Peer-reviewed publications

Most publications are listed in PubMed and the abstracts can be accessed by clicking here. pdfs of most articles are available below.

Since 2002 I have (co)authored 52 peer-reviewed publications (17 in impact factor >10 journals, including 3 in Nature/Science): 18 as first author, 2 as sole author and 3 as senior author. The average impact factor over all publications is 8 (impact factors are given in braces after each entry). I have (co)authored 16 papers with more than 16 citations (H index 16). Citation numbers are given in square brackets after each entry.

1. S. Macgregor, P. M. Visscher, S. Knott, D. Porteous, W. Muir, K. Millar, and D. Blackwood. 2002. Is schizophrenia linked to chromosome 1q? Science, 298:2277a. {IF 2007 26.4} [CITATIONS 10] PDF
2. J. Slate, P. M. Visscher, S. MacGregor, D. Stevens, M. L. Tate, and J. M. Pemberton. 2002. A genome scan for quantitative trait loci in a wild population of red deer (Cervus elaphus). Genetics, 162:1863-1873. {IF 2007 4.0} [CITATIONS 37] PDF
3. S. Macgregor, S. A. Knott, I. White, and P. M. Visscher. 2003 Longitudinal variance-components analysis of the framingham heart study data. BMC Genetics, 4:S22. {IF 2007 1.6} [CITATIONS 4] PDF
4. W. J. Gauderman, S. Macgregor, L. Briollais, K. Scurrah, M. Tobin, T. Park, D. Wang, S. Q. Rao, S. John, and S. Bull. 2003. Longitudinal data analysis in pedigree studies. Genetic Epidemiology, 25:S18-S28. {IF 2007 3.3} [CITATIONS 8] PDF
5. R. Segurado, S. D. Detera-Wadleigh, D. F. Levinson, C. M. Lewis, M. Gill, J. I. Nurnberg, N. Craddock, J. R. DePaulo, M. Baron, E. S. Gershon, J. Ekholm, S. Cichon, G. Turecki, S. Claes, J. R. Kelsoe, P. R. Schofield, R. F. Badenhop, J. Morissette, H. Coon, D. Blackwood, L. A. McInnes, T. Foroud, H. J. Edenberg, T. Reich, J. P. Rice, A. Goate, M. G. McInnis, F. J. McMahon, J. A. Badner, L. R. Goldin, P. Bennett, V. L. Willour, P. P. Zandi, J. J. Liu, C. Gilliam, S. H. Juo, W. H. Berrettini, T. Yoshikawa, L. Peltonen, J. Lonnqvist, M. M. Nothen, J. Schumacher, C. Windemuth, M. Rietschel, P. Propping, W. Maier, M. Alda, P. Grof, G. A. Rouleau, J. Del-Favero, C. Van Broeckhoven, J. Mendlewicz, R. Adolfsson, M. A. Spence, H. Luebbert, L. J. Adams, J. A. Donald, P. B. Mitchell, N. Barden, E. Shink, W. Byerley, W. Muir, P. M. Visscher, S. Macgregor, H. Gurling, G. Kalsi, A. McQuillin, M. A. Escamilla, V. I. Reus, P. Leon, N. B. Freimer, H. Ewald, T. A. Kruse, O. Mors, U. Radhakrishna, J. L. Blouin, S. E. Antonarakis, and N. Akarsu. 2003. Genome scan meta-analysis of schizophrenia and bipolar disorder, part III: Bipolar disorder. American Journal of Human Genetics, 73:49-62. {IF 2007 11.1} [CITATIONS 216] PDF
6. D.J. Porteous, K.L. Evans, J.K. Millar, B.S. Pickard, P.A. Thomson, R. James, S Macgregor, N.R. Wray, P.M. Visscher, W.J. Muir, and D.H. Blackwood. 2004. Genetics of schizophrenia and bipolar affective disorder:strategies to identify candidate genes. Cold Spring Harb Symp Quant Biol. 68:383-394. {IF 2005 0.9} [CITATIONS 3] PDF
