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Lista de obras de Michael C O'Donovan

A Genetic Investigation of Sex Bias in the Prevalence of Attention-Deficit/Hyperactivity Disorder

artículo científico publicado en 2017

A High Proportion of Chromosome 21 Promoter Polymorphisms Influence Transcriptional Activity

article published in 2003

A breakthrough in schizophrenia genetics

artículo científico publicado en 2014

A brief report: de novo copy number variants in children with attention deficit hyperactivity disorder

scientific article published on 12 May 2020

A comparison of four clustering methods for brain expression microarray data

artículo científico publicado en 2008

A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects

A data-driven investigation of relationships between bipolar psychotic symptoms and schizophrenia genome-wide significant genetic loci

artículo científico publicado en 2018

A family based study implicates solute carrier family 1-member 3 (SLC1A3) gene in attention-deficit/hyperactivity disorder

artículo científico publicado en 2005

A family based study of catechol-O-methyltransferase (COMT) and attention deficit hyperactivity disorder (ADHD).

artículo científico publicado en 2005

A family-based study of common polygenic variation and risk of schizophrenia

artículo científico publicado en 2011

A functional polymorphism in the succinate-semialdehyde dehydrogenase (aldehyde dehydrogenase 5 family, member A1) gene is associated with cognitive ability

artículo científico publicado en 2004

A genetic investigation of sex bias in the prevalence of attention deficit hyperactivity disorder

article

A genome-wide association study in individuals of African ancestry reveals the importance of the Duffy-null genotype in the assessment of clozapine-related neutropenia

artículo científico publicado en 2019

A genome-wide study shows a limited contribution of rare copy number variants to Alzheimer's disease risk

artículo científico publicado en 2012

A genomewide linkage study of age at onset in schizophrenia

article

A haplotype implicated in schizophrenia susceptibility is associated with reduced COMT expression in human brain

artículo científico publicado en 2003

A high proportion of polymorphisms in the promoters of brain expressed genes influences transcriptional activity

article

A large replication study and meta-analysis in European samples provides further support for association of AHI1 markers with schizophrenia

artículo científico publicado en 2010

A mega-analysis of genome-wide association studies for major depressive disorder

artículo científico publicado en 2012

A network of dopaminergic gene variations implicated as risk factors for schizophrenia

artículo científico publicado en 2008

A neuropsychological investigation of the genome wide associated schizophrenia risk variant NRGN rs12807809.

artículo científico publicado en 2010

A novel Alzheimer disease locus located near the gene encoding tau protein.

artículo científico publicado en 2015

A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes.

artículo científico publicado en 1993

A population-based study of genetic variation and psychotic experiences in adolescents

artículo científico publicado en 2013

A replicated molecular genetic basis for subtyping antisocial behavior in children with attention-deficit/hyperactivity disorder

artículo científico publicado en 2008

A replication study of JTC bias, genetic liability for psychosis and delusional ideation

artículo científico publicado en 2020

A scan of chromosome 10 identifies a novel locus showing strong association with late-onset Alzheimer disease

artículo científico publicado en 2005

A single nucleotide polymorphism in CHAT influences response to acetylcholinesterase inhibitors in Alzheimer's disease

artículo científico publicado en 2006

A systematic genomewide linkage study in 353 sib pairs with schizophrenia

artículo científico publicado en 2003

ATP2A2 mutations in Darier's disease and their relationship to neuropsychiatric phenotypes

artículo científico publicado en 1999

Absence of de novo point mutations in exons of GRIN2B in a large schizophrenia trio sample

Additive genetic variation in schizophrenia risk is shared by populations of African and European descent

artículo científico publicado en 2013

Adolescent clinical outcomes for young people with attention-deficit hyperactivity disorder

artículo científico publicado en 2010

Advances and retreats in the molecular genetics of major mental illness

artículo científico publicado en 1992

Advances in genetic findings on attention deficit hyperactivity disorder

artículo científico publicado en 2007

Adverse effects from antidepressant treatment: randomised controlled trial of 601 depressed individuals

artículo científico publicado en 2014

All SNPs are not created equal: genome-wide association studies reveal a consistent pattern of enrichment among functionally annotated SNPs

artículo científico publicado en 2013

Allelic expression of APOE in human brain: effects of epsilon status and promoter haplotypes

artículo científico publicado en 2004

Alpha-T-catenin is expressed in human brain and interacts with the Wnt signaling pathway but is not responsible for linkage to chromosome 10 in Alzheimer's disease

artículo científico publicado en 2004

An Analysis of Two Genome-wide Association Meta-analyses Identifies a New Locus for Broad Depression Phenotype

artículo científico publicado en 2016

An association study of common variation at the MAPT locus with late-onset Alzheimer's disease

artículo científico publicado en 2009

An association study of the neurotensin receptor gene with schizophrenia and clozapine response.

artículo científico publicado en 2004

An examination of MUTED as a schizophrenia susceptibility gene

article

An examination of single nucleotide polymorphism selection prioritization strategies for tests of gene-gene interaction

artículo científico publicado en 2011

An inherited duplication at the gene p21 Protein-Activated Kinase 7 (PAK7) is a risk factor for psychosis

artículo científico publicado en 2014

Analysis of 10 independent samples provides evidence for association between schizophrenia and a SNP flanking fibroblast growth factor receptor 2.

artículo científico publicado en 2008

Analysis of CAG/CTG repeat size in Chinese subjects with schizophrenia and bipolar affective disorder using the repeat expansion detection method.

artículo científico publicado en 1998

Analysis of Intellectual Disability Copy Number Variants for Association With Schizophrenia

artículo científico publicado en 2016

Analysis of ProDH, COMT and ZDHHC8 risk variants does not support individual or interactive effects on schizophrenia susceptibility

artículo científico publicado en 2006

Analysis of copy number variation using quantitative interspecies competitive PCR

artículo científico publicado en 2008

Analysis of copy number variations at 15 schizophrenia-associated loci.

artículo científico publicado en 2013

Analysis of exome sequence in 604 trios for recessive genotypes in schizophrenia.

artículo científico publicado en 2015

Analysis of neurogranin (NRGN) in schizophrenia

article published in 2011

Association Between Schizophrenia-Related Polygenic Liability and the Occurrence and Level of Mood-Incongruent Psychotic Symptoms in Bipolar Disorder

artículo científico publicado en 2017

Association analysis of 528 intra-genic SNPs in a region of chromosome 10 linked to late onset Alzheimer's disease

artículo científico publicado en 2008

Association analysis of AKT1 and schizophrenia in a UK case control sample

artículo científico publicado en 2007

Association analysis of NOTCH4 loci in schizophrenia using family and population-based controls

artículo científico publicado en 2001

Association analysis of dynamin-binding protein (DNMBP) on chromosome 10q with late onset Alzheimer's disease in a large caucasian UK sample.

