Published in Nat Genet on December 12, 2010
Bayesian inference analyses of the polygenic architecture of rheumatoid arthritis. Nat Genet (2012) 4.41
New genetic loci link adipose and insulin biology to body fat distribution. Nature (2015) 3.38
Pathogenesis and pathophysiology of endometriosis. Fertil Steril (2012) 2.23
Estimation and partitioning of polygenic variation captured by common SNPs for Alzheimer's disease, multiple sclerosis and endometriosis. Hum Mol Genet (2012) 1.96
Common variants at 6p21.1 are associated with large artery atherosclerotic stroke. Nat Genet (2012) 1.81
Developing symptom-based predictive models of endometriosis as a clinical screening tool: results from a multicenter study. Fertil Steril (2012) 1.50
Extrapelvic endometriosis: a rare entity or an under diagnosed condition? Diagn Pathol (2013) 1.49
Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus. Nat Genet (2013) 1.49
Genome-wide association meta-analysis identifies new endometriosis risk loci. Nat Genet (2012) 1.42
Germline genetic contributions to risk for esophageal adenocarcinoma, Barrett's esophagus, and gastroesophageal reflux. J Natl Cancer Inst (2013) 1.25
Meta-analysis combining new and existing data sets confirms that the TERT-CLPTM1L locus influences melanoma risk. J Invest Dermatol (2011) 1.14
Genome-wide linkage and association analyses implicate FASN in predisposition to Uterine Leiomyomata. Am J Hum Genet (2012) 1.08
Defining future directions for endometriosis research: workshop report from the 2011 World Congress of Endometriosis In Montpellier, France. Reprod Sci (2013) 1.06
Genetic variants in LPL, OASL and TOMM40/APOE-C1-C2-C4 genes are associated with multiple cardiovascular-related traits. BMC Med Genet (2011) 1.06
Endometriosis: a disease that remains enigmatic. ISRN Obstet Gynecol (2013) 1.05
Genome-wide association study link novel loci to endometriosis. PLoS One (2013) 1.05
Human fertility, molecular genetics, and natural selection in modern societies. PLoS One (2015) 1.05
A polymorphism in a let-7 microRNA binding site of KRAS in women with endometriosis. EMBO Mol Med (2012) 1.04
Most common 'sporadic' cancers have a significant germline genetic component. Hum Mol Genet (2014) 1.03
Chronic gastroesophageal reflux disease shares genetic background with esophageal adenocarcinoma and Barrett's esophagus. Hum Mol Genet (2015) 1.01
Molecular network analysis of endometriosis reveals a role for c-Jun-regulated macrophage activation. Sci Transl Med (2014) 0.99
Evidence of a Causal Association Between Insulinemia and Endometrial Cancer: A Mendelian Randomization Analysis. J Natl Cancer Inst (2015) 0.98
Contemporary genetic technologies and female reproduction. Hum Reprod Update (2011) 0.95
MicroRNA 135 regulates HOXA10 expression in endometriosis. J Clin Endocrinol Metab (2011) 0.95
The genetic basis of female reproductive disorders: etiology and clinical testing. Mol Cell Endocrinol (2013) 0.94
Estrogen receptor β regulates endometriotic cell survival through serum and glucocorticoid-regulated kinase activation. Fertil Steril (2016) 0.92
Molecular aspects of development and regulation of endometriosis. Reprod Biol Endocrinol (2014) 0.91
Managing endometriosis-associated infertility. Clin Obstet Gynecol (2011) 0.91
Macrophage migration inhibitory factor antagonist blocks the development of endometriosis in vivo. PLoS One (2012) 0.90
Genetic variants underlying risk of endometriosis: insights from meta-analysis of eight genome-wide association and replication datasets. Hum Reprod Update (2014) 0.90
Nature and nurture of human pain. Scientifica (Cairo) (2013) 0.89
Guidelines for the design, analysis and interpretation of 'omics' data: focus on human endometrium. Hum Reprod Update (2013) 0.89
Fine-mapping of the HNF1B multicancer locus identifies candidate variants that mediate endometrial cancer risk. Hum Mol Genet (2014) 0.87
Genetic variation in the sex hormone metabolic pathway and endometriosis risk: an evaluation of candidate genes. Fertil Steril (2011) 0.87
Genome-wide associations for birth weight and correlations with adult disease. Nature (2016) 0.87
Integrative genomic analysis identifies epigenetic marks that mediate genetic risk for epithelial ovarian cancer. BMC Med Genomics (2014) 0.86
Phenotyping clinical disorders: lessons learned from pelvic organ prolapse. Am J Obstet Gynecol (2012) 0.85
The dynamics of nuclear receptors and nuclear receptor coregulators in the pathogenesis of endometriosis. Hum Reprod Update (2014) 0.85
The Genetics of Infertility: Current Status of the Field. Curr Genet Med Rep (2013) 0.85
Genome-wide enrichment analysis between endometriosis and obesity-related traits reveals novel susceptibility loci. Hum Mol Genet (2014) 0.85
