Novel and known genetic variants for male breast cancer risk at 8q24.21, 9p21.3, 11q13.3 and 14q24.1: Results from a multicenter study in Italy

European Journal of Cancer

Volumn 51, Issue 16, 2015, Pages 2289-2295

  Silvestri, Valentina ^a   Rizzolo, Piera ^a   Scarnò, Marco ^b   Chillemi, Giovanni ^b   Navazio, Anna Sara ^a   Valentini, Virginia ^a   Zelli, Veronica ^a   Zanna, Ines ^c   Saieva, Calogero ^c   Masala, Giovanna ^c   Bianchi, Simonetta ^d   Manoukian, Siranoush ^e   Barile, Monica ^f   Pensotti, Valeria ^g   Peterlongo, Paolo ^g   Varesco, Liliana ^h   Tommasi, Stefania ⁱ   Russo, Antonio ^j   Giannini, Giuseppe ^a   Cortesi, Laura ^k   Viel, Alessandra ^l   Montagna, Marco ^m   Radice, Paolo ^e   Palli, Domenico ^c   Ottini, Laura ^a   more..

^a SAPIENZA UNIVERSITY OF ROME   (Italy)

^b CINECA   (Italy)

^c CANCER RESEARCH AND PREVENTION INSTITUTE ISPO   (Italy)

^d UNIVERSITY OF FLORENCE   (Italy)

^e NATIONAL CANCER INSTITUTE   (Italy)

^f EUROPEAN INSTITUTE OF ONCOLOGY   (Italy)

^g FIRC INSTITUTE OF MOLECULAR ONCOLOGY   (Italy)

^h UNIVERSITY OF GENOA   (Italy)

ⁱ NATIONAL CANCER INSTITUTE GIOVANNI PAOLO II   (Italy)

^j UNIVERSITY OF PALERMO   (Italy)

^k UNIVERSITY OF MODENA AND REGGIO EMILIA   (Italy)

^l CENTRO DI RIFERIMENTO ONCOLOGICO   (Italy)

^m VENETO INSTITUTE OF ONCOLOGY IOV IRCCS   (Italy)

more..

Author keywords

8q24.21; BRCA1 2; Clinical pathologic characteristics; Low penetrance BC alleles; Male breast cancer; SNPs

Indexed keywords

BRCA1 PROTEIN; BRCA2 PROTEIN; EPIDERMAL GROWTH FACTOR RECEPTOR 2; BRCA1 PROTEIN, HUMAN; BRCA2 PROTEIN, HUMAN; TUMOR MARKER;

ADULT; ARTICLE; CANCER RISK; CANCER SUSCEPTIBILITY; CASE CONTROL STUDY; CHROMOSOME 11Q; CHROMOSOME 14Q; CHROMOSOME 8Q; CHROMOSOME 9Q; CONTROLLED STUDY; GENE; GENE LOCUS; GENE MUTATION; GENETIC ASSOCIATION; GENETIC VARIABILITY; GENOTYPE; HETEROZYGOTE; HISTOPATHOLOGY; HUMAN; ITALY; MAJOR CLINICAL STUDY; MALE; MALE BREAST CANCER; MIDDLE AGED; MULTICENTER STUDY; MULTICENTER STUDY (TOPIC); PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; BREAST TUMOR; CHI SQUARE DISTRIBUTION; CHROMOSOME 11; CHROMOSOME 14; CHROMOSOME 8; CHROMOSOME 9; CLINICAL TRIAL; GENE FREQUENCY; GENETIC PREDISPOSITION; GENETICS; HOMOZYGOTE; MULTIVARIATE ANALYSIS; MUTATION; ODDS RATIO; PATHOLOGY; PHENOTYPE; PREDICTIVE VALUE; RISK FACTOR; STATISTICAL MODEL;

BIOMARKERS, TUMOR; BRCA1 PROTEIN; BRCA2 PROTEIN; BREAST NEOPLASMS, MALE; CASE-CONTROL STUDIES; CHI-SQUARE DISTRIBUTION; CHROMOSOMES, HUMAN, PAIR 11; CHROMOSOMES, HUMAN, PAIR 14; CHROMOSOMES, HUMAN, PAIR 8; CHROMOSOMES, HUMAN, PAIR 9; GENE FREQUENCY; GENETIC PREDISPOSITION TO DISEASE; HETEROZYGOTE; HOMOZYGOTE; HUMANS; ITALY; LINEAR MODELS; LOGISTIC MODELS; MALE; MULTIVARIATE ANALYSIS; MUTATION; ODDS RATIO; PHENOTYPE; POLYMORPHISM, SINGLE NUCLEOTIDE; PREDICTIVE VALUE OF TESTS; RISK FACTORS;

EID: 84943657900     PISSN: 09598049     EISSN: 18790852     Source Type: Journal    
DOI: 10.1016/j.ejca.2015.07.020     Document Type: Article

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