Overrepresentation of rare variants in a specific ethnic group may confuse interpretation of association analyses

Author:

Keen-Kim Dianne,Mathews Carol A.,Reus Victor I.,Lowe Thomas L.,Herrera Luis Diego,Budman Cathy L.,Gross-Tsur Varda,Pulver Ann E.,Bruun Ruth D.,Erenberg Gerald,Naarden Allan,Sabatti Chiara,Freimer Nelson B.

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Reference17 articles.

1. Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease;Goate;Nature,1991

2. Multiple rare alleles contribute to low plasma levels of HDL cholesterol;Cohen;Science,2004

3. MEF2A sequence variants and coronary artery disease: a change of heart?;Altshuler;J. Clin. Invest.,2005

4. Family study and segregation analysis of Tourette syndrome: evidence for a mixed model of inheritance;Walkup;Am. J. Hum. Genet.,1996

5. Genetics and epidemiology of Tourette syndrome;Keen-Kim;J. Child Neurol.,2006

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