Genomic insights into the overlap between psychiatric disorders: implications for research and clinical practice
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Title
Genomic insights into the overlap between psychiatric disorders: implications for research and clinical practice
Authors
Keywords
Autism Spectrum Disorder, Schizophrenia, Autism Spectrum Disorder, Bipolar Disorder, Intellectual Disability
Journal
Genome Medicine
Volume 6, Issue 4, Pages 29
Publisher
Springer Nature
Online
2014-04-29
DOI
10.1186/gm546
References
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Note: Only part of the references are listed.- The Research Domain Criteria: moving the goalposts to change the game
- (2014) Joanne L. Doherty et al. BRITISH JOURNAL OF PSYCHIATRY
- De novo mutations in schizophrenia implicate synaptic networks
- (2014) Menachem Fromer et al. NATURE
- A polygenic burden of rare disruptive mutations in schizophrenia
- (2014) Shaun M. Purcell et al. NATURE
- New Ethical Issues for Genetic Counseling in Common Mental Disorders
- (2013) Elliot S. Gershon et al. AMERICAN JOURNAL OF PSYCHIATRY
- Polygenic Risk for Schizophrenia Is Associated with Cognitive Change Between Childhood and Old Age
- (2013) Andrew M. McIntosh et al. BIOLOGICAL PSYCHIATRY
- Reciprocal Duplication of the Williams-Beuren Syndrome Deletion on Chromosome 7q11.23 Is Associated with Schizophrenia
- (2013) Jennifer Gladys Mulle et al. BIOLOGICAL PSYCHIATRY
- The Penetrance of Copy Number Variations for Schizophrenia and Developmental Delay
- (2013) George Kirov et al. BIOLOGICAL PSYCHIATRY
- Reduced burden of very large and rare CNVs in bipolar affective disorder
- (2013) Detelina Grozeva et al. BIPOLAR DISORDERS
- Shared polygenic contribution between childhood attention-deficit hyperactivity disorder and adult schizophrenia
- (2013) Marian L. Hamshere et al. BRITISH JOURNAL OF PSYCHIATRY
- Risk of bipolar disorder and schizophrenia in relatives of people with attention-deficit hyperactivity disorder
- (2013) Henrik Larsson et al. BRITISH JOURNAL OF PSYCHIATRY
- Analysis of copy number variations at 15 schizophrenia-associated loci
- (2013) Elliott Rees et al. BRITISH JOURNAL OF PSYCHIATRY
- Psychopathology and cognition in children with 22q11.2 deletion syndrome
- (2013) Maria Niarchou et al. BRITISH JOURNAL OF PSYCHIATRY
- The internet is parents' main source of information about psychiatric manifestations of 22q11.2 deletion syndrome (22q11.2DS)
- (2013) Marianne B.M. van den Bree et al. European Journal of Medical Genetics
- Global burden of disease attributable to mental and substance use disorders: findings from the Global Burden of Disease Study 2010
- (2013) Harvey A Whiteford et al. LANCET
- Specificity of psychosis, mania and major depression in a contemporary family study
- (2013) C L Vandeleur et al. MOLECULAR PSYCHIATRY
- Evidence that duplications of 22q11.2 protect against schizophrenia
- (2013) E Rees et al. MOLECULAR PSYCHIATRY
- Molecular genetic evidence for overlap between general cognitive ability and risk for schizophrenia: a report from the Cognitive Genomics consorTium (COGENT)
- (2013) T Lencz et al. MOLECULAR PSYCHIATRY
- Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs
- (2013) S Hong Lee et al. NATURE GENETICS
- Genome-wide association analysis identifies 13 new risk loci for schizophrenia
- (2013) Stephan Ripke et al. NATURE GENETICS
- Mortality, ADHD, and Psychosocial Adversity in Adults With Childhood ADHD: A Prospective Study
- (2013) W. J. Barbaresi et al. PEDIATRICS
- Genomics and the classification of mental illness: focus on broader categories
- (2013) Rudolf Uher Genome Medicine
- Examining the Comorbidity Between Attention Deficit Hyperactivity Disorder and Bipolar I Disorder: A Meta-Analysis of Family Genetic Studies
- (2012) Stephen V. Faraone et al. AMERICAN JOURNAL OF PSYCHIATRY
- Intellectual disability and major psychiatric disorders: A continuum of neurodevelopmental causality
- (2012) Michael J. Owen BRITISH JOURNAL OF PSYCHIATRY
- 22q11.2 Deletion Syndrome: Attitudes towards Disclosing the Risk of Psychiatric Illness
- (2012) Nicole Martin et al. Journal of Genetic Counseling
- A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders
- (2012) Flore Zufferey et al. JOURNAL OF MEDICAL GENETICS
- Evidence for a Fragile X Mental Retardation Protein-Mediated Translational Switch in Metabotropic Glutamate Receptor-Triggered Arc Translation and Long-Term Depression
- (2012) F. Niere et al. JOURNAL OF NEUROSCIENCE
- Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study
- (2012) Anita Rauch et al. LANCET
- Using large clinical data sets to infer pathogenicity for rare copy number variants in autism cohorts
