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

Whole exome sequencing identifies monogenic forms of nephritis in a previously unsolved cohort of children with steroid-resistant nephrotic syndrome and hematuria

Pediatric Nephrology(2021)10.1007/s00467-021-05312-4Source: DataRank Database

Whole exome sequencing identifies monogenic forms of nephritis in a previously unsolved cohort of children with steroid-resistant nephrotic syndrome and hematuria is a research paper published in Pediatric Nephrology (2021). On theSindex it has a DataRank of 0. It has been cited 7 times.

N/A

0DataRank · unranked

Scored on demand from live citation data

Open Access7 citations

Download PDF

Cite:

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 (1 grants)Impact (FWCI 0.39)OA: greenTopics (45)IDs (PubMed, OpenAlex)SDGs (2)

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 (2)

Amelie T. van der Ven ORCID,Hongbo Xiao

Live enrichment

PubMed:34762194 OpenAlex:https://openalex.org/W3213995148

national institute of diabetes and digestive and kidney diseases

Grant: 5R01DK076683-15

Discover and functionally characterize full-penetrance causes of nephrosis / FSGS

FWCI

0.39

Citation Percentile

0.6%

Citation Trend

2024

2025

2026

greenLicense: Springer TDM

repositoryhttps://pmc.ncbi.nlm.nih.gov/articles/PMC10043783/pdf/nihms-1881841.pdf

publisherhttps://link.springer.com/content/pdf/10.1007/s00467-021-05312-4.pdf

publisherhttps://link.springer.com/article/10.1007/s00467-021-05312-4/fulltext.html

repositoryhttps://www.ncbi.nlm.nih.gov/pmc/articles/10043783

Fields of Study

Renal Diseases and GlomerulopathiesGenetic and Kidney Cyst DiseasesCell Adhesion Molecules Research0301 basic medicine0303 health sciences03 medical and health sciences0302 clinical medicine

MeSH Terms

Exome SequencingChildDNA Mutational AnalysisHematuriaHumansMutationNephritisNephritis, HereditaryNephrotic SyndromeProteinuriaSteroidsAtypical Hemolytic Uremic Syndrome

Keywords

MedicineNephritic syndromeNephrotic syndromeExome sequencingCohortInternal medicineCiliopathiesNephritisGlomerulonephritisPediatricsGastroenterologyImmunologyGeneticsMutationKidneyPhenotypeGeneBiologyDNA Mutational AnalysisNephritis, HereditaryProteinuriaHumansSteroidsChildAtypical Hemolytic Uremic SyndromeHematuria

Sustainable Development Goals

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