Shih‐hsin Kan

1.3k total citations
47 papers, 873 citations indexed

About

Shih‐hsin Kan is a scholar working on Physiology, Molecular Biology and Rheumatology. According to data from OpenAlex, Shih‐hsin Kan has authored 47 papers receiving a total of 873 indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Physiology, 11 papers in Molecular Biology and 11 papers in Rheumatology. Recurrent topics in Shih‐hsin Kan's work include Lysosomal Storage Disorders Research (29 papers), Glycogen Storage Diseases and Myoclonus (10 papers) and Cellular transport and secretion (6 papers). Shih‐hsin Kan is often cited by papers focused on Lysosomal Storage Disorders Research (29 papers), Glycogen Storage Diseases and Myoclonus (10 papers) and Cellular transport and secretion (6 papers). Shih‐hsin Kan collaborates with scholars based in United States, United Kingdom and India. Shih‐hsin Kan's co-authors include Andrew O.M. Wilkie, David Johnson, Ans M.W. van den Ouweland, Susannah J. Patey, Ben C.J. Hamel, Patricia Dickson, Henk Giele, Grant Gallagher, Steven Q. Le and Grazia M.S. Mancini and has published in prestigious journals such as Journal of Biological Chemistry, Brain and Scientific Reports.

In The Last Decade

Shih‐hsin Kan

40 papers receiving 860 citations

Peers

Countries citing papers authored by Shih‐hsin Kan

Since Specialization

Citations

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

Fields of papers citing papers by Shih‐hsin Kan

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Shih‐hsin Kan. 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 Shih‐hsin Kan. The network helps show where Shih‐hsin Kan may publish in the future.

