Published in PLoS One on March 14, 2013
Physiological and pathophysiological roles for phospholipase D. J Lipid Res (2015) 0.86
Confounding by linkage disequilibrium. J Hum Genet (2013) 0.85
Follow-up to genome-wide linkage and admixture mapping studies implicates components of the extracellular matrix in susceptibility to and size of uterine fibroids. Fertil Steril (2014) 0.84
Evaluation of GWAS candidate susceptibility loci for uterine leiomyoma in the multi-ethnic NIEHS uterine fibroid study. Front Genet (2015) 0.80
Admixture mapping of genetic variants for uterine fibroids. J Hum Genet (2015) 0.79
Fine mapping of the uterine leiomyoma locus on 1q43 close to a lncRNA in the RGS7-FH interval. Endocr Relat Cancer (2015) 0.77
Genetic determinants of uterine fibroid size in the multiethnic NIEHS uterine fibroid study. Int J Mol Epidemiol Genet (2015) 0.75
Correction: Multiple hits for the association of uterine fibroids on human chromosome 1q43. PLoS One (2015) 0.75
Fine Mapping of the Body Fat QTL on Human Chromosome 1q43. PLoS One (2016) 0.75
High cumulative incidence of uterine leiomyoma in black and white women: ultrasound evidence. Am J Obstet Gynecol (2003) 8.59
Germline mutations in FH predispose to dominantly inherited uterine fibroids, skin leiomyomata and papillary renal cell cancer. Nat Genet (2002) 8.19
Uterine fibroids. Lancet (2001) 6.54
Accumulation of Krebs cycle intermediates and over-expression of HIF1alpha in tumours which result from germline FH and SDH mutations. Hum Mol Genet (2005) 4.12
The frequency of uterine leiomyomas. Am J Clin Pathol (1990) 4.00
The complex genetic epidemiology of prostate cancer. Hum Mol Genet (2004) 3.21
Uterine fibroids: the elephant in the room. Science (2005) 3.12
Predisposing gene for early-onset prostate cancer, localized on chromosome 1q42.2-43. Am J Hum Genet (1998) 2.59
Influence of body size and body fat distribution on risk of uterine leiomyomata in U.S. black women. Epidemiology (2005) 2.33
A role for mitochondrial enzymes in inherited neoplasia and beyond. Nat Rev Cancer (2003) 2.26
Why is parity protective for uterine fibroids? Epidemiology (2003) 2.18
Phospholipase D in cell proliferation and cancer. Mol Cancer Res (2003) 2.13
Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways. Nat Genet (2012) 2.12
Post-translational modifications of three members of the human MAP1LC3 family and detection of a novel type of modification for MAP1LC3B. J Biol Chem (2003) 2.06
Epidemiologic contributions to understanding the etiology of uterine leiomyomata. Environ Health Perspect (2000) 1.69
Fumarase: a mitochondrial metabolic enzyme and a cytosolic/nuclear component of the DNA damage response. PLoS Biol (2010) 1.61
Localization of a gene (MCUL1) for multiple cutaneous leiomyomata and uterine fibroids to chromosome 1q42.3-q43. Am J Hum Genet (2001) 1.42
The FH mutation database: an online database of fumarate hydratase mutations involved in the MCUL (HLRCC) tumor syndrome and congenital fumarase deficiency. BMC Med Genet (2008) 1.38
TAGster: efficient selection of LD tag SNPs in single or multiple populations. Bioinformatics (2007) 1.38
Biallelic inactivation of fumarate hydratase (FH) occurs in nonsyndromic uterine leiomyomas but is rare in other tumors. Am J Pathol (2004) 1.37
Familial predisposition to uterine leiomyomas. Int J Gynaecol Obstet (1995) 1.34
Dysregulation of hypoxia pathways in fumarate hydratase-deficient cells is independent of defective mitochondrial metabolism. Hum Mol Genet (2010) 1.33
Hex1: a new human Rad2 nuclease family member with homology to yeast exonuclease 1. Nucleic Acids Res (1998) 1.32
A genome-wide association study identifies three loci associated with susceptibility to uterine fibroids. Nat Genet (2011) 1.31
Association of physical activity with development of uterine leiomyoma. Am J Epidemiol (2006) 1.27
