Analysis of the chromosome X exome in patients with autism spectrum disorders identified novel candidate genes, including TMLHE
出版年份 2012 全文链接
标题
Analysis of the chromosome X exome in patients with autism spectrum disorders identified novel candidate genes, including TMLHE
作者
关键词
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出版物
Translational Psychiatry
Volume 2, Issue 10, Pages e179-e179
出版商
Springer Nature
发表日期
2012-10-23
DOI
10.1038/tp.2012.102
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注意:仅列出部分参考文献,下载原文获取全部文献信息。- SHANK1 Deletions in Males with Autism Spectrum Disorder
- (2012) Daisuke Sato et al. AMERICAN JOURNAL OF HUMAN 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
- A common X-linked inborn error of carnitine biosynthesis may be a risk factor for nondysmorphic autism
- (2012) P. B. S. Celestino-Soper et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Metabolomic analysis reveals that carnitines are key regulatory metabolites in phase transition of the locusts
- (2012) R. Wu et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Genetic and Functional Analyses of SHANK2 Mutations Suggest a Multiple Hit Model of Autism Spectrum Disorders
- (2012) Claire S. Leblond et al. PLoS Genetics
- Genetic Heritability and Shared Environmental Factors Among Twin Pairs With Autism
- (2011) Joachim Hallmayer ARCHIVES OF GENERAL PSYCHIATRY
- Use of array CGH to detect exonic copy number variants throughout the genome in autism families detects a novel deletion in TMLHE
- (2011) Patricia B.S. Celestino-Soper et al. HUMAN MOLECULAR GENETICS
- Mitochondrial dysfunction in autism spectrum disorders: a systematic review and meta-analysis
- (2011) D A Rossignol et al. MOLECULAR PSYCHIATRY
- Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism
- (2011) Stephan J. Sanders et al. NEURON
- Widespread Regulation of miRNA Biogenesis at the Dicer Step by the Cold-Inducible RNA-Binding Protein, RBM3
- (2011) Julie Pilotte et al. PLoS One
- The Genetics of Autism Spectrum Disorders and Related Neuropsychiatric Disorders in Childhood
- (2010) Paul Lichtenstein et al. AMERICAN JOURNAL OF PSYCHIATRY
- Genetic Heterogeneity in Human Disease
- (2010) Jon McClellan et al. CELL
- The X-linked mental retardation gene PHF8 is a histone demethylase involved in neuronal differentiation
- (2010) Jihui Qiu et al. CELL RESEARCH
- PHF8 is a histone H3K9me2 demethylase regulating rRNA synthesis
- (2010) Ziqi Zhu et al. CELL RESEARCH
- Metabolism of acetyl-l-carnitine for energy and neurotransmitter synthesis in the immature rat brain
- (2010) Susanna Scafidi et al. JOURNAL OF NEUROCHEMISTRY
- Systematic resequencing of X-chromosome synaptic genes in autism spectrum disorder and schizophrenia
- (2010) A Piton et al. MOLECULAR PSYCHIATRY
- Functional impact of global rare copy number variation in autism spectrum disorders
- (2010) Dalila Pinto et al. NATURE
- Huwe1 ubiquitin ligase is essential to synchronize neuronal and glial differentiation in the developing cerebellum
- (2010) D. D'Arca et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Screening for Genomic Rearrangements and Methylation Abnormalities of the 15q11-q13 Region in Autism Spectrum Disorders
- (2009) Christel Depienne et al. BIOLOGICAL PSYCHIATRY
- Autism-associated familial microdeletion of Xp11.22
- (2009) Y Qiao et al. CLINICAL GENETICS
- A synaptic trek to autism
- (2009) Thomas Bourgeron CURRENT OPINION IN NEUROBIOLOGY
- Genetics of autistic disorders: review and clinical implications
- (2009) Christine M. Freitag et al. EUROPEAN CHILD & ADOLESCENT PSYCHIATRY
- Solution hybrid selection with ultra-long oligonucleotides for massively parallel targeted sequencing
- (2009) Andreas Gnirke et al. NATURE BIOTECHNOLOGY
- A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation
- (2009) Patrick S Tarpey et al. NATURE GENETICS
- Acylcarnitines: Role in brain
- (2009) Lauren L. Jones et al. PROGRESS IN LIPID RESEARCH
- Serotonin Mediates Behavioral Gregarization Underlying Swarm Formation in Desert Locusts
- (2009) M. L. Anstey et al. SCIENCE
- Genome-Wide Analyses of Exonic Copy Number Variants in a Family-Based Study Point to Novel Autism Susceptibility Genes
- (2009) Maja Bucan et al. PLoS Genetics
- Submicroscopic Duplications of the Hydroxysteroid Dehydrogenase HSD17B10 and the E3 Ubiquitin Ligase HUWE1 Are Associated with Mental Retardation
- (2008) Guy Froyen et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Teneurin-1 is expressed in interconnected regions of the developing brain and is processed in vivo
- (2008) Daniela Kenzelmann et al. BMC DEVELOPMENTAL BIOLOGY
- The HECT-domain ubiquitin ligase Huwe1 controls neural differentiation and proliferation by destabilizing the N-Myc oncoprotein
- (2008) Xudong Zhao et al. NATURE CELL BIOLOGY
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