Sociability and synapse subtype-specific defects in mice lacking SRPX2, a language-associated gene

The central nervous system patterning gene variants associated with clinical symptom severity of autism spectrum disorders

(2017) Yi-Ling Chien et al.   JOURNAL OF THE FORMOSAN MEDICAL ASSOCIATION

Next-generation DNA sequencing identifies novel gene variants and pathways involved in specific language impairment

(2017) Xiaowei Sylvia Chen et al.   Scientific Reports

Insights into the Neural and Genetic Basis of Vocal Communication

(2016) Genevieve Konopka et al.   CELL

Rediscovering area CA2: unique properties and functions

(2016) Serena M. Dudek et al.   NATURE REVIEWS NEUROSCIENCE

The role of neuronal activity and transmitter release on synapse formation

(2014) Laura C Andreae et al.   CURRENT OPINION IN NEUROBIOLOGY

The Matrix Protein Hikaru genki Localizes to Cholinergic Synaptic Clefts and Regulates Postsynaptic Organization in the Drosophila Brain

(2014) M. Nakayama et al.   JOURNAL OF NEUROSCIENCE

The hippocampal CA2 region is essential for social memory

(2014) Frederick L. Hitti et al.   NATURE

Tubacin prevents neuronal migration defects and epileptic activity caused by rat Srpx2 silencing in utero

(2013) Manal Salmi et al.   BRAIN

One-Step Generation of Mice Carrying Mutations in Multiple Genes by CRISPR/Cas-Mediated Genome Engineering

(2013) Haoyi Wang et al.   CELL

One-Step Generation of Mice Carrying Reporter and Conditional Alleles by CRISPR/Cas-Mediated Genome Engineering

(2013) Hui Yang et al.   CELL

FoxP2 Regulates Neurogenesis during Embryonic Cortical Development

(2013) D. Tsui et al.   JOURNAL OF NEUROSCIENCE

Foxp2 Mediates Sex Differences in Ultrasonic Vocalization by Rat Pups and Directs Order of Maternal Retrieval

(2013) J. M. Bowers et al.   JOURNAL OF NEUROSCIENCE

Cell type–specific genetic and optogenetic tools reveal hippocampal CA2 circuits

(2013) Keigo Kohara et al.   NATURE NEUROSCIENCE

The Human Language-Associated Gene SRPX2 Regulates Synapse Formation and Vocalization in Mice

(2013) G. M. Sia et al.   SCIENCE

Multiplex Genome Engineering Using CRISPR/Cas Systems

(2013) L. Cong et al.   SCIENCE

A Competition-Based Mechanism Mediates Developmental Refinement of Tectal Neuron Receptive Fields

(2012) W. Dong et al.   JOURNAL OF NEUROSCIENCE

Autistic-like behaviour and cerebellar dysfunction in Purkinje cell Tsc1 mutant mice

(2012) Peter T. Tsai et al.   NATURE

Patterns and rates of exonic de novo mutations in autism spectrum disorders

(2012) Benjamin M. Neale et al.   NATURE

Motor circuits are required to encode a sensory model for imitative learning

(2012) Todd F Roberts et al.   NATURE NEUROSCIENCE

Neuroligin-1–dependent competition regulates cortical synaptogenesis and synapse number

(2012) Hyung-Bae Kwon et al.   NATURE NEUROSCIENCE

SRPX2 Is a Novel Chondroitin Sulfate Proteoglycan That Is Overexpressed in Gastrointestinal Cancer

(2012) Kaoru Tanaka et al.   PLoS One

FoxP2is significantly associated with schizophrenia and major depression in the Chinese Han Population

(2012) Tao Li et al.   WORLD JOURNAL OF BIOLOGICAL PSYCHIATRY

The Complement Control-Related Genes CSMD1 and CSMD2 Associate to Schizophrenia

(2011) Bjarte Håvik et al.   BIOLOGICAL PSYCHIATRY

Absence of CNTNAP2 Leads to Epilepsy, Neuronal Migration Abnormalities, and Core Autism-Related Deficits

(2011) Olga Peñagarikano et al.   CELL

Cell Type–Specific Three-Dimensional Structure of Thalamocortical Circuits in a Column of Rat Vibrissal Cortex

(2011) Marcel Oberlaender et al.   CEREBRAL CORTEX

CNTNAP2variants affect early language development in the general population

(2011) A. J. O. Whitehouse et al.   GENES BRAIN AND BEHAVIOR

Regulation of MET by FOXP2, Genes Implicated in Higher Cognitive Dysfunction and Autism Risk

