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。Collider scope: when selection bias can substantially influence observed associations
Marcus R. Munafo et al.
INTERNATIONAL JOURNAL OF EPIDEMIOLOGY (2018)
Multi-trait analysis of genome-wide association summary statistics using MTAG
Patrick Turley et al.
NATURE GENETICS (2018)
The nature of nurture: Effects of parental genotypes
Augustine Kong et al.
SCIENCE (2018)
The MR-Base platform supports systematic causal inference across the human phenome
Gibran Hemani et al.
ELIFE (2018)
The UK Biobank resource with deep phenotyping and genomic data
Clare Bycroft et al.
NATURE (2018)
LD Hub: a centralized database and web interface to perform LD score regression that maximizes the potential of summary level GWAS data for SNP heritability and genetic correlation analysis
Jie Zheng et al.
BIOINFORMATICS (2017)
Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variation
Thomas J. Hoffmann et al.
NATURE GENETICS (2017)
The new NHGRI-EBI Catalog of published genome-wide association studies (GWAS Catalog)
Jacqueline MacArthur et al.
NUCLEIC ACIDS RESEARCH (2017)
A comparison of Cox and logistic regression for use in genome-wide association studies of cohort and case-cohort design
James R. Staley et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2017)
Discovery of novel heart rate-associated loci using the Exome Chip
Marten E. van den Berg et al.
HUMAN MOLECULAR GENETICS (2017)
Smoking prevalence and attributable disease burden in 195 countries and territories, 1990-2015: a systematic analysis from the Global Burden of Disease Study 2015
Marissa B. Reitsma et al.
LANCET (2017)
Genetic effects on gene expression across human tissues
Francois Aguet et al.
NATURE (2017)
Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes
James D. McKay et al.
NATURE GENETICS (2017)
Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk
Helen R. Warren et al.
NATURE GENETICS (2017)
Genome-wide association analyses for lung function and chronic obstructive pulmonary disease identify new loci and potential druggable targets
Louise V. Wain et al.
NATURE GENETICS (2017)
An xQTL map integrates the genetic architecture of the human brain's transcriptome and epigenome
Bernard Ng et al.
NATURE NEUROSCIENCE (2017)
Extending the MR-Egger method for multivariable Mendelian randomization to correct for both measured and unmeasured pleiotropy
Jessica M. B. Rees et al.
STATISTICS IN MEDICINE (2017)
Fast and efficient QTL mapper for thousands of molecular phenotypes
Halit Ongen et al.
BIOINFORMATICS (2016)
Reference sequence (RefSeq) database at NCBI: current status, taxonomic expansion, and functional annotation
Nuala A. O'Leary et al.
NUCLEIC ACIDS RESEARCH (2016)
RVTESTS: an efficient and comprehensive tool for rare variant association analysis using sequence data
Xiaowei Zhan et al.
BIOINFORMATICS (2016)
Consistent Estimation in Mendelian Randomization with Some Invalid Instruments Using a Weighted Median Estimator
Jack Bowden et al.
GENETIC EPIDEMIOLOGY (2016)
Genome-wide association study identifies 74 loci associated with educational attainment
Aysu Okbay et al.
NATURE (2016)
SEQMINER: An R-Package to Facilitate the Functional Interpretation of Sequence-Based Associations
Xiaowei Zhan et al.
GENETIC EPIDEMIOLOGY (2015)
Mendelian randomization with invalid instruments: effect estimation and bias detection through Egger regression
Jack Bowden et al.
INTERNATIONAL JOURNAL OF EPIDEMIOLOGY (2015)
Genetic studies of body mass index yield new insights for obesity biology
Adam E. Locke et al.
NATURE (2015)
LD Score regression distinguishes confounding from polygenicity in genome-wide association studies
Brendan K. Bulik-Sullivan et al.
NATURE GENETICS (2015)
Tissue-based map of the human proteome
Mathias Uhlen et al.
SCIENCE (2015)
A Genome-Wide Association Study of a Biomarker of Nicotine Metabolism
Anu Loukola et al.
PLOS GENETICS (2015)
Tobacco smoking is associated with methylation of genes related to coronary artery disease
Rebecca V. Steenaard et al.
CLINICAL EPIGENETICS (2015)
Genome-wide meta-analysis reveals common splice site acceptor variant in CHRNA4 associated with nicotine dependence
D. B. Hancock et al.
TRANSLATIONAL PSYCHIATRY (2015)
Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): a genetic association study in UK Biobank
Louise V. Wain et al.
