Chromosomal microarray analysis in a cohort of underrepresented population identifies SERINC2 as a novel candidate gene for autism spectrum disorder-Reference-Cited by-同舟云学术

Chromosomal microarray analysis in a cohort of underrepresented population identifies SERINC2 as a novel candidate gene for autism spectrum disorder

Published:2017-09-21 Issue:1 Volume:7 Page:
ISSN:2045-2322
Container-title:Scientific Reports
language:en
Short-container-title:Sci Rep

Author:

Hnoonual Areerat,Thammachote Weerin,Tim-Aroon Thipwimol^ORCID,Rojnueangnit Kitiwan,Hansakunachai Tippawan,Sombuntham Tasanawat,Roongpraiwan Rawiwan,Worachotekamjorn Juthamas,Chuthapisith Jariya,Fucharoen Suthat,Wattanasirichaigoon Duangrurdee^ORCID,Ruangdaraganon Nichara,Limprasert Pornprot,Jinawath Natini

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Link

http://www.nature.com/articles/s41598-017-12317-3.pdf

Reference86 articles.

1. Prevalence and Characteristics of Autism Spectrum Disorder Among Children Aged 8 Years - Autism and Developmental Disabilities Monitoring Network, 11 Sites, United States, 2012. MMWR Surveill Summa. 65, 1–23 (2016).

2. Poolsuppasit, S., Panyayong, B., Liknapichitkul, D., Serisathien, P. & Chutha, W. Holistic Care for Thai Autism. J Ment Health Thai. 13, 10–16 (2005).

3. Huguet, G., Ey, E. & Bourgeron, T. The genetic landscapes of autism spectrum disorders. Annu Rev Genomics Hum Genet. 14, 191–213 (2013).

4. Battaglia, A. et al. Confirmation of chromosomal microarray as a first-tier clinical diagnostic test for individuals with developmental delay, intellectual disability, autism spectrum disorders and dysmorphic features. Eur J Paediatr Neurol. 17, 589–599 (2013).

5. Miller, D. T. et al. Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies. Am J Hum Genet. 86, 749–764 (2010).

Cited by 22 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. The Use of CGH Arrays for Identifying Copy Number Variations in Children with Autism Spectrum Disorder;Brain Sciences;2024-03-13

2. De novo copy number variations in candidate genomic regions in patients of severe autism spectrum disorder in Vietnam;PLOS ONE;2024-03-07

3. Identification of Novel Gene variants for Autism Spectrum Disorder in an Indian Patient using Whole Exome Sequencing;2024-03-02

4. Parental Perspectives on Early Life Screening and Genetic Testing for ASD: A Systematic Review;Journal of Autism and Developmental Disorders;2024-02-14

5. Serinc2 deficiency exacerbates sepsis-induced cardiomyopathy by enhancing necroptosis and apoptosis;Biochemical Pharmacology;2023-12