Genetic evidence that lower circulating FSH levels lengthen menstrual cycle, increase age at menopause and impact female reproductive health. Hum Reprod (2016) 0.84
Apolipoprotein E polymorphisms and spontaneous pregnancy loss in patients with endometriosis. Mol Hum Reprod (2012) 0.84
Lack of an association human dioxin detoxification gene polymorphisms with endometriosis in Japanese women: results of a pilot study. Environ Health Prev Med (2012) 0.84
Association between endometriosis and the interleukin 1A (IL1A) locus. Hum Reprod (2014) 0.83
Endometriosis still a challenge. J Med Life (2014) 0.83
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
The Biodemography of Fertility: A Review and Future Research Frontiers. Kolner Z Soz Sozpsychol (2015) 0.83
The future for genetic studies in reproduction. Mol Hum Reprod (2013) 0.81
Evidence of differential allelic effects between adolescents and adults for plasma high-density lipoprotein. PLoS One (2012) 0.81
Shared genetics underlying epidemiological association between endometriosis and ovarian cancer. Hum Mol Genet (2015) 0.81
Allelic Imbalance in Regulation of ANRIL through Chromatin Interaction at 9p21 Endometriosis Risk Locus. PLoS Genet (2016) 0.81
Interplay between Misplaced Müllerian-Derived Stem Cells and Peritoneal Immune Dysregulation in the Pathogenesis of Endometriosis. Obstet Gynecol Int (2013) 0.80
Single-nucleotide polymorphisms in the lysyl oxidase-like protein 4 and complement component 3 genes are associated with increased risk for endometriosis and endometriosis-associated infertility. Fertil Steril (2011) 0.80
Activated glucocorticoid and eicosanoid pathways in endometriosis. Fertil Steril (2012) 0.78
CYP19A1 fine-mapping and Mendelian randomization: estradiol is causal for endometrial cancer. Endocr Relat Cancer (2015) 0.78
Genome-wide association study of susceptibility loci for breast cancer in Sardinian population. BMC Cancer (2015) 0.77
Dysregulated sphingolipid metabolism in endometriosis. J Clin Endocrinol Metab (2014) 0.77
Fine mapping of variants associated with endometriosis in the WNT4 region on chromosome 1p36. Int J Mol Epidemiol Genet (2013) 0.77
CYP19 gene variant confers susceptibility to endometriosis-associated infertility in Chinese women. Exp Mol Med (2014) 0.77
Identification of susceptibility genes for peritoneal, ovarian, and deep infiltrating endometriosis using a pooled sample-based genome-wide association study. Biomed Res Int (2015) 0.77
Coding regions of INHBA, SFRP4 and HOXA10 are not implicated in familial endometriosis linked to chromosome 7p13-15. Mol Hum Reprod (2011) 0.76
Evidence of a genetic link between endometriosis and ovarian cancer. Fertil Steril (2015) 0.76
Failure to detect significant association between estrogen receptor-alpha gene polymorphisms and endometriosis in Japanese women. Environ Health Prev Med (2012) 0.76
Genetic burden associated with varying degrees of disease severity in endometriosis. Mol Hum Reprod (2015) 0.76
Endometriosis is associated with rare copy number variants. PLoS One (2014) 0.76
Methylation of leukocyte DNA and ovarian cancer: relationships with disease status and outcome. BMC Med Genomics (2014) 0.75
Common variants upstream of KDR encoding VEGFR2 and in TTC39B associate with endometriosis. Nat Commun (2016) 0.75
Common variants in the CYP2C19 gene are associated with susceptibility to endometriosis. Fertil Steril (2014) 0.75
Genome-wide genetic analyses highlight mitogen-activated protein kinase (MAPK) signaling in the pathogenesis of endometriosis. Hum Reprod (2017) 0.75
Discover hidden splicing variations by mapping personal transcriptomes to personal genomes. Nucleic Acids Res (2015) 0.75
Association of WNT4 polymorphisms with endometriosis in infertile patients. J Assist Reprod Genet (2015) 0.75
PLINK: a tool set for whole-genome association and population-based linkage analyses. Am J Hum Genet (2007) 209.92
Common SNPs explain a large proportion of the heritability for human height. Nat Genet (2010) 35.02
Common polygenic variation contributes to risk of schizophrenia and bipolar disorder. Nature (2009) 33.26
A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer. Nat Genet (2007) 22.96
Genetic Power Calculator: design of linkage and association genetic mapping studies of complex traits. Bioinformatics (2003) 17.92
Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants. Nat Genet (2007) 12.62
Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls. Nature (2010) 12.27
Endometriosis. Lancet (2004) 8.41
Increased accuracy of artificial selection by using the realized relationship matrix. Genet Res (Camb) (2009) 8.38
A genotype calling algorithm for the Illumina BeadArray platform. Bioinformatics (2007) 8.03
Female development in mammals is regulated by Wnt-4 signalling. Nature (1999) 4.13
