Identification of novel driver risk genes in CNV loci associated with neurodevelopmental disorders-Reference-Cited by-同舟云学术

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Identification of novel driver risk genes in CNV loci associated with neurodevelopmental disorders

Published:2024-07 Issue:3 Volume:5 Page:100316
ISSN:2666-2477
Container-title:Human Genetics and Genomics Advances
language:en
Short-container-title:Human Genetics and Genomics Advances

Author:

Azidane Sara,Gallego Xavier,Durham Lynn,Cáceres Mario,Guney Emre,Pérez-Cano Laura

Funder

Wellcome Trust

Simons Foundation

Hartwell Foundation

Generalitat de Catalunya

Generalitat de Catalunya Agència de Gestió d'Ajuts Universitaris i de Recerca

Publisher

Elsevier BV

Reference50 articles.

1. De novo rates and selection of large copy number variation;Itsara;Genome Res.,2010

2. DNA copy number variation: Main characteristics, evolutionary significance, and pathological aspects;Pos;Biomed. J.,2021

3. An integrated analysis of rare CNV and exome variation in Autism Spectrum Disorder using the Infinium PsychArray;Bacchelli;Sci. Rep.,2020

4. Copy-number variation in the pathogenesis of autism spectrum disorder;Shishido;Psychiatry Clin. Neurosci.,2014

5. The rate of de novo CNVs in healthy controls;Barone,2019

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