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Paper Details

CIViCdb 2022: evolution of an open-access cancer variant interpretation knowledgebase.
Nucleic Acids Res
9
2023
470 genes, CIViC, CIViCdb, cancer, germline
Genetic Variation, High-Throughput Nucleotide Sequencing, Humans, Knowledge Bases, Neoplasms
Author NameAffiliation
Kilannin KrysiakWashington University in St Louis School of Medicine
Kilannin KrysiakWashington University in St Louis School of Medicine
Kilannin KrysiakSiteman Cancer Center, Washington University in St Louis School of Medicine
Kilannin KrysiakMcDonnell Genome Institute, Washington University in St Louis School of Medicine
Arpad M DanosMcDonnell Genome Institute, Washington University in St Louis School of Medicine
Arpad M DanosWashington University in St Louis School of Medicine
Jason SalibaWashington University in St Louis School of Medicine
Joshua F McMichaelMcDonnell Genome Institute, Washington University in St Louis School of Medicine
Joshua F McMichaelMcDonnell Genome Institute, Washington University in St Louis School of Medicine
Adam C CoffmanMcDonnell Genome Institute, Washington University in St Louis School of Medicine
Susanna KiwalaMcDonnell Genome Institute, Washington University in St Louis School of Medicine
Erica K BarnellMcDonnell Genome Institute, Washington University in St Louis School of Medicine
Lana M ShetaMcDonnell Genome Institute, Washington University in St Louis School of Medicine
Cameron J Grisdale
Lynzey KujanMcDonnell Genome Institute, Washington University in St Louis School of Medicine
Shahil P PemaMcDonnell Genome Institute, Washington University in St Louis School of Medicine
Jake LeverUniversity of Glasgow
Sarah RiddUniversity Health Network
Nicholas C SpiesMcDonnell Genome Institute, Washington University in St Louis School of Medicine
Veronica AndricUniversity Health Network
Andreea ChioreanUniversity Health Network
Damian T RiekeCharite - Universitatsmedizin Berlin, corporate member of Freie Universitat Berlin and Humboldt-Universitat zu Berlin
Kaitlin A ClarkMcDonnell Genome Institute, Washington University in St Louis School of Medicine
Caralyn Reisle
Caralyn ReisleUniversity of British Columbia
Ajay C VenigallaWashington University in St Louis School of Medicine
Mark Evans
Payal JaniUniversity Health Network
Hideaki TakahashiNational Cancer Center Hospital East
Avila SudaWashington University in St Louis School of Medicine
Peter HorakNational Center for Tumor Diseases (NCT) Heidelberg and German Cancer Research Center (DKFZ)
Deborah I RitterBaylor College of Medicine, USA Texas Children's Cancer Center, Texas Children's Hospital
Xin ZhouSt. Jude Children's Research Hospital
Xin ZhouSt. Jude Children's Research Hospital
Benjamin J AinscoughMcDonnell Genome Institute, Washington University in St Louis School of Medicine
Sean DelongYork University
Chimene KesserwanNYU Grossman School of Medicine, National Cancer Institute, National Institute of Health
Mario LampingCharite - Universitatsmedizin Berlin, corporate member of Freie Universitat Berlin and Humboldt-Universitat zu Berlin
Haolin ShenWashington University in St Louis School of Medicine
Alex R MarrWashington University in St Louis School of Medicine
My H HoangWashington University in St Louis School of Medicine
Kartik SinghalWashington University in St Louis School of Medicine
Mariam KhanfarWashington University in St Louis School of Medicine
Brian V LiMcDonnell Genome Institute, Washington University in St Louis School of Medicine
Wan-Hsin LinMayo Clinic Florida
Panieh TerrafMemorial Sloan Kettering Cancer Center
Laura B Corson
Yasser SalamaUniversity Health Network
Katie M CampbellMcDonnell Genome Institute, Washington University in St Louis School of Medicine
Kirsten M FarncombeToronto General Hospital Research Institute, University Health Network
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Datasets

CIViCdbClinical interpretation of variants in cancerLink
CIViCdbClinical interpretation of variants in cancerLink