Yoon S. Shin

2.1k total citations
49 papers, 1.2k citations indexed

About

Yoon S. Shin is a scholar working on Rheumatology, Molecular Biology and Clinical Biochemistry. According to data from OpenAlex, Yoon S. Shin has authored 49 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Rheumatology, 17 papers in Molecular Biology and 16 papers in Clinical Biochemistry. Recurrent topics in Yoon S. Shin's work include Glycogen Storage Diseases and Myoclonus (20 papers), Metabolism and Genetic Disorders (16 papers) and Lysosomal Storage Disorders Research (14 papers). Yoon S. Shin is often cited by papers focused on Glycogen Storage Diseases and Myoclonus (20 papers), Metabolism and Genetic Disorders (16 papers) and Lysosomal Storage Disorders Research (14 papers). Yoon S. Shin collaborates with scholars based in Germany, Japan and United States. Yoon S. Shin's co-authors include Teodor Podskarbi, Sung Won Kim, Manfred W. Kilimann, D. Pongratz, Benedikt Schoser, Wolfgang Müller‐Felber, Beate Schlotter‐Weigel, Hanns Lochmüller, Martina Baethmann and Klaus Gempel and has published in prestigious journals such as PEDIATRICS, Annals of Neurology and Scientific Reports.

In The Last Decade

Yoon S. Shin

48 papers receiving 1.2k citations

Peers

Countries citing papers authored by Yoon S. Shin

Since Specialization

Citations

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

Fields of papers citing papers by Yoon S. Shin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Yoon S. Shin. 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 Yoon S. Shin. The network helps show where Yoon S. Shin may publish in the future.

