Harvard Catalyst Profiles

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Christine Edry Seidman, M.D.

Co-Author

This page shows the publications co-authored by Christine Seidman and Raju Kucherlapati.
Connection Strength

0.481
  1. Activation of multiple signaling pathways causes developmental defects in mice with a Noonan syndrome‚Äďassociated Sos1 mutation. J Clin Invest. 2010 Dec; 120(12):4353-65.
    View in: PubMed
    Score: 0.118
  2. Filter-based hybridization capture of subgenomes enables resequencing and copy-number detection. Nat Methods. 2009 Jul; 6(7):507-10.
    View in: PubMed
    Score: 0.107
  3. Shared genetic causes of cardiac hypertrophy in children and adults. N Engl J Med. 2008 May 01; 358(18):1899-908.
    View in: PubMed
    Score: 0.099
  4. The PTPN11 gene is not implicated in nonsyndromic hypertrophic cardiomyopathy. . 2005 Jan 30; 132A(3):333-4.
    View in: PubMed
    Score: 0.079
  5. Mutations in human TBX5 [corrected] cause limb and cardiac malformation in Holt-Oram syndrome. Nat Genet. 1997 Jan; 15(1):30-5.
    View in: PubMed
    Score: 0.045
  6. Spectrum of somatic mitochondrial mutations in five cancers. Proc Natl Acad Sci U S A. 2012 Aug 28; 109(35):14087-91.
    View in: PubMed
    Score: 0.033
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.