Lista de obras -

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

artículo científico publicado en 2012

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

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

artículo científico publicado en 2012

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

Copy number variants in German patients with schizophrenia

artículo científico publicado en 2013

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

article

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

artículo científico publicado en 2009

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

artículo científico publicado en 2012

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

artículo científico publicado en 2013

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 study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder

artículo científico publicado en 2011

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

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

article

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

artículo científico publicado en 2013

Longer telomere length in patients with schizophrenia

artículo científico publicado en 2013

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

artículo científico publicado en 2010

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

artículo científico publicado en 2012

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

artículo científico publicado en 2012

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

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

artículo científico publicado en 2012

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

artículo científico publicado en 2012

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

Lista de obras de

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

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

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

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

Common variants at VRK2 and TCF4 conferring risk of schizophrenia

Common variants conferring risk of schizophrenia

Copy number variants in German patients with schizophrenia

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

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

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

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

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

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

Genome-wide association study reveals two new risk loci for bipolar disorder

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

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

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

Longer telomere length in patients with schizophrenia

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

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

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

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

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

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

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

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