Wei‐De Lin

1.2k total citations
67 papers, 911 citations indexed

About

Wei‐De Lin is a scholar working on Molecular Biology, Genetics and Psychiatry and Mental health. According to data from OpenAlex, Wei‐De Lin has authored 67 papers receiving a total of 911 indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Molecular Biology, 14 papers in Genetics and 9 papers in Psychiatry and Mental health. Recurrent topics in Wei‐De Lin's work include Epilepsy research and treatment (8 papers), Enzyme Structure and Function (7 papers) and Amino Acid Enzymes and Metabolism (7 papers). Wei‐De Lin is often cited by papers focused on Epilepsy research and treatment (8 papers), Enzyme Structure and Function (7 papers) and Amino Acid Enzymes and Metabolism (7 papers). Wei‐De Lin collaborates with scholars based in Taiwan, China and United States. Wei‐De Lin's co-authors include Fuu‐Jen Tsai, I‐Ching Chou, Chang‐Hai Tsai, Chung‐Hsing Wang, Chien‐Chen Lai, Wen-Hwei Hsu, Fuu‐Jen Tsai, Cheng‐Chun Lee, Wan‐Yu Lo and I‐Chieh Chen and has published in prestigious journals such as Applied and Environmental Microbiology, Journal of Agricultural and Food Chemistry and Scientific Reports.

In The Last Decade

Wei‐De Lin

66 papers receiving 895 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Wei‐De Lin Taiwan 17 459 111 85 79 73 67 911
Michael Cardamone Australia 14 479 1.0× 104 0.9× 122 1.4× 35 0.4× 62 0.8× 40 1.0k
Tomoko Nagata Japan 18 347 0.8× 113 1.0× 24 0.3× 69 0.9× 48 0.7× 87 1.0k
Hideto To Japan 21 413 0.9× 137 1.2× 74 0.9× 18 0.2× 67 0.9× 76 1.5k
Yael Lifshitz Israel 17 622 1.4× 58 0.5× 61 0.7× 15 0.2× 92 1.3× 31 1.1k
Colin H. Self United Kingdom 19 676 1.5× 71 0.6× 42 0.5× 60 0.8× 86 1.2× 58 1.6k
Wenxin Li China 22 642 1.4× 211 1.9× 36 0.4× 22 0.3× 167 2.3× 114 1.7k
Ross Dixon United States 21 390 0.8× 54 0.5× 51 0.6× 79 1.0× 61 0.8× 50 1.3k
Viktor Farkas Hungary 18 404 0.9× 70 0.6× 151 1.8× 174 2.2× 17 0.2× 75 982
Nicolò Musso Italy 24 543 1.2× 76 0.7× 46 0.5× 17 0.2× 84 1.2× 90 1.8k
Ian T. Crosby Australia 17 348 0.8× 73 0.7× 48 0.6× 37 0.5× 23 0.3× 47 889

Countries citing papers authored by Wei‐De Lin

Since Specialization
Citations

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

Fields of papers citing papers by Wei‐De Lin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Wei‐De Lin

