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Title
Rare variant association test with multiple phenotypes
Authors
Keywords
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Journal
GENETIC EPIDEMIOLOGY
Volume 41, Issue 3, Pages 198-209
Publisher
Wiley
Online
2016-12-31
DOI
10.1002/gepi.22021
References
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Related references
Note: Only part of the references are listed.- Searching for missing heritability: Designing rare variant association studies
- (2014) O. Zuk et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
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- MultiPhen: Joint Model of Multiple Phenotypes Can Increase Discovery in GWAS
- (2012) Paul F. O’Reilly et al. PLoS One
- The mystery of missing heritability: Genetic interactions create phantom heritability
- (2012) O. Zuk et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Rare-Variant Association Testing for Sequencing Data with the Sequence Kernel Association Test
- (2011) Michael C. Wu et al. AMERICAN JOURNAL OF HUMAN GENETICS
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- Potential etiologic and functional implications of genome-wide association loci for human diseases and traits
- (2009) L. A. Hindorff et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- A Groupwise Association Test for Rare Mutations Using a Weighted Sum Statistic
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- (2008) Peter M Visscher NATURE GENETICS
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- (2008) Elaine R. Mardis TRENDS IN GENETICS
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