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。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)
Prevalence and architecture of de novo mutations in developmental disorders
Jeremy F. McRae et al.
NATURE (2017)
Refining the role of de novo protein-truncating variants in neurodevelopmental disorders by using population reference samples
Jack A. Kosmicki et al.
NATURE GENETICS (2017)
Signatures of positive selection: from selective sweeps at individual loci to subtle allele frequency changes in polygenic adaptation
Wolfgang Stephan
MOLECULAR ECOLOGY (2016)
Detecting recent selective sweeps while controlling for mutation rate and background selection
Christian D. Huber et al.
MOLECULAR ECOLOGY (2016)
Common alleles contribute to schizophrenia in CNV carriers
K. E. Tansey et al.
MOLECULAR PSYCHIATRY (2016)
KEGG as a reference resource for gene and protein annotation
Minoru Kanehisa et al.
NUCLEIC ACIDS RESEARCH (2016)
Reference sequence (RefSeq) database at NCBI: current status, taxonomic expansion, and functional annotation
Nuala A. O'Leary et al.
NUCLEIC ACIDS RESEARCH (2016)
The Reactome pathway Knowledgebase
Antonio Fabregat et al.
NUCLEIC ACIDS RESEARCH (2016)
FINEMAP: efficient variable selection using summary data from genome-wide association studies
Christian Benner et al.
BIOINFORMATICS (2016)
Genetic Markers of Human Evolution Are Enriched in Schizophrenia
Saurabh Srinivasan et al.
BIOLOGICAL PSYCHIATRY (2016)
The Genetic Cost of Neanderthal Introgression
Kelley Harris et al.
GENETICS (2016)
Comprehensive analysis of schizophrenia-associated loci highlights ion channel pathways and biologically plausible candidate causal genes
Tune H. Pers et al.
HUMAN MOLECULAR GENETICS (2016)
Genome-wide analysis of over 106000 individuals identifies 9 neuroticism-associated loci
D. J. Smith et al.
MOLECULAR PSYCHIATRY (2016)
Chromosome conformation elucidates regulatory relationships in developing human brain
Hyejung Won et al.
NATURE (2016)
Analysis of protein-coding genetic variation in 60,706 humans
Monkol Lek 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)
Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders
Tarjinder Singh et al.
NATURE NEUROSCIENCE (2016)
Gene expression elucidates functional impact of polygenic risk for schizophrenia
Menachem Fromer et al.
NATURE NEUROSCIENCE (2016)
Increased burden of ultra-rare protein-altering variants among 4,877 individuals with schizophrenia
Giulio Genovese et al.
NATURE NEUROSCIENCE (2016)
The statistical properties of gene-set analysis
Christiaan A. de Leeuw et al.
NATURE REVIEWS GENETICS (2016)
De Novo Synonymous Mutations in Regulatory Elements Contribute to the Genetic Etiology of Autism and Schizophrenia
Atsushi Takata et al.
NEURON (2016)
Detection of human adaptation during the past 2000 years
Yair Field et al.
SCIENCE (2016)
The Genetic Cost of Neanderthal Introgression
Kelley Harris et al.
GENETICS (2016)
SLC39A8 Deficiency: A Disorder of Manganese Transport and Glycosylation
Julien H. Park et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2015)
Genomic and Network Patterns of Schizophrenia Genetic Variation in Human Evolutionary Accelerated Regions
Ke Xu et al.
MOLECULAR BIOLOGY AND EVOLUTION (2015)
hapbin: An Efficient Program for Performing Haplotype-Based Scans for Positive Selection in Large Genomic Datasets
Colin A. Maclean et al.
MOLECULAR BIOLOGY AND EVOLUTION (2015)
Recombination affects accumulation of damaging and disease-associated mutations in human populations
Julie G. Hussin 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)
LD Score regression distinguishes confounding from polygenicity in genome-wide association studies
Brendan K. Bulik-Sullivan et al.
NATURE GENETICS (2015)
Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways
Colm O'Dushlaine et al.
NATURE NEUROSCIENCE (2015)
Systems biology and gene networks in neurodevelopmental and neurodegenerative disorders
Neelroop N. Parikshak et al.
NATURE REVIEWS GENETICS (2015)
Novel Findings from CNVs Implicate Inhibitory and Excitatory Signaling Complexes in Schizophrenia
Andrew J. Pocklington et al.
