Varaico: Literature-Extracted Genetic Variants

Gene:FSHR
Variant:p.A307T
Back to variants list

FSHR

NM_000145.4:p.A307T

Associated Papers

Descriptive overview of gene variants potentially affecting female infertility treatments: A systematic review.

Martinez-Martinez A et al.

Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie, 2026

The Impact of FSHR Mutations on Female Ovarian Function and Pregnancy Outcomes: A Systematic Review.

Qu Z et al.

Biology of Reproduction, 2025

Metformin-Driven Activation of Polymorphic Follicle-Stimulating Hormone Receptors for Polycystic Ovary Syndrome Treatment: A Computational Study.

Alzahrani KJ

Medical Science Monitor : International Medical Journal of Experimental and Clinical Research, 2025

Women with FSHR-inactivating mutations causing resistant ovarian syndrome benefit from oocyte in-vitro maturation.

Li XF et al.

Reproductive Biomedicine Online, 2025

Identification of genetic variants in patients with primary and secondary amenorrhea.

Bai F et al.

Saudi Medical Journal, 2025

Pharmacological Characterization of Dopamine Receptor DRD1 Variants and Exploration of Their Allosteric Activation.

Wu C et al.

Biochemistry, 2025

Infertility management in resistant ovary syndrome: a review.

Yi H et al.

Frontiers in Endocrinology, 2025

The Impact of FSHR Polymorphisms (rs6165 and rs6166) on Ovarian Response to Stimulation in Infertile Women with Diminished Ovarian Reserve.

Hoang TTT et al.

The Application of Clinical Genetics, 2025

Testing the role of unstimulated in vitro maturation for potential development of immature oocytes in women with oocyte maturation abnormalities

Kalyoncu Ş et al.

Journal of the Turkish German Gynecological Association, 2024

Recurrent somatic mutations of FAT family cadherins induce an aggressive phenotype and poor prognosis in anaplastic large cell lymphoma.

Villa M et al.

British Journal of Cancer, 2024

39478125 (PubMed )
Supplement: 41416_2024_2881_MOESM1_ESM.pdf

Prevalence of FSH-R Asn680Ser and Ala307Thr receptor polymorphism and their correlation with ART outcomes among infertile Indian-Asian women-a prospective cohort study.

Mahey R et al.

Journal of Human Genetics, 2024

Follicle-Stimulating Hormone Receptor and Estrogen Receptor Gene Polymorphisms in Women With Discordant Follicle-Stimulating Hormone and Anti-Mullerian Hormone Levels.

Aktaş G et al.

Cureus, 2024

The relationship between primary ovarian insufficiency and gene variations: a prospective case-control study.

Gündüz R et al.

Women & Health, 2024

Novel NARS2 variants in a patient with early-onset status epilepticus: case study and literature review.

Yang N et al.

Bmc Pediatrics, 2024

38310242 (PubMed )
Supplement: 12887_2024_4553_MOESM1_ESM.xlsx › trio.hg38.filter

Genetic Variants of Steroidogenesis and Gonadotropin Pathways and Polycystic Ovary Syndrome Susceptibility: A Systematic Review and Meta-analysis.

Sharma P et al.

Metabolic Syndrome and Related Disorders, 2024

Whole exome sequencing reveals novel candidate variants for endometriosis utilizing multiple affected members in a single family.

Kina BG et al.

Molecular Genetics & Genomic Medicine, 2024

38013616 (PubMed )
Supplement: MGG3-12-e2312-s002.docx

TUBB8 mutations as a cause of oocyte maturation abnormalities: presentation of oocyte and embryo profiles and novel mutations.

Ebru H et al.

Reproductive Biomedicine Online, 2023

Involvement of SYCP2L and TDRD3 gene variants on ovarian reserve and reproductive outcomes: a cross-sectional study.

Rosa IR et al.

Jbra Assisted Reproduction, 2023

Polymorphisms in FSHR modulating susceptibility to polycystic ovary syndrome: an updated meta-analysis.

Kaur M et al.

Journal of Ovarian Research, 2023

Ala307Thr variation modulates FSHR structure and impairs its binding affinity for FSH: Implications in polycystic ovarian syndrome.

Amin A et al.

Cell Biochemistry and Function, 2023

Association of FSHR and DENND1A polymorphisms with polycystic ovary syndrome: a meta-analysis.

Larsen CB et al.

