Works by Ha, Nguyen Hai

Results: 42
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    Rare and novel variants of PRKN and PINK1 genes in Vietnamese patients with early‐onset Parkinson's disease.

    Published in:
    Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 10, p. 1, doi. 10.1002/mgg3.1463
    By:
    • Ton, Nguyen Dang;
    • Thuan, Nguyen Duc;
    • Thuong, Ma Thi Huyen;
    • Ngoc, Tran Thi Bich;
    • Nhung, Vu Phuong;
    • Hoa, Nguyen Thi Thanh;
    • Nam, Nguyen Hoai;
    • Dung, Hoang Thi;
    • Son, Nhu Dinh;
    • Ba, Nguyen Van;
    • Bac, Nguyen Duy;
    • Tai, Tran Ngoc;
    • Dung, Le Thi Kim;
    • Hung, Nguyen Trong;
    • Duong, Nguyen Thuy;
    • Ha, Nguyen Hai;
    • Hai, Nong Van
    Publication type:
    Article
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    Investigating demic versus cultural diffusion and sex bias in the spread of Austronesian languages in Vietnam.

    Published in:
    PLoS ONE, 2024, v. 19, n. 6, p. 1, doi. 10.1371/journal.pone.0304964
    By:
    • Thao, Dinh Huong;
    • Dinh, Tran Huu;
    • Mitsunaga, Shigeki;
    • Duy, La Duc;
    • Phuong, Nguyen Thanh;
    • Anh, Nguyen Phuong;
    • Anh, Nguyen Tho;
    • Duc, Bui Minh;
    • Hue, Huynh Thi Thu;
    • Ha, Nguyen Hai;
    • Ton, Nguyen Dang;
    • Hübner, Alexander;
    • Pakendorf, Brigitte;
    • Stoneking, Mark;
    • Inoue, Ituro;
    • Duong, Nguyen Thuy;
    • Hai, Nong Van
    Publication type:
    Article
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    Polymorphic analysis of CYP2C9 gene in Vietnamese population.

    Published in:
    Molecular Biology Reports, 2018, v. 45, n. 5, p. 893, doi. 10.1007/s11033-018-4235-3
    By:
    • Vu, Nhung Phuong;
    • Ma, Thuong Thi Huyen;
    • Tran, Ngoc Thi Bich;
    • Huynh, Hue Thi Thu;
    • Nguyen, Ton Dang;
    • Nguyen, Duong Thuy;
    • Van Nong, Hai;
    • Lee, Ming Ta Michael;
    • Nguyen, Ha Hai
    Publication type:
    Article
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    Genetic analyses of Vietnamese patients with oculocutaneous albinism.

    Published in:
    Journal of Clinical Laboratory Analysis, 2022, v. 36, n. 9, p. 1, doi. 10.1002/jcla.24625
    By:
    • Thuong, Ma Thi Huyen;
    • Anh, Luong Thi Lan;
    • Nhung, Vu Phuong;
    • Ngoc, Tran Thi Bich;
    • Lan, Hoang Thu;
    • Phuong, Doan Kim;
    • Ha, Nguyen Hai;
    • Van Hai, Nong;
    • Ton, Nguyen Dang
    Publication type:
    Article
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    CYP2C19 genetic polymorphism in the Vietnamese population.

    Published in:
    Annals of Human Biology, 2019, v. 46, n. 6, p. 491, doi. 10.1080/03014460.2019.1687750
    By:
    • Vu, Nhung Phuong;
    • Nguyen, Hoa Thi Thanh;
    • Tran, Ngoc Thi Bich;
    • Nguyen, Ton Dang;
    • Huynh, Hue Thi Thu;
    • Nguyen, Xuan Thi;
    • Nguyen, Duong Thuy;
    • Nong, Hai Van;
    • Nguyen, Ha Hai
    Publication type:
    Article
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    Whole genome sequencing and mutation rate analysis of trios with paternal dioxin exposure.

