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Lista de obras de Sven Cichon

1q21.1 distal copy number variants are associated with cerebral and cognitive alterations in humans

artículo científico publicado en 2021

4th Pediatric Allergy and Asthma Meeting (PAAM)

artículo científico publicado en 2016

A Genome-Wide Association Study Suggests Novel Loci Associated with a Schizophrenia-Related Brain-Based Phenotype

artículo científico publicado en 2013

A case of hereditary angio-oedema type III presenting with C1-inhibitor cleavage and a missense mutation in the F12 gene

article

A common microdeletion affecting a hippocampus- and amygdala-specific isoform of tryptophan hydroxylase 2 is not associated with affective disorders

artículo científico publicado en 2014

A common risk variant in CACNA1C supports a sex-dependent effect on longitudinal functioning and functional recovery from episodes of schizophrenia-spectrum but not bipolar disorder

artículo científico publicado en 2015

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

A family-based and case–control association study of trace amine receptor genes on chromosome 6q23 in bipolar affective disorder

article

A genetic deconstruction of neurocognitive traits in schizophrenia and bipolar disorder

artículo científico publicado en 2013

A genome screen for genes predisposing to bipolar affective disorder detects a new susceptibility locus on 8q

article

A genome-wide association study confirms PNPLA3 and identifies TM6SF2 and MBOAT7 as risk loci for alcohol-related cirrhosis

artículo científico publicado en 2015

A genome-wide association study for late-onset Alzheimer's disease using DNA pooling

artículo científico publicado en 2008

A genome-wide association study implicates diacylglycerol kinase eta (DGKH) and several other genes in the etiology of bipolar disorder

artículo científico publicado en 2008

A genome-wide association study in 574 schizophrenia trios using DNA pooling

scientific journal article

A genome-wide association study of anorexia nervosa

artículo científico publicado en 2014

A genome-wide association study of attempted suicide.

artículo científico publicado en 2011

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 new susceptibility locus for bipolar affective disorder in PAR1 on Xp22.3/Yp11.3

A possible susceptibility locus for bipolar affective disorder in chromosomal region 10q25–q26

article by Sven Cichon et al published 27 April 2001 in Molecular Psychiatry

A reappraisal of the association between Dysbindin (DTNBP1) and schizophrenia in a large combined case-control and family-based sample of German ancestry

artículo científico publicado en 2010

A serine to glycine substitution at position 9 in the extracellular N-terminal part of the dopamine D3 receptor protein: No role in the genetic predisposition to bipolar affective disorder

scientific article published on 01 March 1993

A summary statistic approach to sequence variation in noncoding regions of six schizophrenia-associated gene loci

artículo científico publicado en 2006

A systematic association mapping on chromosome 6q in bipolar affective disorder--evidence for the melanin-concentrating-hormone-receptor-2 gene as a risk factor for bipolar affective disorder

artículo científico publicado en 2010

Agonist Binding to Chemosensory Receptors: A Systematic Bioinformatics Analysis

artículo científico publicado en 2017

Allelic differences between Europeans and Chinese for CREB1 SNPs and their implications in gene expression regulation, hippocampal structure and function, and bipolar disorder susceptibility.

scientific article published on 09 April 2013

Altered Functional Subnetwork During Emotional Face Processing: A Potential Intermediate Phenotype for Schizophrenia

artículo científico publicado en 2016

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

artículo científico publicado en 2016

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 genome-wide significant bipolar disorder genes in borderline personality disorder

artículo científico publicado en 2014

Analysis of shared heritability in common disorders of the brain

artículo científico publicado en 2018

Analysis of the Influence of microRNAs in Lithium Response in Bipolar Disorder.

artículo científico publicado en 2018

Analysis of the joint effect of SNPs to identify independent loci and allelic heterogeneity in schizophrenia GWAS data

artículo científico publicado en 2017

Angio-oedema induced by oestrogen contraceptives is mediated by bradykinin and is frequently associated with urticaria.

artículo científico publicado en 2012

Assessment of Response to Lithium Maintenance Treatment in Bipolar Disorder: A Consortium on Lithium Genetics (ConLiGen) Report

artículo científico publicado en 2013

Association Study of Nonsynonymous Single Nucleotide Polymorphisms in Schizophrenia

article by Noa Carrera et al published January 2012 in Biological Psychiatry

Association analysis of Neuregulin 1 candidate regions in schizophrenia and bipolar disorder

article

Association analysis of the dopamine D2 receptor gene in Tourette's syndrome using the haplotype relative risk method

article

Association between a polymorphism in the pseudoautosomal X-linked gene SYBL1 and bipolar affective disorder

artículo científico publicado en 2002

Association between a promoter dopamine D2 receptor gene variant and the personality trait detachment

artículo científico publicado en 2003

Association between copy number variants in 16p11.2 and major depressive disorder in a German case-control sample

artículo científico publicado en 2012

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

artículo científico publicado en 2011

Association between neuropeptide Y receptor Y2 promoter variant rs6857715 and major depressive disorder

artículo científico publicado en 2016

Association between schizophrenia and common variation in neurocan (NCAN), a genetic risk factor for bipolar disorder

artículo científico publicado en 2012

Association of Copy Number Variation of the 15q11.2 BP1-BP2 Region With Cortical and Subcortical Morphology and Cognition

artículo científico publicado en 2019

Association of Polygenic Score for Schizophrenia and HLA Antigen and Inflammation Genes With Response to Lithium in Bipolar Affective Disorder: A Genome-Wide Association Study.

