PhenoScanner: a database of human genotype–phenotype associations-Reference-Cited by-同舟云学术

PhenoScanner: a database of human genotype–phenotype associations

Published:2016-06-17 Issue:20 Volume:32 Page:3207-3209
ISSN:1367-4803
Container-title:Bioinformatics
language:en
Short-container-title:Bioinformatics

Author:

Staley James R.,Blackshaw James,Kamat Mihir A.,Ellis Steve,Surendran Praveen,Sun Benjamin B.,Paul Dirk S.,Freitag Daniel,Burgess Stephen,Danesh John,Young Robin,Butterworth Adam S.

Publisher

Oxford University Press (OUP)

Subject

Computational Mathematics,Computational Theory and Mathematics,Computer Science Applications,Molecular Biology,Biochemistry,Statistics and Probability

Link

http://academic.oup.com/bioinformatics/article-pdf/32/20/3207/

Reference9 articles.

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3. Burgess S. Thompson S.G. (2015) Mendelian Randomization: Methods for Using Genetic Variants in Causal Estimation. Chapman & Hall, Boca Raton, FL, USA.

4. A second generation human haplotype map of over 3.1 million SNPs

5. Cardiometabolic effects of genetic upregulation of the interleukin 1 receptor antagonist: a Mendelian randomisation analysis

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