Genetic architectures of psychiatric disorders: the emerging picture and its implications
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Title
Genetic architectures of psychiatric disorders: the emerging picture and its implications
Authors
Keywords
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Journal
NATURE REVIEWS GENETICS
Volume 13, Issue 8, Pages 537-551
Publisher
Springer Nature
Online
2012-07-10
DOI
10.1038/nrg3240
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Note: Only part of the references are listed.- Five Years of GWAS Discovery
- (2012) Peter M. Visscher et al. AMERICAN JOURNAL OF HUMAN GENETICS
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- (2012) Jean Addington et al. Annual Review of Clinical Psychology
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- (2012) Dheeraj Malhotra et al. CELL
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- (2012) Benjamin M. Neale et al. NATURE
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- (2012) Stephan J. Sanders et al. NATURE
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- (2012) Brian J. O’Roak et al. NATURE
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- (2012) S Hong Lee et al. NATURE GENETICS
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- (2012) Eli A Stahl et al. NATURE GENETICS
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- (2012) Adam Kiezun et al. NATURE GENETICS
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- (2012) Patrick F Sullivan NATURE MEDICINE
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- (2012) D. G. MacArthur et al. SCIENCE
- Ten Years of Pathway Analysis: Current Approaches and Outstanding Challenges
- (2012) Purvesh Khatri et al. PLoS Computational Biology
- Genome-wide significant association between alcohol dependence and a variant in the ADH gene cluster
- (2011) Josef Frank et al. ADDICTION BIOLOGY
- Genomewide Association Analysis of Symptoms of Alcohol Dependence in the Molecular Genetics of Schizophrenia (MGS2) Control Sample
- (2011) Kenneth S. Kendler et al. ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH
- Genome-wide association studies identify genetic loci related to alcohol consumption in Korean men
- (2011) Inkyung Baik et al. AMERICAN JOURNAL OF CLINICAL NUTRITION
- Genome-wide Association Study Identifies Genetic Variation in Neurocan as a Susceptibility Factor for Bipolar Disorder
- (2011) Sven Cichon et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Copy Number Variants in Schizophrenia: Confirmation of Five Previous Findings and New Evidence for 3q29 Microdeletions and VIPR2 Duplications
- (2011) Douglas F. Levinson et al. AMERICAN JOURNAL OF PSYCHIATRY
- Genome-Wide Analysis of Copy Number Variants in Attention Deficit Hyperactivity Disorder: The Role of Rare Variants and Duplications at 15q13.3
- (2011) Nigel M. Williams et al. AMERICAN JOURNAL OF PSYCHIATRY
- Investigating the Contribution of Common Genetic Variants to the Risk and Pathogenesis of ADHD
- (2011) Evangelia Stergiakouli et al. AMERICAN JOURNAL OF PSYCHIATRY
- The Serotonin Transporter Promoter Variant (5-HTTLPR), Stress, and Depression Meta-analysis Revisited
- (2011) Katja Karg et al. ARCHIVES OF GENERAL PSYCHIATRY
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- (2011) Jon Arcelus ARCHIVES OF GENERAL PSYCHIATRY
- Alzheimer's disease genetics: lessons to improve disease modelling: Table 1
- (2011) Rita J. Guerreiro et al. BIOCHEMICAL SOCIETY TRANSACTIONS
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- (2011) Andrew C. Heath et al. BIOLOGICAL PSYCHIATRY
- Life stress, 5-HTTLPR and mental disorder: findings from a 30-year longitudinal study
- (2011) David M. Fergusson et al. BRITISH JOURNAL OF PSYCHIATRY
- Ischemic Preconditioning Effect of Prodromal Angina Is Attenuated in Acute Myocardial Infarction Patients With Hypertensive Left Ventricular Hypertrophy
- (2011) Toshiharu Takeuchi et al. CIRCULATION JOURNAL
- Analysis of genetic deletions and duplications in the University College London bipolar disorder case control sample
- (2011) Andrew McQuillin et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Common variants at VRK2 and TCF4 conferring risk of schizophrenia
- (2011) Stacy Steinberg et al. HUMAN MOLECULAR GENETICS
- Chromosome 1p21.3 microdeletions comprising DPYD and MIR137 are associated with intellectual disability
- (2011) M. H. Willemsen et al. JOURNAL OF MEDICAL GENETICS
- Meta-Analysis of Genome-Wide Association Studies of Attention-Deficit/Hyperactivity Disorder
- (2011) Benjamin M. Neale et al. JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY
- A family-based study of common polygenic variation and risk of schizophrenia
- (2011) D M Ruderfer et al. MOLECULAR PSYCHIATRY
- Don't give up on GWAS
- (2011) P Sullivan et al. MOLECULAR PSYCHIATRY
- Alzheimer risk associated with a copy number variation in the complement receptor 1 increasing C3b/C4b binding sites
- (2011) N Brouwers et al. MOLECULAR PSYCHIATRY
