, Borecki IB, Deloukas P, Frayling TM, Groop LC, Haritunians T, Hunter DJ, Kaplan RC, North KE, O'Connell JR, Peltonen L, Schlessinger D, Strachan DP, Hirschhorn JN, Assimes TL, Wichmann HE, Thorsteinsdottir U, van Duijn CM, Stefansson K, Cupples LA, Loos RJ, Barroso I, McCarthy MI, Fox CS, Mohlke KL, Lindgren CM: Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. Nature Genetics 42(11):949-960, 2010 [PDF unavailable] [PubMed] [More...]
 Speliotes EK, Willer CJ, Berndt SI, Monda KL, Thorleifsson G, Jackson AU, Allen HL, Lindgren CM, Luan J, Magi R, Randall JC, Vedantam S, Winkler TW, Qi L, Workalemahu T, Heid IM, Steinthorsdottir V, Stringham HM, Weedon MN, Wheeler E, Wood AR, Ferreira T, Weyant RJ, Segre AV, Estrada K, Liang L, Nemesh J, Park JH, Gustafsson S, Kilpelainen TO, Yang J, Bouatia-Naji N, Esko T, Feitosa MF, Kutalik Z, Mangino M, Raychaudhuri S, Scherag A, Smith AV, Welch R, Zhao JH, Aben KK, Absher DM, Amin N, Dixon AL, Fisher E, Glazer NL, Goddard ME, Heard-Costa NL, Hoesel V, Hottenga JJ, Johansson A, Johnson T, Ketkar S, Lamina C, Li S, Moffatt MF, Myers RH, Narisu N, Perry JR, Peters MJ, Preuss M, Ripatti S, Rivadeneira F, Sandholt C, Scott LJ, Timpson NJ, Tyrer JP, van Wingerden S, Watanabe RM, White CC, Wiklund F, Barlassina C, Chasman DI, Cooper MN, Jansson JO, Lawrence RW, Pellikka N, Prokopenko I, Shi J, Thiering E, Alavere H, Alibrandi MT, Almgren P, Arnold AM, Aspelund T, Atwood LD, Balkau B, Balmforth AJ, Bennett AJ, Ben-Shlomo Y, Bergman RN, Bergmann S, Biebermann H, Blakemore AI, Boes T, Bonnycastle LL, Bornstein SR, Brown MJ, Buchanan TA, Busonero F, Campbell H, Cappuccio FP, Cavalcanti-Proenca C, Chen YD, Chen CM, Chines PS, Clarke R, Coin L, Connell J, Day IN, Heijer MD, Duan J, Ebrahim S, Elliott P, Elosua R, Eiriksdottir G, Erdos MR, Eriksson JG, Facheris MF, Felix SB, Fischer-Posovszky P, Folsom AR, Friedrich N, Freimer NB, Fu M, Gaget S, Gejman PV, Geus EJ, Gieger C, Gjesing AP, Goel A, Goyette P, Grallert H, Grassler J, Greenawalt DM, Groves CJ, Gudnason V, Guiducci C, Hartikainen AL, Hassanali N, Hall AS, Havulinna AS, Hayward C, Heath AC, Hengstenberg C, Hicks AA, Hinney A, Hofman A, Homuth G, Hui J, Igl W, Iribarren C, Isomaa B, Jacobs KB, Jarick I, Jewell E, John U, Jorgensen T, Jousilahti P, Jula A, Kaakinen M, Kajantie E, Kaplan LM, Kathiresan S, Kettunen J, Kinnunen L, Knowles JW, Kolcic I, Konig IR, Koskinen S, Kovacs P, Kuusisto J, Kraft P, Kvaloy K, Laitinen J, Lantieri O, Lanzani C, Launer LJ, Lecoeur C, Lehtimaki T, Lettre G, Liu J, Lokki ML, Lorentzon M, Luben RN, Ludwig B, MAGIC, Manunta P, Marek D, Marre M, Martin NG, McArdle WL, McCarthy A, McKnight B, Meitinger T, Melander O, Meyre D, Midthjell K, Montgomery GW, Morken MA, Morris AP, Mulic R, Ngwa JS, Nelis M, Neville MJ, Nyholt DR, O'Donnell CJ, O'Rahilly S, Ong KK, Oostra B, Pare G, Parker AN, Perola M, Pichler I, Pietilainen KH, Platou CG, Polasek O, Pouta A, Rafelt S, Raitakari O, Rayner NW, Ridderstrale M, Rief W, Ruokonen A, Robertson NR, Rzehak P, Salomaa V, Sanders AR, Sandhu MS, Sanna S, Saramies J, Savolainen MJ, Scherag S, Schipf S, Schreiber S, Schunkert H, Silander K, Sinisalo J, Siscovick DS, Smit JH, Soranzo N, Sovio U, Stephens J, Surakka I, Swift AJ, Tammesoo ML, Tardif JC, Teder-Laving M, Teslovich TM, Thompson JR, Thomson B, Tonjes A, Tuomi T, van Meurs JB, van Ommen GJ, Vatin V, Viikari J, Visvikis-Siest S, Vitart V, Vogel CI, Voight BF, Waite LL, Wallaschofski H, Walters GB, Widen E, Wiegand S, Wild SH, Willemsen G, Witte DR, Witteman JC, Xu J, Zhang Q, Zgaga L, Ziegler A, Zitting P, Beilby JP, Farooqi IS, Hebebrand J, Huikuri HV, James AL, Kahonen M, Levinson DF, Macciardi F, Nieminen MS, Ohlsson C, Palmer LJ, Ridker PM, Stumvoll M, Beckmann JS, Boeing H, Boerwinkle E, Boomsma DI, Caulfield MJ, Chanock SJ, Collins FS, Cupples LA, Smith GD, Erdmann J, Froguel P, Gronberg H, Gyllensten U, Hall P, Hansen T, Harris TB, Hattersley AT, Hayes RB, Heinrich J, Hu FB, Hveem K, Illig T, Jarvelin MR, Kaprio J, Karpe F, Khaw KT, Kiemeney LA, Krude H, Laakso M, Lawlor DA, Metspalu A, Munroe PB, Ouwehand WH, Pedersen O, Penninx BW, Peters A, Pramstaller PP, Quertermous T, Reinehr T, Rissanen A, Rudan I, Samani NJ, Schwarz PE, Shuldiner AR, Spector TD, Tuomilehto J, Uda M, Uitterlinden A, Valle TT, Wabitsch M, Waeber G, Wareham NJ, Watkins H, on behalf of Procardis Consortium, Wilson JF, Wright AF, Zillikens MC, Chatterjee N, McCarroll SA, Purcell S, Schadt EE, Visscher PM, Assimes TL, Borecki IB, Deloukas P, Fox CS, Groop LC, Haritunians T, Hunter DJ, Kaplan RC, Mohlke KL, O'Connell JR, Peltonen L, Schlessinger D, Strachan DP, van Duijn CM, Wichmann HE, Frayling TM, Thorsteinsdottir U, Abecasis GR, Barroso I, Boehnke M, Stefansson K, North KE, I McCarthy M, Hirschhorn JN, Ingelsson E, Loos RJ: Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index. Nature Genetics 42(11):937-948, 2010 [PDF unavailable] [PubMed] [More...]
 Visscher PM, Yang J, Goddard ME: A Commentary on 'Common SNPs Explain a Large Proportion of the Heritability for Human Height' by Yang et al. (2010). Twin Research and Human Genetics 13(6):517-524, 2010 [PDF unavailable] [PubMed] [More...]