    Published in:
    Human Mutation, 2018, v. 39, n. 10, p. 1384, doi. 10.1002/humu.23585
    By:
    • Ton, Nguyen Dang;
    • Nakagawa, Hidewaki;
    • Ha, Nguyen Hai;
    • Duong, Nguyen Thuy;
    • Nhung, Vu Phuong;
    • Hien, Le Thi Thu;
    • Hue, Huynh Thi Thu;
    • Hoang, Nguyen Huy;
    • Wong, Jing Hao;
    • Nakano, Kaoru;
    • Maejima, Kazuhiro;
    • Sasaki‐Oku, Aya;
    • Tsunoda, Tatsuhiko;
    • Fujimoto, Akihiro;
    • Van Hai, Nong
    Publication type:
    Article
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    Whole-genome mutational landscape of liver cancers displaying biliary phenotype reveals hepatitis impact and molecular diversity.

    Published in:
    Nature Communications, 2015, v. 6, n. 1, p. 6120, doi. 10.1038/ncomms7120
    By:
    • Fujimoto, Akihiro;
    • Furuta, Mayuko;
    • Shiraishi, Yuichi;
    • Gotoh, Kunihito;
    • Kawakami, Yoshiiku;
    • Arihiro, Koji;
    • Nakamura, Toru;
    • Ueno, Masaki;
    • Ariizumi, Shun-ichi;
    • Hai Nguyen, Ha;
    • Shigemizu, Daichi;
    • Abe, Tetsuo;
    • Boroevich, Keith A.;
    • Nakano, Kaoru;
    • Sasaki, Aya;
    • Kitada, Rina;
    • Maejima, Kazihiro;
    • Yamamoto, Yujiro;
    • Tanaka, Hiroko;
    • Shibuya, Tetsuo
    Publication type:
    Article
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    Whole Genome Sequencing of a Vietnamese Family from a Dioxin Contamination Hotspot Reveals Novel Variants in the Son with Undiagnosed Intellectual Disability.

    Published in:
    International Journal of Environmental Research & Public Health, 2018, v. 15, n. 12, p. 2629, doi. 10.3390/ijerph15122629
    By:
    • Nguyen, Dang Ton;
    • Nguyen, Hai Ha;
    • Nguyen, Thuy Duong;
    • Nguyen, Thi Thanh Hoa;
    • Nakano, Kaoru;
    • Maejima, Kazuhiro;
    • Sasaki-Oku, Aya;
    • Nguyen, Van Ba;
    • Nguyen, Duy Bac;
    • Le, Bach Quang;
    • Wong, Jing Hao;
    • Tsunoda, Tatsuhiko;
    • Nakagawa, Hidewaki;
    • Fujimoto, Akihiro;
    • Nong, Van Hai
    Publication type:
    Article
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    Whole-genome sequencing of liver cancers identifies etiological influences on mutation patterns and recurrent mutations in chromatin regulators.

    Published in:
    Nature Genetics, 2012, v. 44, n. 7, p. 760, doi. 10.1038/ng.2291
    By:
    • Fujimoto, Akihiro;
    • Totoki, Yasushi;
    • Abe, Tetsuo;
    • Boroevich, Keith A;
    • Hosoda, Fumie;
    • Nguyen, Ha Hai;
    • Aoki, Masayuki;
    • Hosono, Naoya;
    • Kubo, Michiaki;
    • Miya, Fuyuki;
    • Arai, Yasuhito;
    • Takahashi, Hiroyuki;
    • Shirakihara, Takuya;
    • Nagasaki, Masao;
    • Shibuya, Tetsuo;
    • Nakano, Kaoru;
    • Watanabe-Makino, Kumiko;
    • Tanaka, Hiroko;
    • Nakamura, Hiromi;
    • Kusuda, Jun
    Publication type:
    Article
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    ISG15 deficiency features a complex cellular phenotype that responds to treatment with itaconate and derivatives.

    Published in:
    Clinical & Translational Medicine, 2022, v. 12, n. 7, p. 1, doi. 10.1002/ctm2.931
    By:
    • Waqas, Syed Fakhar‐ul‐Hassnain;
    • Sohail, Aaqib;
    • Nguyen, Ariane Hai Ha;
    • Usman, Abdulai;
    • Ludwig, Tobias;
    • Wegner, Andre;
    • Malik, Muhammad Nasir Hayat;
    • Schuchardt, Sven;
    • Geffers, Robert;
    • Winterhoff, Moritz;
    • Merkert, Sylvia;
    • Martin, Ulrich;
    • Olmer, Ruth;
    • Lachmann, Nico;
    • Pessler, Frank
    Publication type:
    Article
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