Harvard Catalyst Profiles

Contact, publication, and social network information about Harvard faculty and fellows.

Steven A. McCarroll, Ph.D.

Co-Author

This page shows the publications co-authored by Steven McCarroll and Daniel MacArthur.
Connection Strength

0.724
  1. A whole-genome sequence study identifies genetic risk factors for neuromyelitis optica. Nat Commun. 2018 05 16; 9(1):1929.
    View in: PubMed
    Score: 0.190
  2. Quantifying prion disease penetrance using large population control cohorts. Sci Transl Med. 2016 Jan 20; 8(322):322ra9.
    View in: PubMed
    Score: 0.162
  3. A systematic survey of loss-of-function variants in human protein-coding genes. Science. 2012 Feb 17; 335(6070):823-8.
    View in: PubMed
    Score: 0.123
  4. Whole-genome analysis of human embryonic stem cells enables rational line selection based on genetic variation. Cell Stem Cell. 2022 Mar 03; 29(3):472-486.e7.
    View in: PubMed
    Score: 0.062
  5. The Genetic Landscape of Diamond-Blackfan Anemia. Am J Hum Genet. 2019 Feb 07; 104(2):356.
    View in: PubMed
    Score: 0.050
  6. The Genetic Landscape of Diamond-Blackfan Anemia. Am J Hum Genet. 2018 12 06; 103(6):930-947.
    View in: PubMed
    Score: 0.049
  7. A Loss-of-Function Splice Acceptor Variant in IGF2 Is Protective for Type 2 Diabetes. Diabetes. 2017 11; 66(11):2903-2914.
    View in: PubMed
    Score: 0.045
  8. Analysis of protein-coding genetic variation in 60,706 humans. Nature. 2016 08 18; 536(7616):285-91.
    View in: PubMed
    Score: 0.042
Connection Strength
The connection strength for co-authors is the sum of the scores for each of their shared publications.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.
Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.