Lista de obras - Anjene M. Addington - Dominio Público Uruguay

22q11 deletion syndrome in childhood onset schizophrenia: an update

scientific article published on 01 March 2004

A novel frameshift mutation in UPF3B identified in brothers affected with childhood onset schizophrenia and autism spectrum disorders.

artículo científico publicado en 2010

Annual research review: impact of advances in genetics in understanding developmental psychopathology.

artículo científico publicado en 2011

Association of the dopamine receptor D4 (DRD4) gene 7-repeat allele with children with attention-deficit/hyperactivity disorder (ADHD): an update

artículo científico publicado en 2007

Autism spectrum disorders and childhood-onset schizophrenia: clinical and biological contributions to a relation revisited

artículo científico publicado en 2009

Catechol-o-methyl transferase (COMT) val158met polymorphism and adolescent cortical development in patients with childhood-onset schizophrenia, their non-psychotic siblings, and healthy controls.

artículo científico publicado en 2011

Convergence of advances in genomics, team science, and repositories as drivers of progress in psychiatric genomics

artículo científico publicado en 2015

De novo mutations in the gene encoding the synaptic scaffolding protein SHANK3 in patients ascertained for schizophrenia

artículo científico publicado en 2010

Direct measure of the de novo mutation rate in autism and schizophrenia cohorts

artículo científico publicado en 2010

Dysbindin (DTNBP1, 6p22.3) is associated with childhood-onset psychosis and endophenotypes measured by the Premorbid Adjustment Scale (PAS).

artículo científico publicado en 2005

Epidemiology of unexplained fatigue and major depression in the community: the Baltimore ECA follow-up, 1981-1994.

artículo científico publicado en 2001

GAD1 (2q31.1), which encodes glutamic acid decarboxylase (GAD67), is associated with childhood-onset schizophrenia and cortical gray matter volume loss

artículo científico publicado en 2005

Genome-wide scan of bipolar disorder in 65 pedigrees: supportive evidence for linkage at 8q24, 18q22, 4q32, 2p12, and 13q12

article

Longitudinally mapping the influence of sex and androgen signaling on the dynamics of human cortical maturation in adolescence

artículo científico publicado en 2010

Microduplications of 16p11.2 are associated with schizophrenia

artículo científico publicado en 2009

Molecular genetic studies of ADHD: 1991 to 2004

Mutations in SYNGAP1 in autosomal nonsyndromic mental retardation

artículo científico publicado en 2009

Neuregulin 1 (8p12) and childhood-onset schizophrenia: susceptibility haplotypes for diagnosis and brain developmental trajectories.

artículo científico publicado en 2006

Novel autism subtype-dependent genetic variants are revealed by quantitative trait and subphenotype association analyses of published GWAS data

artículo científico publicado en 2011

Pervasive developmental disorder and childhood-onset schizophrenia: comorbid disorder or a phenotypic variant of a very early onset illness?

artículo científico publicado en 2004

Polymorphisms in the 13q33.2 gene G72/G30 are associated with childhood-onset schizophrenia and psychosis not otherwise specified

artículo científico publicado en 2004

Polymorphisms of the dopamine D4 receptor, clinical outcome, and cortical structure in attention-deficit/hyperactivity disorder.

artículo científico publicado en 2007

Publisher Correction: Whole genome sequencing in psychiatric disorders: the WGSPD consortium.

artículo científico publicado en 2018

Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia

artículo científico publicado en 2008

Segmental uniparental isodisomy on 5q32-qter in a patient with childhood-onset schizophrenia

artículo científico publicado en 2006

Sequencing and analyzing the t(1;7) reciprocal translocation breakpoints associated with a case of childhood-onset schizophrenia/autistic disorder

artículo científico publicado en 2007

Sex chromosome anomalies in childhood onset schizophrenia: an update.

artículo científico publicado en 2008

Sleep disturbances in childhood-onset schizophrenia

artículo científico publicado en 2006

Support for association between ADHD and two candidate genes: NET1 and DRD1.

artículo científico publicado en 2005

Systematic resequencing of X-chromosome synaptic genes in autism spectrum disorder and schizophrenia.

artículo científico publicado en 2010

The Influence of Microdeletions and Microduplications of 16p11.2 on Global Transcription Profiles.

artículo científico publicado en 2015

The Open Translational Science in Schizophrenia (OPTICS) project: an open-science project bringing together Janssen clinical trial and NIMH data.