LANCET RESPIRATORY MEDICINE (2015)
RAREMETAL: fast and powerful meta-analysis for rare variants
Shuang Feng et al.
BIOINFORMATICS (2014)
Variants in two adjacent genes, EGLN2 and CYP2A6, influence smoking behavior related to disease risk via different mechanisms
A. Joseph Bloom et al.
HUMAN MOLECULAR GENETICS (2014)
Biological insights from 108 schizophrenia-associated genetic loci
Stephan Ripke et al.
NATURE (2014)
The genetic architecture of psychophysiological phenotypes
Marcus R. Munafo et al.
PSYCHOPHYSIOLOGY (2014)
Efficient Design for Mendelian Randomization Studies: Subsample and 2-Sample Instrumental Variable Estimators
Brandon L. Pierce et al.
AMERICAN JOURNAL OF EPIDEMIOLOGY (2013)
Predicting the Functional, Molecular, and Phenotypic Consequences of Amino Acid Substitutions using Hidden Markov Models
Hashem A. Shihab et al.
HUMAN MUTATION (2013)
Genome-wide SNP and CNV analysis identifies common and low-frequency variants associated with severe early-onset obesity
Eleanor Wheeler et al.
NATURE GENETICS (2013)
REV3L 3′UTR 460 T>C polymorphism in microRNA target sites contributes to lung cancer susceptibility
S. Zhang et al.
ONCOGENE (2013)
A Comprehensive Family-Based Replication Study of Schizophrenia Genes
Karolina A. Aberg et al.
JAMA PSYCHIATRY (2013)
Family-based association study of ADHD and genes increasing the risk for smoking behaviours
Geeta A. Thakur et al.
ARCHIVES OF DISEASE IN CHILDHOOD (2012)
Haplotypes with Copy Number and Single Nucleotide Polymorphisms in CYP2A6 Locus Are Associated with Smoking Quantity in a Japanese Population
Natsuhiko Kumasaka et al.
PLOS ONE (2012)
Rare-Variant Association Testing for Sequencing Data with the Sequence Kernel Association Test
Michael C. Wu et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2011)
Genetic Polymorphisms in 15q25 and 19q13 Loci, Cotinine Levels, and Risk of Lung Cancer in EPIC
Maria N. Timofeeva et al.
CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION (2011)
Quality control parameters on a large dataset of regionally dissected human control brains for whole genome expression studies
Daniah Trabzuni et al.
JOURNAL OF NEUROCHEMISTRY (2011)
GENOMIC MEDICINE Genomics of Cardiovascular Disease
Christopher J. O'Donnell et al.
NEW ENGLAND JOURNAL OF MEDICINE (2011)
Genome-wide association study of smoking behaviours in patients with COPD
Mateusz Siedlinski et al.
THORAX (2011)
METAL: fast and efficient meta-analysis of genomewide association scans
Cristen J. Willer et al.
BIOINFORMATICS (2010)
An Evaluation of Statistical Approaches to Rare Variant Analysis in Genetic Association Studies
Andrew P. Morris et al.
GENETIC EPIDEMIOLOGY (2010)
Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior
Thorgeir E. Thorgeirsson et al.
NATURE GENETICS (2010)
Genome-wide meta-analyses identify multiple loci associated with smoking behavior
Helena Furberg et al.
NATURE GENETICS (2010)
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index
Elizabeth K. Speliotes et al.
NATURE GENETICS (2010)
A method and server for predicting damaging missense mutations
Ivan A. Adzhubei et al.
NATURE METHODS (2010)
Association of serum cotinine level with a cluster of three nicotinic acetylcholine receptor genes (CHRNA3/CHRNA5/CHRNB4) on chromosome 15
Kaisu Keskitalo et al.
HUMAN MOLECULAR GENETICS (2009)
Risk for nicotine dependence and lung cancer is conferred by mRNA expression levels and amino acid change in CHRNA5
Jen C. Wang et al.
HUMAN MOLECULAR GENETICS (2009)
ConsensusPathDB-a database for integrating human functional interaction networks
Atanas Kamburov et al.
NUCLEIC ACIDS RESEARCH (2009)
A Groupwise Association Test for Rare Mutations Using a Weighted Sum Statistic
Bo Eskerod Madsen et al.
PLOS GENETICS (2009)
Heritability of smoking initiation and nicotine dependence
J Vink et al.
BEHAVIOR GENETICS (2005)
Statistical significance for genomewide studies
JD Storey et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2003)
分享论文
