Impact of on-site clinical genetics consultations on diagnostic rate in children and young adults with autism spectrum disorder-Reference-Cited by-同舟云学术

Impact of on-site clinical genetics consultations on diagnostic rate in children and young adults with autism spectrum disorder

Published:2019-08-07 Issue:1 Volume:10 Page:
ISSN:2040-2392
Container-title:Molecular Autism
language:en
Short-container-title:Molecular Autism

Author:

Munnich Arnold,Demily Caroline^ORCID,Frugère Lisa,Duwime Charlyne,Malan Valérie,Barcia Giulia,Vidal Céline,Throo Emeline,Besmond Claude,Hubert Laurence,Roland-Manuel Gilles,Malen Jean-Pierre,Ferreri Mélanie,Hanein Sylvain,Thalabard Jean-Christophe,Boddaert Nathalie,Assouline Moïse

Publisher

Springer Science and Business Media LLC

Subject

Psychiatry and Mental health,Developmental Biology,Developmental Neuroscience,Molecular Biology

Link

http://link.springer.com/content/pdf/10.1186/s13229-019-0284-2.pdf

Reference23 articles.

1. Charman T. The new genetics of autism: a translational opportunity? Lancet Psychiatry. 2015;10:856–7.

2. Lai MC, Lombardo MV, Baron-Cohen S. Autism. Lancet. 2014;383:896–910.

3. American Psychiatric Association. Diagnostic and Statistical Manual of Mental Disorders. 5th Edn. Washington, DC: American Psychiatric Association; 2013.

4. Leroy C, Jacquemont ML, Doray B. Xq25 duplication: the crucial role of the STAG2 gene in this novel human cohesinopathy. Clin Genet. 2016;89:68–73.

5. Kearney HM, Thorland EC, Brown KK, Quintero-Rivera F, South ST. Working Group of the American College of Medical Genetics Laboratory Quality Assurance Committee. American College of Medical Genetics standards and guidelines for interpretation and reporting of postnatal constitutional copy number variants. Genet Med 2011; 13:680–685.

Cited by 32 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. Fluorescence Signal Enhancement-Based On-Site Single-Molecule Sensing: A Review;IEEE Sensors Journal;2024-07-01

2. CNVs in Patients with Neurodevelopmental Disorders: Meta-Analysis;Russian Journal of Genetics;2024-05

3. Detection of autism spectrum disorder-related pathogenic trio variants by a novel structure-based approach;Molecular Autism;2024-04-03

4. A cohort study of neurodevelopmental disorders and/or congenital anomalies using high resolution chromosomal microarrays in southern Brazil highlighting the significance of ASD;Scientific Reports;2024-02-14

5. Reanalysis of Trio Whole-Genome Sequencing Data Doubles the Yield in Autism Spectrum Disorder: De Novo Variants Present in Half;International Journal of Molecular Sciences;2024-01-18