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Jonathan Rosand, M.D.

Co-Author

This page shows the publications co-authored by Jonathan Rosand and Kathryn Rexrode.
Connection Strength

0.272
  1. Subtype Specificity of Genetic Loci Associated With Stroke in 16?664 Cases and 32?792 Controls. Circ Genom Precis Med. 2019 07; 12(7):e002338.
    View in: PubMed
    Score: 0.053
  2. Publisher Correction: Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes. Nat Genet. 2019 Jul; 51(7):1192-1193.
    View in: PubMed
    Score: 0.053
  3. Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes. Nat Genet. 2018 04; 50(4):524-537.
    View in: PubMed
    Score: 0.048
  4. Genetic variation at 16q24.2 is associated with small vessel stroke. Ann Neurol. 2017 Mar; 81(3):383-394.
    View in: PubMed
    Score: 0.045
  5. Pathogenic ischemic stroke phenotypes in the NINDS-stroke genetics network. Stroke. 2014 Dec; 45(12):3589-96.
    View in: PubMed
    Score: 0.038
  6. Stroke Genetics Network (SiGN) study: design and rationale for a genome-wide association study of ischemic stroke subtypes. Stroke. 2013 Oct; 44(10):2694-702.
    View in: PubMed
    Score: 0.035
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.