- (2012) D Moreno-De-Luca et al. MOLECULAR PSYCHIATRY
- Patterns and rates of exonic de novo mutations in autism spectrum disorders
- (2012) Benjamin M. Neale et al. NATURE
- De novo mutations revealed by whole-exome sequencing are strongly associated with autism
- (2012) Stephan J. Sanders et al. NATURE
- Estimating the proportion of variation in susceptibility to schizophrenia captured by common SNPs
- (2012) S Hong Lee et al. NATURE GENETICS
- De Novo Gene Disruptions in Children on the Autistic Spectrum
- (2012) Ivan Iossifov et al. NEURON
- Diagnostic Exome Sequencing in Persons with Severe Intellectual Disability
- (2012) Joep de Ligt et al. NEW ENGLAND JOURNAL OF MEDICINE
- Psychiatry, The Pharmaceutical Industry, and The Road to Better Therapeutics
- (2012) H. C. Fibiger SCHIZOPHRENIA BULLETIN
- Association between schizophrenia and common variation in neurocan (NCAN), a genetic risk factor for bipolar disorder
- (2012) Thomas W. Mühleisen et al. SCHIZOPHRENIA RESEARCH
- 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
- Maternally Derived Microduplications at 15q11-q13: Implication of Imprinted Genes in Psychotic Illness
- (2011) Andrés Ingason et al. AMERICAN JOURNAL OF PSYCHIATRY
- 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
- What causes attention deficit hyperactivity disorder?
- (2011) Anita Thapar et al. ARCHIVES OF DISEASE IN CHILDHOOD
- Prevalence and Correlates of Bipolar Spectrum Disorder in the World Mental Health Survey Initiative
- (2011) Kathleen R. Merikangas et al. ARCHIVES OF GENERAL PSYCHIATRY
- 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
- Microdeletion/microduplication of proximal 15q11.2 between BP1 and BP2: a susceptibility region for neurological dysfunction including developmental and language delay
- (2011) Rachel D. Burnside et al. HUMAN GENETICS
- Genome-wide association analysis of copy number variation in recurrent depressive disorder
- (2011) J J H Rucker et al. MOLECULAR PSYCHIATRY
- De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia
- (2011) G Kirov et al. MOLECULAR PSYCHIATRY
- Exome sequencing supports a de novo mutational paradigm for schizophrenia
- (2011) Bin Xu et al. NATURE GENETICS
- Increased exonic de novo mutation rate in individuals with schizophrenia
- (2011) Simon L Girard et al. NATURE GENETICS
- Genome-wide association study identifies five new schizophrenia loci
- (2011) NATURE GENETICS
- Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations
- (2011) Brian J O'Roak et al. NATURE GENETICS
- Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4
- (2011) NATURE GENETICS
- A copy number variation morbidity map of developmental delay
- (2011) Gregory M Cooper et al. NATURE GENETICS
- High Frequencies of De Novo CNVs in Bipolar Disorder and Schizophrenia
- (2011) Dheeraj Malhotra et al. NEURON
- Rare De Novo and Transmitted Copy-Number Variation in Autistic Spectrum Disorders
- (2011) Dan Levy et al. NEURON
- Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism
- (2011) Stephan J. Sanders et al. NEURON
- Microdeletions of 3q29 Confer High Risk for Schizophrenia
- (2010) Jennifer Gladys Mulle 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
- GCTA: A Tool for Genome-wide Complex Trait Analysis
- (2010) Jian Yang et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Rare Copy Number VariantsA Point of Rarity in Genetic Risk for Bipolar Disorder and SchizophreniaRare Copy Number Variants
- (2010) Detelina Grozeva ARCHIVES OF GENERAL PSYCHIATRY
- Impaired Intellect and Memory
- (2010) Timothea Toulopoulou et al. ARCHIVES OF GENERAL PSYCHIATRY
- The Kraepelinian dichotomy – going, going … but still not gone
- (2010) Nick Craddock et al. BRITISH JOURNAL OF PSYCHIATRY
- Shared heritability of attention-deficit/hyperactivity disorder and autism spectrum disorder
- (2010) Nanda N. J. Rommelse et al. EUROPEAN CHILD & ADOLESCENT PSYCHIATRY
- 15q11.2 microdeletion – Seven new patients with delayed development and/or behavioural problems
- (2010) C. von der Lippe et al. European Journal of Medical Genetics
- Array-based technology and recommendations for utilization in medical genetics practice for detection of chromosomal abnormalities
- (2010) Melanie Manning et al. GENETICS IN MEDICINE
- Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis
- (2010) Nigel M Williams et al. LANCET
- 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
- Toward New Approaches to Psychotic Disorders: The NIMH Research Domain Criteria Project
- (2010) B. N. Cuthbert et al. SCHIZOPHRENIA BULLETIN
- Cognitive decline in schizophrenia from childhood to midlife: A 33-year longitudinal birth cohort study
