Shuan‐Pei Lin

3.5k total citations
163 papers, 2.1k citations indexed

About

Shuan‐Pei Lin is a scholar working on Genetics, Physiology and Molecular Biology. According to data from OpenAlex, Shuan‐Pei Lin has authored 163 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 61 papers in Genetics, 47 papers in Physiology and 46 papers in Molecular Biology. Recurrent topics in Shuan‐Pei Lin's work include Lysosomal Storage Disorders Research (44 papers), Genomic variations and chromosomal abnormalities (31 papers) and Prenatal Screening and Diagnostics (24 papers). Shuan‐Pei Lin is often cited by papers focused on Lysosomal Storage Disorders Research (44 papers), Genomic variations and chromosomal abnormalities (31 papers) and Prenatal Screening and Diagnostics (24 papers). Shuan‐Pei Lin collaborates with scholars based in Taiwan, United States and United Kingdom. Shuan‐Pei Lin's co-authors include Chih‐Kuang Chuang, Hsiang‐Yu Lin, Ming‐Ren Chen, Dau‐Ming Niu, Chih‐Ping Chen, Wayseen Wang, Hung‐Chang Lee, Schu‐Rern Chern, Chao Huang and Tuen-Jen Wang and has published in prestigious journals such as Journal of Clinical Investigation, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

Shuan‐Pei Lin

159 papers receiving 2.0k citations

Peers

Countries citing papers authored by Shuan‐Pei Lin

Since Specialization

Citations

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

Fields of papers citing papers by Shuan‐Pei Lin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Shuan‐Pei Lin. 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 Shuan‐Pei Lin. The network helps show where Shuan‐Pei Lin may publish in the future.