artículo científico publicado en 2009

Association analysis of monoamine oxidase a and attention deficit hyperactivity disorder

artículo científico publicado en 2003

Association analysis of the glial cell line-derived neurotrophic factor (GDNF) gene in schizophrenia

artículo científico publicado en 2007

Association analysis of the proneurotensin gene and bipolar disorder

artículo científico publicado en 2000

Association at SYNE1 in both bipolar disorder and recurrent major depression

artículo científico publicado en 2012

Association between PRODH and schizophrenia is not confirmed

artículo científico publicado en 2003

Association between TCF4 and schizophrenia does not exert its effect by common nonsynonymous variation or by influencing cis-acting regulation of mRNA expression in adult human brain

artículo científico publicado en 2011

Association between functional psychosis and expanded CAG/CTG repeats is not explained by health stratification

article

Association between genetic variation in a region on chromosome 11 and schizophrenia in large samples from Europe

artículo científico publicado en 2011

Association of Genetic Risk Variants With Attention-Deficit/Hyperactivity Disorder Trajectories in the General Population.

artículo científico publicado en 2016

Association of Genetic Risk for Schizophrenia With Nonparticipation Over Time in a Population-Based Cohort Study

artículo científico publicado en 2016

Association of Whole-Genome and NETRIN1 Signaling Pathway–Derived Polygenic Risk Scores for Major Depressive Disorder and White Matter Microstructure in the UK Biobank

scholarly article by Miruna C. Barbu et al published July 2018 in Biological Psychiatry: Cognitive Neuroscience and Neuroimaging

Association of copy number variation across the genome with neuropsychiatric traits in the general population

artículo científico publicado en 2018

Association of the dopamine D4 receptor gene 7-repeat allele with neuropsychological test performance of children with ADHD.

artículo científico publicado en 2004

Association of the paternally transmitted copy of common Valine allele of the Val66Met polymorphism of the brain-derived neurotrophic factor (BDNF) gene with susceptibility to ADHD.

artículo científico publicado en 2005

Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants

artículo científico publicado en 2007

Association studies between risk for late-onset Alzheimer's disease and variants in insulin degrading enzyme

artículo científico publicado en 2005

Association studies of 23 positional/functional candidate genes on chromosome 10 in late-onset Alzheimer's disease

artículo científico publicado en 2007

Association study in the 5q31-32 linkage region for schizophrenia using pooled DNA genotyping

artículo científico publicado en 2008

Associations between polygenic risk for schizophrenia and brain function during probabilistic learning in healthy individuals

artículo científico publicado en 2015

At-risk variant in TCF7L2 for type II diabetes increases risk of schizophrenia

artículo científico publicado en 2011

Atypical antipsychotics elevate dopamine D3 but not D1 or D2 receptor mRNA levels in rat brain

scholarly article by P.R. Buckland et al published September 1992 in European Neuropsychopharmacology

Author Correction: Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

scientific article published on 01 September 2019

Authors' reply

Authors' reply

Bi-directional changes in the levels of messenger RNAs encoding gamma-aminobutyric acidA receptor alpha subunits after flurazepam treatment

artículo científico publicado en 1992

Bias in the genomic distribution of CAG and CTG trinucleotide repeats

artículo científico publicado en 1997

Biological overlap of attention-deficit/hyperactivity disorder and autism spectrum disorder: evidence from copy number variants

artículo científico publicado en 2014

Bipolar disorder and polymorphisms in the dysbindin gene (DTNBP1).

artículo científico publicado en 2005

Blind Analysis of Denaturing High-Performance Liquid Chromatography as a Tool for Mutation Detection

article

Both splicing variants of the dopamine D2 receptor mRNA are up-regulated by antipsychotic drugs

artículo científico publicado en 1993

CAG repeat length in the hKCa3 gene and symptom dimensions in schizophrenia

article

CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1

artículo científico publicado en 2014

CTG18.1 and ERDA-1 CAG/CTG repeat size in bipolar disorder

artículo científico publicado en 1999

CUX2, a potential regulator of NCAM expression: genomic characterization and analysis as a positional candidate susceptibility gene for bipolar disorder

artículo científico publicado en 2001

Candidate gene association study of insulin signaling genes and Alzheimer's disease: evidence for SOS2, PCK1, and PPARgamma as susceptibility loci

artículo científico publicado en 2007

Candidate-gene association studies of schizophrenia

artículo científico publicado en 1999

Case-control association study of 59 candidate genes reveals the DRD2 SNP rs6277 (C957T) as the only susceptibility factor for schizophrenia in the Bulgarian population.

artículo científico publicado en 2009

Case-control association study of 65 candidate genes revealed a possible association of a SNP of HTR5A to be a factor susceptible to bipolar disease in Bulgarian population

artículo científico publicado en 2009

Catechol O-methyltransferase gene variant and birth weight predict early-onset antisocial behavior in children with attention-deficit/hyperactivity disorder

artículo científico publicado en 2005

Changes in dopa decarboxylase mRNA but not tyrosine hydroxylase mRNA levels in rat brain following antipsychotic treatment

artículo científico publicado en 1992

Changes in dopamine D1, D2 and D3 receptor mRNA levels in rat brain following antipsychotic treatment

artículo científico publicado en 1992

Characterisation, mutation detection, and association analysis of alternative promoters and 5' UTRs of the human dopamine D3 receptor gene in schizophrenia.

artículo científico publicado en 2002

Characterization of a family with rare deletions in CNTNAP5 and DOCK4 suggests novel risk loci for autism and dyslexia

artículo científico publicado en 2010

Cheap, accurate and rapid allele frequency estimation of single nucleotide polymorphisms by primer extension and DHPLC in DNA pools

artículo científico publicado en 2000

Chromosome 22 deletion syndrome and schizophrenia

artículo científico publicado en 2006

Chromosome 22q11 deletions, velo-cardio-facial syndrome and early-onset psychosis

article

Cis- and trans- loci influence expression of the schizophrenia susceptibility gene DTNBP1.

artículo científico publicado en 2008

Cis-effects on gene expression in the human prenatal brain associated with genetic risk for neuropsychiatric disorders

artículo científico publicado en 2020

Clinical and cognitive characteristics of children with attention-deficit hyperactivity disorder, with and without copy number variants

artículo científico publicado en 2011

Clozapine and sulpiride up-regulate dopamine D3 receptor mRNA levels

artículo científico publicado en 1993

Clustering of metabolic comorbidity in schizophrenia: a genetic contribution?

artículo científico publicado en 2005

Cognitive Characterization of Schizophrenia Risk Variants Involved in Synaptic Transmission: Evidence of CACNA1C's Role in Working Memory

artículo científico publicado en 2017

Cognitive Performance Among Carriers of Pathogenic Copy Number Variants: Analysis of 152,000 UK Biobank Subjects

artículo científico publicado en 2016

Cognitive analysis of schizophrenia risk genes that function as epigenetic regulators of gene expression

artículo científico publicado en 2016

Cognitive mechanisms underlying reading and spelling development in five European orthographies

article

Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder

artículo científico publicado en 2008

Common alleles contribute to schizophrenia in CNV carriers.

artículo científico publicado en 2015

Common polygenic variation contributes to risk of schizophrenia and bipolar disorder

artículo científico publicado en 2009

Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection.

artículo científico publicado en 2018

Common variant at 16p11.2 conferring risk of psychosis.

