The Human Phenotype Ontology in 2017-Reference-Cited by-同舟云学术

The Human Phenotype Ontology in 2017

Published:2016-11-28 Issue:D1 Volume:45 Page:D865-D876
ISSN:0305-1048
Container-title:Nucleic Acids Research
language:en
Short-container-title:Nucleic Acids Res

Author:

Köhler Sebastian,Vasilevsky Nicole A.^ORCID,Engelstad Mark,Foster Erin,McMurry Julie,Aymé Ségolène,Baynam Gareth,Bello Susan M.,Boerkoel Cornelius F.,Boycott Kym M.,Brudno Michael,Buske Orion J.,Chinnery Patrick F.,Cipriani Valentina,Connell Laureen E.,Dawkins Hugh J.S.,DeMare Laura E.,Devereau Andrew D.,de Vries Bert B.A.,Firth Helen V.,Freson Kathleen,Greene Daniel,Hamosh Ada,Helbig Ingo,Hum Courtney,Jähn Johanna A.,James Roger,Krause Roland,F. Laulederkind Stanley J.^ORCID,Lochmüller Hanns,Lyon Gholson J.,Ogishima Soichi,Olry Annie,Ouwehand Willem H.,Pontikos Nikolas,Rath Ana,Schaefer Franz,Scott Richard H.,Segal Michael,Sergouniotis Panagiotis I.,Sever Richard,Smith Cynthia L.,Straub Volker,Thompson Rachel,Turner Catherine,Turro Ernest,Veltman Marijcke W.M.,Vulliamy Tom,Yu Jing,von Ziegenweidt Julie,Zankl Andreas,Züchner Stephan,Zemojtel Tomasz,Jacobsen Julius O.B.,Groza Tudor,Smedley Damian,Mungall Christopher J.,Haendel Melissa,Robinson Peter N.

Publisher

Oxford University Press (OUP)

Subject

Genetics

Link

http://academic.oup.com/nar/article-pdf/45/D1/D865/8846656/gkw1039.pdf

Reference103 articles.

1. The Human Phenotype Ontology: A Tool for Annotating and Analyzing Human Hereditary Disease

2. Navigating the Phenotype Frontier: The Monarch Initiative

3. Representation of rare diseases in health information systems: The orphanet approach to serve a wide range of end users

4. Phenotype matters

5. Phenotype Ontologies and Cross-Species Analysis for Translational Research

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