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Publications by Dale R. Nyholt

 
55.
54. Holliday EG*, Nyholt DR*, Tirupati S, John S, Ramachandran P, Ramamurti M, Ramadoss AJ, Jeyagurunathan A, Kottiswaran S, Smith H, Filippich C, Nertney D, Watkins WS, Jorde LB, Thara R, Mowry BJ. [*equal contributors].
Strong evidence for a novel schizophrenia risk locus in 1p31.1 in homogeneous pedigrees from Tamil Nadu, India.
Am J Psychiat [in press].
53. Nyholt DR, Gillespie NA, Merikangas KR, Treloar SA, Martin NG, Montgomery GW.
Common Genetic Influences Underlie Comorbidity of Migraine and Endometriosis.
Genet Epidemiol [in press]. 
52. Montgomery GW, Nyholt DR, Zhao ZZ, Treloar SA, Kennedy SH, Zondervan KT.
The Search for Genes Contributing to Endometriosis Risk.
Hum Reprod Update 2008 Jun 5; [Epub ahead of print].
51. Ligthart L*, Nyholt DR*, Hottenga JJ, Distel MA, Willemsen G, Boomsma DI. [*equal contributors].
A genome-wide linkage scan provides evidence for both new and previously reported loci influencing common migraine.
Am J Med Genet B (Neuropsychiatric Genetics). 2008 Mar 24; [Epub ahead of print].
50. Holliday EG, Mowry BJ, Nyholt DR.
A reanalysis of 409 European-Ancestry and African American schizophrenia pedigrees reveals significant linkage to 8p23.3 with evidence of locus heterogeneity.
Am J Med Genet B (Neuropsychiatric Genetics). 2008 Mar 24; [Epub ahead of print].
49. Zhao ZZ, Pollock PM, Thomas S, Treloar SA, Nyholt DR, Montgomery GW.
Common variation in fibroblast growth factor receptor 2 coding region is not associated with endometriosis risk.
Hum Reprod. 2008 23(7):1661-1668.
48. 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 two large cohorts from Australia and the Netherlands.
Arch Gen Psychiat. 2008 65(6):649-658.
47. Anttila V* Nyholt DR*, Kallela M, Artto V, Vepsäläinen S, Jakkula E, Wennerström A, Tikka-Kleemola P, Kaunisto MA, Hämäläinen E, Widén E, Terwilliger J, Merikangas K, Montgomery GW, Martin NG, Daly M, Kaprio J, Peltonen L, Färkkila M, Wessman M, Palotie A. [*equal contributors].
Consistently replicating locus linked to migraine on 10q22-q23.
Am J Hum Genet. 2008 82(5):1051-1063. 
46. 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 5,815 sibling pairs.
Eur J Hum Genet. 2008 16(4):516-524.
45. Visscher PM, Andrew T, Nyholt DR.
Genome-wide association studies of quantitative traits with related individuals: little (power) lost but much to be gained.
Eur J Hum Genet. 2008 16(3):387-390.
44. Zhao ZZ, Nyholt DR, Le L, Thomas S, Engwerda C, Randall L, Treloar SA, Montgomery GW.
Genetic variation in tumour necrosis factor and lymphotoxin is not associated with endometriosis in an Australian sample.
Hum Reprod. 2007 22(9):2389-2397.
43. Treloar SA, Zhao ZZ, Le L, Zondervan KT, Martin NG, Kennedy SH, Nyholt DR, Montgomery GW.
Variants in EMX2 and PTEN do not contribute to risk of endometriosis. 
Mol Hum Reprod. 2007 13(8):587-594.
42. Distel MA, Ligthart L, Willemsen G, Nyholt DR, Trull TJ, Boomsma DI.
Personality, health and lifestyle in a questionnaire family study: a comparison between highly cooperative and less cooperative families. 
Twin Res Hum Genet. 2007 10(2):348-353.
41. Souter VL, Parisi MA, Nyholt DR, Kapur KP, Opheim KE, Gunther DF, Mitchell ME, Glass IA, Montgomery GW.
A case of true hermaphroditism reveals an usual mechanism of twinning.
Hum Genet. 2007 121(2):179-185. 
40. Zondervan KT, Treloar SA, Lin J, Weeks DE, Nyholt DR, Mangion J, MacKay IJ, Cardon LR, Martin NG, Kennedy SH, Montgomery GW.
Significant evidence of one or more susceptibility loci for endometriosis with near-Mendelian inheritance on chromosome 7p13-15.
Hum Reprod. 2007 22(3):717-728. 
39 Nyholt DR.
ssSNPer: identifying statistically similar SNPs to aid interpretation of genetic association studies. 
Bioinformatics 2006 22(23):2960-2961.
38. Zhao ZZ, Nyholt DR, Le L, Martin NG, James MR, Treloar SA, Montgomery GW.
KRAS variation and risk of endometriosis. 
Mol Hum Reprod. 2006 12(11):671-676.
37. Holliday EG, Handoko HY, James MR, McGrath JJ, Nertney DA, Tirupati S, Thara R, Levinson DF, Mowry BJ, Nyholt DR.
Association study of the dystrobrevin-binding gene with schizophrenia in Australian and Indian samples.
