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Defining Disease in the Genomics Era
Author(s) -
Larissa K. Temple,
Robin S. McLeod,
Steven Gallinger,
James G. Wright
Publication year - 2001
Publication title -
science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 12.556
H-Index - 1186
eISSN - 1095-9203
pISSN - 0036-8075
DOI - 10.1126/science.1062938
Subject(s) - genomics , disease , genetic variation , variation (astronomy) , human genome , biology , genome , human disease , human genetic variation , genetics , computational biology , evolutionary biology , medicine , gene , pathology , physics , astrophysics
With sequencing of the human genome complete and comparative analyses of genetic variations among individuals well under way, there is increasing uncertainty about which variations are associated with disease. In a Science and Society Essay, Temple and colleagues discuss the need for an explicit definition of disease that takes into consideration possible risks and adverse consequences associated with genetic variations, while at the same time acknowledging that a disease cannot be defined by a single genetic variation.

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