 Lee SH, Nyholt DR, Macgregor S, Henders AK, Zondervan KT, Montgomery GW, Visscher PM: A simple and fast two-locus quality control test to detect false positives due to batch effects in genome-wide association studies. Genetic Epidemiology 34(8):854-862, 2010 [PDF unavailable] [PubMed] [More...]
 Visscher PM, McEvoy BP, Yang J: From Galton to GWAS: quantitative genetics of human height. Genetics research 92(5-6):371-379, 2010 [PDF unavailable] [PubMed] [More...]
2009
 Visscher PM: Whole genome approaches to quantitative genetics. Genetica 136:351-358, 2009 [PDF unavailable] [PubMed] [More...]
 Luciano M, Gow AJ, Taylor MD, Hayward C, Harris SE, Campbell H, Porteous DJ, Starr JM, Visscher PM, Deary IJ: Apolipoprotein E is not Related to Memory Abilities at 70 Years of Age. Behavior Genetics 39:6-14, 2009 [PDF unavailable] [PubMed] [More...]
 Nyholt DR, Yu CE, Visscher PM: On Jim Watson's APOE status: genetic information is hard to hide. European Journal of Human Genetics 17:147-149, 2009 [PDF unavailable] [PubMed] [More...]
 Benyamin B, McRae AF, Zhu G, Gordon S, Henders AK, Palotie A, Peltonen L, Martin NG, Montgomery GW, Whitfield JB, Visscher PM: Variants in TF and HFE Explain approximately 40% of Genetic Variation in Serum-Transferrin Levels. American Journal of Human Genetics 84:60-65, 2009 [PDF unavailable] [PubMed] [More...]
 Luciano M, Miyajima F, Lind PA, Bates TC, Horan M, Harris SE, Wright MJ, Ollier WE, Hayward C, Pendleton N, Gow AJ, Visscher PM, Starr JM, Deary IJ, Martin NG, Payton A: Variation in the Dysbindin gene and normal cognitive function in three independent population samples. Genes, brain, and behavior 8:218-227, 2009 [PDF unavailable] [PubMed] [More...]
 Houlihan LM, Harris SE, Luciano M, Gow AJ, Starr JM, Visscher PM, Deary IJ: Replication study of candidate genes for cognitive abilities: the Lothian Birth Cohort 1936. Genes, brain, and behavior 8:238-247, 2009 [PDF unavailable] [PubMed] [More...]
 Kaminsky ZA, Tang T, Wang SC, Ptak C, Oh GH, Wong AH, Feldcamp LA, Virtanen C, Halfvarson J, Tysk C, McRae AF, Visscher PM, Montgomery GW, Gottesman II, Martin NG, Petronis A: DNA methylation profiles in monozygotic and dizygotic twins. Nature Genetics 41(2):240-245, 2009 [PDF unavailable] [PubMed] [More...]
 Chenoweth SF, Visscher PM: Association Mapping in Outbred Populations: Power and Efficiency When Genotyping Parents and Phenotyping Progeny. Genetics 181:755-765, 2009 [PDF unavailable] [PubMed] [More...]
 Benyamin B, Visscher PM, McRae AF: Family-based genome-wide association studies. Pharmacogenomics 10(2):181-190, 2009 [PDF unavailable] [PubMed] [More...]
 Hayes BJ, Visscher PM, Goddard ME: Increased accuracy of artificial selection by using the realized relationship matrix. Genetical Research 91(1):47-60, 2009 [PDF unavailable] [PubMed] [More...]
 McEvoy BP, Montgomery GW, McRae AF, Ripatti S, Perola M, Spector TD, Cherkas L, Ahmadi KR, Boomsma D, Willemsen G, Hottenga JJ, Pedersen NL, Magnusson PKE, Kyvik KO, Christensen K, Kaprio J, Heikkila K, Palotie A, Widen E, Muilu J, Syvanen A-C, Liljedahl U, Hardiman O, Cronin S, Peltonen L, Martin NG, Visscher PM: Geographical structure and differential natural selection among North European populations. Genome Research 19:804-814, 2009 [PDF unavailable] [PubMed] [More...]
 Luciano M, Gow AJ, Harris SE, Hayward C, Allerhand M, Starr JM, Visscher PM, Deary IJ: Cognitive ability at age 11 and 70 years, information processing speed, and APOE variation: The Lothian Birth Cohort 1936 study. Psychology and Aging 24(1):129-138, 2009 [PDF unavailable] [PubMed] [More...]
 Posthuma D, de Koning, Dolan C, Goddard ME, Visscher PM: A note on permutation tests for genetic association analysis of quantitative traits when variances are heterogeneous. Genetic Epidemiology 33:710-716, 2009 [PDF unavailable] [PubMed] [More...]
 Byrne EM, McRae AF, Duffy DL, Zhao ZZ, Martin NG, Wright MJ, Montgomery GW, Visscher PM: Association Study of Common Mitochondrial Variants and Cognitive Ability. Behavior Genetics 39:504-512, 2009 [PDF unavailable] [PubMed] [More...]
 Evans DM, Visscher PM, Wray NR: Harnessing the Information Contained Within Genome-wide Association Studies to Improve Individual Prediction of Complex Disease Risk. Human Molecular Genetics 18:3525-3531, 2009 [PDF unavailable] [PubMed] [More...]
 International Schizophrenia Consortium, Purcell SM, Wray NR, Stone JL, Visscher PM, O'Donovan MC, Sullivan PF, Sklar P: Common polygenic variation contributes to risk of schizophrenia and bipolar disorder. Nature 2009 [PDF unavailable] [PubMed] [More...]
 Keller MC, McRae AF, McGaughran JM, Visscher PM, Martin NG, Montgomery GW: Non-pathological paternal isodisomy of chromosome 2 detected from a genome-wide SNP scan. American journal of medical genetics. Part A 149A(8):1823-1826, 2009 [PDF unavailable] [PubMed] [More...]
 Visscher PM, Hill WG: The limits of individual identification from sample allele frequencies: theory and statistical analysis. PLoS Genetics 5(10):e1000628, 2009 [PDF unavailable] [PubMed] [More...]
 Byrne EM, McRae AF, Duffy DL, Zhao ZZ, Martin NG, Whitfield JB, Visscher PM, Montgomery GW: Family-based mitochondrial association study of traits related to type 2 diabetes and the metabolic syndrome in adolescents. Diabetologia 52(11):2359-2368, 2009 [PDF unavailable] [PubMed] [More...]
 Benyamin B, Ferreira MA, Willemsen G, Gordon SD, Middelberg RPS, McEvoy BP, Hottenga JJ, Henders AK, Campbell MJ, Wallace L, Frazer IH, Heath AC, de Geus EJC, Nyholt DR, Visscher PM, Penninx BW, Boomsma DI, Martin NG, Montgomery GW, Whitfield JB: Common variants in TMPRSS6 are associated with iron status and erythrocyte volume. Nature Genetics 41:1173-1175, 2009 [PDF unavailable] [PubMed] [More...]
 Nagamine Y, Pong-Wong R, Visscher PM, Haley CS: Detection of multiple quantitative trait loci and their pleiotropic effects in outbred pig populations. Genetics, selection, evolution 41:44, 2009 [PDF unavailable] [PubMed] [More...]
 McEvoy BP, Visscher PM: Genetics of human height. Economics and human biology 7(3):294-306, 2009 [PDF unavailable] [PubMed] [More...]
 Manolio TA, Collins FS, Cox NJ, Goldstein DB, Hindorff LA, Hunter DJ, McCarthy MI, Ramos EM, Cardon LR, Chakravarti A, Cho JH, Guttmacher AE, Kong A, Kruglyak L, Mardis E, Rotimi CN, Slatkin M, Valle D, Whittemore AS, Boehnke M, Clark AG, Eichler EE, Gibson G, Haines JL, Mackay TF, McCarroll SA, Visscher PM: Finding the missing heritability of complex diseases. Nature 461(7265):747-753, 2009 [PDF unavailable] [PubMed] [More...]
 Craig JE, Hewitt AW, McMellon AE, Henders AK, Ma L, Wallace L, Sharma S, Burdon KP, Visscher PM, Montgomery GW, Macgregor S: Rapid inexpensive genome-wide association using pooled whole blood. Genome Research 19:2075-2080, 2009 [PDF unavailable] [PubMed] [More...]
 Visscher PM, Montgomery GW: Genome-wide association studies and human disease: from trickle to flood. JAMA 302(18):2028-2029, 2009 [PDF unavailable] [PubMed] [More...]
 Knight HM, Pickard BS, Maclean A, Malloy MP, Soares DC, McRae AF, Condie A, White A, Hawkins W, McGhee K, van Beck M, Macintyre DJ, Starr JM, Deary IJ, Visscher PM, Porteous DJ, Cannon RE, St Clair D, Muir WJ, Blackwood DH: A Cytogenetic Abnormality and Rare Coding Variants Identify ABCA13 as a Candidate Gene in Schizophrenia, Bipolar Disorder, and Depression. American Journal of Human Genetics 85:833-846, 2009 [PDF unavailable] [PubMed] [More...]
2008
 Edmonds CJ, Isaacs EB, Rogers M, Lanigan J, Singhal A, Lucas A, Gringras P, Denton J, Visscher PM, Deary IJ: Inspection Time and cognitive abilities in twins aged 7 to 17 years: age-related changes, heritability and genetic covariance. Intelligence 36:210-225, 2008 [PDF unavailable]
 Wray NR, Middeldorp CM, Birley AJ, Gordon SD, Sullivan PF, Visscher PM, Nyholt DR, Willemsen G, de Geus EJC, Slagboom PE, Montgomery GW, Martin NG, Boomsma DI: Genome-wide linkage analysis of multiple measures of neuroticism of 2 large cohorts from Australia and the Netherlands. Archives of General Psychiatry 65(6):649-658, 2008 [PDF unavailable] [PubMed] [More...]
 Benyamin B, Perola M, Cornes BK, Madden PAF, Palotie A, Nyholt DR, Montgomery GW, Peltonen L, Martin NG, Visscher PM: Within-family outliers: segregating alleles or environmental effects? A linkage analysis of height from 5815 sibling pairs. European Journal of Human Genetics 16(4):516-524, 2008 [PDF unavailable] [PubMed] [More...]
 Macgregor S, Zhao ZZ, Henders A, Martin NG, Montgomery GW, Visscher PM: Highly cost-efficient genome-wide association studies using DNA pools and dense SNP arrays. Nucleic Acids Research 36(6):e35, 2008 [PDF unavailable] [PubMed] [More...]
 Anderson CA, Maclean A, Dunnigan MG, Pelosi AJ, Murray V, McKee I, McDonald G, Burt DW, Morrice DR, Muir WJ, Visscher PM, Blackwood DHR: A genome-wide linkage study in families with major depression and co-morbid unexplained swelling. American journal of medical genetics. Part B, Neuropsychiatric genetics 147(3):356-362, 2008 [PDF unavailable] [PubMed] [More...]
 Gratten J, Wilson AJ, McRae AF, Beraldi D, Visscher PM, Pemberton JM, Slate J: A localized negative genetic correlation constrains microevolution of coat color in wild sheep. Science 319(5861):318-320, 2008 [PDF unavailable] [PubMed] [More...]
 Visscher PM, Gordon S, Neale MC: Power of the classical twin design revisited: II detection of common environmental variance. Twin Research and Human Genetics 11(1):48-54, 2008 [PDF unavailable] [PubMed] [More...]
 Nagamine Y, Nirasawa K, Takahashi H, Sasaki O, Ishii K, Minezawa M, Oda S, Visscher PM, Furukawa T: Estimation of the time of divergence between Japanese Mishima island cattle and other cattle populations using microsatellite DNA markers. Journal of Heredity 99(2):202-207, 2008 [PDF unavailable] [PubMed] [More...]
 Avendano S, Visscher PM, Villanueva B: Response to selection from using identified genes and quadratic indices in two-traits breeding goals. Spanish Journal Of Agricultural Research 6:88-97, 2008 [PDF unavailable]
 Visscher PM, Hill WG, Wray NR: Heritability in the genomics era--concepts and misconceptions. Nature Reviews Genetics 9(4):255-266, 2008 [PDF unavailable] [PubMed] [More...]
 Visscher PM, Andrew T, Nyholt DR: Genome-wide association studies of quantitative traits with related individuals: little (power) lost but much to be gained. European Journal of Human Genetics 16(3):387-390, 2008 [PDF unavailable] [PubMed] [More...]
 Hill WG, Goddard ME, Visscher PM: Data and theory point to mainly additive genetic variance for complex traits. PLoS Genetics 4(2): e1000008, 2008 [PDF unavailable] [PubMed] [More...]
 Visscher PM: Sizing up human height variation. Nature Genetics 40(5):489-490, 2008 [PDF unavailable] [PubMed] [More...]
 McRae AF, Byrne EM, Zhao ZZ, Montgomery GW, Visscher PM: Power and SNP Tagging in Whole Mitochondrial Genome Association Studies. Genome Research 18:911-917, 2008 [PDF unavailable] [PubMed] [More...]
 Keith JM, McRae AF, Duffy DL, Mengersen K, Visscher PM: Calculation of IBD probabilities with dense SNP or sequence data. Genetic Epidemiology (epub 20/03/2008) 2008 [PDF unavailable] [PubMed] [More...]
 Webbink D, Martin NG, Visscher PM: Does teenage childbearing increase smoking, drinking and body size? Journal of Health Economics 27:888-903, 2008 [PDF unavailable] [PubMed] [More...]
 Luciano M, Lind PA, Deary IJ, Payton A, Posthuma D, Butcher LM, Bochdanovits Z, Whalley LJ, Visscher PM, Harris SE, Polderman TJ, Davis OS, Wright MJ, Starr JM, de Geus EJC, Bates TC, Montgomery GW, Boomsma DI, Martin NG, Plomin R: Testing replication of a 5-SNP set for general cognitive ability in six population samples. European Journal of Human Genetics 16:1388-1395, 2008 [PDF unavailable] [PubMed] [More...]
 Dolezal M, Schwarzenbacher H, Soller M, Solkner J, Visscher PM: Multiple-marker mapping for selective DNA pooling within large families. Journal of Dairy Science 91(7):2864-2873, 2008 [PDF unavailable] [PubMed] [More...]
 Ayub M, Irfan M, Maclean A, Naeem F, Macgregor S, Visscher PM, Muir W, Blackwood D: Linkage analysis in a large family from Pakistan with depression and a high incidence of consanguineous marriages. Human Heredity 66(3):190-198, 2008 [PDF unavailable] [PubMed] [More...]
 Byrne EM, McRae AF, Zhao ZZ, Martin NG, Montgomery GW, Visscher PM: The use of common mitochondrial variants to detect and characterise population structure in the Australian population: implications for genome-wide association studies. European Journal of Human Genetics 16(11):1396-1403, 2008 [PDF unavailable] [PubMed] [More...]
