Woon-Chee Yee

1.9k total citations
33 papers, 1.5k citations indexed

About

Woon-Chee Yee is a scholar working on Cellular and Molecular Neuroscience, Neurology and Molecular Biology. According to data from OpenAlex, Woon-Chee Yee has authored 33 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Cellular and Molecular Neuroscience, 14 papers in Neurology and 13 papers in Molecular Biology. Recurrent topics in Woon-Chee Yee's work include Peripheral Neuropathies and Disorders (12 papers), Hereditary Neurological Disorders (10 papers) and Myasthenia Gravis and Thymoma (6 papers). Woon-Chee Yee is often cited by papers focused on Peripheral Neuropathies and Disorders (12 papers), Hereditary Neurological Disorders (10 papers) and Myasthenia Gravis and Thymoma (6 papers). Woon-Chee Yee collaborates with scholars based in United States, Singapore and Canada. Woon-Chee Yee's co-authors include Alan Pestronk, Albert R. La Spada, Roland Spiegel, I Hausmanowa-Pétrusewicz, Kenneth H. Fischbeck, Carolyn L. Warner, Anita E. Harding, Jeffrey L. Elliott, David R. Cornblath and Eva L. Feldman and has published in prestigious journals such as Nature Genetics, Biomaterials and Neurology.

In The Last Decade

Woon-Chee Yee

32 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Woon-Chee Yee United States 19 891 667 500 138 127 33 1.5k
Tomohisa Furuta Japan 20 314 0.4× 397 0.6× 524 1.0× 240 1.7× 80 0.6× 65 1.3k
Eiichiro Mukai Japan 14 844 0.9× 751 1.1× 647 1.3× 300 2.2× 47 0.4× 19 1.5k
Haesun A. Kim United States 18 834 0.9× 353 0.5× 604 1.2× 89 0.6× 29 0.2× 25 1.6k
Feza Deymeer Türkiye 25 427 0.5× 751 1.1× 659 1.3× 196 1.4× 34 0.3× 88 1.5k
Kevin J. Felice United States 23 350 0.4× 686 1.0× 643 1.3× 501 3.6× 77 0.6× 65 1.7k
Joachim Schessl Germany 22 386 0.4× 310 0.5× 622 1.2× 165 1.2× 43 0.3× 43 1.2k
S. Tokiguchi Japan 19 310 0.3× 568 0.9× 546 1.1× 160 1.2× 178 1.4× 50 1.5k
Jean‐Christophe Antoine France 25 454 0.5× 1.7k 2.6× 302 0.6× 120 0.9× 98 0.8× 64 2.1k
Sylvie Tuffery‐Giraud France 26 432 0.5× 444 0.7× 1.2k 2.5× 269 1.9× 62 0.5× 72 2.0k
Maria J. Crowe United States 12 465 0.5× 273 0.4× 318 0.6× 162 1.2× 49 0.4× 15 1.5k

Countries citing papers authored by Woon-Chee Yee

Since Specialization
Citations

This map shows the geographic impact of Woon-Chee Yee'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 Woon-Chee Yee with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Woon-Chee Yee more than expected).

Fields of papers citing papers by Woon-Chee Yee

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Woon-Chee Yee. 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 Woon-Chee Yee. The network helps show where Woon-Chee Yee may publish in the future.