artículo científico publicado en 2017

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 polygenic score for major depression with response to lithium in patients with bipolar disorder

artículo científico publicado en 2020

Association study between genetic variants at the PIP5K2A gene locus and schizophrenia and bipolar affective disorder

article

Association study between genetic variants at the VAMP2 and VAMP3 loci and bipolar affective disorder

artículo científico publicado en 2008

Association study between two variants in the DOPA decarboxylase gene in bipolar and unipolar affective disorder

artículo científico publicado en 2002

Association study of 20 genetic variants at the D-amino acid oxidase gene in schizophrenia

article

Association study of a functional promoter polymorphism in theXBP1 gene and schizophrenia

article

Association study of the GRIA1 and CLINT1 (Epsin 4) genes in a German schizophrenia sample

article

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

artículo científico publicado en 2011

Bipolar disorder risk alleles in children with ADHD.

artículo científico publicado en 2013

Bipolar multiplex families have an increased burden of common risk variants for psychiatric disorders

Brain function in carriers of a genome-wide supported bipolar disorder variant

artículo científico publicado en 2010

Brain-derived neurotrophic factor gene (BDNF) variants and schizophrenia: an association study

artículo científico publicado en 2006

Brain-specific tryptophan hydroxylase 2 (TPH2): a functional Pro206Ser substitution and variation in the 5'-region are associated with bipolar affective disorder

artículo científico publicado en 2007

Brief report: no association between premorbid adjustment in adult-onset schizophrenia and genetic variation in Dysbindin

artículo científico publicado en 2008

CLCN2 variants in idiopathic generalized epilepsy

artículo científico publicado en 2009

CNTF and psychiatric disorders

Can long-range microsatellite data be used to predict short-range linkage disequilibrium?

artículo científico publicado en 2002

Candidate gene analysis of the human natural killer-1 carbohydrate pathway and perineuronal nets in schizophrenia: B3GAT2 is associated with disease risk and cortical surface area

artículo científico publicado en 2010

Caspase recruitment domain 15 gene haplotypes in sarcoidosis

article

Cloning, genomic organization, alternative transcripts and mutational analysis of the gene responsible for autosomal recessive universal congenital alopecia

artículo científico publicado en 1998

Cognitive state and connectivity effects of the genome-wide significant psychosis variant in ZNF804A.

artículo científico publicado en 2010

Combined analysis from eleven linkage studies of bipolar disorder provides strong evidence of susceptibility loci on chromosomes 6q and 8q

artículo científico publicado en 2005

Common and rare variant analysis in early-onset bipolar disorder vulnerability

artículo científico publicado en 2014

Common and rare variant association analyses in Amyotrophic Lateral Sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

artículo científico

Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

artículo científico

Common functional variants of the glutamatergic system in Autism spectrum disorder with high and low intellectual abilities

artículo científico publicado en 2017

Common genetic variants and gene-expression changes associated with bipolar disorder are over-represented in brain signaling pathway genes

artículo científico publicado en 2012

Common genetic variants influence human subcortical brain structures

artículo científico publicado en 2015

Common obesity risk alleles in childhood attention-deficit/hyperactivity disorder.

artículo científico publicado en 2013

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

artículo científico publicado en 2012

Common variants at 2q11.2, 8q21.3, and 11q13.2 are associated with major mood disorders.

artículo científico publicado en 2017

Common variants at VRK2 and TCF4 conferring risk of schizophrenia

artículo científico publicado en 2011

Common variants conferring risk of schizophrenia

artículo científico publicado en 2009

Common variants on 8p12 and 1q24.2 confer risk of schizophrenia

artículo científico publicado en 2011

Common variation in NCAN, a risk factor for bipolar disorder and schizophrenia, influences local cortical folding in schizophrenia

artículo científico publicado en 2014

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

Contact system activation in patients with HAE and normal C1 inhibitor function

artículo científico publicado en 2013

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

artículo científico publicado en 2016

Convergent Lines of Evidence Support LRP8 as a Susceptibility Gene for Psychosis

artículo científico publicado en 2015

Converging Evidence for Epistasis between ANK3 and Potassium Channel Gene KCNQ2 in Bipolar Disorder