7. S. Macgregor, P. M. Visscher, S. Knott, P. Thompson, D. Porteous, K. Millar, D. Blackwood, W. Muir. 2004. A genome scan and follow-up study identify a bipolar disorder susceptibility locus on chromosome 1q42. Molecular Psychiatry, 9:1083-90. {IF 2007 10.9} [CITATIONS 53] PDF
8. E.K. Green, R. Raybould, S. MacGregor, K. Gordon-Smith, J. Heron, S. Hyde, D. Grozeva, M. L. Hamshere, N. Williams, Michael J Owen, Michael C O'Donovan., L. Jones, I. Jones, G. Kirov, N. Craddock. 2005. Operation of the Schizophrenia Susceptibility Gene, Neuregulin 1, Across Traditional Diagnostic Boundaries to Increase Risk for Bipolar Disorder. Archives of General Psychiatry, 62 (6): 642. {IF 2007 16.0} [CITATIONS 102] PDF
9. R. Raybould, E. K. Green, S. MacGregor, K. Gordon-Smith, J. Heron, S. Hyde, S. Caesar, I. Nikolov, N. Williams, L. Jones, M. C. O'Donovan, M. J. Owen, I. Jones, G. Kirov, N. Craddock. 2005. Bipolar Disorder and polymorphisms in the dysbindin gene (DTNBP1). Biological Psychiatry,57, 7, 696-701. {IF 2007 8.5} [CITATIONS 45] PDF
10. S. Macgregor, S.K. Knott, I. White, P. Visscher. 2005. QTL Analysis of longitudinal quantitative trait data in complex pedigrees. Genetics, 171(3):1365-1376. {IF 2007 4.0} [CITATIONS 12] PDF
11. Williams HJ, Glaser B, Williams NM, Zammit S, Macgregor S, Murphy KC, Kirov G, Owen MJ, O'Donovan MC. 2005. No association between Schizophrenia and polymorphisms in COMT in two large samples. American Journal of Psychiatry, 162:1736-1738. {IF 2007 9.1} [CITATIONS 42] PDF
12. M.L. Hamshere, S. Macgregor, V. Moskvina, I. Nikolov, P. Holmans. 2005. Covariate linkage analysis of GAW14 simulated data incorporating subclinical phenotype, sex, population, parent-of-origin, and interaction. BMC Genetics, 6(Suppl 1):S45. {IF 2007 1.6} [CITATIONS 3] PDF
13. N.M. Williams, E.K. Green, S. Macgregor, S. Dwyer, N. Norton, H. Williams, R. Raybould, D. Grozeva, M. Hamshere, S. Zammit, L. Jones, A. Cardno, G. Kirov, I. Jones, M.C.O'Donovan, M.J.Owen, N. Craddock. 2006. Variation at the DAOA/G30 locus influences susceptibility to major mood episodes but not psychosis in schizophrenia and bipolar disorder. Archives of General Psychiatry, 63:366-373. {IF 2007 16.0} [CITATIONS 68] PDF
14. S. Macgregor, S.A. Knott, P.M. Visscher. 2006. False disease region identification from identity-by-descent haplotype sharing in the presence of phenocopies. Twin Research and Human Genetics, 9(1):9-17. {IF 2007 1.5} [CITATIONS 0] PDF
15. E.K. Green, R. Raybould, S. Macgregor, S. Hyde, A. Young, M. O'Donovan, M. Owen, G. Kirov, L. Jones, I. Jones, N. Craddock. 2006. Genetic variation of brain-derived neurotrophic factor (BDNF) in bipolar disorder. Case-control study of over 3000 individuals from the UK. British Journal of Psychiatry, 188(1). {IF 2007 5.5} [CITATIONS 47] PDF
16. *D. Harold, *S. MacGregor, C. E Patterson, P. Hollingworth, P. Moore, M.J. Owen, J. Williams, M. O'Donovan, P. Passmore, S. McIlroy and L. Jones *JOINT FIRST AUTHORS. 2006. A single nucleotide polymorphism in CHAT influences response to acetylcholinesterase inhibitors in Alzheimer's Disease. Pharmacogenetics and Genomics, 16(2):75-77. {IF 2007 5.8} [CITATIONS 6] PDF
17. S. Macgregor, N. Craddock, P.A. Holmans. 2006. Use of phenotypic covariates in association analysis by sequential addition of cases. European Journal of Human Genetics, 14(5):529-34. {IF 2007 4.0} [CITATIONS 9] PDF
18. S. Macgregor, P.M. Visscher, G. Montgomery. 2006. Analysis of pooled DNA samples on high density arrays without prior knowledge of differential hybridization rates. Nucleic Acids Research, 34(7):e55. {IF 2007 7.0} [CITATIONS 23] PDF
19. S. Macgregor and I.A. Khan. 2006. GAIA: An easy-to-use web-based application for interaction analysis of case-control data. BMC Medical Genetics, 7(1):34. {IF 2007 2.4} [CITATIONS 8] PDF
20. E. Forty, L. Jones, S. Macgregor, S. Caesar, C. Cooper, A. Hough, L. Dean, S. Dave, A. Farmer, P. McGuffin, S. Brewster, N. Craddock, I. Jones. 2006. Familiality of Postpartum Depression in Unipolar Disorder: Results of a Family Study. Am. J. Psychiat., 163(9):1549-53. {IF 2007 9.1} [CITATIONS 21] PDF
21. L. Georgieva, V. Moskvina, T. Peirce, N. Norton, N. Bray, L. Jones, P. Holmans, S. Macgregor, S. Zammit, J. Wilkinson, H. Williams, I. Nikolov, N. Williams, D. Ivanov, K.L. Davis, V. Haroutunian, J. D. Buxbaum, N. Craddock, G. Kirov, M.J. Owen, M.C. O'Donovan. 2006. Convergent evidence that oligodendrocyte lineage transcription factor 2 (OLIG2) and interacting genes influence susceptibility to schizophrenia. Proceedings of the National Academy of Sciences of the United States of America (PNAS), 103(33):12469-12474. {IF 2007 9.6} [CITATIONS 30] PDF
22. S. Macgregor, B. Cornes, N.G. Martin, P.M. Visscher. 2006. Bias, precision and heritability of self-reported and clinically measured height in Australian twins. Human Genetics, 120: 571-580. {IF 2007 4.0} [CITATIONS 19] PDF
23. S. Macgregor. 2007. Most pooling variation in array based DNA pooling is attributable to array error rather than pool construction error. European Journal of Human Genetics 15: 501-504. {IF 2007 4.0} [CITATIONS 13] PDF
24. P.M. Visscher, S. Macgregor, B. Benyamin, G. Zhu, S. Gordon, S. Medland, W.G. Hill, J. Hottenga, G. Willemsen, D.I. Boomsma, Y. Liu, H. Deng, G.W. Montgomery, N.G. Martin. 2007. Genome Partitioning of Genetic Variation for Height from 11,214 Sibling Pairs. American Journal of Human Genetics, 81:1104-1110. {IF 2007 11.1} [CITATIONS 15] PDF
25. S. Macgregor, Z.Z. Zhao, A. Henders, N.G. Martin, G.W. Montgomery, P.M. Visscher. 2008. Highly cost efficient genome wide association studies using DNA pools and dense SNP arrays,  Nucleic Acids Research, 36(6):e35. {IF 2007 7.0} [CITATIONS 17] PDF
26. S. Macgregor. 2008. Optimal two stage hypothesis testing for family based genome wide association studies. American Journal of Human Genetics, 82:797-799. {IF 2007 11.1} [CITATIONS 1] PDF
27. P. Lind, S. Macgregor, G.W. Montgomery, A. C. Heath, N.G. Martin, J.B. Whitfield. 2008 Effects of GABRA2 Variation on Physiological, Psychomotor and Subjective Responses in the Alcohol Challenge Twin Study. Twin Research and Human Genetics, 11(2):174-82. {IF 2007 1.5} [CITATIONS 2]. PDF
