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

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 8 papers. Top paper: Exome copy number variant detection, analysis, and classification in a large cohort of families with undiagnosed rare genetic disease.

25 citations

Alba Sanchis‐Juan, Kathryn Russell, Samantha Baxter, Katherine R. Chao, Moriel Singer‐Berk +59 more

5 citations

Megan Loew, Kathryn Russell, Brooklee Lightsey Tynes, Belinda N. Mandrell, Sara M. Witcraft +3 more

4 citations

Melanie Morse, Ibrahim Qaddoumi, Sean Phipps, Valerie McLaughlin Crabtree, Rachel C. Brennan +7 more

8 citations

Gabrielle Lemire, Maha S. Zaki, Mariel Wissman, Wathone Win, S. White +70 more

1 citations

Alba Sanchis‐Juan, Kathryn Russell, Samantha Baxter, Katherine R. Chao, Moriel Singer‐Berk +59 more

8 citations

Megan Othus, Carole Shaw, Kathryn Russell, Anna B. Halpern, Jacob Appelbaum +5 more

6 citations

Andrew J. Paladino, Kathryn Russell, Rebecca Rupff, Jamilla Griffith, Yujiao Mai +4 more

0 citations

Helene Starks, Lindsey Bandini, T. Harrington, Mary‐Elizabeth M. Percival, Roland B. Walter +6 more