Kon‐Ping Lin

834 total citations
31 papers, 480 citations indexed

About

Kon‐Ping Lin is a scholar working on Neurology, Cellular and Molecular Neuroscience and Molecular Biology. According to data from OpenAlex, Kon‐Ping Lin has authored 31 papers receiving a total of 480 indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Neurology, 11 papers in Cellular and Molecular Neuroscience and 7 papers in Molecular Biology. Recurrent topics in Kon‐Ping Lin's work include Peripheral Neuropathies and Disorders (8 papers), Hereditary Neurological Disorders (8 papers) and Botulinum Toxin and Related Neurological Disorders (6 papers). Kon‐Ping Lin is often cited by papers focused on Peripheral Neuropathies and Disorders (8 papers), Hereditary Neurological Disorders (8 papers) and Botulinum Toxin and Related Neurological Disorders (6 papers). Kon‐Ping Lin collaborates with scholars based in Taiwan, United States and Malaysia. Kon‐Ping Lin's co-authors include Yi‐Chung Lee, Bing‐Wen Soong, Chih‐Chao Yang, Pang‐Hsien Tu, I‐Hui Lee, Jong‐Ling Fuh, Ming‐Hong Chang, Zin‐An Wu, Yo‐Tsen Liu and Kwong‐Kum Liao and has published in prestigious journals such as PLoS ONE, Neurology and Neurobiology of Aging.

In The Last Decade

Kon‐Ping Lin

31 papers receiving 471 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Kon‐Ping Lin Taiwan	13	263	163	145	96	91	31	480
Andrea Legati Italy	17	113 0.4×	509 3.1×	74 0.5×	35 0.4×	60 0.7×	41	762
J Rafałowska Poland	12	188 0.7×	137 0.8×	58 0.4×	101 1.1×	82 0.9×	44	390
Chiho Ishida Japan	14	223 0.8×	219 1.3×	116 0.8×	49 0.5×	52 0.6×	44	507
Gianna Berti Italy	13	77 0.3×	222 1.4×	103 0.7×	11 0.1×	77 0.8×	31	404
Michelle M. Mezei Canada	10	158 0.6×	165 1.0×	36 0.2×	76 0.8×	35 0.4×	19	326
Kalliopi Marinou Italy	12	472 1.8×	170 1.0×	117 0.8×	189 2.0×	79 0.9×	14	660
Emily P. McCann Australia	12	373 1.4×	213 1.3×	34 0.2×	156 1.6×	89 1.0×	18	508
Ulf Drugge Sweden	11	118 0.4×	328 2.0×	89 0.6×	23 0.2×	9 0.1×	26	501
Karima Ghorab France	11	194 0.7×	190 1.2×	205 1.4×	29 0.3×	50 0.5×	19	476
Ilaria Di Donato Italy	13	312 1.2×	197 1.2×	35 0.2×	9 0.1×	192 2.1×	23	596

Countries citing papers authored by Kon‐Ping Lin

Since Specialization

Citations

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

Fields of papers citing papers by Kon‐Ping Lin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kon‐Ping Lin

This figure shows the co-authorship network connecting the top 25 collaborators of Kon‐Ping Lin. A scholar is included among the top collaborators of Kon‐Ping 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 Kon‐Ping Lin. Kon‐Ping 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

Low, Soon-Chai, Nor Ashikin Md Sari, Cheng‐Yin Tan, et al.. (2021). Hereditary transthyretin amyloidosis in multi-ethnic Malaysians. Neuromuscular Disorders. 31(7). 642–650. 4 indexed citations

Lin, Kon‐Ping, et al.. (2020). Clinical characteristics of Taiwanese patients with Hereditary spastic paraplegia type 5. Annals of Clinical and Translational Neurology. 7(4). 486–496. 12 indexed citations

Tsai, Pei‐Chien, Yi‐Chu Liao, Po‐Lin Chen, et al.. (2017). Investigating CCNF mutations in a Taiwanese cohort with amyotrophic lateral sclerosis. Neurobiology of Aging. 62. 243.e1–243.e6. 13 indexed citations

Lin, Kon‐Ping, et al.. (2017). Acute Sensory Neuronopathy following Enterovirus Infection in a 3-Year-Old Girl. Neuropediatrics. 48(3). 190–193. 2 indexed citations