artículo científico publicado en 2013

Copy number variants in German patients with schizophrenia

artículo científico publicado en 2013

Copy number variations of chromosome 16p13.1 region associated with schizophrenia

artículo científico publicado en 2009

Correction: Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia

artículo científico publicado en 2020

DRD4 exon 3 variants are not associated with symptomatology of major psychoses in a German population

artículo científico publicado en 2004

Detecting significant genotype-phenotype association rules in bipolar disorder: market research meets complex genetics

article

Disruption of the neurexin 1 gene is associated with schizophrenia

artículo científico publicado en 2009

Dissection of phenotype reveals possible association between schizophrenia and Glutamate Receptor Delta 1 (GRID1) gene promoter

artículo científico publicado en 2009

Distinct loci in the CHRNA5/CHRNA3/CHRNB4 gene cluster are associated with onset of regular smoking

artículo científico publicado en 2013

Dopamine D2 receptor molecular variant and schizophrenia

artículo científico publicado en 1994

Dopamine D4 receptor gene (DRD4) variants and schizophrenia: meta-analyses

artículo científico publicado en 2003

Dual association of a TRKA polymorphism with schizophrenia.

artículo científico publicado en 2011

Duplications in RB1CC1 are associated with schizophrenia; identification in large European sample sets.

artículo científico publicado en 2013

Effects of a genome-wide supported psychosis risk variant on neural activation during a theory-of-mind task

artículo científico publicado en 2010

Effects of exogenous agmatine in human leukemia HMC-1 and HL-60 cells on proliferation, polyamine metabolism and cell cycle

artículo científico publicado en 2011

Effects of the circadian rhythm gene period 1 (per1) on psychosocial stress-induced alcohol drinking.

artículo científico publicado en 2011

Efficient region-based test strategy uncovers genetic risk factors for functional outcome in bipolar disorder

scientific article published on 29 November 2018

Efficient strategy for detecting gene × gene joint action and its application in schizophrenia

artículo científico publicado en 2013

Enzymatic assays for the diagnosis of bradykinin-dependent angioedema

artículo científico publicado en 2013

Epigenetic alteration of the dopamine transporter gene in alcohol-dependent patients is associated with age.

artículo científico publicado en 2012

Epistatic interaction of genetic depression risk variants in the human subgenual cingulate cortex during memory encoding

artículo científico

Erratum: Corrigendum: Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis

scholarly article published in Nature Genetics

Erratum: Genome-wide association study meta-analysis of European and Asian-ancestry samples identifies three novel loci associated with bipolar disorder

article

European collaborative study of early-onset bipolar disorder: Evidence for genetic heterogeneity on 2q14 according to age at onset

article

Evaluation of linkage of bipolar affective disorder to chromosome 18 in a sample of 57 German families

article

Evidence for a relationship between genetic variants at the brain-derived neurotrophic factor (BDNF) locus and major depression

artículo científico publicado en 2005

Evidence for linkage of spelling disability to chromosome 15

artículo científico publicado en 1998

Examination of G72 and D-amino-acid oxidase as genetic risk factors for schizophrenia and bipolar affective disorder

artículo científico publicado en 2004

Excess of homozygosity at the dopamine D3 receptor gene in schizophrenia not confirmed

artículo científico publicado en 1993

Exome chip analyses in adult attention deficit hyperactivity disorder.

artículo científico publicado en 2016

Expanding the range of ZNF804A variants conferring risk of psychosis

artículo científico publicado en 2010

Expert and self-assessment of lifetime symptoms and diagnosis of major depressive disorder in large-scale genetic studies in the general population: comparison of a clinical interview and a self-administered checklist

artículo científico

Factor XII missense mutation THR328LYS in three Brazilian families

article

Family-based association studies of alpha-adrenergic receptor genes in chromosomal regions with linkage to bipolar affective disorder

artículo científico publicado en 2004

Feasible and Successful: Genome-Wide Interaction Analysis Involving All 1.9 × 1011 Pair-Wise Interaction Tests

article

Functional Subclone Profiling for Prediction of Treatment-Induced Intratumor Population Shifts and Discovery of Rational Drug Combinations in Human Glioblastoma

artículo científico publicado en 2016

Functional impact of a recently identified quantitative trait locus for hippocampal volume with genome-wide support

artículo científico publicado en 2013

Functional neuroimaging effects of recently discovered genetic risk loci for schizophrenia and polygenic risk profile in five RDoC subdomains

artículo científico publicado en 2017

Further evidence for age of onset being an indicator for severity in bipolar disorder

article

Further evidence for the impact of a genome-wide-supported psychosis risk variant in ZNF804A on the Theory of Mind Network

artículo científico publicado en 2013

G72 and its association with major depression and neuroticism in large population-based groups from Germany.

artículo científico publicado en 2008

GLRB allelic variation associated with agoraphobic cognitions, increased startle response and fear network activation: a potential neurogenetic pathway to panic disorder.

artículo científico publicado en 2017

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

artículo científico publicado en 2010

GWAS for executive function and processing speed suggests involvement of the CADM2 gene.

artículo científico publicado en 2015

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

artículo científico publicado en 2019

GWAS-based pathway analysis differentiates between fluid and crystallized intelligence.

artículo científico publicado en 2014

Gender-specific association of variants in the AKR1C1 gene with dimensional anxiety in patients with panic disorder: additional evidence for the importance of neurosteroids in anxiety?

artículo científico publicado en 2014

Gene expression is stable in a complete CIB1 knockout keratinocyte model

scientific article published on 11 September 2020

Gene set enrichment analysis and expression pattern exploration implicate an involvement of neurodevelopmental processes in bipolar disorder

artículo científico publicado en 2017

Gene variants associated with schizophrenia in a Norwegian genome-wide study are replicated in a large European cohort

scientific journal article

Gene-based analysis of regionally enriched cortical genes in GWAS data sets of cognitive traits and psychiatric disorders

artículo científico publicado en 2012

Genetic Architecture of Subcortical Brain Structures in Over 40,000 Individuals Worldwide

scholarly article published 28 August 2017

Genetic Contribution to Alcohol Dependence: Investigation of a Heterogeneous German Sample of Individuals with Alcohol Dependence, Chronic Alcoholic Pancreatitis, and Alcohol-Related Cirrhosis

artículo científico

Genetic and functional abnormalities of the melatonin biosynthesis pathway in patients with bipolar disorder

artículo científico publicado en 2012

Genetic architecture of subcortical brain structures in 38,851 individuals

scientific article published on 21 October 2019

Genetic association between the phospholipase A2 gene and unipolar affective disorder: a multicentre case???control study

article

Genetic effects influencing risk for major depressive disorder in China and Europe

artículo científico publicado en 2017

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

artículo científico publicado en 2013

Genetic risk for schizophrenia impacts Theory-of-Mind-related brain activation

scientific article published on 01 April 2011

Genetic variants associated with response to lithium treatment in bipolar disorder: a genome-wide association study

artículo científico publicado en 2016

Genetic variation at the synaptic vesicle gene SV2A is associated with schizophrenia

artículo científico publicado en 2012

Genetic variation in the human androgen receptor gene is the major determinant of common early-onset androgenetic alopecia

artículo científico publicado en 2005

Genetic variation of the FAT gene at 4q35 is associated with bipolar affective disorder.

artículo científico publicado en 2007

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

artículo científico publicado en 2017

Genetics of structural connectivity and information processing in the brain

artículo científico publicado en 2016

Geneties of Schizophrenia and Bipolar Affective Disorder

Genome scan meta-analysis of schizophrenia and bipolar disorder, part III: Bipolar disorder

artículo científico publicado en 2003

Genome-Wide Association Study Reveals First Locus for Anorexia Nervosa and Metabolic Correlations

scholarly article

Genome-wide analysis implicates microRNAs and their target genes in the development of bipolar disorder

artículo científico publicado en 2015

Genome-wide analysis of rare copy number variations reveals PARK2 as a candidate gene for attention-deficit/hyperactivity disorder

artículo científico publicado en 2012

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

artículo científico publicado en 2018

Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis

artículo científico publicado en 2016

Genome-wide association analysis of age at onset and psychotic symptoms in bipolar disorder

artículo científico publicado en 2011

Genome-wide association data provide further support for an association between 5-HTTLPR and major depressive disorder

artículo científico publicado en 2012

Genome-wide association for major depressive disorder: a possible role for the presynaptic protein piccolo

artículo científico publicado en 2008

Genome-wide association of mood-incongruent psychotic bipolar disorder

artículo científico publicado en 2012

Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis

artículo científico publicado en 2009

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

artículo científico publicado en 2019

Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa.

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 two susceptibility loci for nonsyndromic cleft lip with or without cleft palate

artículo científico publicado en 2009

Genome-wide association study implicates NDST3 in schizophrenia and bipolar disorder

scientific article published on January 2013

Genome-wide association study in German patients with attention deficit/hyperactivity disorder

artículo científico publicado en 2011

Genome-wide association study meta-analysis of European and Asian-ancestry samples identifies three novel loci associated with bipolar disorder

artículo científico publicado en 2011

Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder

artículo científico publicado en 2016

Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder

article

Genome-wide association study of alcohol dependence

scientific journal article

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 more than 40,000 bipolar disorder cases provides new insights into the underlying biology

artículo científico publicado en 2021

Genome-wide association study of suicide attempts in mood disorder patients

artículo científico publicado en 2010

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 association study reveals two new risk loci for bipolar disorder

artículo científico publicado en 2014

Genome-wide association-, replication-, and neuroimaging study implicates HOMER1 in the etiology of major depression

artículo científico publicado en 2010

Genome-wide mapping of genetic determinants influencing DNA methylation and gene expression in human hippocampus

artículo científico publicado en 2017

Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci

scientific journal article

Genome-wide scan for genes involved in bipolar affective disorder in 70 European families ascertained through a bipolar type I early-onset proband: supportive evidence for linkage at 3p14

artículo científico publicado en 2006

Genome-wide significant association between a 'negative mood delusions' dimension in bipolar disorder and genetic variation on chromosome 3q26.1.

