Pilot corpus: NIH-funded biomedical datasets. Any DOI can be scored on demand — network effects sharpen as coverage grows.

Diminished DNA binding affinity of DMRT1 caused by heterozygous DM domain mutations is a cause of male infertility

Human Molecular Genetics(2025)10.1093/hmg/ddae197Source: DataRank Database

Diminished DNA binding affinity of DMRT1 caused by heterozygous DM domain mutations is a cause of male infertility is a research paper published in Human Molecular Genetics (2025). On theSindex it has a DataRank of 0.

N/A

0DataRank · unranked

Scored on demand from live citation data

Open Access0 citations

Download PDF

Cite:

Linked data & code

ensembl dbgap pdb

DataRank reads this dataset's downstream impact straight off the citation graph — no black box, no proprietary weighting. How is this computed?

›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Pipeline:MetadataData-paper checkEnrichmentCitation networkScoring

Enrichment:Funding (7 grants)Impact (FWCI 0.00)OA: greenTopics (49)IDs (PubMed, PMC, OpenAlex)Annotations (3)SDGs (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)

FAIR checklist signals are shown for context only and do not affect DataRank scoring.

Run a calibrated FAIR evaluation for this paper →

We only score data papers we can read in full — never from an abstract alone.

Authors (27)

Helen Castillo‐Madeen,Monika Logara Klarić ORCID,Antun Barišić,Lovro Trgovec-Greif,Mark W. Murphy

Live enrichment

PubMed:39777458 PMC:PMC11891871 OpenAlex:https://openalex.org/W4406135811

US National Institutes of Health

Grant: GM127379

US National Institutes of Health

Grant: R01HD078641

US National Institutes of Health

Grant: P50HD096723

Estonian Research Council

Grant: PRG1021

NIGMS NIH HHS

Grant: R01 GM127379

Scientific Center of Excellence for Reproductive and Regenerative Medicine, Republic of Croatia

FWCI

0.00

Citation Percentile

0.0%

greenLicense: https://academic.oup.com/pages/standard-publication-reuse-rights

repositoryhttps://pmc.ncbi.nlm.nih.gov/articles/PMC11891871/pdf/ddae197.pdf

publisherhttps://academic.oup.com/hmg/article-pdf/34/6/481/61371136/ddae197.pdf

repositoryhttps://pmc.ncbi.nlm.nih.gov/articles/PMC11891871/

journalhttps://doi.org/10.1093/hmg/ddae197

Fields of Study

CRISPR and Genetic EngineeringGenetic and Clinical Aspects of Sex Determination and Chromosomal AbnormalitiesAnimal Genetics and ReproductionHumansMaleTranscription FactorsInfertility, MaleMutationFemaleAdultAzoospermiaMolecular Dynamics SimulationDNAHeterozygoteProtein DomainsExome SequencingProtein BindingGenetic Predisposition to DiseasePrimary Ovarian InsufficiencyAzoospermia, Nonobstructive

MeSH Terms

Protein DomainsExome SequencingAdultDNAFemaleHeterozygoteHumansInfertility, MaleMaleMutationProtein BindingTranscription FactorsPrimary Ovarian InsufficiencyGenetic Predisposition to DiseaseAzoospermiaMolecular Dynamics Simulation

Keywords

BiologyGeneticsHeterozygote advantageInfertilityMale infertilityMutationDNAMolecular biologyGeneAllelePregnancyDMRT1Exome Sequencing

Sustainable Development Goals

SDG 0: Good health and well-being

Diminished DNA binding affinity of DMRT1 caused by heterozygous DM domain mutations is a cause of male infertility

FAIR Checklist

Authors (27)

Funding (7 grants)

Impact

Open Access

Topics

Annotations (Europe PMC)