Soong, Bing‐Wen, Pang‐Hsien Tu, Kon‐Ping Lin, et al.. (2012). A hexanucleotide repeat expansion in C9ORF72 causes familial and sporadic ALS in Taiwan. Neurobiology of Aging. 33(9). 2232.e11–2232.e18. 45 indexed citations

Lin, Kon‐Ping, Bing‐Wen Soong, Chih‐Chao Yang, et al.. (2011). The Mutational Spectrum in a Cohort of Charcot-Marie-Tooth Disease Type 2 among the Han Chinese in Taiwan. PLoS ONE. 6(12). e29393–e29393. 80 indexed citations

Lee, Yi‐Chung, Kon‐Ping Lin, Ming‐Hong Chang, et al.. (2010). Cellular characterization of MPZ mutations presenting with diverse clinical phenotypes. Journal of Neurology. 257(10). 1661–1668. 12 indexed citations

Soong, Bing‐Wen, et al.. (2010). FUS, TARDBP, and SOD1 mutations in a Taiwanese cohort with familial ALS. Neurobiology of Aging. 32(3). 553.e13–553.e21. 59 indexed citations

Lee, Yi‐Chung, et al.. (2009). Population-specific spectrum of NOTCH3 mutations, MRI features and founder effect of CADASIL in Chinese. Journal of Neurology. 256(2). 249–255. 69 indexed citations

10.

Lee, Yi‐Chung, Chunhua Yu, Kon‐Ping Lin, et al.. (2008). MPZ mutation G123S characterization. Neurology. 70(4). 273–277. 12 indexed citations

11.

Liu, Yo‐Tsen, et al.. (2007). Transthyretin Ala97Ser in Chinese–Taiwanese patients with familial amyloid polyneuropathy: Genetic studies and phenotype expression. Journal of the Neurological Sciences. 267(1-2). 91–99. 32 indexed citations

12.

Lin, Kon‐Ping, et al.. (2004). Guillain–Barré syndrome coexisting with pericarditis or nephrotic syndrome after influenza vaccination. Clinical Neurology and Neurosurgery. 106(2). 136–138. 18 indexed citations

13.

Nakamura, Makoto, Kon‐Ping Lin, Shuji Ito, Hiroko Terasaki, & Yoshihiro Miyake. (2003). Novel GRM6 Mutations and Clinical Phenotype in Japanese Patients With Complete Congenital Stationary Night Blindness. Investigative Ophthalmology & Visual Science. 44(13). 2314–2314. 1 indexed citations

14.

Liu, Yi‐Chung, Zin‐An Wu, Shuu‐Jiun Wang, Din‐E Shan, & Kon‐Ping Lin. (1998). Transient syndrome of continuous muscle fiber activity associated with staphylococcal infection. Movement Disorders. 13(3). 609–611. 3 indexed citations

15.

Lin, Kon‐Ping, et al.. (1998). Heterogeneity of antibody specificity in Taiwanese patients with polyneuropathy and IgM paraproteinemia. Journal of Biomedical Science. 5(6). 441–445. 1 indexed citations

16.

Lin, Kon‐Ping, et al.. (1996). Polyneuropathy associated with acute monoblastic leukemia: a case report.. Journal of the Chinese Medical Association. 58(6). 435–438. 1 indexed citations

17.

Wang, Shuu‐Jiun, Kwong‐Kum Liao, Hung‐Hsiang Liou, et al.. (1994). Sympathetic skin response and R–R interval variation in chronic uremic patients. Muscle & Nerve. 17(4). 411–418. 35 indexed citations

18.

Lin, Kon‐Ping, et al.. (1993). Myokymia and neuromyotonia of the tongue: a case report of complication of irradiation.. Journal of the Chinese Medical Association. 52(6). 413–415. 3 indexed citations

19.

Lin, Kon‐Ping, Shang‐Yeong Kwan, Shaoyin Chen, et al.. (1993). Generalized Neuropathy in Taiwan: An Etiologic Survey. Neuroepidemiology. 12(5). 257–261. 21 indexed citations

20.

Lin, Kon‐Ping, et al.. (1993). Myoclonus associated with hyperthyroidism and thymoma: a case report.. PubMed. 51(2). 138–40. 2 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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