artículo científico publicado en 2012

Genome-wide significant association between alcohol dependence and a variant in the ADH gene cluster

artículo científico publicado en 2011

Genome-wide study of association and interaction with maternal cytomegalovirus infection suggests new schizophrenia loci

artículo científico publicado en 2013

Genome-wide survey implicates the influence of copy number variants (CNVs) in the development of early-onset bipolar disorder

artículo científico publicado en 2011

Genomewide association studies: history, rationale, and prospects for psychiatric disorders

artículo científico publicado en 2009

Genomewide scan and fine-mapping linkage studies in four European samples with bipolar affective disorder suggest a new susceptibility locus on chromosome 1p35-p36 and provides further evidence of loci on chromosome 4q31 and 6q24.

artículo científico publicado en 2005

Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

article

Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

artículo científico publicado en 2017

Genotype-phenotype association mining in bipolar disorder: market research meets complex genetics

article

Genotype-phenotype studies in bipolar disorder showing association between the DAOA/G30 locus and persecutory delusions: a first step toward a molecular genetic classification of psychiatric phenotypes.

artículo científico publicado en 2005

Glutamate receptor δ 1 (GRID1) genetic variation and brain structure in schizophrenia

artículo científico publicado en 2012

Haplotype interaction analysis of unlinked regions.

artículo científico publicado en 2005

Hereditary Angioedema with Normal C1 Inhibitor and F12 Mutations in 42 Brazilian Families

artículo científico publicado en 2017

Hereditary angioedema with normal C1 inhibitor gene in a family with affected women and men is associated with the p.Thr328Lys mutation in the F12 gene

article

High frequencies of de novo CNVs in bipolar disorder and schizophrenia

artículo científico publicado en 2011

Hippocampal and frontolimbic function as intermediate phenotype for psychosis: evidence from healthy relatives and a common risk variant in CACNA1C.

artículo científico publicado en 2013

Hippocampal function in healthy carriers of the CLU Alzheimer's disease risk variant

artículo científico publicado en 2011

Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease

artículo científico publicado en 2012

Human metabotropic glutamate receptor 2 gene (GRM2): chromosomal sublocalization (3p21.1-p21.2) and genomic organization

artículo científico publicado en 2002

Hypotrichosis simplex of the scalp is associated with nonsense mutations in CDSN encoding corneodesmosin

artículo científico publicado en 2003

Identification of ADHD risk genes in extended pedigrees by combining linkage analysis and whole-exome sequencing

article

Identification of a Bipolar Disorder Vulnerable Gene CHDH at 3p21.1.

artículo científico publicado en 2016

Identification of common variants associated with human hippocampal and intracranial volumes

artículo científico publicado en 2012

Identification of increased genetic risk scores for schizophrenia in treatment-resistant patients

artículo científico publicado en 2014

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

artículo científico publicado en 2008

Identification of mutations in the human hairless gene in two new families with congenital atrichia

artículo científico publicado en 2007

Identification of pleiotropy at the gene level between psychiatric disorders and related traits

artículo científico publicado en 2021

Identification of rare variants in KCTD13 at the schizophrenia risk locus 16p11.2.

scientific article published on 23 September 2016

Identification of shared risk loci and pathways for bipolar disorder and schizophrenia

artículo científico publicado en 2017

Identification of two novel polymorphisms and a rare deletion variant in the human dopamine D4 receptor gene

scientific journal article

Identifying bipolar disorder susceptibility loci in a densely affected pedigree

artículo científico publicado en 2012

Imaging genetics of FOXP2 in dyslexia

artículo científico publicado en 2011

Imaging genetics of FOXP2 in dyslexia

artículo científico publicado en 2012

Impact of a cis-associated gene expression SNP on chromosome 20q11.22 on bipolar disorder susceptibility, hippocampal structure and cognitive performance

artículo científico publicado en 2015

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

artículo científico publicado en 2013

Increased activity of coagulation factor XII (Hageman factor) causes hereditary angioedema type III

artículo científico publicado en 2006

Increased genetic vulnerability to smoking at CHRNA5 in early-onset smokers

artículo científico publicado en 2012

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 age and cognitive performance on resting-state brain networks of older adults in a population-based cohort

artículo científico publicado en 2017

Integrated pathway-based approach identifies association between genomic regions at CTCF and CACNB2 and schizophrenia

artículo científico publicado en 2014

Integration of transcriptomic and cytoarchitectonic data implicates a role for MAOA and TAC1 in the limbic-cortical network.