artículo científico publicado en 2012

Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease

artículo científico publicado en 2011

Common variants at VRK2 and TCF4 conferring risk of schizophrenia

artículo científico publicado en 2011

Comparative genome hybridization suggests a role for NRXN1 and APBA2 in schizophrenia

artículo científico publicado en 2008

Comparative sequencing of the proneurotensin gene and association studies in schizophrenia

article

Complement factor H Y402H polymorphism is not associated with late-onset Alzheimer's disease

artículo científico publicado en 2007

Complement system biomarkers in first episode psychosis

artículo científico publicado en 2017

Comprehensive analysis of schizophrenia-associated loci highlights ion channel pathways and biologically plausible candidate causal genes

artículo científico publicado en 2016

Conditional GWAS analysis to identify disorder-specific SNPs for psychiatric disorders

artículo científico publicado en 2020

Consensus paper of the WFSBP Task Force on Genetics: Genetics, epigenetics and gene expression markers of major depressive disorder and antidepressant response

artículo científico publicado en 2016

Constance E. Lieber, Theodore R. Stanley, and the Enduring Impact of Philanthropy on Psychiatry Research

artículo científico publicado en 2016

Contrasting genetic architectures of schizophrenia and other complex diseases using fast variance-components analysis

artículo científico publicado en 2015

Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects

artículo científico publicado en 2016

Convergent Evidence for 2′,3′-Cyclic Nucleotide 3′-Phosphodiesterase as a Possible Susceptibility Gene for Schizophrenia

article

Convergent evidence that oligodendrocyte lineage transcription factor 2 (OLIG2) and interacting genes influence susceptibility to schizophrenia

artículo científico publicado en 2006

Convergent functional genomics of schizophrenia: from comprehensive understanding to genetic risk prediction.

artículo científico publicado en 2012

Convergent patterns of association between phenylalanine hydroxylase variants and schizophrenia in four independent samples

artículo científico publicado en 2009

Copy number variants and therapeutic response to antidepressant medication in major depressive disorder

artículo científico publicado en 2014

Copy number variation in bipolar disorder

artículo científico publicado en 2015

Copy number variation in schizophrenia in Sweden

artículo científico publicado en 2014

Copy number variation in schizophrenia in the Japanese population

artículo científico publicado en 2009

Correction: The genomic basis of mood instability: identification of 46 loci in 363,705 UK Biobank participants, genetic correlation with psychiatric disorders, and association with gene expression and function

artículo científico publicado en 2019

DAPK1 variants are associated with Alzheimer's disease and allele-specific expression

artículo científico publicado en 2006

DISC1 exon 11 rare variants found more commonly in schizoaffective spectrum cases than controls

artículo científico publicado en 2011

DISC1 mRNA expression is not influenced by common Cis-acting regulatory polymorphisms or imprinting.

artículo científico publicado en 2008

DNA Pooling: a tool for large-scale association studies

artículo científico publicado en 2002

DNA pooling as a tool for large-scale association studies in complex traits

artículo científico publicado en 2004

De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia.

artículo científico publicado en 2011

De novo CNVs in bipolar affective disorder and schizophrenia

artículo científico publicado en 2014

De novo mutation in schizophrenia

artículo científico publicado en 2012

De novo mutations identified by exome sequencing implicate rare missense variants in SLC6A1 in schizophrenia

scientific article published on 13 January 2020

De novo mutations in schizophrenia implicate synaptic networks

artículo científico publicado en 2014

De novo rates and selection of schizophrenia-associated copy number variants

artículo científico publicado en 2011

Detailed analysis of the relative power of direct and indirect association studies and the implications for their interpretation

artículo científico publicado en 2007

Determination of the genomic structure and mutation screening in schizophrenic individuals for five subunits of the N-methyl-D-aspartate glutamate receptor

artículo científico publicado en 2002

Developmental Profile of Psychiatric Risk Associated With Voltage-Gated Cation Channel Activity

artículo científico publicado en 2021

Discovery and statistical genotyping of copy-number variation from whole-exome sequencing depth

artículo científico publicado en 2012

Dynamic expression of genes associated with schizophrenia and bipolar disorder across development

scientific article published on 04 February 2019

Dysbindin modulates brain function during visual processing in children.

artículo científico publicado en 2009

Dysbindin-1 and schizophrenia: from genetics to neuropathology

artículo científico publicado en 2004

Effect of cytochrome CYP2C19 metabolizing activity on antidepressant response and side effects: Meta-analysis of data from genome-wide association studies

Effects of DTNBP1 genotype on brain development in children

article

Effects of MiR-137 genetic risk score on brain volume and cortical measures in patients with schizophrenia and controls

artículo científico publicado en 2018

Effects of differential genotyping error rate on the type I error probability of case-control studies

artículo científico

Erratum: Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease

scholarly article published in Nature Genetics

Erratum: Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease

article

Erratum: Genome-wide haplotype association study identifies the FRMD4A gene as a risk locus for Alzheimer's disease

article

Erratum: Genome-wide significant associations in schizophrenia to ITIH3/4, CACNA1C and SDCCAG8, and extensive replication of associations reported by the Schizophrenia PGC

scholarly article published in Molecular Psychiatry

Estimating Effect Sizes and Expected Replication Probabilities from GWAS Summary Statistics

artículo científico publicado en 2016

Estimating Exposome Score for Schizophrenia Using Predictive Modeling Approach in Two Independent Samples: The Results From the EUGEI Study

artículo científico publicado en 2019

Evaluation of a susceptibility gene for schizophrenia: genotype based meta-analysis of RGS4 polymorphisms from thirteen independent samples

artículo científico publicado en 2006

Evaluation of an approximation method for assessment of overall significance of multiple-dependent tests in a genomewide association study

artículo científico publicado en 2011

Evidence for novel susceptibility genes for late-onset Alzheimer's disease from a genome-wide association study of putative functional variants

article

Evidence for rare and common genetic risk variants for schizophrenia at protein kinase C, alpha

artículo científico publicado en 2009

Evidence of Common Genetic Overlap Between Schizophrenia and Cognition.

artículo científico publicado en 2015

Evidence that a DISC1 frame-shift deletion associated with psychosis in a single family may not be a pathogenic mutation

artículo científico publicado en 2006

Evidence that common variation in NEDD9 is associated with susceptibility to late-onset Alzheimer's and Parkinson's disease

artículo científico publicado en 2008

Evidence that duplications of 22q11.2 protect against schizophrenia

artículo científico publicado en 2013

Evidence that interaction between neuregulin 1 and its receptor erbB4 increases susceptibility to schizophrenia

artículo científico publicado en 2006

Evidence that putative ADHD low risk alleles at SNAP25 may increase the risk of schizophrenia

artículo científico publicado en 2009

Evidence that variation in the oligodendrocyte lineage transcription factor 2 (OLIG2) gene is associated with psychosis in Alzheimer's disease

artículo científico publicado en 2009

Evidence to suggest biased phenotypes in children with Attention Deficit Hyperactivity Disorder from completely ascertained trios

article

Evidence, and replication thereof, that molecular-genetic and environmental risks for psychosis impact through an affective pathway

artículo científico publicado en 2020

Examining for association between candidate gene polymorphisms in the dopamine pathway and attention-deficit hyperactivity disorder: a family-based study

artículo científico publicado en 2001

Examining pathways between genetic liability for schizophrenia and patterns of tobacco and cannabis use in adolescence

artículo científico publicado en 2020

Examining the independent and joint effects of molecular genetic liability and environmental exposures in schizophrenia: results from the EUGEI study

scientific article published on 01 June 2019

Exclusion of expansion of 50 CAG/CTG trinucleotide repeats in bipolar disorder

scientific article published on 01 August 1997

Exclusion of the Darier's disease gene, ATP2A2, as a common susceptibility gene for bipolar disorder

artículo científico publicado en 2001

Exome arrays capture polygenic rare variant contributions to schizophrenia.

