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QIMR Neurogenetics Laboratory Homepage > Dale's Homepage > Publications for Dale R. Nyholt

Publications by Dale R. Nyholt

 

77.

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.

Am J Hum Genet. 2010 87(1):139-145. [Suppl]

76.

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.

Nat Genet. 2010 42(7):565-569. [Suppl]

75.

Ligthart L, Nyholt DR, Penninx BW, Boomsma DI.

The Shared Genetics of Migraine and Anxious Depression.

Headache. 2010 Jun 10. [Epub ahead of print]

74.

Painter JN, Willemsen G, Nyholt D, Hoekstra C, Duffy DL, Henders AK, Wallace L, Healey S, Cannon-Albright LA, Skolnick M, Martin NG, Boomsma DI, Montgomery GW.

A genome wide linkage scan for dizygotic twinning in 525 families of mothers of dizygotic twins.

Hum Reprod. 2010 25(6):1569-1580.

73.

Medland SE, Zayats T, Glaser B, Nyholt DR, Gordon SD, Wright MJ, Montgomery GW, Campbell MJ, Henders AK, Timpson NJ, Peltonen L, Wolke D, Ring SM, Deloukas P, Martin NG, Smith GD, Evans DM.

A Variant in LIN28B Is Associated with 2D:4D Finger-Length Ratio, a Putative Retrospective Biomarker of Prenatal Testosterone Exposure.

Am J Hum Genet. 2010 86(4):519-525. [Suppl]

72.

Nyholt DR.

Letter to the Editor: Further evidence is required to confirm association between CACNA1C gene variants and bipolar affective disorder.

Psychol Med. 2010 40(4):702-704.

71.

Ferreira MA, Mangino M, Brumme CJ, Zhao ZZ, Medland SE, Wright MJ, Nyholt DR, Gordon S, Campbell M, McEvoy BP, Henders A, Evans DM, Lanchbury JS, Pereyra F; International HIV Controllers Study, Walker BD, Haas DW, Soranzo N, Spector TD, de Bakker PI, Frazer IH, Montgomery GW, Martin NG.

Quantitative Trait Loci for CD4:CD8 Lymphocyte Ratio Are Associated with Risk of Type 1 Diabetes and HIV-1 Immune Control.

Am J Hum Genet. 2010 86(1):88-92. [Suppl]

70.

Medland SE, Nyholt DR, Painter JN, McEvoy BP, McRae AF, Zhu G, Gordon SD, Ferreira MAR, Wright MJ, Henders AK, Campbell MJ, Duffy DL, Hansell NK, Macgregor S, Slutske WS, Heath AC, Montgomery GW, Martin NG.

Common Variants in the Trichohyalin Gene Are Associated with Straight Hair in Europeans.

Am J Hum Genet. 2009 85(5):750-755. [Suppl]

69.

Ferreira MA, Hottenga JJ, Warrington NM, Medland SE, Willemsen G, Lawrence RW, Gordon S, de Geus EJ, Henders AK, Smit JH, Campbell MJ, Wallace L, Evans DM, Wright MJ, Nyholt DR, James AL, Beilby JP, Penninx BW, Palmer LJ, Frazer IH, Montgomery GW, Martin NG, Boomsma DI.

Sequence Variants in Three Loci Influence Monocyte Counts and Erythrocyte Volume.

Am J Hum Genet. 2009 85(5):745-749. [Suppl]

68.

Benyamin B, Ferreira MA, Willemsen G, Gordon S, Middelberg RP, McEvoy BP, Hottenga JJ, Henders AK, Campbell MJ, Wallace L, Frazer IH, Heath AC, de Geus EJ, 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.

Nat Genet. 2009 41(11):1173-1175. [Suppl]

67.

Kolz M, Johnson T, Sanna S, Teumer A, Vitart V, Perola M, Mangino M, Albrecht E, Wallace C, Farrall M, Johansson A, Nyholt DR, Aulchenko Y, Beckmann JS, Bergmann S, Bochud M, Brown M, Campbell H; EUROSPAN Consortium, Connell J, Dominiczak A, Homuth G, Lamina C, McCarthy MI; ENGAGE Consortium, Meitinger T, Mooser V, Munroe P, Nauck M, Peden J, Prokisch H, Salo P, Salomaa V, Samani NJ, Schlessinger D, Uda M, Völker U, Waeber G, Waterworth D, Wang-Sattler R, Wright AF, Adamski J, Whitfield JB, Gyllensten U, Wilson JF, Rudan I, Pramstaller P, Watkins H; PROCARDIS Consortium, Doering A, Wichmann HE; KORA Study, Spector TD, Peltonen L, Völzke H, Nagaraja R, Vollenweider P, Caulfield M; WTCCC, Illig T, Gieger C.

Meta-Analysis of 28,141 Individuals Identifies Common Variants within Five New Loci That Influence Uric Acid Concentrations.

PLoS Genet. 2009 Jun;5(6):e1000504.

66.

Cornes BK, Medland SE, Lind PA, Nyholt DR, Montgomery GW, Martin NG.

Genetic variation in female BMI increases with number of children born but failure to replicate association between GNβ3 variants and increased BMI in parous females.
Twin Res Hum Genet. 2009 12(3):276-285.

