PRICKLE1 Interaction with SYNAPSIN I Reveals a Role in Autism Spectrum Disorders

Mechanisms of prickle1a function in zebrafish epilepsy and retinal neurogenesis

(2013) X. Mei et al.   Disease Models & Mechanisms

Neuroethologically delineated differences in the seizure behavior of Synapsin 1 and Synapsin 2 knock-out mice

(2012) Lars Etholm et al.   EPILEPSY RESEARCH

Mutations in Prickle Orthologs Cause Seizures in Flies, Mice, and Humans

(2011) Hirotaka Tao et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Dystrophic Serotonin Axons in Postmortem Brains from Young Autism Patients

(2011) Efrain C. Azmitia et al.   Anatomical Record-Advances in Integrative Anatomy and Evolutionary Biology

SYN1 loss-of-function mutations in autism and partial epilepsy cause impaired synaptic function

(2011) Anna Fassio et al.   HUMAN MOLECULAR GENETICS

Mouse model of Timothy syndrome recapitulates triad of autistic traits

(2011) P. L. Bader et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Association of MouseDlg4(PSD-95) Gene Deletion and HumanDLG4Gene Variation With Phenotypes Relevant to Autism Spectrum Disorders and Williams' Syndrome

(2010) Michael Feyder et al.   AMERICAN JOURNAL OF PSYCHIATRY

RNG105 Deficiency Impairs the Dendritic Localization of mRNAs for Na+/K+ ATPase Subunit Isoforms and Leads to the Degeneration of Neuronal Networks

(2010) N. Shiina et al.   JOURNAL OF NEUROSCIENCE

PRICKLE1 progressive myoclonus epilepsy in Southern Italy

(2010) C. Criscuolo et al.   MOVEMENT DISORDERS

The synapsins: Key actors of synapse function and plasticity

(2010) F. Cesca et al.   PROGRESS IN NEUROBIOLOGY

Yeast Two-Hybrid, a Powerful Tool for Systems Biology

(2009) Anna Brückner et al.   INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES

A de novo 1p34.2 microdeletion identifies the synaptic vesicle gene RIMS3 as a novel candidate for autism

(2009) R. A. Kumar et al.   JOURNAL OF MEDICAL GENETICS

Circadian rhythms and sleep in children with autism

(2009) Gena Glickman   NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS

Common increase of GATA-3 level in PC-12 cells by three teratogens causing autism spectrum disorders

(2009) Ujjwal K. Rout et al.   NEUROSCIENCE RESEARCH

Mouse prickle1, the homolog of a PCP gene, is essential for epiblast apical-basal polarity

(2009) H. Tao et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

A Homozygous Mutation in Human PRICKLE1 Causes an Autosomal-Recessive Progressive Myoclonus Epilepsy-Ataxia Syndrome

(2008) Alexander G. Bassuk et al.   AMERICAN JOURNAL OF HUMAN 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

Valproic acid regulates catecholaminergic pathways by concentration-dependent threshold effects on TH mRNA synthesis and degradation

(2008) Antoni D'Souza et al.   BRAIN RESEARCH

Mutations in the calcium-related gene IL1RAPL1 are associated with autism

(2008) A. Piton et al.   HUMAN MOLECULAR GENETICS

Expression of the neurosecretory process in pc12 cells is governed by rest

(2008) Rosalba D’Alessandro et al.   JOURNAL OF NEUROCHEMISTRY

Advances in autism genetics: on the threshold of a new neurobiology

(2008) Brett S. Abrahams et al.   NATURE REVIEWS GENETICS

Comprehensive behavioral phenotyping of calpastatin-knockout mice

(2008) Ryuichi Nakajima et al.   Molecular Brain