Shuan‐Pei Lin

3.5k citations

163 papers · 2.1k indexed · h-index 26

Physiology top 5%
- Lysosomal Storage Disorders Research 44
Genetics top 5%
- Genomic variations and chromosomal abnormalities 31
- Genetic Syndromes and Imprinting 14
Rheumatology top 5%
- Glycogen Storage Diseases and Myoclonus 14
Genetics top 5%
- Genomic variations and chromosomal abnormalities 31
- Genetic Syndromes and Imprinting 14
Pediatrics, Perinatology and Child Health top 5%
- Prenatal Screening and Diagnostics 24
Epidemiology
- Trypanosoma species research and implications 21
Plant Science
- Chromosomal and Genetic Variations 11
Organic Chemistry
- Carbohydrate Chemistry and Synthesis 11

Co-authors: Chih‐Kuang Chuang Hsiang‐Yu Lin Ming‐Ren Chen Dau‐Ming Niu Chih‐Ping Chen Wayseen Wang Hung‐Chang Lee Schu‐Rern Chern
Cited by: Physiology Genetics Rheumatology
Partner nations: Taiwan United States United Kingdom

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

The 25 scholars most cited alongside Shuan‐Pei Lin, 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 Shuan‐Pei Lin Line = papers co-authored together Shuan‐Pei Lin links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Understanding Genetic Screening: Harnessing Health Information to Prevent Disease Risks Chung‐Lin Lee,Chih‐Kuang Chuang,Huei‐Ching Chiu,Ya-Hui Chang,Yuan-Rong Tu,Yun‐Ting Lo,Hsiang‐Yu Lin,Shuan‐Pei Lin	2025	4
2	Endoscopic and Image Analysis of the Airway in Patients with Mucopolysaccharidosis Type IVA Yi-Hao Lee,Chin‐Hui Su,Che-Yi Lin,Hsiang‐Yu Lin,Shuan‐Pei Lin,Chih‐Kuang Chuang,Kuo‐Sheng Lee	2023	2
3	Utility of whole‐exome sequencing for patients with multiple congenital anomalies with or without intellectual disability/developmental delay in East Asia population Rai‐Hseng Hsu,Chen‐Hao Lee,Yin‐Hsiu Chien,Shuan‐Pei Lin,Miao‐Zi Hung,Nai‐Chi Chen,Yi‐Lin Lin,Wuh‐Liang Hwu,Ni‐Chung Lee	2023	2
4	A phase I/II study on intracerebroventricular tralesinidase alfa in patients with Sanfilippo syndrome type B Nicole Muschol,Anja F. Koehn,Katharina von Cossel,İlyas Okur,Fatih Süheyl Ezgü,Paul Harmatz,María José de Castro López,María L. Couce,Shuan‐Pei Lin,Spyros Batzios,Maureen Cleary,Martha Solano,Igor Nestrašil,Bella Kaufman,Adam J. Shaywitz,Stephen M. Maricich,Bernice Kuca,Joseph Kovalchin,Eric Zanelli	2022	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 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	2016	9
6	Recurrent spontaneous subserosal hematoma of ileum causing intestinal obstruction in a patient with menkes disease Shu-Chao Weng,Chyong-Hsin Hsu,Nien-Lu Wang,Shuan‐Pei Lin,Chuen‐Bin Jiang	2016	2
7	Cardiovascular abnormalities in Taiwanese patients with mucopolysaccharidosis Shan‐Miao Lin,(unknown),Hsiang‐Yu Lin,Chih‐Kuang Chuang,Shuan‐Pei Lin,Ming‐Ren Chen	2014	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 Chih‐Ping Chen,Pu-Tsui Wang,Shuan‐Pei Lin,Schu‐Rern Chern,Yuting Chen,Peih-Shan Wu,Yu‐Ling Kuo,Wenlin Chen,Wayseen Wang	2014	11
9	Assessment of bone mineral density by dual energy x-ray absorptiometry in patients with mucopolysaccharidoses Hsiang‐Yu Lin,Shou‐Chuan Shih,Chih‐Kuang Chuang,Ming‐Ren Chen,Dau‐Ming Niu,Shuan‐Pei Lin	2013	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 Chih‐Ping Chen,Kwui-Shuai Hwang,Her‐Young Su,Shuan‐Pei Lin,Yi‐Ning Su,Schu‐Rern Chern,Jun-Wei Su,Yu-Ting Chen,Wenlin Chen,Wayseen Wang	2013	14
