Related references
Note: Only part of the references are listed.Conditional GWAS analysis to identify disorder-specific SNPs for psychiatric disorders
Enda M. Byrne et al.
MOLECULAR PSYCHIATRY (2021)
A combined analysis of genetically correlated traits identifies 187 loci and a role for neurogenesis and myelination in intelligence
W. D. Hill et al.
MOLECULAR PSYCHIATRY (2019)
Genome-Wide Association Study Detected Novel Susceptibility Genes for Schizophrenia and Shared Trans-Populations/Diseases Genetic Effect
Masashi Ikeda et al.
SCHIZOPHRENIA BULLETIN (2019)
Defining the Genetic, Genomic, Cellular, and Diagnostic Architectures of Psychiatric Disorders
Patrick F. Sullivan et al.
CELL (2019)
Identification of common genetic risk variants for autism spectrum disorder
Jakob Grove et al.
NATURE GENETICS (2019)
Genome-wide meta-analysis of depression identifies 102 independent variants and highlights the importance of the prefrontal brain regions
David M. Howard et al.
NATURE NEUROSCIENCE (2019)
Genome-wide association study identifies 30 loci associated with bipolar disorder
Eli A. Stahl et al.
NATURE GENETICS (2019)
Reconciling S-LDSC and LDAK functional enrichment estimates
Steven Gazal et al.
NATURE GENETICS (2019)
Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa
Hunna J. Watson et al.
NATURE GENETICS (2019)
Bivariate causal mixture model quantifies polygenic overlap between complex traits beyond genetic correlation
Oleksandr Frei et al.
NATURE COMMUNICATIONS (2019)
Pleiotropic Meta-Analysis of Cognition, Education, and Schizophrenia Differentiates Roles of Early Neurodevelopmental and Adult Synaptic Pathways
Max Lam et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2019)
Extreme Polygenicity of Complex Traits Is Explained by Negative Selection
Luke J. O'Connor et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2019)
Comparative genetic architectures of schizophrenia in East Asian and European populations
Max Lam et al.
NATURE GENETICS (2019)
Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders
Phil H. Lee et al.
CELL (2019)
Multivariate genome-wide analyses of the well-being spectrum
Bart M. L. Baselmans et al.
NATURE GENETICS (2019)
Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder
Ditte Demontis et al.
NATURE GENETICS (2019)
Trans-ethnic association study of blood pressure determinants in over 750,000 individuals
Ayush Giri et al.
NATURE GENETICS (2019)
The NHGRI-EBI GWAS Catalog of published genome-wide association studies, targeted arrays and summary statistics 2019
Annalisa Buniello et al.
NUCLEIC ACIDS RESEARCH (2019)
Interrogating the Genetic Determinants of Tourette's Syndrome and Other Tic Disorders Through Genome-Wide Association Studies
Dongmei Yu et al.
AMERICAN JOURNAL OF PSYCHIATRY (2019)
Revealing the complex genetic architecture of obsessive-compulsive disorder using meta-analysis
Paul D. Arnold et al.
MOLECULAR PSYCHIATRY (2018)
Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes
Douglas M. Ruderfer et al.
CELL (2018)
Transformation of Summary Statistics from Linear Mixed Model Association on All-or-None Traits to Odds Ratio
Luke R. Lloyd-Jones et al.
GENETICS (2018)
Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression
Naomi R. Wray et al.
NATURE GENETICS (2018)
Signatures of negative selection in the genetic architecture of human complex traits
Jian Zeng et al.
NATURE GENETICS (2018)
Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence
Jeanne E. Savage et al.
NATURE GENETICS (2018)
Meta-analysis of genome-wide association studies for neuroticism in 449,484 individuals identifies novel genetic loci and pathways
Mats Nagel et al.
NATURE GENETICS (2018)
Multi-trait analysis of genome-wide association summary statistics using MTAG
Patrick Turley et al.
NATURE GENETICS (2018)
Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection
Antonio F. Pardinas et al.
NATURE GENETICS (2018)
Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals
James J. Lee et al.
NATURE GENETICS (2018)
Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function
Gail Davies et al.
NATURE COMMUNICATIONS (2018)
Identifying gene targets for brain-related traits using transcriptomic and methylomic data from blood
Ting Qi et al.
NATURE COMMUNICATIONS (2018)
Causal associations between risk factors and common diseases inferred from GWAS summary data
Zhihong Zhu et al.
NATURE COMMUNICATIONS (2018)
Transformation of Summary Statistics from Linear Mixed Model Association on All-or-None Traits to Odds Ratio
Luke R. Lloyd-Jones et al.
GENETICS (2018)
Estimation of complex effect-size distributions using summary-level statistics from genome-wide association studies across 32 complex traits
Yan Zhang et al.
NATURE GENETICS (2018)
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits
Evangelos Evangelou et al.
