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Paper Details

Patterns and functional implications of rare germline variants across 12 cancer types.
Nat Commun
200
2015
AML, ATM, BAP1, BRCA1, BRCA1 rare missense variants, BRCA1/2, BRIP1, Cancer, FANCM, MSH6, PALB2, RAD51C, RAD51C/D, acute myeloid leukaemia, cancer, cancer genes, cancer-susceptibility-associated genes, cancers, germline cancer susceptibility variants, ovarian cancer, rare, rare germline variants, stomach and endometrial cancers, stomach cancer, tumour
Author NameAffiliation
Charles LuThe McDonnell Genome Institute, Washington University in St. Louis
Michael C WendlThe McDonnell Genome Institute, Washington University in St. Louis
Michael C WendlWashington University in St. Louis
Michael C WendlWashington University in St. Louis
Michael C WendlThe McDonnell Genome Institute, Washington University in St. Louis
Michael C WendlWashington University in St. Louis
Michael C WendlWashington University in St. Louis
Jiayin WangThe McDonnell Genome Institute, Washington University in St. Louis
Jiayin WangWashington University in St. Louis
Michael D McLellanThe McDonnell Genome Institute, Washington University in St. Louis
Michael D McLellanThe McDonnell Genome Institute, Washington University in St. Louis
Kuan-Lin HuangThe McDonnell Genome Institute, Washington University in St. Louis
Kuan-Lin HuangWashington University in St. Louis
Kuan-Lin HuangThe McDonnell Genome Institute, Washington University in St. Louis
Kuan-Lin HuangWashington University in St. Louis
Matthew A WyczalkowskiThe McDonnell Genome Institute, Washington University in St. Louis
Matthew A WyczalkowskiWashington University in St. Louis
Matthew A WyczalkowskiThe McDonnell Genome Institute, Washington University in St. Louis
Matthew A WyczalkowskiWashington University in St. Louis
Reyka G JayasingheThe McDonnell Genome Institute, Washington University in St. Louis
Reyka G JayasingheWashington University in St. Louis
Reyka G JayasingheThe McDonnell Genome Institute, Washington University in St. Louis
Reyka G JayasingheWashington University in St. Louis
Qunyuan ZhangThe McDonnell Genome Institute, Washington University in St. Louis
Beifang NiuThe McDonnell Genome Institute, Washington University in St. Louis
Kai YeThe McDonnell Genome Institute, Washington University in St. Louis
Kai YeWashington University in St. Louis
Robert S FultonThe McDonnell Genome Institute, Washington University in St. Louis
Robert S FultonWashington University in St. Louis
Robert S FultonThe McDonnell Genome Institute, Washington University in St. Louis
Robert S FultonWashington University in St. Louis
Joshua F McMichaelThe McDonnell Genome Institute, Washington University in St. Louis
Joshua F McMichaelThe McDonnell Genome Institute, Washington University in St. Louis
Cyriac KandothThe McDonnell Genome Institute, Washington University in St. Louis
Daniel C KoboldtThe McDonnell Genome Institute, Washington University in St. Louis
Christopher A MillerThe McDonnell Genome Institute, Washington University in St. Louis
James M EldredThe McDonnell Genome Institute, Washington University in St. Louis
David E LarsonThe McDonnell Genome Institute, Washington University in St. Louis
David E LarsonWashington University in St. Louis
Bradley A OzenbergerThe McDonnell Genome Institute, Washington University in St. Louis
Bradley A OzenbergerWashington University in St. Louis
Bradley A OzenbergerThe McDonnell Genome Institute, Washington University in St. Louis
Bradley A OzenbergerWashington University in St. Louis
Ramaswamy GovindanWashington University in St. Louis
Ramaswamy GovindanSiteman Cancer Center, Washington University in St Louis
Matthew J WalterWashington University in St. Louis
Matthew J WalterSiteman Cancer Center, Washington University in St Louis
Matthew J EllisWashington University in St. Louis
Matthew J EllisSiteman Cancer Center, Washington University in St Louis
Elaine R MardisThe McDonnell Genome Institute, Washington University in St. Louis
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