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Large scale genotype- and phenotype-driven machine learning in Von Hippel-Lindau disease.
Chiorean, Andreea; Farncombe, Kirsten M; Delong, Sean; Andric, Veronica; Ansar, Safa; Chan, Clarissa; Clark, Kaitlin; Danos, Arpad M; Gao, Yizhuo; Giles, Rachel H; Goldenberg, Anna; Jani, Payal; Krysiak, Kilannin; Kujan, Lynzey; Macpherson, Samantha; Maher, Eamonn R; McCoy, Liam G; Salama, Yasser; Saliba, Jason; Sheta, Lana; Griffith, Malachi; Griffith, Obi L; Erdman, Lauren; Ramani, Arun; Kim, Raymond H.
Affiliation
  • Chiorean A; Department of Medicine, Division of Medical Oncology, University Health Network, Toronto, Ontario, Canada.
  • Farncombe KM; Toronto General Hospital Research Institute, University Health Network, Toronto, Ontario, Canada.
  • Delong S; Department of Medicine, Division of Medical Oncology, University Health Network, Toronto, Ontario, Canada.
  • Andric V; Department of Medicine, Division of Medical Oncology, University Health Network, Toronto, Ontario, Canada.
  • Ansar S; Department of Medicine, Division of Medical Oncology, University Health Network, Toronto, Ontario, Canada.
  • Chan C; Department of Medicine, Division of Medical Oncology, University Health Network, Toronto, Ontario, Canada.
  • Clark K; Department of Medicine, Division of Oncology, Washington University School of Medicine, Washington University, St. Louis, Missouri, USA.
  • Danos AM; McDonnell Genome Institute, Washington University School of Medicine, Missouri, St. Louis, USA.
  • Gao Y; Department of Medicine, Division of Oncology, Washington University School of Medicine, Washington University, St. Louis, Missouri, USA.
  • Giles RH; McDonnell Genome Institute, Washington University School of Medicine, Missouri, St. Louis, USA.
  • Goldenberg A; Department of Medicine, Division of Medical Oncology, University Health Network, Toronto, Ontario, Canada.
  • Jani P; International Kidney Cancer Coalition, Duivendrecht-Amsterdam, Duivendrecht, The Netherlands.
  • Krysiak K; Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.
  • Kujan L; Department of Medicine, Division of Medical Oncology, University Health Network, Toronto, Ontario, Canada.
  • Macpherson S; Department of Medicine, Division of Oncology, Washington University School of Medicine, Washington University, St. Louis, Missouri, USA.
  • Maher ER; McDonnell Genome Institute, Washington University School of Medicine, Missouri, St. Louis, USA.
  • McCoy LG; Department of Medicine, Division of Oncology, Washington University School of Medicine, Washington University, St. Louis, Missouri, USA.
  • Salama Y; McDonnell Genome Institute, Washington University School of Medicine, Missouri, St. Louis, USA.
  • Saliba J; Department of Medicine, Division of Medical Oncology, University Health Network, Toronto, Ontario, Canada.
  • Sheta L; Department of Medical Genetics, University of Cambridge, Cambridge, UK.
  • Griffith M; NIHR Cambridge Biomedical Research Centre, Cambridge Biomedical Campus, Cambridge, UK.
  • Griffith OL; Department of Medicine, Division of Medical Oncology, University Health Network, Toronto, Ontario, Canada.
  • Erdman L; Department of Medicine, Division of Medical Oncology, University Health Network, Toronto, Ontario, Canada.
  • Ramani A; Department of Medicine, Division of Oncology, Washington University School of Medicine, Washington University, St. Louis, Missouri, USA.
  • Kim RH; McDonnell Genome Institute, Washington University School of Medicine, Missouri, St. Louis, USA.
Hum Mutat ; 43(9): 1268-1285, 2022 09.
Article in En | MEDLINE | ID: mdl-35475554

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Adrenal Gland Neoplasms / Von Hippel-Lindau Disease Type of study: Diagnostic_studies / Prognostic_studies Limits: Humans Language: En Journal: Hum Mutat Journal subject: GENETICA MEDICA Year: 2022 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Adrenal Gland Neoplasms / Von Hippel-Lindau Disease Type of study: Diagnostic_studies / Prognostic_studies Limits: Humans Language: En Journal: Hum Mutat Journal subject: GENETICA MEDICA Year: 2022 Document type: Article Affiliation country: