Paul Wuh-Liang Hwu (Wuh-Liang Hwu)

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 27

Top Venues

Gene therapy

Orphanet journal of rare diseases

International journal of neonatal screening

Journal of biomedical science

National Taiwan University Hospital

National Taiwan University (PHD)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

National Taiwan University Hospital

Taiwan

Attending Physician :: Department of Medical Genetics

National Taiwan University Hospital

Taiwan

Professor :: Department of Pediatrics

National Taiwan University Hospital

Taiwan

pres Professor :: Department of Pediatrics

Mayo Clinic

United States

Visiting Scientist :: Department of Medical Genetics

National Taiwan University Hospital

Taiwan

pres Attending Physician :: Department of Medical Genetics and Pediatrics

National Taiwan University Hospital

Taiwan

Director :: Department of Medical Genetics

National Taiwan University Hospital

Taiwan

Associated Professor :: Department of Pediatrics

National Taiwan University Hospital

Taiwan

Assistant Professor :: Department of Pediatrics

National Taiwan University Hospital

Taiwan

Assistant Professor :: College of Medicine

National Taiwan University Hospital

Taiwan

Lecturer :: Department of Pediatrics

Johns Hopkins University

United States

Postdoctoral Fellow :: Department of Genetics

National Taiwan University Hospital

Taiwan

Residency :: Department of Pediatrics

Education History

National Taiwan University

Taiwan

PHD :: Institute of Molecular Medicine

Publications

Paul Wuh-Liang Hwu, Karine Chang, Yu-Han Liu, Hao-Chun Wang, Ni-Chung Lee, Yin-Hsiu Chien
Gene therapy corrects the neurological deficits of mice with sialidosis. Gene therapy 31 (5-6) (2024)
Hui-Min Lee, Saadet Mercimek-Andrews, Gabriella Horvath, Diana Marchese, Richard E Poulin, Alexis Krolick, Kati-Lyn Tierney, Jasmine Turna, Judy Wei, Paul Wuh-Liang Hwu
A position statement on the post gene-therapy rehabilitation of aromatic I-amino acid decarboxylase deficiency patients. Orphanet journal of rare diseases 19 (1) (2024)
Paul Wuh-Liang Hwu
Gene therapy for ultrarare diseases: a geneticist's perspective. Journal of biomedical science 31 (1) (2024)
Paul Wuh-Liang Hwu, Karine Chang, Yu-Han Liu, Hao-Chun Wang, Ni-Chung Lee, Yin-Hsiu Chien
Gene therapy corrects the neurological deficits of mice with sialidosis. Gene therapy (2024)
Hui-Min Lee, Saadet Mercimek-Andrews, Gabriella Horvath, Diana Marchese, Richard E Poulin, Alexis Krolick, Kati-Lyn Tierney, Jasmine Turna, Judy Wei, Paul Wuh-Liang Hwu
A position statement on the post gene-therapy rehabilitation of aromatic I-amino acid decarboxylase deficiency patients. Orphanet journal of rare diseases 19 (1) (2024)
Paul Wuh-Liang Hwu, Karine Chang, Yu-Han Liu, Hao-Chun Wang, Ni-Chung Lee, Yin-Hsiu Chien
Gene therapy corrects the neurological deficits of mice with sialidosis. Gene therapy (2024)
Paul Wuh-Liang Hwu, Karine Chang, Yu-Han Liu, Hao-Chun Wang, Ni-Chung Lee, Yin-Hsiu Chien
Gene therapy corrects the neurological deficits of mice with sialidosis. Gene therapy 31 (5-6) (2024)
