Claudine Isaacs

发表

Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus

A. Whittemore, S. Cross, R. Nussbaum, 2016, Breast Cancer Research.

Germline mutations in CDH1 are infrequent in women with early-onset or familial lobular breast cancers

O. Olopade, M. Southey, P. Miron, 2010, Journal of Medical Genetics.

Genetic Epidemiology

K. Humphreys, O. Olopade, B. Karlan, 2011, Methods in Molecular Biology.

Colorectal-cancer incidence and mortality with screening flexible sigmoidoscopy.

Mark P Purdue, Barnett S Kramer, John K Gohagan, 2012, The New England journal of medicine.

q 31 . 2 and in ZNF 365 are associated with breast cancer risk for BRCA 1 and / or BRCA 2 mutation carriers

V. Pankratz, F. Couch, B. Bonanni, 2012 .

Common breast cancer susceptibility alleles are associated with tumor subtypes in BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2.

B. Bonanni, O. Olopade, B. Karlan, 2012 .

Genetic Epidemiology

K. Humphreys, O. Olopade, B. Karlan, 2020, Methods in Molecular Biology.

Hereditary Breast Cancer

T. Rebbeck, C. Isaacs, Claudine Isaacs, 2007, Cancer Plus.

Association of type and location of BRCA1 and BRCA2 mutations with risk of breast and ovarian cancer.

A. Whittemore, F. Couch, B. Bonanni, 2015 .

Association of Rad51 polymorphism with DNA repair in BRCA1 mutation carriers and sporadic breast cancer risk

J. Freudenheim, J. Nie, C. Marian, 2011, BMC Cancer.

Supplement use during an intergroup clinical trial for breast cancer (S0221)

G. Hortobagyi, C. Isaacs, J. Unger, 2013, Breast Cancer Research and Treatment.

Association of Rad51 polymorphism with DNA repair in BRCA1 mutation carriers and sporadic breast cancer risk

S. Edge, J. Freudenheim, C. Isaacs, 2011, BMC Cancer.