GeneYenta specifications


Unique identifier OMICS_14130
Name GeneYenta
Interface Web user interface
Restrictions to use None
Programming languages Javascript
Database management system MySQL
Computer skills Basic
Stability Stable
Maintained Yes


  • Primates
    • Homo sapiens



  • person_outline Wyeth Wasserman <>

Publication for GeneYenta

GeneYenta in publication

PMCID: 4850887
PMID: 27148566
DOI: 10.1101/mcs.a000372

[…] among the groups and projects using the hpo are the u.k. 100,000 genomes project (rare diseases), the canadian care for rare, phenomecentral (, the case matching system geneyenta (), the u.s. national institutes of health undiagnosed diseases program and network, and the sanger institute's deciphering developmental disorders (ddd) () and decipher () databases. […]

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GeneYenta institution(s)
Department of Medical Genetics, Centre for Molecular Medicine and Therapeutics, Child and Family Research Institute, University of British Columbia, Vancouver, BC, Canada; Department of Medical Genetics, University of British Columbia, Vancouver, BC, Canada; Stanford University, Stanford, CA, USA
GeneYenta funding source(s)
British Columbia Children’s Hospital Foundation as 1st Collaborative Area of Innovation; Genome BC (SOF-195); BC Clinical Genomics Network (#00032); the Canadian Institutes of Health Research (#301221); Canadian Institutes of Health Research Studentship Award; Genome BC and Genome Canada (ABC4DE Project).

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