 Anderson CA, Zhu G, Falchi M, van den Berg M, Treloar SA, Spector TD, Martin NG, Boomsma DI, Visscher PM, Montgomery GW: A genome-wide linkage scan for age at menarche in three populations of European descent. Journal of Clinical Endocrinology and Metabolism 93(10):3965-3970, 2008 [PDF unavailable] [PubMed] [More...]
 Oldmeadow C, Wood I, Mengersen K, Visscher PM, Martin NG, Duffy DL: Investigation of the relationship between smoking and appendicitis in Australian twins. Annals of Epidemiology 18(8):631-636, 2008 [PDF unavailable] [PubMed] [More...]
 Wray NR, Goddard ME, Visscher PM: Prediction of individual genetic risk of complex disease. Current opinion in genetics & development 18:257-263, 2008 [PDF unavailable] [PubMed] [More...]
 Hur YM, Kaprio J, Iacono WG, Boomsma DI, McGue M, Silventoinen K, Martin NG, Luciano M, Visscher PM, Rose RJ, He M, Ando J, Ooki S, Nonaka K, Lin CC, Lajunen HR, Cornes BK, Bartels M, van Beijsterveldt CE, Cherny SS, Mitchell K: Genetic influences on the difference in variability of height, weight and body mass index between Caucasian and East Asian adolescent twins. International Journal of Obesity 32:1455-1467, 2008 [PDF unavailable] [PubMed] [More...]
 Stone JL, O'Donovan MC, Gurling H, Kirov GK, Blackwood DHR, Corvin A, Craddock NJ, Gill M, Hultman CM, Lichtenstein P, McQuillin A, Pato CN, Ruderfer DM, Owen MJ, St Clair D, Sullivan PF, Scolnick EM, Korn J, Macgregor S, Morris DW, O'Dushlaine CT, Daly MJ, Visscher PM, Holmans PA, Sklar P, Purcell SM: Rare chromosomal deletions and duplications increase risk of schizophrenia. Nature Epub 2008 Jul 30:237-241, 2008 [PDF unavailable] [PubMed] [More...]
 Macgregor S, Hottenga JJ, Lind PA, Suchiman HE, Willemsen G, Slagboom PE, Montgomery GW, Martin NG, Visscher PM, Boomsma DI: Vitamin d receptor gene polymorphisms have negligible effect on human height. Twin Research and Human Genetics 11(5):488-494, 2008 [PDF unavailable] [PubMed] [More...]
 Lee SH, van der Werf JH, Hayes BJ, Goddard ME, Visscher PM: Predicting unobserved phenotypes for complex traits from whole-genome SNP data. PLoS Genetics 4(10):e1000231, 2008 [PDF unavailable] [PubMed] [More...]
 Hasselbalch AL, Benyamin B, Visscher PM, Heitmann BL, Kyvik KO, Sorensen TI: Common Genetic Components of Obesity Traits and Serum Leptin. Obesity (Silver Spring, Md.) 16:2723-2729, 2008 [PDF unavailable] [PubMed] [More...]
 Webbink D, Posthuma D, Boomsma DI, de Geus EJC, Visscher PM: Do twins have lower cognitive ability than singletons? Intelligence 36:539-547, 2008 [PDF unavailable]
 Sved JA, McRae AF, Visscher PM: Divergence between human populations estimated from linkage disequilibrium. American Journal of Human Genetics 83(6):737-743, 2008 [PDF unavailable] [PubMed] [More...]
2007
 Beraldi D, McRae AF, Gratten J, Pilkington JG, Slate J, Visscher PM, Pemberton JM: Quantitative trait loci (QTL) mapping of resistance to strongyles and coccidia in the free-living Soay sheep (Ovis aries). International Journal for Parasitology 37(1):121-129, 2007 [PDF unavailable] [PubMed] [More...]
 Gratten J, Beraldi D, Lowder BV, McRae AF, Visscher PM, Pemberton JM, Slate J: Compelling evidence that a single nucleotide substitution in TYRP1 is responsible for coat-colour polymorphism in a free-living population of Soay sheep. Proceedings of the Royal Society B: Biological Sciences 274(1610):619-626, 2007 [PDF unavailable] [PubMed] [More...]
 Ivkovic V, Vitart V, Rudan I, Janicijevic B, Smolej-Narancic N, Skaric-Juric T, Barbalic M, Polasek O, Kolcic I, Biloglav Z, Visscher PM, Hayward C, Hastie ND, Anderson N, Campbell H, Wright AF, Rudan P, Deary IJ: The Eysenck personality factors: psychometric structure, reliability, heritability and phenotypic and genetic correlations with psychological distress in an isolated Croatian population. Personality and Individual Differences 42(1):123-133, 2007 [PDF unavailable]
 Tenesa A, Navarro P, Hayes BJ, Duffy DL, Clarke GM, Goddard ME, Visscher PM: Recent human effective population size estimated from linkage disequilibrium. Genome Research 17(4):520-526, 2007 [PDF unavailable] [PubMed] [More...]
 Beraldi D, McRae AF, Gratten J, Slate J, Visscher PM, Pemberton J: Mapping quantitative trait Loci underlying fitness-related traits in a free-living sheep population. Evolution 61(6):1403-1416, 2007 [PDF unavailable] [PubMed] [More...]
 Wood IA, Visscher PM, Mengersen K: Classification based upon gene expression data: bias and precision of error rates. Bioinformatics 23(11):1363-1370, 2007 [PDF unavailable] [PubMed] [More...]
 Webbink D, Hay D, Visscher PM: Does sharing the same class in school improve cognitive abilities of twins? Twin Research and Human Genetics 10(4):573-580, 2007 [PDF unavailable] [PubMed] [More...]
 Benyamin B, Sorensen TIA, Schousboe K, Fenger M, Visscher PM, Kyvik KO: Are there common genetic and environmental factors behind the endophenotypes associated with the metabolic syndrome? Diabetologia 50(9):1880-1888, 2007 [PDF unavailable] [PubMed] [More...]
 Perola M, Sammalisto S, Hiekkalinna T, Martin NG, Visscher PM, Montgomery GW, Benyamin B, Harris JR, Boomsma D, Willemsen G, Hottenga JJ, Christensen K, Kyvik KO, Sorensen TI, Pedersen NL, Magnusson PK, Spector TD, Widen E, Silventoinen K, Kaprio J, Palotie A, Peltonen L, GenomEUtwin Project: Combined Genome Scans for Body Stature in 6,602 European Twins: Evidence for Common Caucasian Loci. PLoS Genetics 3(6):1019-1028, 2007 [PDF unavailable] [PubMed] [More...]
 Benyamin B, Martin ICA, Cheung CC, Buckley MF, Thomson PC, Visscher PM, Moran C: Bodyweight QTL on mouse chromosomes 4 and 11 by selective genotyping: regression v. maximum likelihood. Australian Journal of Experimental Agriculture 47(6):677-682, 2007 [PDF unavailable]
 Anderson CA, Duffy DL, Martin NG, Visscher PM: Estimation of variance components for age at menarche in twin families. Behavior Genetics 37(5):668-677, 2007 [PDF unavailable] [PubMed] [More...]
 Wray NR, Birley AJ, Sullivan PK, Visscher PM, Martin NG: Genetic and phenotypic stability of measures of neuroticism over 22 years. Twin Research and Human Genetics 10(5):695-702, 2007 [PDF unavailable] [PubMed] [More...]
 Visscher PM, Macgregor S, Benyamin B, Zhu G, Gordon S, Medland SE, Hill WG, Hottenga JJ, Willemsen G, Boomsma DI, Liu YZ, Deng HW, Montgomery GW, Martin NG: Genome Partitioning of Genetic Variation for Height from 11,214 Sibling Pairs. American Journal of Human Genetics 81(5):1104-1110, 2007 [PDF unavailable] [PubMed] [More...]
 Wray NR, Goddard ME, Visscher PM: Prediction of individual genetic risk to disease from genome-wide association studies. Genome Research 17(10):1520-1528, 2007 [PDF unavailable] [PubMed] [More...]
 Thornblad TA, Elliott KS, Jowett J, Visscher PM: Prioritization of positional candidate genes using multiple web-based software tools. Twin Research and Human Genetics 10(6):861-870, 2007 [PDF unavailable] [PubMed] [More...]
 Deary IJ, Gow AJ, Taylor MD, Corley J, Brett C, Wilson V, Campbell H, Whalley LJ, Visscher PM, Porteous DJ, Starr JM: The Lothian Birth Cohort 1936: a study to examine influences on cognitive ageing from age 11 to age 70 and beyond. BMC Geriatrics 7:1-12, 2007 [PDF unavailable] [PubMed] [More...]
 McRae AF, Matigian NA, Vadlamudi L, Mulley JC, Mowry B, Martin NG, Berkovic SF, Hayward NK, Visscher PM: Replicated effects of sex and genotype on gene expression in human lymphoblastoid cell lines. Human Molecular Genetics 16(4):364-373, 2007 [PDF unavailable] [PubMed] [More...]
2006
 Visscher PM, Duffy DL: The value of relatives with phenotypes but missing genotypes in association studies for quantitative traits. Genetic Epidemiology 30(1):30-36, 2006 [PDF unavailable]
 Macgregor S, Knott SA, Visscher PM: False disease region identification from identity-by-descent haplotype sharing in the presence of phenocopies. Twin Research and Human Genetics 9(1):9-16, 2006 [PDF unavailable] [PubMed] [More...]
 Visscher PM, Medland SE, Ferreira MA, Morley KI, Zhu G, Cornes BK, Montgomery GW, Martin NG: Assumption-Free Estimation of Heritability from Genome-Wide Identity-by-Descent Sharing between Full Siblings. PLoS Genetics 2(3):316-325, 2006 [PDF unavailable] [PubMed] [More...]
 Macgregor S, Visscher PM, Montgomery GW: Analysis of pooled DNA samples on high density arrays without prior knowledge of differential hybridization rates. Nucleic Acids Research 34(7): 2006 [PDF unavailable] [PubMed] [More...]
 Beraldi D, McRae AF, Gratten J, Slate J, Visscher PM, Pemberton JM: Development of a Linkage Map and Mapping of Phenotypic Polymorphisms in a Free-living Population of Soay Sheep (Ovis aries). Genetics 173(3):1521-1537, 2006 [PDF unavailable] [PubMed] [More...]
 Anderson CA, McRae AF, Visscher PM: A simple linear regression method for quantitative trait loci linkage analysis with censored observations. Genetics 173(3):1735-1745, 2006 [PDF unavailable] [PubMed] [More...]
 Benyamin B, Deary IJ, Visscher PM: Precision and bias of a normal finite mixture distribution model to analyze twin data when zygosity is unknown: simulations and application to IQ phenotypes on a large sample of twin pairs. Behavior Genetics 36(6):935-946, 2006 [PDF unavailable] [PubMed] [More...]
 Webbink D, Roeleveld J, Visscher PM: Identification of Twin Pairs from Large Population Based Samples. Twin Research and Human Genetics 9(4):496-500, 2006 [PDF unavailable]
 Visscher PM: Variation of Estimates of SNP and Haplotype Diversity and Linkage Disequilibrium in samples from the same population due to Experimental and Evolutionary Sample Size. Annals of Human Genetics 70:1-8, 2006 [PDF unavailable]
 Visscher PM: A note on the asymptotic distribution of likelihood ratio tests to test variance components. Twin Research and Human Genetics 9(4):490-495, 2006 [PDF unavailable]
 Visscher PM, Hill WG: Estimation of Recombination Rate and Detection of Recombination Hotspots from Dense SNP Trio Data. Genetics 173(4):2415-2417, 2006 [PDF unavailable]
 Macgregor S, Cornes BK, Martin NG, Visscher PM: Bias, precision and heritability of self-reported and clinically measured height in Australian twins. Human Genetics 120(4):571-580, 2006 [PDF unavailable] [PubMed] [More...]
 Montgomery GW, Zhu G, Hottenga JJ, Duffy DL, Heath AC, Boomsma DI, Martin NG, Visscher PM: HLA and Genomewide Allele Sharing in Dizygotic Twins. American Journal of Human Genetics 79(6):1052-1058, 2006 [PDF unavailable] [PubMed] [More...]
 Navarro P, Visscher PM, Chatziplis D, Koerhuis ANM, Haley CS: Genetic parameters for blood oxygen saturation, body weight and breast conformation in 4 meat-type chicken lines. British Poultry Science 47(6):659-670, 2006 [PDF unavailable]
 Navarro P, Visscher PM, Chatziplis D, Koerhuis ANM, Haley CS: Segregation analysis of blood oxygen saturation in broilers suggests a major gene influence on ascites. British Poultry Science 47(6):671-684, 2006 [PDF unavailable]
 Gordon S, Visscher PM: Residual linkage: Why do linkage peaks not disappear after an association study? Human Genetics 121(1):77-82, 2006 [PDF unavailable]
 Ferreira MA, Visscher PM, Martin NG, Duffy DL: A simple method to localise pleiotropic susceptibility loci using univariate linkage analyses of correlated traits. European Journal of Human Genetics 14(8):953-962, 2006 [PDF unavailable] [PubMed] [More...]
 Posthuma D, Visscher PM, Willemsen G, Zhu G, Martin NG, Slagboom PE, de Geus EJC, Boomsma DI: Replicated linkage for eye color on 15q using comparative ratings of sibling pairs. Behavior Genetics 36(1):12-17, 2006 [PDF unavailable] [PubMed] [More...]
2005
 Tenesa A, Visscher PM, Carothers A, Knott SA: Marker and trait based analysis of QTL using selective genotyping. Behavior Genetics 35(2):219-228, 2005 [PDF unavailable]
 Visscher PM, Haley CS, Ewald H, Mors O, Egeland J, Thiel B, Ginns E, Muir W, Blackwood DHR: Joint multi-population analysis for genetic linkage of bipolar disorder or "wellness" to chromosome 4p. American Journal of Medical Genetics 133:18-24, 2005 [PDF unavailable]
 McRae AF, Bishop SC, Walling GA, Wilson AD, Visscher PM: Mapping of Multiple Quantitative Trait Loci for Growth and Carcass Traits in a Complex Commercial Sheep Pedigree. Animal Science 80:135-141, 2005 [PDF unavailable]
 Navarro P, Visscher PM, Knott SA, Burt DW, Hocking P, Haley CS: Mapping quantitative trait loci affecting organ weights and blood variables in a broiler-layer cross. British Poultry Science 46(4):430-442, 2005 [PDF unavailable]
 Benyamin B, Wilson V, Whalley LJ, Visscher PM, Deary IJ: Large consistent estimates of IQ heritability in two entire populations of 11-year-olds from 1932 and 1947. Behavior Genetics 35(5):525-534, 2005 [PDF unavailable]
 Wall E, Visscher PM, Hospital F, Woolliams JA: Genomic contributions in livestock gene introgression programmes. Genetics Selection Evolution 37(3):291-313, 2005 [PDF unavailable]
 McRae AF, Pemberton JM, Visscher PM: Modeling linkage disequilibrium in natural populations: the example of the Soay sheep population of St. Kilda, Scotland. Genetics 171(1):251-258, 2005 [PDF unavailable] [PubMed] [More...]
