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

Gabriele Richard

ORCID: 0000-0003-1976-9672
Biochemistry, 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 2%percentile
3.3Author DataRank

Indexed papers

3in 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 3 indexed papers 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.

Axenfeld-Rieger syndrome: more than meets the eye

Journal of Medical Genetics(2022)10.1136/jmg-2022-108646
Top 12%
1.7DataRank
Top 12%81 citations

Mohit Maheshwari, Jenina Capasso, Hüban Atilla, Lubica Dudakova, Samuel Thompson +22 more

Papers

Driven by 5 papers — median percentile 81. Top paper: “Axenfeld-Rieger syndrome: more than meets the eye”.

Axenfeld-Rieger syndrome: more than meets the eye

Journal of Medical Genetics(2022)10.1136/jmg-2022-108646
Top 12%
1.7DataRank
Top 12%81 citations

Mohit Maheshwari, Jenina Capasso, Hüban Atilla, Lubica Dudakova, Samuel Thompson +22 more

Deciphering the genetic architecture and ethnographic distribution of IRD in three ethnic populations by whole genome sequence analysis

PLoS Genetics(2021)10.1371/journal.pgen.1009848
Top 19%
1.1DataRank
Top 19%36 citations

Adda Villanueva, Angel Soto‐Hermida, Jacque L. Duncan, Hiroko Matsui, Shyamanga Borooah +24 more

Harmonizing the Collection of Clinical Data on Genetic Testing Requisition Forms to Enhance Variant Interpretation in Hypertrophic Cardiomyopathy (HCM)

Journal of Molecular Diagnostics(2021)10.1016/j.jmoldx.2021.01.014
Top 40%
0.481DataRank
Top 40%8 citations

Alexander Ing, Christian Antolik, Christina Austin‐Tse, Linnea M. Baudhuin, Lucas Bronicki +25 more

Case Series of Nizon‐Isidor Syndrome by Heterozygous Variants in MED12L With Further Evidence of Mitotic Instability in One Case With Diploid–Triploid Mosaicism

American Journal of Medical Genetics Part A(2025)10.1002/ajmg.a.64233
N/A
0.104DataRank · unranked
1 citations

Kimberly Ezell, Deanna S. Bell, Brian Corner, Ashley McMinn, Joy D. Cogan +16 more

Mutation update: Variants of the ENPP1 gene in pathologic calcification, hypophosphatemic rickets, and cutaneous hypopigmentation with punctate keratoderma

Human Mutation(2022)10.1002/humu.24391
N/A
0DataRank · unranked
11 citations

Michael A. Levine, Gabriele Richard, Michelle M. Morrow, Elizabeth K. Flynn, Jouni Uitto +2 more