Co-authorship network of co-authors of Shih‐hsin Kan

This figure shows the co-authorship network connecting the top 25 collaborators of Shih‐hsin Kan. A scholar is included among the top collaborators of Shih‐hsin Kan 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 Shih‐hsin Kan. Shih‐hsin Kan 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	Generation of an infantile GM1 gangliosidosis induced pluripotent stem cell line (CHOCi005-A) for disease modeling and therapeutic testing 2024 ·Stem Cell Research ·(unknown), (unknown), Shih‐hsin Kan, (unknown), (unknown), Raymond Wang	1
2	Tranexamic Acid With Acid Suppression Versus Acid Suppression Alone as Therapy for Upper Gastrointestinal Bleeding: A Meta‐Analysis of Randomized Controlled Trials 2024 ·Journal of Gastroenterology and Hepatology ·Shih‐hsin Kan, (unknown), (unknown), Mei‐Ju Chi	0
3	Base editing rescues acid α-glucosidase function in infantile-onset Pompe disease patient-derived cells 2024 ·Molecular Therapy — Nucleic Acids ·(unknown), Shih‐hsin Kan, (unknown), (unknown), (unknown), Raymond Wang	3
4	Human iPSC-derived neural stem cells engraft and improve pathophysiology of MPS I mice 2024 ·Molecular Therapy — Methods & Clinical Development ·(unknown), Shih‐hsin Kan, Alexander E. Stover, (unknown), Edwin S. Monuki, Raymond Wang, Philip H. Schwartz	0
5	Intra-Articular AAV9 α-l-Iduronidase Gene Replacement in the Canine Model of Mucopolysaccharidosis Type I 2023 ·PubMed ·Raymond Wang, Shih‐hsin Kan, Haoyue Zhang, Jodi D. Smith, (unknown), Elizabeth Snella, Jackie K. Jens, Sarah P. Young, Patricia Dickson, N. Matthew Ellinwood	0
6	CRISPR-mediated generation and characterization of a Gaa homozygous c.1935C>A (p.D645E) Pompe disease knock-in mouse model recapitulating human infantile onset-Pompe disease 2022 ·Scientific Reports ·Shih‐hsin Kan, (unknown), (unknown), (unknown), Nancy D. Dalton, (unknown), (unknown), Jeremy Davis‐Turak, Jonathan Neumann, Raymond Wang	7
7	Impaired mitophagy in Sanfilippo a mice causes hypertriglyceridemia and brown adipose tissue activation 2022 ·Journal of Biological Chemistry ·(unknown), William C. Lamanna, Chrissa A. Dwyer, Daniel R. Sandoval, Ariane Pessentheiner, (unknown), Stéphane Sarrazin, Jon C. Gonzales, Shih‐hsin Kan, Alexander Y. Andreyev, (unknown), Bryan E. Thacker, Charles A. Glass, Patricia Dickson, Raymond Wang, Scott B. Selleck, Jeffrey D. Esko, Philip L.S.M. Gordts	3
8	Biochemical evaluation of intracerebroventricular rhNAGLU-IGF2 enzyme replacement therapy in neonatal mice with Sanfilippo B syndrome 2021 ·Molecular Genetics and Metabolism ·Shih‐hsin Kan, (unknown), Steven Q. Le, (unknown), (unknown), Jonathan D. Cooper, Roger Lawrence, Mark S. Sands, Brett E. Crawford, Patricia Dickson	2
9	Neuropathology of murine Sanfilippo D syndrome 2021 ·Molecular Genetics and Metabolism ·(unknown), Steven Q. Le, Shih‐hsin Kan, (unknown), Patricia Dickson, Jonathan D. Cooper	3
10	Genetically Corrected iPSC-Derived Neural Stem Cell Grafts Deliver Enzyme Replacement to Affect CNS Disease in Sanfilippo B Mice 2018 ·Molecular Therapy — Methods & Clinical Development ·(unknown), (unknown), Shih‐hsin Kan, Steven Q. Le, Valentina Sanghez, Jonathan D. Cooper, Patricia Dickson, Michelina Iacovino	10
11	A Humoral Immune Response Alters the Distribution of Enzyme Replacement Therapy in Murine Mucopolysaccharidosis Type I 2017 ·Molecular Therapy — Methods & Clinical Development ·Steven Q. Le, Shih‐hsin Kan, (unknown), Valentina Sanghez, Martin Egeland, (unknown), Terence M. Doherty, (unknown), Michelina Iacovino, Jonathan D. Cooper, Mark S. Sands, Patricia Dickson	11
12	Behavioral deficits and cholinergic pathway abnormalities in male Sanfilippo B mice 2016 ·Behavioural Brain Research ·Shih‐hsin Kan, Steven Q. Le, (unknown), (unknown), Jesse D. Cushman, Mark S. Sands, Patricia Dickson	6
13	A novel, long-lived, and highly engraftable immunodeficient mouse model of mucopolysaccharidosis type I 2015 ·Molecular Therapy — Methods & Clinical Development ·(unknown), Alexander E. Stover, (unknown), David J. Brick, Hubert E. Nethercott, (unknown), Omar Khalid, Andrew M.S. Wong, Jonathan D. Cooper, James V. Jester, Edwin S. Monuki, (unknown), Steven Q. Le, Shih‐hsin Kan, Patricia Dickson, Philip H. Schwartz	15
14	Intra-articular enzyme replacement therapy with rhIDUA is safe, well-tolerated, and reduces articular GAG storage in the canine model of mucopolysaccharidosis type I 2014 ·Molecular Genetics and Metabolism ·Raymond Wang, (unknown), Michael F. McEntee, Shih‐hsin Kan, Calogera M. Simonaro, William C. Lamanna, Roger Lawrence, N. Matthew Ellinwood, (unknown), Steven Q. Le, Patricia Dickson, Jeffrey D. Esko	14
15	Innate immune system activation in MPS I canine vascular disease 2014 ·Molecular Genetics and Metabolism ·(unknown), Steven Q. Le, Shih‐hsin Kan, Patricia Dickson, Raymond Wang	0
16	Immune response to intrathecal enzyme replacement therapy in mucopolysaccharidosis I patients 2013 ·Pediatric Research ·(unknown), Steven Q. Le, Shih‐hsin Kan, Hermes Garbán, David E. Naylor, Anton Mlikotic, Ilkka Kaitila, Paul Harmatz, Agnes Chen, Patricia Dickson	19
17	Genetic screening of 202 individuals with congenital limb malformations and requiring reconstructive surgery 2009 ·Journal of Medical Genetics ·Dominic Furniss, Shih‐hsin Kan, Indira B. Taylor, David Johnson, (unknown), Henk Giele, Andrew O.M. Wilkie	28
18	An acceptor splice site mutation in HOXD13 results in variable hand, but consistent foot malformations 2003 ·American Journal of Medical Genetics Part A ·Shih‐hsin Kan, David Johnson, Henk Giele, Andrew O.M. Wilkie	27
19	Missense Mutations in the Homeodomain of HOXD13 Are Associated with Brachydactyly Types D and E 2003 ·The American Journal of Human Genetics ·David Johnson, Shih‐hsin Kan, Michael Oldridge, Richard C. Trembath, Philippe Roche, Robert Esnouf, Henk Giele, Andrew O.M. Wilkie	76
20	FGFs, their receptors, and human limb malformations: Clinical and molecular correlations 2002 ·American Journal of Medical Genetics ·Andrew O.M. Wilkie, Susannah J. Patey, Shih‐hsin Kan, Ans M.W. van den Ouweland, Ben C.J. Hamel	140

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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