 Uimari P, Kontkanen O, Visscher PM, Pirskanen M, Fuentes R, Salonen JT: Genome-wide linkage disequilibrium from 100,000 SNPs in the East Finland founder population. Twin Research and Human Genetics 8(3):185-197, 2005 [PDF unavailable]
 Montgomery GW, Campbell MJ, Dickson PA, Herbert S, Siemering K, Ewen-White KR, Visscher PM, Martin NG: Estimation of the rate of SNP genotyping errors from DNA extracted from different tissues. Twin Research and Human Genetics 8(4):346-352, 2005 [PDF unavailable] [PubMed] [More...]
 Macgregor S, Knott SA, White I, Visscher PM: Quantitative trait locus analysis of longitudinal quantitative trait data in complex pedigrees. Genetics 171(3):1365-1376, 2005 [PDF unavailable] [PubMed] [More...]
 Charlesworth B, Keightley P, Visscher PM: Introduction: population genetics, quantitative genetics and animal improvement: papers in honour of William (Bill) Hill. Philosophical Transactions of the Royal Society B-Biological Sciences 360:1365-1366, 2005 [PDF unavailable]
 Ferreira MA, O'Gorman L, Le Souef P, Burton PR, Toelle BG, Robertson CF, Visscher PM, Martin NG, Duffy DL: Robust estimation of experimentwise p values applied to a genome scan of multiple asthma traits identifies a new region of significant linkage on chromosome 20q13. American Journal of Human Genetics 77(6):1075-1085, 2005 [PDF unavailable] [PubMed] [More...]
2004
 Thomas S, Porteous D, Visscher PM: Efficiency of Direct Haplotyping versus Genotyping in Association Studies. Genetic Epidemiology 26(2):116-124, 2004 [PDF unavailable]
 Nagamine Y, Visscher PM, Haley CS: QTL detection and allelic effects for growth and fat traits in outbred pig populations. Genetics Selection Evolution 36(1):83-96, 2004 [PDF unavailable]
 Schousboe K, Visscher PM, Erbas B, Kyvik KO, Hopper JL, Henriksen JE, Heitmann BL, S?rensen TIA: Twin Study of Genetic and Environmental Influences on Adult Body Size, Shape and Composition. International Journal of Obesity 28(1):39-48, 2004 [PDF unavailable]
 Tenesa A, Wright AF, Knott SA, Carothers AD, Hayward C, Angius A, Persico I, Maestrale G, Hastie ND, Pirastu M, Visscher PM: Extent of linkage disequilibrium in a Sardinian sub-isolate: sampling and methodological considerations. Human Molecular Genetics 13(1):25-33, 2004 [PDF unavailable]
 Nsengimana J, Baret PV, Haley CS, Visscher PM: Linkage disequilibrium in the domesticated pig. Genetics 166(3):1395-1404, 2004 [PDF unavailable]
 Visscher PM, Goddard ME: Prediction of the confidence interval of QTL location. Behavior Genetics 34(4):477-482, 2004 [PDF unavailable]
 Deary IJ, Whiteman MC, Pattie A, Starr JM, Hayward C, Wright AF, Visscher PM, Tynan MC, Whalley LJ: Apolipoprotein E gene variability and cognitive functions at age 79: Follow up of the Scottish Mental Survey 1932. Psychology and Aging 19(2):367-371, 2004 [PDF unavailable]
 Walling GA, Visscher PM, Wilson AD, McTeir BL, Simm G, Bishop SC: Mapping of quantitative trait loci for growth and carcass traits in commercial sheep populations. Journal of Animal Science 82(8):2234-2245, 2004 [PDF unavailable]
 Yu X, Knott SA, Visscher PM: Theoretical and Empirical Power of Regression and Maximum-Likelihood Methods to Map Quantitative Trait Loci in General Pedigrees. American Journal of Human Genetics 75(1):17-26, 2004 [PDF unavailable]
 Macgregor S, Visscher PM, Knott SA, Thomson P, Porteous DJ, Millar JK, Devon RS, Blackwood DHR, Muir WJ: A genome scan and follow-up study identify a bipolar disorder susceptibility locus on chromosome 1q42. Molecular Psychiatry 9(12):1083-1090, 2004 [PDF unavailable]
 Visscher PM: Power of the classical twin design revisited. Twin Research 7(5):505-512, 2004 [PDF unavailable]
 Visscher PM, Wray NR: Conventional Multipoint Nonparametric Linkage Analysis is not Necessarily Inherently Biased. American Journal of Human Genetics 75(4):718-720, 2004 [PDF unavailable]
 Visscher PM, Benyamin B, White I: The Use of Linear Mixed Models to Estimate Variance Components from Data on Twin Pairs by Maximum Likelihood. Twin Research 7(6):670-674, 2004 [PDF unavailable] [PubMed] [More...]
2003
 Tenesa A, Knott SA, Carothers A, Williams JL, Smith D, Visscher PM: Estimation of linkage disequilibrium in a sample of the United Kingdom dairy cattle population using unphased genotypes. Journal of Animal Science 81(3):617-623, 2003 [PDF unavailable]
 Hayes B, Visscher PM, McPartlan H, Goddard ME: Novel multi-locus measure of linkage disequilibrium to estimate past effective population size. Genome Research 13(4):635-643, 2003 [PDF unavailable]
 Hernandez-Sanchez J, Haley CS, Visscher PM: Power of QTL detection using assocation tests with family controls. European Journal of Human Genetics 11(11):819-827, 2003 [PDF unavailable]
 Nagamine Y, Haley CS, Sewalem A, Visscher PM: QTL variation for growth and obesity between and within lines of pigs (Sus Scrofa). Genetics 164(2):629-635, 2003 [PDF unavailable]
 Visscher PM, Le Hellard S: A Simple Method to Analyse SNP-based Association Studies Using DNA Pools. Genetic Epidemiology 24(4):291-296, 2003 [PDF unavailable]
 Tenesa A, Knott SA, Carothers A, Visscher PM: Power of linkage disequilibrium maping to detect a quantitative trait locus (QTL) in selected samples of unrelated individuals. Annals of Human Genetics 67:557-566, 2003 [PDF unavailable]
 Schousboe K, Visscher PM, Henriksen JE, Hopper JL, S?rensen TIA, Kyvik KO: Twin Study of Genetic and Environmental Influences on Glucose Tolerance and Indices of Insulin Sensitivity and Secretion. Diabetologia 46(9):1276-1283, 2003 [PDF unavailable]
 Visscher PM, Tynan M, Whiteman MC, Pattie A, White I, Hayward C, Wright AF, Starr JM, Whalley LJ, Deary IJ: Lack of association between polymorphisms in angiotensin-converting-enzyme and methylenetetrahydrofolate reductase genes and normal cognitive ageing in humans. Neuroscience Letters 347(3):175-178, 2003 [PDF unavailable]
 Hernandez-Sanchez J, Visscher PM, Plastow G, Haley CS: Candidate gene analysis for quantitative traits using the transmission disequilibrium test: The example of the Melanocortin 4-Receptor in pigs. Genetics 164(2):637-644, 2003 [PDF unavailable]
 Segurado R, Detera-Wadleigh SD, Levinson DF, Lewis CM, Gill M, Nurnberger JI Jr, Craddock N, DePaulo JR, Baron M, Gershon ES, Ekholm J, Cichon S, Turecki G, Claes S, Kelsoe JR, Schofield PR, Badenhop RF, Morissette J, Coon H, Blackwood DHR, McInnes LA, Foroud T, Edenberg HJ, Reich T, Rice JP, Goate A, McInnis MG, McMahon FJ, Badner JA, Goldin LR, Bennett P, Willour VL, Zandi PP, Liu J, Gilliam C, Juo SH, Berrettini WH, Yoshikawa T, Peltonen L, Lonnqvist J, Nothen MM, Schumacher J, Windemuth C, Rietschel M, Propping P, Maier W, Alda M, Grof P, Rouleau GA, Del-Favero J, Van Broeckhoven C, Mendlewicz J, Adolfsson R, Spence MA, Luebbert H, Adams LJ, Donald JA, Mitchell PB, Barden N, Shink E, Byerley W, Muir W, Visscher PM, Macgregor S, Gurling H, Kalsi G, McQuillin A, Escamilla MA, Reus VI, Leon P, Freimer NB, Ewald H, Kruse TA, Mors O, Radhakrishna U, Blouin JL, Antonarakis SE, Akarsu N: Genome scan meta-analysis of schizophrenia and bipolar disorder, part III: Bipolar disorder. American Journal of Human Genetics 73(1):49-62, 2003 [PDF unavailable] [PubMed] [More...]
