Si Houn Hahn

3.3k citations

81 papers · 2.4k indexed · h-index 27

Impact in

Clinical Biochemistry top 0.2%
- Metabolism and Genetic Disorders
Sensory Systems top 2%
- Hearing, Cochlea, Tinnitus, Genetics

Papers in

Clinical Biochemistry 28
- Metabolism and Genetic Disorders 28
Biochemistry 10
- Amino Acid Enzymes and Metabolism 9

Co-authors: Valeria Vasta Piero Rinaldo Irene J. Chang Dietrich Matern Mark J Magera Keehyun Park Sídney M. Gospe Kateřina Sadílková
Journals: Molecular Genetics and Metabolism (13 papers)Genetics in Medicine (7 papers)Journal of Inherited Metabolic Disease (4 papers)Human Mutation (3 papers)Clinical Chemistry (3 papers)
Partner nations: United States South Korea Germany

In The Last Decade

Si Houn Hahn

80 papers receiving 2.3k citations

Peers

Countries citing papers authored by Si Houn Hahn

Since Specialization

Citations

This map shows the geographic impact of Si Houn Hahn'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 Si Houn Hahn with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Si Houn Hahn more than expected).

Fields of papers citing papers by Si Houn Hahn

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Si Houn Hahn. 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 Si Houn Hahn. The network helps show where Si Houn Hahn may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Si Houn Hahn, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Si Houn Hahn Line = papers co-authored together Si Houn Hahn links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	The Mini-COMET Clinical Trial: Safety and Efficacy of Avalglucosidase Alfa after 97 Weeks of Treatment in Children with Infantile-Onset Pompe Disease Previously Treated with Alglucosidase Alfa The Journal of Pediatrics ·David Kronn, James Davison, Alexander Broomfield, Anaïs Brassier, François Labarthe, Si Houn Hahn, Satoko Kumada, Hirotaka Ohki, S. Grace Prakalapakorn, Catherine Wilson, Kristina An Haack, N. Asli, Susan Richards, Susan Sparks, Nicolas Hoffmann, Tianyue Zhou, Yin‐Hsiu Chien, Priya S. Kishnani	2025	0
2	ER-associated degradation in cystinosis pathogenesis and the prospects of precision medicine Journal of Clinical Investigation ·TAKEKAZU KOSAKI, Shirley Seltzer, Xi Yang, Jess G. Thoene, Si Houn Hahn, Ming Li	2023	4
3	Oncogenic signaling pathways and hallmarks of cancer in Korean patients with acral melanoma Computers in Biology and Medicine ·Frederico Serpa Santana Ferra, Hee Joo Kim, Yeeun Lee, Povar Mj, Sungwon Jung, Jin Sook Lee, Si Houn Hahn, Adam J. Criblez, Joo Young Roh, Seungyoon Nam	2023	3
4	A rapid and non-invasive proteomic analysis using DBS and buccal swab for multiplexed second-tier screening of Pompe disease and Mucopolysaccharidosis type I Molecular Genetics and Metabolism ·Tong Zhang, R C Stehle, Donghao Li, Christopher J. Collins, Alejandro Valderrama-Martínez, Jenny Thies, Irene J. Chang, Christina Lam, Angela Sun, Anna I. Scott, Koyano Wataru, L. Jeanty, Hamid Khaledi, Michael H. Gelb, Si Houn Hahn	2022	8
5	Safety and efficacy of avalglucosidase alfa in individuals with infantile-onset Pompe disease enrolled in the phase 2, open-label Mini-COMET study: The 6-month primary analysis report Genetics in Medicine ·Priya S. Kishnani, David Kronn, Anaïs Brassier, Alexander Broomfield, James Davison, Si Houn Hahn, Satoko Kumada, François Labarthe, Hirotaka Ohki, Shungo Nakayama, S. Grace Prakalapakorn, Kristina An Haack, Barbara Kittner, Vincensia Stefanny Trenggono, Susan Sparks, Catherine Wilson, Atef Zaher, Yin‐Hsiu Chien	2022	28
6	Motor Responses in Pediatric Pompe Disease in the ADVANCE Participant Cohort Journal of Neuromuscular Diseases ·Tina Duong, Priya S. Kishnani, Kristina An Haack, Meredith C. Foster, James B. Gibson, Catherine Wilson, Si Houn Hahn, Richard E. Hillman, David Kronn, Nancy D. Leslie, Loren Peña, Susan Sparks, David W. Stockton, Pranoot Tanpaiboon, John Day	2022	3
7	Clinical characteristics and genotypes in the ADVANCE baseline data set, a comprehensive cohort of US children and adolescents with Pompe disease Genetics in Medicine ·Priya S. Kishnani, James B. Gibson, Michael J. Gambello, Richard E. Hillman, David W. Stockton, David Kronn, Nancy D. Leslie, Loren Peña, Pranoot Tanpaiboon, John Day, Raymond Wang, Jennifer Goldstein, Kristina An Haack, Susan Sparks, Yang Zhao, Si Houn Hahn	2019	9
8	Rapid Multiplexed Proteomic Screening for Primary Immunodeficiency Disorders From Dried Blood Spots Frontiers in Immunology ·Christopher J. Collins, Irene J. Chang, Sunhee Jung, Donghao Li, Jeffrey R. Whiteaker, Gesmar Rodrigues Silva Segundo, Troy R. Torgerson, Hans D. Ochs, Amanda G. Paulovich, Si Houn Hahn	2018	22
9	A Korean Case of β-Ureidopropionase Deficiency Presenting with Intractable Seizure, Global Developmental Delay, and Microcephaly JIMD Reports ·Jun Hwa Lee, André B. P. Kuilenburg, N. G. G. M. Abeling, Valeria Vasta, Si Houn Hahn	2014	9
10	In vitro correction of disorders of lysosomal transport by microvesicles derived from baculovirus-infected Spodoptera cells Molecular Genetics and Metabolism ·Jess G. Thoene, Thomas J. Goss, Sun Quan-she, Dubravka Bojić Bultrini, Francisca N’Kuli, Patrick Van Deŕ Smissen, Pierre J. Courtoy, Si Houn Hahn	2013	13
11	Targeted exome sequencing for mitochondrial disorders reveals high genetic heterogeneity BMC Medical Genetics ·А.Л. Петречук, Valeria Vasta, John S. Penn, سامیة عبد الحفیظ یعقوب, Si Houn Hahn	2013	43
12	Preliminary investigation of the use of newborn dried blood spots for screening pyridoxine-dependent epilepsy by LC-MS/MS Molecular Genetics and Metabolism ·Sunhee Jung, Sérgio Bexiga, Sídney M. Gospe, Si Houn Hahn	2013	24
13	Next‐generation sequencing for mitochondrial diseases: A wide diagnostic spectrum Pediatrics International ·Valeria Vasta, J. Lawrence Merritt, Russell P. Saneto, Si Houn Hahn	2012	55
14	An Exceptional Family with Three Consecutive Generations Affected by Wilson Disease JIMD Reports ·James T. Bennett, Kathleen B. Schwarz, Phillip D. Swanson, Si Houn Hahn	2012	12
15	Infantile Periorificial and Intertriginous Dermatitis Preceding Sepsis‐Like Respiratory Failure Pediatric Dermatology ·Xiaozu Wu, K. KATSURADA, Si Houn Hahn, Kathleen Patterson, Heather A. Brandling‐Bennett	2011	8
16	Quality improvement of mitochondrial respiratory chain complex enzyme assays using Caenorhabditis elegans Genetics in Medicine ·Monika Tausend, David R. Thorburn, Lee-Jun Wong, Georgirene D. Vladutiu, Richard Haas, Thuy Le, Charles L. Hoppel, Margaret M. Sedensky, Philip G. Morgan, Si Houn Hahn	2011	17
17	Assay to Measure Oxidized and Reduced Forms of CoQ by LC–MS/MS Methods in molecular biology ·Si Houn Hahn, Muhammad Djabir D, Valeria Vasta	2011	9
18	Screening of newborns and high-risk group of children for inborn metabolic disorders using tandem mass spectrometry in South Korea: a three-year report Clinica Chimica Acta ·Junyun Liao, (unknown), 张明波, Seungwoo Kang, Dong Hwan Lee, Han‐Wook Yoo, Won‐Ki Min, Baki KURTİ, Son Moon Shin, Jong‐Won Kim, Junghan Song, Ho Joo Yoon, Niedya Inten Suwono, Si Houn Hahn	2005	68
19	Effect of metal ions on the stability of metallothionein in the degradation by cellular fractions in vitro Experimental & Molecular Medicine ·Si Houn Hahn, Ook Joon Yoo, William A. Gahl	2001	14
20	Acute Tyrosinemia Type 1 in a 5 Month Old Korean Boy Si Houn Hahn, Ki Soo Pai, Ki‐Bum Lee, Cabaleiro Goas M, Ok Hwa Kim, Sophie Schudel, Umesh Chandra Reddy Koduru, Seiji Yamaguchi	1996	1