GWAMA: software for genome-wide association meta-analysis. BMC Bioinformatics (2010) 4.11
Curses--winner's and otherwise--in genetic epidemiology. Epidemiology (2008) 3.19
Common variants in the trichohyalin gene are associated with straight hair in Europeans. Am J Hum Genet (2009) 3.18
Revised American Fertility Society classification of endometriosis: 1985. Fertil Steril (1985) 3.05
A single SNP in an evolutionary conserved region within intron 86 of the HERC2 gene determines human blue-brown eye color. Am J Hum Genet (2008) 3.00
Incidence of laparoscopically confirmed endometriosis by demographic, anthropometric, and lifestyle factors. Am J Epidemiol (2004) 2.72
A major quantitative-trait locus for mole density is linked to the familial melanoma gene CDKN2A: a maximum-likelihood combined linkage and association analysis in twins and their sibs. Am J Hum Genet (1999) 2.15
24-h uric acid excretion and the risk of kidney stones. Kidney Int (2007) 2.14
Endometriosis: cost estimates and methodological perspective. Hum Reprod Update (2007) 2.00
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
HOX gene expression is altered in the endometrium of women with endometriosis. Hum Reprod (1999) 1.72
What makes a good case-control study? Design issues for complex traits such as endometriosis. Hum Reprod (2002) 1.59
The search for genes contributing to endometriosis risk. Hum Reprod Update (2008) 1.58
A genome-wide association study identifies genetic variants in the CDKN2BAS locus associated with endometriosis in Japanese. Nat Genet (2010) 1.57
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
Genetic influences on endometriosis in an Australian twin sample. sueT@qimr.edu.au. Fertil Steril (1999) 1.51
Genetic and environmental contributions to size, color, shape, and other characteristics of melanocytic naevi in a sample of adolescent twins. Genet Epidemiol (1999) 1.51
Estimating relatedness between individuals in general populations with a focus on their use in conservation programs. Genetics (2006) 1.49
Genetic factors contribute to the risk of developing endometriosis. Hum Reprod (2002) 1.42
The International Endogene Study: a collection of families for genetic research in endometriosis. Fertil Steril (2002) 1.28
Chronic gynecological conditions reported by US women: findings from the National Health Interview Survey, 1984 to 1992. Am J Public Health (1996) 1.28
Aberrant methylation at HOXA10 may be responsible for its aberrant expression in the endometrium of patients with endometriosis. Am J Obstet Gynecol (2005) 1.26
Health-related quality of life measurement in women with common benign gynecologic conditions: a systematic review. Am J Obstet Gynecol (2002) 1.23
WNT4 is required for normal ovarian follicle development and female fertility. FASEB J (2010) 1.19
Familial aggregation of endometriosis in a large pedigree of rhesus macaques. Hum Reprod (2004) 1.18
Endometriosis in monozygotic twins. Fertil Steril (1997) 1.13
A prospective study of body size during childhood and early adulthood and the incidence of endometriosis. Hum Reprod (2010) 1.10
The genetic basis of endometriosis. Curr Opin Obstet Gynecol (2001) 1.07
Genetic variation in tumour necrosis factor and lymphotoxin is not associated with endometriosis in an Australian sample. Hum Reprod (2007) 1.06
Wnt4/5a signalling coordinates cell adhesion and entry into meiosis during presumptive ovarian follicle development. Hum Mol Genet (2010) 1.06
Heritability and molecular genetic studies of endometriosis. Ann N Y Acad Sci (2002) 0.96
Deeply infiltrating endometriosis is a disease whereas mild endometriosis could be considered a non-disease. Ann N Y Acad Sci (1994) 0.94
Common variation in the fibroblast growth factor receptor 2 gene is not associated with endometriosis risk. Hum Reprod (2008) 0.89
The genetics of endometriosis. J Reprod Med (1998) 0.83
A second generation human haplotype map of over 3.1 million SNPs. Nature (2007) 85.39
Finding the missing heritability of complex diseases. Nature (2009) 67.95
Common SNPs explain a large proportion of the heritability for human height. Nat Genet (2010) 35.02
Common polygenic variation contributes to risk of schizophrenia and bipolar disorder. Nature (2009) 33.26
Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes. Science (2007) 32.97
Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. Nat Genet (2008) 30.20
Biological, clinical and population relevance of 95 loci for blood lipids. Nature (2010) 28.21
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index. Nat Genet (2010) 23.08
A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer. Nat Genet (2007) 22.96
Six new loci associated with body mass index highlight a neuronal influence on body weight regulation. Nat Genet (2008) 22.35