Phospholipase D-structure, regulation and function. Rev Physiol Biochem Pharmacol (2002) 1.23
Involvement of fumarate hydratase in nonsyndromic uterine leiomyomas: genetic linkage analysis and FISH studies. Genes Chromosomes Cancer (2004) 1.19
Growth factors and cytokines in uterine leiomyomas. Semin Reprod Endocrinol (1996) 1.17
Low frequency of somatic mutations in the FH/multiple cutaneous leiomyomatosis gene in sporadic leiomyosarcomas and uterine leiomyomas. Br J Cancer (2002) 1.08
Utilizing HapMap and tagging SNPs. Methods Mol Med (2008) 1.07
Fumarate hydratase enzyme activity in lymphoblastoid cells and fibroblasts of individuals in families with hereditary leiomyomatosis and renal cell cancer. J Med Genet (2006) 1.07
Expression profiling in progressive stages of fumarate-hydratase deficiency: the contribution of metabolic changes to tumorigenesis. Cancer Res (2010) 1.05
Involvement of Exo1b in DNA damage-induced apoptosis. Nucleic Acids Res (2009) 0.98
Reduced expression of fumarate hydratase in clear cell renal cancer mediates HIF-2α accumulation and promotes migration and invasion. PLoS One (2011) 0.97
A quantitative trait locus for body fat on chromosome 1q43 in French Canadians: linkage and association studies. Obesity (Silver Spring) (2006) 0.95
Mitochondrial import of human and yeast fumarase in live mammalian cells: retrograde translocation of the yeast enzyme is mainly caused by its poor targeting sequence. Biochem Biophys Res Commun (2006) 0.93
A genome-wide linkage scan for steroids and SHBG levels in black and white families: the HERITAGE Family Study. J Clin Endocrinol Metab (2002) 0.91
SNPs in Multi-species Conserved Sequences (MCS) as useful markers in association studies: a practical approach. BMC Genomics (2007) 0.89
[Genetic analysis of the predisposition to uterine myoma. Prevalence and morbidity]. Genetika (1989) 0.89
A single nucleotide polymorphism in EXO1 gene is associated with cervical cancer susceptibility in Chinese patients. Int J Gynecol Cancer (2012) 0.87
Genetic variation in metabolic genes, occupational solvent exposure, and risk of non-hodgkin lymphoma. Am J Epidemiol (2011) 0.87
Differential metabolic consequences of fumarate hydratase and respiratory chain defects. Biochim Biophys Acta (2008) 0.86
A proportional hazards model for incidence and induced remission of disease. Biometrics (2002) 0.85
PCAP is the major known prostate cancer predisposing locus in families from south and west Europe. Eur J Hum Genet (2001) 0.84
Results of a high-resolution genome screen of 437 Alzheimer's disease families. Hum Mol Genet (2003) 3.00
Direct determination of molecular haplotypes by chromosome microdissection. Nat Methods (2010) 2.21
Prediction of protein function using protein-protein interaction data. J Comput Biol (2003) 2.15
Two-dimensional transcriptome profiling: identification of messenger RNA isoform signatures in prostate cancer from archived paraffin-embedded cancer specimens. Cancer Res (2006) 2.11
Stem cell pathways contribute to clinical chemoresistance in ovarian cancer. Clin Cancer Res (2011) 2.03
Drinking and drinking patterns and health status in the general population of five areas of China. Alcohol Alcohol (2003) 1.76
Role of activating FcγR gene polymorphisms in Kawasaki disease susceptibility and intravenous immunoglobulin response. Circ Cardiovasc Genet (2012) 1.65
Haplotype-association analysis. Adv Genet (2008) 1.55
Domain dynamics during ferroelectric switching. Science (2011) 1.51
Altered DNA methylation profile in idiopathic pulmonary fibrosis. Am J Respir Crit Care Med (2012) 1.47
Smooth muscle cell-specific runx2 deficiency inhibits vascular calcification. Circ Res (2012) 1.45
Project among African-Americans to explore risks for schizophrenia (PAARTNERS): recruitment and assessment methods. Schizophr Res (2006) 1.19
