Sihoun Hahn

1.3k total citations
23 papers, 340 citations indexed

About

Sihoun Hahn is a scholar working on Clinical Biochemistry, Molecular Biology and Nutrition and Dietetics. According to data from OpenAlex, Sihoun Hahn has authored 23 papers receiving a total of 340 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Clinical Biochemistry, 8 papers in Molecular Biology and 5 papers in Nutrition and Dietetics. Recurrent topics in Sihoun Hahn's work include Metabolism and Genetic Disorders (9 papers), Trace Elements in Health (5 papers) and Biochemical and Molecular Research (4 papers). Sihoun Hahn is often cited by papers focused on Metabolism and Genetic Disorders (9 papers), Trace Elements in Health (5 papers) and Biochemical and Molecular Research (4 papers). Sihoun Hahn collaborates with scholars based in United States, South Korea and Japan. Sihoun Hahn's co-authors include Piero Rinaldo, Dietrich Matern, Craig L. Bennett, Ian A. Glass, Sídney M. Gospe, Thomas Brewster, Silvia Tortorelli, Tina M. Cowan, Barbara K. Burton and Sarah C. Grünert and has published in prestigious journals such as The American Journal of Human Genetics, Journal of Hepatology and The Journal of Pediatrics.

In The Last Decade

Sihoun Hahn

22 papers receiving 333 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Sihoun Hahn United States 9 247 219 88 63 50 23 340
T. Baykal Türkiye 14 237 1.0× 228 1.0× 61 0.7× 41 0.7× 88 1.8× 18 449
Emanuela Scolamiero Italy 10 172 0.7× 212 1.0× 67 0.8× 26 0.4× 79 1.6× 14 374
Elizabeth Wenz United States 12 289 1.2× 100 0.5× 116 1.3× 47 0.7× 107 2.1× 21 353
Persephone Augoustides‐Savvopoulou Greece 10 227 0.9× 233 1.1× 38 0.4× 101 1.6× 123 2.5× 17 430
Roland Posset Germany 10 386 1.6× 238 1.1× 117 1.3× 94 1.5× 89 1.8× 18 468
H. Niederhoff Germany 10 118 0.5× 135 0.6× 32 0.4× 26 0.4× 25 0.5× 44 304
Marta Camilot Italy 12 66 0.3× 157 0.7× 60 0.7× 14 0.2× 42 0.8× 29 385
Geoffrey Sherwood Canada 7 165 0.7× 326 1.5× 25 0.3× 26 0.4× 14 0.3× 11 478
Yuichi Mushimoto Japan 12 222 0.9× 262 1.2× 45 0.5× 32 0.5× 75 1.5× 30 425
Keow Giak Sim Australia 12 399 1.6× 335 1.5× 112 1.3× 64 1.0× 105 2.1× 13 512

