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

Genome-wide association study on coronary artery disease in type 1 diabetes suggests beta-defensin 127 as a risk locus

Cardiovascular Research(2020)10.1093/cvr/cvaa045Source: DataRank Database

Genome-wide association study on coronary artery disease in type 1 diabetes suggests beta-defensin 127 as a risk locus is a research paper published in Cardiovascular Research (2020). On theSindex it has a DataRank of 0. It has been cited 28 times.

N/A

0DataRank · unranked

Scored on demand from live citation data

Open Access28 citations

Download PDF

Cite:

Linked data & code

refsnp

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 (25 grants)Impact (FWCI 3.36)OA: bronzeTopics (64)Linked Datasets (2)DataCite Reuse (2)IDs (PubMed, PMC, OpenAlex)Annotations (1)SDGs (2)

FAIR Checklist

Context only (not used in score)

Findable (2/2)

Has DOI
Indexed in repositories

Accessible (1/2)

Open Access

Interoperable (2/2)

DataCite relations
Linked datasets

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 (15)

Niina Sandholm ORCID,David-Alexandre Trégouët ORCID,Romain Charmet ORCID,Amy Jayne McKnight ORCID,Tarunveer S. Ahluwalia ORCID

Live enrichment

PubMed:32077919 PMC:PMC8453280 OpenAlex:https://openalex.org/W3007141561

Novo Nordisk Fonden

Grant: NNF14OC0013659

Novo Nordisk Fonden

Grant: NNF18OC0052457

Novo Nordisk Foundation

Grant: NNFOC0013659

Helsinki University Central Hospital Research Funds (EVO) and Academy of Finland

Grant: 316664

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

Diabetic Nephropathy Collaborative Research Initiative

Grant: 17-2013-7

Steno Diabetes Center Copenhagen (SDCC)

Grant: SDCC 3.A Complications

Helsinki University Central Hospital Research Funds (EVO) and 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)

Public Health Agency

Grant: STL/4760/13

Helsinki University Central Hospital Research Funds (EVO) and Academy of Finland

Grant: 299200

Genetic dissection of the pathogenesis of diabetic complications

NIDDK NIH HHS

Grant: R01 DK105154

Health Research Board

Grant: unidentified

unidentified

Science Foundation Ireland

Grant: 15/IA/3152

Discovery of an integrated risk profile for chronic kidney disease and development of a clinical biomarker panel for personalising medicine

Finnish Foundation for Cardiovascular Research

Health Research Board, Science Foundation Ireland

NIH

Ida Montini Foundation

Liv och Hälsa Society

Wilhelm och Else Stockmann Foundation

EFSD award supported by EFSD/Sanofi European Diabetes Research Programme in Macrovascular Complications

Medical Research Council

Northern Ireland Public Health Agency

European Foundation for the Study of Diabetes (EFSD) Young Investigator Research Award funds

Region Ile de France

FinnDiane project were supported by the Folkhälsan Research Foundation

Juvenile Diabetes Research Foundation

FWCI

3.36

Citation Percentile

0.9%

Citation Trend

2020

2021

2022

2023

2024

2025

bronzeLicense: OUP Standard Publication Reuse

journalhttps://academic.oup.com/cardiovascres/article-pdf/117/2/600/40418965/cvaa045.pdf

publisherhttps://academic.oup.com/cardiovascres/article-pdf/117/2/600/40418965/cvaa045.pdf

journalhttps://doi.org/10.1093/cvr/cvaa045

repositoryhttps://pubmed.ncbi.nlm.nih.gov/32077919

repositoryhttps://pure.qub.ac.uk/en/publications/ba65d1b3-5f7e-4af1-8e49-636bcbf40248

Fields of Study

Genetic Associations and EpidemiologyDiabetes and associated disordersAdipokines, Inflammation, and Metabolic Diseases0301 basic medicine03 medical and health sciences0303 health sciences

MeSH Terms

AdultAgedCoronary Artery DiseaseDiabetes Mellitus, Type 1FemaleFinlandHumansMaleMiddle AgedPhenotypePromoter Regions, GeneticRegistriesRisk FactorsCase-Control StudiesRisk AssessmentGenetic Predisposition to DiseasePolymorphism, Single Nucleotidebeta-DefensinsGenome-Wide Association StudyGenetic LociRNA, Long Noncoding

Keywords

Coronary artery diseaseLocus (genetics)Diabetes mellitusMedicineType 2 diabetesGenome-wide association studyDefensinInternal medicineDiseaseBETA (programming language)CardiologyGeneticsBiologyGeneEndocrinologyGenotypeSingle-nucleotide polymorphismCardiovascular diseasetype 1 diabetesAdultMalePolymorphism, Single NucleotideRisk AssessmentRisk FactorsHumansGenetic Predisposition to DiseaseRegistriesPromoter Regions, GeneticFinlandAgedMiddle AgedDiabetes Mellitus, Type 1PhenotypeGenetic LociCase-Control StudiesFemaleRNA, Long Noncoding

Sustainable Development Goals

SDG 3: 3. Good healthSDG 0: Good health and well-being

Additional file 1 of Whole-exome sequencing identifies novel protein-altering variants associated with serum apolipoprotein and lipid concentrations

10.6084/m9.figshare.21622433.v1figshare

Additional file 1 of Whole-exome sequencing identifies novel protein-altering variants associated with serum apolipoprotein and lipid concentrations

10.6084/m9.figshare.21622433figshare