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Abstract

Genetic mapping provides a powerful approach to identify genes and biological processes underlying any trait influenced by inheritance, including human diseases. We discuss the intellectual foundations of genetic mapping of Mendelian and complex traits in humans, examine lessons emerging from linkage analysis of Mendelian diseases and genome-wide association studies of common diseases, and discuss questions and challenges that lie ahead.

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Science
Volume 322 | Issue 5903
7 November 2008

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Published in print: 7 November 2008

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Supporting Online Material
www.sciencemag.org/cgi/content/full/322/5903/881/DC1
Table S1

Authors

Affiliations

David Altshuler* [email protected]
Broad Institute of Harvard and MIT, Cambridge, MA 02142, USA.
Center for Human Genetic Research and Department of Medicine, Massachusetts General Hospital, Boston, MA 02114, USA.
Department of Molecular Biology, Massachusetts General Hospital, Boston, MA 02114, USA.
Department of Genetics, Harvard Medical School, Boston, MA 02114, USA.
Department of Medicine, Harvard Medical School, Boston, MA 02114, USA.
Mark J. Daly* [email protected]
Broad Institute of Harvard and MIT, Cambridge, MA 02142, USA.
Center for Human Genetic Research and Department of Medicine, Massachusetts General Hospital, Boston, MA 02114, USA.
Department of Medicine, Harvard Medical School, Boston, MA 02114, USA.
Eric S. Lander* [email protected]
Broad Institute of Harvard and MIT, Cambridge, MA 02142, USA.
Department of Systems Biology, Harvard Medical School, Boston, MA 02114, USA.
Department of Biology, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.
Whitehead Institute for Biomedical Research, Cambridge, MA 02142, USA.

Notes

*
To whom correspondence should be addressed. E-mail: [email protected] (D.A.); [email protected] (M.J.D.); [email protected] (E.S.L.)

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