Countries citing papers authored by Sihoun Hahn

Since Specialization
Citations

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

Fields of papers citing papers by Sihoun Hahn

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sihoun Hahn

This figure shows the co-authorship network connecting the top 25 collaborators of Sihoun Hahn. A scholar is included among the top collaborators of Sihoun Hahn 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 Sihoun Hahn. Sihoun Hahn is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Weiss, Karl Heinz, Michael L. Schilsky, Anna Członkowska, et al.. (2022). O01 Efficacy and safety of ALXN1840 versus standard of care in Wilson disease: primary results from an ongoing phase 3, randomized, controlled, rater-blinded trial. Abstracts. A1–A1. 1 indexed citations
2.
Scott, Anna I., S.M. Sullivan, Irene J. Chang, et al.. (2020). Tutorial: Triheptanoin and Nutrition Management for Treatment of Long‐Chain Fatty Acid Oxidation Disorders. Journal of Parenteral and Enteral Nutrition. 45(2). 230–238. 14 indexed citations
3.
Kishnani, Priya S., John Day, Michael J. Gambello, et al.. (2016). Clinical characteristics and genotypes in the ADVANCE baseline dataset, a comprehensive cohort of us children and youth with Pompe disease. Molecular Genetics and Metabolism. 117(2). S68–S68. 1 indexed citations
4.
Marshall, M., et al.. (2016). Reality of outpatient care with medical compression stockings. Phlebologie. 45(4). 207–214.
5.
Wang, Guo-Li, Jing Wang, Ganka Douglas, et al.. (2011). Expanded molecular features of carnitine acyl-carnitine translocase (CACT) deficiency by comprehensive molecular analysis. Molecular Genetics and Metabolism. 103(4). 349–357. 23 indexed citations
6.
Vasta, Valeria, et al.. (2011). The role of DMQ9 in the long-lived mutant clk-1. Mechanisms of Ageing and Development. 132(6-7). 331–339. 22 indexed citations
7.
Bennett, Craig L., et al.. (2008). Prevalence of ALDH7A1 mutations in 18 North American pyridoxine‐dependent seizure (PDS) patients. Epilepsia. 50(5). 1167–1175. 63 indexed citations
8.
Merritt, J. Lawrence, et al.. (2008). 38. Quality-of-life changes in MPS II patients receiving enzyme replacement therapy. Molecular Genetics and Metabolism. 93(2). 23–24. 1 indexed citations
9.
Ensenauer, Regina, Jerry Vockley, Jörn Oliver Sass, et al.. (2004). A Common Mutation Is Associated with a Mild, Potentially Asymptomatic Phenotype in Patients with Isovaleric Acidemia Diagnosed by Newborn Screening. The American Journal of Human Genetics. 75(6). 1136–1142. 100 indexed citations
10.
Tortorelli, Silvia, Sihoun Hahn, Tina M. Cowan, et al.. (2004). The urinary excretion of glutarylcarnitine is an informative tool in the biochemical diagnosis of glutaric acidemia type I. Molecular Genetics and Metabolism. 84(2). 137–143. 47 indexed citations
11.
Rinaldo, Piero, et al.. (2003). Mutation analysis of copper transporter genes in patients with ethylmalonic encephalopathy, mitochondriopathies and copper deficiency phenotypes. Journal of Inherited Metabolic Disease. 26(1). 55–66. 8 indexed citations
12.
Hahn, Sihoun, et al.. (2001). Development of a Screening Kit for Early Diagnosis and Prevention of Wilson`s Disease. 44(12). 1374–1380. 1 indexed citations
13.
Hahn, Sihoun, et al.. (2001). Identification of Four Novel Mutations in Classical Menkes Disease and Successful Prenatal DNA Diagnosis. Molecular Genetics and Metabolism. 73(1). 86–90. 15 indexed citations
14.
Hong, Kyeong‐Man, et al.. (2000). Novel 67-bp insertional mutation in theASS gene in a patient with citrullinemia. Human Mutation. 15(6). 585–585. 6 indexed citations
15.
Hong, Kyeong‐Man, et al.. (2000). The First Successful Prenatal Diagnosis on a Korean Family with Citrullinemia. Molecules and Cells. 10(6). 692–694. 6 indexed citations
16.
17.
Hong, Kyeong‐Man, et al.. (2000). Mutation Analysis of Korean Patients with Citrullinemia. Molecules and Cells. 10(4). 465–468. 12 indexed citations
18.
Hong, Kyeong‐Man, et al.. (2000). The First Successful Prenatal Diagnosis on a Korean Family with Citrullinemia. Molecules and Cells. 10(6). 692–694. 4 indexed citations
19.
Hahn, Sihoun, Eunha Lee, Jo Won Jung, et al.. (1999). Very long chain acyl coenzyme A dehydrogenase deficiency in a 5-month-old Korean boy: Identification of a novel mutation. The Journal of Pediatrics. 135(2). 250–253. 4 indexed citations
20.
Hahn, Sihoun & W. A. Gahl. (1993). Copper Effects on Metal Regulatory Factors of Cultured Human Fibroblasts. Biochemical Medicine and Metabolic Biology. 50(3). 346–357. 1 indexed citations

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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