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

Mengmeng ShiXinyi LengYing LiZihan ChenYe CaoTiffany ChungBonaventure Ym IpVincent Hl IpYannie Oy SooFlorence Sy FanSze Ho MaKaren MaAnne Y Y ChanLisa Wc AuHowan LeungAlexander Y LauVincent Ct MokKwong Wai ChoyZirui DongThomas W Leung

Published in: Stroke and vascular neurology (2021)

Our GS study suggests a role of rare genomic variants with various variant types contributing to the development of ICAD in Chinese patients.

Keyphrases

copy number
genome wide
dna methylation
single cell
gene expression