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Paper Details

Clinically relevant combined effect of polygenic background, rare pathogenic germline variants, and family history on colorectal cancer incidence.
BMC Med Genomics
6
2023
APC, CRC, CRC susceptibility genes, FH, MLH1, MSH2, MSH6, PMS2, PRS, colorectal cancer, common variants, risk
Author NameAffiliation
Markus M N??thenInstitute of Human Genetics, University of Bonn
Markus M N??thenInstitute of Human Genetics, University of Bonn
Andreas J ForstnerInstitute of Human Genetics, University of Bonn
Andreas J ForstnerUniversity of Marburg
Andreas J ForstnerInstitute of Neuroscience and Medicine (INM-1), Research Center Julich
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