NATURE GENETICS (2018)
The UK Biobank resource with deep phenotyping and genomic data
Clare Bycroft et al.
NATURE (2018)
Heritability informed power optimization (HIPO) leads to enhanced detection of genetic associations across multiple traits
Guanghao Qi et al.
PLOS GENETICS (2018)
Dissecting the genetics of complex traits using summary association statistics
Bogdan Pasaniuc et al.
NATURE REVIEWS GENETICS (2017)
UniProt: the universal protein knowledgebase
Alex Bateman et al.
NUCLEIC ACIDS RESEARCH (2017)
Missing heritability: is the gap closing? An analysis of 32 complex traits in the Lifelines Cohort Study
Ilja M. Nolte et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2017)
Association analysis identifies 65 new breast cancer risk loci
Kyriaki Michailidou et al.
NATURE (2017)
Genetic effects on gene expression across human tissues
Francois Aguet et al.
NATURE (2017)
Linkage disequilibrium-dependent architecture of human complex traits shows action of negative selection
Steven Gazal et al.
NATURE GENETICS (2017)
Genome-wide association analysis identifies 30 new susceptibility loci for schizophrenia
Zhiqiang Li et al.
NATURE GENETICS (2017)
Statistical correction of the Winner's Curse explains replication variability in quantitative trait genome-wide association studies
Cameron Palmer et al.
PLOS GENETICS (2017)
Reference sequence (RefSeq) database at NCBI: current status, taxonomic expansion, and functional annotation
Nuala A. O'Leary et al.
NUCLEIC ACIDS RESEARCH (2016)
GWIS: Genome-Wide Inferred Statistics for Functions of Multiple Phenotypes
Harold A. Nieuwboer et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2016)
Genome-wide association study identifies 74 loci associated with educational attainment
Aysu Okbay et al.
NATURE (2016)
Schizophrenia risk from complex variation of complement component 4
Aswin Sekar et al.
NATURE (2016)
Integration of summary data from GWAS and eQTL studies predicts complex trait gene targets
Zhihong Zhu et al.
NATURE GENETICS (2016)
Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations
Jimmy Z. Liu et al.
NATURE GENETICS (2015)
Partitioning heritability by functional annotation using genome-wide association summary statistics
Hilary K. Finucane et al.
NATURE GENETICS (2015)
An atlas of genetic correlations across human diseases and traits
Brendan Bulik-Sullivan et al.
NATURE GENETICS (2015)
Second-generation PLINK: rising to the challenge of larger and richer datasets
Christopher C. Chang et al.
GIGASCIENCE (2015)
Cancer Statistics, 2014
Rebecca Siegel et al.
CA-A CANCER JOURNAL FOR CLINICIANS (2014)
Genetics of rheumatoid arthritis contributes to biology and drug discovery
Yukinori Okada et al.
NATURE (2014)
Biological insights from 108 schizophrenia-associated genetic loci
Stephan Ripke et al.
NATURE (2014)
Measuring missing heritability: Inferring the contribution of common variants
David Golan et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2014)
Estimating and interpreting FST: The impact of rare variants
Gaurav Bhatia et al.
GENOME RESEARCH (2013)
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs
S. Hong Lee et al.
NATURE GENETICS (2013)
High Trans-ethnic Replicability of GWAS Results Implies Common Causal Variants
Urko M. Marigorta et al.
PLOS GENETICS (2013)
A Subset-Based Approach Improves Power and Interpretation for the Combined Analysis of Genetic Association Studies of Heterogeneous Traits
Samsiddhi Bhattacharjee et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2012)
Increasing Incidence and Prevalence of the Inflammatory Bowel Diseases With Time, Based on Systematic Review
Natalie A. Molodecky et al.
GASTROENTEROLOGY (2012)
Interpreting Meta-Analyses of Genome-Wide Association Studies
Buhm Han et al.
PLOS GENETICS (2012)
Estimating Missing Heritability for Disease from Genome-wide Association Studies
Sang Hong Lee et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2011)
Kruppel-like transcription factors in the nervous system: Novel players in neurite outgrowth and axon regeneration
Darcie L. Moore et al.
MOLECULAR AND CELLULAR NEUROSCIENCE (2011)
Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease
Heribert Schunkert et al.
NATURE GENETICS (2011)
Analyze Multivariate Phenotypes in Genetic Association Studies by Combining Univariate Association Tests
Qiong Yang et al.
GENETIC EPIDEMIOLOGY (2010)
Meta-Analysis of Genome-wide Association Studies with Overlapping Subjects
Dan-Yu Lin et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2009)
NDUFA2 complex I mutation leads to Leigh disease
Saskia J. G. Hoefs et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2008)
Expression of Kruppel-like factor 5 gene in human brain and association of the gene with the susceptibility to schizophrenia
Masaya Yanagi et al.
SCHIZOPHRENIA RESEARCH (2008)
Share Paper