- (2010) William S. Kremen et al. SCHIZOPHRENIA RESEARCH
- Meta-analytic Evidence for Familial Coaggregation of Schizophrenia and Bipolar Disorder
- (2009) Jared X. Van Snellenberg et al. ARCHIVES OF GENERAL PSYCHIATRY
- Recurrent Rearrangements in Synaptic and Neurodevelopmental Genes and Shared Biologic Pathways in Schizophrenia, Autism, and Mental Retardation
- (2009) Audrey Guilmatre et al. ARCHIVES OF GENERAL PSYCHIATRY
- The Role of DNA Copy Number Variation in Schizophrenia
- (2009) Gloria W.C. Tam et al. BIOLOGICAL PSYCHIATRY
- Copy Number Variation in Schizophrenia in the Japanese Population
- (2009) Masashi Ikeda et al. BIOLOGICAL PSYCHIATRY
- Prevalence of autism-spectrum conditions: UK school-based population study
- (2009) Simon Baron-Cohen et al. BRITISH JOURNAL OF PSYCHIATRY
- Nine patients with a microdeletion 15q11.2 between breakpoints 1 and 2 of the Prader–Willi critical region, possibly associated with behavioural disturbances
- (2009) Marianne Doornbos et al. European Journal of Medical Genetics
- Support for the involvement of large copy number variants in the pathogenesis of schizophrenia
- (2009) George Kirov et al. HUMAN MOLECULAR GENETICS
- Microdeletion 15q13.3: a locus with incomplete penetrance for autism, mental retardation, and psychiatric disorders
- (2009) S Ben-Shachar et al. JOURNAL OF MEDICAL GENETICS
- Recurrent reciprocal 16p11.2 rearrangements associated with global developmental delay, behavioural problems, dysmorphism, epilepsy, and abnormal head size
- (2009) M. Shinawi et al. JOURNAL OF MEDICAL GENETICS
- Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcome
- (2009) B W M van Bon et al. JOURNAL OF MEDICAL GENETICS
- Psychiatric Disorders in Children With Autism Spectrum Disorders: Prevalence, Comorbidity, and Associated Factors in a Population-Derived Sample
- (2009) Emily Simonoff et al. JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY
- Common genetic determinants of schizophrenia and bipolar disorder in Swedish families: a population-based study
- (2009) Paul Lichtenstein et al. LANCET
- Strong genetic evidence for a selective influence of GABAA receptors on a component of the bipolar disorder phenotype
- (2009) N Craddock et al. MOLECULAR PSYCHIATRY
- Copy number variations of chromosome 16p13.1 region associated with schizophrenia
- (2009) A Ingason 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
- Microduplications of 16p11.2 are associated with schizophrenia
- (2009) Shane E McCarthy et al. NATURE GENETICS
- Neurexin 1 (NRXN1) Deletions in Schizophrenia
- (2009) G. Kirov et al. SCHIZOPHRENIA BULLETIN
- Relationship between clinical and neuropsychological characteristics in child and adolescent first degree relatives of subjects with schizophrenia
- (2009) Elena de la Serna et al. SCHIZOPHRENIA RESEARCH
- Advanced Paternal Age Is Associated with Impaired Neurocognitive Outcomes during Infancy and Childhood
- (2009) Sukanta Saha et al. PLOS MEDICINE
- Advanced Parental Age and the Risk of Autism Spectrum Disorder
- (2008) M. S. Durkin et al. AMERICAN JOURNAL OF EPIDEMIOLOGY
- Disruption of Neurexin 1 Associated with Autism Spectrum Disorder
- (2008) Hyung-Goo Kim et al. AMERICAN JOURNAL OF HUMAN GENETICS
- A 15q13.3 microdeletion segregating with autism
- (2008) Alistair T Pagnamenta et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Microdeletion/duplication at 15q13.2q13.3 among individuals with features of autism and other neuropsychiatric disorders
- (2008) D T Miller et al. JOURNAL OF MEDICAL GENETICS
- Singleton deletions throughout the genome increase risk of bipolar disorder
- (2008) D Zhang et al. MOLECULAR PSYCHIATRY
- Rare chromosomal deletions and duplications increase risk of schizophrenia
- (2008) Jennifer L. Stone et al. NATURE
- Large recurrent microdeletions associated with schizophrenia
- (2008) Hreinn Stefansson et al. NATURE
- Strong association of de novo copy number mutations with sporadic schizophrenia
- (2008) Bin Xu et al. NATURE GENETICS
- Identification of loci associated with schizophrenia by genome-wide association and follow-up
- (2008) Michael C O'Donovan et al. NATURE GENETICS
- Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities
- (2008) Nicola Brunetti-Pierri et al. NATURE GENETICS
- Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder
- (2008) Manuel A R Ferreira et al. NATURE GENETICS
- Association between Microdeletion and Microduplication at 16p11.2 and Autism
- (2008) Lauren A. Weiss et al. NEW ENGLAND JOURNAL OF MEDICINE
- Rare Structural Variants Disrupt Multiple Genes in Neurodevelopmental Pathways in Schizophrenia
- (2008) T. Walsh et al. SCIENCE
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