相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。Evidence for contribution of common genetic variants within chromosome 8p21.2-8p21.1 to restricted and repetitive behaviors in autism spectrum disorders
Yu Tao et al.
BMC GENOMICS (2016)
Chromosome conformation elucidates regulatory relationships in developing human brain
Hyejung Won et al.
NATURE (2016)
Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population
Elise B. Robinson et al.
NATURE GENETICS (2016)
Enhancer-promoter interactions are encoded by complex genomic signatures on looping chromatin
Sean Whalen et al.
NATURE GENETICS (2016)
Social Responsiveness, an Autism Endophenotype: Genomewide Significant Linkage to Two Regions on Chromosome 8
Jennifer K. Lowe et al.
AMERICAN JOURNAL OF PSYCHIATRY (2015)
Identification of causal genes for complex traits
Farhad Hormozdiari et al.
BIOINFORMATICS (2015)
Common genetic variants influence human subcortical brain structures
Derrek P. Hibar et al.
NATURE (2015)
Synaptic, transcriptional and chromatin genes disrupted in autism
Silvia De Rubeis et al.
NATURE (2014)
A polygenic burden of rare disruptive mutations in schizophrenia
Shaun M. Purcell et al.
NATURE (2014)
Most genetic risk for autism resides with common variation
Trent Gaugler et al.
NATURE GENETICS (2014)
Comparison of Methods to Account for Relatedness in Genome-Wide Association Studies with Family-Based Data
Jakris Eu-ahsunthornwattana et al.
PLOS GENETICS (2014)
QTL replication and targeted association highlight the nerve growth factor gene for nonverbal communication deficits in autism spectrum disorders
A. T-H Lu et al.
MOLECULAR PSYCHIATRY (2013)
Subcategories of Restricted and Repetitive Behaviors in Children with Autism Spectrum Disorders
Somer L. Bishop et al.
JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS (2013)
Prohibitin Reduces Mitochondrial Free Radical Production and Protects Brain Cells from Different Injury Modalities
Ping Zhou et al.
JOURNAL OF NEUROSCIENCE (2012)
The long-range interaction landscape of gene promoters
Amartya Sanyal et al.
NATURE (2012)
Genome-wide efficient mixed-model analysis for association studies
Xiang Zhou et al.
NATURE GENETICS (2012)
EnigmaVis: Online Interactive Visualization of Genome-Wide Association Studies of the Enhancing NeuroImaging Genetics through Meta-Analysis (ENIGMA) Consortium
Nic M. Novak et al.
TWIN RESEARCH AND HUMAN GENETICS (2012)
Loss of Prohibitin Membrane Scaffolds Impairs Mitochondrial Architecture and Leads to Tau Hyperphosphorylation and Neurodegeneration
Carsten Merkwirth et al.
PLOS GENETICS (2012)
Genetic Heritability and Shared Environmental Factors Among Twin Pairs With Autism
Joachim Hallmayer et al.
ARCHIVES OF GENERAL PSYCHIATRY (2011)
Basal Ganglia Morphometry and Repetitive Behavior in Young Children with Autism Spectrum Disorder
Annette Estes et al.
AUTISM RESEARCH (2011)
Neurobiology of obsessive-compulsive disorder: insights into neural circuitry dysfunction through mouse genetics
Jonathan T. Ting et al.
CURRENT OPINION IN NEUROBIOLOGY (2011)
Spatio-temporal transcriptome of the human brain
Hyo Jung Kang et al.
NATURE (2011)
Dlx5 and Dlx6 Regulate the Development of Parvalbumin-Expressing Cortical Interneurons
Yanling Wang et al.
JOURNAL OF NEUROSCIENCE (2010)
Variance component model to account for sample structure in genome-wide association studies
Hyun Min Kang et al.
NATURE GENETICS (2010)
Genome-wide linkage analyses of two repetitive behavior phenotypes in Utah pedigrees with autism spectrum disorders
Dale S. Cannon et al.
MOLECULAR AUTISM (2010)
The pathophysiology of restricted repetitive behavior
Mark Lewis et al.
JOURNAL OF NEURODEVELOPMENTAL DISORDERS (2009)
Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene
Maricela Alarcon et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2008)
Autism: Many Genes, Common Pathways?
Daniel H. Geschwind
CELL (2008)
Prohibitins control cell proliferation and apoptosis by regulating OPA1-dependent cristae morphogenesis in mitochondria
Carsten Merkwirth et al.
GENES & DEVELOPMENT (2008)
High density SNP association study of a major autism linkage region on chromosome 17
Jennifer L. Stone et al.
HUMAN MOLECULAR GENETICS (2007)
Mapping autism risk loci using genetic linkage and chromosomal rearrangements
Peter Szatmari et al.
NATURE GENETICS (2007)
Animal models of restricted repetitive behavior in autism
Mark H. Lewis et al.
BEHAVIOURAL BRAIN RESEARCH (2007)
Quantitative trait locus analysis of nonverbal communication in autism spectrum disorder
GK Chen et al.
MOLECULAR PSYCHIATRY (2006)
Striatal volume on magnetic resonance imaging and repetitive behaviors in autism
E Hollander et al.
BIOLOGICAL PSYCHIATRY (2005)
Replication of autism linkage:: Fine-mapping peak at 17q21
RM Cantor et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2005)
Factor analysis of restricted and repetitive behaviors in autism using the Autism Diagnostic Interview-R
ML Cuccaro et al.
CHILD PSYCHIATRY & HUMAN DEVELOPMENT (2003)
Fine mapping of Autistic disorder to chromosome 15q11-q13 by use of phenotypic subtypes
YJ Shao et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2003)
Evidence for a language quantitative trait locus on chromosome 7q in multiplex autism families
M Alarcon et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2002)
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)