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Rapid Communication | Open Access

Clinically relevant variants detected in Chinese children with global developmental delay/intellectual disability: An exome-wide sequencing study

Yimeng Qiaoa,b,c,1, Nan Lvd,1, Tongchuan Lie,1, Ye Chenga,1, Yunqian Lia, Jiqiang Dongd, Meimei Hand, Yang Gud, Qing Shangd( ), Qinghe Xinga,f( )
Children’s Hospital of Fudan University and Institutes of Biomedical Sciences of Fudan University, Shanghai 201102, China
Henan Key Laboratory of Child Brain Injury, Department of Pediatrics, The 3rd Affiliated Hospital of Zhengzhou University and Institute of Neuroscience, Zhengzhou, Henan 450052, China
NHC Key Laboratory of Birth Defects Prevention, Henan Key Laboratory of Population Defects Prevention, Zhengzhou, Henan 450002, China
Children’s Hospital Affiliated to Zhengzhou University, Henan Children’s Hospital, Zhengzhou Children’s Hospital, Zhengzhou, Henan 450053, China
Puyang Maternity and Child Care Centers, Puyang, Henan 457005, China
Shanghai Center for Women and Children’s Health, Shanghai 201102, China

Peer review under responsibility of Chongqing Medical University.

1 These authors contributed equally to this work.

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Genes & Diseases
Volume 12 Issue 4,
July 2025
Article number: 101389
DOI: 10.1016/j.gendis.2024.101389

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Cite this article:
Qiao Y, Lv N, Li T, et al. Clinically relevant variants detected in Chinese children with global developmental delay/intellectual disability: An exome-wide sequencing study. Genes & Diseases, 2025, 12(4): 101389. https://doi.org/10.1016/j.gendis.2024.101389

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Received: 30 January 2024
Published: 09 August 2024
© 2024 The Authors.

This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).