TSHZ3 deletion causes an autism syndrome and defects in cortical projection neurons

Metabolic, synaptic and behavioral impact of 5-week chronic deep brain stimulation in hemiparkinsonian rats

(2015) Carine Chassain et al.   JOURNAL OF NEUROCHEMISTRY

PANTHER version 10: expanded protein families and functions, and analysis tools

(2015) Huaiyu Mi et al.   NUCLEIC ACIDS RESEARCH

Satb2 Regulates the Differentiation of Both Callosal and Subcerebral Projection Neurons in the Developing Cerebral Cortex

(2014) Dino P. Leone et al.   CEREBRAL CORTEX

Behavioral Abnormalities and Circuit Defects in the Basal Ganglia of a Mouse Model of 16p11.2 Deletion Syndrome

(2014) Thomas Portmann et al.   Cell Reports

19q13.11 microdeletion concomitant with ins(2;19)(p25.3;q13.1q13.4)dn in a boy: potential role of UBA2 in the associated phenotype

(2014) Carlos Venegas-Vega et al.   Molecular Cytogenetics

Phenotypic and molecular characterization of 19q12q13.1 deletions: A report of five patients

(2013) Shimul Chowdhury et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Coexpression Networks Implicate Human Midfetal Deep Cortical Projection Neurons in the Pathogenesis of Autism

(2013) A. Jeremy Willsey et al.   CELL

Integrative Functional Genomic Analyses Implicate Specific Molecular Pathways and Circuits in Autism

(2013) Neelroop N. Parikshak et al.   CELL

Functional and structural connectivity of frontostriatal circuitry in Autism Spectrum Disorder

(2013) Sonja Delmonte et al.   Frontiers in Human Neuroscience

Deletions in 16q24.2 are associated with autism spectrum disorder, intellectual disability and congenital renal malformation

(2013) Gregory Ryan Handrigan et al.   JOURNAL OF MEDICAL GENETICS

Teashirt 3 Regulates Development of Neurons Involved in Both Respiratory Rhythm and Airflow Control

(2013) X. Caubit et al.   JOURNAL OF NEUROSCIENCE

Modeling Transformations of Neurodevelopmental Sequences across Mammalian Species

(2013) A. D. Workman et al.   JOURNAL OF NEUROSCIENCE

Autism

(2013) Meng-Chuan Lai et al.   LANCET

Corticostriatal connectivity and its role in disease

(2013) Gordon M. G. Shepherd   NATURE REVIEWS NEUROSCIENCE

Expression profiling of mouse subplate reveals a dynamic gene network and disease association with autism and schizophrenia

(2013) Anna Hoerder-Suabedissen et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

TopHat2: accurate alignment of transcriptomes in the presence of insertions, deletions and gene fusions

(2013) Daehwan Kim et al.   GENOME BIOLOGY

Complex autism spectrum disorder in a patient with a 17q12 microduplication

(2012) Tracy Brandt et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Anatomic and Molecular Development of Corticostriatal Projection Neurons in Mice

(2012) U. Shivraj Sohur et al.   CEREBRAL CORTEX

Transcriptional co-regulation of neuronal migration and laminar identity in the neocortex

(2012) K. Y. Kwan et al.   DEVELOPMENT

19q13.11 cryptic deletion: description of two new cases and indication for a role of WTIP haploinsufficiency in hypospadias

(2012) Simone Gana et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

19q13 microdeletion syndrome: Further refining the critical region

(2012) Francesca Forzano et al.   European Journal of Medical Genetics

Fast gapped-read alignment with Bowtie 2

(2012) Ben Langmead et al.   NATURE METHODS

The Autism Sequencing Consortium: Large-Scale, High-Throughput Sequencing in Autism Spectrum Disorders

(2012) Joseph D. Buxbaum et al.   NEURON

Autism-like socio-communicative deficits and stereotypies in mice lacking heparan sulfate