28. M. Ayub, M.Irfan, A. Maclean, F. Naeem, S. MacGregor, P.M. Visscher, W. Muir, D. Blackwood. 2008. Linkage analysis in a large family from Pakistan with depression and a high incidence of consanguineous marriages, Human Heredity, 66(3):190-198. {IF 2007 2.2} [CITATIONS 1] PDF
29. K. M. Brown*, S MacGregor*, G. W. Montgomery, D. W. Craig, Z. Z. Zhao, K. Iyadurai, A. Henders, N. Homer, M. Campbell, M. Stark, S. Thomas, H. Schmid, E. A Holland, E. M. Gillanders, D. L. Duffy, J. A. Maskiell, J. Jetann, M. Ferguson, D. A. Stephan, A. E. Cust, D. Whiteman, A. Green, H. Olsson, S. Puig, P. Ghiorzo, J. Hansson, F. Demenais, A. M. Goldstein, N. A. Gruis, D. E. Elder, J. Newton Bishop, R. F. Kefford, G. G. Giles, B. K. Armstrong, J. F. Aitken, J. L. Hopper, N. G. Martin, J. M. Trent, G. J. Mann, N. K. Hayward 2008 *JOINT FIRST AUTHORS – CORRESPONDING AUTHOR, S. MACGREGOR. Common sequence variants on 20q11.22 confer melanoma susceptibility, Nature Genetics, 40(7):838-40. {IF 2007 25.6} [CITATIONS 36]. PDF
30. S. Macgregor, J.J. Hottenga, P.A. Lind, H.E.D. Suchiman, G. Willemsen, P.E. Slagboom, G.W. Montgomery, N.G. Martin, P.M. Visscher, D.I. Boomsma. 2008. Vitamin D receptor gene polymorphisms have negligible effect on human height, Twin Research and Human Genetics,  11(5):488-494. {IF 2007 1.5} [CITATIONS 0]. PDF
31. P. A. Lind*, S. MacGregor*, A. Agrawal, G. W. Montgomery, A. C. Heath, N. G. Martin, J. B. Whitfield. 2008 *JOINT FIRST AUTHORS. The Role of GABRA2 in Alcohol Dependence, Smoking and Illicit Drug Use in an Australian Population Sample, Alcoholism: Clinical and Experimental Research. 32(10):1-11. {IF 2007 3.2} [CITATIONS 5]. PDF
32. The International Schizophrenia Consortium, comprising; J. L. Stone, M. C. O’Donovan, H. Gurling, G. K. Kirov, D. H. R. Blackwood, A. Corvin, N. J. Craddock, M. Gill, C. M. Hultman, P. Lichtenstein, A. McQuillin, C. N. Pato1, D. M. Ruderfer, M. J. Owen, D. St Clair, P. F. Sullivan, E. M. Scolnick, D. M. Ruderfer, J. Korn, S. Macgregor, D. W. Morris, C. T. O’Dushlaine, M. J. Daly, P. M. Visscher, P. A. Holmans, P. Sklar, S. M. Purcell 2008 Rare chromosomal deletions and duplications increase risk of schizophrenia, Nature 455(7210):237-241. {IF 2007 28.8} [CITATIONS 148]. PDF PDFsupplementary
33. B. P. Zietsch, K. I. Morley, S. N. Shekar, K. J. H. Verweij, M. C. Keller, S. Macgregor, M. J. Wright, J. M. Bailey, N. G. Martin. 2008. Genetic factors predisposing to homosexuality may increase mating success in heterosexuals, Evolution and Human Behavior, 29(6), 424-433. {IF 2007 2.5} [CITATIONS 5]. PDF
34. R. Kaneva, V. Milanova, D. Angelicheva, S. MacGregor, C. Kostov, R Vladimirova, S Aleksiev, M Angelova, V Stoyanova, A Loh, J Hallmayer, L Kalaydjieva, A Jablensky. 2009. Bipolar Disorder in the Bulgarian Gypsies: Genetic Heterogeneity in a Young Founder Population, Am J Med Genet Part B, 150B(2):191-201 {IF 2007 4.2} [CITATIONS 0]. PDF
