GeneMatcher: A Matching Tool for Connecting Investigators with an Interest in the Same Gene
Author:
Affiliation:
1. Institute of Genetic Medicine; Johns Hopkins University School of Medicine; Baltimore Maryland
2. FS Consulting; Salem Massachusetts
Funder
NHGRI
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Reference5 articles.
1. Exome sequencing reveals pathogenic mutations in 91 strains of mice with Mendelian disorders;Fairfield;Genome Res.,2015
2. PhenoDB: a new web-based tool for the collection, storage, and analysis of phenotypic features;Hamosh;Hum Mutat,2013
3. The Human Phenotype Ontology project: linking molecular biology and disease through phenotype data;Köhler;Nucleic Acids Res,2014
4. New tools for Mendelian disease gene identification: PhenoDB variant analysis module; and GeneMatcher, a web-based tool for linking investigators with an interest in the same gene;Sobreira;Hum Mutat,2015
5. Molecular findings among patients referred for clinical whole-exome sequencing;Yang;JAMA,2014
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