Browsing Universität Ulm / Medizin by Person "Aalfs, Cora M."

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A Nonsynonymous Polymorphism in IRS1 Modifies Risk of Developing Breast and Ovarian Cancers in BRCA1 and Ovarian Cancer in BRCA2 Mutation Carriers

Ding, Yuan C. et al. (2012)

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An original phylogenetic approach identified mitochondrial haplogroup T1a1 as inversely associated with breast cancer risk in BRCA2 mutation carriers

Blein, Sophie et al. (2015)

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Assessing Associations between the AURKA-HMMR-TPX2-TUBG1 Functional Module and Breast Cancer Risk in BRCA1/2 Mutation Carriers

Blanco, Ignacio et al. (2015)

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Associations of common breast cancer susceptibility alleles with risk of breast cancer subtypes in BRCA1 and BRCA2 mutation carriers

Kuchenbaecker, Karoline B. et al. (2014)

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Breast Cancer Risk and 6q22.33: Combined Results from Breast Cancer Association Consortium and Consortium of Investigators on Modifiers of BRCA1/2

Kirchhoff, Tomas et al. (2012)

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Common Breast Cancer Susceptibility Alleles and the Risk of Breast Cancer for BRCA1 and BRCA2 Mutation Carriers: Implications for Risk Prediction

Antoniou, Antonis C. et al. (2010)

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Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers

Antoniou, Antonis C. et al. (2009)

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Evidence for SMAD3 as a modifier of breast cancer risk in BRCA2 mutation carriers

Walker, Logan C. et al. (2010)

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Height and Body Mass Index as Modifiers of Breast Cancer Risk in BRCA1/2 Mutation Carriers: A Mendelian Randomization Study

Qian, Frank et al. (2019)

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Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer

Phelan, Catherine M. et al. (2017)

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Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer

Milne, Roger L. et al. (2017)

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Interplay between BRCA1 and RHAMM Regulates Epithelial Apicobasal Polarization and May Influence Risk of Breast Cancer

Maxwell, Christopher A. et al. (2011)

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Large scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants: An ENIGMA resource to support clinical variant classification

Parsons, Michael T. et al. (2019)

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Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations

Rebbeck, Timothy R. et al. (2018)

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Mutations in SPRTN cause early onset hepatocellular carcinoma, genomic instability and progeroid features

Lessel, Davor et al. (2014)

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Ovarian Cancer Susceptibility Alleles and Risk of Ovarian Cancer in BRCA1 and BRCA2 Mutation Carriers

Ramus, Susan J. et al. (2012)

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The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer

Figlioli, Gisella et al. (2019)

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