Overlapping 16p13.11 deletion and gain of copies variations associated with childhood onset psychosis include genes with mechanistic implications for autism associated pathways: Two case reports

Exome sequencing and genome-wide copy number variant mapping reveal novel associations with sensorineural hereditary hearing loss

(2015) Rajini R Haraksingh et al.   BMC GENOMICS

Distal Xq28 microdeletions: Clarification of the spectrum of contiguous gene deletions involvingABCD1,BCAP31, andSLC6A8with a new case and review of the literature

(2014) Amy R.U.L. Calhoun et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

ANK3 gene expression in bipolar disorder and schizophrenia

(2014) Katrine Verena Wirgenes et al.   BRITISH JOURNAL OF PSYCHIATRY

TPH2 gene polymorphisms in the regulatory region are associated with paranoid schizophrenia in Northern Han Chinese

(2014) X.M. Xu et al.   GENETICS AND MOLECULAR RESEARCH

Relationship between genetic polymorphisms in the DRD5 gene and paranoid schizophrenia in northern Han Chinese

(2014) Y. Zhao et al.   GENETICS AND MOLECULAR RESEARCH

Sequencing and expression analyses of the synaptic lipid raft adapter gene PAG1 in schizophrenia

(2014) Shabeesh Balan et al.   JOURNAL OF NEURAL TRANSMISSION

Pleiotropic genes for metabolic syndrome and inflammation

(2014) Aldi T. Kraja et al.   MOLECULAR GENETICS AND METABOLISM

De novo mutations in schizophrenia implicate chromatin remodeling and support a genetic overlap with autism and intellectual disability

(2014) S E McCarthy et al.   MOLECULAR PSYCHIATRY

Copy number variation in schizophrenia in Sweden

(2014) J P Szatkiewicz et al.   MOLECULAR PSYCHIATRY

Genetic pleiotropy between multiple sclerosis and schizophrenia but not bipolar disorder: differential involvement of immune-related gene loci

(2014) O A Andreassen et al.   MOLECULAR PSYCHIATRY

The Neurology of mTOR

(2014) Jonathan O. Lipton et al.   NEURON

The expression and roles of Nde1 and Ndel1 in the adult mammalian central nervous system

(2014) Z. Pei et al.   NEUROSCIENCE

A competitive PCR assay confirms the association of a copy number variation in the VIPR2 gene with schizophrenia in Han Chinese

(2014) Jianmin Yuan et al.   SCHIZOPHRENIA RESEARCH

Resequencing and association study of the NFKB activating protein-like gene (NKAPL) in schizophrenia

(2014) Shih-Fen Chen et al.   SCHIZOPHRENIA RESEARCH

DNA hypermethylation of serotonin transporter gene promoter in drug naïve patients with schizophrenia

(2014) Hamid Mostafavi Abdolmaleky et al.   SCHIZOPHRENIA RESEARCH

Genomic insights into the overlap between psychiatric disorders: implications for research and clinical practice

(2014) Joanne L Doherty et al.   Genome Medicine

Ubiquitin-proteasome dependent degradation of GABAAα1 in autism spectrum disorder

(2014) Amanda Crider et al.   Molecular Autism

Transcriptional targets of the schizophrenia risk gene MIR137

(2014) A L Collins et al.   Translational Psychiatry

Mutations in BCAP31 Cause a Severe X-Linked Phenotype with Deafness, Dystonia, and Central Hypomyelination and Disorganize the Golgi Apparatus

(2013) Pierre Cacciagli et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Analysis of copy number variations at 15 schizophrenia-associated loci

(2013) Elliott Rees et al.   BRITISH JOURNAL OF PSYCHIATRY

Efficient Strategy for Detecting Gene × Gene Joint Action and Its Application in Schizophrenia

(2013) Sungho Won et al.   GENETIC EPIDEMIOLOGY

The ubiquitin–proteasome system as a critical regulator of synaptic plasticity and long-term memory formation

(2013) Timothy J. Jarome et al.   NEUROBIOLOGY OF LEARNING AND MEMORY

Dysfunction of the Ubiquitin Proteasome and Ubiquitin-Like Systems in Schizophrenia

(2013) María D Rubio et al.   NEUROPSYCHOPHARMACOLOGY

Male-Biased Autosomal Effect of 16p13.11 Copy Number Variation in Neurodevelopmental Disorders

(2013) Maria Tropeano et al.   PLoS One

Chronic Exposure of Mutant DISC1 Mice to Lead Produces Sex-Dependent Abnormalities Consistent With Schizophrenia and Related Mental Disorders: A Gene-Environment Interaction Study

(2013) Bagrat Abazyan et al.   SCHIZOPHRENIA BULLETIN

Evidence of allelic imbalance in the schizophrenia susceptibility gene ZNF804A in human dorsolateral prefrontal cortex

(2013) Ilaria Guella et al.   SCHIZOPHRENIA RESEARCH

Activity-Dependent Growth of New Dendritic Spines Is Regulated by the Proteasome

(2012) Andrew M. Hamilton et al.   NEURON

Copy number variations in neurodevelopmental disorders

(2012) Hannah M. Grayton et al.   PROGRESS IN NEUROBIOLOGY

Expression and Biochemical Characterization of the Human Enzyme N-Terminal Asparagine Amidohydrolase

(2011) Jason R. Cantor et al.   BIOCHEMISTRY

16p13.11 duplication is a risk factor for a wide spectrum of neuropsychiatric disorders

(2011) Arivudainambi Ramalingam et al.   JOURNAL OF HUMAN GENETICS

Rare Deletions at 16p13.11 Predispose to a Diverse Spectrum of Sporadic Epilepsy Syndromes

(2010) Erin L. Heinzen et al.   AMERICAN JOURNAL OF HUMAN GENETICS

LIS1 and NudE Induce a Persistent Dynein Force-Producing State

(2010) Richard J. McKenney et al.   CELL

Phenotypic manifestations of copy number variation in chromosome 16p13.11

(2010) Sandesh C Sreenath Nagamani et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Behavioural phenotyping assays for mouse models of autism

(2010) Jill L. Silverman et al.   NATURE REVIEWS NEUROSCIENCE

Copy number variations of chromosome 16p13.1 region associated with schizophrenia

(2009) A Ingason et al.   MOLECULAR PSYCHIATRY

Microduplications of 16p11.2 are associated with schizophrenia

(2009) Shane E McCarthy et al.   NATURE GENETICS

DISC1, PDE4B, and NDE1 at the centrosome and synapse

(2008) Nicholas J. Bradshaw et al.   BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS

Ndel1 Controls the Dynein-mediated Transport of Vimentin during Neurite Outgrowth

(2008) Su Yeon Shim et al.   JOURNAL OF BIOLOGICAL CHEMISTRY