标题
Phenome-wide association studies (PheWASs) for functional variants
作者
关键词
-
出版物
EUROPEAN JOURNAL OF HUMAN GENETICS
Volume 23, Issue 4, Pages 523-529
出版商
Springer Nature
发表日期
2014-07-30
DOI
10.1038/ejhg.2014.123
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- Genome- and Phenome-Wide Analyses of Cardiac Conduction Identifies Markers of Arrhythmia Risk
- (2013) Marylyn D. Ritchie et al. CIRCULATION
- A PheWAS approach in studying HLA-DRB1*1501
- (2013) S J Hebbring et al. GENES AND IMMUNITY
- A genome- and phenome-wide association study to identify genetic variants influencing platelet count and volume and their pleiotropic effects
- (2013) Khader Shameer et al. HUMAN GENETICS
- The challenges, advantages and future of phenome-wide association studies
- (2013) Scott J. Hebbring IMMUNOLOGY
- Cumulative association between age-related macular degeneration and less studied genetic variants in PLEKHA1/ARMS2/HTRA1: a meta and gene-cluster analysis
- (2013) Weihong Yu et al. MOLECULAR BIOLOGY REPORTS
- Systematic comparison of phenome-wide association study of electronic medical record data and genome-wide association study data
- (2013) Joshua C Denny et al. NATURE BIOTECHNOLOGY
- Phenome-Wide Association Study (PheWAS) for Detection of Pleiotropy within the Population Architecture using Genomics and Epidemiology (PAGE) Network
- (2013) Sarah A. Pendergrass et al. PLoS Genetics
- Associations of autoantibodies, autoimmune risk alleles, and clinical diagnoses from the electronic medical records in rheumatoid arthritis cases and non-rheumatoid arthritis controls
- (2012) Katherine P. Liao et al. ARTHRITIS AND RHEUMATISM
- NMD: a multifaceted response to premature translational termination
- (2012) Stephanie Kervestin et al. NATURE REVIEWS MOLECULAR CELL BIOLOGY
- A Systematic Survey of Loss-of-Function Variants in Human Protein-Coding Genes
- (2012) D. G. MacArthur et al. SCIENCE
- Variants Near FOXE1 Are Associated with Hypothyroidism and Other Thyroid Conditions: Using Electronic Medical Records for Genome- and Phenome-wide Studies
- (2011) Joshua C. Denny et al. AMERICAN JOURNAL OF HUMAN GENETICS
- The eMERGE Network: A consortium of biorepositories linked to electronic medical records data for conducting genomic studies
- (2011) Catherine A McCarty et al. BMC Medical Genomics
- Knowledge-Driven Multi-Locus Analysis Reveals Gene-Gene Interactions Influencing HDL Cholesterol Level in Two Independent EMR-Linked Biobanks
- (2011) Stephen D. Turner et al. PLoS One
- PheWAS: demonstrating the feasibility of a phenome-wide scan to discover gene-disease associations
- (2010) J. C. Denny et al. BIOINFORMATICS
- Genome-wide association study of conduct disorder symptomatology
- (2010) D M Dick et al. MOLECULAR PSYCHIATRY
- A map of human genome variation from population-scale sequencing
- (2010) Richard M. Durbin et al. NATURE
- Non-Synonymous and Synonymous Coding SNPs Show Similar Likelihood and Effect Size of Human Disease Association
- (2010) Rong Chen et al. PLoS One
- Genetics and genomics of ankylosing spondylitis
- (2009) Gethin P. Thomas et al. IMMUNOLOGICAL REVIEWS
- A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke
- (2009) Daniel F Gudbjartsson et al. NATURE GENETICS
- The Human Gene Mutation Database: 2008 update
- (2009) Peter D Stenson et al. Genome Medicine
- CC2D2A Is Mutated in Joubert Syndrome and Interacts with the Ciliopathy-Associated Basal Body Protein CEP290
- (2008) Nicholas T. Gorden et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Risk variants for atrial fibrillation on chromosome 4q25 associate with ischemic stroke
- (2008) Solveig Gretarsdottir et al. ANNALS OF NEUROLOGY
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