NEURON (2015)
Complex trait architecture: the pleiotropic model revisited
T-L. North et al.
SCIENTIFIC REPORTS (2015)
MAGMA: Generalized Gene-Set Analysis of GWAS Data
Christiaan A. de Leeuw et al.
PLOS COMPUTATIONAL BIOLOGY (2015)
Premature Mortality Among Adults With Schizophrenia in the United States
Mark Olfson et al.
JAMA PSYCHIATRY (2015)
Gene Ontology Consortium: going forward
J. A. Blake et al.
NUCLEIC ACIDS RESEARCH (2015)
OMIM.org: Online Mendelian Inheritance in Man (OMIM®), an online catalog of human genes and genetic disorders
Joanna S. Amberger et al.
NUCLEIC ACIDS RESEARCH (2015)
Ensembl 2015
Fiona Cunningham et al.
NUCLEIC ACIDS RESEARCH (2015)
CrossMap: a versatile tool for coordinate conversion between genome assemblies
Hao Zhao et al.
BIOINFORMATICS (2014)
Analysis of copy number variations at 15 schizophrenia-associated loci
Elliott Rees et al.
BRITISH JOURNAL OF PSYCHIATRY (2014)
Improving the Power of GWAS and Avoiding Confounding from Population Stratification with PC-Select
George Tucker et al.
GENETICS (2014)
Analysis of the Human Tissue-specific Expression by Genome-wide Integration of Transcriptomics and Antibody-based Proteomics
Linn Fagerberg et al.
MOLECULAR & CELLULAR PROTEOMICS (2014)
Copy number variation in schizophrenia in Sweden
J. P. Szatkiewicz et al.
MOLECULAR PSYCHIATRY (2014)
De novo mutations in schizophrenia implicate synaptic networks
Menachem Fromer et al.
NATURE (2014)
A polygenic burden of rare disruptive mutations in schizophrenia
Shaun M. Purcell et al.
NATURE (2014)
The genomic landscape of Neanderthal ancestry in present-day humans
Sriram Sankararaman et al.
NATURE (2014)
Biological insights from 108 schizophrenia-associated genetic loci
Stephan Ripke et al.
NATURE (2014)
A framework for the interpretation of de novo mutation in human disease
Kaitlin E. Samocha et al.
NATURE GENETICS (2014)
Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility
Anubha Mahajan et al.
NATURE GENETICS (2014)
The Mouse Genome Database: integration of and access to knowledge about the laboratory mouse
Judith A. Blake et al.
NUCLEIC ACIDS RESEARCH (2014)
The NHGRI GWAS Catalog, a curated resource of SNP-trait associations
Danielle Welter et al.
NUCLEIC ACIDS RESEARCH (2014)
Reappraising the long-term course and outcome of psychotic disorders: the AESOP-10 study
C. Morgan et al.
PSYCHOLOGICAL MEDICINE (2014)
The evolutionary paradox and the missing heritability of schizophrenia
Jenny van Dongen et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS (2013)
Detecting Natural Selection in Genomic Data
Joseph J. Vitti et al.
ANNUAL REVIEW OF GENETICS, VOL 47 (2013)
Selection and Adaptation in the Human Genome
Wenqing Fu et al.
ANNUAL REVIEW OF GENOMICS AND HUMAN GENETICS, VOL 14 (2013)
Identifying Recent Adaptations in Large-Scale Genomic Data
Sharon R. Grossman et al.
CELL (2013)
Learning Natural Selection from the Site Frequency Spectrum
Roy Ronen et al.
GENETICS (2013)
Background Selection 20 Years on
Brian Charlesworth
JOURNAL OF HEREDITY (2013)
Genome-wide association analysis identifies 13 new risk loci for schizophrenia
Stephan Ripke et al.
NATURE GENETICS (2013)
Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease
Jean-Charles Lambert et al.
NATURE GENETICS (2013)
Fecundity of Patients With Schizophrenia, Autism, Bipolar Disorder, Depression, Anorexia Nervosa, or Substance Abuse vs Their Unaffected Siblings
Robert A. Power et al.
JAMA PSYCHIATRY (2013)
A Better Coefficient of Determination for Genetic Profile Analysis
Sang Hong Lee et al.
