Rare copy number variants are common in young children with autism spectrum disorder-Reference-Cited by-同舟云学术

Rare copy number variants are common in young children with autism spectrum disorder

Published:2015-03-11 Issue:6 Volume:104 Page:610-618
ISSN:0803-5253
Container-title:Acta Paediatrica
language:en
Short-container-title:Acta Paediatr

Author:

Eriksson Mats Anders¹²³,Liedén Agne⁴⁵,Westerlund Joakim⁶,Bremer Anna⁷,Wincent Josephine⁴,Sahlin Ellika⁴⁵,Gillberg Christopher³,Fernell Elisabeth³,Anderlid Britt-Marie⁴⁵

Affiliation:

1. Department of Women's and Children's Health; Karolinska Institutet; Stockholm Sweden

2. Department of Neuropediatrics; Astrid Lindgren's Children's Hospital; Karolinska University Hospital; Stockholm Sweden

3. Gillberg Neuropsychiatry Centre; Sahlgrenska Academy; Gothenburg University; Gothenburg Sweden

4. Department of Molecular Medicine and Surgery and Centre for Molecular Medicine; Karolinska Institutet; Stockholm Sweden

5. Department of Clinical Genetics; Karolinska University Hospital; Stockholm Sweden

6. Department of Psychology; Stockholm University; Stockholm Sweden

7. Division of Clinical Genetics; University Hospital; Linköping Sweden

Publisher

Wiley

Subject

General Medicine,Pediatrics, Perinatology and Child Health

Reference34 articles.

1. The genetic landscapes of autism spectrum disorders;Huguet;Annu Rev Genomics Hum Genet,2013

2. Global variation in copy number in the human genome;Redon;Nature,2006

3. Detection and characterization of copy number variation in autism spectrum disorder;Marshall;Methods Mol Biol,2012

4. Functional impact of global rare copy number variation in autism spectrum disorders;Pinto;Nature,2010

5. Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism;Sanders;Neuron,2011

Cited by 19 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. Toward 3D facial analysis for recognizing Mendelian causes of autism spectrum disorder;Clinical Genetics;2024-07-26

2. Loss of CNTNAP2 Alters Human Cortical Excitatory Neuron Differentiation and Neural Network Development;Biological Psychiatry;2023-11

3. Prenatal Diagnosis of a de novo 2q14.3-q22.1 Deletion with Complex Chromosomal Rearrangement;Molecular Syndromology;2023-09-18

4. Screening for FMR1 CGG Repeat Expansion in Thai Patients with Autism Spectrum Disorder;BioMed Research International;2021-12-08

5. Copy number variations in a Brazilian cohort with autism spectrum disorders highlight the contribution of cell adhesion genes;Clinical Genetics;2021-11-15