35. S. Macgregor, P.A. Lind, K.K. Bucholz, N.K. Hansell, P.A. Madden, M.M. Richter, G.W. Montgomery, N.G. Martin, A.C. Heath, J.B. Whitfield. 2009. Associations of ADH and ALDH2 gene variation with self report alcohol reactions, consumption and dependence: an integrated analysis. Hum Mol Genet. 18(3):580-93. {IF 2007 7.8} [CITATIONS 9] PDF
36. E.K. Green, D. Grozeva, R. Raybould, G. Elvidge, S. Macgregor, I. Craig, A. Farmer, P. McGuffin, L. Forty, L. Jones, I. Jones, M.C. O'Donovan, M.J. Owen, G. Kirov, N. Craddock. 2009. P2RX7: A bipolar and unipolar disorder candidate susceptibility gene? Am J Med Genet B Neuropsychiatr Genet., 150B(8):1063-9. {IF 2007 4.2} [CITATIONS 0] PDF
37. The International Schizophrenia Consortium; S.M. Purcell, N.R. Wray, J.L. Stone, P.M. Visscher, M.C. O’Donovan, P.F. Sullivan, P. Sklar, D.M. Ruderfer, A. McQuillin, D.W. Morris, A. Corvin, C.T. O'Dushlaine, P.A.Holmans, S. MacGregor, H.Gurling, D.H.R. Blackwood, N.J. Craddock, M.Gill, C.M. Hultman, G. K. Kirov, P. Lichtenstein,  M.J. Owen, C.N. Pato, E.M. Scolnick, D. St. Clair. 2009. Common polygenic variation contributes to risk of schizophrenia and overlaps with bipolar disorder, Nature, 460(7256), 748-752. {IF 2007 28.8}. [CITATIONS 31] PDF PDFsupplementary
38. J.E. Craig, A.W. Hewitt, A.E. McMellon, A.K. Henders, L. Ma, L. Wallace, S. Sharma, K.P. Burdon, P.M. Visscher, G.W. Montgomery, S. MacGregor. 2009 Rapid inexpensive genome-wide association using pooled whole blood, Genome Research, 19:2075-2080. {IF 2008 10.2} [CITATIONS 0]. PDF
39. S.E. Medland, D.R. Nyholt, J.N. Painter, B.P. McEvoy, A.F. McRae,Gu Zhu, S.D. Gordon, N.R. Wray, M.A.R. Ferreira, M.J. Wright, A.K. Henders, M.J. Campbell, D.L. Duffy, N.K. Hansell, S. Macgregor,W.S. Slutske, A.C. Heath, G.W. Montgomery, N.G. Martin. 2009 Common variants in the Trichohyalin gene are associated with straight hair in Europeans, American Journal of Human Genetics, 85:750-755 {IF 2007 11.} [CITATIONS 0]. PDF
40. S. Macgregor, C. Bellis, R.A. Lea, H. Cox, T. Dyer, J. Blangero, P.M. Visscher, L.R. Griffiths. 2010. Legacy of Mutiny on the Bounty: Founder Effect and Admixture on Norfolk Island, European Journal of Human Genetics, 18: 67-72. {IF 2007 4.0} [CITATIONS 0] PDF
41. B.P. McEvoy, Z.Z. Zhao, S. Macgregor, C. Bellis, R.A. Lea, H. Cox, G.W. Montgomery, L.R. Griffiths, P.M. Visscher. European and Polynesian Admixture in the Norfolk Island Population, Heredity, accepted Nov 2009 {IF 2008 3.8} [CITATIONS 0]. PDF
42. P.A. Lind*, S. Macgregor*, J.M. Vink*, M.L. Pergadia*, N.K. Hansell, M.H.M. de Moor, A.B. Smit, J.J. Hottenga, M.M. Richter, A.C. Heath, N.G. Martin, G. Willemsen, E.J.C. de Geus, N. Vogelzangs, B.W. Penninx, J.B. Whitfield, G.W. Montgomery, D.I. Boomsma and P.A.F. Madden 2010 *JOINT FIRST AUTHORS A Genomewide Association Study of Nicotine and Alcohol Dependence in Australian and Dutch Populations, Twin Research and Human Genetics, 13(1):10-29. {IF 2007 1.5} [CITATIONS 0]. PDF