artículo científico publicado en 2018

Interaction Testing and Polygenic Risk Scoring to Estimate the Association of Common Genetic Variants With Treatment Resistance in Schizophrenia

artículo científico publicado en 2022

Investigating polygenic burden in age at disease onset in bipolar disorder: Findings from an international multicentric study

Investigation of the human serotonin 6 (5HT6) receptor gene in bipolar affective disorder and schizophrenia

article

Investigation of the human serotonin 6 [5-HT6] receptor gene in bipolar affective disorder and schizophrenia

artículo científico publicado en 2000

Investigation of the involvement of MIR185 and its target genes in the development of schizophrenia

artículo científico publicado en 2014

Investigation of the role of TCF4 rare sequence variants in schizophrenia

artículo científico publicado en 2015

Investigation of the tryptophan hydroxylase 2 gene in bipolar I disorder in the Romanian population

artículo científico publicado en 2008

Involvement of the atrial natriuretic peptide transcription factor GATA4 in alcohol dependence, relapse risk and treatment response to acamprosate

artículo científico publicado en 2011

Is there a phenotypic difference between probands in case-control versus family-based association studies?

Key susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24.

artículo científico publicado en 2009

Lack of genetic association between the phospholipase A2 gene and bipolar mood disorder in a European multicentre case-control study.

artículo científico publicado en 2006

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

Large recurrent microdeletions associated with schizophrenia

artículo científico publicado en 2008

Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease

artículo científico publicado en 2011

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

artículo científico publicado en 2016

Levetiracetam resistance: Synaptic signatures & corresponding promoter SNPs in epileptic hippocampi

artículo científico publicado en 2013

Linkage-disequilibrium-based binning affects the interpretation of GWASs

artículo científico publicado en 2012

Linking single nucleotide polymorphisms

artículo científico publicado en 2002

Localization of a gene for syndactyly type 1 to chromosome 2q34-q36.

artículo científico publicado en 2000

Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis

artículo científico publicado en 2009

Mapping genomic loci implicates genes and synaptic biology in schizophrenia

artículo científico publicado en 2022

Marie Unna hereditary hypotrichosis: Identification of a U2HR mutation in the family from the original 1925 report

Mast cells increase vascular permeability by heparin-initiated bradykinin formation in vivo

artículo científico publicado en 2011

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

artículo científico publicado en 2011

Meta-analysis and brain imaging data support the involvement of VRK2 (rs2312147) in schizophrenia susceptibility

artículo científico publicado en 2012

Meta-analysis identifies seven susceptibility loci involved in the atopic march

artículo científico publicado en 2015

Meta-analysis of genome-wide association data identifies a risk locus for major mood disorders on 3p21.1.

artículo científico publicado en 2010

Meta-analysis of two genome-wide association studies of bipolar disorder reveals important points of agreement

artículo científico publicado en 2008

Metabotropic glutamate receptor 3 (GRM3) gene variation is not associated with schizophrenia or bipolar affective disorder in the German population

artículo científico publicado en 2002

MicroRNA hsa-miR-4717-5p regulates RGS2 and may be a risk factor for anxiety-related traits

artículo científico publicado en 2015

Microduplications of 16p11.2 are associated with schizophrenia

artículo científico publicado en 2009

Molecular genetic overlap in bipolar disorder, schizophrenia, and major depressive disorder

artículo científico publicado en 2012

Monoamine related functional gene variants and relationships to monoamine metabolite concentrations in CSF of healthy volunteers

artículo científico publicado en 2004

Mood-incongruent psychosis in bipolar disorder: conditional linkage analysis shows genome-wide suggestive linkage at 1q32.3, 7p13 and 20q13.31

article

Multi-ancestry genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitis

artículo científico publicado en 2015

Multiple independent loci at chromosome 15q25.1 affect smoking quantity: a meta-analysis and comparison with lung cancer and COPD.

artículo científico publicado en 2010

Neural mechanisms of a genome-wide supported psychosis variant

artículo científico publicado en 2009

Neuregulin 3 is associated with attention deficits in schizophrenia and bipolar disorder

artículo científico publicado en 2012

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

artículo científico publicado en 2015

New findings in the genetics of major psychoses

artículo científico publicado en 2010

No Reliable Association between Runs of Homozygosity and Schizophrenia in a Well-Powered Replication Study

artículo científico publicado en 2016

No association between a promoter dopamine D(4) receptor gene variant and schizophrenia.

artículo científico publicado en 2001

No association between genetic variants at the DGCR2 gene and schizophrenia in a German sample

article

No association between genetic variants at the GLYT2 gene and bipolar affective disorder and schizophrenia

artículo científico publicado en 2006

No association between genetic variants at the GRIN1 gene and bipolar disorder in a German sample.

