Role of the cytoplasmic isoform of RBFOX1/A2BP1 in establishing the architecture of the developing cerebral cortex

SIL1, a causative cochaperone gene of Marinesco-Sjogren syndrome, plays an essential role in establishing the architecture of the developing cerebral cortex

(2014) Y. Inaguma et al.   EMBO Molecular Medicine

Analysis of RBFOX1 gene expression in lymphoblastoid cell lines of Italian discordant autism spectrum disorders sib-pairs

(2014) Paola Prandini et al.   MOLECULAR AND CELLULAR PROBES

HITS-CLIP and Integrative Modeling Define the Rbfox Splicing-Regulatory Network Linked to Brain Development and Autism

(2014) Sebastien M. Weyn-Vanhentenryck et al.   Cell Reports

Biochemical and morphological characterization of A2BP1 in neuronal tissue

(2013) Nanako Hamada et al.   JOURNAL OF NEUROSCIENCE RESEARCH

RBFOX1 regulates both splicing and transcriptional networks in human neuronal development

(2012) Brent L. Fogel et al.   HUMAN MOLECULAR GENETICS

Autism genetics: searching for specificity and convergence

(2012) Jamee M Berg et al.   GENOME BIOLOGY

Developmental Expression Mapping of a Gene Implicated in Multiple Neurodevelopmental Disorders, A2bp1 (Fox1)

(2011) Elizabeth A.D. Hammock et al.   DEVELOPMENTAL NEUROSCIENCE

Rare structural variation of synapse and neurotransmission genes in autism

(2011) X Gai et al.   MOLECULAR PSYCHIATRY

Transcriptomic analysis of autistic brain reveals convergent molecular pathology

(2011) Irina Voineagu et al.   NATURE

The splicing regulator Rbfox1 (A2BP1) controls neuronal excitation in the mammalian brain

(2011) Lauren T Gehman et al.   NATURE GENETICS

Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism

(2011) Stephan J. Sanders et al.   NEURON

Septin 14 Is Involved in Cortical Neuronal Migration via Interaction with Septin 4

(2010) Tomoyasu Shinoda et al.   MOLECULAR BIOLOGY OF THE CELL

Dysbindin-1, WAVE2 and Abi-1 form a complex that regulates dendritic spine formation

(2010) H Ito et al.   MOLECULAR PSYCHIATRY

Functional impact of global rare copy number variation in autism spectrum disorders

(2010) Dalila Pinto et al.   NATURE

Inhibition of N-methyl-d-aspartate receptor activity resulted in aberrant neuronal migration caused by delayed morphological development in the mouse neocortex

(2010) S. Uchino et al.   NEUROSCIENCE

Fox-3 and PSF interact to activate neural cell-specific alternative splicing

(2010) Kee K. Kim et al.   NUCLEIC ACIDS RESEARCH

Integrative Modeling Defines the Nova Splicing-Regulatory Network and Its Combinatorial Controls

(2010) C. Zhang et al.   SCIENCE

Genetic utility of broadly defined bipolar schizoaffective disorder as a diagnostic concept

(2009) M. L. Hamshere et al.   BRITISH JOURNAL OF PSYCHIATRY

An inducible change in Fox-1/A2BP1 splicing modulates the alternative splicing of downstream neuronal target exons

(2009) J.-A. Lee et al.   GENES & DEVELOPMENT

Interaction of a multi-domain adaptor protein, vinexin, with a Rho-effector, Rhotekin

(2009) Koh-ichi Nagata et al.   Medical Molecular Morphology

Developmental Control of CaV1.2 L-Type Calcium Channel Splicing by Fox Proteins

(2009) Z. Z. Tang et al.   MOLECULAR AND CELLULAR BIOLOGY

Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes

(2009) J Elia et al.   MOLECULAR PSYCHIATRY

Genome-Wide Analyses of Exonic Copy Number Variants in a Family-Based Study Point to Novel Autism Susceptibility Genes

(2009) Maja Bucan et al.   PLoS Genetics

Cell-Autonomous Roles of ARX in Cell Proliferation and Neuronal Migration during Corticogenesis

(2008) G. Friocourt et al.   JOURNAL OF NEUROSCIENCE

Strong association of de novo copy number mutations with sporadic schizophrenia

(2008) Bin Xu et al.   NATURE GENETICS