Dau‐Ming Niu

4.6k total citations
173 papers, 3.2k citations indexed

About

Dau‐Ming Niu is a scholar working on Physiology, Molecular Biology and Epidemiology. According to data from OpenAlex, Dau‐Ming Niu has authored 173 papers receiving a total of 3.2k indexed citations (citations by other indexed papers that have themselves been cited), including 88 papers in Physiology, 54 papers in Molecular Biology and 50 papers in Epidemiology. Recurrent topics in Dau‐Ming Niu's work include Lysosomal Storage Disorders Research (84 papers), Trypanosoma species research and implications (44 papers) and Glycogen Storage Diseases and Myoclonus (35 papers). Dau‐Ming Niu is often cited by papers focused on Lysosomal Storage Disorders Research (84 papers), Trypanosoma species research and implications (44 papers) and Glycogen Storage Diseases and Myoclonus (35 papers). Dau‐Ming Niu collaborates with scholars based in Taiwan, United States and Brazil. Dau‐Ming Niu's co-authors include Hsiang‐Yu Lin, Chih‐Kuang Chuang, Ming‐Ren Chen, Ting‐Rong Hsu, Shuan‐Pei Lin, Wuh‐Liang Hwu, Chuan-Chi Chiang, Chuan‐Hong Kao, Chia‐Feng Yang and Ching‐Yuang Lin and has published in prestigious journals such as SHILAP Revista de lepidopterología, The Journal of Immunology and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Dau‐Ming Niu

167 papers receiving 3.1k citations

Peers

Countries citing papers authored by Dau‐Ming Niu

Since Specialization

Citations

This map shows the geographic impact of Dau‐Ming Niu's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Dau‐Ming Niu with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Dau‐Ming Niu more than expected).

Fields of papers citing papers by Dau‐Ming Niu

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Dau‐Ming Niu. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Dau‐Ming Niu. The network helps show where Dau‐Ming Niu may publish in the future.

