A Novel Stratification Method in Linkage Studies to Address Inter- and Intra-Family Heterogeneity in Autism
出版年份 2013 全文链接
标题
A Novel Stratification Method in Linkage Studies to Address Inter- and Intra-Family Heterogeneity in Autism
作者
关键词
-
出版物
PLoS One
Volume 8, Issue 6, Pages e67569
出版商
Public Library of Science (PLoS)
发表日期
2013-06-27
DOI
10.1371/journal.pone.0067569
参考文献
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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。- An atypical 0.8 Mb inherited duplication of 22q11.2 associated with psychomotor impairment
- (2012) Céline Pebrel-Richard et al. European Journal of Medical Genetics
- A Noncoding RNA Antisense to Moesin at 5p14.1 in Autism
- (2012) T. Kerin et al. Science Translational Medicine
- Evidence for involvement of GNB1L in autism
- (2011) Ying-Zhang Chen et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS
- Tbx1: identification of a 22q11.2 gene as a risk factor for autism spectrum disorder in a mouse model
- (2011) Takeshi Hiramoto et al. HUMAN MOLECULAR GENETICS
- Novel Autism Subtype-Dependent Genetic Variants Are Revealed by Quantitative Trait and Subphenotype Association Analyses of Published GWAS Data
- (2011) Valerie W. Hu et al. PLoS One
- Novel variants of the SHANK3 gene in Japanese autistic patients with severe delayed speech development
- (2011) Chikako Waga et al. PSYCHIATRIC GENETICS
- Information from cochlear potentials and genetic mutations helps localize the lesion site in auditory neuropathy
- (2011) Rosamaria Santarelli Genome Medicine
- A double hit implicates DIAPH3 as an autism risk gene
- (2010) J A S Vorstman et al. MOLECULAR PSYCHIATRY
- Novel clustering of items from the Autism Diagnostic Interview-Revised to define phenotypes within autism spectrum disorders
- (2009) Valerie W. Hu et al. Autism Research
- Gene expression profiling differentiates autism case-controls and phenotypic variants of autism spectrum disorders: evidence for circadian rhythm dysfunction in severe autism
- (2009) Valerie W. Hu et al. Autism Research
- The effect of the COMT val158met polymorphism on neural correlates of semantic verbal fluency
- (2009) Axel Krug et al. EUROPEAN ARCHIVES OF PSYCHIATRY AND CLINICAL NEUROSCIENCE
- Family-based studies indicate association ofEngrailed 2gene with autism in an Indian population
- (2009) B. Sen et al. GENES BRAIN AND BEHAVIOR
- Linkage and linkage disequilibrium scan for autism loci in an extended pedigree from Finland
- (2009) Helena Kilpinen et al. HUMAN MOLECULAR GENETICS
- 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
- Diminished dosage of 22q11 genes disrupts neurogenesis and cortical development in a mouse model of 22q11 deletion/DiGeorge syndrome
- (2009) D. W. Meechan et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Linkage, Association, and Gene-Expression Analyses Identify CNTNAP2 as an Autism-Susceptibility Gene
- (2008) Maricela Alarcón et al. AMERICAN JOURNAL OF HUMAN GENETICS
- The association analysis of RELN and GRM8 genes with autistic spectrum disorder in chinese han population
- (2007) Hui Li et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS
- Association of the ENGRAILED 2 (EN2) gene with autism in Chinese Han population
- (2007) Lifang Wang et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS
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