artículo científico publicado en 2016

Expanded CAG repeats in schizophrenia and bipolar disorder

artículo científico publicado en 1995

Expanded CAG/CTG repeats in bipolar disorder: No correlation with phenotypic measures of illness severity

artículo científico publicado en 1997

Expression analysis in a rat psychosis model identifies novel candidate genes validated in a large case-control sample of schizophrenia.

artículo científico publicado en 2015

Factor structure of autistic traits in children with ADHD.

artículo científico publicado en 2014

Failure to confirm association betweenPIK4CAand psychosis in 22q11.2 deletion syndrome

artículo científico publicado en 2010

Finding schizophrenia genes

artículo científico publicado en 2005

Fine mapping of ZNF804A and genome-wide significant evidence for its involvement in schizophrenia and bipolar disorder

artículo científico publicado en 2010

Fine-mapping reveals novel alternative splicing of the dopamine transporter

artículo científico publicado en 2010

Follow-up of genetic linkage findings on chromosome 16p13: evidence of association of N-methyl-D aspartate glutamate receptor 2A gene polymorphism with ADHD.

artículo científico publicado en 2004

Formalising recall by genotype as an efficient approach to detailed phenotyping and causal inference.

artículo científico publicado en 2018

Functional SNPs are enriched for schizophrenia association signals

artículo científico publicado en 2013

Functional analysis of human promoter polymorphisms

artículo científico publicado en 2003

Functional analysis of polymorphisms in the promoter regions of genes on 22q11.

artículo científico publicado en 2004

Functional gene group analysis identifies synaptic gene groups as risk factor for schizophrenia.

artículo científico publicado en 2011

Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia

artículo científico publicado en 2006

Further support for an association between a polymorphic CAG repeat in the hKCa3 gene and schizophrenia.

artículo científico publicado en 1998

GENetic and clinical predictors of treatment response in depression: the GenPod randomised trial protocol

artículo científico publicado en 2008

GWA study data mining and independent replication identify cardiomyopathy-associated 5 (CMYA5) as a risk gene for schizophrenia

artículo científico publicado en 2010

GWAS of Suicide Attempt in Psychiatric Disorders and Association With Major Depression Polygenic Risk Scores.

artículo científico publicado en 2019

Gender differences in CNV burden do not confound schizophrenia CNV associations.

artículo científico publicado en 2016

Gene expression imputation across multiple brain regions provides insights into schizophrenia risk

article

Gene ontology analysis of GWA study data sets provides insights into the biology of bipolar disorder

artículo científico publicado en 2009

Gene-wide analyses of genome-wide association data sets: evidence for multiple common risk alleles for schizophrenia and bipolar disorder and for overlap in genetic risk

artículo científico publicado en 2009

Gene-wide analysis detects two new susceptibility genes for Alzheimer's disease

artículo científico publicado en 2014

Genes for schizophrenia and bipolar disorder? Implications for psychiatric nosology

artículo científico publicado en 2005

Genetic Risk Factors for Schizophrenia

Genetic architectures of psychiatric disorders: the emerging picture and its implications

artículo científico publicado en 2012

Genetic association of FMRP targets with psychiatric disorders

artículo científico publicado en 2020

Genetic association of the APP binding protein 2 gene (APBB2) with late onset Alzheimer disease

artículo científico publicado en 2005

Genetic differences between five European populations

artículo científico

Genetic evidence implicates the immune system and cholesterol metabolism in the aetiology of Alzheimer's disease

artículo científico publicado en 2010

Genetic identification of brain cell types underlying schizophrenia

scientific article published on 21 May 2018

Genetic influences on schizophrenia and subcortical brain volumes: large-scale proof of concept

artículo científico publicado en 2016

Genetic liability to schizophrenia is negatively associated with educational attainment in UK Biobank

artículo científico publicado en 2019

Genetic mapping approaches in neuropsychiatry

Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

artículo científico publicado en 2019

Genetic overlap between Alzheimer's disease and Parkinson's disease at the MAPT locus

artículo científico publicado en 2015

Genetic pleiotropy between multiple sclerosis and schizophrenia but not bipolar disorder: differential involvement of immune-related gene loci

artículo científico publicado en 2014

Genetic predictors of antidepressant side effects: a grouped candidate gene approach in the Genome-Based Therapeutic Drugs for Depression (GENDEP) study

artículo científico publicado en 2014

Genetic predictors of response to serotonergic and noradrenergic antidepressants in major depressive disorder: a genome-wide analysis of individual-level data and a meta-analysis

artículo científico publicado en 2012

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

artículo científico publicado en 2013

Genetic risk for attention-deficit/hyperactivity disorder contributes to neurodevelopmental traits in the general population

artículo científico publicado en 2014

Genetic risk for schizophrenia: convergence on synaptic pathways involved in plasticity

artículo científico publicado en 2014

Genetic susceptibility for bipolar disorder and response to antidepressants in major depressive disorder

artículo científico publicado en 2013

Genetic utility of broadly defined bipolar schizoaffective disorder as a diagnostic concept

artículo científico publicado en 2009

Genetic variants in the ErbB4 gene are associated with white matter integrity

artículo científico publicado en 2011

Genetic variation of brain-derived neurotrophic factor (BDNF) in bipolar disorder: case-control study of over 3000 individuals from the UK.

artículo científico publicado en 2006

Genetically predicted complement component 4A expression: effects on memory function and middle temporal lobe activation.

artículo científico publicado en 2018

Genetics and the brain: many pathways to enlightenment

artículo científico publicado en 2009

Genetics of schizophrenia

Genetics of schizophrenia: A consensus paper of the WFSBP Task Force on Genetics

artículo científico publicado en 2017

Genetics of self-reported risk-taking behaviour, trans-ethnic consistency and relevance to brain gene expression

article

Genome scan meta-analysis of schizophrenia and bipolar disorder, part II: Schizophrenia

artículo científico publicado en 2003

Genome screen for loci influencing age at onset and rate of decline in late onset Alzheimer's disease

artículo científico publicado en 2005

Genome wide significant linkage in schizophrenia conditioning on occurrence of depressive episodes

artículo científico publicado en 2005

Genome-wide Association Study Identifies Genetic Variation in Neurocan as a Susceptibility Factor for Bipolar Disorder

artículo científico publicado en 2011

Genome-wide analyses for personality traits identify six genomic loci and show correlations with psychiatric disorders

artículo científico publicado en 2016

Genome-wide analysis in UK Biobank identifies four loci associated with mood instability and genetic correlation with major depressive disorder, anxiety disorder and schizophrenia

artículo científico publicado en 2017

Genome-wide analysis of copy number variants in attention deficit hyperactivity disorder: the role of rare variants and duplications at 15q13.3.

