The ongoing dissection of the genetic architecture of autistic spectrum disorder
Published 2011 View Full Article
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Title
The ongoing dissection of the genetic architecture of autistic spectrum disorder
Authors
Keywords
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Journal
Molecular Autism
Volume 2, Issue 1, Pages 12
Publisher
Springer Nature
Online
2011-08-17
DOI
10.1186/2040-2392-2-12
References
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Related references
Note: Only part of the references are listed.- Autism Spectrum Disorders and Epigenetics
- (2011) Daria Grafodatskaya et al. JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY
- Direct Measure of the De Novo Mutation Rate in Autism and Schizophrenia Cohorts
- (2010) Philip Awadalla et al. AMERICAN JOURNAL OF HUMAN GENETICS
- De Novo Mutations in FOXP1 in Cases with Intellectual Disability, Autism, and Language Impairment
- (2010) Fadi F. Hamdan et al. AMERICAN JOURNAL OF HUMAN GENETICS
- A genome-wide scan for common alleles affecting risk for autism
- (2010) R. Anney et al. HUMAN MOLECULAR GENETICS
- Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls
- (2010) NATURE
- Functional impact of global rare copy number variation in autism spectrum disorders
- (2010) Dalila Pinto et al. NATURE
- The Genetics of Child Psychiatric Disorders: Focus on Autism and Tourette Syndrome
- (2010) Matthew W. State NEURON
- Key role for gene dosage and synaptic homeostasis in autism spectrum disorders
- (2010) Roberto Toro et al. TRENDS IN GENETICS
- Fragile X and autism: Intertwined at the molecular level leading to targeted treatments
- (2010) Randi Hagerman et al. Molecular Autism
- Genetics of autistic disorders: review and clinical implications
- (2009) Christine M. Freitag et al. EUROPEAN CHILD & ADOLESCENT PSYCHIATRY
- A genome-wide linkage and association scan reveals novel loci for autism
- (2009) Lauren A. Weiss et al. NATURE
- Common genetic variants on 5p14.1 associate with autism spectrum disorders
- (2009) Kai Wang et al. NATURE
- Structural Variation of Chromosomes in Autism Spectrum Disorder
- (2008) Christian R. Marshall et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Novel de novo SHANK3 mutation in autistic patients
- (2008) Julie Gauthier et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS
- Mutations in the calcium-related gene IL1RAPL1 are associated with autism
- (2008) A. Piton et al. HUMAN MOLECULAR GENETICS
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