🏆 Finalist — NIH Data Sharing Index (“S-Index”) Challenge

Daniah Beleford

University of California, San Francisco

ORCID: 0000-0003-1766-1094

Also affiliated with University of California San Diego, Rady Children's Hospital-San Diego, UCSF Benioff Children's Hospital, University of California, Davis

MedicineBiochemistry, Genetics and Molecular Biology

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 5%percentile
0.572Author DataRank

Indexed papers

1in pilot corpus
datarank_citation_only_1hop_v6· scope data_onlyMethodology
Why this DataRank?

An author's DataRank is the sum of the DataRanks of all 1 indexed paper attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

Top data-sharing exemplar

The highest-impact dataset this researcher has shared, ranked by DataRank — the single contribution doing the most to lift their data-sharing standing.

BCL11A intellectual developmental disorder: defining the clinical spectrum and genotype-phenotype correlations

European Journal of Human Genetics(2024)10.1038/s41431-024-01701-z
Top 34%
0.572DataRank
Top 34%16 citations

Felice D’Arco, Kimberly A. Aldinger, Constance Smith‐Hicks, Christiane Zweier, Gyri Aasland Gradek +69 more

Papers

Driven by 9 papers — median percentile 66. Top paper: “Application of full-genome analysis to diagnose rare monogenic disorders”.

Application of full-genome analysis to diagnose rare monogenic disorders

npj Genomic Medicine(2021)10.1038/s41525-021-00241-5
N/A
0.598DataRank · unranked
53 citations

Monica Penon‐Portmann, K. Wong, Michal Levy‐Sakin, Michelle Verghese, Anne Slavotinek +15 more

BCL11A intellectual developmental disorder: defining the clinical spectrum and genotype-phenotype correlations

European Journal of Human Genetics(2024)10.1038/s41431-024-01701-z
Top 34%
0.572DataRank
Top 34%16 citations

Felice D’Arco, Kimberly A. Aldinger, Constance Smith‐Hicks, Christiane Zweier, Gyri Aasland Gradek +69 more

PTPN14, a modifier of HHT, protects SMAD4 from ubiquitination and turnover to potentiate BMP9 signaling in endothelial cells

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.09.29.462397
N/A
0.208DataRank · unranked
3 citations

Daniah Beleford, Mark A. Taylor, Sugandha Basu, Xinjian Cen, Suprita Trilok +4 more

Biallelic variants in the RNA exosome gene EXOSC5 are associated with developmental delays, short stature, cerebellar hypoplasia and motor weakness

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.04.01.839274
N/A
0DataRank · unranked
1 citations

Doriana Misceo, Stephanie Htun, Linda Mathisen, Eirik Frengen, Michelle Foreman +16 more

BCL11A intellectual developmental disorder: defining the clinical spectrum and genotype-phenotype correlations

medRxiv(2021)10.1101/2021.09.06.21262776
N/A
0DataRank · unranked
8 citations

Felice D’Arco, Kimberly A. Aldinger, Constance Smith‐Hicks, Christiane Zweier, Gyri Aasland Gradek +64 more

Biallelic variants in the RNA exosome gene EXOSC5 are associated with developmental delays, short stature, cerebellar hypoplasia and motor weakness

Human Molecular Genetics(2020)10.1093/hmg/ddaa108
N/A
0DataRank · unranked
37 citations

Doriana Misceo, Stephanie Htun, Linda Mathisen, Eirik Frengen, Michelle Foreman +18 more

BCL11A intellectual developmental disorder: defining the clinical spectrum and genotype-phenotype correlations

UNC Libraries(2024)10.17615/2254-fj45
N/A
0DataRank · unranked
0 citations

Rolph Pfundt, Birgit Elisabeth Kristiansen, Mary J. Green, Sally Ann Lynch, Amanda Openshaw +67 more

A missense variant, p.(Ile269Asn), in MC4R as a secondary finding in a child with BCL11A-related intellectual disability

European Journal of Medical Genetics(2020)10.1016/j.ejmg.2020.103969
N/A
0DataRank · unranked
5 citations

Jessica Van Ziffle, Uğur Hodoğlugil, Anne Slavotinek, Daniah Beleford

Application of Full Genome Analysis to Diagnose Rare Monogenic Disorders

medRxiv(2020)10.1101/2020.10.22.20216531
N/A
0DataRank · unranked
9 citations

Monica Penon‐Portmann, K. Wong, Michal Levy‐Sakin, Michelle Verghese, Anne Slavotinek +15 more