Lista de obras - Elliott Rees - Dominio Público Uruguay

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

artículo científico publicado en 2012

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 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

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

artículo científico publicado en 2015

Associations Between Schizophrenia Polygenic Liability, Symptom Dimensions, and Cognitive Ability in Schizophrenia

artículo científico publicado en 2021

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

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

artículo científico publicado en 2016

Common alleles contribute to schizophrenia in CNV carriers.

artículo científico publicado en 2015

Copy number variation in bipolar disorder

artículo científico publicado en 2015

Copy number variation in schizophrenia in Sweden

artículo científico publicado en 2014

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 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

Erratum: Common alleles contribute to schizophrenia in CNV carriers

scholarly article published in Molecular Psychiatry

Evidence that duplications of 22q11.2 protect against schizophrenia

artículo científico publicado en 2013

Exome arrays capture polygenic rare variant contributions to schizophrenia.

artículo científico publicado en 2016

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

artículo científico publicado en 2016

Genetic disruption of voltage-gated calcium channels in psychiatric and neurological disorders

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

artículo científico publicado en 2017

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

artículo científico publicado en 2016

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

artículo científico publicado en 2013

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

artículo científico publicado en 2015

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

artículo científico publicado en 2015

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

artículo científico publicado en 2016

Pathogenic copy number variants and SCN1A mutations in patients with intellectual disability and childhood-onset epilepsy

artículo científico publicado en 2016

Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome

artículo científico publicado en 2017

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

artículo científico publicado en 2016

Schizophrenia copy number variants and associative learning

artículo científico publicado en 2016

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

artículo científico publicado en 2017

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

artículo científico publicado en 2013

Lista de obras de Elliott Rees

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

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

Analysis of Intellectual Disability Copy Number Variants for Association With Schizophrenia

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

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

Associations Between Schizophrenia Polygenic Liability, Symptom Dimensions, and Cognitive Ability in Schizophrenia

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

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

Common alleles contribute to schizophrenia in CNV carriers.

Copy number variation in bipolar disorder

Copy number variation in schizophrenia in Sweden

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

De novo CNVs in bipolar affective disorder and schizophrenia

De novo mutation in schizophrenia

De novo mutations in schizophrenia implicate synaptic networks

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

Erratum: Common alleles contribute to schizophrenia in CNV carriers

Evidence that duplications of 22q11.2 protect against schizophrenia

Exome arrays capture polygenic rare variant contributions to schizophrenia.

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

Genetic disruption of voltage-gated calcium channels in psychiatric and neurological disorders

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

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

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

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

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

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

Pathogenic copy number variants and SCN1A mutations in patients with intellectual disability and childhood-onset epilepsy

Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome

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

Schizophrenia copy number variants and associative learning

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

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