Lista de obras -

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

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

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

artículo científico publicado en 2016

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

article

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

artículo científico publicado en 2013

Genome-wide association study of multiplex schizophrenia pedigrees.

artículo científico publicado en 2012

Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

artículo científico publicado en 2017

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

scientific article published on 23 September 2016

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

artículo científico publicado en 2022

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

article

Investigation of the human serotonin receptor gene HTR3B in bipolar affective and schizophrenic patients

artículo científico publicado en 2004

Mapping genomic loci implicates genes and synaptic biology in schizophrenia

artículo científico publicado en 2022

Neurocognitive functioning in patients with first-episode schizophrenia: results of a prospective 15-year follow-up study

scientific article published on 18 June 2019

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

artículo científico publicado en 2002

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 serotonin 1F receptor gene in patients with bipolar affective disorder and schizophrenia

article

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

article

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

scientific article published on 04 February 2020

Lista de obras de

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

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

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

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

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

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

Genome-wide association study of multiplex schizophrenia pedigrees.

Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

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

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

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

Investigation of the human serotonin receptor gene HTR3B in bipolar affective and schizophrenic patients

Mapping genomic loci implicates genes and synaptic biology in schizophrenia

Neurocognitive functioning in patients with first-episode schizophrenia: results of a prospective 15-year follow-up study

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

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

Systematic screening for mutations in the human serotonin 1F receptor gene in patients with bipolar affective disorder and schizophrenia

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

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