Genome-wide linkage analysis of 723 affected relative pairs with late-onset Alzheimer's disease. Hum Mol Genet (2007) 1.16
Length bias correction for RNA-seq data in gene set analyses. Bioinformatics (2011) 1.15
Vitamin D deficiency is associated with decreased lung function in Chinese adults with asthma. Respiration (2010) 1.13
The role of the fat mass and obesity associated gene (FTO) in breast cancer risk. BMC Med Genet (2011) 1.12
Haplotype inference for present-absent genotype data using previously identified haplotypes and haplotype patterns. Bioinformatics (2007) 1.09
Comparison of measures of marker informativeness for ancestry and admixture mapping. BMC Genomics (2011) 1.07
Highly efficient photoluminescent graphene oxide with tunable surface properties. Chem Commun (Camb) (2010) 1.06
Prediction of protein function using protein-protein interaction data. Proc IEEE Comput Soc Bioinform Conf (2002) 1.05
Constitutively decreased TGFBR1 allelic expression is a common finding in colorectal cancer and is associated with three TGFBR1 SNPs. J Exp Clin Cancer Res (2010) 1.05
Neuregulin-1 polymorphism in late onset Alzheimer's disease families with psychoses. Am J Med Genet B Neuropsychiatr Genet (2005) 1.05
Haplotype-based methods for detecting uncommon causal variants with common SNPs. Genet Epidemiol (2012) 1.04
Haplotype kernel association test as a powerful method to identify chromosomal regions harboring uncommon causal variants. Genet Epidemiol (2013) 1.04
Polymorphisms of ADIPOQ and ADIPOR1 and prostate cancer risk. Metabolism (2011) 1.02
High-resolution whole-genome haplotyping using limited seed data. Nat Methods (2013) 1.01
Practical Consideration of Genotype Imputation: Sample Size, Window Size, Reference Choice, and Untyped Rate. Stat Interface (2011) 1.01
Oral delivery of tumor-targeting Salmonella exhibits promising therapeutic efficacy and low toxicity. Cancer Sci (2009) 0.98
Genotype calling from next-generation sequencing data using haplotype information of reads. Bioinformatics (2012) 0.98
Pharmacogenetic association of the APOA1/C3/A4/A5 gene cluster and lipid responses to fenofibrate: the genetics of lipid-lowering drugs and diet network study. Pharmacogenet Genomics (2009) 0.97
MAASE: an alternative splicing database designed for supporting splicing microarray applications. RNA (2005) 0.96
Calmodulin mediates Fas-induced FADD-independent survival signaling in pancreatic cancer cells via activation of Src-extracellular signal-regulated kinase (ERK). J Biol Chem (2011) 0.96
Microarray analysis. Methods Mol Biol (2007) 0.94
Association between vitamin D insufficiency and the risk for gestational diabetes mellitus in pregnant Chinese women. Biomed Environ Sci (2012) 0.94
Increased expression of thymidylate synthetase (TS), ubiquitin specific protease 10 (USP10) and survivin is associated with poor survival in glioblastoma multiforme (GBM). J Neurooncol (2006) 0.94
Defining haplotype blocks and tag single-nucleotide polymorphisms in the human genome. Hum Mol Genet (2003) 0.93
The influence of human leukocyte antigen class I alleles and their population frequencies on human immunodeficiency virus type 1 control among African Americans. Hum Immunol (2011) 0.93
Further evidence of a maternal parent-of-origin effect on chromosome 10 in late-onset Alzheimer's disease. Am J Med Genet B Neuropsychiatr Genet (2006) 0.92
Prognostic value of IL-27 polymorphisms and the susceptibility to epithelial ovarian cancer in a Chinese population. Immunogenetics (2013) 0.91
The SCARB1 gene is associated with lipid response to dietary and pharmacological interventions. J Hum Genet (2008) 0.90
A genome-wide association study of host genetic determinants of the antibody response to Anthrax Vaccine Adsorbed. Vaccine (2012) 0.90
