Tomas Kirchhoff

发表

Common alleles at 6q25.1 and 1p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriers.

Christiana Kartsonaki, Mads Thomassen, Etienne Rouleau, 2011, Human molecular genetics.

Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers

Mads Thomassen, Nina Ditsch, Vijai Joseph, 2012, Breast Cancer Research.

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

Mads Thomassen, Nina Ditsch, Dieter Niederacher, 2009, Human molecular genetics.

Identification of a BRCA2-Specific Modifier Locus at 6p24 Related to Breast Cancer Risk

Mads Thomassen, Julian Peto, Peter A. Fasching, 2013, PLoS genetics.

Functional and genomic approaches reveal an ancient CHEK2 allele associated with breast cancer in the Ashkenazi Jewish population.

Kenneth Offit, Tom Walsh, T. Walsh, 2005, Human molecular genetics.

A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor–negative breast cancer in the general population

Christiana Kartsonaki, Mads Thomassen, Julian Peto, 2010, Nature Genetics.

Correction: Common Genetic Variants and Modification of Penetrance of BRCA2-Associated Breast Cancer

Joshua M. Korn, Christiana Kartsonaki, Amanda B. Spurdle, 2010, PLoS Genetics.

1147PDGermline determinants of immune related adverse events (irAEs) in melanoma immunotherapy response

Iman Osman, J. S. Weber, Tomas Kirchhoff, 2017 .

Mutation burden as a potential prognostic marker of melanoma progression and survival.

Adriana Heguy, A. Heguy, T. Kirchhoff, 2017 .

The signatures of autozygosity among patients with colorectal cancer.

Jurg Ott, Kenneth Offit, Francis Barany, 2008, Cancer research.

Analysis of genetic variation in Ashkenazi Jews by high density SNP genotyping

Eleazar Eskin, Kenneth Offit, Kirk E Lohmueller, 2008, BMC Genetics.

Genetic Polymorphisms in Vitamin D Metabolism and Signaling Genes and Risk of Breast Cancer: A Nested Case-Control Study

Eva Lundin, Tomas Axelsson, Göran Hallmans, 2015, PloS one.

Common breast cancer susceptibility alleles and the risk of breast cancer for BRCA1 and BRCA2 mutation carriers: implications for risk prediction.

Mads Thomassen, Etienne Rouleau, Dieter Niederacher, 2010, Cancer research.

Melanoma risk loci as determinants of melanoma recurrence and survival

Yongzhao Shao, Justin Rendleman, David Polsky, 2013, Journal of Translational Medicine.