The BRCA1 Ashkenazi founder mutations occur on common haplotypes and are not highly correlated with anonymous single nucleotide polymorphisms likely to be used in genome-wide case-control association studies

BMC Genetics

Volumn 8, Issue , 2007, Pages

  Pereira, Lutécia H M ^a   Pineda, Marbin A ^a   Rowe, William H ^a   Fonseca, Libia R ^b   Greene, Mark H ^a   Offit, Kenneth ^c   Ellis, Nathan A ^d   Zhang, Jinghui ^a   Collins, Andrew ^e   Struewing, Jeffery P ^a  

^a NATIONAL CANCER INSTITUTE   (United States)

^b FLORIDA INTERNATIONAL UNIVERSITY   (United States)

^c MEMORIAL SLOAN KETTERING CANCER CENTER   (United States)

^d UNIVERSITY OF CHICAGO   (United States)

^e UNIVERSITY OF SOUTHAMPTON   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

BRCA1 PROTEIN;

AFRICAN AMERICAN; ARTICLE; BREAST CANCER; BREAST CARCINOGENESIS; CANCER RISK; CASE CONTROL STUDY; CHILD; CONTROLLED STUDY; CORRELATION COEFFICIENT; FEMALE; GENE DELETION; GENE LINKAGE DISEQUILIBRIUM; GENE MUTATION; GENETIC CORRELATION; GENETIC MARKER; GENETIC RISK; GENETIC SUSCEPTIBILITY; HUMAN; JEW; MAJOR CLINICAL STUDY; MUTATIONAL ANALYSIS; OVARY CANCER; POPULATION GENETICS; RISK ASSESSMENT; SINGLE NUCLEOTIDE POLYMORPHISM; BREAST TUMOR; ETHNOLOGY; FOUNDER EFFECT; GENETIC PREDISPOSITION; GENETICS; GENOME; HAPLOTYPE; OVARY TUMOR; TUMOR SUPPRESSOR GENE;

BREAST NEOPLASMS; CASE-CONTROL STUDIES; FEMALE; FOUNDER EFFECT; GENES, BRCA1; GENETIC PREDISPOSITION TO DISEASE; GENOME, HUMAN; HAPLOTYPES; HUMANS; JEWS; LINKAGE DISEQUILIBRIUM; OVARIAN NEOPLASMS; POLYMORPHISM, SINGLE NUCLEOTIDE; SEQUENCE DELETION;

EID: 36549023516     PISSN: None     EISSN: 14712156     Source Type: Journal    
DOI: 10.1186/1471-2156-8-68     Document Type: Article

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