Related references
Note: Only part of the references are listed.Detection and replication of epistasis influencing transcription in humans
Gibran Hemani et al.
NATURE (2014)
Exploiting SNP Correlations within Random Forest for Genome-Wide Association Studies
Vincent Botta et al.
PLOS ONE (2014)
Pharmacogenetics of antidepressant drugs: An update after almost 20 years of research
Chiara Fabbri et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS (2013)
An Exhaustive Epistatic SNP Association Analysis on Expanded Wellcome Trust Data
Christoph Lippert et al.
SCIENTIFIC REPORTS (2013)
Five Years of GWAS Discovery
Peter M. Visscher et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2012)
Gene set enrichment analysis: performance evaluation and usage guidelines
Jui-Hung Hung et al.
BRIEFINGS IN BIOINFORMATICS (2012)
Genomics and Pharmacogenomics of Brain Disorders
Ramon Cacabelos et al.
CURRENT PHARMACEUTICAL BIOTECHNOLOGY (2012)
Ten Years of Pathway Analysis: Current Approaches and Outstanding Challenges
Purvesh Khatri et al.
PLOS COMPUTATIONAL BIOLOGY (2012)
Testing SNPs and sets of SNPs for importance in association studies
Holger Schwender et al.
BIOSTATISTICS (2011)
'The missing genes: what happened to the heritability of psychiatric disorders?'
T. J. Crow
MOLECULAR PSYCHIATRY (2011)
Strategies for Genetic Studies of Complex Diseases
Kai Wang et al.
CELL (2010)
Genetic Heterogeneity in Human Disease
Jon McClellan et al.
CELL (2010)
Evidence of statistical epistasis between DISC1, CIT and NDEL1 impacting risk for schizophrenia: biological validation with functional neuroimaging
Kristin K. Nicodemus et al.
HUMAN GENETICS (2010)
Genomewide Association Studies and Assessment of the Risk of Disease
Teri A. Manolio
NEW ENGLAND JOURNAL OF MEDICINE (2010)
The GeneMANIA prediction server: biological network integration for gene prioritization and predicting gene function
David Warde-Farley et al.
NUCLEIC ACIDS RESEARCH (2010)
The Role of Genetics in the Etiology of Schizophrenia
Pablo V. Gejman et al.
PSYCHIATRIC CLINICS OF NORTH AMERICA (2010)
Finding the missing heritability of complex diseases
Teri A. Manolio et al.
NATURE (2009)
Common Genetic Variation and Human Traits
David B. Goldstein
NEW ENGLAND JOURNAL OF MEDICINE (2009)
Genetic Interactions Between Transcription Factors Cause Natural Variation in Yeast
Justin Gerke et al.
SCIENCE (2009)
PLINK: A tool set for whole-genome association and population-based linkage analyses
Shaun Purcell et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2007)
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
Paul R. Burton et al.
NATURE (2007)
Evidence for statistical epistasis between catechol-O-methyltransferase (COMT) and polymorphisms in RGS4, G72 (DAOA), GRM3, and DISC1: influence on risk of schizophrenia
Kristin K. Nicodemus et al.
HUMAN GENETICS (2007)
The Haplotype Map of the human genome: a revolution in the genetics of complex diseases
Alexandre Montpetit et al.
M S-MEDECINE SCIENCES (2006)
Genome-wide strategies for detecting multiple loci that influence complex diseases
J Marchini et al.
NATURE GENETICS (2005)
Share Paper