GENETIC EPIDEMIOLOGY (2012)
The Effects of Deleterious Mutations on Evolution at Linked Sites
Brian Charlesworth
GENETICS (2012)
De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia
G. Kirov et al.
MOLECULAR PSYCHIATRY (2012)
Including known covariates can reduce power to detect genetic effects in case-control studies
Matti Pirinen et al.
NATURE GENETICS (2012)
De Novo Gene Disruptions in Children on the Autistic Spectrum
Ivan Iossifov et al.
NEURON (2012)
Birth-Cohort Effects in the Association Between Personality and Fertility
Markus Jokela
PSYCHOLOGICAL SCIENCE (2012)
Choice of population structure informative principal components for adjustment in a case-control study
Gina M. Peloso et al.
BMC GENETICS (2011)
Physical health disparities and mental illness: the scandal of premature mortality
Graham Thornicroft
BRITISH JOURNAL OF PSYCHIATRY (2011)
FMRP Stalls Ribosomal Translocation on mRNAs Linked to Synaptic Function and Autism
Jennifer C. Darnell et al.
CELL (2011)
Fecundability among women with type 1 and type 2 diabetes in the Norwegian Mother and Child Cohort Study
K. W. Whitworth et al.
DIABETOLOGIA (2011)
Common variants on 8p12 and 1q24.2 confer risk of schizophrenia
Yongyong Shi et al.
NATURE GENETICS (2011)
Genome-wide association study identifies five new schizophrenia loci
Stephan Ripke et al.
NATURE GENETICS (2011)
Accounting for Population Stratification in Practice: A Comparison of the Main Strategies Dedicated to Genome-Wide Association Studies
Matthieu Bouaziz et al.
PLOS ONE (2011)
METAL: fast and efficient meta-analysis of genomewide association scans
Cristen J. Willer et al.
BIOINFORMATICS (2010)
Integrating common and rare genetic variation in diverse human populations
David M. Altshuler et al.
NATURE (2010)
ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data
Kai Wang et al.
NUCLEIC ACIDS RESEARCH (2010)
Quantitative proteomics of the Cav2 channel nano-environments in the mammalian brain
Catrin Swantje Mueller et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2010)
Selection at Linked Sites Shapes Heritable Phenotypic Variation in C. elegans
Matthew V. Rockman et al.
SCIENCE (2010)
The role of genetic variation in the causation of mental illness: an evolution-informed framework
R. Uher
MOLECULAR PSYCHIATRY (2009)
Targeted tandem affinity purification of PSD-95 recovers core postsynaptic complexes and schizophrenia susceptibility proteins
Esperanza Fernandez et al.
MOLECULAR SYSTEMS BIOLOGY (2009)
Widespread Genomic Signatures of Natural Selection in Hominid Evolution
Graham McVicker et al.
PLOS GENETICS (2009)
Pointwise testing with functional data using the Westfall-Young randomization method
Dennis D. Cox et al.
BIOMETRIKA (2008)
Natural selection on genes that underlie human disease susceptibility
Ran Blekhman et al.
CURRENT BIOLOGY (2008)
Schizophrenia: A Concise Overview of Incidence, Prevalence, and Mortality
John McGrath et al.
EPIDEMIOLOGIC REVIEWS (2008)
The Hill-Robertson effect: evolutionary consequences of weak selection and linkage in finite populations
J. M. Comeron et al.
HEREDITY (2008)
Genome-wide detection and characterization of positive selection in human populations
Pardis C. Sabeti et al.
NATURE (2007)
Lifetime prevalence of psychotic and bipolar I disorders in a general population
Jonna Perala et al.
ARCHIVES OF GENERAL PSYCHIATRY (2007)
Positive natural selection in the human lineage
P. C. Sabeti et al.
SCIENCE (2006)
The proteomes of neurotransmitter receptor complexes form modular networks with distributed functionality underlying plasticity and behaviour
Andrew J. Pocklington et al.
MOLECULAR SYSTEMS BIOLOGY (2006)
Schizophrenia as one extreme of a sexually selected fitness indicator
A Shaner et al.
SCHIZOPHRENIA RESEARCH (2004)
Human disease genes: patterns and predictions
NGC Smith et al.
GENE (2003)
Synaptic multiprotein complexes associated with 5-HT2C receptors:: a proteomic approach
C Bécamel et al.
EMBO JOURNAL (2002)
分享论文