(2012) F. Irie et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

The Emerging Biology of Autism Spectrum Disorders

(2012) M. W. State et al.   SCIENCE

Multiplex Targeted Sequencing Identifies Recurrently Mutated Genes in Autism Spectrum Disorders

(2012) B. J. O'Roak et al.   SCIENCE

Spatio-temporal transcriptome of the human brain

(2011) Hyo Jung Kang et al.   NATURE

Shank3 mutant mice display autistic-like behaviours and striatal dysfunction

(2011) João Peça et al.   NATURE

TBR1 directly represses Fezf2 to control the laminar origin and development of the corticospinal tract

(2011) W. Han et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

A noise-reduction GWAS analysis implicates altered regulation of neurite outgrowth and guidance in autism

(2011) John P Hussman et al.   Molecular Autism

Refining the phenotype associated withMEF2Chaploinsufficiency

(2010) F Novara et al.   CLINICAL GENETICS

SFARI Gene: an evolving database for the autism research community

(2010) S. Banerjee-Basu et al.   Disease Models & Mechanisms

Copy number variations associated with autism spectrum disorders contribute to a spectrum of neurodevelopmental disorders

(2010) Jill A Rosenfeld et al.   GENETICS IN MEDICINE

Neuroligin-1 Deletion Results in Impaired Spatial Memory and Increased Repetitive Behavior

(2010) J. Blundell et al.   JOURNAL OF NEUROSCIENCE

Renal malformations associated with mutations of developmental genes: messages from the clinic

(2010) Shazia Adalat et al.   PEDIATRIC NEPHROLOGY

Ciliary Neurotrophic Factor Protects Striatal Neurons against Excitotoxicity by Enhancing Glial Glutamate Uptake

(2010) Corinne Beurrier et al.   PLoS One

Tbr1 regulates regional and laminar identity of postmitotic neurons in developing neocortex

(2010) F. Bedogni et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Refining the critical region of the novel 19q13.11 microdeletion syndrome to 750 Kb

(2009) J H M Schuurs-Hoeijmakers et al.   JOURNAL OF MEDICAL GENETICS

19q13.11 deletion syndrome: a novel clinically recognisable genetic condition identified by array comparative genomic hybridisation

(2009) V Malan et al.   JOURNAL OF MEDICAL GENETICS

Common genetic variants on 5p14.1 associate with autism spectrum disorders

(2009) Kai Wang et al.   NATURE

Analysis of TSHZ2 and TSHZ3 genes in congenital pelvi-ureteric junction obstruction

(2009) D. Jenkins et al.   NEPHROLOGY DIALYSIS TRANSPLANTATION

Small Deletions of SATB2 Cause Some of the Clinical Features of the 2q33.1 Microdeletion Syndrome

(2009) Jill A. Rosenfeld et al.   PLoS One

Marble burying reflects a repetitive and perseverative behavior more than novelty-induced anxiety

(2009) Alexia Thomas et al.   PSYCHOPHARMACOLOGY

FOXG1 Is Responsible for the Congenital Variant of Rett Syndrome

(2008) Francesca Ariani et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Teashirt 3 is necessary for ureteral smooth muscle differentiation downstream of SHH and BMP4

(2008) X. Caubit et al.   DEVELOPMENT

Ctip2 Controls the Differentiation of Medium Spiny Neurons and the Establishment of the Cellular Architecture of the Striatum

(2008) P. Arlotta et al.   JOURNAL OF NEUROSCIENCE

Satb2 Is a Postmitotic Determinant for Upper-Layer Neuron Specification in the Neocortex

(2008) Olga Britanova et al.   NEURON

SOX5 Controls the Sequential Generation of Distinct Corticofugal Neuron Subtypes

(2008) Tina Lai et al.   NEURON

Transcription factor MEF2C influences neural stem/progenitor cell differentiation and maturation in vivo

(2008) H. Li et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

SOX5 postmitotically regulates migration, postmigratory differentiation, and projections of subplate and deep-layer neocortical neurons

(2008) K. Y. Kwan et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA