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

Evidence for chromosome 2p16.3 polycystic ovary syndrome susceptibility locus in affected women of European ancestry.

The Journal of clinical endocrinology and metabolism - 1 Jan 2013

Mutharasan Priscilla, Galdones Eugene, Peñalver Bernabé Beatriz, Garcia Obed A, Jafari Nadereh, Shea Lonnie D, Woodruff Teresa K, Legro Richard S, Dunaif Andrea, Urbanek Margrit

Abstract excerpt

CONTEXT: A previous genome-wide association study in Chinese women with polycystic ovary syndrome (PCOS) identified a region on chromosome 2p16.3 encoding the LH/choriogonadotropin receptor (LHCGR) and FSH receptor (FSHR) genes as a reproducible PCOS susceptibility locus. OBJECTIVE: The objective of the study was to determine the role of the LHCGR and/or FSHR gene in the etiology of PCOS in women of European...

Read the complete abstract on PubMed

Topics

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

Share to Chromosomes, Human, Pair 2
Share to Genetic Loci

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Linkage Disequilibrium

Share to Polycystic Ovary Syndrome

Share to Receptors, FSH

Share to Receptors, LH

Share to United States

Share to White People

Source

Open in PubMed Open full text

Identifiers

PMID: 23118426
DOI: 10.1210/jc.2012-2471
PMCID: PMC3537106

Genes

FSHR
LHCGR

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

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

Evidence for chromosome 2p16.3 polycystic ovary syndrome susceptibility locus in affected women of European ancestry.PMID 23118426Read ↗

Genome-wide association study identifies susceptibility loci for polycystic ovary syndrome on chromosome 2p16.3, 2p21 and 9q33.3.Semantic proximity Read ↗

Genetic association between LHCGR variants and polycystic ovary syndrome: a meta-analysis.Semantic proximity Read ↗

Genome-wide association of polycystic ovary syndrome implicates alterations in gonadotropin secretion in European ancestry populations.Semantic proximity Read ↗

Genome-wide association study identified new susceptibility loci for polycystic ovary syndrome.Semantic proximity Read ↗

Further investigation in europeans of susceptibility variants for polycystic ovary syndrome discovered in genome-wide association studies of Chinese individuals.Semantic proximity Read ↗

Han Chinese polycystic ovary syndrome risk variants in women of European ancestry: relationship to FSH levels and glucose tolerance.Semantic proximity Read ↗

Replication study and meta-analysis of selected genetic variants and polycystic ovary syndrome susceptibility in Asian population.Semantic proximity Read ↗

Susceptibility loci for polycystic ovary syndrome on chromosome 2p16.3, 2p21, and 9q33.3 in a cohort of Caucasian women.Semantic proximity Read ↗

Genome-wide association study identifies eight new risk loci for polycystic ovary syndrome.Semantic proximity Read ↗

Molecular genetics of polycystic ovary syndrome: an update.Semantic proximity Read ↗

Genetics of polycystic ovary syndrome.Semantic proximity Read ↗

Association study between FSHR Ala307Thr and Ser680Asn variants and polycystic ovary syndrome (PCOS) in Northern Chinese Han women.Semantic proximity Read ↗

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