Effect of sedation on pain perception. Anesthesiology (2013) 0.90
Association between IL6 -174G/C and cancer: A meta-analysis of 105,482 individuals. Exp Ther Med (2012) 0.89
Sonic Hedgehog pathway is essential for neuroblastoma cell proliferation and tumor growth. Mol Cell Biochem (2012) 0.89
Detecting susceptibility genes in case-control studies using set association. BMC Genet (2003) 0.89
A Bayesian hierarchical model for detecting haplotype-haplotype and haplotype-environment interactions in genetic association studies. Hum Hered (2011) 0.89
Human leukocyte antigen class I supertypes and HIV-1 control in African Americans. J Virol (2009) 0.88
TGFBR1 haplotypes and risk of non-small-cell lung cancer. Cancer Res (2009) 0.88
Case-control association analysis of rheumatoid arthritis with candidate genes using related cases. BMC Proc (2007) 0.87
A two-SNP IL-6 promoter haplotype is associated with increased lung cancer risk. J Cancer Res Clin Oncol (2012) 0.87
Salivary Actinomyces naeslundii genospecies 2 and Lactobacillus casei levels predict pregnancy outcomes. J Periodontol (2005) 0.87
Interleukin-17 gene polymorphisms are associated with bladder cancer in a Chinese Han population. Mol Carcinog (2012) 0.87
Selecting additional tag SNPs for tolerating missing data in genotyping. BMC Bioinformatics (2005) 0.86
The FCRL3-169CT promoter single-nucleotide polymorphism, which is associated with systemic lupus erythematosus in a Japanese population, predicts expression of receptor protein on CD19+ B cells. Arthritis Rheum (2009) 0.86
Genotypic characteristics of multidrug-resistant Escherichia coli isolates associated with urinary tract infections. APMIS (2014) 0.86
Syndecan-1 overexpression is associated with nonluminal subtypes and poor prognosis in advanced breast cancer. Am J Clin Pathol (2013) 0.85
Determinants of access to antenatal care and birth outcomes in Kumasi, Ghana. J Epidemiol Glob Health (2013) 0.85
CD226 Gly307Ser association with multiple autoimmune diseases: a meta-analysis. Hum Immunol (2012) 0.85
Prostatic alpha-linolenic acid (ALA) is positively associated with aggressive prostate cancer: a relationship which may depend on genetic variation in ALA metabolism. PLoS One (2012) 0.84
The Fc receptor-like 3 gene polymorphisms and susceptibility to autoimmune diseases: an updated meta-analysis. Autoimmunity (2013) 0.84
Elevated interleukin-18 serum levels in chronic schizophrenia: Association with psychopathology. J Psychiatr Res (2012) 0.84
Functional polymorphism of hOGG1 gene is associated with type 2 diabetes mellitus in Chinese population. Mol Cell Endocrinol (2010) 0.84
Genes and biochemical pathways in human skeletal muscle affecting resting energy expenditure and fuel partitioning. J Appl Physiol (1985) (2010) 0.84
Detecting epistatic interactions contributing to human gene expression using the CEPH family data. BMC Proc (2007) 0.84
The TLR9 gene polymorphisms and the risk of cancer: evidence from a meta-analysis. PLoS One (2013) 0.84
Packet randomized experiments for eliminating classes of confounders. Eur J Clin Invest (2015) 0.83
GJB2 and GJB6 mutations in children with congenital cytomegalovirus infection. Pediatr Res (2007) 0.83
Establishment of a highly sensitive sandwich enzyme-linked immunosorbent assay specific for ovomucoid from hen's egg white. J Agric Food Chem (2007) 0.83
Fcγ receptor IIIa single-nucleotide polymorphisms and haplotypes affect human IgG binding and are associated with lupus nephritis in African Americans. Arthritis Rheumatol (2014) 0.82
Frequencies of circulating IL-17-producing CD4+CD161+ T cells and CD4+CD161+ T cells correlate with disease activity in rheumatoid arthritis. Mod Rheumatol (2014) 0.82
System-level factors as predictors of adherence to clinical appointment schedules in antiretroviral therapy in Cambodia. AIDS Care (2015) 0.82
