The WNT2 gene polymorphism associated with speech delay inherent to autism-Reference-Cited by-同舟云学术

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The WNT2 gene polymorphism associated with speech delay inherent to autism

Published:2012-09 Issue:5 Volume:33 Page:1533-1540
ISSN:0891-4222
Container-title:Research in Developmental Disabilities
language:en
Short-container-title:Research in Developmental Disabilities

Author:

Lin Ping-I,Chien Yi-Ling,Wu Yu-Yu,Chen Chia-Hsiang,Gau Susan Shur-Fen,Huang Yu-Shu,Liu Shih-Kai,Tsai Wen-Che,Chiu Yen-Nan

Publisher

Elsevier BV

Subject

Clinical Psychology,Developmental and Educational Psychology

Reference43 articles.

1. Evidence for a language quantitative trait locus on chromosome 7q in multiplex autism families;Alarcon;American Journal of Human Genetics,2002

2. Quantitative genome scan and ordered-subsets analysis of autism endophenotypes support language QTLs;Alarcon;Molecular Psychiatry,2005

3. Molecular genetics and animal models in autistic disorder;Andres;Brain Research Bulletin,2002

4. A genome-wide scan for common alleles affecting risk for autism;Anney;Human Molecular Genetics,2010

5. Incorporating language phenotypes strengthens evidence of linkage to autism;Bradford;American Journal of Medical Genetics,2001

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1. Three Decades of Valproate: A Current Model for Studying Autism Spectrum Disorder;Current Neuropharmacology;2024-02

2. Genetic Aspects of Speech Disorders in Children;Neuroscience and Behavioral Physiology;2024-02

3. Genetic aspects of speech disorders in children;Zhurnal nevrologii i psikhiatrii im. S.S. Korsakova;2023

4. Roles of Wnt Signaling Pathway and ROR2 Receptor in Embryonic Development: An Update Review Article;Epigenetics Insights;2022-01

5. Principal Molecular Pathways Affected in Autism Spectrum Disorder;Nutritional Neurosciences;2022

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