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Human Genomics|October 10, 2024
Fast and accurate DNASeq variant calling workflow composed of LUSH toolkitTaifu Wang, Youjin Zhang, Haoling Wang, et al.
Human Genomics|October 8, 2024
Comprehensive analysis of NGS-based expanded carrier screening and follow-up in southern and southwestern China: results from 3024 Chinese individualsQinlin Huang, Juan Wen, Hongyun Zhang, et al.
Human Genomics|August 17, 2024
Shaping the future of kidney genetics in Australia: proceedings from the KidGen policy implementation workshop 2023Amali Mallawaarachchi, Erik Biros, Trudie Harris, et al.
Human Genomics|August 7, 2024
Public perceptions of international genetic information sharing for biomedical research in China: a case study of the social media debate on the article "A Pangenome Reference of 36 Chinese Populations" published in NatureZhangyu Wang, Meng Wang, Li Du
Human Genomics|July 29, 2024
Clinical outcomes of patients with mut-type methylmalonic acidemia identified through expanded newborn screening in ChinaShiying Ling, Shengnan Wu, Ruixue Shuai, et al.
Human Genomics|October 30, 2024
Novel FLNC variants in pediatric cardiomyopathy: an insight into disease mechanismsRui Dong, Xin Zhou, Haiyan Zhang, et al.
Human Genomics|May 13, 2025
A survey on mutation spectrum in Iranian patients with limb-girdle muscular dystrophiesSheyda Khalilian, Mohadeseh Fathi, Raheleh Tangestani, et al.
Human Genomics|May 12, 2025
Prognostic significance of clonal hematopoiesis in STEMI: a 10-year follow-up reveals high-risk gene mutationsWen-Lang Fan, Jih-Kai Yeh, Li-Ching Hsieh, et al.
Human Genomics|April 26, 2025
Functional analyses of splice site variants in TCF12Angela Borst, Tilmann Schweitzer, Denise Horn, et al.
Human Genomics|March 29, 2025
Tapping natures rhythm: the role of season in mitochondrial function and genetics in the UK biobankAnastasios Papadam, Mihail Mihov, Adriana Koller, et al.
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