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Association of Coding Variants in Hydroxysteroid 17-beta Dehydrogenase 14 (HSD17B14) with Reduced Progression to End Stage Kidney Disease in Type 1 Diabetes

Journal of the American Society of Nephrology(2021)10.1681/asn.2020101457Source: DataRank Database

Association of Coding Variants in Hydroxysteroid 17-beta Dehydrogenase 14 (HSD17B14) with Reduced Progression to End Stage Kidney Disease in Type 1 Diabetes is a research paper published in Journal of the American Society of Nephrology (2021). On theSindex it has a DataRank of 0.575. It has been cited 15 times, with 9 citing works in its 1-hop citation network.

N/A

0.575DataRank · unranked

Scored on demand from live citation data

Open Access15 citations · 9 citing works in its network

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›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Pipeline:MetadataData-paper checkEnrichmentCitation networkScoring

Enrichment:Funding (31 grants)OA: greenTopics (84)IDs (PubMed)

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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DataRank Breakdown

Base Score 72%Citation Network 28%

Base Score Contribution

0.416

From this paper's citation signal

Citation Network Contribution

0.159

From 7 citing papers with measurable signal

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Top 5 citers driving the network score

Ranked by each citer's contribution to N(p) — log1p(C_q) divided by its reference count — out of 9 citers.

Expression and localization of HSD17B13 along mouse urinary tract
American Journal of Physiology-Renal Physiology20243 citations24 referencesContributes 0.058
Identification of ferroptosis-related genes and pathways in diabetic kidney disease using bioinformatics analysis
Scientific Reports202217 citations59 referencesContributes 0.049
DNA methyltransferase 1 (DNMT1) promotes cyst growth and epigenetic age acceleration in autosomal dominant polycystic kidney disease
Kidney International202413 citations58 referencesContributes 0.046
17β-hydroxysteroid dehydrogenases in the progression of nonalcoholic fatty liver disease
Pharmacology & Therapeutics202320 citations156 referencesContributes 0.020
PheCode-guided multi-modal topic modeling of electronic health records improves disease incidence prediction and GWAS discovery from UK Biobank
medRxiv20251 citations49 referencesContributes 0.014

Authors (35)

Erkka Valo ORCID,Takaharu Ichimura ORCID,Tarunveer S. Ahluwalia ORCID,Christian Dina ORCID,Rachel G. Miller ORCID

Live enrichment

PubMed:34261756

JDRF

Grant: (3-SRA-2018-529-M-B)

JDRF

Grant: (17-2013-8)

JDRF

Grant: 6-2010-550

JDRF

Grant: 1-2008-1018

National Institutes of Health

Grant: DK-041526

Joslin Diabetes Research Center

Grant: P30 DK036836

JDRF

Grant: 17-2013-7

Novo Nordisk Foundation

Grant: OC0013659

Academy of Finland

Grant: 275614

Next-generation genetic studies for the discovery of rare variants associated with the development of diabetic complications with specific focus on nephropathy in type 1 diabetes (FinnDiane)

Academy of Finland

Grant: 299200

Genetic dissection of the pathogenesis of diabetic complications

Academy of Finland

Grant: 316664

Genetic and metabolomics dissection of the pathogenesis of diabetic complications The Finnish Diabetic Nephropathy Study (FinnDiane)

Helsinki University Hospital Research Funds

Grant: TYH2018207

NIDDK

Grant: DK34818

NIDDK

Grant: NEI EY016379

NIH-NIDDK

Grant: R37 DK39773

NIH-NIDDK

Grant: R01 DK072381

NCATS/NIDDK

Grant: UG TR002155

Claude D. Pepper Older Americans Independence Center

Grant: AG08808

Novo Nordisk Foundation

Grant: unidentified

unidentified

NEI NIH HHS

Grant: R01 EY016379

NIDDK NIH HHS

Grant: DP3 DK108220

NIDDK NIH HHS

Grant: R37 DK039773

NIDDK NIH HHS

Grant: R01 DK041526

NIDDK NIH HHS

Grant: R01 DK076077

NIDDK NIH HHS

Grant: R01 DK034818

NIDDK NIH HHS

Grant: R01 DK105821

NIA NIH HHS

Grant: P30 AG024824

NIA NIH HHS

Grant: P60 AG008808

NIDDK NIH HHS

Grant: R01 DK087635

NCATS NIH HHS

Grant: UG3 TR002155

NIDDK NIH HHS

Grant: R37 DK034818

green

repositoryhttps://www.ncbi.nlm.nih.gov/pmc/articles/8722802

publisherhttps://www.ovid.com/10.1681/ASN.2020101457

repositoryhttp://hdl.handle.net/10138/353497

https://doi.org/10.1681/asn.2020101457

https://pubmed.ncbi.nlm.nih.gov/34261756

Fields of Study

0301 basic medicine03 medical and health sciences0302 clinical medicine17-Hydroxysteroid DehydrogenasesAdultAnimalsCase-Control StudiesDiabetes Mellitus, Type 1Diabetic NephropathiesDisease ProgressionExomeFemaleGene ExpressionGenetic VariationHumansKidney Failure, ChronicKidney Tubules, ProximalMaleMiceMiddle AgedProtein Structural ElementsReperfusion InjuryRetrospective StudiesSurvival Rate

MeSH Terms

17-Hydroxysteroid DehydrogenasesAdultAnimalsCase-Control StudiesDiabetes Mellitus, Type 1Diabetic NephropathiesDisease ProgressionExomeFemaleGene ExpressionGenetic VariationHumansKidney Failure, ChronicKidney Tubules, ProximalMaleMiceMiddle AgedProtein Structural ElementsReperfusion InjuryRetrospective StudiesSurvival Rate

Keywords

Gene-based testsAdultMaleGENESGENETICS17-Hydroxysteroid Dehydrogenasestype 1 diabetesNEPHROPATHYDURATIONhydroxysteroid 17-beta dehydrogenase 14Gene ExpressionDiabetic nephropathyKidney Tubules, ProximalMiceAnimalsHumansDiabetic NephropathiesExomeGENOME-WIDE ASSOCIATIONDiabetic kidney diseasePREDICTORSRetrospective StudiesRISKCOMPLICATIONSEnd stage kidney diseaseMICROALBUMINURIArare variantsGenetic VariationMiddle AgedGeneral medicine, internal medicine and other clinical medicineRENAL DECLINEDiabetes Mellitus, Type 1[SDV.SPEE] Life Sciences [q-bio]/Santé publique et épidémiologieCase-Control StudiesReperfusion InjuryDisease ProgressionKidney Failure, ChronicFemaleProtein Structural Elements