artículo científico publicado en 2006

No association between the D-aspartate oxidase locus and schizophrenia

artículo científico publicado en 2009

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

artículo científico publicado en 2005

No association between the serine racemase gene (SRR) and bipolar disorder in a German case-control sample

artículo científico publicado en 2007

No association between the serine racemase gene (SRR) and schizophrenia in a German case-control sample.

artículo científico publicado en 2007

No evidence for DUP25 in patients with panic disorder using a quantitative real-time PCR approach.

artículo científico publicado en 2003

No evidence for an association between variants at the gamma-amino-n-butyric acid type A receptor beta2 locus and schizophrenia

artículo científico publicado en 2007

No evidence for an association between variants at the proline dehydrogenase locus and schizophrenia or bipolar affective disorder

artículo científico publicado en 2005

No evidence for an involvement of copy number variation in ABCA13 in schizophrenia, bipolar disorder, or major depressive disorder

artículo científico publicado en 2013

No evidence for association between NOTCH4 and schizophrenia in a large family-based and case???control association analysis

article

Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia

Novel genetic loci associated with hippocampal volume

scientific article published on 18 January 2017

Novel genetic loci underlying human intracranial volume identified through genome-wide association

artículo científico publicado en 2016

P.1.003 Multiple single nucleotide polymorphisms of schizophrenia-related DISC1 gene in lithium-treated patients with bipolar affective disorder

article

Polymorphic imprinting of the serotonin-2A (5-HT2A) receptor gene in human adult brain

artículo científico publicado en 1998

Polymorphism of Human Complement Component C6: An Amino Acid Substitution (GLU/ALA) within the Second Thrombospondin Repeat Differentiates between the Two Common Allotypes C6A and C6B

scientific article published on 01 July 1993

Polymorphisms in SREBF1 and SREBF2, two antipsychotic-activated transcription factors controlling cellular lipogenesis, are associated with schizophrenia in German and Scandinavian samples

artículo científico publicado en 2008

Possible association between genetic variants at the GRIN1 gene and schizophrenia with lifetime history of depressive symptoms in a German sample.

artículo científico publicado en 2007

Possible association of different G72/G30 SNPs with mood episodes and persecutory delusions in bipolar I Romanian patients

artículo científico publicado en 2010

Promoter variants determine γ-aminobutyric acid homeostasis-related gene transcription in human epileptic hippocampi.

artículo científico publicado en 2011

Psychiatric Genomics: An Update and an Agenda

artículo científico publicado en 2017

Psychiatric Genomics: An Update and an Agenda

RETRACTED: Identification of gene ontologies linked to prefrontal-hippocampal functional coupling in the human brain

artículo científico publicado en 2014

Reduced anxiety and depression-like behaviours in the circadian period mutant mouse afterhours

artículo científico publicado en 2012

Reduced cortical thickness is associated with the glutamatergic regulatory gene risk variant DAOA Arg30Lys in schizophrenia

artículo científico publicado en 2011

Replication of brain function effects of a genome-wide supported psychiatric risk variant in the CACNA1C gene and new multi-locus effects

artículo científico publicado en 2014

Replication of functional serotonin receptor type 3A and B variants in bipolar affective disorder: a European multicenter study

artículo científico publicado en 2012

Replication study and meta-analysis in European samples supports association of the 3p21.1 locus with bipolar disorder

artículo científico publicado en 2012

Reply

Reply to “Replication of association of 3p21.1 with susceptibility to bipolar disorder but not major depression”

Resequencing and follow-up of neurexin 1 (NRXN1) in schizophrenia patients

Retraction for Dixson et al., Identification of gene ontologies linked to prefrontal-hippocampal functional coupling in the human brain

artículo científico publicado en 2014

Rs6295 promoter variants of the serotonin type 1A receptor are differentially activated by c-Jun in vitro and correlate to transcript levels in human epileptic brain tissue.

artículo científico publicado en 2013

Segment-wise genome-wide association analysis identifies a candidate region associated with schizophrenia in three independent samples

artículo científico publicado en 2012

Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders

artículo científico publicado en 2022

Shared genetic etiology between alcohol dependence and major depressive disorder.

artículo científico publicado en 2018

Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studies

artículo científico publicado en 2020

Single nucleotide variation analysis in 65 candidate genes for CNS disorders in a representative sample of the European population

artículo científico publicado en 2003

Smoking behaviour: investigation of the coaction of environmental and genetic risk factors

artículo científico publicado en 2014

Strauch et al reply

artículo científico publicado en 2000

Striatal response to reward anticipation: evidence for a systems-level intermediate phenotype for schizophrenia

artículo científico publicado en 2014

Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia

artículo científico publicado en 2005

Studies in humans and mice implicate neurocan in the etiology of mania

artículo científico publicado en 2012

Studying variability in human brain aging in a population-based German cohort—rationale and design of 1000BRAINS

artículo científico publicado en 2014

Supporting evidence for LRRTM1 imprinting effects in schizophrenia.