- Genome-wide survey implicates the influence of copy number variants (CNVs) in the development of early-onset bipolar disorder
- (2011) L Priebe et al. MOLECULAR PSYCHIATRY
- Genome-wide association studies establish that human intelligence is highly heritable and polygenic
- (2011) G Davies et al. MOLECULAR PSYCHIATRY
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- (2011) G Kirov et al. MOLECULAR PSYCHIATRY
- A high-resolution map of human evolutionary constraint using 29 mammals
- (2011) Kerstin Lindblad-Toh et al. NATURE
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- (2011) Eric S. Lander NATURE
- Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus
- (2011) Sébastien Jacquemont et al. NATURE
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- (2011) Vladimir Vacic et al. NATURE
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- (2011) Christie D. Fowler et al. NATURE
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- (2011) Pamela Y. Collins et al. NATURE
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- (2011) Irina Voineagu et al. NATURE
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- (2011) Bin Xu et al. NATURE GENETICS
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- (2011) Gerome Breen et al. NATURE GENETICS
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- (2011) Yongyong Shi et al. NATURE GENETICS
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- (2011) NATURE GENETICS
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- KEGG for integration and interpretation of large-scale molecular data sets
- (2011) M. Kanehisa et al. NUCLEIC ACIDS RESEARCH
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- (2011) S. Treusch et al. SCIENCE
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- (2010) Howard J. Edenberg et al. ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH
- Functional Gene Group Analysis Reveals a Role of Synaptic Heterotrimeric G Proteins in Cognitive Ability
- (2010) Dina Ruano et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Deletion 17q12 Is a Recurrent Copy Number Variant that Confers High Risk of Autism and Schizophrenia
- (2010) Daniel Moreno-De-Luca et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Prioritizing GWAS Results: A Review of Statistical Methods and Recommendations for Their Application
- (2010) Rita M. Cantor et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Genetics of Early Onset Cognitive Impairment
- (2010) Hans Hilger Ropers Annual Review of Genomics and Human Genetics
- Suggestion of Roles for Both Common and Rare Risk Variants in Genome-wide Studies of Schizophrenia
- (2010) Michael J. Owen et al. ARCHIVES OF GENERAL PSYCHIATRY
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- (2010) Detelina Grozeva ARCHIVES OF GENERAL PSYCHIATRY
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- (2010) R. Anney et al. HUMAN MOLECULAR GENETICS
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- (2010) G. Orozco et al. HUMAN MOLECULAR GENETICS
- Massively parallel sequencing and rare disease
- (2010) S. B. Ng et al. HUMAN MOLECULAR GENETICS
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- (2010) Jon McClellan et al. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION
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- (2010) Sudha Seshadri JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION
- Cross talk between microRNA and epigenetic regulation in adult neurogenesis
- (2010) Keith E. Szulwach et al. JOURNAL OF CELL BIOLOGY
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- (2010) Nigel M Williams et al. LANCET
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- (2010) K Wang et al. MOLECULAR PSYCHIATRY
- Fine mapping of ZNF804A and genome-wide significant evidence for its involvement in schizophrenia and bipolar disorder
- (2010) H J Williams et al. MOLECULAR PSYCHIATRY
- Functional impact of global rare copy number variation in autism spectrum disorders
- (2010) Dalila Pinto et al. NATURE
- Hundreds of variants clustered in genomic loci and biological pathways affect human height
- (2010) Hana Lango Allen et al. NATURE
- A map of human genome variation from population-scale sequencing
- (2010) Richard M. Durbin et al. NATURE
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- (2010) Richard S Houlston et al. NATURE GENETICS
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- (2010) Francis J McMahon et al. NATURE GENETICS
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- (2010) Thorgeir E Thorgeirsson et al. NATURE GENETICS
- Genome-wide meta-analyses identify multiple loci associated with smoking behavior
- (2010) NATURE GENETICS
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- (2010) Clare Turnbull et al. NATURE GENETICS
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- (2010) Elizabeth K Speliotes et al. NATURE GENETICS
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- (2010) Jian Yang et al. NATURE GENETICS