artículo científico publicado en 2012

Genome-wide analysis of over 106 000 individuals identifies 9 neuroticism-associated loci.

artículo científico publicado en 2016

Genome-wide analysis of self-reported risk-taking behaviour and cross-disorder genetic correlations in the UK Biobank cohort.

artículo científico publicado en 2018

Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression

artículo científico publicado en 2018

Genome-wide association analysis identifies 13 new risk loci for schizophrenia

artículo científico publicado en 2013

Genome-wide association analysis identifies 30 new susceptibility loci for schizophrenia

artículo científico publicado en 2017

Genome-wide association identifies a common variant in the reelin gene that increases the risk of schizophrenia only in women

artículo científico publicado en 2008

Genome-wide association studies in psychiatry: lessons from early studies of non-psychiatric and psychiatric phenotypes

artículo científico publicado en 2008

Genome-wide association study identifies 30 loci associated with bipolar disorder.

artículo científico publicado en 2019

Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder

artículo científico publicado en 2011

Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease

artículo científico publicado en 2009

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

artículo científico publicado en 2007

Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls

artículo científico publicado en 2010

Genome-wide association study of borderline personality disorder reveals genetic overlap with bipolar disorder, major depression and schizophrenia

artículo científico

Genome-wide association study of dietary intake in the UK biobank study and its associations with schizophrenia and other traits

artículo científico publicado en 2020

Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology

artículo científico publicado en 2021

Genome-wide association study of multiplex schizophrenia pedigrees.

artículo científico publicado en 2012

Genome-wide association study of schizophrenia in a Japanese population

artículo científico publicado en 2010

Genome-wide association study on bipolar disorder in the Bulgarian population

scientific journal article

Genome-wide association study reveals greater polygenic loading for schizophrenia in cases with a family history of illness

artículo científico publicado en 2015

Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia

artículo científico publicado en 2016

Genome-wide haplotype association study identifies the FRMD4A gene as a risk locus for Alzheimer's disease

artículo científico publicado en 2012

Genome-wide linkage analysis of 723 affected relative pairs with late-onset Alzheimer's disease

article

Genome-wide significant associations in schizophrenia to ITIH3/4, CACNA1C and SDCCAG8, and extensive replication of associations reported by the Schizophrenia PGC.

artículo científico publicado en 2012

Genome-wide significant locus for Research Diagnostic Criteria Schizoaffective Disorder Bipolar type

artículo científico publicado en 2017

Genomewide Linkage Scan in Schizoaffective Disorder

artículo científico publicado en 2005

Genotype effects of CHRNA7, CNR1 and COMT in schizophrenia: interactions with tobacco and cannabis use.

artículo científico publicado en 2007

Genotype link with extreme antisocial behavior: the contribution of cognitive pathways

artículo científico publicado en 2010

Genotyping single nucleotide polymorphisms by primer extension and high performance liquid chromatography

artículo científico publicado en 1999

Haplotypes at the dystrobrevin binding protein 1 (DTNBP1) gene locus mediate risk for schizophrenia through reduced DTNBP1 expression

artículo científico publicado en 2005

High loading of polygenic risk for ADHD in children with comorbid aggression

artículo científico publicado en 2013

Hypothesis-driven candidate genes for schizophrenia compared to genome-wide association results

artículo científico publicado en 2011

IGF1, growth pathway polymorphisms and schizophrenia: A pooling study

artículo científico publicado en 2007

Identification in 2 independent samples of a novel schizophrenia risk haplotype of the dystrobrevin binding protein gene (DTNBP1).

artículo científico publicado en 2004

Identification of a potential bipolar risk haplotype in the gene encoding the winged-helix transcription factor RFX4.

artículo científico publicado en 2005

Identification of loci associated with schizophrenia by genome-wide association and follow-up

artículo científico publicado en 2008

Identification of novel candidate genes for treatment response to risperidone and susceptibility for schizophrenia: integrated analysis among pharmacogenomics, mouse expression, and genetic case-control association approaches

artículo científico publicado en 2009

Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis

artículo científico publicado en 2013

Identifying gene-environment interactions in schizophrenia: contemporary challenges for integrated, large-scale investigations

artículo científico publicado en 2014

Identifying mechanisms that underlie links between COMT genotype and aggression in male adolescents with ADHD.

artículo científico publicado en 2015

Implication of a rare deletion at distal 16p11.2 in schizophrenia

artículo científico publicado en 2013

Improved detection of common variants associated with schizophrenia and bipolar disorder using pleiotropy-informed conditional false discovery rate

artículo científico publicado en 2013

Improved detection of common variants associated with schizophrenia by leveraging pleiotropy with cardiovascular-disease risk factors

artículo científico publicado en 2013

Improving classification of psychoses

artículo científico publicado en 2016

Increased familial risk and genomewide significant linkage for Alzheimer's disease with psychosis

artículo científico publicado en 2007

Independent estimation of the frequency of rare CNVs in the UK population confirms their role in schizophrenia

artículo científico publicado en 2011

Independent evidence for the selective influence of GABA(A) receptors on one component of the bipolar disorder phenotype

artículo científico publicado en 2010

Influence of NOS1 on verbal intelligence and working memory in both patients with schizophrenia and healthy control subjects

artículo científico publicado en 2009

Integrative functional genomic analysis of human brain development and neuropsychiatric risks

scientific article published on 01 December 2018

Interaction between the ADAM12 and SH3MD1 genes may confer susceptibility to late-onset Alzheimer's disease

artículo científico publicado en 2007

Investigating cis-acting regulatory variation using assays of relative allelic expression

scientific article published on 01 August 2006

Investigating the contribution of common genetic variants to the risk and pathogenesis of ADHD.

artículo científico publicado en 2012

Investigating the genetic architecture of general and specific psychopathology in adolescence

artículo científico publicado en 2018

Investigating the genetic underpinnings of early-life irritability

artículo científico publicado en 2017

Investigation of rare non-synonymous variants at ABCA13 in schizophrenia and bipolar disorder

artículo científico publicado en 2011

Involvement of expanded trinucleotide repeats in common diseases

artículo científico publicado en 1996

Is COMT a susceptibility gene for schizophrenia?

artículo científico publicado en 2007

Is the dysbindin gene (DTNBP1) a susceptibility gene for schizophrenia?

artículo científico publicado en 2005

Jumping To Conclusions, General Intelligence, And Psychosis Liability: Findings From The Multicentric EU-GEI Case-Control Study

Lack of effect of antidepressant drugs on the levels of mRNAs encoding serotonergic receptors, synthetic enzymes and 5HT transporter.

artículo científico publicado en 1994

Lack of effect of chronic antipsychotic treatment on dopamine D5 receptor mRNA level

artículo científico publicado en 1992

Lack of functional promoter polymorphisms in genes involved in glutamate neurotransmission.

artículo científico publicado en 2003

Lack of support for a genetic association of the XBP1 promoter polymorphism with bipolar disorder in probands of European origin

artículo científico publicado en 2004

Letter to the Editor: Strong evidence for multiple psychosis susceptibility genes – a rejoinder to Crow

article

Levels of GABAa receptor subunit mRNA in rat brain following flurazepam treatment.

