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Analysis of copy number variation in men with non‐obstructive azoospermia

Andrology(2022)10.1111/andr.13267Source: DataRank Database

Analysis of copy number variation in men with non‐obstructive azoospermia is a research paper published in Andrology (2022). On theSindex it has a DataRank of 0. It has been cited 12 times.

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Open Access12 citations

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Enrichment:Funding (4 grants)Impact (FWCI 1.51)OA: hybridTopics (40)IDs (PubMed, PMC, OpenAlex)Annotations (1)

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 (19)

Rebecca Wabschke,Albrecht Röpke ORCID,Marius Wöste ORCID,Christian Rückert ORCID,S. Perrey

Live enrichment

PubMed:36041235 PMC:PMC9605881 OpenAlex:https://openalex.org/W4293698208

National Institutes of Health

Grant: P50 HD096723

National Institutes of Health

Grant: R21 HD080755

National Institutes of Health

Grant: 5P50HD096723-04

Genetics of Male Infertility: A Marker of Overall Health

National Institutes of Health

Grant: 1R21HD080755-01A1

Genomic signatures of X-linked and autosomal candidate-genes in azoospermia

FWCI

1.51

Citation Percentile

0.8%

Citation Trend

2023

2024

2025

2026

hybridLicense: cc-by-nc

journalhttps://onlinelibrary.wiley.com/doi/pdfdirect/10.1111/andr.13267

publisherhttps://onlinelibrary.wiley.com/doi/pdfdirect/10.1111/andr.13267

publisherhttps://onlinelibrary.wiley.com/doi/pdf/10.1111/andr.13267

publisherhttps://onlinelibrary.wiley.com/doi/full-xml/10.1111/andr.13267

journalhttps://doi.org/10.1111/andr.13267

Fields of Study

Genetic and Clinical Aspects of Sex Determination and Chromosomal AbnormalitiesGenomic variations and chromosomal abnormalitiesPrenatal Screening and Diagnostics0301 basic medicine0303 health sciences03 medical and health sciences

MeSH Terms

HomozygoteHumansMaleNucleotidesAzoospermiaDNA Copy Number Variations

Keywords

Copy-number variationAzoospermiaGeneticsBiologyMale infertilityMeiosisGeneCandidate geneComparative genomic hybridizationInfertilityMissense mutationAllelePhenotypeGenomeMeiotic arrestNon-obstructive azoospermiaCnvWesScoSyce1MaleCancer ResearchDNA Copy Number VariationsNucleotidesTopic 1: Genes, Cells and Cell-Based MedicineHomozygoteHumansArticle

Analysis of copy number variation in men with non‐obstructive azoospermia

FAIR Checklist

Authors (19)

Funding (4 grants)

Impact

Open Access

Topics

Annotations (Europe PMC)