 Macgregor S, Knott SA, White I, Visscher PM, Framingham Heart Study: Longitudinal variance-components analysis of the Framingham Heart Study data. BMC Genetics 4(1): 2003 [PDF unavailable] [PubMed] [More...]
2002
 Villanueva B, Verspoor E, Visscher PM: Parental assignment in fish using microsatellite genetic markers with finite numbers of parents and offspring. Animal Genetics 33(1):33-41, 2002 [PDF unavailable]
 Yazdi MH, Visscher PM, Ducrocq VP, Thompson R: Heritability, Reliability of Genetic Evaluations and Response to Selection in Proportional Hazard Models. Journal of Dairy Science 85(6):1563-1577, 2002 [PDF unavailable]
 Seaton G, Knott SA, Kearsey MJ, Haley CS, Visscher PM: QTL Express: user-friendly software to map quantitative trait loci in outbred populations. Bioinformatics 18(2):339-340, 2002 [PDF unavailable]
 Walling GA, Haley CS, Perez-Enciso M, Thompson R, Visscher PM: On the mapping of QTL at marker and non-marker locations. Genetical Research 79(1):97-106, 2002 [PDF unavailable]
 Jaffrezic F, White IMS, Thompson R, Visscher PM: Contrasting models for lactation curve analysis. Journal of Dairy Science 85(4):968-975, 2002 [PDF unavailable]
 Le Hellard S, Ballereau SJ, Visscher PM, Torrance HS, Pinson J, Morris SW, Thomson ML, Semple CAM, Muir WJ, Blackwood DHR, Porteous DJ, Evans KL: SNP genotyping on pooled DNAs: comparison of genotyping technologies and a semi automated method for data storage. Nucleic Acids Research 30(15):e741-10, 2002 [PDF unavailable]
 Nagamine Y, Knott SA, Visscher PM, Haley CS: Simple deterministic identity-by-descent coefficients and estimation of QTL allelic effects in full and half-sibs. Genetical Research 80(3):237-243, 2002 [PDF unavailable]
 Visscher PM: Increased rate of twins among affected sib pairs. American Journal of Human Genetics 71(4):995-996, 2002 [PDF unavailable]
 Visscher PM, Haley CS, Knott SA: In: Statistical modelling and analysis of genetic data. Journal of the Royal Statistical Society Series B : Statistical Methodology 737-775, 2002 [PDF unavailable]
 Argente MJ, Blasco A, Ortega JA, Haley CS, Visscher PM: Analyses for the presence of a major genen affecting uterine capacity in unilaterallly ovariectomised rabbits. Genetics 163(3):1061-1068, 2002 [PDF unavailable]
 Macgregor S, Visscher PM, Knott S, Porteous D, Muir W, Millar K, Blackwood D: Is schizophrenia linked to chromosome 1q? Science 298(5602):2277, 2002 [PDF unavailable] [PubMed] [More...]
 Visscher PM, Woolliams JA, Smith D, Williams J: Estimation of the pedigree error rate in the UK dairy population using microsatellite markers and the impact on selection. Journal of Dairy Science 85(9):2368-2375, 2002 [PDF unavailable]
 Slate J, Visscher PM, Macgregor S, Stevens D, Tate ML, Pemberton JM: A Genome Scan for Quantitative Trait Loci in a Wild Population of Red Deer (Cervus elaphus). Genetics 162(4):1863-1873, 2002 [PDF unavailable]
2001
 Blackwood DHR, Visscher PM, Muir WJ: Genetic studies of bipolar affective disorder in large families. British Journal of Psychiatry 178(Suppl. 41):S134-S136, 2001 [PDF unavailable]
 Visscher PM, Smith D, Hall SJG, Williams JL: A viable herd of genetically uniform cattle. Nature 409(6818):303-303, 2001 [PDF unavailable]
 Visscher PM, Haley CS: True and false positive peaks in genomewide scans: The long and the short of it. Genetic Epidemiology 20:409-14, 2001 [PDF unavailable]
 Roughsedge T, Brotherstone S, Visscher PM: Bias and power in the estimation of a maternal family variance component in the presence of incomplete and incorrect pedigree information. Journal of Dairy Science 84(4):944-950, 2001 [PDF unavailable]
 Visscher PM, Hopper JL: Power of regression and maximum likelihood methods to map QTL from sib-pair and DZ twin data. Annals of Human Genetics 65:583-601, 2001 [PDF unavailable]
 Visscher PM, Yazdi MH, Jackson AD, Schalling M, Lindblad K, Yuan QP, Porteous D, Muir WJ, Blackwood DHR: Genetic Survival Analysis of Age-at-Onset of Bipolar Disorder. Evidence for Anticipation or a cohort Effect in Families. Psychiatric Genetics 11(3):129-137, 2001 [PDF unavailable]
2000
 Visscher PM, Whittaker JC, Jansen RC: Mapping multiple QTL of different effects: comparison of a simple sequential testing strategy and multiple QTL mapping. Molecular Breeding 6:11-24, 2000 [PDF unavailable]
 Lubbers R, Brotherstone S, Ducrocq VP, Visscher PM: A comparison of a linear and proportional hazards approach to analyse discrete longevity data in dairy cows. Animal Science 70:197-206, 2000 [PDF unavailable]
 Roughsedge T, Brotherstone S, Visscher PM: Effects of cow families on type traits in dairy cattle. Animal Science 70:391-398, 2000 [PDF unavailable]
 Walling GA, Visscher PM, Andersson L, Rothschild MF, Wang L, Moser G, Groenen MAM, Bidanel JP, Cepica S, Archibald AL, Geldermann H, De Koning DJ, Milan D, Haley CS: Combined Analyses of Data From Quantitative Trait Loci Mapping Studies: Chromosome 4 Effects on Porcine Growth and Fatness. Genetics 155(3):1369-1378, 2000 [PDF unavailable]
 Roughsedge T, Visscher PM, Brotherstone S: Effects of cow families on production traits in dairy cattle. Animal Science 71:49-57, 2000 [PDF unavailable]
 George AW, Visscher PM, Haley CS: Mapping quantitative trait loci in complex pedigrees: A two step variance component approach. Genetics 156(4):2081-2092, 2000 [PDF unavailable]
1999
 Roughsedge T, Brotherstone S, Visscher PM: Estimation of variance of maternal lineage effects at the Langhill dairy herd. Animal Science 68:79-86, 1999 [PDF unavailable]
 Visscher PM, Haley CS, Heath SC, Muir WJ, Blackwood DHR: Detecting QTLs for uni and bipolar disorder using a variance component method. Psychiatric Genetics 9(2):75-84, 1999 [PDF unavailable]
 Visscher PM: Speedcongenics: accelerated genome recovery using genetic markers. Genetical Research 74(1):81-85, 1999 [PDF unavailable]
 Roughsedge T, Brotherstone S, Visscher PM: Quantifying genetic contributions to a dairy cattle population using pedigree analysis. Livestock Production Science 60(2-3):359-369, 1999 [PDF unavailable]
 Slate J, Pemberton JM, Visscher PM: Power to detect QTL in a free-living polygynous ruminant population. Heredity 83:327-336, 1999 [PDF unavailable]