Co-authorship network of co-authors of Dau‐Ming Niu

This figure shows the co-authorship network connecting the top 25 collaborators of Dau‐Ming Niu. A scholar is included among the top collaborators of Dau‐Ming Niu based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Dau‐Ming Niu. Dau‐Ming Niu is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Two decades of experience of the Fabry Outcome Survey provides further confirmation of the long-term effectiveness of agalsidase alfa enzyme replacement therapy 2025 ·Molecular Genetics and Metabolism Reports ·Uma Ramaswami, Guillem Pintos‐Morell, Christoph Kampmann, Kathy Nicholls, Dau‐Ming Niu, Ricardo Reisin, Michael L. West, Christina Anagnostopoulou, (unknown), (unknown), (unknown), Derralynn Hughes, Roberto Giugliani	3
2	Prognostic Implications of Left Ventricular Hypertrophy and Mechanical Function in Fabry Disease: A Longitudinal Cohort Study 2024 ·Journal of the American Society of Echocardiography ·(unknown), Ling Kuo, Shih‐Hsien Sung, Dau‐Ming Niu, Wen‐Chung Yu	6
3	Consensus recommendations for the treatment and management of patients with Fabry disease on migalastat: a modified Delphi study 2023 ·Frontiers in Medicine ·Daniel G. Bichet, Robert J. Hopkin, (unknown), Sridhar R. Allam, Yin‐Hsiu Chien, Roberto Giugliani, Staci Kallish, (unknown), Olivier Lidove, Dau‐Ming Niu, (unknown), Juan Politei, (unknown), Roser Torrá, Camilla Tøndel, Derralynn Hughes	10
4	Association of Fabry Disease with Hearing Loss, Tinnitus, and Sudden Hearing Loss: A Nationwide Population-Based Study 2022 ·Journal of Clinical Medicine ·Yen‐Fu Cheng, Sudha Xirasagar, (unknown), Dau‐Ming Niu, Herng‐Ching Lin	5
5	The benefits and challenges of family genetic testing in rare genetic diseases—lessons from Fabry disease 2021 ·Molecular Genetics & Genomic Medicine ·Dominique P. Germain, Sergey Moiseev, Fernando Suárez‐Obando, (unknown), (unknown), Gheona Altarescu, Fellype Carvalho Barreto, (unknown), (unknown), И. А. Максимова, (unknown), Sheela Nampoothiri, (unknown), Dau‐Ming Niu, Juan Politei, Long‐Sun Ro, Dũng Chí Vũ, Nan Chen, Sergey I. Kutsev	30
6	Airway abnormalities in very early treated infantile‐onset Pompe disease: A large‐scale survey by flexible bronchoscopy 2020 ·American Journal of Medical Genetics Part A ·Chia‐Feng Yang, Dau‐Ming Niu, Shyh‐Kuan Tai, (unknown), (unknown), Lingyi Huang, (unknown)	10
7	Cardiac Evaluation Using Two-Dimensional Speckle-Tracking Echocardiography and Conventional Echocardiography in Taiwanese Patients with Mucopolysaccharidoses 2020 ·Diagnostics ·Hsiang‐Yu Lin, Chih‐Kuang Chuang, Chung‐Lin Lee, Ming‐Ren Chen, Kuo‐Tzu Sung, (unknown), (unknown), Charles Jia‐Yin Hou, Dau‐Ming Niu, Tung‐Ming Chang, Chung‐Lieh Hung, (unknown), (unknown)	10
8	Very rare condition of multiple Gaucheroma: A case report and review of the literature 2019 ·Molecular Genetics and Metabolism Reports ·(unknown), Dau‐Ming Niu, (unknown), (unknown), (unknown), (unknown), Hsuan-Chieh Liao, Chuan-Chi Chiang, Hui‐Chen Ho, (unknown), Chia‐Feng Yang	15
9	Mucopolysaccharidosis III in Taiwan: Natural history, clinical and molecular characteristics of 28 patients diagnosed during a 21‐year period 2018 ·American Journal of Medical Genetics Part A ·Hsiang‐Yu Lin, Chih‐Kuang Chuang, Chung‐Lin Lee, (unknown), (unknown), Pao Chin Chiu, Dau‐Ming Niu, Yi‐Ya Fang, (unknown), Fuu‐Jen Tsai, Wuh‐Liang Hwu, Shio Jean Lin, Tung‐Ming Chang	23
10	Cardiac structure and function and effects of enzyme replacement therapy in patients with mucopolysaccharidoses I, II, IVA and VI 2016 ·Molecular Genetics and Metabolism ·Hsiang‐Yu Lin, Chih‐Kuang Chuang, (unknown), (unknown), (unknown), Chung‐Lieh Hung, (unknown), Pao Chin Chiu, Wen-Hui Tsai, Dau‐Ming Niu, Fuu‐Jen Tsai, Shio Jean Lin, Wuh‐Liang Hwu, Ju-Li Lin, (unknown), (unknown)	34
11	AB067. Glucose tetrasaccharide (Glc4) level in urine sample as a biomarker for Pompe patients. 2015 ·Annals of Translational Medicine ·Chun‐Kai Huang, Hsuan-Chieh Liao, (unknown), Ya‐Chi Chen, Chia‐Feng Yang, Dau‐Ming Niu	1
12	A novel mutation of KCNJ11 gene in a patient with permanent neonatal diabetes mellitus 2014 ·Diabetes Research and Clinical Practice ·Wei‐Lun Chang, (unknown), (unknown), Dau‐Ming Niu, Chih‐Yang Chiu, Tjin‐Shing Jap	3
13	A novel mutation of ABCG5 gene in a Turkish boy with phytosterolemia presenting with macrotrombocytopenia and stomatocytosis 2014 ·Pediatric Blood & Cancer ·Zühre Kaya, Dau‐Ming Niu, Aslı Yorulmaz, Aziz Tekin, Türkiz Gursel	15
14	Assessment of bone mineral density by dual energy x-ray absorptiometry in patients with mucopolysaccharidoses 2013 ·Orphanet Journal of Rare Diseases ·Hsiang‐Yu Lin, Shou‐Chuan Shih, Chih‐Kuang Chuang, Ming‐Ren Chen, Dau‐Ming Niu, Shuan‐Pei Lin	32
15	TLR2 Agonists Enhance CD8+Foxp3+ Regulatory T Cells and Suppress Th2 Immune Responses during Allergen Immunotherapy 2010 ·The Journal of Immunology ·Yi‐Giien Tsai, Kuender D. Yang, Dau‐Ming Niu, Jien‐Wen Chien, Ching‐Yuang Lin	56
16	Enzyme replacement therapy for mucopolysaccharidosis VI—experience in Taiwan 2010 ·Journal of Inherited Metabolic Disease ·Hsiang‐Yu Lin, Ming‐Ren Chen, Chih‐Kuang Chuang, Chih‐Ping Chen, Dar‐Shong Lin, Yin‐Hsiu Chien, (unknown), Fuu‐Jen Tsai, (unknown), Shio‐Jean Lin, Wuh‐Liang Hwu, Dau‐Ming Niu, Ni‐Chung Lee	23
17	Six New Mutations of the Thyroglobulin Gene Discovered in Taiwanese Children Presenting with Thyroid Dyshormonogenesis 2009 ·The Journal of Clinical Endocrinology & Metabolism ·Dau‐Ming Niu, (unknown), (unknown), (unknown), (unknown), Chuan‐Hong Kao, (unknown), (unknown), Tjin‐Shing Jap	30
18	Incidence of the mucopolysaccharidoses in Taiwan, 1984–2004 2009 ·American Journal of Medical Genetics Part A ·Hsiang‐Yu Lin, Chih‐Kuang Chuang, Dau‐Ming Niu, Ming‐Ren Chen, Fuu‐Jen Tsai, Mei‐Chyn Chao, (unknown), Shio‐Jean Lin, Li‐Ping Tsai, Wuh‐Liang Hwu, Ju‐Li Lin	150
19	Dysregulation of C/EBPα by mutant Huntingtin causes the urea cycle deficiency in Huntington's disease 2007 ·Human Molecular Genetics ·Ming‐Chang Chiang, Huimei Chen, Yi-Hsin Lee, (unknown), (unknown), Bing‐Wen Soong, Chiung‐Mei Chen, Yih‐Ru Wu, Chin‐San Liu, Dau‐Ming Niu, Jer‐Yuarn Wu, Yuan-Tsong Chen, Yijuang Chern	80
20	Clinical Features of Ehlers-Danlos Syndrome 2006 ·Journal of the Formosan Medical Association ·(unknown), Shuan‐Pei Lin, Ming‐Ren Chen, Dau‐Ming Niu	58

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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