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Bi-allelic Mutations in M1AP Are a Frequent Cause of Meiotic Arrest and Severely Impaired Spermatogenesis Leading to Male Infertility

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.06.010Source: DataRank Database

Bi-allelic Mutations in M1AP Are a Frequent Cause of Meiotic Arrest and Severely Impaired Spermatogenesis Leading to Male Infertility is a research paper published in The American Journal of Human Genetics (2020). On theSindex it has a DataRank of 0. It has been cited 105 times.

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Open Access105 citations

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omim hpa refseq uniprot doi

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›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

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Enrichment:Funding (7 grants)Impact (FWCI 21.25)OA: bronzeTopics (85)IDs (PubMed, PMC, OpenAlex)Annotations (5)SDGs (1)

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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 (34)

Sehime Gulsun Temel ORCID,Liina Nagirnaja ORCID,Manon S. Oud ORCID,Alexandra M. Lopes ORCID,Godfried W. van der Heijden ORCID

Live enrichment

PubMed:32673564 PMC:PMC7413853 OpenAlex:https://openalex.org/W3041109538

Deutsche Forschungsgemeinschaft

Grant: DFG CRU326

Wellcome Trust

Grant: 209451/Z/17/Z

NICHD NIH HHS

Grant: P50 HD096723

NIH HHS

Grant: P51 OD011092

NICHD NIH HHS

Grant: R01 HD078641

Deutsche Forschungsgemeinschaft

Grant: unidentified

unidentified

National Institutes of Health

Grant: 5R01HD078641-05

GENOMICS OF SPERMATOGENIC IMPAIRMENT

FWCI

21.25

Citation Percentile

1.0%

Citation Trend

2020

2021

2022

2023

2024

2025

2026

bronzeLicense: Elsevier Non-Commercial

journalhttp://www.cell.com/article/S0002929720301981/pdf

publisherhttp://www.cell.com/article/S0002929720301981/pdf

journalhttps://doi.org/10.1016/j.ajhg.2020.06.010

repositoryhttps://pubmed.ncbi.nlm.nih.gov/32673564

repositoryhttp://europepmc.org/pmc/articles/PMC7413853

Fields of Study

Prenatal Screening and DiagnosticsRenal and related cancersGenomics and Rare Diseases0301 basic medicine03 medical and health sciences0303 health sciencesAdultAllelesAnimalsAzoospermiaCell Cycle CheckpointsHomozygoteHumansInfertility, MaleMaleMeiosisMiceMutationPhenotypeProteinsSpermatogenesisSpermatozoaTestisTurkeyExome SequencingAzoospermia, Nonobstructive

MeSH Terms

Exome SequencingAdultAllelesAnimalsHomozygoteHumansInfertility, MaleMaleMeiosisMutationPhenotypeProteinsSpermatogenesisSpermatozoaTestisTurkeyMiceAzoospermiaCell Cycle Checkpoints

Keywords

SpermatogenesisMeiosisInfertilityMale infertilityAlleleBiologyGeneticsMedicineAndrologyGenePregnancyMeiotic arrestNon-obstructive azoospermiaOligozoospermiaSpermatogenic FailureCryptozoospermiaM1apMeiosis 1 Associated ProteinRadboudumc 18: Healthcare improvement science RIHS: Radboud Institute for Health SciencesAdultMaleTurkeyRadboud University Medical CenterMiceGynaecology - Radboud University Medical CenterTestisExome SequencingAnimalsHumansAllelesInfertility, MaleAzoospermiaRadboudumc 7: Neurodevelopmental disorders DCMN: Donders Center for Medical NeuroscienceHomozygoteProteinsCell Cycle CheckpointsSpermatozoaPhenotypeMutationHuman Genetics - Radboud University Medical Center

Sustainable Development Goals

SDG 0: Good health and well-being

Bi-allelic Mutations in M1AP Are a Frequent Cause of Meiotic Arrest and Severely Impaired Spermatogenesis Leading to Male Infertility

FAIR Checklist

Authors (34)

Funding (7 grants)

Impact

Open Access

Topics

Annotations (Europe PMC)