 Visscher PM, Haley CS: On the efficiency of marker-assisted introgression. Animal Science 68:59-68, 1999 [PDF unavailable]
1998
 Visscher PM: On the sampling variance of intraclass correlations and genetic correlations. Genetics 149(3):1605-1614, 1998 [PDF unavailable]
 Haley CS, Visscher PM: Strategies to utilise marker-QTL information. Journal of Dairy Science 81(Suppl. 2):85-97, 1998 [PDF unavailable]
 Walling G, Visscher PM, Haley CS: A comparison of bootstrap methods to construct confidence intervals in QTL mapping. Genetical Research 71(2):171-180, 1998 [PDF unavailable]
 Baret PV, Knott SA, Visscher PM: On the use of regression and maximum likelihood for QTL mapping in halfsib designs. Genetical Research 72(2):149-158, 1998 [PDF unavailable]
 Visscher PM, Haley CS: Power of a chromosomal test to detect genetic variation using genetic markers. Heredity 81:317-326, 1998 [PDF unavailable]
 Lebreton CM, Visscher PM, Haley CS, Semikhodskii A, Quarrie SA: A Nonparametric Bootstrap Method for Testing Close Linkage vs. Pleiotropy of Coincident Quantitative Trait Loci. Genetics 150(2):931-943, 1998 [PDF unavailable]
 Walling GA, Archibald AL, Cattermole JA, Downing AC, Finlayson HA, Nicholson D, Visscher PM, Walker CA, Haley CS: Mapping of quantitative trait loci on porcine chromosome 4. Animal Genetics 29(6):415-424, 1998 [PDF unavailable]
 Lebreton CM, Visscher PM: Empirical nonparametric bootstrap strategies in quantitative trait loci mapping: Conditioning on the genetic model. Genetics 148(1):525-535, 1998 [PDF unavailable]
 De Koning DJ, Visscher PM, Knott SA, Haley CS: A strategy for QTL detection in half sib populations. Animal Science 67:257-268, 1998 [PDF unavailable]
1997
 Van Heelsum AM, Visscher PM, Haley CS: Marker assisted introgression using non-unique marker alleles. I. Selection on presence of linked marker alleles. Animal Genetics 28(3):181-187, 1997 [PDF unavailable]
 Van Heelsum AM, Haley CS, Visscher PM: Marker assisted introgression using non-unique marker alleles. II. Selection on probability of presence of the introgressed allele. Animal Genetics 28(3):188-194, 1997 [PDF unavailable]
 Visscher PM, Mackinnon M, Haley CS: Efficiency of marker-assisted selection. Animal Biotechnology 8(1):99-106, 1997 [PDF unavailable]
1996
 Bowman P, Visscher PM, Goddard ME: Customized selection indices for dairy bulls in Australia. Animal Science 62:393-403, 1996 [PDF unavailable]
 Visscher PM: Proportion of the variation in genetic composition in backcrossing programs explained by genetic markers. Journal of Heredity 87(2):136-138, 1996 [PDF unavailable]
 Visscher PM, Haley CS: Detection of putative quantitative trait loci in line crosses under infinitesimal genetic models. Theoretical and Applied Genetics 93(5-6):691-702, 1996 [PDF unavailable]
 Visscher PM, Thompson R, Haley CS: Confidence intervals in QTL mapping by bootstrapping. Genetics 143(2):1013-1020, 1996 [PDF unavailable]
 Visscher PM, Haley CS, Knott SA: Mapping QTLs for binary traits in backcross and F2 populations. Genetical Research 68(1):55-63, 1996 [PDF unavailable]
 Whittaker JC, Thompson R, Visscher PM: On the mapping of QTL by regression of phenotype on marker-type. Heredity 77:23-32, 1996 [PDF unavailable]
 Visscher PM, Haley CS, Thompson R: Marker Assisted Introgression in Backcross Breeding Programs. Genetics 144(4):1923-1932, 1996 [PDF unavailable]
1995
 Visscher PM, Goddard ME: Genetic parameters for Milk Yield, Survival Workability, and type traits for Australian Dairy Cattle. Journal of Dairy Science 78(1):205-220, 1995 [PDF unavailable]
 Visscher PM, Goddard ME: Genetic analyses of profit for Australian Dairy Cattle. Animal Science 61:9-18, 1995 [PDF unavailable]
 Visscher PM: Bias in multiple genetic correlation from half-sib designs. Genetics Selection Evolution 27(4):335-345, 1995 [PDF unavailable]
 Visscher PM, Haley CS: Utilizing genetic markers in pig breeding programmes. Animal Breeding Abstracts 63:1-8, 1995 [PDF unavailable]
 Visscher PM, Thompson R: Haplotype frequencies of linked loci in backcross populations derived from inbred lines. Heredity 75:644-649, 1995 [PDF unavailable]
1994
 Visscher PM, Bowman P, Goddard ME: Breeding objectives for pasture based dairy production systems. Livestock Production Science 40(2):123-137, 1994 [PDF unavailable]
 Thompson R, Crump RE, Juga Y, Visscher PM: Bivariate animal models using scaling and transformation. Genetics Selection Evolution 27(1):33-42, 1994 [PDF unavailable]
1993
 Visscher PM, Goddard ME: Fixed and random contemporary groups. Journal of Dairy Science 76(5):1444-1454, 1993 [PDF unavailable]
1992
 Visscher PM, Hill WG: Heterogeneity of variance and dairy cattle breeding. Animal Production 55:321-329, 1992 [PDF unavailable]
 Visscher PM: Power of likelihood ratio tests for heterogeneity of intraclass correlation and variance in balanced half-sib designs. Journal of Dairy Science 75(5):1320-1330, 1992 [PDF unavailable]
 Visscher PM, Thompson R: Comparisons between genetic variances estimated from different types of relatives in dairy cattle. Animal Production 55:315-320, 1992 [PDF unavailable]
 Visscher PM, Thompson R: Univariate and multivariate parameter estimates for milk production traits using an animal model. I. Description and results of REML analyses. Genetics Selection Evolution 24(5):415-430, 1992 [PDF unavailable]
 Visscher PM, Hill WG, Thompson R: Univariate and multivariate parameter estimates for milk production traits using an animal model. II Efficiency of selection when using simplified covariance structures. Genetics Selection Evolution 24(5):431-447, 1992 [PDF unavailable]
1991
 Visscher PM: On the estimation of variances within herd-mean production groups. Journal of Dairy Science 74(6):1987-1992, 1991 [PDF unavailable]
 Visscher PM, Thompson R, Hill WG: Estimation of genetic and environmental variances for fat yield in individual herds and an investigation into heterogeneity of variance between herds. Livestock Production Science 28(4):273-290, 1991 [PDF unavailable]
 
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