( en | de | ru )

 

Disambiguation of "Sutter, Christian"

Author of the publication

copydeleteadd this publication to your clipboard
Low-risk variants FGFR2, TNRC9 and LSP1 in German familial breast cancer patients

, , , , , , , , , , , , , , , , , , , , , , and . International journal of cancer. Journal international du cancer, 126 (12): 2858–2862 (2010)

Please choose a person to relate this publication to

To differ between persons with the same name, the academic degree and the title of an important publication will be displayed. You can also use the button next to the name to display some publications already assigned to the person.

Christian Sutter

Christian Sutter

Wolfgang Sutter

Kurt Sutter

Kurt Sutter

 

Other publications of authors with the same name

Common breast cancer susceptibility alleles and the risk of breast cancer for BRCA1 and BRCA2 mutation carriers: implications for risk prediction, , , , , , , , , and 168 other author(s). Cancer research, 70 (23): 9742–9754 (2010)Eight novel MSH6 germline mutations in patients with familial and nonfamilial colorectal cancer selected by loss of protein expression in tumor tissue, , , , , , , , , and 4 other author(s). Human mutation, 23 (3): 285 (2004)Ovarian cancer susceptibility alleles and risk of ovarian cancer in BRCA1 and BRCA2 mutation carriers, , , , , , , , , and 176 other author(s). Human mutation, 33 (4): 690–702 (2012)Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk, , , , , , , , , and 252 other author(s). PLoS genetics, 9 (3): e1003212 (2013)Common breast cancer susceptibility alleles are associated with tumour subtypes in BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2, , , , , , , , , and 172 other author(s). Breast cancer research : BCR, 13 (6): R110 (2011)Identification of a DMBT1 polymorphism associated with increased breast cancer risk and decreased promoter activity, , , , , , , , , and 17 other author(s). Human mutation, 31 (1): 60–66 (2010)Common variants of the BRCA1 wild-type allele modify the risk of breast cancer in BRCA1 mutation carriers, , , , , , , , , and 99 other author(s). Human molecular genetics, 20 (23): 4732–4747 (2011)Polymorphisms in BRCA2 resulting in aberrant codon-usage and their analysis on familial breast cancer risk, , , , , , , , , and 4 other author(s). Breast cancer research and treatment, 118 (2): 407–413 (2009)Low-risk variants FGFR2, TNRC9 and LSP1 in German familial breast cancer patients, , , , , , , , , and 13 other author(s). International journal of cancer. Journal international du cancer, 126 (12): 2858–2862 (2010)Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers, , , , , , , , , and 171 other author(s). Breast cancer research : BCR, 14 (1): R33 (2012)