Related references
Note: Only part of the references are listed.Systematic resequencing of X-chromosome synaptic genes in autism spectrum disorder and schizophrenia
A. Piton et al.
MOLECULAR PSYCHIATRY (2011)
Mutation screening of melatonin-related genes in patients with autism spectrum disorders
Lina Jonsson et al.
BMC MEDICAL GENOMICS (2010)
Association of the oxytocin receptor (OXTR) gene polymorphisms with autism spectrum disorder (ASD) in the Japanese population
Xiaoxi Liu et al.
JOURNAL OF HUMAN GENETICS (2010)
Functional impact of global rare copy number variation in autism spectrum disorders
Dalila Pinto et al.
NATURE (2010)
Mutations in the SHANK2 synaptic scaffolding gene in autism spectrum disorder and mental retardation
Simone Berkel et al.
NATURE GENETICS (2010)
Xenopus Meiotic Microtubule-Associated Interactome
Vincent Gache et al.
PLOS ONE (2010)
Rare Variants Create Synthetic Genome-Wide Associations
Samuel P. Dickson et al.
PLOS BIOLOGY (2010)
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)
Asymmetric centrosome inheritance maintains neural progenitors in the neocortex
Xiaoqun Wang et al.
NATURE (2009)
Protein structure prediction on the Web: a case study using the Phyre server
Lawrence A. Kelley et al.
NATURE PROTOCOLS (2009)
Human Splicing Finder: an online bioinformatics tool to predict splicing signals
Francois-Olivier Desmet et al.
NUCLEIC ACIDS RESEARCH (2009)
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)
Heterogeneous association between engrailed-2 and autism in the CPEA network
Camille W. Brune et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS (2008)
Familial deletion within NLGN4 associated with autism and Tourette syndrome
Amy Lawson-Yuen et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2008)
Epigenetics, brain evolution and behaviour
Eric B. Keverne et al.
FRONTIERS IN NEUROENDOCRINOLOGY (2008)
Association between microdeletion and microduplication at 16p11.2 and autism
Lauren A. Weiss et al.
NEW ENGLAND JOURNAL OF MEDICINE (2008)
Mutations in the pericentrin (PCNT) gene cause primordial dwarfism
Anita Rauch et al.
SCIENCE (2008)
Identifying autism loci and genes by tracing recent shared ancestry
Eric M. Morrow et al.
SCIENCE (2008)
Mutations in pericentrin cause Seckel syndrome with defective ATR-dependent DNA damage signaling
Elen Griffith et al.
NATURE GENETICS (2008)
Contribution of SHANK3 mutations to autism spectrum disorder
Rainald Moessner et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2007)
Genetic mechanisms underlying abnormal neuronal migration in classical lissencephaly
Geraldine Kerjan et al.
TRENDS IN GENETICS (2007)
Competing interactions between Micro-RNAs determine neural progenitor survival and proliferation after ethanol exposure:: Evidence from an ex vivo model of the fetal cerebral cortical neuroepithelium
Pratheesh Sathyan et al.
JOURNAL OF NEUROSCIENCE (2007)
A unified genetic theory for sporadic and inherited autism
Xiaoyue Zhao et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2007)
The centrosome in neuronal development
Holden R. Higginbotham et al.
TRENDS IN NEUROSCIENCES (2007)
Association of the oxytocin receptor gene (OXTR) in Caucasian children and adolescents with autism
Suma Jacob et al.
NEUROSCIENCE LETTERS (2007)
Most rare missense alleles are deleterious in humans: Implications for complex disease and association studies
Gregory V. Kryukov et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2007)
15q11-13 GABAA receptor genes are normally biallelically expressed in brain yet are subject to epigenetic dysregulation in autism-spectrum disorders
Amber Hogart et al.
HUMAN MOLECULAR GENETICS (2007)
Mapping autism risk loci using genetic linkage and chromosomal rearrangements
Peter Szatmari et al.
NATURE GENETICS (2007)
Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders
Christelle M. Durand et al.
NATURE GENETICS (2007)
High frequency of neurexin 1β signal peptide structural variants in patients with autism
Jinong Feng et al.
NEUROSCIENCE LETTERS (2006)
Evidence for multiple loci from a genome scan of autism kindreds
G. D. Schellenberg et al.
MOLECULAR PSYCHIATRY (2006)
Aspm specifically maintains symmetric proliferative divisions of neuroepithelial cells
Jennifer L. Fish et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2006)
A heterogeneity-based genome search meta-analysis for autism-spectrum disorders
TA Trikalinos et al.
MOLECULAR PSYCHIATRY (2006)
Support for the homeobox transcription factor gene ENGRAILED 2 as an autism spectrum disorder susceptibility locus
R Benayed et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2005)
PMUT:: a web-based tool for the annotation of pathological mutations on proteins
C Ferrer-Costa et al.
BIOINFORMATICS (2005)
Positive association of the oxytocin receptor gene (OXTR) with autism in the Chinese Han population
SP Wu et al.
BIOLOGICAL PSYCHIATRY (2005)
Allelic variation in gene expression in thyroid tissue
HL He et al.
THYROID (2005)
Analysis of IMGSAC autism susceptibility loci: evidence for sex limited and parent of origin specific effects
JA Lamb et al.
JOURNAL OF MEDICAL GENETICS (2005)
Cortical neurons arise in symmetric and asymmetric division zones and migrate through specific phases
SC Noctor et al.
NATURE NEUROSCIENCE (2004)
Proteomic characterization of the human centrosome by protein correlation profiling
JS Andersen et al.
NATURE (2003)
Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism
S Jamain et al.
NATURE GENETICS (2003)
Defining the autism minimum candidate gene region on chromosome 7
HB Hutcheson et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS (2003)
Neuroscience - New directions in neuronal migration
ME Hatten
SCIENCE (2002)
Human non-synonymous SNPs: server and survey
V Ramensky et al.
NUCLEIC ACIDS RESEARCH (2002)
Regional meta-analysis of published data supports linkage of autism with markers on chromosome 7
JA Badner et al.
MOLECULAR PSYCHIATRY (2002)
Evidence for a language quantitative trait locus on chromosome 7q in multiplex autism families
M Alarcon et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2002)
Family-based tests of association in the presence of linkage
SL Lake et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2000)
A unified approach to adjusting association tests for population admixture with arbitrary pedigree structure and arbitrary missing marker information
D Rabinowitz et al.
HUMAN HEREDITY (2000)
The Autism Diagnostic Observation Schedule-Generic: A standard measure of social and communication deficits associated with the spectrum of autism
C Lord et al.
JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS (2000)
Share Paper