Genome-wide association study of prostate cancer identifies a second risk locus at 8q24. Nat Genet (2007) 21.18
GCTA: a tool for genome-wide complex trait analysis. Am J Hum Genet (2010) 20.73
Hundreds of variants clustered in genomic loci and biological pathways affect human height. Nature (2010) 20.01
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. Nat Genet (2010) 17.89
Multiple loci identified in a genome-wide association study of prostate cancer. Nat Genet (2008) 17.65
Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. Nat Genet (2010) 17.38
Genome-wide detection and characterization of positive selection in human populations. Nature (2007) 17.27
Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. Nat Genet (2010) 16.96
Identification of ten loci associated with height highlights new biological pathways in human growth. Nat Genet (2008) 16.25
Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease. Nature (2012) 16.13
Common variants near MC4R are associated with fat mass, weight and risk of obesity. Nat Genet (2008) 15.94
Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility. Nat Genet (2007) 13.74
Cholinergic nicotinic receptor genes implicated in a nicotine dependence association study targeting 348 candidate genes with 3713 SNPs. Hum Mol Genet (2006) 13.16
Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants. Nat Genet (2007) 12.62
Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. Nat Genet (2008) 12.32
Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls. Nature (2010) 12.27
Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes. Nat Genet (2012) 11.09
Estimating missing heritability for disease from genome-wide association studies. Am J Hum Genet (2011) 8.95
Genome partitioning of genetic variation for complex traits using common SNPs. Nat Genet (2011) 8.57
Meta-analysis and imputation refines the association of 15q25 with smoking quantity. Nat Genet (2010) 8.55
Prediction of individual genetic risk to disease from genome-wide association studies. Genome Res (2007) 8.48
A versatile gene-based test for genome-wide association studies. Am J Hum Genet (2010) 8.44
A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1). Nat Genet (2009) 8.39
Escalation of drug use in early-onset cannabis users vs co-twin controls. JAMA (2003) 8.29
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. Nat Genet (2013) 8.02
Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47. Nat Genet (2011) 7.98
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
Novel genes identified in a high-density genome wide association study for nicotine dependence. Hum Mol Genet (2006) 7.90
Genome-wide association analysis identifies 13 new risk loci for schizophrenia. Nat Genet (2013) 7.44
Newly discovered breast cancer susceptibility loci on 3p24 and 17q23.2. Nat Genet (2009) 7.30
Data and theory point to mainly additive genetic variance for complex traits. PLoS Genet (2008) 7.15
Assumption-free estimation of heritability from genome-wide identity-by-descent sharing between full siblings. PLoS Genet (2006) 7.13
Mapping cis- and trans-regulatory effects across multiple tissues in twins. Nat Genet (2012) 6.97
Recent human effective population size estimated from linkage disequilibrium. Genome Res (2007) 6.79
Sizing up human height variation. Nat Genet (2008) 6.66
Powerful SNP-set analysis for case-control genome-wide association studies. Am J Hum Genet (2010) 6.60
Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior. Nat Genet (2010) 6.49
Heritability of adult body height: a comparative study of twin cohorts in eight countries. Twin Res (2003) 6.43
A mega-analysis of genome-wide association studies for major depressive disorder. Mol Psychiatry (2012) 6.34
Heterogeneity of breast cancer associations with five susceptibility loci by clinical and pathological characteristics. PLoS Genet (2008) 6.22
The metabochip, a custom genotyping array for genetic studies of metabolic, cardiovascular, and anthropometric traits. PLoS Genet (2012) 6.15
DNA methylation profiles in monozygotic and dizygotic twins. Nat Genet (2009) 5.99
The architecture of gene regulatory variation across multiple human tissues: the MuTHER study. PLoS Genet (2011) 5.95
Genome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distribution. PLoS Genet (2009) 5.81
Performance of common genetic variants in breast-cancer risk models. N Engl J Med (2010) 5.79
Estimating the proportion of variation in susceptibility to schizophrenia captured by common SNPs. Nat Genet (2012) 5.78
Two-stage two-locus models in genome-wide association. PLoS Genet (2006) 5.60
Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array. Nat Genet (2013) 5.58
Conditional and joint multiple-SNP analysis of GWAS summary statistics identifies additional variants influencing complex traits. Nat Genet (2012) 5.55