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Frontiers in Genetics|October 30, 2023
Novel mutations in the SGCA gene in unrelated Vietnamese patients with limb-girdle muscular dystrophies diseaseNam Chung Tran, Nguyen Thi Kim Lien, Thanh Dat Ta, et al.Diagnostics (Basel, Switzerland)|October 29, 2025
Identifying Pathogenic Variants in Vietnamese Children with Functional Single Ventricle Based on Whole-Exome SequencingLe Trong Tu, Nguyen Thi Kim Lien, Nguyen Van Tung, et al.3 Biotech|November 27, 2023
Draft genome sequencing of halotolerant bacterium Salinicola sp. DM10 unravels plant growth-promoting potentialsNgoc-Lan Nguyen, Vu Van Dung, Nguyen Van Tung, et al.Journal of Fungi (Basel, Switzerland)|May 24, 2024
Genome Characteristics of the Endophytic Fungus Talaromyces sp. DC2 Isolated from Catharanthus roseus (L.) G. DonNguyen Duc Quan, Ngoc-Lan Nguyen, Tran Thi Huong Giang, et al.Diagnostics (Basel, Switzerland)|September 14, 2024
Identifying the Pathogenic Variants in Heart Genes in Vietnamese Sudden Unexplained Death Victims by Next-Generation SequencingTho Nguyen Tat, Nguyen Thi Kim Lien, Hung Luu Sy, et al.Frontiers in Genetics|June 12, 2026
Case Report: A case series of using whole exome sequencing to detect novel variants in Vietnamese patients with inborn errors of immunityNguyen Thi Kim Lien, Nguyen Van Tung, Le Thi Minh Huong, et al.Diagnostics (Basel, Switzerland)|July 12, 2025
Novel Splice Variant in the HES7 Gene in Vietnamese Patient with Spondylocostal Dysostosis 4: A Case Report and Literature ReviewHa Minh Nguyen, Nguyen Thi Kim Lien, Thinh Huy Tran, et al.Frontiers in Pediatrics|March 6, 2023
Case Report: Novel rare mutation c.6353C > G in the ABCA12 gene causing harlequin ichthyosis identified by whole exome sequencingVan Khanh Tran, Quang Minh Diep, Qiu Zilong, et al.Medicine|November 8, 2025
Novel variants related to extreme elevation of serum IgE in Vietnamese patients with primary immunodeficiency: Case reportLe Thi Minh Huong, Nguyen Thi Kim Lien, Nguyen Thi Van Anh, et al.Frontiers in Pediatrics|December 25, 2024
Case Report: A novel hemizygous missense PDHA1 variant in a Vietnamese boy with pyruvate dehydrogenase E1-alpha deficiencyThi Thanh Ngan Nguyen, Nguyen Ngoc Khanh, Chi Dung Vu, et al.Pageof 3