about
Novel autism subtype-dependent genetic variants are revealed by quantitative trait and subphenotype association analyses of published GWAS dataDirect measure of the de novo mutation rate in autism and schizophrenia cohortsDe novo mutations in the gene encoding the synaptic scaffolding protein SHANK3 in patients ascertained for schizophrenia.Microduplications of 16p11.2 are associated with schizophreniaAutism spectrum disorders and childhood-onset schizophrenia: clinical and biological contributions to a relation revisitedConvergence of advances in genomics, team science, and repositories as drivers of progress in psychiatric genomicsRare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophreniaLongitudinally mapping the influence of sex and androgen signaling on the dynamics of human cortical maturation in adolescence.A novel frameshift mutation in UPF3B identified in brothers affected with childhood onset schizophrenia and autism spectrum disorders.Association of the dopamine receptor D4 (DRD4) gene 7-repeat allele with children with attention-deficit/hyperactivity disorder (ADHD): an update.Transcriptome profiling of UPF3B/NMD-deficient lymphoblastoid cells from patients with various forms of intellectual disability.Sex chromosome anomalies in childhood onset schizophrenia: an update.Catechol-o-methyl transferase (COMT) val158met polymorphism and adolescent cortical development in patients with childhood-onset schizophrenia, their non-psychotic siblings, and healthy controls.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.Annual research review: impact of advances in genetics in understanding developmental psychopathology.Sequencing and analyzing the t(1;7) reciprocal translocation breakpoints associated with a case of childhood-onset schizophrenia/autistic disorder.Segmental uniparental isodisomy on 5q32-qter in a patient with childhood-onset schizophrenia.GAD1 (2q31.1), which encodes glutamic acid decarboxylase (GAD67), is associated with childhood-onset schizophrenia and cortical gray matter volume loss.Support for association between ADHD and two candidate genes: NET1 and DRD1.Whole genome sequencing in psychiatric disorders: the WGSPD consortium.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.Polymorphisms in the 13q33.2 gene G72/G30 are associated with childhood-onset schizophrenia and psychosis not otherwise specified.Neuregulin 1 (8p12) and childhood-onset schizophrenia: susceptibility haplotypes for diagnosis and brain developmental trajectories.Sleep disturbances in childhood-onset schizophrenia.Dysbindin (DTNBP1, 6p22.3) is associated with childhood-onset psychosis and endophenotypes measured by the Premorbid Adjustment Scale (PAS).Pervasive developmental disorder and childhood-onset schizophrenia: comorbid disorder or a phenotypic variant of a very early onset illness?Polymorphisms of the dopamine D4 receptor, clinical outcome, and cortical structure in attention-deficit/hyperactivity disorder.Epidemiology of unexplained fatigue and major depression in the community: the Baltimore ECA follow-up, 1981-1994.Publisher Correction: Whole genome sequencing in psychiatric disorders: the WGSPD consortium.The Open Translational Science in Schizophrenia (OPTICS) project: an open-science project bringing together Janssen clinical trial and NIMH data.Molecular genetic studies of ADHD: 1991 to 2004Genome-wide scan of bipolar disorder in 65 pedigrees: supportive evidence for linkage at 8q24, 18q22, 4q32, 2p12, and 13q1222q11 deletion syndrome in childhood onset schizophrenia: an updateThe identification of OCD-related subgroups based on comorbidity
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P50
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wetenschapper
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հետազոտող
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Anjene M. Addington
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Anjene M. Addington
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Anjene M. Addington
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Anjene M. Addington
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Anjene M. Addington
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Anjene M. Addington
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Anjene M. Addington
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Anjene M. Addington
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Anjene M. Addington
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Anjene M. Addington
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Anjene M. Addington
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Anjene M. Addington
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P106
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6603020927
P31
P496
0000-0001-7770-299X