Related references
Note: Only part of the references are listed.CNV Workshop: an integrated platform for high-throughput copy number variation discovery and clinical diagnostics
Xiaowu Gai et al.
BMC BIOINFORMATICS (2010)
Mice lacking synapsin III show abnormalities in explicit memory and conditioned fear
B. Porton et al.
GENES BRAIN AND BEHAVIOR (2010)
Mechanisms of mosaicism, chimerism and uniparental disomy identified by single nucleotide polymorphism array analysis
Laura K. Conlin et al.
HUMAN MOLECULAR GENETICS (2010)
Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes
J. Elia et al.
MOLECULAR PSYCHIATRY (2010)
Functional impact of global rare copy number variation in autism spectrum disorders
Dalila Pinto et al.
NATURE (2010)
Autism genetics: emerging data from genome-wide copy-number and single nucleotide polymorphism scans
Lauren A. Weiss
EXPERT REVIEW OF MOLECULAR DIAGNOSTICS (2009)
High-resolution mapping and analysis of copy number variations in the human genome: A data resource for clinical and research applications
Tamim H. Shaikh et al.
GENOME RESEARCH (2009)
A genome-wide linkage and association scan reveals novel loci for autism
Lauren A. Weiss et al.
NATURE (2009)
Common genetic variants on 5p14.1 associate with autism spectrum disorders
Kai Wang et al.
NATURE (2009)
Autism genome-wide copy number variation reveals ubiquitin and neuronal genes
Joseph T. Glessner et al.
NATURE (2009)
Copy-number variants in neurodevelopmental disorders: promises and challenges
Alison K. Merikangas et al.
TRENDS IN GENETICS (2009)
The emerging role of synaptic cell-adhesion pathways in the pathogenesis of autism spectrum disorders
Catalina Betancur et al.
TRENDS IN NEUROSCIENCES (2009)
Genome-Wide Analyses of Exonic Copy Number Variants in a Family-Based Study Point to Novel Autism Susceptibility Genes
Maja Bucan et al.
PLOS GENETICS (2009)
Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene
Maricela Alarcon et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2008)
A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism
Dan E. Arking et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2008)
Extensive copy-number variation of the human olfactory receptor gene family
Janet M. Young et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2008)
Neuregulin 1 in neural development, synaptic plasticity and schizophrenia
Lin Mei et al.
NATURE REVIEWS NEUROSCIENCE (2008)
High-Resolution Copy-Number Variation Map Reflects Human Olfactory Receptor Diversity and Evolution
Yehudit Hasin et al.
PLOS GENETICS (2008)
PICK1-ICA69 heteromeric BAR domain complex regulates synaptic targeting and surface expression of AMPA receptors
Mian Cao et al.
JOURNAL OF NEUROSCIENCE (2007)
A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene
Hakon Hakonarson et al.
NATURE (2007)
Evolutionary dynamics of olfactory receptor genes in Drosophila species
Masafumi Nozawa et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2007)
Mapping autism risk loci using genetic linkage and chromosomal rearrangements
Peter Szatmari et al.
NATURE GENETICS (2007)
Recent advances in the genetics of autism
Abha R. Gupta et al.
BIOLOGICAL PSYCHIATRY (2007)
qBase relative quantification framework and software for management and automated analysis of real-time quantitative PCR data
Jan Hellemans et al.
GENOME BIOLOGY (2007)
Molecular mechanisms of schizophrenia
Undine E. Lang et al.
CELLULAR PHYSIOLOGY AND BIOCHEMISTRY (2007)
Significant linkage and association between a functional (GT)n polymorphism in promoter of the N-methyl-D-aspartate receptor subunit gene (GRIN2A) and schizophrenia
Jinsong Tang et al.
NEUROSCIENCE LETTERS (2006)
Association of a functional deficit of the BKCa channel, a synaptic regulator of neuronal excitability, with autism and mental retardation
Frederic Laumonnier et al.
AMERICAN JOURNAL OF PSYCHIATRY (2006)
Genetic heterogeneity between the three components of the autism spectrum:: A twin study
Angelica Ronald et al.
JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY (2006)
Immunolocalization of the Ca2+-activated K+ channel Slo1 in axons and nerve terminals of mammalian brain and cultured neurons
H Misonou et al.
JOURNAL OF COMPARATIVE NEUROLOGY (2006)
Examination of ancestry and ethnic affiliation using highly informative diallelic DNA markers: application to diverse and admixed populations and implications for clinical epidemiology and forensic medicine
N Yang et al.
HUMAN GENETICS (2005)
Candidate-gene screening and association analysis at the autism-susceptibility locus on chromosome 16p:: Evidence of association at GRIN2A and ABAT
G Barnby et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2005)
The Mammalian Phenotype Ontology as a tool for annotating, analyzing and comparing phenotypic information
CL Smith et al.
GENOME BIOLOGY (2005)
Cerebellar ataxia and Purkinje cell dysfunction caused by Ca2+-activated K+ channel deficiency
M Sausbier et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2004)
Postnatal neurodevelopmental disorders: Meeting at the synapse?
HY Zoghbi
SCIENCE (2003)
α-neurexins couple Ca2+ channels to synaptic vesicle exocytosis
M Missler et al.
NATURE (2003)
The Autism Genetic Resource Exchange: A resource for the study of autism and related neuropsychiatric conditions
DH Geschwind et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2001)
Share Paper
