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

Association analysis of FMR1 genetic variants and primary ovarian insufficiency in South Indian women with a novel approach of CGG repeats classification.

European journal of medical genetics - 1 Dec 2020

Komaravalli Prasanna Latha, Rani S Vasantha, Dalal Ashwin, Jahan Parveen

Abstract excerpt

Around 20-28% of FMR1gene CGG premutation (PM) carriers are at augmented risk towards an infertility related disorder, Fragile X-associated primary ovarian insufficiency (FXPOI). Except the effect of CGG repeats, reports are not available on the mechanism through which the cis-acting variations, namely, SNPs involved in POI susceptibility. Addressing the hypothesis that the FMR1 gene polymorphisms [CGG repeats,...

Read the complete abstract on PubMed

Topics

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

Share to Fragile X Mental Retardation Protein
Share to India

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Polymorphism, Single Nucleotide

Share to Primary Ovarian Insufficiency

Share to Trinucleotide Repeat Expansion

Source

Identifiers

PMID: 33039683
DOI: 10.1016/j.ejmg.2020.104081

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

Association analysis of FMR1 genetic variants and primary ovarian insufficiency in South Indian women with a novel approach of CGG repeats classification.PMID 33039683Read ↗

Association between fragile X premutation and premature ovarian failure: a case-control study and meta-analysis.Semantic proximity Read ↗

The significance of FMR1 CGG repeats in Chinese women with premature ovarian insufficiency and diminished ovarian reserve.Semantic proximity Read ↗

Does the presence of AGG interruptions within the CGG repeat tract have a protective effect on the fertility phenotype of female FMR1 premutation carriers?Semantic proximity Read ↗

Large-scale analysis of FMR1 CGG repeat length and risk of premature ovarian insufficiency in over 92 000 women.Semantic proximity Read ↗

Ovarian dysfunction and FMR1 alleles in a large Italian family with POF and FRAXA disorders: case report.Semantic proximity Read ↗

Stratification of the risk of ovarian dysfunction by studying the complexity of intermediate and premutation alleles of the FMR1 gene.Semantic proximity Read ↗

Premature ovarian insufficiency: clinical orientations for genetic testing and genetic counselingSemantic proximity Read ↗

PGT-M for Premature Ovarian Failure Related to CGG Repeat Expansion of the FMR1 Gene.Semantic proximity Read ↗

Molecular Characterization of FMR1 Gene by TP-PCR in Women of Reproductive Age and Women with Premature Ovarian Insufficiency.Semantic proximity Read ↗

FMR1 and the continuum of primary ovarian insufficiency.Semantic proximity Read ↗

FMR1 premutation: not only important in premature ovarian failure but also in diminished ovarian reserve.Semantic proximity Read ↗

Genetic Etiologic Analysis in 74 Chinese Han Women with Idiopathic Premature Ovarian Insufficiency by Combined Molecular Genetic TestingSemantic proximity Read ↗

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