This figure shows the co-authorship network connecting the top 25 collaborators of Wei‐De Lin. A scholar is included among the top collaborators of Wei‐De 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 Wei‐De Lin. Wei‐De Lin is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Lin, Wei‐De, et al.. (2025). Impact of neutrophil percentage-to-albumin ratio on mortality in iron-deficiency anemia patients: a retrospective study using MIMIC-IV database. European journal of medical research. 30(1). 4–4. 1 indexed citations
2.
Lin, Wei‐De, Bilan Lin, Junfan Chen, et al.. (2024). Impact of unintentional weight loss on 30-day mortality in intensive care unit sepsis patients: a retrospective cohort study. Scientific Reports. 14(1). 31535–31535. 1 indexed citations
3.
Lin, Wei‐De, Wen‐Ling Liao, Wei-Cheng Chen, et al.. (2024). Genome-wide association study identifies novel susceptible loci and evaluation of polygenic risk score for chronic obstructive pulmonary disease in a Taiwanese population. BMC Genomics. 25(1). 607–607. 1 indexed citations
4.
Chang, Yu‐Tzu, et al.. (2023). Genetic Testing in Children with Developmental and Epileptic Encephalopathies: A Review of Advances in Epilepsy Genomics. Children. 10(3). 556–556. 11 indexed citations
5.
Lin, Wei‐De, Fuu‐Jen Tsai, & Chung‐Hsing Wang. (2023). Identification of a novel deletion mutation in PHKA2 in a taiwanese patient with type IXa glycogen storage disease. Pediatrics & Neonatology. 64(4). 465–467. 2 indexed citations
6.
Cheng, Chi‐Fung, Wen‐Miin Liang, Chung‐Hsing Wang, et al.. (2022). Your height affects your health: genetic determinants and health-related outcomes in Taiwan. BMC Medicine. 20(1). 250–250. 16 indexed citations
7.
Lin, Wei‐De, Fuu‐Jen Tsai, & I‐Ching Chou. (2022). Current understanding of the genetics of Tourette syndrome. Biomedical Journal. 45(2). 271–279. 15 indexed citations
8.
Chen, Yng‐Tay, et al.. (2021). Author Correction: NT5C2 methylation regulatory interplay between DNMT1 and insulin receptor in type 2 diabetes. Scientific Reports. 11(1). 6961–6961.
9.
Lin, Chien‐Heng, et al.. (2019). Epilepsy and Neurodevelopmental Outcomes in Children With Etiologically Diagnosed Central Nervous System Infections: A Retrospective Cohort Study. Frontiers in Neurology. 10. 528–528. 16 indexed citations
10.
Lin, Chien‐Heng, et al.. (2018). Epileptic spasms in PPP1CB-associated Noonan-like syndrome: a case report with clinical and therapeutic implications. BMC Neurology. 18(1). 150–150. 8 indexed citations
11.
Zhu, Hongyan, Ziyi Wang, Yuxiao Zhao, et al.. (2016). Parkinson’s disease-like forelimb akinesia induced by BmK I, a sodium channel modulator. Behavioural Brain Research. 308. 166–176. 7 indexed citations
12.
Chou, I‐Ching, et al.. (2016). A case of Pitt-Hopkins syndrome presented with Angelman-like syndromic phenotypes. Biomedicine. 6(4). 25–25. 5 indexed citations
13.
Lin, Wei‐De, et al.. (2015). Identification and Characterization of Mutations in the CLCN7 Gene in a Taiwanese Patient with Infantile Malignant Osteopetrosis. Pediatrics & Neonatology. 57(2). 155–157. 3 indexed citations
14.
Chou, I‐Ching, et al.. (2014). Successful control with carbamazepine of family with paroxysmal kinesigenic dyskinesia of PRRT2 mutation. Biomedicine. 4(2). 15–15. 10 indexed citations
15.
Wang, Chung‐Hsing, Wei‐De Lin, DA-TIAN BAU, I‐Ching Chou, & Fuu‐Jen Tsai. (2011). Genetic and clinical profiles of spondylocostal dysostosis patients in Taiwan. American Journal of Medical Genetics Part A. 155(12). 3132–3135. 3 indexed citations
16.
Chou, I‐Ching, Chung‐Hsing Wang, Wei‐De Lin, Chang‐Hai Tsai, & Fuu‐Jen Tsai. (2011). Association study in Taiwanese girls with precocious puberty. Journal of Pediatric Endocrinology and Metabolism. 24(1-2). 103–4. 8 indexed citations
17.
Chen, I‐Chieh, et al.. (2009). Lysine racemase: a novel non-antibiotic selectable marker for plant transformation. Plant Molecular Biology. 72(1-2). 153–169. 28 indexed citations
18.
Chien, Shu‐Chin, et al.. (2009). Rare rearrangements: A “jumping satellite” in one family and autosomal location of the SRY gene in an XX male. American Journal of Medical Genetics Part A. 149A(12). 2775–2781. 6 indexed citations
19.
Lo, Hsueh‐Hsia, Shih‐Kuang Hsu, Wei‐De Lin, Nei‐Li Chan, & Wen-Hwei Hsu. (2005). Asymmetrical Synthesis of l-Homophenylalanine Using Engineered Escherichia coli Aspartate Aminotransferase. Biotechnology Progress. 21(2). 411–415. 30 indexed citations
20.
Lin, Wei‐De, et al.. (2001). Identification of a polymorphism (D168N) in the XRP2 gene in Chinese. Human Mutation. 17(4). 354–354. 4 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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