Jbra Assisted Reproduction, 2023

The Ala307Thr polymorphism of the follicle-stimulating hormone receptor (FSHR) gene is associated with the dose of recombinant FSH received during IVF/ICSI treatment.

Dieamant F et al.

Jbra Assisted Reproduction, 2023

Association Between Follicle-Stimulating Hormone Receptor (FSHR) rs6166 and Estrogen Receptor 1 (ESR1) rs2234693 Polymorphisms and Polycystic Ovary Syndrome Risk, Phenotype, and Reproductive Outcomes in an Infertile Portuguese Population.

Vieira IH et al.

Cureus, 2023

The Effect of the Allelics of Ser680Asn Polymorphisms of Follicle-Stimulating Hormone Receptor Gene in IVF/ICSI Cycles: a Systematic Review and Meta-analysis.

Prodromidou A et al.

Reproductive Sciences (thousand Oaks, Calif.), 2023

Cytogenetic screening of chromosomal abnormalities and genetic analysis of FSH receptor Ala307Thr and Ser680Asn genes in amenorrheic patients.

Kanaan BA et al.

Peerj, 2023

Current understanding of the genomic abnormities in premature ovarian failure: chance for early diagnosis and management.

Yang X et al.

Frontiers in Medicine, 2023

Impact of Follicle Stimulating Hormone Receptor (FSHR) Polymorphism on the Efficiency of Co-Treatment with Growth Hormone in a Group of Infertile Women from Romania.

Surcel M et al.

Diagnostics (basel, Switzerland), 2022

Functional characterization of naturally-occurring constitutively activating/inactivating mutations in equine follicle-stimulating hormone receptor.

Byambaragchaa M et al.

Animal Bioscience, 2022

Mutational Landscape Screening Through Comprehensive In Silico Analysis for Polycystic Ovarian Syndrome-Related Genes.

Dhar S et al.

Reproductive Sciences (thousand Oaks, Calif.), 2022

Variants Ala307Ala and Ser680Ser of 307 and 680 FSHr polymorphisms negatively influence on assisted reproductive techniques outcome and determine high probability of non-pregnancy in Caucasian patients.

Monge-Ochoa B et al.

Journal of Assisted Reproduction and Genetics, 2021

The role of polymorphism in various potential genes on polycystic ovary syndrome susceptibility and pathogenesis.

Chaudhary H et al.

Journal of Ovarian Research, 2021

Utilization of in vitro maturation in cases with a FSH receptor mutation.

Benammar A et al.

Journal of Assisted Reproduction and Genetics, 2021

Reduced FSH and LH action: implications for medically assisted reproduction.

Bosch E et al.

Human Reproduction (oxford, England), 2021

Association of FSHR gene polymorphisms with endometriosis in women visiting tertiary-care hospitals of Lahore, Pakistan.

Liaqat I et al.

Jpma. the Journal of the Pakistan Medical Association, 2021

Pharmacogenomic Biomarkers of Follicle-Stimulating Hormone Receptor Malfunction in Females with Impaired Ovarian Response-A Genetic Survey.

Tafazoli A et al.

Journal of Clinical Medicine, 2021

One4Two®: An Integrated Molecular Approach to Optimize Infertile Couples' Journey.

D'Argenio V et al.

Genes, 2021

Investigation of the FSHR, CYP11, and INSR Mutations and Polymorphisms in Iranian Infertile Women with Polycystic Ovary Syndrome (PCOS).

Seyed Abutorabi E et al.

Reports of Biochemistry & Molecular Biology, 2021

Prioritization of candidate genes for a South African family with Parkinson's disease using in-silico tools.

Sebate B et al.

Plos One, 2021

33770142 (PubMed )
Supplement: pone.0249324.s003.xlsx › 8772__III-8__

Effect of Genetic Variants of Gonadotropins and Their Receptors on Ovarian Stimulation Outcomes: A Delphi Consensus.

Conforti A et al.

Frontiers in Endocrinology, 2021

Follicle-stimulating hormone receptor gene polymorphisms of ovarian reserve markers in Romanian population.

Tănase AE et al.

Experimental and Therapeutic Medicine, 2020

Oncology and Pharmacogenomics Insights in Polycystic Ovary Syndrome: An Integrative Analysis.

Yumiceba V et al.

Frontiers in Endocrinology, 2020

1–50 of 135 papers
Select a paper to view details
UCSC Genome Browser·Imprint·Privacy·Terms·Feedback·Email Updates·

Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."