Kon-Ping Lin

3.5k total citations
16 papers, 388 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 16 papers receiving a total of 388 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Neurology, 7 papers in Cellular and Molecular Neuroscience and 2 papers in Molecular Biology. Recurrent topics in Kon-Ping Lin's work include Hereditary Neurological Disorders (5 papers), Genetic Neurodegenerative Diseases (4 papers) and Neurological diseases and metabolism (2 papers). Kon-Ping Lin is often cited by papers focused on Hereditary Neurological Disorders (5 papers), Genetic Neurodegenerative Diseases (4 papers) and Neurological diseases and metabolism (2 papers). Kon-Ping Lin collaborates with scholars based in Taiwan, United States and India. Kon-Ping Lin's co-authors include Yi‐Chung Lee, Bing‐Wen Soong, Pei‐Chien Tsai, Shuu‐Jiun Wang, Yi‐Chu Liao, Wei-Shu Wang, Muh‐Hwa Yang, Chueh‐Chuan Yen, Po‐Min Chen and Tzeon-Jye Chiou and has published in prestigious journals such as PLoS ONE, NeuroImage and Neurology.

In The Last Decade

Kon-Ping Lin

16 papers receiving 377 citations

Peers

Kon-Ping Lin
Kon-Ping Lin
Citations per year, relative to Kon-Ping Lin Kon-Ping Lin (= 1×) peers Eduardo Gutiérrez‐Rivas

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

16 of 16 papers shown
1.
Lin, Kon-Ping, et al.. (2019). Cellular secretion and cytotoxicity of transthyretin mutant proteins underlie late-onset amyloidosis and neurodegeneration. Cellular and Molecular Life Sciences. 77(7). 1421–1434. 13 indexed citations
2.
Wang, Yen-Feng, Chih‐Chao Yang, Yu‐Chuan Tsai, et al.. (2019). Development and validation of a Taiwan version of the DN4-T questionnaire. Journal of the Chinese Medical Association. 82(8). 623–627. 12 indexed citations
3.
Yang, Chih‐Chao, Yu‐Chuan Tsai, Kon-Ping Lin, et al.. (2017). Development and validation of a Taiwan version of the ID Pain questionnaire (ID Pain-T). Journal of the Chinese Medical Association. 81(1). 12–17. 11 indexed citations
4.
Liao, Yi‐Chu, et al.. (2017). Clinical and Molecular Characterization of PMP22 point mutations in Taiwanese patients with Inherited Neuropathy. Scientific Reports. 7(1). 15363–15363. 11 indexed citations
5.
Tsai, Pei‐Chien, Chou‐Ching K. Lin, Yo-Tsen Liu, et al.. (2016). Clinical and Molecular Characterization of BSCL2 Mutations in a Taiwanese Cohort with Hereditary Neuropathy. PLoS ONE. 11(1). e0147677–e0147677. 19 indexed citations
6.
Chen, Wei‐Ti, et al.. (2016). Acute Disseminated Encephalomyelitis After Influenza Vaccination: A Case Report. Critical Care Nurse. 36(3). e1–e6. 4 indexed citations
7.
Wu, Ming-Ling, et al.. (2015). Neurotoxicity associated with exposure to 1-bromopropane in golf-club cleansing workers. Clinical Toxicology. 53(8). 823–826. 10 indexed citations
8.
Soong, Bing‐Wen, Kon-Ping Lin, Chou‐Ching K. Lin, et al.. (2014). Extensive molecular genetic survey of Taiwanese patients with amyotrophic lateral sclerosis. Neurobiology of Aging. 35(10). 2423.e1–2423.e6. 45 indexed citations
9.
Tsai, Pei‐Chien, Yen‐Hua Huang, Hung-Ta Wu, et al.. (2014). A novel TFG mutation causes Charcot-Marie-Tooth disease type 2 and impairs TFG function. Neurology. 83(10). 903–912. 39 indexed citations
10.
Soong, Bing‐Wen, Yen‐Hua Huang, Pei‐Chien Tsai, et al.. (2013). Exome Sequencing Identifies GNB4 Mutations as a Cause of Dominant Intermediate Charcot-Marie-Tooth Disease. The American Journal of Human Genetics. 92(3). 422–430. 37 indexed citations
11.
Lai, Tzu-Hsien, Ren-Shyan Liu, Bang‐Hung Yang, et al.. (2013). Cerebral involvement in spinal and bulbar muscular atrophy (Kennedy's disease): A pilot study of PET. Journal of the Neurological Sciences. 335(1-2). 139–144. 24 indexed citations
12.
Wang, Shuu‐Jiun, et al.. (2011). A proposed mechanism of superficial siderosis supported by surgical and neuroimaging findings. Medical Hypotheses. 76(6). 823–826. 23 indexed citations
13.
Lee, Yi‐Chung, et al.. (2010). Clinical characterization and genetic analysis of a possible novel type of dominant Charcot-Marie-Tooth disease. Neuromuscular Disorders. 20(8). 534–539. 4 indexed citations
14.
Lin, Peng-Chan, Ming-Yang Lee, Wei-Shu Wang, et al.. (2006). N-acetylcysteine has neuroprotective effects against oxaliplatin-based adjuvant chemotherapy in colon cancer patients: preliminary data. Supportive Care in Cancer. 14(5). 484–487. 89 indexed citations
15.
Lin, Yung‐Yang, Yang‐Hsin Shih, Jen‐Chuen Hsieh, et al.. (2003). Differential effects of stimulus intensity on peripheral and neuromagnetic cortical responses to median nerve stimulation. NeuroImage. 20(2). 909–917. 40 indexed citations
16.
Lee, Yi‐Chung, Yau‐Huei Wei, Jiing-Feng Lirng, et al.. (2002). Wernicke’s Encephalopathy in a Patient with Multiple Symmetrical Lipomatosis and the A8344G Mutation of Mitochondrial DNA. European Neurology. 47(2). 126–128. 7 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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