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- (2010) Andre Franke et al. NATURE GENETICS
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- (2010) Jason Z Liu et al. NATURE GENETICS
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- (2010) Benjamin F Voight et al. NATURE GENETICS
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- (2010) Elizabeth T. Cirulli et al. NATURE REVIEWS GENETICS
- Missing heritability and strategies for finding the underlying causes of complex disease
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- (2010) Albert-László Barabási et al. NATURE REVIEWS GENETICS
- Duplication of amyloid precursor protein (APP), but not prion protein (PRNP) gene is a significant cause of early onset dementia in a large UK series
- (2010) Daniel McNaughton et al. NEUROBIOLOGY OF AGING
- The Psychiatric GWAS Consortium: Big Science Comes to Psychiatry
- (2010) Patrick F. Sullivan NEURON
- Genetic Evidence Implicates the Immune System and Cholesterol Metabolism in the Aetiology of Alzheimer's Disease
- (2010) Lesley Jones et al. PLoS One
- A genome-wide association study of alcohol dependence
- (2010) L. J. Bierut et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
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- (2010) G. Miller SCIENCE
- MicroRNA miR-137 Regulates Neuronal Maturation by Targeting Ubiquitin Ligase Mind Bomb-1
- (2010) Richard D. Smrt et al. STEM CELLS
- Rare Variants Create Synthetic Genome-Wide Associations
- (2010) Samuel P. Dickson et al. PLOS BIOLOGY
- Consistent Association of Type 2 Diabetes Risk Variants Found in Europeans in Diverse Racial and Ethnic Groups
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- (2010) Soumya Raychaudhuri et al. PLoS Genetics
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- (2010) Dan L. Nicolae et al. PLoS Genetics
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- (2010) Nancy L. Saccone et al. PLoS Genetics
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- (2009) Peter Holmans et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Population Analysis of Large Copy Number Variants and Hotspots of Human Genetic Disease
- (2009) Andy Itsara et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Genomewide Association Studies: History, Rationale, and Prospects for Psychiatric Disorders
- (2009) AMERICAN JOURNAL OF PSYCHIATRY
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- (2009) Deqiong Ma et al. ANNALS OF HUMAN GENETICS
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- (2009) Ling Zhong et al. EMBO JOURNAL
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- (2009) Neil Risch et al. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION
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- (2009) John Attia et al. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION
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- (2009) M. Shinawi et al. JOURNAL OF MEDICAL GENETICS
- Common genetic determinants of schizophrenia and bipolar disorder in Swedish families: a population-based study
- (2009) Paul Lichtenstein et al. LANCET
- The moderation by the serotonin transporter gene of environmental adversity in the etiology of depression: 2009 update
- (2009) R Uher et al. MOLECULAR PSYCHIATRY
- The bipolar disorder risk allele at CACNA1C also confers risk of recurrent major depression and of schizophrenia
- (2009) E K Green et al. MOLECULAR PSYCHIATRY
- A genome-wide linkage and association scan reveals novel loci for autism
- (2009) Lauren A. Weiss et al. NATURE
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- (2009) Kai Wang et al. NATURE
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- (2009) Jean-Charles Lambert et al. NATURE GENETICS
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- (2009) Denise Harold et al. NATURE GENETICS
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- (2009) Joel N. Hirschhorn NEW ENGLAND JOURNAL OF MEDICINE
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- (2009) Huaiyu Mi et al. NUCLEIC ACIDS RESEARCH
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- (2009) L. A. Hindorff et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Genome-wide association studies: a primer
- (2009) A. Corvin et al. PSYCHOLOGICAL MEDICINE
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- (2009) N. R. Wray et al. SCHIZOPHRENIA BULLETIN
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- (2008) Itsik Pe'er et al. GENETIC EPIDEMIOLOGY
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- (2008) P. I.W. de Bakker et al. HUMAN MOLECULAR GENETICS
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- (2008) D Zhang et al. MOLECULAR PSYCHIATRY
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- (2008) M Y M Ng et al. MOLECULAR PSYCHIATRY
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- (2008) P Sklar et al. MOLECULAR PSYCHIATRY
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- (2008) MOLECULAR PSYCHIATRY
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