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Bidirectional disruption of GNAS transcripts causes broad methylation defects in pseudohypoparathyroidism type 1B

Proceedings of the National Academy of Sciences(2025)10.1073/pnas.2423271122Source: DataRank Database

Bidirectional disruption of GNAS transcripts causes broad methylation defects in pseudohypoparathyroidism type 1B is a research paper published in Proceedings of the National Academy of Sciences (2025). On theSindex it has a DataRank of 0. It has been cited 3 times.

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Open Access3 citations

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›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Pipeline:MetadataData-paper checkEnrichmentCitation networkScoring

Enrichment:Funding (6 grants)Impact (FWCI 2.70)OA: hybridTopics (43)IDs (PubMed, PMC, OpenAlex)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)

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Authors (9)

Monica Reyes,Anna Ryabets‐Lienhard,Barbara Gales,Agnès Linglart ORCID,Danny E. Miller ORCID

Live enrichment

PubMed:40249781 PMC:PMC12037034 OpenAlex:https://openalex.org/W4409580808

HHS | NIH | National Institute of Diabetes and Digestive and Kidney Diseases

Grant: R01DK046718

HHS | NIH | National Institute of Diabetes and Digestive and Kidney Diseases

Grant: R01DK121776

Uehara Memorial Foundation

Grant: Fellowship

Japan Society for the Promotion of Science London

Grant: 19K20170

HHS | NIH | National Institute of Diabetes and Digestive and Kidney Diseases

Grant: R01DK140244

HHS | National Institutes of Health

Grant: DP5OD033357

FWCI

2.70

Citation Percentile

0.9%

Citation Trend

2025

2026

hybridLicense: cc-by-nc-nd

journalhttps://doi.org/10.1073/pnas.2423271122

publisherhttps://doi.org/10.1073/pnas.2423271122

publisherhttps://pnas.org/doi/pdf/10.1073/pnas.2423271122

repositoryhttps://pubmed.ncbi.nlm.nih.gov/40249781

repositoryhttps://www.ncbi.nlm.nih.gov/pmc/articles/12037034

Fields of Study

Genetic Syndromes and ImprintingGenomics and Rare DiseasesBlood groups and transfusionPseudohypoparathyroidismDNA MethylationChromograninsHumansGTP-Binding Protein alpha Subunits, GsEpigenesis, GeneticAnimalsMiceSyntaxin 16FemaleMaleRetroelements

MeSH Terms

AnimalsChromograninsFemaleHumansMalePseudohypoparathyroidismRetroelementsDNA MethylationGTP-Binding Protein alpha Subunits, GsEpigenesis, GeneticMiceSyntaxin 16

Keywords

GNAS complex locusPseudohypoparathyroidismMethylationDifferentially methylated regionsBiologyDNA methylationEpigeneticsGeneticsInternal medicineMedicineGeneGene expressionParathyroid hormoneRetrotransposongenomic imprintingGnas

Sustainable Development Goals

SDG 0: Good health and well-being