Protocadherin α (PCDHA) as a novel susceptibility gene for autism

A Anitha, I Thanseem, K Nakamura, K Yamada… - Journal of Psychiatry and …, 2013 - jpn.ca
Background: Synaptic dysfunction has been shown to be involved in the pathogenesis of
autism. We hypothesized that the protocadherin α gene cluster (PCDHA), which is involved …

Association of the neuronal cell adhesion molecule (NRCAM) gene variants with autism

T Marui, I Funatogawa, S Koishi… - International Journal …, 2009 - academic.oup.com
Autism is a severe neurodevelopmental disorder of early childhood. Genetic factors play an
important role in the aetiology of the disorder. In this study, we considered the NRCAM gene …

[HTML][HTML] Association between genetic variants in DUSP15, CNTNAP2, and PCDHA genes and risk of childhood autism spectrum disorder

F Fang, M Ge, J Liu, Z Zhang, H Yu, S Zhu, L Xu… - Behavioural …, 2021 - hindawi.com
Objective. Genetic factors play an important role in the development of autism spectrum
disorder (ASD). This case-control study was to determine the association between childhood …

Sociability deficits and altered amygdala circuits in mice lacking Pcdh10, an autism associated gene

H Schoch, AS Kreibich, SL Ferri, RS White… - Biological …, 2017 - Elsevier
Background Behavioral symptoms in individuals with autism spectrum disorder (ASD) have
been attributed to abnormal neuronal connectivity, but the molecular bases of these …

Expression and genetic variability of PCDH11Y, a gene specific to Homo sapiens and candidate for susceptibility to psychiatric disorders

CM Durand, C Kappeler, C Betancur… - American Journal of …, 2006 - Wiley Online Library
Synaptogenesis, the formation of functional synapses, is a crucial step for the development
of the central nervous system. Among the genes involved in this process are cell adhesion …

[HTML][HTML] Segregated expressions of autism risk genes Cdh11 and Cdh9 in autism-relevant regions of developing cerebellum

C Wang, YH Pan, Y Wang, G Blatt, XB Yuan - Molecular Brain, 2019 - Springer
Results of recent genome-wide association studies (GWAS) and whole genome sequencing
(WGS) highlighted type II cadherins as risk genes for autism spectrum disorders (ASD). To …

Neurotransmitter systems and neurotrophic factors in autism: association study of 37 genes suggests involvement of DDC

C Toma, A Hervás, N Balmaña, M Salgado… - The World Journal of …, 2013 - Taylor & Francis
Objectives. Neurotransmitter systems and neurotrophic factors can be considered strong
candidates for autism spectrum disorder (ASD). The serotoninergic and dopaminergic …

[HTML][HTML] A systematic review of common genetic variation and biological pathways in autism spectrum disorder

DA Rodriguez-Gomez, DP Garcia-Guaqueta… - BMC neuroscience, 2021 - Springer
Background Autism spectrum disorder (ASD) is a complex neurodevelopmental condition
characterized by persistent deficits in social communication and interaction. Common …

[HTML][HTML] Current knowledge on the genetics of autism and propositions for future research

T Bourgeron - Comptes rendus biologies, 2016 - Elsevier
Autism spectrum disorders (ASD) are a heterogeneous group of neuropsychiatric disorders
characterized by problems in social communication, as well as by the presence of restricted …

[HTML][HTML] Exome sequencing analysis of Japanese autism spectrum disorder case-control sample supports an increased burden of synaptic function-related genes

H Kimura, M Nakatochi, B Aleksic, J Guevara… - Translational …, 2022 - nature.com
Autism spectrum disorder (ASD) is a highly heritable, complex disorder in which rare
variants contribute significantly to disease risk. Although many genes have been associated …