Co-authorship network of co-authors of Yoon S. Shin

This figure shows the co-authorship network connecting the top 25 collaborators of Yoon S. Shin. A scholar is included among the top collaborators of Yoon S. Shin 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 Yoon S. Shin. Yoon S. Shin 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	Muscle diffusion MRI reveals autophagic buildup in a mouse model for Pompe disease 2023 ·Scientific Reports ·(unknown), (unknown), Xavier Helluy, Martijn Froeling, (unknown), (unknown), Denise Manahan‐Vaughan, Robert Rehmann, (unknown), Frank Jacobsen, Andreas Roos, Yoon S. Shin, Anne Schänzer, Matthias Vorgerd, Lara Schlaffke	4
2	Bond Ratings, Corporate Governance, and Cost of Debt: The Case of Korea 2016 ·Journal of Asian Finance Economics and Business ·(unknown), (unknown), Yoon S. Shin	5
3	Novel AGL mutation in a Turkish patient with glycogen storage disease type IIIa 2010 ·Pediatrics International ·Yoshiko Aoyama, (unknown), Tetsu Ebara, Toshio Murase, Yoon S. Shin, Teodor Podskarbi, (unknown), Mübeccel Demirkol, Gülden Gökçay, Minoru Okubo	2
4	Congenital ocular malformations (lens subluxation, pupillary displacement, cataract, myopia) and classic galactosaemia associated with Q188R and /or G1391A mutations 2010 ·Acta Ophthalmologica ·Nicole Eter, Yoon S. Shin, Claudia Auw‐Haedrich, Uta Tacke	1
5	Molecular features of 23 patients with glycogen storage disease type III in Turkey: a novel mutation p.R1147G associated with isolated glucosidase deficiency, along with 9 AGL mutations 2009 ·Journal of Human Genetics ·Yoshiko Aoyama, (unknown), Mübeccel Demirkol, Tetsu Ebara, Toshio Murase, Teodor Podskarbi, Yoon S. Shin, Gülden Gökçay, Minoru Okubo	21
6	Egyptian glycogen storage disease type III – identification of six novel AGL mutations, including a large 1.5 kb deletion and a missense mutation p.L620P with subtype IIId 2009 ·Clinical Chemistry and Laboratory Medicine (CCLM) ·(unknown), (unknown), Mortada El‐Shabrawi, Yoshiko Aoyama, Tetsu Ebara, Toshio Murase, Teodor Podskarbi, Yoon S. Shin, Minoru Okubo	9
7	Molecular analysis of the AGL gene: heterogeneity of mutations in patients with glycogen storage disease type III from Germany, Canada, Afghanistan, Iran, and Turkey 2006 ·Journal of Human Genetics ·(unknown), (unknown), Matthias Vorgerd, Yoshiko Aoyama, Tetsu Ebara, Toshio Murase, Masato Odawara, Teodor Podskarbi, Yoon S. Shin, Minoru Okubo	39
8	Delayed or late-onset type II glycogenosis with globular inclusions 2005 ·Acta Neuropathologica ·(unknown), (unknown), Arpad von Moers, Gisela Stoltenburg‐Didinger, Yoon S. Shin, Teodor Podskarbi, (unknown), Dominique S. Tews, Hans H. Goebel	19
9	Molecular characterization of Egyptian patients with glycogen storage disease type IIIa 2005 ·Journal of Human Genetics ·(unknown), (unknown), Yoshiko Aoyama, (unknown), Tetsu Ebara, Toshio Murase, Yoon S. Shin, Minoru Okubo	13
10	Oligosymptomatic Cornea Verticillata in a Heterozygote for Fabry Disease 2003 ·Cornea ·(unknown), Teodor Podskarbi, Yoon S. Shin, Ines Lanzl	4
11	Muscle glycogenosis with low phosphorylase kinase activity: mutations in PHKA1, PHKG1 or six other candidate genes explain only a minority of cases 2003 ·European Journal of Human Genetics ·Barbara Burwinkel, Bin Hu, (unknown), Paula R. Clemens, Shimon Moses, Yoon S. Shin, D. Pongratz, Matthias Vorgerd, Manfred W. Kilimann	38
12	An Unexpectedly High Frequency of Hypergalactosemia in an Immigrant Bosnian Population Revealed by Newborn Screening 2002 ·Pediatric Research ·(unknown), Julia B. Hennermann, Barbara Vetter, Luitgard M. Neumann, Yoon S. Shin, Ariane Söling, E. Mönch, Andreas E. Kulozik	11
13	Characteristics of l-ornithine: 2-oxoacid aminotransferase and potential prenatal diagnosis of gyrate atrophy of the choroid and retina by first trimester chorionic villus sampling 2000 ·Clinica Chimica Acta ·Wulf Röschinger, W. Endres, Yoon S. Shin	0
14	Classical galactosemia and mutations at the galactose-1-phosphate uridyl transferase (GALT) gene 1999 ·Human Mutation ·Linda Tyfield, Juergen Reichardt, (unknown), David T. Croke, Louis J. Elsas, Wolfgang Strobl, Libor Kozák, Turgay Coşkun, Giuseppe Novelli, Yoshiyuki Okano, Cezary Żekanowski, Yoon S. Shin, (unknown)	104
15	Familiäre Katarakt bei Galaktitol-Erhöhung im Plasma ohne bekannten Enzymdefekt 1999 ·Klinische Monatsblätter für Augenheilkunde ·(unknown), Gabriele C. Gusek-Schneider, Anselm Jünemann, F. K. Jansen, Yoon S. Shin	1
16	Mutations in the Liver Glycogen Phosphorylase Gene (PYGL) Underlying Glycogenosis Type VI (Hers Disease) 1998 ·The American Journal of Human Genetics ·Barbara Burwinkel, H. D. Bakker, (unknown), Shimon Moses, Yoon S. Shin, Manfred W. Kilimann	71
17	A new mutation of the glucose-6-phosphatase gene in a 4-year-old girl with oligosymptomatic glycogen storage disease type 1a 1998 ·The Journal of Pediatrics ·Klaus Keller, (unknown), Teodor Podskarbi, L. Bindl, Michael J. Lentze, Yoon S. Shin	21
18	Three missense mutations in the galactose-1-phosphate uridyltransferase gene of three families with mild galactosaemia 1996 ·European Journal of Pediatrics ·Yoon S. Shin, Birgit Gathof, Teodor Podskarbi, (unknown), (unknown), Ursula Gresser	12
19	Localization of a New Type of X-Linked Liver Glycogenosis to the Chromosomal Region Xp22 Containing the Liver α-Subunit of Phosphorylase Kinase (PHKA2) 1994 ·Genomics ·Jan Hendrickx, Paul Coucke, M. C. Hors‐Cayla, Gerrit Smit, Yoon S. Shin, J. Deutsch, Jan Smeıtınk, Ruud Berger, Philip Lee, John Fernandes, Patrick J. Willems	22
20	A mild juvenile variant of type IV glycogenosis 1992 ·Brain and Development ·E. Reusche, Fuat Aksu, Hans H. Goebel, Yoon S. Shin, Tadaaki Yokota, Heinz Reichmann	34

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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