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Identifying susceptibility genes for primary ovarian insufficiency on the high-risk genetic background of a fragile X premutation

Fertility and Sterility(2021)10.1016/j.fertnstert.2021.04.021Source: DataRank Database

Identifying susceptibility genes for primary ovarian insufficiency on the high-risk genetic background of a fragile X premutation is a research paper published in Fertility and Sterility (2021). On theSindex it has a DataRank of 0. It has been cited 6 times.

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Open Access6 citations

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datarank_citation_only_1hop_v6· scope data_onlyMethodology

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Enrichment:Funding (10 grants)Impact (FWCI 0.76)OA: bronzeTopics (84)IDs (PubMed, PMC, OpenAlex)Annotations (1)SDGs (2)

FAIR Checklist

Context only (not used in score)

Findable (1/2)

Has DOI

Accessible (1/2)

Open Access

Interoperable (0/2)

Reusable (0/3)

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Authors (23)

J. Christopher Rounds ORCID,Krista Charen,Lisa Shubeck,Heather S. Hipp ORCID,Jessica B. Spencer ORCID

Live enrichment

PubMed:34016428 PMC:PMC8494118 OpenAlex:https://openalex.org/W3162423831

University of Utah School of Medicine

Grant: R01 HD099487

NINDS NIH HHS

Grant: U54 NS091859

NICHD NIH HHS

Grant: P50 HD103573

National Institutes of Health

Grant: 5R01HD099487-05

Primary Ovarian Insufficiency: Etiology and Comorbid Disease

National Institutes of Health

Grant: 5P50HD103573-03

Clinical Translational Research Center for Neurodevelopmental Disorders

EMORY UNIVERSITY

Eunice Kennedy Shriver National Institute of Child Health and Human Development

National Institutes of Health

University of North Carolina at Chapel Hill

National Institute of Mental Health

FWCI

0.76

Citation Percentile

0.7%

Citation Trend

2021

2022

2025

bronzeLicense: CC BY NC ND

journalhttps://www.fertstert.org/article/S0015-0282(21)00307-1/pdf

publisherhttps://www.fertstert.org/article/S0015-0282(21)00307-1/pdf

publisherhttps://api.elsevier.com/content/article/PII:S0015028221003071?httpAccept=text/xml

publisherhttps://api.elsevier.com/content/article/PII:S0015028221003071?httpAccept=text/plain

journalhttps://doi.org/10.1016/j.fertnstert.2021.04.021

Fields of Study

Genetics and Neurodevelopmental DisordersGenetic and Clinical Aspects of Sex Determination and Chromosomal AbnormalitiesUbiquitin and proteasome pathways0301 basic medicine03 medical and health sciences0303 health sciencesAdultAge FactorsAnimalsAnimals, Genetically ModifiedCase-Control StudiesDrosophila melanogasterFemaleFertilityFragile X Messenger Ribonucleoprotein 1Genetic BackgroundGenetic Predisposition to DiseaseGenome-Wide Association StudyHumansMenopauseMiddle AgedMutationOvaryPhenotypePrimary Ovarian InsufficiencyRisk AssessmentRisk Factors

MeSH Terms

Genetic BackgroundAdultAge FactorsAnimalsDrosophila melanogasterFemaleFertilityHumansMenopauseMiddle AgedMutationOvaryPhenotypeRisk FactorsCase-Control StudiesPrimary Ovarian InsufficiencyRisk AssessmentGenetic Predisposition to DiseaseAnimals, Genetically ModifiedFragile X Messenger Ribonucleoprotein 1Fragile X Mental Retardation ProteinGenome-Wide Association Study

Keywords

Fragile xGeneticsGenePrimary (astronomy)MedicinePremature ovarian insufficiencyBiologyBioinformaticsInternal medicinePrimary Ovarian InsufficiencySumo1FxpoiFragile X-associated DisordersKrr1Adult610Risk AssessmentArticleAnimals, Genetically ModifiedAnimalsHumansGenetic Predisposition to DiseaseFragile X Messenger Ribonucleoprotein 1OvaryAge FactorsMiddle AgedDrosophila melanogasterFertilityPhenotypeCase-Control StudiesMutationFemaleMenopauseGenetic BackgroundGenome-Wide Association Study

Sustainable Development Goals

SDG 3: 3. Good healthSDG 0: Good health and well-being

Identifying susceptibility genes for primary ovarian insufficiency on the high-risk genetic background of a fragile X premutation

FAIR Checklist

Authors (23)

Funding (10 grants)

Impact

Open Access

Topics

Annotations (Europe PMC)