标题
De novo TBR1 mutations in sporadic autism disrupt protein functions
作者
关键词
-
出版物
Nature Communications
Volume 5, Issue 1, Pages -
出版商
Springer Nature
发表日期
2014-09-18
DOI
10.1038/ncomms5954
参考文献
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。- TBR1is the candidate gene for intellectual disability in patients with a 2q24.2 interstitial deletion
- (2014) Orazio Palumbo et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Reelin gene variants and risk of autism spectrum disorders: An integrated meta-analysis
- (2014) Zhenling Wang et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS
- A de novo 2.3Mb deletion in 2q24.2q24.3 in a 20-month-old developmentally delayed girl
- (2014) V. Belengeanu et al. GENE
- Tbr1 haploinsufficiency impairs amygdalar axonal projections and results in cognitive abnormality
- (2014) Tzyy-Nan Huang et al. NATURE NEUROSCIENCE
- Coexpression Networks Implicate Human Midfetal Deep Cortical Projection Neurons in the Pathogenesis of Autism
- (2013) A. Jeremy Willsey et al. CELL
- Integrative Functional Genomic Analyses Implicate Specific Molecular Pathways and Circuits in Autism
- (2013) Neelroop N. Parikshak et al. CELL
- Autism-Associated Neuroligin-3 Mutations Commonly Disrupt Tonic Endocannabinoid Signaling
- (2013) Csaba Földy et al. NEURON
- Using Whole-Exome Sequencing to Identify Inherited Causes of Autism
- (2013) Timothy W. Yu et al. NEURON
- The role of AUTS2 in neurodevelopment and human evolution
- (2013) Nir Oksenberg et al. TRENDS IN GENETICS
- Neurogenomics of speech and language disorders: the road ahead
- (2013) Pelagia Deriziotis et al. GENOME BIOLOGY
- Sequencing Chromosomal Abnormalities Reveals Neurodevelopmental Loci that Confer Risk across Diagnostic Boundaries
- (2012) Michael E. Talkowski et al. CELL
- Individual common variants exert weak effects on the risk for autism spectrum disorders
- (2012) Richard Anney et al. HUMAN MOLECULAR GENETICS
- Patterns and rates of exonic de novo mutations in autism spectrum disorders
- (2012) Benjamin M. Neale et al. NATURE
- De novo mutations revealed by whole-exome sequencing are strongly associated with autism
- (2012) Stephan J. Sanders et al. NATURE
- Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations
- (2012) Brian J. O’Roak et al. NATURE
- De Novo Gene Disruptions in Children on the Autistic Spectrum
- (2012) Ivan Iossifov et al. NEURON
- Phenotypic Heterogeneity of Genomic Disorders and Rare Copy-Number Variants
- (2012) Santhosh Girirajan et al. NEW ENGLAND JOURNAL OF MEDICINE
- Multiplex Targeted Sequencing Identifies Recurrently Mutated Genes in Autism Spectrum Disorders
- (2012) B. J. O'Roak et al. SCIENCE
- Genetic Heritability and Shared Environmental Factors Among Twin Pairs With Autism
- (2011) Joachim Hallmayer ARCHIVES OF GENERAL PSYCHIATRY
- Phenotypic spectrum associated with CASK loss-of-function mutations
- (2011) U. Moog et al. JOURNAL OF MEDICAL GENETICS
- Tbr1 and Fezf2 Regulate Alternate Corticofugal Neuronal Identities during Neocortical Development
- (2011) W. L. McKenna et al. JOURNAL OF NEUROSCIENCE
- Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations
- (2011) Brian J O'Roak et al. NATURE GENETICS
- TBR1 directly represses Fezf2 to control the laminar origin and development of the corticospinal tract
- (2011) W. Han et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Protein Interactome Reveals Converging Molecular Pathways Among Autism Disorders
- (2011) Y. Sakai et al. Science Translational Medicine
- A Population Genetic Approach to Mapping Neurological Disorder Genes Using Deep Resequencing
- (2011) Rachel A. Myers et al. PLoS Genetics
- Tbr1 regulates regional and laminar identity of postmitotic neurons in developing neocortex
- (2010) F. Bedogni et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- The forkhead transcription factors, Foxp1 and Foxp2, identify different subpopulations of projection neurons in the mouse cerebral cortex
- (2009) T. Hisaoka et al. NEUROSCIENCE
- FOXP2 as a molecular window into speech and language
- (2009) Simon E. Fisher et al. TRENDS IN GENETICS
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