artículo científico publicado en 1992

Leveraging Genomic Annotations and Pleiotropic Enrichment for Improved Replication Rates in Schizophrenia GWAS.

artículo científico publicado en 2016

Linkage disequilibrium mapping provides further evidence of a gene for reading disability on chromosome 6p21.3-22.

artículo científico publicado en 2003

Linked polymorphisms upstream of exons 1 and 2 of the human cholecystokinin gene are not associated with schizophrenia or bipolar disorder.

artículo científico publicado en 1998

Localization of bipolar susceptibility locus by molecular genetic analysis of the chromosome 12q23-q24 region in two pedigrees with bipolar disorder and Darier's disease

artículo científico publicado en 2005

Low gene expression conferred by association of an allele of the 5-HT2C receptor gene with antipsychotic-induced weight gain

artículo científico publicado en 2005

Maternally derived microduplications at 15q11-q13: implication of imprinted genes in psychotic illness

artículo científico publicado en 2011

Mental disorders of known aetiology and precision medicine in psychiatry: a promising but neglected alliance.

artículo científico publicado en 2016

Meta-Analysis of Genome-Wide Association Studies of Attention-Deficit/Hyperactivity Disorder ⬇️

artículo científico publicado el 1 de agosto de 2010

Meta-analysis of 32 genome-wide linkage studies of schizophrenia.

artículo científico publicado en 2008

Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease

artículo científico publicado en 2013

Meta-analysis of COMT val158met in panic disorder: ethnic heterogeneity and gender specificity

artículo científico publicado en 2007

Meta-analysis of genetic association with diagnosed Alzheimer's disease identifies novel risk loci and implicates Abeta, Tau, immunity and lipid processing

Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder.

artículo científico publicado en 2010

Methylation QTLs in the developing brain and their enrichment in schizophrenia risk loci

artículo científico publicado en 2015

Methylomic trajectories across human fetal brain development

artículo científico publicado en 2015

MiR-137-derived polygenic risk: effects on cognitive performance in patients with schizophrenia and controls

artículo científico publicado en 2017

Microduplications of 16p11.2 are associated with schizophrenia

artículo científico publicado en 2009

Molecular genetic contribution to the developmental course of attention-deficit hyperactivity disorder.

artículo científico publicado en 2008

Mosaic copy number variation in schizophrenia

artículo científico publicado en 2013

Most genome-wide significant susceptibility loci for schizophrenia and bipolar disorder reported to date cross-traditional diagnostic boundaries

artículo científico publicado en 2010

Multicenter linkage study of schizophrenia loci on chromosome 22q.

artículo científico publicado en 2004

Mutation intolerant genes and targets of FMRP are enriched for nonsynonymous alleles in schizophrenia

artículo científico publicado en 2017

Mutation screening and LD mapping in the VCFS deleted region of chromosome 22q11 in schizophrenia using a novel DNA pooling approach

artículo científico publicado en 2002

Mutation screening of SCN2A in schizophrenia and identification of a novel loss-of-function mutation

artículo científico publicado en 2015

Mutation screening of the 3q29 microdeletion syndrome candidate genes DLG1 and PAK2 in schizophrenia

artículo científico publicado en 2011

Mutation screening of the KCNN3 gene reveals a rare frameshift mutation

artículo científico publicado en 2001

Mutation screening of theDTNBP1exonic sequence in 669 schizophrenics and 710 controls using high-resolution melting analysis

artículo científico publicado en 2010

Mutations in ATP2A2, encoding a Ca2+ pump, cause Darier disease

artículo científico publicado en 1999

Neurexin 1 (NRXN1) deletions in schizophrenia

artículo científico publicado en 2009

Neurocognitive abilities in the general population and composite genetic risk scores for attention-deficit hyperactivity disorder

artículo científico publicado en 2014

Neurodevelopmental hypothesis of schizophrenia

artículo científico publicado en 2011

Neuroprotective effect of lithium on hippocampal volumes in bipolar disorder independent of long-term treatment response

artículo científico publicado en 2013

Neuropsychological effects of the CSMD1 genome-wide associated schizophrenia risk variant rs10503253.

artículo científico publicado en 2013

New data and an old puzzle: the negative association between schizophrenia and rheumatoid arthritis

artículo científico publicado en 2015

New findings from genetic association studies of schizophrenia

artículo científico publicado en 2009

New insights into the pharmacogenomics of antidepressant response from the GENDEP and STAR*D studies: rare variant analysis and high-density imputation.

artículo científico publicado en 2017

No Evidence for Enrichment in Schizophrenia for Common Allelic Associations at Imprinted Loci

artículo científico publicado en 2015

No association between schizophrenia and polymorphisms in COMT in two large samples

artículo científico publicado en 2005

No association between the putative functional ZDHHC8 single nucleotide polymorphism rs175174 and schizophrenia in large European samples

artículo científico publicado en 2005

No evidence for association between a non-synonymous polymorphism in the gene encoding human metabotropic glutamate receptor 7 and schizophrenia

artículo científico publicado en 2000

No evidence for association between polymorphisms in GRM3 and schizophrenia

artículo científico publicado en 2005

No evidence for expanded polyglutamine sequences in bipolar disorder and schizophrenia.

artículo científico publicado en 1997

No evidence of association between Catechol-O-Methyltransferase (COMT) Val158Met genotype and performance on neuropsychological tasks in children with ADHD: a case-control study

artículo científico publicado en 2004

No evidence of association between HLA-DRB1 and attention deficit hyperactivity disorder

artículo científico publicado en 2003

No evidence of association from transmission disequilibrium analysis of the hKCa3 gene in bipolar disorder

article

No evidence of association of two 5HT transporter gene polymorphisms and attention deficit hyperactivity disorder

artículo científico publicado en 2003

No evidence that extended tracts of homozygosity are associated with Alzheimer's disease

artículo científico publicado en 2011

No evidence that rare coding variants in ZNF804A confer risk of schizophrenia.

artículo científico publicado en 2010

No major schizophrenia locus detected on chromosome 1q in a large multicenter sample

artículo científico publicado en 2002

No support for association between the dopamine transporter (DAT1) gene and ADHD.

artículo científico publicado en 2005

Non-random mating, parent-of-origin, and maternal-fetal incompatibility effects in schizophrenia

artículo científico publicado en 2012

Novel Findings from CNVs Implicate Inhibitory and Excitatory Signaling Complexes in Schizophrenia

artículo científico publicado en 2015

Novel genetic advances in schizophrenia: an interview with Michael O'Donovan

artículo científico publicado en 2015

Operation of the schizophrenia susceptibility gene, neuregulin 1, across traditional diagnostic boundaries to increase risk for bipolar disorder

artículo científico publicado en 2005

P2RX7: A bipolar and unipolar disorder candidate susceptibility gene?

artículo científico publicado en 2009

POLARIS: Polygenic LD-adjusted risk score approach for set-based analysis of GWAS data.

artículo científico publicado en 2018

Parental Origin of Interstitial Duplications at 15q11.2-q13.3 in Schizophrenia and Neurodevelopmental Disorders.