artículo científico publicado en 2018

The identification of OCD-related subgroups based on comorbidity

artículo científico publicado en 2003

The influence of uridine diphosphate glucuronosyl transferase 1A promoter polymorphisms, beta-globin gene haplotype, co-inherited alpha-thalassemia trait and Hb F on steady-state serum bilirubin levels in sickle cell anemia

artículo científico publicado en 2005

Transcriptome profiling of UPF3B/NMD-deficient lymphoblastoid cells from patients with various forms of intellectual disability.

artículo científico publicado en 2011

Whole genome sequencing in psychiatric disorders: the WGSPD consortium.

artículo científico publicado en 2017

Lista de obras de Anjene M. Addington

22q11 deletion syndrome in childhood onset schizophrenia: an update

A novel frameshift mutation in UPF3B identified in brothers affected with childhood onset schizophrenia and autism spectrum disorders.

Annual research review: impact of advances in genetics in understanding developmental psychopathology.

Association of the dopamine receptor D4 (DRD4) gene 7-repeat allele with children with attention-deficit/hyperactivity disorder (ADHD): an update

Autism spectrum disorders and childhood-onset schizophrenia: clinical and biological contributions to a relation revisited

Catechol-o-methyl transferase (COMT) val158met polymorphism and adolescent cortical development in patients with childhood-onset schizophrenia, their non-psychotic siblings, and healthy controls.

Convergence of advances in genomics, team science, and repositories as drivers of progress in psychiatric genomics

De novo mutations in the gene encoding the synaptic scaffolding protein SHANK3 in patients ascertained for schizophrenia

Direct measure of the de novo mutation rate in autism and schizophrenia cohorts

Dysbindin (DTNBP1, 6p22.3) is associated with childhood-onset psychosis and endophenotypes measured by the Premorbid Adjustment Scale (PAS).

Epidemiology of unexplained fatigue and major depression in the community: the Baltimore ECA follow-up, 1981-1994.

GAD1 (2q31.1), which encodes glutamic acid decarboxylase (GAD67), is associated with childhood-onset schizophrenia and cortical gray matter volume loss

Genome-wide scan of bipolar disorder in 65 pedigrees: supportive evidence for linkage at 8q24, 18q22, 4q32, 2p12, and 13q12

Longitudinally mapping the influence of sex and androgen signaling on the dynamics of human cortical maturation in adolescence

Microduplications of 16p11.2 are associated with schizophrenia

Molecular genetic studies of ADHD: 1991 to 2004

Mutations in SYNGAP1 in autosomal nonsyndromic mental retardation

Neuregulin 1 (8p12) and childhood-onset schizophrenia: susceptibility haplotypes for diagnosis and brain developmental trajectories.

Novel autism subtype-dependent genetic variants are revealed by quantitative trait and subphenotype association analyses of published GWAS data

Pervasive developmental disorder and childhood-onset schizophrenia: comorbid disorder or a phenotypic variant of a very early onset illness?

Polymorphisms in the 13q33.2 gene G72/G30 are associated with childhood-onset schizophrenia and psychosis not otherwise specified

Polymorphisms of the dopamine D4 receptor, clinical outcome, and cortical structure in attention-deficit/hyperactivity disorder.

Publisher Correction: Whole genome sequencing in psychiatric disorders: the WGSPD consortium.

Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia

Segmental uniparental isodisomy on 5q32-qter in a patient with childhood-onset schizophrenia

Sequencing and analyzing the t(1;7) reciprocal translocation breakpoints associated with a case of childhood-onset schizophrenia/autistic disorder

Sex chromosome anomalies in childhood onset schizophrenia: an update.

Sleep disturbances in childhood-onset schizophrenia

Support for association between ADHD and two candidate genes: NET1 and DRD1.

Systematic resequencing of X-chromosome synaptic genes in autism spectrum disorder and schizophrenia.

The Influence of Microdeletions and Microduplications of 16p11.2 on Global Transcription Profiles.

The Open Translational Science in Schizophrenia (OPTICS) project: an open-science project bringing together Janssen clinical trial and NIMH data.

The identification of OCD-related subgroups based on comorbidity

The influence of uridine diphosphate glucuronosyl transferase 1A promoter polymorphisms, beta-globin gene haplotype, co-inherited alpha-thalassemia trait and Hb F on steady-state serum bilirubin levels in sickle cell anemia

Transcriptome profiling of UPF3B/NMD-deficient lymphoblastoid cells from patients with various forms of intellectual disability.

Whole genome sequencing in psychiatric disorders: the WGSPD consortium.