Follow-up mapping supports the evidence for linkage in the candidate region at 9q22 in the NIMH Alzheimer's disease Genetics Initiative cohort. Am J Med Genet B Neuropsychiatr Genet (2007) 0.82
Analysis of IL-17 gene polymorphisms in Chinese patients with dilated cardiomyopathy. Hum Immunol (2013) 0.82
Multiple genetic variants associated with primary biliary cirrhosis in a Han Chinese population. Clin Rev Allergy Immunol (2015) 0.82
A family-based association study of the MOG gene with schizophrenia in the Chinese population. Schizophr Res (2005) 0.82
Tamoxifen enhances therapeutic effects of gemcitabine on cholangiocarcinoma tumorigenesis. Lab Invest (2011) 0.82
Identification and validation of PROM1 and CRTC2 mutations in lung cancer patients. Mol Cancer (2014) 0.81
Efficient ratiometric fluorescence probe based on dual-emission quantum dots hybrid for on-site determination of copper ions. Anal Chem (2013) 0.81
Intensive insulin therapy increases sex hormone-binding globulin in newly diagnosed type 2 diabetic patients. Eur J Endocrinol (2014) 0.81
AluYb8 insertion in the MUTYH gene is related to increased 8-OHdG in genomic DNA and could be a risk factor for type 2 diabetes in a Chinese population. Mol Cell Endocrinol (2010) 0.81
A candidate gene approach for virally induced cancer with application to HIV-related Kaposi's sarcoma. Int J Cancer (2013) 0.81
Electrochemiluminescence energy transfer-promoted ultrasensitive immunoassay using near-infrared-emitting CdSeTe/CdS/ZnS quantum dots and gold nanorods. Sci Rep (2013) 0.81
A common mutation of the MYH gene is associated with increased DNA oxidation and age-related diseases. Free Radic Biol Med (2009) 0.80
[A highly sensitive enzyme-linked immunosorbent assay for measurement of leptin secretion in human adipocytes]. Zhonghua Yi Xue Za Zhi (2008) 0.80
Factors associated with the acceptability of male circumcision among men in Jamaica. PLoS One (2013) 0.80
Genome-wide association studies of rheumatoid arthritis data via multiple hypothesis testing methods for correlated tests. BMC Proc (2009) 0.80
Admixture Mapping of Subclinical Atherosclerosis and Subsequent Clinical Events Among African Americans in 2 Large Cohort Studies. Circ Cardiovasc Genet (2017) 0.80
A Sequence Kernel Association Test for Dichotomous Traits in Family Samples under a Generalized Linear Mixed Model. Hum Hered (2015) 0.80
[Effect of bodyweight on the onset of puberty of female children and adolescents]. Zhongguo Yi Xue Ke Xue Yuan Xue Bao (2010) 0.80
Highly selective and sensitive detection of mercuric ion based on a visual fluorescence method. Anal Chem (2012) 0.80
On a family-based haplotype pattern mining method for linkage disequilibrium mapping. Pac Symp Biocomput (2002) 0.80
Increased frequency of HLA-B44 in recurrent sinopulmonary infections (RESPI). Clin Immunol (2006) 0.80
[Clinical analysis of four cases of hepatic veno-occlusive disease caused by Gynura segetum (Lour.) Merr]. Zhonghua Gan Zang Bing Za Zhi (2007) 0.80
Application of truncated immunodominant polypeptide from hepatitis E virus (HEV) ORF2 in an assay to exclude nonspecific binding in detecting anti-HEV immunoglobulin M. J Clin Microbiol (2009) 0.80
Similarity-based multimarker association tests for continuous traits. Ann Hum Genet (2012) 0.79
Antenatal care attendance, a surrogate for pregnancy outcome? The case of Kumasi, Ghana. Matern Child Health J (2014) 0.79
Prognostic value of serum nicotinamide phosphoribosyltransferase in patients with bladder cancer. Croat Med J (2014) 0.79
Structure of tumor necrosis factor-alpha haploblocks in European populations. Immunogenetics (2013) 0.79
Rare-Variant Kernel Machine Test for Longitudinal Data from Population and Family Samples. Hum Hered (2016) 0.78