Whole-exome sequencing in a family with a monozygotic twin pair concordant for autism spectrum disorder and a follow-up study-Reference-Cited by-同舟云学术

Whole-exome sequencing in a family with a monozygotic twin pair concordant for autism spectrum disorder and a follow-up study

Published:2015-09 Issue:1-2 Volume:229 Page:599-601
ISSN:0165-1781
Container-title:Psychiatry Research
language:en
Short-container-title:Psychiatry Research

Author:

Egawa Jun,Watanabe Yuichiro,Sugimoto Atsunori,Nunokawa Ayako,Shibuya Masako,Igeta Hirofumi,Inoue Emiko,Hoya Satoshi,Orime Naoki,Hayashi Taketsugu,Sugiyama Toshiro,Someya Toshiyuki

Funder

Grant-in-Aid for Scientific Research

Publisher

Elsevier BV

Subject

Biological Psychiatry,Psychiatry and Mental health

Reference7 articles.

1. A detailed association analysis between the tryptophan hydroxylase 2 (TPH2) gene and autism spectrum disorders in a Japanese population;Egawa;Psychiatry Res.,2012

2. Most genetic risk for autism resides with common variation;Gaugler;Nat. Genet.,2014

3. Rare truncating variations and risk of autism spectrum disorder: whole-exome sequencing of a multiplex family and follow-up study in a Japanese population;Inoue;Psychiatry Clin. Neurosci.,2015

4. Johnson, C.N., Damo, S.M., Chazin, W.J., 2014. EF-Hand Calcium-Binding Proteins. eLS 10.1002/9780470015902.a0003056.pub3.

5. WD-repeat proteins: structure characteristics, biological function, and their involvement in human diseases;Li;Cell. Mol. Life Sci.,2001

Cited by 6 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. Rare Pathogenic Variants Identified in Whole Exome Sequencing of Monozygotic Twins With Autism Spectrum Disorder;Pediatric Neurology;2024-09

2. Technical strategy for monozygotic twin discrimination by single-nucleotide variants;International Journal of Legal Medicine;2024-01-10

3. ASD Phenotype—Genotype Associations in Concordant and Discordant Monozygotic and Dizygotic Twins Stratified by Severity of Autistic Traits;International Journal of Molecular Sciences;2019-08-03

4. Family studies to find rare high risk variants in migraine;The Journal of Headache and Pain;2017-03-02

5. RareUNC13Bvariations and risk of schizophrenia: Whole-exome sequencing in a multiplex family and follow-up resequencing and a case-control study;American Journal of Medical Genetics Part B: Neuropsychiatric Genetics;2016-03-14