About Si Houn Hahn

Si Houn Hahn is a scholar working on Clinical Biochemistry, Biochemistry, Nutrition and Dietetics, Hematology and Rheumatology, having authored 81 papers that have together received 2.4k indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (28 papers), Trace Elements in Health (17 papers), Mitochondrial Function and Pathology (16 papers), Lysosomal Storage Disorders Research (13 papers), Heavy Metal Exposure and Toxicity (11 papers), Iron Metabolism and Disorders (10 papers), Amino Acid Enzymes and Metabolism (9 papers) and Neonatal Health and Biochemistry (9 papers). The work is most often cited by research in Clinical Biochemistry (801 citations), Sensory Systems (160 citations), Biochemistry (220 citations), Nutrition and Dietetics (450 citations) and Hematology (265 citations). Si Houn Hahn has collaborated with scholars based in United States, South Korea and Germany. Frequent co-authors include Valeria Vasta, Piero Rinaldo, Irene J. Chang, Dietrich Matern, Mark J Magera, Keehyun Park, Sídney M. Gospe, Kateřina Sadílková, James Lymp and Jean M. Lacey. Their work appears in journals such as Molecular Genetics and Metabolism, Genetics in Medicine, Journal of Inherited Metabolic Disease, Human Mutation and Clinical Chemistry.

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