Paul Wuh-Liang Hwu
Gene therapy for ultrarare diseases: a geneticist's perspective. Journal of biomedical science 31 (1) (2024)
Hui-Min Lee, Saadet Mercimek-Andrews, Gabriella Horvath, Diana Marchese, Richard E Poulin, Alexis Krolick, Kati-Lyn Tierney, Jasmine Turna, Judy Wei, Paul Wuh-Liang Hwu
A position statement on the post gene-therapy rehabilitation of aromatic I-amino acid decarboxylase deficiency patients. Orphanet journal of rare diseases 19 (1) (2024)
Rai-Hseng Hsu, Hui-An Chen, Yin-Hsiu Chien, Paul Wuh-Liang Hwu, Ju-Li Lin, Hui-Ling Weng, Yi-Ting Lin, Yu-Ching Lin, Hung-Chang Lee
Bedtime extended release cornstarch improves biochemical profile and sleep quality for patients with glycogen storage disease type Ia. Molecular genetics & genomic medicine (2023)
Meng-Ju Melody Tsai, Miao-Zi Hung, Yi-Lin Lin, Hung-Chang Lee, Yin-Hsiu Chien, Paul Wuh-Liang Hwu
Curated incidence of lysosomal storage diseases from the Taiwan Biobank. NPJ genomic medicine 8 (1) (2023)
Paul Wuh-Liang Hwu, Rai-Hseng Hsu, Mei-Hsin Li, Hui-Min Lee, Hui-An Chen, Ni-Chung Lee, Yin-Hsiu Chien
Aromatic l-amino acid decarboxylase deficiency in Taiwan. JIMD reports 64 (5) (2023)
Rai-Hseng Hsu, Chen-Hao Lee, Yin-Hsiu Chien, Shuan-Pei Lin, Miao-Zi Hung, Nai-Chi Chen, Yi-Lin Lin, Paul Wuh-Liang Hwu, Hung-Chang Lee
Utility of whole-exome sequencing for patients with multiple congenital anomalies with or without intellectual disability/developmental delay in East Asia population. Molecular genetics & genomic medicine (2023)
Thomas O Crawford, Kathryn J Swoboda, Darryl C De Vivo, Enrico Silvio Bertini, Paul Wuh-Liang Hwu, Richard S Finkel, Janbernd Kirschner, Nancy L Kuntz, Aledie Navas Nazario, Julie A Parsons, Astrid Pechmann, Monique M Ryan, Russell J Butterfield, Haluk A Topaloglu, Tawfeg Ben-Omran, Valeria Ada Sansone, Yuh-Jyh Jong, Francy Shu, Cong Zhu, Stephanie Raynaud, Tiffany R Lago, Angela D Paradis, Richard Foster, Russell Chin, Zdenek Berger, null null
Continued benefit of nusinersen initiated in the presymptomatic stage of spinal muscular atrophy: 5-year update of the NURTURE study. Muscle & nerve (2023)
Yu-Shan Huang, Ching Hsu, Yu-Chang Chune, I-Cheng Liao, Hsin Wang, Yi-Lin Lin, Paul Wuh-Liang Hwu, Hung-Chang Lee, Feipei Lai
Diagnosis of a Single-Nucleotide Variant in Whole-Exome Sequencing Data for Patients With Inherited Diseases: Machine Learning Study Using Artificial Intelligence Variant Prioritization. JMIR bioinformatics and biotechnology 3 (1) (2022)
Yu-Shan Huang, Ching Hsu, Yu-Chang Chune, I-Cheng Liao, Hsin Wang, Yi-Lin Lin, Paul Wuh-Liang Hwu, Hung-Chang Lee, Feipei Lai
Diagnosis of a Single-Nucleotide Variant in Whole-Exome Sequencing Data for Patients With Inherited Diseases: Machine Learning Study Using Artificial Intelligence Variant Prioritization. JMIR bioinformatics and biotechnology 3 (1) (2022)
Paul Wuh-Liang Hwu, Karl Kiening, Irina Anselm, David R Compton, Takeshi Nakajima, Thomas Opladen, Phillip L Pearl, Agathe Roubertie, Thomas Roujeau, Shin-Ichi Muramatsu