artículo científico publicado en 2016

Permutation-based approaches do not adequately allow for linkage disequilibrium in gene-wide multi-locus association analysis

artículo científico publicado en 2012

Pharmacogenetics of antidepressant response: A polygenic approach

artículo científico publicado en 2017

Phenotype evaluation and genomewide linkage study of clinical variables in schizophrenia

artículo científico publicado en 2011

Phenotypic Manifestation of Genetic Risk for Schizophrenia During Adolescence in the General Population

artículo científico publicado en 2016

Phenotypic and genetic complexity of psychosis

artículo científico publicado en 2007

Phenotypic variation between parent-offspring trios and non-trios in genetic studies of schizophrenia

artículo científico publicado en 2005

Phenotypic variations on the theme of CNVs

Pleiotropic Effects of Trait-Associated Genetic Variation on DNA Methylation: Utility for Refining GWAS Loci.

artículo científico publicado en 2017

Polygenic Overlap Between C-Reactive Protein, Plasma Lipids, and Alzheimer Disease

artículo científico publicado en 2015

Polygenic dissection of diagnosis and clinical dimensions of bipolar disorder and schizophrenia

artículo científico publicado en 2013

Polygenic dissection of the bipolar phenotype

artículo científico publicado en 2011

Polygenic risk for schizophrenia and season of birth within the UK Biobank cohort

scientific article published on 04 March 2018

Polygenic transmission and complex neuro developmental network for attention deficit hyperactivity disorder: genome-wide association study of both common and rare variants ⬇️

artículo científico publicado en 2013

Polymorphism of the 5-HT transporter and response to antidepressants: randomised controlled trial

artículo científico publicado en 2011

Polymorphisms in the phosphate and tensin homolog gene are not associated with late-onset Alzheimer's disease

artículo científico publicado en 2006

Pooled DNA genotyping on Affymetrix SNP genotyping arrays

artículo científico publicado en 2006

Predictors of developmental dyslexia in European orthographies with varying complexity

artículo científico

Premature mortality among people with severe mental illness — New evidence from linked primary care data

artículo científico publicado en 2018

Promoter polymorphisms in glutathione-S-transferase genes affect transcription

artículo científico publicado en 2004

Promoting Measured Genes and Measured Environments: On the Importance of Careful Statistical Analyses and Biological Relevance—Reply

article

Psychiatric Genomics: An Update and an Agenda

artículo científico publicado en 2017

Psychiatric Genomics: An Update and an Agenda

Psychiatric gene discoveries shape evidence on ADHD's biology

artículo científico publicado en 2015

Psychiatric genetics: back to the future

artículo científico publicado en 2000

Psychiatric genetics: what's new in 2015?

artículo científico publicado en 2016

Psychopathy trait scores in adolescents with childhood ADHD: the contribution of genotypes affecting MAOA, 5HTT and COMT activity.

artículo científico publicado en 2009

Psychopathy traits in adolescents with childhood attention-deficit hyperactivity disorder

artículo científico publicado en 2009

Psychosis genetics: modeling the relationship between schizophrenia, bipolar disorder, and mixed (or "schizoaffective") psychoses

artículo científico publicado en 2009

Psychosis susceptibility gene ZNF804A and cognitive performance in schizophrenia

artículo científico publicado en 2010

Publisher Correction: Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection

artículo científico publicado en 2019

Publisher Correction: Gene expression imputation across multiple brain regions provides insights into schizophrenia risk

scientific article published on 01 June 2019

Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis

artículo científico publicado en 2010

Rare chromosomal deletions and duplications increase risk of schizophrenia

artículo científico publicado en 2008

Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease

artículo científico publicado en 2017

Rare copy number variants: a point of rarity in genetic risk for bipolar disorder and schizophrenia

artículo científico publicado en 2010

Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders.

artículo científico publicado en 2016

Reasons for discontinuing clozapine: A cohort study of patients commencing treatment

artículo científico publicado en 2016

Recent genomic advances in schizophrenia

artículo científico publicado en 2011

Reciprocal duplication of the Williams-Beuren syndrome deletion on chromosome 7q11.23 is associated with schizophrenia

artículo científico publicado en 2013

Reduced burden of very large and rare CNVs in bipolar affective disorder

artículo científico publicado en 2013

Refining the attention deficit hyperactivity disorder phenotype for molecular genetic studies

artículo científico publicado en 2006

Repeat sizes at CAG/CTG loci CTG18.1, ERDA1 and TGC13-7a in schizophrenia

artículo científico publicado en 2000

Replicated evidence that endophenotypic expression of schizophrenia polygenic risk is greater in healthy siblings of patients compared to controls, suggesting gene-environment interaction. The EUGEI study

scientific article published on 15 August 2019

Replication of bipolar disorder susceptibility alleles and identification of two novel genome-wide significant associations in a new bipolar disorder case-control sample

scientific article published on 16 October 2012

Reply to Bertram et al.

artículo científico publicado en 2006

Response to 'Predicting the diagnosis of autism spectrum disorder using gene pathway analysis'.

artículo científico publicado en 2013

Risk variant of oligodendrocyte lineage transcription factor 2 is associated with reduced white matter integrity

artículo científico publicado en 2012

SORL1 variants and risk of late-onset Alzheimer's disease

artículo científico publicado en 2008

Schizophrenia

article

Schizophrenia and functional polymorphisms in the MAOA and COMT genes: no evidence for association or epistasis.

artículo científico publicado en 2002

Schizophrenia and the neurodevelopmental continuum:evidence from genomics

artículo científico publicado en 2017

Schizophrenia copy number variants and associative learning

artículo científico publicado en 2016

Schizophrenia genetic variants are not associated with intelligence

artículo científico publicado en 2013

Schizophrenia genetics: advancing on two fronts

scientific article published on April 2009

Schizophrenia genetics: building the foundations of the future

artículo científico publicado en 2014

Schizophrenia genetics: emerging themes for a complex disorder.

artículo científico publicado en 2014

Schizophrenia genetics: new insights from new approaches

artículo científico publicado en 2009

Schizophrenia polygenic risk score and psychotic risk detection-Authors' reply

artículo científico publicado en 2017

Schizophrenia risk alleles and neurodevelopmental outcomes in childhood: a population-based cohort study

artículo científico publicado en 2016

Schizophrenia risk variants modulate white matter volume across the psychosis spectrum: evidence from two independent cohorts

artículo científico publicado en 2015

Schizophrenia susceptibility alleles are enriched for alleles that affect gene expression in adult human brain ⬇️

artículo científico publicado el 22 de febrero de 2011

Schizophrenia two-hit hypothesis in velo-cardio facial syndrome

artículo científico publicado en 2013

Schizophrenia: a genetic disorder of the synapse?

artículo científico publicado en 2005

Schizophrenia: complex genetics, not fairy tales.

artículo científico publicado en 2008

Schizophrenia: genes at last?

artículo científico publicado en 2005

Screening ABCG1, the human homologue of the Drosophila white gene, for polymorphisms and association with bipolar affective disorder.

artículo científico publicado en 2001

Screening the human protocadherin 8 (PCDH8) gene in schizophrenia.