artículo científico publicado en 2009

Susceptibility variants for male-pattern baldness on chromosome 20p11.

artículo científico publicado en 2008

Systematic Integration of Brain eQTL and GWAS Identifies ZNF323 as a Novel Schizophrenia Risk Gene and Suggests Recent Positive Selection Based on Compensatory Advantage on Pulmonary Function

artículo científico publicado en 2015

Systematic analysis of glutamatergic neurotransmission genes in alcohol dependence and adolescent risky drinking behavior

artículo científico publicado en 2008

Systematic screening for DNA sequence variation in the coding region of the human dopamine transporter gene (DAT1)

artículo científico publicado en 2000

Systematic screening for mutations in the 5′-regulatory region of the human dopamine D1 receptor (DRD1) gene in patients with schizophrenia and bipolar affective disorder

article

Systematic screening for mutations in the human N-methyl-D-aspartate receptor 1 gene in schizophrenic patients from the German population

artículo científico publicado en 2004

Systematic screening for mutations in the promoter and the coding region of the 5-HT1A gene

article

TLR4, ATF-3 and IL8 inflammation mediator expression correlates with seizure frequency in human epileptic brain tissue

artículo científico publicado en 2013

TMEM132D, a new candidate for anxiety phenotypes: evidence from human and mouse studies

artículo científico publicado en 2010

The DISC locus and schizophrenia: evidence from an association study in a central European sample and from a meta-analysis across different European populations

artículo científico publicado en 2009

The DTNBP1 (dysbindin) gene contributes to schizophrenia, depending on family history of the disease

artículo científico publicado en 2003

The G72/G30 gene locus in psychiatric disorders: a challenge to diagnostic boundaries?

artículo científico publicado en 2006

The International Consortium on Lithium Genetics (ConLiGen): an initiative by the NIMH and IGSLI to study the genetic basis of response to lithium treatment

artículo científico publicado en 2010

The KMO allele encoding Arg452 is associated with psychotic features in bipolar disorder type 1, and with increased CSF KYNA level and reduced KMO expression

artículo científico publicado en 2013

The catechol-O-methyl transferase (COMT) gene and its potential association with schizophrenia: findings from a large German case-control and family-based sample

artículo científico publicado en 2010

The complement control-related genes CSMD1 and CSMD2 associate to schizophrenia

artículo científico publicado en 2011

The first genomewide interaction and locus-heterogeneity linkage scan in bipolar affective disorder: strong evidence of epistatic effects between loci on chromosomes 2q and 6q.

artículo científico publicado en 2007

The genetic architecture of the human cerebral cortex

The genetic architecture of the human cerebral cortex

artículo científico publicado en 2020

The hairless gene in androgenetic alopecia: results of a systematic mutation screening and a family-based association approach

scientific article (publication date: April 2002)

The neuronal transporter gene SLC6A15 confers risk to major depression

artículo científico publicado en 2011

The opioid peptides enkephalin and beta-endorphin in alcohol dependence

artículo científico publicado en 2008

The protocadherin 17 gene affects cognition, personality, amygdala structure and function, synapse development and risk of major mood disorders

artículo científico publicado en 2017

Trans-ancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders

scholarly article published 10 March 2018

Transancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders

artículo científico publicado en 2018

Two variants in Ankyrin 3 (ANK3) are independent genetic risk factors for bipolar disorder

artículo científico publicado en 2009

VEGF Gene Haplotypes Are Associated With Sarcoidosis

article

Variant 1859G-->A (Arg620Gln) of the "hairless" gene: absence of association with papular atrichia or androgenic alopecia

artículo científico publicado en 2001

Volition diminishes genetically mediated amygdala hyperreactivity

artículo científico publicado en 2009

Whole-exome sequencing of 81 individuals from 27 multiply affected bipolar disorder families

scientific article published on 04 February 2020

XRCC5 as a risk gene for alcohol dependence: evidence from a genome-wide gene-set-based analysis and follow-up studies in Drosophila and humans

artículo científico publicado en 2014

ZNF804A and cortical structure in schizophrenia: in vivo and postmortem studies

artículo científico publicado en 2013

ZNF804A genetic variation (rs1344706) affects brain grey but not white matter in schizophrenia and healthy subjects

artículo científico publicado en 2014

αCaMKII autophosphorylation controls the establishment of alcohol drinking behavior

artículo científico publicado en 2013

“Association study of a functional promoter polymorphism in theXBP1 gene and schizophrenia,” American Journal Of Medical Genetics Part B (Neuropsychiatric Genetics) 141B:71–75 (2006)

article

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