Gene therapy in the putamen for curing AADC deficiency and Parkinson's disease. EMBO molecular medicine 13 (9) (2021)
Ngoc Thi Bich Can, Dien Minh Tran, Thao Phuong Bui, Khanh Ngoc Nguyen, Nguyen Huy Hoang, Nguyen Van Tung, Paul Wuh-Liang Hwu, Shunji Tomatsu, Dung Chi Vu
Molecular Analysis of Vietnamese Patients with Mucopolysaccharidosis Type I. Life (Basel, Switzerland) 11 (11) (2021)
Chih-Ling Chen, Chien-Nan Lee, Yin-Hsiu Chien, Paul Wuh-Liang Hwu, Tung-Ming Chang, Hung-Chang Lee
Novel Compound Heterozygous Variants in TBCD Gene Associated with Infantile Neurodegenerative Encephalopathy. Children (Basel, Switzerland) 8 (12) (2021)
Yin-Hsiu Chien, Ni-Chung Lee, Pin-Wen Chen, Hui-Ying Yeh, Michael H Gelb, Pao-Chin Chiu, Shao-Yin Chu, Chen-Hao Lee, An-Ru Lee, Paul Wuh-Liang Hwu
Newborn screening for Morquio disease and other lysosomal storage diseases: results from the 8-plex assay for 70,000 newborns. Orphanet journal of rare diseases 15 (1) (2020)
Paul Wuh-Liang Hwu, Yin-Hsiu Chien
Development of Newborn Screening for Pompe Disease. International journal of neonatal screening 6 (1) (2020)
Szu-Ju Chen, Bo-Chin Lee, Hung-Chang Lee, Yin-Hsiu Chien, Paul Wuh-Liang Hwu, Chin-Hsien Lin
Clinical, radiological, and genetic characteristics in patients with Huntington's disease in a Taiwanese cohort. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 183 (6) (2020)
Shu-Chuan Chiang, Yin-Hsiu Chien, Kai-Ling Chang, Ni-Chung Lee, Paul Wuh-Liang Hwu
The Timely Needs for Infantile Onset Pompe Disease Newborn Screening-Practice in Taiwan. International journal of neonatal screening 6 (2) (2020)
Chung-Lin Lee, Louis Tan Hock-Cheong Tan, Hsiang-Yu Lin, Paul Wuh-Liang Hwu, Hung-Chang Lee, Yin-Hsiu Chien, Chih-Kuang Chuang, Mei-Hwan Wu, Jou-Kou Wang, Shao-Yin Chu, Ju-Li Lin, Fu-Sung Lo, Pen-Hua Su, Chia-Chi Hsu, Yu-Yuan Ko, Ming-Ren Chen, Hui-Ching Chiu, Shuan-Pei Lin
Cardiac manifestations and gene mutations of patients with RASopathies in Taiwan. American journal of medical genetics. Part A 182 (2) (2019)
Hsiang-Yu Lin, Chung-Lin Lee, Pao Chin Chiu, Dau-Ming Niu, Fuu-Jen Tsai, Paul Wuh-Liang Hwu, Shio Jean Lin, Ju-Li Lin, Tung-Ming Chang, Chih-Kuang Chuang, Shuan-Pei Lin
Relationships among Height, Weight, Body Mass Index, and Age in Taiwanese Children with Different Types of Mucopolysaccharidoses. Diagnostics (Basel, Switzerland) 9 (4) (2019)
Ni-Chung Lee, Yin-Hsiu Chien, Paul Wuh-Liang Hwu
A review of aromatic l-amino acid decarboxylase (AADC) deficiency in Taiwan. American journal of medical genetics. Part C, Seminars in medical genetics 181 (2) (2019)
Shu-Chuan Chiang, Pin-Wen Chen, Paul Wuh-Liang Hwu, An-Ju Lee, Li-Chu Chen, Ni-Chung Lee, Li-Yan Chiou, Yin-Hsiu Chien
Performance of the Four-Plex Tandem Mass Spectrometry Lysosomal Storage Disease Newborn Screening Test: The Necessity of Adding a 2nd Tier Test for Pompe Disease. International journal of neonatal screening 4 (4) (2018)

Paul Wuh-Liang Hwu.css-eqlu8i{font-size:small;padding-left:4px;} (Wuh-Liang Hwu)

Publication Activity (10 Years)

Top Topics

Top Venues

Paul Wuh-Liang Hwu (Wuh-Liang Hwu)