Co-authorship network of co-authors of Woon-Chee Yee

This figure shows the co-authorship network connecting the top 25 collaborators of Woon-Chee Yee. A scholar is included among the top collaborators of Woon-Chee Yee 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 Woon-Chee Yee. Woon-Chee Yee 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.
Spaendonck‐Zwarts, Karin Y. van, Anneke J. van der Kooi, Maarten P. van den Berg, et al.. (2012). Recurrent and founder mutations in the Netherlands: the cardiac phenotype of DES founder mutations p.S13F and p.N342D. Netherlands Heart Journal. 20(5). 219–228. 19 indexed citations
2.
Yee, Woon-Chee, et al.. (2008). Correction of dystrophia myotonica type 1 pre-mRNA transcripts by artificial trans-splicing. Gene Therapy. 16(2). 211–217. 25 indexed citations
3.
Pramono, Zacharias Aloysius Dwi, et al.. (2008). Characterization of a novel S13F desmin mutation associated with desmin myopathy and heart block in a Chinese family. Neuromuscular Disorders. 18(2). 178–182. 21 indexed citations
4.
Yee, Woon-Chee. (2008). Two eminently treatable genetic metabolic myopathies. Neurology India. 56(3). 333–333. 2 indexed citations
5.
Yee, Woon-Chee, et al.. (2007). G.P.8.15 Limb girdle muscular dystrophy 2G and novel TCAP mutations in ethnic Chinese. Neuromuscular Disorders. 17(9-10). 814–814. 15 indexed citations
6.
Pramono, Zacharias Aloysius Dwi, et al.. (2007). M.P.4.17 Late onset multiple acyl-CoA dehydrogenase deficiency (MADD) associated with novel ETFDH mutations in two Chinese patients. Neuromuscular Disorders. 17(9-10). 864–864.
7.
Wang, Xu, Chaoyang Wang, Jieming Zeng, et al.. (2005). Gene Transfer to Dorsal Root Ganglia by Intrathecal Injection: Effects on Regeneration of Peripheral Nerves. Molecular Therapy. 12(2). 314–320. 56 indexed citations
8.
Pestronk, Alan, Rati Choksi, Woon-Chee Yee, et al.. (1998). Serum antibodies to heparan sulfate glycosaminoglycans in Guillain–Barré syndrome and other demyelinating polyneuropathies. Journal of Neuroimmunology. 91(1-2). 204–209. 11 indexed citations
9.
Connolly, Anne M., et al.. (1997). Serum IgM Monoclonal Autoantibody Binding to the 301 to 314 Amino Acid Epitope of Beta-tubulin. Neurology. 48(1). 243–248. 14 indexed citations
10.
Nevo, Yoram, Alan Pestronk, Andrew J. Kornberg, et al.. (1996). Childhood chronic inflammatory demyelinating neuropathies. Neurology. 47(1). 98–102. 78 indexed citations
11.
Pestronk, Alan, et al.. (1995). Myopathy and paraproteinemia with serum igm binding to a high‐ molecular‐weight muscle fiber surface protein. Annals of Neurology. 37(1). 41–46. 3 indexed citations
12.
Pestronk, Alan, et al.. (1994). Rapidly evolving myopathy with myosin‐deficient muscle fibers. Annals of Neurology. 35(3). 273–279. 58 indexed citations
13.
Belsham, Denise D., et al.. (1992). Analysis of the CAG repeat region of the androgen receptor gene in a kindred with X-linked spinal and bulbar muscular atrophy. Journal of the Neurological Sciences. 112(1-2). 133–138. 27 indexed citations
14.
Spada, Albert R. La, Anita E. Harding, Carolyn L. Warner, et al.. (1992). Meiotic stability and genotype – phenotype correlation of the trinucleotide repeat in X–linked spinal and bulbar muscular atrophy. Nature Genetics. 2(4). 301–304. 280 indexed citations
15.
Kryger, Meir H., et al.. (1991). Central sleep apnoea in congenital muscular dystrophy.. Journal of Neurology Neurosurgery & Psychiatry. 54(8). 710–712. 10 indexed citations
16.
Pestronk, Alan, Vinay Chaudhry, Eva L. Feldman, et al.. (1990). Lower motor neuron syndromes defined by patterns of weakness, nerve conduction abnormalities, and high titers of antiglycolipid antibodies. Annals of Neurology. 27(3). 316–326. 185 indexed citations
17.
Alderson, Kathy, Woon-Chee Yee, & Alan Pestronk. (1989). Reorganization of intrinsic components in the distal motor axon during outgrowth. Journal of Neurocytology. 18(4). 541–552. 4 indexed citations
18.
Yee, Woon-Chee, et al.. (1989). Neuropathy in igM? paraproteinemia. Acta Neuropathologica. 78(1). 57–64. 39 indexed citations
19.
Yee, Woon-Chee, Andreas Hahn, & J. J. Gilbert. (1988). Adult onset scapuloperoneal myopathy: diagnostic value of nerve morphometry and multiple muscle biopsies.. Journal of Neurology Neurosurgery & Psychiatry. 51(6). 808–813. 4 indexed citations
20.
Yee, Woon-Chee, et al.. (1988). Effect of ketoleucine treatment on atrophy of skeletal muscle. Experimental Neurology. 99(1). 1–9. 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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