Lista de obras - Sophie E Legge - Dominio Público Uruguay

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

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 retrospective study of intramuscular clozapine prescription for treatment initiation and maintenance in treatment-resistant psychosis

scientific article published on 01 July 2020

Analysis of Intellectual Disability Copy Number Variants for Association With Schizophrenia

artículo científico publicado en 2016

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

artículo científico publicado en 2013

Antipsychotic polypharmacy and augmentation strategies prior to clozapine initiation: a historical cohort study of 310 adults with treatment-resistant schizophrenic disorders

artículo científico publicado en 2016

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

Clinical indicators of treatment-resistant psychosis

artículo científico publicado en 2019

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

artículo científico publicado en 2018

Common schizophrenia alleles are enriched in mutation-intolerant genes and maintained by background selection

article

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

artículo científico publicado en 2016

Effects of genomic copy number variants penetrant for schizophrenia on cortical thickness and surface area in healthy individuals: analysis of the UK Biobank

artículo científico publicado en 2020

Evidence that duplications of 22q11.2 protect against schizophrenia

artículo científico publicado en 2013

Examining cognition across the bipolar/schizophrenia diagnostic spectrum

artículo científico publicado en 2018

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

artículo científico publicado en 2016

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

artículo científico publicado en 2016

Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

article

Impact of schizophrenia genetic liability on the association between schizophrenia and physical illness: data-linkage study

artículo científico publicado en 2020

Missed opportunities: mental disorder in children of parents with depression

artículo científico publicado en 2012

Polygenic risk for schizophrenia and subcortical brain anatomy in the UK Biobank cohort

scientific article published on 09 September 2020

Predictors of Nonhospitalization and Functional Response in Clozapine Treatment: A Nationwide, Population-Based Cohort Study.

artículo científico publicado en 2017

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

artículo científico publicado en 2019

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

artículo científico publicado en 2016

The Duffy-null genotype and risk of infection

artículo científico publicado en 2020

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

artículo científico publicado en 2013

Lista de obras de Sophie E Legge

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

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

A retrospective study of intramuscular clozapine prescription for treatment initiation and maintenance in treatment-resistant psychosis

Analysis of Intellectual Disability Copy Number Variants for Association With Schizophrenia

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

Antipsychotic polypharmacy and augmentation strategies prior to clozapine initiation: a historical cohort study of 310 adults with treatment-resistant schizophrenic disorders

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

Clinical indicators of treatment-resistant psychosis

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

Common schizophrenia alleles are enriched in mutation-intolerant genes and maintained by background selection

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

Effects of genomic copy number variants penetrant for schizophrenia on cortical thickness and surface area in healthy individuals: analysis of the UK Biobank

Evidence that duplications of 22q11.2 protect against schizophrenia

Examining cognition across the bipolar/schizophrenia diagnostic spectrum

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

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

Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

Impact of schizophrenia genetic liability on the association between schizophrenia and physical illness: data-linkage study

Missed opportunities: mental disorder in children of parents with depression

Polygenic risk for schizophrenia and subcortical brain anatomy in the UK Biobank cohort

Predictors of Nonhospitalization and Functional Response in Clozapine Treatment: A Nationwide, Population-Based Cohort Study.

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

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

The Duffy-null genotype and risk of infection

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