43. Y. Lu, D.P. Dimasi , P.G. Hysi, A.W. Hewitt, K.P. Burdon, T. Toh, J.B. Ruddle, Y. Li, P. Mitchell, P.R. Healey, G.W. Montgomery, T.D. Spector, N.G. Martin, T.L. Young, C.J. Hammond, S. MacGregor*, D. Mackey*, J. Craig* 2010 *JOINT SENIOR AUTHORS. Common Genetic Variants near the Brittle Cornea Syndrome Locus ZNF469 Influence the Blinding Disease Risk Factor Central Corneal Thickness., in press, accepted March 2010, PLoS Genet. {IF 2008 8.8}
44. S. Macgregor, A.W. Hewitt, P.G. Hysi, J.B. Ruddle, S.E. Medland, A.K. Henders, S.D. Gordon, T. Andrew, B. McEvoy, P.G. Sanfilippo, F. Carbonaro, V. Tah, Y. Li, S.L. Bennett, J.E. Craig, G.W. Montgomery, K. Tran-Viet , N.L. Brown, T.D. Spector, N.G. Martin, T.L. Young, C.J. Hammond, D.A. Mackey. Genome-wide association identifies ATOH7 as a major gene determining human optic disc size, in press, accepted April 2010, Human Molecular Genetics. {IF 2007 7.8} PDF
45. S.E. Johnatty, J. Beesley, X. Chen, S. Macgregor, D.L. Duffy, A.B. Spurdle, A. deFazio, N. Gava, P.M. Webb, Australian Ovarian Cancer Study Group, Australian Cancer Study (Ovarian Cancer), M. Rossing, J.A. Doherty, M.T. Goodman, G. Lurie, P. J. Thompson, L.R. Wilkens, R.B. Ness, K.B. Moysich, J.C. Claude, S. Wang-Gohrke, D.W. Cramer, K.L. Terry, S.E. Hankinson, S.S. Tworoger, M. Garcia-Closas, H. Yang, J. Lissowska, S.J. Chanock, P. D. Pharoah, H. Song, A.S. Whitemore, C.L. Pearce, D.O. Stram, A.H. Wu, M.C. Pike, S.A. Gayther, S.J. Ramus, U. Menon, A. Gentry-Maharaj, H. Anton-Culver, A. Ziogas, E. Hogdall, S. Kruger-Kjaer, C. Hogdall, A. Berchuck , J.M. Schildkraut, E.S. Iversen, P. G. Moorman, C.M. Phelan, T.A. Sellers, J.M. Cunningham, R.A. Vierkant, D.N. Rider, E.L. Goode, I. Haviv, G. Chenevix-Trench. 2010 Evaluation of candidate stromal epithelial cross-talk genes identifies association between risk of serous ovarian cancer and TERT, a cancer susceptibility “hot-spot”, PLoS Genet. e1001016. {IF 2008 8.8} [CITATIONS 0]. PDF
46. K.S. Elliott, E. Zeggini, M.I. McCarthy, J. Gudmundsson, P. Sulem, S. N. Stacey, S. Thorlacius, L. Amundadottir, H. Grönberg, J. Xu, V. Gaborieau, R.A. Eeles, D. E. Neal, J. L. Donovan, F. C. Hamdy, K. Muir, S. Hwang, M.R. Spitz, B. Zanke, L. Carvajal-Carmona, K.M. Brown, Australian Melanoma Family Study Investigators, N. Hayward, S. Macgregor, I.P. Tomlinson, M. Lemire, C.I. Amos, J.M. Murabito, W.B. Isaacs, D.F. Easton, P. Brennan, The PanScan Consortium, R.B Barkardottir, D.F. Gudbjartsson, T. Rafnar, S. J. Chanock, D.J. Hunter, K. Stefansson & J.P. Ioannidis.2010 Evaluation of association of HNF1B variants with diverse cancers: collaborative analysis of data from 19 genome-wide association studies, PLoS ONE 28;5(5):e10858. [CITATIONS 0]. PDF
47. J.Z. Liu, A.F. Mcrae, D.R. Nyholt, S.E. Medland, N.R. Wray, K.M. Brown, Australian Melanoma Family Study Investigators, N.K. Hayward, G.W. Montgomery, P.M. Visscher, N.G. Martin, S. Macgregor. 2010. A versatile gene-based test for genome-wide association studies, American Journal of Human Genetics, 87(1), 139-145. {IF 2007 11.1}  [CITATIONS 0]. PDF