artículo científico publicado en 2002

Searching for susceptibility genes in schizophrenia

artículo científico publicado en 2001

Sequence variation in the CHAT locus shows no association with late-onset Alzheimer's disease

artículo científico publicado en 2003

Serotonergic system and attention deficit hyperactivity disorder (ADHD): a potential susceptibility locus at the 5-HT(1B) receptor gene in 273 nuclear families from a multi-centre sample

artículo científico publicado en 2002

Severity of depression and response to antidepressants: GENPOD randomised controlled trial

artículo científico publicado en 2011

Sex differences in gene expression in the human fetal brain

article

Shared genetic influences between attention-deficit/hyperactivity disorder (ADHD) traits in children and clinical ADHD.

artículo científico publicado en 2015

Shared polygenic contribution between childhood attention-deficit hyperactivity disorder and adult schizophrenia

artículo científico publicado en 2013

Steroid sulfatase is a potential modifier of cognition in attention deficit hyperactivity disorder

artículo científico publicado en 2011

Streamlined analysis of pooled genotype data in SNP-based association studies

artículo científico publicado en 2005

Strong bias in the location of functional promoter polymorphisms

artículo científico publicado en 2005

Strong evidence for association between the dystrobrevin binding protein 1 gene (DTNBP1) and schizophrenia in 488 parent-offspring trios from Bulgaria

artículo científico publicado en 2004

Strong evidence that GNB1L is associated with schizophrenia

artículo científico publicado en 2007

Strong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia

artículo científico publicado en 2005

Strong genetic evidence for a selective influence of GABAA receptors on a component of the bipolar disorder phenotype

artículo científico publicado en 2008

Structural variations in attention-deficit hyperactivity disorder – Authors' reply

artículo científico publicado en 2011

Substantial linkage disequilibrium across the insulin-degrading enzyme locus but no association with late-onset Alzheimer's disease.

artículo científico publicado en 2001

Suggestion of roles for both common and rare risk variants in genome-wide studies of schizophrenia

artículo científico publicado en 2010

Support for RGS4 as a susceptibility gene for schizophrenia

artículo científico publicado en 2004

Support for genetic variation in neuregulin 1 and susceptibility to schizophrenia

artículo científico publicado en 2003

Support for neuregulin 1 as a susceptibility gene for bipolar disorder and schizophrenia

artículo científico publicado en 2008

Support for the involvement of large copy number variants in the pathogenesis of schizophrenia

artículo científico publicado en 2009

Symptom dimensions and the Kraepelinian dichotomy

scientific article published on 01 April 2007

T128. THE ASSOCIATION BETWEEN GENETIC RISK FOR SCHIZOPHRENIA AND PATTERNS OF CIGARETTE AND CANNABIS USE IN ADOLESCENCE.

artículo científico publicado en 2018

TCF4, schizophrenia, and Pitt-Hopkins Syndrome

artículo científico publicado en 2010

TCTEX1D2 mutations underlie Jeune asphyxiating thoracic dystrophy with impaired retrograde intraflagellar transport ⬇️

artículo científico publicado en 2015

Tbx1 haploinsufficiency is linked to behavioral disorders in mice and humans: implications for 22q11 deletion syndrome

artículo científico publicado en 2006

Testing for gene x environment interaction effects in attention deficit hyperactivity disorder and associated antisocial behavior.

artículo científico publicado en 2008

The Duffy-null genotype and risk of infection

artículo científico publicado en 2020

The ENCODE project: implications for psychiatric genetics

artículo científico publicado en 2013

The bipolar disorder risk allele at CACNA1C also confers risk of recurrent major depression and of schizophrenia

artículo científico publicado en 2010

The catechol-O-methyl transferase (COMT) gene as a candidate for psychiatric phenotypes: evidence and lessons

artículo científico publicado en 2006

The contribution of gene-environment interaction to psychopathology.

artículo científico publicado en 2007

The contribution of rare variants to risk of schizophrenia in individuals with and without intellectual disability.

artículo científico publicado en 2017

The effect of age and the H1c MAPT haplotype on MAPT expression in human brain

article

The effects of antidepressant drugs on kainate receptor mRNA levels

artículo científico publicado en 1991

The genetics of attention deficit hyperactivity disorder

artículo científico publicado en 2005

The genetics of developmental dyslexia

artículo científico publicado en 2006

The genetics of schizophrenia and bipolar disorder: dissecting psychosis

artículo científico publicado en 2005

The genomic basis of mood instability: identification of 46 loci in 363,705 UK Biobank participants, genetic correlation with psychiatric disorders, and association with gene expression and function

artículo científico publicado en 2019

The high affinity neurotensin receptor gene (NTSR1): comparative sequencing and association studies in schizophrenia

article

The impact of schizophrenia and mood disorder risk alleles on emotional problems: investigating change from childhood to middle age.

artículo científico publicado en 2017

The implications of the shared genetics of psychiatric disorders

artículo científico publicado en 2016

The molecular genetics of schizophrenia.

artículo científico publicado en 1996

The molecular genetics of schizophrenia: new findings promise new insights

artículo científico publicado en 2004

The penetrance of copy number variations for schizophrenia and developmental delay.

artículo científico publicado en 2013

The relative contribution of common and rare genetic variants to ADHD

artículo científico publicado en 2015

The role of the major histocompatibility complex region in cognition and brain structure: a schizophrenia GWAS follow-up

artículo científico publicado en 2013

The role of variation at AβPP, PSEN1, PSEN2, and MAPT in late onset Alzheimer's disease

artículo científico publicado en 2012

The serotonin-2A receptor gene locus does not contain common polymorphism affecting mRNA levels in adult brain

artículo científico publicado en 2004

The synapse in schizophrenia

artículo científico

Towards diagnostic markers for the psychoses

artículo científico publicado en 2016

Transcriptome-wide association study of schizophrenia and chromatin activity yields mechanistic disease insights

article

Tryptophan pyrrolase gene expression in an alcohol preferring and non-preferring mouse strain

article

Ubiquilin 1 polymorphisms are not associated with late-onset Alzheimer's disease

artículo científico publicado en 2006

Universal, robust, highly quantitative SNP allele frequency measurement in DNA pools

artículo científico publicado en 2002

Validity of the concept of minor depression in a developing country setting

artículo científico publicado en 2008

Variants of dopamine and serotonin candidate genes as predictors of response to risperidone treatment in first-episode schizophrenia

artículo científico publicado en 2008

Variation at the DAOA/G30 locus influences susceptibility to major mood episodes but not psychosis in schizophrenia and bipolar disorder

artículo científico publicado en 2006

Variation at the GABAA receptor gene, Rho 1 (GABRR1) associated with susceptibility to bipolar schizoaffective disorder

artículo científico publicado en 2010

Variation in tau isoform expression in different brain regions and disease states

artículo científico publicado en 2013

Variation in the protocadherin gamma A gene cluster

artículo científico publicado en 2003

Wake-up call for British psychiatry

artículo científico publicado en 2008

What have we learned from the Psychiatric Genomics Consortium

artículo científico publicado en 2015

Whole genome association study in a homogenous population in Shandong peninsula of China reveals JARID2 as a susceptibility gene for schizophrenia

artículo científico publicado en 2009

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