|
|
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.
|
|
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