| Extreme phenotypic diversity and nonpenetrance in families with the LMNA gene mutation R644C J Rankin, M Auer‐Grumbach, W Bagg, K Colclough, NT Duong, ... American journal of medical genetics Part A 146 (12), 1530-1542, 2008 | 138 | 2008 |
| The LINC complex and human disease P Meinke, TD Nguyen, MS Wehnert Biochemical Society Transactions 39 (6), 1693-1697, 2011 | 115 | 2011 |
| Identification of mutational hot spots in LMNA encoding lamin A/C in patients with familial dilated cardiomyopathy A Perrot, S Hussein, V Ruppert, HHJ Schmidt, MS Wehnert, NT Duong, ... Basic research in cardiology 104, 90-99, 2009 | 96 | 2009 |
| Nesprins: tissue-specific expression of epsilon and other short isoforms NT Duong, GE Morris, LT Lam, Q Zhang, CA Sewry, CM Shanahan, I Holt PloS one 9 (4), e94380, 2014 | 88 | 2014 |
| Extensive ethnolinguistic diversity in Vietnam reflects multiple sources of genetic diversity D Liu, NT Duong, ND Ton, N Van Phong, B Pakendorf, N Van Hai, ... Molecular biology and evolution 37 (9), 2503-2519, 2020 | 74 | 2020 |
| New ZMPSTE24 (FACE1) mutations in patients affected with restrictive dermopathy or related progeroid syndromes and mutation update CL Navarro, V Esteves-Vieira, S Courrier, A Boyer, T Duong Nguyen, ... European Journal of Human Genetics 22 (8), 1002-1011, 2014 | 63 | 2014 |
| Complete human mtDNA genome sequences from Vietnam and the phylogeography of Mainland Southeast Asia NT Duong, E Macholdt, ND Ton, L Arias, R Schröder, N Van Phong, ... Scientific Reports 8 (1), 11651, 2018 | 41 | 2018 |
| Regulation of dendritic cell function by insulin/IGF-1/PI3K/Akt signaling through klotho expression NT Xuan, NH Hoang, VP Nhung, NT Duong, NH Ha, NV Hai Journal of Receptors and Signal Transduction 37 (3), 297-303, 2017 | 39 | 2017 |
| Restrictive dermopathy: a rare laminopathy M Thill, TD Nguyen, M Wehnert, D Fischer, I Hausser, S Braun, C Jackisch Archives of gynecology and obstetrics 278, 201-208, 2008 | 34 | 2008 |
| Specific localization of nesprin-1-α2, the short isoform of nesprin-1 with a KASH domain, in developing, fetal and regenerating muscle, using a new monoclonal antibody I Holt, NT Duong, Q Zhang, LT Lam, CA Sewry, K Mamchaoui, ... BMC cell biology 17, 1-16, 2016 | 32 | 2016 |
| The paternal and maternal genetic history of Vietnamese populations E Macholdt, L Arias, NT Duong, ND Ton, N Van Phong, R Schröder, ... European Journal of Human Genetics 28 (5), 636-645, 2020 | 24 | 2020 |
| Whole genome sequencing and mutation rate analysis of trios with paternal dioxin exposure ND Ton, H Nakagawa, NH Ha, NT Duong, VP Nhung, LTT Hien, HTT Hue, ... Human Mutation 39 (10), 1384-1392, 2018 | 20 | 2018 |
| Polymorphisms of ABCG2 and SLC22A12 Genes Associated with Gout Risk in Vietnamese Population N Thuy Duong, N Thy Ngoc, N Tran Minh Thang, B Thi Hoai Phuong, ... Medicina 55 (1), 8, 2019 | 17 | 2019 |
| Rare and novel variants of PRKN and PINK1 genes in Vietnamese patients with early‐onset Parkinson’s disease ND Ton, ND Thuan, MTH Thuong, TTB Ngoc, VP Nhung, NTT Hoa, ... Molecular genetics & genomic medicine 8 (10), e1463, 2020 | 16 | 2020 |
| Clinical, radiographic, and genetic characteristics of hypohidrotic ectodermal dysplasia: A cross‐sectional study. VTN Ngoc, NT Duong, DT Chu, LM Hang, DH Viet, NM Duc, LQ Anh, ... Clinical genetics 94 (5), 2018 | 12 | 2018 |
| Huong le CL Navarro, V Esteves-Vieira, S Courrier, A Boyer, T Duong Nguyen TT, Meinke, P., Schroder, W., Cormier-Daire, V., Sznajer, Y., Amor, DJ …, 2014 | 9 | 2014 |
| Identification of novel missense mutations associated with non-syndromic syndactyly in two vietnamese trios by whole exome sequencing NT Ngoc, NT Duong, ND Ton, HH Duc, LTL Anh, N Van Hai Clinica Chimica Acta 506, 16-21, 2020 | 7 | 2020 |
| Cockayne syndrome without UV-sensitivity in Vietnamese siblings with novel ERCC8 variants NT Duong, TH Dinh, BS Möhl, S Hintze, DTT Ha, ND Ngoc, VC Dung, ... Aging (Albany NY) 14 (13), 5299, 2022 | 6 | 2022 |
| Characterization of newly isolated thermotolerant yeasts and evaluation of their potential for use in Cayratia trifolia wine production DTK Tien, HX Phong, M Yamada, HT Toan, NTP Dung Vietnam Journal of Science, Technology and Engineering 61 (1), 68-73, 2019 | 6 | 2019 |
| X-linked Emery-Dreifuss muscular dystrophy with lamin A deficiency and IBM inclusions. A Fidzianska, I Niebroj-Dobosz, A Madej-Pilarczyk, NT Duong, M Wehnert Clinical Neuropathology 29 (2), 78-83, 2010 | 6 | 2010 |
Nong Van Hai (Van Hai Nong)Professor & Senior Researcher, Institute of Genome Research (IGR), VAST, Hanoi, Vietnam在 igr.ac.vn 的电子邮件经过验证