Co-authorship network of co-authors of Shuan‐Pei Lin

This figure shows the co-authorship network connecting the top 25 collaborators of Shuan‐Pei Lin. A scholar is included among the top collaborators of Shuan‐Pei Lin 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 Shuan‐Pei Lin. Shuan‐Pei Lin 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	Understanding Genetic Screening: Harnessing Health Information to Prevent Disease Risks 2025 ·International Journal of Medical Sciences ·Chung‐Lin Lee, Chih‐Kuang Chuang, (unknown), Ya-Hui Chang, (unknown), (unknown), Hsiang‐Yu Lin, Shuan‐Pei Lin	4
2	Endoscopic and Image Analysis of the Airway in Patients with Mucopolysaccharidosis Type IVA 2023 ·Journal of Personalized Medicine ·(unknown), Chin‐Hui Su, (unknown), Hsiang‐Yu Lin, Shuan‐Pei Lin, Chih‐Kuang Chuang, Kuo‐Sheng Lee	2
3	Utility of whole‐exome sequencing for patients with multiple congenital anomalies with or without intellectual disability/developmental delay in East Asia population 2023 ·Molecular Genetics & Genomic Medicine ·Rai‐Hseng Hsu, (unknown), Yin‐Hsiu Chien, Shuan‐Pei Lin, (unknown), (unknown), (unknown), Wuh‐Liang Hwu, Ni‐Chung Lee	2
4	A phase I/II study on intracerebroventricular tralesinidase alfa in patients with Sanfilippo syndrome type B 2022 ·Journal of Clinical Investigation ·Nicole Muschol, (unknown), (unknown), İlyas Okur, Fatih Süheyl Ezgü, Paul Harmatz, (unknown), María L. Couce, Shuan‐Pei Lin, Spyros Batzios, Maureen Cleary, (unknown), Igor Nestrašil, Bella Kaufman, Adam J. Shaywitz, Stephen M. Maricich, (unknown), Joseph Kovalchin, Eric Zanelli	9
5	Molecular cytogenetic characterization of an inv dup(15) chromosome presenting as a small supernumerary marker chromosome associated with the inv dup(15) syndrome 2016 ·Taiwanese Journal of Obstetrics and Gynecology ·Chih‐Ping Chen, Shuan‐Pei Lin, Schu‐Rern Chern, Peih-Shan Wu, Yen-Ni Chen, Shin-Wen Chen, Chen‐Chi Lee, Dai‐Dyi Town, Chien-Wen Yang, Wayseen Wang	9
6	Recurrent spontaneous subserosal hematoma of ileum causing intestinal obstruction in a patient with menkes disease 2016 ·Medicine ·(unknown), (unknown), Nien-Lu Wang, Shuan‐Pei Lin, Chuen‐Bin Jiang	2
7	Cardiovascular abnormalities in Taiwanese patients with mucopolysaccharidosis 2014 ·Molecular Genetics and Metabolism ·(unknown), (unknown), Hsiang‐Yu Lin, Chih‐Kuang Chuang, Shuan‐Pei Lin, Ming‐Ren Chen	26
8	Interphase FISH on uncultured amniocytes at repeat amniocentesis for rapid diagnosis of true mosaicism in a case of level II mosaicism involving trisomy 21 in a single colony from an in situ culture of amniocytes 2014 ·Taiwanese Journal of Obstetrics and Gynecology ·Chih‐Ping Chen, (unknown), Shuan‐Pei Lin, Schu‐Rern Chern, Yuting Chen, Peih-Shan Wu, (unknown), Wenlin Chen, Wayseen Wang	11
9	Assessment of bone mineral density by dual energy x-ray absorptiometry in patients with mucopolysaccharidoses 2013 ·Orphanet Journal of Rare Diseases ·Hsiang‐Yu Lin, Shou‐Chuan Shih, Chih‐Kuang Chuang, Ming‐Ren Chen, Dau‐Ming Niu, Shuan‐Pei Lin	32
10	Prenatal diagnosis and molecular cytogenetic characterization of a de novo interstitial duplication of 14q (14q31.3→q32.12) associated with abnormal maternal serum biochemistry 2013 ·Taiwanese Journal of Obstetrics and Gynecology ·Chih‐Ping Chen, (unknown), Her‐Young Su, Shuan‐Pei Lin, Yi‐Ning Su, Schu‐Rern Chern, Jun-Wei Su, Yu-Ting Chen, Wenlin Chen, Wayseen Wang	14
11	Functional independence of Taiwanese children with VACTERL association 2012 ·American Journal of Medical Genetics Part A ·(unknown), Shuan‐Pei Lin, Hsiang‐Yu Lin, (unknown), Jui‐Hsing Chang, Hsin‐An Kao, Han‐Yang Hung, (unknown), Hung‐Chang Lee, Ming‐Ren Chen, (unknown)	5
12	Current diagnosis and management of mucopolysaccharidosis VI in the Asia-Pacific region 2012 ·Molecular Genetics and Metabolism ·Wuh‐Liang Hwu, Torayuki Okuyama, (unknown), (unknown), Xuefan Gu, Joannie Hui, Motomichi Kosuga, Shuan‐Pei Lin, Lock Hock Ngu, (unknown), Akemi Tanaka, Meow‐Keong Thong, Duangrurdee Wattanasirichaigoon, Pornswan Wasant, Jim McGill	5
13	Intravenous Pamidronate Therapy in Taiwanese Patients with Osteogenesis Imperfecta 2008 ·Pediatrics & Neonatology ·Hsiang‐Yu Lin, Shuan‐Pei Lin, Chih‐Kuang Chuang, Ming‐Ren Chen, Chia-Ying Chang	9
14	X-linked Myotubular Myopathy with a Novel MTM1 Mutation in a Taiwanese Child 2008 ·Journal of the Formosan Medical Association ·Chia-Ying Chang, Shuan‐Pei Lin, Hsiang‐Yu Lin, Chih‐Kuang Chuang, Che‐Sheng Ho, Yi‐Ning Su	2
15	Prenatal sonographic findings of Klippel‐Trénaunay‐Weber syndrome 2007 ·Journal of Clinical Ultrasound ·Chih‐Ping Chen, Shuan‐Pei Lin, Tung‐Yao Chang, Hung‐Chang Lee, Han‐Yang Hung, Hsiang‐Yu Lin, Jian‐Pei Huang, Wayseen Wang	12
16	Clinical Features of Ehlers-Danlos Syndrome 2006 ·Journal of the Formosan Medical Association ·(unknown), Shuan‐Pei Lin, Ming‐Ren Chen, Dau‐Ming Niu	58
17	Cardiovascular changes in mucopolysaccharidoses in Taiwan 2005 ·Acta Cardiologica ·Ming‐Ren Chen, Shuan‐Pei Lin, (unknown), (unknown)	32
18	Polymorphism of Transmembrane Region of MICA Gene and Kawasaki Disease 2000 ·PubMed ·Chao Huang, Yann‐Jinn Lee, Ming‐Ren Chen, (unknown), Shuan‐Pei Lin, (unknown), (unknown), Jan‐Gowth Chang	36
19	Analysis of the mRNA transcripts of the survival motor neuron (SMN) gene in the tissue of an SMA fetus and the peripheral blood mononuclear cells of normals, carriers and SMA patients 2000 ·Journal of the Neurological Sciences ·Yuh‐Jyh Jong, Jan‐Gowth Chang, Shuan‐Pei Lin, (unknown), Jyh‐Chwan Wang, Chih‐Peng Chang, Cheng‐Chun Lee, Hung Li, Hsiu-Mei Hsieh-Li, Chang‐Hai Tsai	23
20	Molecular analysis of survival motor neuron (SMN) and neuronal apoptosis inhibitory protein (NAIP) genes of spinal muscular atrophy patients and their parents 1997 ·Human Genetics ·Jan‐Gowth Chang, Yuh‐Jyh Jong, Shuan‐Pei Lin, Bing‐Wen Soong, Chang‐Hai Tsai, Tse-Yen Yang, Chih‐Peng Chang, (unknown)	23

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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