Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

BET1L and TNRC6B associate with uterine fibroid risk among European Americans.

Human genetics - 1 Aug 2013

Edwards Todd L, Michels Kara A, Hartmann Katherine E, Velez Edwards Digna R

Abstract excerpt

Uterine fibroid (UFs) affect 77 % of women by menopause and account for $9.4 billion in healthcare costs each year. Although UFs are heritable, genetic risk is poorly understood. The first genome-wide association study (GWAS) of UFs was recently performed in a Japanese population, with reported genome-wide significance for single nucleotide polymorphisms (SNPs) across three chromosomal regions. We tested these...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Case-Control Studies
Share to Genome-Wide Association Study
Share to Haplotypes

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Leiomyoma

Share to Polymorphism, Single Nucleotide

Share to Risk Factors

Share to RNA-Binding Proteins

Share to White People

Source

Open in PubMed Open full text

Identifiers

PMID: 23604678
DOI: 10.1007/s00439-013-1306-3
PMCID: PMC3715562

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

BET1L and TNRC6B associate with uterine fibroid risk among European Americans.PMID 23604678Read ↗

Variants in BET1L and TNRC6B associate with increasing fibroid volume and fibroid type among European Americans.Semantic proximity Read ↗

Association of BET1L and TNRC6B with uterine leiomyoma risk and its relevant clinical features in Han Chinese population.Semantic proximity Read ↗

Uterine fibroid polygenic risk score (PRS) associates and predicts risk for uterine fibroid.Semantic proximity Read ↗

A multi-stage genome-wide association study of uterine fibroids in African Americans.Semantic proximity Read ↗

GWAS of five gynecologic diseases and cross-trait analysis in JapaneseSemantic proximity Read ↗

Uterine Fibroids: Bridging Genomic Defects and Chronic InflammationSemantic proximity Read ↗

GWAS-Significant Loci and Uterine Fibroids Risk: Analysis of Associations, Gene-Gene and Gene-Environmental Interactions.Semantic proximity Read ↗

Risk of uterine leiomyoma based on BET1L rs2280543 single nucleotide polymorphism and vegetarian diet.Semantic proximity Read ↗

Genetic predisposition to uterine leiomyoma is determined by loci for genitourinary development and genome stabilitySemantic proximity Read ↗

Cross-Tissue Regulatory Network Analyses Reveal Novel Susceptibility Genes and Potential Mechanisms for EndometriosisSemantic proximity Read ↗

Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis.Semantic proximity Read ↗

Genome-wide meta-analysis identifies novel risk loci for uterine fibroids within and across multiple ancestry groups.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.