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Early‐onset diabetes mellitus as a presenting feature of Werner's syndrome in an Indian family

Molecular Genetics & Genomic Medicine(2023)10.1002/mgg3.2299Source: DataRank Database

Early‐onset diabetes mellitus as a presenting feature of Werner's syndrome in an Indian family is a research paper published in Molecular Genetics & Genomic Medicine (2023). On theSindex it has a DataRank of 0. It has been cited 1 time.

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Open Access1 citations

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›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Pipeline:MetadataData-paper checkEnrichmentCitation networkScoring

Enrichment:Funding (5 grants)Impact (FWCI 0.12)OA: goldTopics (64)IDs (PubMed, PMC, OpenAlex)Annotations (2)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)

Chao Xing ORCID,Vinaya Simha ORCID,Anil K. Agarwal ORCID,Xunzhi Zhang ORCID,Leena Lekkala

Live enrichment

PubMed:37815015 PMC:PMC10767583 OpenAlex:https://openalex.org/W4387473348

National Institutes of Health

Grant: R01‐DK105448

NIDDK NIH HHS

Grant: R01 DK105448

NIH HHS

Grant: R01-DK105448

National Institutes of Health

Grant: 5R01DK105448-07

Genetic and Metabolic Basis of Familial Lipodystrophies

Southwestern Medical Foundation

FWCI

0.12

Citation Percentile

0.5%

Citation Trend

2026

goldLicense: cc-by-nc-nd

journalhttps://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/mgg3.2299

GOLDhttps://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/mgg3.2299

publisherhttps://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/mgg3.2299

publisherhttps://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.2299

journalhttps://doi.org/10.1002/mgg3.2299

Fields of Study

Cancer-related Molecular PathwaysWnt/β-catenin signaling in development and cancerMitochondrial Function and PathologyMedicine0303 health sciences03 medical and health sciencesMaleChildAdolescentHumansAdultYoung AdultWerner SyndromeOsteoporosisDNA HelicasesDiabetes Mellitus, Type 1Diabetes Mellitus, Type 2

MeSH Terms

AdolescentAdultChildDiabetes Mellitus, Type 1Diabetes Mellitus, Type 2DNA HelicasesHumansMaleOsteoporosisWerner SyndromeYoung Adult

Keywords

Werner syndromeProbandMedicineConsanguinityAcanthosis nigricansShort statureExome sequencingFamily historyType 2 Diabetes MellitusAge of onsetDiabetes mellitusPediatricsGeneticsEndocrinologyInternal medicineBiologyMutationGeneInsulin resistanceDiseaseHelicaseLipodystrophyWerner's SyndromeWrnMyxoid Malignant Peripheral Nerve Sheath TumorMaleAdultAdolescentDNA HelicasesOriginal ArticlesYoung AdultDiabetes Mellitus, Type 1Diabetes Mellitus, Type 2HumansOsteoporosisChild

Sustainable Development Goals

SDG 0: Good health and well-being

Early‐onset diabetes mellitus as a presenting feature of Werner's syndrome in an Indian family

FAIR Checklist

Authors (9)

Funding (5 grants)

Impact

Open Access

Topics

Annotations (Europe PMC)