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

Alexandra C Martin-Geary

Centre for Human Genetics

ORCID: 0000-0002-5818-1962

Also affiliated with Open Data Institute, University of Oxford

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 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 3 papers. Top paper: “Systematic identification of disease-causing promoter and untranslated region variants in 8,040 undiagnosed individuals with rare disease”.

Systematic identification of disease-causing promoter and untranslated region variants in 8,040 undiagnosed individuals with rare disease

medRxiv(2023)10.1101/2023.09.12.23295416

N/A

0DataRank · unranked

6 citations

Alexander J. M. Blakes, Ruebena Dawes, Scott D. Findlay, Jenny Lord, Susan Walker +17 more

De novo variants in the non-coding spliceosomal snRNA gene RNU4-2 are a frequent cause of syndromic neurodevelopmental disorders

medRxiv(2024)10.1101/2024.04.07.24305438

N/A

0DataRank · unranked

10 citations

Ruebena Dawes, Hyung Chul Kim, Sarah L. Stenton, Susan Walker, Alicia Ljungdahl +92 more

Aberrant splicing prediction during human organ development

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.07.16.665183

N/A

0DataRank · unranked

0 citations

Александр Неверов, Alexandra C Martin-Geary, Shubhankar Londhe, Carina Schröder, Vicente A. Yépez +3 more