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 β papers, authors, and institutions outside the pilot are not represented. Methodology.
Driven by 1 paper. Top paper: βBTB domain mutations perturbing KCTD15 oligomerisation cause a distinctive frontonasal dysplasia syndromeβ.
David A. Cruz Walma, Daniel M. Pinkas, Rebecca S Tooze, Joshua C. Bufton, William Richardson +13 more