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Genome sequencing reveals the role of rare genomic variants in Chinese patients with symptomatic intracranial atherosclerotic disease

Authors

  • Mengmeng Shi Department of Obstetrics and Gynaecology, The Chinese University of Hong Kong, Hong Kong, ChinaKey Laboratory for Regenerative Medicine, Ministry of Education (Shenzhen Base), Shenzhen Research Institute, The Chinese University of Hong Kong, Shenzhen, ChinaHong Kong Hub of Paediatric Excellence, The Chinese University of Hong Kong, Hong Kong, China PubMed articlesGoogle scholar articles
  • Xinyi Leng Department of Medicine and Therapeutics, The Chinese University of Hong Kong, Prince of Wales Hospital, Hong Kong, China PubMed articlesGoogle scholar articles
  • Ying Li Department of Obstetrics and Gynaecology, The Chinese University of Hong Kong, Hong Kong, ChinaKey Laboratory for Regenerative Medicine, Ministry of Education (Shenzhen Base), Shenzhen Research Institute, The Chinese University of Hong Kong, Shenzhen, ChinaHong Kong Hub of Paediatric Excellence, The Chinese University of Hong Kong, Hong Kong, China PubMed articlesGoogle scholar articles
  • Zihan Chen Department of Obstetrics and Gynaecology, The Chinese University of Hong Kong, Hong Kong, ChinaKey Laboratory for Regenerative Medicine, Ministry of Education (Shenzhen Base), Shenzhen Research Institute, The Chinese University of Hong Kong, Shenzhen, ChinaHong Kong Hub of Paediatric Excellence, The Chinese University of Hong Kong, Hong Kong, China PubMed articlesGoogle scholar articles
  • Ye Cao Department of Obstetrics and Gynaecology, The Chinese University of Hong Kong, Hong Kong, ChinaDepartment of Paediatrics, The Chinese University of Hong Kong, Hong Kong, China PubMed articlesGoogle scholar articles
  • Tiffany Chung Department of Medicine and Therapeutics, The Chinese University of Hong Kong, Prince of Wales Hospital, Hong Kong, China PubMed articlesGoogle scholar articles
  • Bonaventure YM Ip Department of Medicine and Therapeutics, The Chinese University of Hong Kong, Prince of Wales Hospital, Hong Kong, China PubMed articlesGoogle scholar articles
  • Vincent HL Ip Department of Medicine and Therapeutics, The Chinese University of Hong Kong, Prince of Wales Hospital, Hong Kong, China PubMed articlesGoogle scholar articles
  • Yannie OY Soo Department of Medicine and Therapeutics, The Chinese University of Hong Kong, Prince of Wales Hospital, Hong Kong, China PubMed articlesGoogle scholar articles
  • Florence SY Fan Department of Medicine and Therapeutics, The Chinese University of Hong Kong, Prince of Wales Hospital, Hong Kong, China PubMed articlesGoogle scholar articles
  • Sze Ho Ma Department of Medicine and Therapeutics, The Chinese University of Hong Kong, Prince of Wales Hospital, Hong Kong, China PubMed articlesGoogle scholar articles
  • Karen Ma Department of Medicine and Therapeutics, The Chinese University of Hong Kong, Prince of Wales Hospital, Hong Kong, China PubMed articlesGoogle scholar articles
  • Anne Y Y Chan Department of Medicine and Therapeutics, The Chinese University of Hong Kong, Prince of Wales Hospital, Hong Kong, China PubMed articlesGoogle scholar articles
  • Lisa WC Au Department of Medicine and Therapeutics, The Chinese University of Hong Kong, Prince of Wales Hospital, Hong Kong, China PubMed articlesGoogle scholar articles
  • Howan Leung Department of Medicine and Therapeutics, The Chinese University of Hong Kong, Prince of Wales Hospital, Hong Kong, China PubMed articlesGoogle scholar articles
  • Alexander Y Lau Department of Medicine and Therapeutics, The Chinese University of Hong Kong, Prince of Wales Hospital, Hong Kong, China PubMed articlesGoogle scholar articles
  • Vincent CT Mok Department of Medicine and Therapeutics, The Chinese University of Hong Kong, Prince of Wales Hospital, Hong Kong, China PubMed articlesGoogle scholar articles
  • Kwong Wai Choy Department of Obstetrics and Gynaecology, The Chinese University of Hong Kong, Hong Kong, ChinaKey Laboratory for Regenerative Medicine, Ministry of Education (Shenzhen Base), Shenzhen Research Institute, The Chinese University of Hong Kong, Shenzhen, ChinaHong Kong Hub of Paediatric Excellence, The Chinese University of Hong Kong, Hong Kong, ChinaThe Chinese University of Hong Kong-Baylor College of Medicine Joint Center For Medical Genetics, The Chinese University of Hong Kong, Hong Kong, China PubMed articlesGoogle scholar articles
  • Zirui Dong Department of Obstetrics and Gynaecology, The Chinese University of Hong Kong, Hong Kong, ChinaKey Laboratory for Regenerative Medicine, Ministry of Education (Shenzhen Base), Shenzhen Research Institute, The Chinese University of Hong Kong, Shenzhen, ChinaHong Kong Hub of Paediatric Excellence, The Chinese University of Hong Kong, Hong Kong, China PubMed articlesGoogle scholar articles
  • Thomas W Leung Department of Medicine and Therapeutics, The Chinese University of Hong Kong, Prince of Wales Hospital, Hong Kong, China PubMed articlesGoogle scholar articles
  1. Correspondence to Dr Zirui Dong; elvisdong{at}cuhk.edu.hk; Professor Thomas W Leung; drtleung{at}cuhk.edu.hk
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Citation

Shi M, Leng X, Li Y, et al
Genome sequencing reveals the role of rare genomic variants in Chinese patients with symptomatic intracranial atherosclerotic disease

Publication history

  • Received June 4, 2021
  • Accepted October 27, 2021
  • First published December 8, 2021.
  • Supplementary Data

    This web only file has been produced by the BMJ Publishing Group from an electronic file supplied by the author(s) and has not been edited for content.

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