Combined effect of low-penetrant SNPs on breast cancer risk

British Journal of Cancer

Volumn 106, Issue 2, 2012, Pages 389-396

  Harlid, S ^a   Ivarsson, M I L ^b   Butt, S ^c   Grzybowska, E ^d   Eyfjord J E ^e   Lenner, P ^f   Forsti A ^a,g   Hemminki, K ^a,g   Manjer, J ^c   Dillner, J ^a,h   Carlson, J ^a  

^a LUND UNIVERSITY   (Sweden)

^b Wallenberg Laboratory   (Sweden)

^c LUND UNIVERSITY HOSPITAL   (Sweden)

^d INSTITUTE OF ONCOLOGY   (Poland)

^e UNIVERSITY OF ICELAND   (Iceland)

^f UMEÅ UNIVERSITY HOSPITAL   (Sweden)

^g GERMAN CANCER RESEARCH CENTER DKFZ   (Germany)

^h KAROLINSKA UNIVERSITY HOSPITAL   (Sweden)

Author keywords

breast cancer; common variants; hereditability; multiple risk allele GWA replication

Indexed keywords

ADULT; AGED; ALLELE; ARTICLE; BREAST CANCER; CANCER RISK; CONTROLLED STUDY; GENETIC ASSOCIATION; GENOTYPE; HUMAN; LOGISTIC REGRESSION ANALYSIS; MAJOR CLINICAL STUDY; MATRIX ASSISTED LASER DESORPTION IONIZATION TIME OF FLIGHT MASS SPECTROMETRY; POSTMENOPAUSE; PREMENOPAUSE; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM;

AGED; AGED, 80 AND OVER; BASE SEQUENCE; BREAST NEOPLASMS; DNA PRIMERS; FEMALE; GENETIC PREDISPOSITION TO DISEASE; HUMANS; LOGISTIC MODELS; MIDDLE AGED; POLYMORPHISM, SINGLE NUCLEOTIDE; PROSPECTIVE STUDIES; SWEDEN;

EID: 84856415225     PISSN: 00070920     EISSN: 15321827     Source Type: Journal    
DOI: 10.1038/bjc.2011.461     Document Type: Article

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