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Paper Details

Multiple rare variants in high-risk pancreatic cancer-related genes may increase risk for pancreatic cancer in a subset of patients with and without germline CDKN2A mutations.
Hum Genet
22
2016
ATM, ATM variants, CDKN2A, CDKN2A factors, CPA1, MLH1, MSH2, MSH6, PC, PC-related genes, PMS2, digestive system tumors, high, high-risk pancreatic cancer-related genes, melanoma, mismatch repair, mismatch repair genes, pancreatic cancer, patients
Author NameAffiliation
Xiaohong R YangNational Cancer Institute, National Institutes of Health
Xiaohong R YangNational Cancer Institute, National Institutes of Health
Melissa RotunnoNational Cancer Institute, National Institutes of Health
Melissa RotunnoNational Cancer Institute, National Institutes of Health
Hunter BennettNational Cancer Institute, National Institutes of Health
Hunter BennettNational Cancer Institute, National Institutes of Health
Aurelie VogtNational Cancer Institute, National Institutes of Health
Aurelie VogtFrederick National Laboratory for Cancer Research, Inc.
Aurelie VogtNational Cancer Institute, National Institutes of Health
Aurelie VogtFrederick National Laboratory for Cancer Research, Inc.
Laurie BurdettNational Cancer Institute, National Institutes of Health
Laurie BurdettFrederick National Laboratory for Cancer Research, Inc.
Laurie BurdettNational Cancer Institute, National Institutes of Health
Laurie BurdettFrederick National Laboratory for Cancer Research, Inc.
Belynda HicksNational Cancer Institute, National Institutes of Health
Belynda HicksFrederick National Laboratory for Cancer Research, Inc.
Belynda HicksNational Cancer Institute, National Institutes of Health
Belynda HicksFrederick National Laboratory for Cancer Research, Inc.
Meredith YeagerNational Cancer Institute, National Institutes of Health
Meredith YeagerFrederick National Laboratory for Cancer Research, Inc.
Meredith YeagerNational Cancer Institute, National Institutes of Health
Meredith YeagerFrederick National Laboratory for Cancer Research, Inc.
Stephen J ChanockNational Cancer Institute, National Institutes of Health
Stephen J ChanockNational Cancer Institute, National Institutes of Health
Maria Teresa LandiNational Cancer Institute, National Institutes of Health
Margaret A TuckerNational Cancer Institute, National Institutes of Health
Margaret A TuckerNational Cancer Institute, National Institutes of Health
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