Twin Res Hum Genet. 2006 9(4):531-539.
36. Anttila V, Kallela M, Oswell G, Kaunisto MA, Nyholt DR, Hämäläinen E, Havanka H, Ilmavirta M, Terwilliger J, Sobel E, Peltonen L, Kaprio J, Färkkilä M, Wessman M, Palotie A.
Trait components provide tools to dissect the genetic susceptibility of migraine.
Am J Hum Genet. 2006 79(1):85-99.
35. Nyholt DR.
On the probability of dizygotic twins being concordant for two alleles at multiple polymorphic loci.
Twin Res Hum Genet. 2006 9(2):194-197.
34. Ligthart L, Boomsma DI, Martin NG, Stubbe JH, Nyholt DR.
Migraine with aura and migraine without aura are not distinct entities: further evidence from a large Dutch population study.
Twin Res Hum Genet. 2006 9(1):54-63.
33. Warner J, Nyholt DR, Busfield F, Epstein M, Burgess J, Stranks S, Hill P, Perry-Keene D, Learoyd D, Robinson B, Teh BT, Prins JB, Cardinal JW.
Familial isolated hyperparathyroidism is linked to a 1.7 Mb region on chromosome 2p13.3-14.
J Med Genet. 2006 43(3):e12.
32. Mah S, Nelson MR, DeLisi LE, Reneland RH, Markward N, James MR, Nyholt DR, Hayward N, Handoko H, Mowry B, Kammerer S, Braun A.
Identification of the PLXNA2 as a Candidate for Susceptibility to Schizophrenia.
Mol Psychiatry. 2006 11(5):471-478.
31. Nyholt DR.
Evaluation of Nyholt's procedure for multiple testing correction - Authors reply.
Hum Hered. 2005 60(1):61-62.
30. Zhao ZZ, Nyholt DR, James MR, Mayne R, Treloar SA, Montgomery GW.
A comparison of DNA pools constructed following whole genome amplification for two-stage SNP genotyping designs.
Twin Res Hum Genet. 2005 8(4):353-361.
29. Nyholt DR, Morley KI, Ferreira MAR, Medland SE, Boomsma DI, Heath AC, Merikangas KR, Montgomery GW, Martin NG.
Genomewide significant linkage to migrainous headache on chromosome 5q21.
Am J Hum Genet. 2005 77(3):500-512.
28. Treloar SA, Wicks J, Nyholt DR, Montgomery GW, Bahlo M, Smith V, Dawson G, Mackay IJ, Weeks DE, Bennett ST, Carey A, Ewen-White KR, Duffy DL, O'Connor DT, Barlow D, Martin NG, Kennedy SH.
Genomewide linkage study in 1,176 affected sister pair families identifies a significant susceptibility locus for endometriosis on chromosome 10q26.
Am J Hum Genet. 2005 77(3):365-376.
27. Holliday E, Mowry B, Chant D, Nyholt D.
The importance of modelling heterogeneity in complex disease: application to NIMH Schizophrenia Genetics Initiative data.
Hum Genet. 2005 117(2-3):160-167.
26. Lea RA, Nyholt DR, Curtain RP, Ovcaric M, Sciascia R, Bellis C, Macmillan J, Quinlan S, Gibson RA, McCarthy LC, Riley JH, Smithies YJ, Kinrade S, Griffiths LR.
A genome-wide scan provides evidence for loci influencing a severe heritable form of common migraine.
Neurogenetics. 2005 6(2):67-72.
25. Evans DM, Kirk KM, Nyholt DR, Novac C, Martin NG.
Teenage acne is influenced by genetic factors. 
Br J Dermatol 2005 152(3):579-581.
24. Handoko HY*, Nyholt DR*, Hayward NK, Nertney DA, Hannah DE, Windus LC, McCormack CM, Smith HJ, Filippich C, James MR, Mowry BJ. [*equal contributors].
Separate and interacting effects within the catechol-O-methyltransferase (COMT) are associated with schizophrenia.
Mol Psychiatry. 2005 10(6):589-597. [Supplementary Information]
23. Nyholt DR.
A simple correction for multiple testing for SNPs in linkage disequilibrium with each other.
Am J Hum Genet. 2004 74(4):765-769.
22.   Nyholt DR, Gillespie NA, Heath AC, Merikangas KR, Duffy DL, Martin NG.
Latent class analysis does not support migraine with aura and migraine without aura as separate entities. 
Genet Epidemiol. 2004 26(3):231-244. 
21.   Nyholt DR, Gillespie NA, Heath AC, Martin NG.
The Genetic Basis of Male Pattern Baldness. 
J Invest Dermatol. 2003 121(6):1561-1564. 
20.   Mulder E, van Baal C, Gaist D, Kallela M, Kaprio J, Svensson DA, Nyholt DR, Martin NG, MacGregor AJ, Cherkas LF, Boomsma DI, Palotie A.
Genetic and environmental influences on migraine: a twin study across six countries. 
Twin Res. 2003 6(5):422-431.
