Molecular and network disruptions in neurodevelopment uncovered by single cell transcriptomics analysis of CHD8 heterozygous cerebral organoids-Reference-Cited by-同舟云学术

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Molecular and network disruptions in neurodevelopment uncovered by single cell transcriptomics analysis of CHD8 heterozygous cerebral organoids

Published:2024-07 Issue:14 Volume:10 Page:e34862
ISSN:2405-8440
Container-title:Heliyon
language:en
Short-container-title:Heliyon

Author:

Astorkia Maider,Liu Yang^ORCID,Pedrosa Erika M.,Lachman Herbert M.,Zheng Deyou^ORCID

Funder

NIH

Publisher

Elsevier BV

Reference51 articles.

1. Sequencing chromosomal abnormalities reveals neurodevelopmental loci that confer risk across diagnostic boundaries;Talkowski;Cell,2012

2. Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations;O ’ Roak;Nature,2012

3. Multiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disorders;O'Roak;Science,2012

4. Patterns and rates of exonic de novo mutations in autism spectrum disorders;Neale;Nat,2012

5. Excess of rare, inherited truncating mutations in autism;Krumm;Nat. Genet.,2015

Cited by 1 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. CHD8 gene; minority participation in research; machine-learning autism screen;The Transmitter;2024

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