65.

Holliday EG, McLean DE, Nyholt DR, Mowry BJ.
Susceptibility locus on chromosome 1q23-25 for a schizophrenia subtype resembling deficit schizophrenia identified by latent class analysis
Arch Gen Psychiat. 2009 66(10):1058-1067.

64.

Wieser T, Dresler K, Evers S, Gaul C, König D, Hölzl D, Berger K, Nyholt D, Deufel T.
No influence of 5-HTTLPR gene polymorphism on migraine symptomatology, comorbid depression, and chronification.
Headache 2009 Apr 27. [Epub ahead of print].

63.

Chen CC, Keith JM, Nyholt DR, Martin NG, Mengersen KL.
Bayesian latent trait modeling of migraine symptom data.
Hum Genet. 2009 126(2):277-288.

62.

Chen CC, Mengersen KL, Keith JM, Martin NG, Nyholt DR. 
Linkage and heritability analysis of migraine symptom groupings: a comparison of three different clustering methods on twin data. 
Hum Genet. 2009 125(5-6):591-604.

61.

Cornes BK, Lind PA, Medland SE, Montgomery GW, Nyholt DR, Martin NG.
Replication of the association of common rs9939609 variant of FTO with increased BMI in an Australian adult twin population but no evidence for Gene by Environment (G×E) Interaction. 
Int J Obesity. 2009 33(1):75-79.

60.

Nyholt DR, Yu C-E, Visscher PM.
On Jim Watson’s APOE status: genetic information is hard to hide.
Eur J Hum Genet. 2009 17(2):147-149.

59.

Hillmer AM, Brockschmidt FF, Hanneken S, Eigelshoven S, Steffens M, Flaquer A, Herms A, Becker T, Kortüm A-K, Nyholt DR, Zhao ZZ, Montgomery GW, Martin NG, Mühleisen TW, Alblas MA, Moebus S, Jöckel K-H, Bröcker-Preuss M, Erbel R, Reinartz R, Betz RC, Cichon S, Propping P, Baur MP, Wienker TF, Kruse R, Nöthen MM.
A genome-wide association scan identifies new susceptibility variants for male pattern baldness on chromosome 20p11.
Nat Genet. 2008 40(11):1279-1281.

58.

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. 2009 166(2):206-215. Erratum in: Am J Psychiatry. 2009 166(2):238.

57.

Medland SE, Duffy DL, Wright MJ, Geffen GM, Hay DA, Levy F, van-Beijsterveldt CEM, Willemsen G, Townsend GC, White V, Hewitt AW, Mackey DA, Bailey JM, Slutske WS, Nyholt DR, Treloar SA, Martin NG, Boomsma DI.
Genetic influences on handedness: data from 25,732 Australian and Dutch twin families.
Neuropsychologia 2009 47(2):330-337.

56.

Nyholt DR, LaForge KS, Kallela M, Alakurtti K, Anttila V, Farkkila M, Hamalainen E, Kaprio J, Kaunisto MA, Heath AC, Montgomery GW, Gobel H, Todt U, Ferrari MD, Launer LJ, Frants RR, Terwindt GM, de Vries B, Verschuren WMM, Brand J, Freilinger T, Pfaffenrath V, Straube A, Ballinger DG, Zhan Y, Daly MJ, Cox DR, Dichgans M, van den Maagdenberg AMJM, Kubisch C, Martin NG, Wessman M, Peltonen L, Palotie A.
A high-density association screen of 155 ion transport genes for involvement with common migraine.
Hum Mol Genet. 2008 17(21):3318-3331.

55.

Zhao ZZ, Nyholt DR, Thomas S, Treloar SA, Montgomery GW.
Polymorphisms in the vascular endothelial growth factor gene and the risk of familial endometriosis.
Mol Hum Reprod. 2008 14(9):531-538.

54.

Nyholt DR, Gillespie NA, Merikangas KR, Treloar SA, Martin NG, Montgomery GW.
Common Genetic Influences Underlie Comorbidity of Migraine and Endometriosis.
Genet Epidemiol. 2009 33(2):105-113. 

53.

Zhao ZZ, Nyholt DR, Le L, Treloar SA, Montgomery GW.
Common Variation in the CYP17A1 and IFIT1 Genes on Chromosome 10 Does Not Contribute to the Risk of Endometriosis.
TORSJ. 2008 1: 35-40.

52.

Montgomery GW, Nyholt DR, Zhao ZZ, Treloar SA, Painter JN, Missmer SA, Kennedy SH, Zondervan KT.
The Search for Genes Contributing to Endometriosis Risk.
Hum Reprod Update. 2008 14(5):447-457.

51.

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.

50.

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. 

49.

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 147B(7):1186-1195.

48.

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 147B(7):1080-1088.

47.

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.

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.

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.

42.

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.

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 semaphorin receptor PLXNA2 as a Candidate for Susceptibility to Schizophrenia.
Mol Psychiatry. 2006 11(5):471-478.

31.

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.

30.

Nyholt DR.
Evaluation of Nyholt's procedure for multiple testing correction - Authors reply.
Hum Hered. 2005 60(1):61-62.

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 A. 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. 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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