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

Chantal Farra

Saint Joseph University

ORCID: 0000-0003-3200-1086
Medicine

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 2 papers. Top paper: “A synonymous variant in MYO15A enriched in the Ashkenazi Jewish population causes autosomal recessive hearing loss due to abnormal splicing”.

A synonymous variant in MYO15A enriched in the Ashkenazi Jewish population causes autosomal recessive hearing loss due to abnormal splicing

European Journal of Human Genetics(2021)10.1038/s41431-020-00790-w
N/A
0DataRank · unranked
17 citations

Chayada Tangshewinsirikul, Kevin T. Booth, Héla Azaiez, Devorah Yefet, Adina Quint +23 more

PI4K2A deficiency causes innate error in intracellular trafficking with developmental and epileptic‐dyskinetic encephalopathy

Annals of Clinical and Translational Neurology(2022)10.1002/acn3.51634
N/A
0DataRank · unranked
24 citations

Joshua G. Pemberton, Elizabeth Ferrer, Tony Yammine, Chantal Farra, Mohammad Hasan Mohammadi +13 more