19.   Souter VL, Kapur RP, Nyholt DR, Skogerboe K, Myerson D, Ton CC, Opheim KE, Easterling TR, Shields LE, Montgomery GW, Glass IA.
A report of dizygous monochorionic twins.
N Engl J Med. 2003 349(2):154-158.
18.   Heath AC, Nyholt DR, Neuman R, Madden PA, Bucholz KK, Todd RD, Nelson EC, Montgomery GW, Martin NG.
Zygosity diagnosis in the absence of genotypic data: an approach using latent class analysis.
Twin Res. 2003 6(1):22-26. 
17.   Lea RA, Shepherd AG, Curtain RP, Nyholt DR, Quinlan S, Brimage PJ, Griffiths LR.
A typical migraine susceptibility region localizes to chromosome 1q31.
Neurogenetics. 2002 4(1):17-22. 
16.   Nyholt DR.
GENEHUNTER: your 'one-stop shop' for statistical genetic analysis?
Hum Hered. 2002 53(1):2-7. Review. 
15.   Chenevix-Trench G, Spurdle AB, Gatei M, Kelly H, Marsh A, Chen X, Donn K, Cummings M, Nyholt D, Jenkins MA, Scott C, Pupo GM, Dork T, Bendix R, Kirk J, Tucker K, McCredie MR, Hopper JL, Sambrook J, Mann GJ, Khanna KK.
Dominant negative ATM mutations in breast cancer families.
J Natl Cancer Inst. 2002 94(3):205-215. 
14.   Li W, Nyholt DR.
Marker selection by Akaike information criterion and Bayesian information criterion.
Genet Epidemiol. 2001 21(Suppl 1):S272-S277. 
13.   Nyholt DR.
Genetic case-control association studies--correcting for multiple testing.
Hum Genet. 2001 Nov;109(5):564-567. 
12.   Liu J*, Nyholt DR*, Magnussen P, Parano E, Pavone P, Geschwind D, Lord C, Iversen P, Hoh J, Ott J, Gilliam TC; Autism Genetic Resource Exchange Consortium. [*equal contributors]
A genomewide screen for autism susceptibility loci.
Am J Hum Genet. 2001 69(2):327-340.
11.   Simonic I, Nyholt DR, Gericke GS, Gordon D, Matsumoto N, Ledbetter DH, Ott J, Weber JL.
Further evidence for linkage of Gilles de la Tourette syndrome (GTS) susceptibility loci on chromosomes 2p11, 8q22 and 11q23-24 in South African Afrikaners.
Am J Med Genet. 2001 105(2):163-167. 
10.   Nyholt DR, Curtain RP, Griffiths LR.
Familial typical migraine: significant linkage and localization of a gene to Xq24-28.
Hum Genet. 2000 107(1):18-23. 
9.   Nyholt DR.
All LODs are not created equal.
Am J Hum Genet. 2000 67(2):282-288. 
8.   Wang WY, Glenn CL, Zhang W, Benjafield AV, Nyholt DR, Morris BJ.
Exclusion of angiotensinogen gene in molecular basis of human hypertension: sibpair linkage and association analyses in Australian anglo-caucasians.
Am J Med Genet. 1999 87(1):53-60. 
7.   Benjafield AV, Jeyasingam CL, Nyholt DR, Griffiths LR, Morris BJ.
G-protein beta3 subunit gene (GNB3) variant in causation of essential hypertension.
Hypertension. 1998 32(6):1094-1097. 
6.   Nyholt DR, Lea RA, Goadsby PJ, Brimage PJ, Griffiths LR.
Familial typical migraine: linkage to chromosome 19p13 and evidence for genetic heterogeneity.
Neurology. 1998 50(5):1428-1432. 
5.   Nyholt DR, Dawkins JL, Brimage PJ, Goadsby PJ, Nicholson GA, Griffiths LR.
Evidence for an X-linked genetic component in familial typical migraine.
Hum Mol Genet. 1998 7(3):459-463. 
4.   Rutherford S, Nyholt DR, Curtain RP, Quinlan SR, Gaffney PT, Morris BJ, Griffiths LR.
Association of a low density lipoprotein receptor microsatellite variant with obesity.
Int J Obes Relat Metab Disord. 1997 21(11):1032-1037. 
3.   Griffiths LR, Nyholt DR, Curtain RP, Goadsby PJ, Brimage PJ.
Migraine association and linkage studies of an endothelial nitric oxide synthase (NOS3) gene polymorphism.
Neurology. 1997 49(2):614-7. Erratum in: Neurology 1997 49(5):1489.
2.   Nyholt DR, Curtain RP, Gaffney PT, Brimage P, Goadsby PJ, Griffiths LR.
Migraine association and linkage analyses of the human 5-hydroxytryptamine (5HT2A) receptor gene.
Cephalalgia. 1996 16(7):463-467. 
1.   Griffiths LR, Nyholt DR, Curtain RP, Gaffney PT, Morris BJ.
Cross-sectional study of a microsatellite marker in the low density lipoprotein receptor gene in obese normotensives.
Clin Exp Pharmacol Physiol. 1995 22(6-7):496-498. 

 

 
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