11	Functional independence of Taiwanese children with VACTERL association Hsin‐Yi Lin,Shuan‐Pei Lin,Hsiang‐Yu Lin,Chyong‐Hsin Hsu,Jui‐Hsing Chang,Hsin‐An Kao,Han‐Yang Hung,Chun‐Chih Peng,Hung‐Chang Lee,Ming‐Ren Chen,Jeng‐Daw Tsai	2012	5
12	Current diagnosis and management of mucopolysaccharidosis VI in the Asia-Pacific region Wuh‐Liang Hwu,Torayuki Okuyama,Wai Man But,Sylvia Estrada,Xuefan Gu,Joannie Hui,Motomichi Kosuga,Shuan‐Pei Lin,Lock Hock Ngu,Huiping Shi,Akemi Tanaka,Meow‐Keong Thong,Duangrurdee Wattanasirichaigoon,Pornswan Wasant,Jim McGill	2012	5
13	Intravenous Pamidronate Therapy in Taiwanese Patients with Osteogenesis Imperfecta Hsiang‐Yu Lin,Shuan‐Pei Lin,Chih‐Kuang Chuang,Ming‐Ren Chen,Chia-Ying Chang	2008	9
14	X-linked Myotubular Myopathy with a Novel MTM1 Mutation in a Taiwanese Child Chia-Ying Chang,Shuan‐Pei Lin,Hsiang‐Yu Lin,Chih‐Kuang Chuang,Che‐Sheng Ho,Yi‐Ning Su	2008	2
15	Prenatal sonographic findings of Klippel‐Trénaunay‐Weber syndrome Chih‐Ping Chen,Shuan‐Pei Lin,Tung‐Yao Chang,Hung‐Chang Lee,Han‐Yang Hung,Hsiang‐Yu Lin,Jian‐Pei Huang,Wayseen Wang	2007	12
16	Clinical Features of Ehlers-Danlos Syndrome Jui‐Lung Yen,Shuan‐Pei Lin,Ming‐Ren Chen,Dau‐Ming Niu	2006	58
17	Cardiovascular changes in mucopolysaccharidoses in Taiwan Ming‐Ren Chen,Shuan‐Pei Lin,Haw‐Kwei Hwang,Chang-Hsien Yu	2005	32
18	Polymorphism of Transmembrane Region of MICA Gene and Kawasaki Disease Chao Huang,Yann‐Jinn Lee,Ming‐Ren Chen,Chyong-Hsin Hsu,Shuan‐Pei Lin,Tseng-Chen Sung,Shih-Chuan Chang,Jan‐Gowth Chang	2000	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 Yuh‐Jyh Jong,Jan‐Gowth Chang,Shuan‐Pei Lin,Tzu-Yao Yang,Jyh‐Chwan Wang,Chih‐Peng Chang,Cheng‐Chun Lee,Hung Li,Hsiu-Mei Hsieh-Li,Chang‐Hai Tsai	2000	23
20	Molecular analysis of survival motor neuron (SMN) and neuronal apoptosis inhibitory protein (NAIP) genes of spinal muscular atrophy patients and their parents Jan‐Gowth Chang,Yuh‐Jyh Jong,Shuan‐Pei Lin,Bing‐Wen Soong,Chang‐Hai Tsai,Tse-Yen Yang,Chih‐Peng Chang,Wen-Shin Wang	1997	23

About Shuan‐Pei Lin

Shuan‐Pei Lin is a scholar working on Genetics, Physiology and Pediatrics, Perinatology and Child Health, having authored 163 papers that have together received 2.1k indexed citations. Recurring topics across this work include Lysosomal Storage Disorders Research (44 papers), Genomic variations and chromosomal abnormalities (31 papers), Prenatal Screening and Diagnostics (24 papers), Trypanosoma species research and implications (21 papers), Genetic Syndromes and Imprinting (14 papers), Glycogen Storage Diseases and Myoclonus (14 papers), Chromosomal and Genetic Variations (11 papers) and Carbohydrate Chemistry and Synthesis (11 papers). The work is most often cited by research in Physiology (683 citations), Genetics (609 citations) and Rheumatology (284 citations). Shuan‐Pei Lin has collaborated with scholars based in Taiwan, United States and United Kingdom. Frequent 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.

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