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Paper Details

Large scale genotype- and phenotype-driven machine learning in Von Hippel-Lindau disease.
Hum Mutat
4
2022
Author NameAffiliation
Kirsten M FarncombeToronto General Hospital Research Institute, University Health Network
Arpad M DanosWashington University School of Medicine, Washington University
Arpad M DanosMcDonnell Genome Institute, Washington University School of Medicine
Rachel H Giles
Kilannin KrysiakWashington University School of Medicine, Washington University
Kilannin KrysiakMcDonnell Genome Institute, Washington University School of Medicine
Lynzey KujanWashington University School of Medicine, Washington University
Lynzey KujanMcDonnell Genome Institute, Washington University School of Medicine
Yasser SalamaUniversity Health Network
Jason SalibaWashington University School of Medicine, Washington University
Jason SalibaMcDonnell Genome Institute, Washington University School of Medicine
Lana M ShetaWashington University School of Medicine, Washington University
Lana M ShetaMcDonnell Genome Institute, Washington University School of Medicine
Malachi GriffithWashington University School of Medicine, Washington University
Malachi GriffithMcDonnell Genome Institute, Washington University School of Medicine
Obi L GriffithWashington University School of Medicine, Washington University
Obi L GriffithMcDonnell Genome Institute, Washington University School of Medicine
Lauren ErdmanThe Hospital for Sick Children
Raymond H KimPrincess Margaret Cancer Centre, University Health Network and Sinai Health System
Raymond H KimDivision of Clinical and Metabolic Genetics, The Hospital for Sick Children
Raymond H KimOntario Institute for Cancer Research
Raymond H KimUniversity of Toronto
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Datasets

Human Phenotype OntologyStandardized vocabulary of phenotypic abnormalities in human diseaseLink
Human Phenotype OntologyStandardized vocabulary of phenotypic abnormalities in human diseaseLink
Human Phenotype OntologyStandardized vocabulary of phenotypic abnormalities in human diseaseLink
Human Phenotype OntologyStandardized vocabulary of phenotypic abnormalities in human diseaseLink
Human Phenotype OntologyStandardized vocabulary of phenotypic abnormalities in human diseaseLink
Human Phenotype OntologyStandardized vocabulary of phenotypic abnormalities in human diseaseLink
Human Phenotype OntologyStandardized vocabulary of phenotypic abnormalities in human diseaseLink
Human Phenotype OntologyStandardized vocabulary of phenotypic abnormalities in human diseaseLink
Human Phenotype OntologyStandardized vocabulary of phenotypic abnormalities in human diseaseLink
Human Phenotype OntologyStandardized vocabulary of phenotypic abnormalities in human diseaseLink
Human Phenotype OntologyStandardized vocabulary of phenotypic abnormalities in human diseaseLink
Human Phenotype OntologyStandardized vocabulary of phenotypic abnormalities in human diseaseLink
Human Phenotype OntologyStandardized vocabulary of phenotypic abnormalities in human diseaseLink
Human Phenotype OntologyStandardized vocabulary of phenotypic abnormalities in human diseaseLink
Human Phenotype OntologyStandardized vocabulary of phenotypic abnormalities in human diseaseLink