标题
A genome-wide scan for common alleles affecting risk for autism
作者
关键词
-
出版物
HUMAN MOLECULAR GENETICS
Volume 19, Issue 20, Pages 4072-4082
出版商
Oxford University Press (OUP)
发表日期
2010-07-28
DOI
10.1093/hmg/ddq307
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。- Functional impact of global rare copy number variation in autism spectrum disorders
- (2010) Dalila Pinto et al. NATURE
- Divergent impact of the polysialyltransferases ST8SiaII and ST8SiaIV on polysialic acid expression in immature neurons and interneurons of the adult cerebral cortex
- (2010) J. Nacher et al. NEUROSCIENCE
- A genome-wide association study of alcohol dependence
- (2010) L. J. Bierut et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Genome-Wide Association Studies of MRI-Defined Brain Infarcts
- (2010) Stéphanie Debette et al. STROKE
- A Unified Approach to Genotype Imputation and Haplotype-Phase Inference for Large Data Sets of Trios and Unrelated Individuals
- (2009) Brian L. Browning et al. AMERICAN JOURNAL OF HUMAN GENETICS
- A Genome-wide Association Study of Autism Reveals a Common Novel Risk Locus at 5p14.1
- (2009) Deqiong Ma et al. ANNALS OF HUMAN GENETICS
- Imbalance of neural cell adhesion molecule and polysialyltransferase alleles causes defective brain connectivity
- (2009) Herbert Hildebrandt et al. BRAIN
- Prevalence of autism-spectrum conditions: UK school-based population study
- (2009) Simon Baron-Cohen et al. BRITISH JOURNAL OF PSYCHIATRY
- NovelPTENmutations in neurodevelopmental disorders and macrocephaly
- (2009) A Orrico et al. CLINICAL GENETICS
- The prevalence of PTEN mutations in a clinical pediatric cohort with autism spectrum disorders, developmental delay, and macrocephaly
- (2009) Elizabeth A Varga et al. GENETICS IN MEDICINE
- Phenotypic spectrum associated with de novo and inherited deletions and duplications at 16p11.2 in individuals ascertained for diagnosis of autism spectrum disorder
- (2009) B. A. Fernandez et al. JOURNAL OF MEDICAL 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
- Autism genome-wide copy number variation reveals ubiquitin and neuronal genes
- (2009) Joseph T. Glessner et al. NATURE
- Epidemiology of Pervasive Developmental Disorders
- (2009) Eric Fombonne PEDIATRIC RESEARCH
- Elucidating the genetic architecture of familial schizophrenia using rare copy number variant and linkage scans
- (2009) B. Xu et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Genetic Architecture of Transcript-Level Variation in Humans
- (2008) Shiwei Duan et al. AMERICAN JOURNAL OF HUMAN GENETICS
- On the Use of General Control Samples for Genome-wide Association Studies: Genetic Matching Highlights Causal Variants
- (2008) Diana Luca et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Structural Variation of Chromosomes in Autism Spectrum Disorder
- (2008) Christian R. Marshall et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Genome-wide Linkage Analyses of Quantitative and Categorical Autism Subphenotypes
- (2008) Xiao-Qing Liu et al. BIOLOGICAL PSYCHIATRY
- Learning-associated regulation of polysialylated neural cell adhesion molecule expression in the rat prefrontal cortex is region-, cell type- and paradigm-specific
- (2008) Judith P. F. ter Horst et al. EUROPEAN JOURNAL OF NEUROSCIENCE
- Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis
- (2008) Sergio E. Baranzini et al. HUMAN MOLECULAR GENETICS
- Copy-number variations associated with neuropsychiatric conditions
- (2008) Edwin H. Cook Jr et al. NATURE
- Advances in autism genetics: on the threshold of a new neurobiology
- (2008) Brett S. Abrahams et al. NATURE REVIEWS GENETICS
- Association between Microdeletion and Microduplication at 16p11.2 and Autism
- (2008) Lauren A. Weiss et al. NEW ENGLAND JOURNAL OF MEDICINE
Publish scientific posters with Peeref
Peeref publishes scientific posters from all research disciplines. Our Diamond Open Access policy means free access to content and no publication fees for authors.
Learn MoreFind the ideal target journal for your manuscript
Explore over 38,000 international journals covering a vast array of academic fields.
Search