(2011) Z. Mukamel et al.   JOURNAL OF NEUROSCIENCE

Foxp2 Regulates Gene Networks Implicated in Neurite Outgrowth in the Developing Brain

(2011) Sonja C. Vernes et al.   PLoS Genetics

FOXP2 gene and language impairment in schizophrenia: association and epigenetic studies

(2010) Amparo Tolosa et al.   BMC Medical Genetics

Refining the phenotype associated withMEF2Chaploinsufficiency

(2010) F Novara et al.   CLINICAL GENETICS

The structure of innate vocalizations in Foxp2-deficient mouse pups

(2010) S. Gaub et al.   GENES BRAIN AND BEHAVIOR

Molecular networks implicated in speech-related disorders: FOXP2 regulates the SRPX2/uPAR complex

(2010) Patrice Roll et al.   HUMAN MOLECULAR GENETICS

The Sushi Domains of GABAB Receptors Function as Axonal Targeting Signals

(2010) B. Biermann et al.   JOURNAL OF NEUROSCIENCE

Synaptic and Vesicular Coexistence of VGLUT and VGAT in Selected Excitatory and Inhibitory Synapses

(2010) J.-F. Zander et al.   JOURNAL OF NEUROSCIENCE

Rapid spine stabilization and synaptic enhancement at the onset of behavioural learning

(2010) Todd F. Roberts et al.   NATURE

Behavioural phenotyping assays for mouse models of autism

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

Social Cognition and the Evolution of Language: Constructing Cognitive Phylogenies

(2010) W. Tecumseh Fitch et al.   NEURON

The cognitive niche: Coevolution of intelligence, sociality, and language

(2010) S. Pinker   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

A Humanized Version of Foxp2 Affects Cortico-Basal Ganglia Circuits in Mice

(2009) Wolfgang Enard et al.   CELL

MEF2C haploinsufficiency caused by either microdeletion of the 5q14.3 region or mutation is responsible for severe mental retardation with stereotypic movements, epilepsy and/or cerebral malformations

(2009) N. Le Meur et al.   JOURNAL OF MEDICAL GENETICS

The subcellular organization of neocortical excitatory connections

(2009) Leopoldo Petreanu et al.   NATURE

Human-specific transcriptional regulation of CNS development genes by FOXP2

(2009) Genevieve Konopka et al.   NATURE

A secreted complement-control-related protein ensures acetylcholine receptor clustering

(2009) Marie Gendrel et al.   NATURE

The forkhead transcription factors, Foxp1 and Foxp2, identify different subpopulations of projection neurons in the mouse cerebral cortex

(2009) T. Hisaoka et al.   NEUROSCIENCE

FOXP2 as a molecular window into speech and language

(2009) Simon E. Fisher et al.   TRENDS IN GENETICS

Linkage, Association, and Gene-Expression Analyses Identify CNTNAP2 as an Autism-Susceptibility Gene

(2008) Maricela Alarcón et al.   AMERICAN JOURNAL OF HUMAN GENETICS

A Common Genetic Variant in the Neurexin Superfamily Member CNTNAP2 Increases Familial Risk of Autism

(2008) Dan E. Arking et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Molecular Cytogenetic Analysis and Resequencing of Contactin Associated Protein-Like 2 in Autism Spectrum Disorders

(2008) Betul Bakkaloglu et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Impaired Synaptic Plasticity and Motor Learning in Mice with a Point Mutation Implicated in Human Speech Deficits

(2008) Matthias Groszer et al.   CURRENT BIOLOGY

Conservation and diversity of Foxp2 expression in muroid rodents: Functional implications

(2008) Polly Campbell et al.   JOURNAL OF COMPARATIVE NEUROLOGY

A Functional Genetic Link between Distinct Developmental Language Disorders

(2008) Sonja C. Vernes et al.   NEW ENGLAND JOURNAL OF MEDICINE

Ultrasonic vocalization impairment of Foxp2 (R552H) knockin mice related to speech-language disorder and abnormality of Purkinje cells

(2008) E. Fujita et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Reduced social interaction and ultrasonic communication in a mouse model of monogenic heritable autism

(2008) S. Jamain et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Abnormal social behaviors in mice lacking Fgf17

(2007) K. Scearce-Levie et al.   GENES BRAIN AND BEHAVIOR