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

James T. Neal

Broad Institute

ORCID: 0000-0002-3962-8570

Also affiliated with Foundation Center, Novo Nordisk (United States)

Biochemistry, Genetics and Molecular BiologyMedicine

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: “Massively parallel phenotyping of variant impact in cancer with Perturb-seq reveals a shift in the spectrum of cell states induced by somatic mutations”.

Massively parallel phenotyping of variant impact in cancer with Perturb-seq reveals a shift in the spectrum of cell states induced by somatic mutations

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.11.16.383307

N/A

0.673DataRank · unranked

12 citations

James T. Neal, Emily Shea, Pratiksha I. Thakore, Livnat Jerby-Arnon, Danielle Dionne +15 more

Author Correction: Massively parallel phenotyping of coding variants in cancer with Perturb-seq

Nature Biotechnology(2022)10.1038/s41587-022-01495-9

N/A

0.133DataRank · unranked

1 citations

James T. Neal, Emily Shea, Pratiksha I. Thakore, Livnat Jerby-Arnon, Danielle Dionne +17 more

Massively parallel assessment of human variants with base editor screens

Cell(2021)10.1016/j.cell.2021.01.012

N/A

0DataRank · unranked

333 citations

Mudra Hegde, Christian Fagre, Peter C. DeWeirdt, Annabel K. Sangree, Zsofia M Szegletes +9 more