PubRank

Dale R Nyholt

Author PubWeight™ 218.79‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Common SNPs explain a large proportion of the heritability for human height. Nat Genet 2010 35.02
2 Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index. Nat Genet 2010 23.08
3 Hundreds of variants clustered in genomic loci and biological pathways affect human height. Nature 2010 20.01
4 A versatile gene-based test for genome-wide association studies. Am J Hum Genet 2010 8.44
5 Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. Nat Genet 2013 8.02
6 Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. Nat Genet 2010 7.94
7 A mega-analysis of genome-wide association studies for major depressive disorder. Mol Psychiatry 2012 6.34
8 Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations. PLoS Genet 2009 4.97
9 Genomic inflation factors under polygenic inheritance. Eur J Hum Genet 2011 4.89
10 GWAS of 126,559 individuals identifies genetic variants associated with educational attainment. Science 2013 4.71
11 Identification of seven loci affecting mean telomere length and their association with disease. Nat Genet 2013 3.87
12 Common variants in the trichohyalin gene are associated with straight hair in Europeans. Am J Hum Genet 2009 3.18
13 Identification of IL6R and chromosome 11q13.5 as risk loci for asthma. Lancet 2011 3.03
14 A quantitative-trait genome-wide association study of alcoholism risk in the community: findings and implications. Biol Psychiatry 2011 2.87
15 FTO genotype is associated with phenotypic variability of body mass index. Nature 2012 2.77
16 Genome-wide association study identifies susceptibility loci for open angle glaucoma at TMCO1 and CDKN2B-AS1. Nat Genet 2011 2.42
17 Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1. Nat Genet 2010 2.35
18 Common variants in TMPRSS6 are associated with iron status and erythrocyte volume. Nat Genet 2009 2.29
19 Genetic and environmental influences on migraine: a twin study across six countries. Twin Res 2003 2.22
20 Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways. Nat Genet 2012 2.12
21 Genome-wide association study identifies a locus at 7p15.2 associated with endometriosis. Nat Genet 2010 2.04
22 Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption. Proc Natl Acad Sci U S A 2011 2.01
23 Estimation and partitioning of polygenic variation captured by common SNPs for Alzheimer's disease, multiple sclerosis and endometriosis. Hum Mol Genet 2012 1.96
24 Susceptibility variants for male-pattern baldness on chromosome 20p11. Nat Genet 2008 1.80
25 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 1.76
26 A report of dizygous monochorionic twins. N Engl J Med 2003 1.73
27 Meta-analysis of telomere length in 19,713 subjects reveals high heritability, stronger maternal inheritance and a paternal age effect. Eur J Hum Genet 2013 1.72
28 On Jim Watson's APOE status: genetic information is hard to hide. Eur J Hum Genet 2008 1.67
29 Genome-wide association analysis identifies susceptibility loci for migraine without aura. Nat Genet 2012 1.64
30 The search for genes contributing to endometriosis risk. Hum Reprod Update 2008 1.58
31 A simple and fast two-locus quality control test to detect false positives due to batch effects in genome-wide association studies. Genet Epidemiol 2010 1.57
32 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 2009 1.51
33 Genome-wide association study identifies a new melanoma susceptibility locus at 1q21.3. Nat Genet 2011 1.46
34 Genetic basis of male pattern baldness. J Invest Dermatol 2003 1.36
35 Genetic influences on handedness: data from 25,732 Australian and Dutch twin families. Neuropsychologia 2008 1.34
36 KRAS variation and risk of endometriosis. Mol Hum Reprod 2006 1.33
37 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 1.32
38 Sequence variants in three loci influence monocyte counts and erythrocyte volume. Am J Hum Genet 2009 1.28
39 Association between ORMDL3, IL1RL1 and a deletion on chromosome 17q21 with asthma risk in Australia. Eur J Hum Genet 2010 1.27
40 Migraine with aura and migraine without aura are not distinct entities: further evidence from a large Dutch population study. Twin Res Hum Genet 2006 1.25
41 Within-family outliers: segregating alleles or environmental effects? A linkage analysis of height from 5815 sibling pairs. Eur J Hum Genet 2008 1.25
42 Genome-wide association studies of quantitative traits with related individuals: little (power) lost but much to be gained. Eur J Hum Genet 2008 1.16
43 Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases. PLoS Genet 2012 1.14
44 Personality, health and lifestyle in a questionnaire family study: a comparison between highly cooperative and less cooperative families. Twin Res Hum Genet 2007 1.13
45 A genome-wide association study of Cloninger's temperament scales: implications for the evolutionary genetics of personality. Biol Psychol 2010 1.12
46 Zygosity diagnosis in the absence of genotypic data: an approach using latent class analysis. Twin Res 2003 1.08
47 Genome-wide linkage and association analyses implicate FASN in predisposition to Uterine Leiomyomata. Am J Hum Genet 2012 1.08
48 Genetic variation in tumour necrosis factor and lymphotoxin is not associated with endometriosis in an Australian sample. Hum Reprod 2007 1.06
