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Stephen Schaffner, Ph.D.

Co-Author

This page shows the publications co-authored by Stephen Schaffner and Mark Daly.
Connection Strength

0.244
  1. Calibrating a coalescent simulation of human genome sequence variation. Genome Res. 2005 Nov; 15(11):1576-83.
    View in: PubMed
    Score: 0.082
  2. Searching for missing heritability: designing rare variant association studies. Proc Natl Acad Sci U S A. 2014 Jan 28; 111(4):E455-64.
    View in: PubMed
    Score: 0.036
  3. Integrating common and rare genetic variation in diverse human populations. Nature. 2010 Sep 02; 467(7311):52-8.
    View in: PubMed
    Score: 0.029
  4. A second generation human haplotype map of over 3.1 million SNPs. Nature. 2007 Oct 18; 449(7164):851-61.
    View in: PubMed
    Score: 0.023
  5. Genome-wide detection and characterization of positive selection in human populations. Nature. 2007 Oct 18; 449(7164):913-8.
    View in: PubMed
    Score: 0.023
  6. An integrated haplotype map of the human major histocompatibility complex. Am J Hum Genet. 2003 Sep; 73(3):580-90.
    View in: PubMed
    Score: 0.018
  7. Human genome sequence variation and the influence of gene history, mutation and recombination. Nat Genet. 2002 Sep; 32(1):135-42.
    View in: PubMed
    Score: 0.016
  8. The structure of haplotype blocks in the human genome. Science. 2002 Jun 21; 296(5576):2225-9.
    View in: PubMed
    Score: 0.016
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.