48. P.G. Hysi, T.L. Young, D.A. Mackey, T. Andrew, A. Fernández-Medarde, A.M. Solouki, AW. Hewitt, S. Macgregor, J.R. Vingerling, Y. Li, M.K. Ikram, L.Y. Fai, P.C. Sham, L. Manyes, A. Porteros, M. C. Lopes, F. Carbonaro, S.J. Fahy, N.G. Martin, C.M. van Duijn, T.D. Spector, J. S. Rahi, E.Santos, C.C.W. Klaver, C.J. Hammond. 2010. A genome-wide association study for myopia and refractive error identifies a susceptibility locus at 15q25. Advanced online publication, 12^th September 2010, Nature Genetics.{IF 2007 25.6} [CITATIONS 0]. PDF PDFsupplementary
49. G. Thorleifsson, G.B. Walters, A.W. Hewitt, G. Masson, A. Helgason, A. DeWan, A. Sigurdsson, A. Jonasdottir, S.A. Gudjonsson, K.P. Magnusson, H. Stefansson, D.S.C. Lam,P.O. S. Tam, G.J. Gudmundsdottir, L. Southgate, K.P. Burdon, M.S. Gottfredsdottir, M.A. Aldred, P. Mitchell, D. St Clair, D.A. Collier, N. Tang, O. Sveinsson, S. Macgregor, N.G. Martin, A.J. Cree, J. Gibson, A. MacLeod, A. Jacob, S. Ennis, T.L. Young, J.C.N. Chan, W.S.S. Karwatowski, C.J. Hammond, K. Thordarson, M. Zhang, C. Wadelius, A.J. Lotery, R.C. Trembath, C.P. Pang, J. Hoh, J.E. Craig, A. Kong, D.A. Mackey, F. Jonasson, U. Thorsteinsdottir, K. Stefansson. Common variants near CAV1 and CAV2 are associated with primary open angle glaucoma. Advanced online publication, 12^th September 2010, Nature Genetics.{IF 2007 25.6} [CITATIONS 0]. PDF PDFsupplementary
50. M.K. Ikram, S. Xueling, R.A. Jensen, M. F. Cotch, A.W. Hewitt, M.A. Ikram, J.J. Wang, R. Klein, B.E.K. Klein, M.M.B. Breteler, N. Cheung, G. Liew, P. Mitchell, A.G. Uitterlinden, F. Rivadeneira, A. Hofman, P.T.V.M. de Jong, C.M. van Duijn, L. Kao, C. Cheng, A.V. Smith, N. L. Glazer, T. Lumley, B. McKnight, B.M. Psaty, F. Jonasson, G. Eiriksdottir, T.Aspelund, Global BPgen Consortium, T.B. Harris, L. J. Launer, K.D. Taylor, X.Li, S.K. Iyengar, Q. Xi, T.A. Sivakumaran, D.A. Mackey, S. MacGregor, N.G. Martin, T.L. Young, J.C. Bis, K.L. Wiggins, S.R. Heckbert, C. J. Hammond, T.Andrew, S.Fahy, J. Attia, E.G. Holliday, R. J. Scott, F.M.A. Islam, J.I. Rotter, A.K.McAuley, E. Boerwinkle, E.S. Tai, V. Gudnason, D.S. Siscovick, J.R. Vingerling, T.Y. Wong. Four Novel Loci (19q13, 6q24, 12q24 and 5q14) Influence the Microcirculation in Vivo. In press, accepted August 2010, PLoS Genet.. {IF 2008 8.8}  [CITATIONS 0].
51. J.N. Painter, C.A. Anderson, D.R. Nyholt, S. Macgregor, J. Lin, S.H. Lee , A. Lambert, Z.Z. Zhao, F. Roseman, Qu. Guo, S.D. Gordon, L. Wallace, A.K. Henders, P.M. Visscher, P. Kraft , N.G. Martin, A.P. Morris, S.A. Treloar, S.H. Kennedy, S.A. Missmer, G.W. Montgomery, K.T. Zondervan. Genome-wide association study identifies a locus at 7p15.2 associated with endometriosis, In press, accepted October 2010, Nat Genetics {IF 2007 25.6} [CITATIONS 0].

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Non-peer-reviewed publications

1.      S. Macgregor. 2010. Invited Commentary: Optimal selection of markers from DNA pooling experiments. Behavior Genetics, 40(1), 46-47. {IF 2008 3.3} [CITATIONS 0]. PDF