49 Meta-analysis of genome-wide association for migraine in six population-based European cohorts. Eur J Hum Genet 2011 1.04
50 Inference of the genetic architecture underlying BMI and height with the use of 20,240 sibling pairs. Am J Hum Genet 2013 1.04
51 Telomere length in circulating leukocytes is associated with lung function and disease. Eur Respir J 2013 1.04
52 Consistently replicating locus linked to migraine on 10q22-q23. Am J Hum Genet 2008 0.99
53 A genome-wide association study of sleep habits and insomnia. Am J Med Genet B Neuropsychiatr Genet 2013 0.98
54 Loci affecting gamma-glutamyl transferase in adults and adolescents show age × SNP interaction and cardiometabolic disease associations. Hum Mol Genet 2011 0.98
55 A comparison of DNA pools constructed following whole genome amplification for two-stage SNP genotyping designs. Twin Res Hum Genet 2005 0.97
56 A typical migraine susceptibility region localizes to chromosome 1q31. Neurogenetics 2002 0.95
57 Genome-wide linkage analysis of multiple measures of neuroticism of 2 large cohorts from Australia and the Netherlands. Arch Gen Psychiatry 2008 0.94
58 A genome-wide association study of caffeine-related sleep disturbance: confirmation of a role for a common variant in the adenosine receptor. Sleep 2012 0.94
59 Genetic risk score analysis indicates migraine with and without comorbid depression are genetically different disorders. Hum Genet 2013 0.94
60 A case of true hermaphroditism reveals an unusual mechanism of twinning. Hum Genet 2006 0.93
61 Significant evidence of one or more susceptibility loci for endometriosis with near-Mendelian inheritance on chromosome 7p13-15. Hum Reprod 2006 0.93
62 Variants in EMX2 and PTEN do not contribute to risk of endometriosis. Mol Hum Reprod 2007 0.93
63 Susceptibility locus on chromosome 1q23-25 for a schizophrenia subtype resembling deficit schizophrenia identified by latent class analysis. Arch Gen Psychiatry 2009 0.92
64 GWAS of butyrylcholinesterase activity identifies four novel loci, independent effects within BCHE and secondary associations with metabolic risk factors. Hum Mol Genet 2011 0.91
65 High-density fine-mapping of a chromosome 10q26 linkage peak suggests association between endometriosis and variants close to CYP2C19. Fertil Steril 2011 0.89
66 Polymorphisms in the vascular endothelial growth factor gene and the risk of familial endometriosis. Mol Hum Reprod 2008 0.89
67 Common variation in the fibroblast growth factor receptor 2 gene is not associated with endometriosis risk. Hum Reprod 2008 0.89
68 Genome-wide meta-analysis of common variant differences between men and women. Hum Mol Genet 2012 0.88
69 The shared genetics of migraine and anxious depression. Headache 2010 0.87
70 Association study of the dystrobrevin-binding gene with schizophrenia in Australian and Indian samples. Twin Res Hum Genet 2006 0.86
71 Educational attainment: a genome wide association study in 9538 Australians. PLoS One 2011 0.86
72 A genome-wide linkage scan provides evidence for both new and previously reported loci influencing common migraine. Am J Med Genet B Neuropsychiatr Genet 2008 0.86
73 Androgenetic alopecia: identification of four genetic risk loci and evidence for the contribution of WNT signaling to its etiology. J Invest Dermatol 2013 0.85
74 Migraine symptomatology and major depressive disorder. Cephalalgia 2010 0.84
75 Strong evidence for a novel schizophrenia risk locus on chromosome 1p31.1 in homogeneous pedigrees from Tamil Nadu, India. Am J Psychiatry 2008 0.83
76 Heritability and genome-wide linkage analysis of migraine in the genetic isolate of Norfolk Island. Gene 2011 0.83
77 No evidence for genetic association with the let-7 microRNA-binding site or other common KRAS variants in risk of endometriosis. Hum Reprod 2012 0.83
78 Common Variation in the CYP17A1 and IFIT1 Genes on Chromosome 10 Does Not Contribute to the Risk of Endometriosis. Open Reprod Sci J 2008 0.81
79 Variation in BMPR1B, TGFRB1 and BMPR2 and control of dizygotic twinning. Twin Res Hum Genet 2011 0.80
80 Unique X-linked familial FSGS with co-segregating heart block disorder is associated with a mutation in the NXF5 gene. Hum Mol Genet 2013 0.80
81 Linkage and heritability analysis of migraine symptom groupings: a comparison of three different clustering methods on twin data. Hum Genet 2009 0.80
82 Bayesian latent trait modeling of migraine symptom data. Hum Genet 2009 0.79
83 Evaluation of polymorphisms in predicted target sites for micro RNAs differentially expressed in endometriosis. Mol Hum Reprod 2010 0.79
84 Corrigendum: Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine. Nat Genet 2016 0.77
85 Fine mapping of variants associated with endometriosis in the WNT4 region on chromosome 1p36. Int J Mol Epidemiol Genet 2013 0.77
86 Letter to the editor: Further evidence is required to confirm association between CACNA1C gene variants and bipolar affective disorder. Psychol Med 2010 0.75
87 Genetic variation in female BMI increases with number of children born but failure to replicate association between GNbeta3 variants and increased BMI in parous females. Twin Res Hum Genet 2009 0.75
88 Corrigendum: Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis. Nat Commun 2015 0.75
89 Association mapping. Methods Mol Biol 2011 0.75