The clinical significance of small copy number variants in neurodevelopmental disorders-Reference-Cited by-同舟云学术

The clinical significance of small copy number variants in neurodevelopmental disorders

Published:2014-08-08 Issue:10 Volume:51 Page:677-688
ISSN:0022-2593
Container-title:Journal of Medical Genetics
language:en
Short-container-title:J Med Genet

Author:

Asadollahi Reza,Oneda Beatrice,Joset Pascal,Azzarello-Burri Silvia,Bartholdi Deborah,Steindl Katharina,Vincent Marie,Cobilanschi Joana,Sticht Heinrich,Baldinger Rosa,Reissmann Regina,Sudholt Irene,Thiel Christian T,Ekici Arif B,Reis André,Bijlsma Emilia K,Andrieux Joris,Dieux Anne,FitzPatrick David,Ritter Susanne,Baumer Alessandra,Latal Beatrice,Plecko Barbara,Jenni Oskar G,Rauch Anita

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference60 articles.

1. Genomic rearrangements and gene copy-number alterations as a cause of nervous system disorders;Lee;Neuron,2006

2. A de novo convergence of autism genetics and molecular neuroscience;Krumm;Trends Neurosci,2014

3. Genetics of early onset cognitive impairment;Ropers;Annu Rev Genomics Hum Genet,2010

4. Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies;Miller;Am J Hum Genet,2010

5. Origins and functional impact of copy number variation in the human genome;Conrad;Nature,2010

Cited by 73 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. Low‐pass whole genome sequencing as a cost‐effective alternative to chromosomal microarray analysis for low‐ and middle‐income countries;American Journal of Medical Genetics Part A;2024-06-25

2. Severe manifestation of Rauch‐Azzarello syndrome associated with biallelic deletion of CTNND2;Clinical Genetics;2024-04-11

3. Low-pass whole genome sequencing as a cost-effective alternative to chromosomal microarray analysis for low- and middle-income countries;2023-12-28

4. Impact of Copy Number Variants and Polygenic Risk Scores on Psychopathology in the UK Biobank;Biological Psychiatry;2023-10

5. A pilot study on glutamate receptor and carrier gene variants and risk of childhood autism spectrum;Metabolic Brain Disease;2023-08-14