Ling T. Guo

1.6k total citations
74 papers, 1.2k citations indexed

About

Ling T. Guo is a scholar working on Molecular Biology, Cell Biology and Surgery. According to data from OpenAlex, Ling T. Guo has authored 74 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 59 papers in Molecular Biology, 20 papers in Cell Biology and 16 papers in Surgery. Recurrent topics in Ling T. Guo's work include Muscle Physiology and Disorders (44 papers), Tissue Engineering and Regenerative Medicine (11 papers) and Congenital heart defects research (10 papers). Ling T. Guo is often cited by papers focused on Muscle Physiology and Disorders (44 papers), Tissue Engineering and Regenerative Medicine (11 papers) and Congenital heart defects research (10 papers). Ling T. Guo collaborates with scholars based in United States, China and Canada. Ling T. Guo's co-authors include G. Diane Shelton, Eva Engvall, Andrew P. Mizisin, Ju Chen, Jianlin Zhang, Theodore Friedmann, Katie M. Minor, Richard L. Lieber, J K Yee and Aritoshi Iida and has published in prestigious journals such as Proceedings of the National Academy of Sciences, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

Ling T. Guo

72 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ling T. Guo United States 19 880 258 213 167 130 74 1.2k
Ellen van Beusekom Netherlands 10 1.1k 1.2× 187 0.7× 273 1.3× 134 0.8× 93 0.7× 15 1.4k
Frances A. Lemckert Australia 21 753 0.9× 310 1.2× 310 1.5× 73 0.4× 317 2.4× 27 1.9k
Terri G. Thompson United States 13 891 1.0× 271 1.1× 156 0.7× 92 0.6× 331 2.5× 15 1.2k
Alexis R. Demonbreun United States 25 1.2k 1.4× 318 1.2× 89 0.4× 109 0.7× 217 1.7× 59 1.7k
Helen M. Phillips United Kingdom 19 784 0.9× 298 1.2× 144 0.7× 129 0.8× 159 1.2× 34 1.2k
Koichi Ojima Japan 25 1.1k 1.3× 499 1.9× 137 0.6× 147 0.9× 209 1.6× 64 1.7k
Nena J. Winand United States 17 1.1k 1.3× 288 1.1× 339 1.6× 171 1.0× 170 1.3× 27 1.5k
Steven C. Miller United States 11 1.2k 1.3× 201 0.8× 157 0.7× 117 0.7× 64 0.5× 19 1.5k
Bradley L. Hodges United States 25 954 1.1× 210 0.8× 526 2.5× 103 0.6× 97 0.7× 30 1.5k
Shin’ichiro Yasunaga Japan 21 741 0.8× 143 0.6× 237 1.1× 103 0.6× 52 0.4× 60 1.7k

Countries citing papers authored by Ling T. Guo

Since Specialization
Citations

This map shows the geographic impact of Ling T. Guo'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 Ling T. Guo with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ling T. Guo more than expected).

Fields of papers citing papers by Ling T. Guo

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ling T. Guo. 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 Ling T. Guo. The network helps show where Ling T. Guo may publish in the future.

Co-authorship network of co-authors of Ling T. Guo

This figure shows the co-authorship network connecting the top 25 collaborators of Ling T. Guo. A scholar is included among the top collaborators of Ling T. Guo 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 Ling T. Guo. Ling T. Guo 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.
2.
Wang, Xing, et al.. (2024). Effects of radiofrequency field from 5G communication on fecal microbiome and metabolome profiles in mice. Scientific Reports. 14(1). 3571–3571. 4 indexed citations
3.
Marks, Stanley L., et al.. (2024). Feline dystrophin-deficient muscular dystrophy misdiagnosed as Toxoplasma myositis. Journal of Feline Medicine and Surgery Open Reports. 10(2). 4132964691–4132964691. 1 indexed citations
4.
Shelton, G. Diane, James R. Mickelson, Steven G. Friedenberg, et al.. (2024). Variants in CLCN1 and PDE4C Associated with Muscle Hypertrophy, Dysphagia, and Gait Abnormalities in Young French Bulldogs. Animals. 14(5). 722–722. 1 indexed citations
5.
Chen, Annie V., Katie M. Minor, Steven G. Friedenberg, et al.. (2023). Novel COL6A3 frameshift variant in American Staffordshire Terrier dogs with Ullrich-like congenital muscular dystrophy. Journal of Veterinary Internal Medicine. 37(6). 2504–2509. 2 indexed citations
6.
Mickelson, James R., Katie M. Minor, Ling T. Guo, et al.. (2021). Sarcoglycan A mutation in miniature dachshund dogs causes limb-girdle muscular dystrophy 2D. Skeletal Muscle. 11(1). 9 indexed citations
7.
Shelton, G. Diane, et al.. (2021). Congenital dyserythropoiesis and polymyopathy without cardiac disease in male Labrador retriever littermates. Journal of Veterinary Internal Medicine. 35(5). 2409–2414. 3 indexed citations
8.
Tsai, Kate L., Karen M. Vernau, Beverly K. Sturges, et al.. (2019). Congenital myasthenic syndrome in Golden Retrievers is associated with a novel COLQ mutation. Journal of Veterinary Internal Medicine. 34(1). 258–265. 4 indexed citations
9.
Shelton, G. Diane, Katie M. Minor, Kefeng Li, et al.. (2019). A Mutation in the Mitochondrial Aspartate/Glutamate Carrier Leads to a More Oxidizing Intramitochondrial Environment and an Inflammatory Myopathy in Dutch Shepherd Dogs. Journal of Neuromuscular Diseases. 6(4). 485–501. 14 indexed citations
10.
Michaels, Jennifer, et al.. (2017). Congenital Myasthenic Syndrome in a Mixed Breed Dog. Frontiers in Veterinary Science. 4. 173–173. 2 indexed citations
11.
Chan, Adriano, Jingjing Jiang, Ling T. Guo, et al.. (2015). Nitrocobinamide, a New Cyanide Antidote That Can Be Administered by Intramuscular Injection. Journal of Medicinal Chemistry. 58(4). 1750–1759. 38 indexed citations
12.
Levine, Jonathan M., Katie M. Minor, Ling T. Guo, et al.. (2014). A COLQ Missense Mutation in Labrador Retrievers Having Congenital Myasthenic Syndrome. PLoS ONE. 9(8). e106425–e106425. 20 indexed citations
13.
Marioni‐Henry, Katia, et al.. (2013). Sarcolemmal Specific Collagen VI Deficient Myopathy in a Labrador Retriever. Journal of Veterinary Internal Medicine. 28(1). 243–249. 12 indexed citations
14.
Costa, Ronaldo C. da, et al.. (2011). Multisystem Cranial Polyneuritis and Ganglionitis in a Dog. Journal of Veterinary Internal Medicine. 25(5). 1161–1165. 6 indexed citations
15.
Guo, Ling T., Steven A. Moore, Sonia Vanina Forcales, Eva Engvall, & G. Diane Shelton. (2010). Evaluation of commercial dysferlin antibodies on canine, mouse and human skeletal muscle. Neuromuscular Disorders. 20(12). 820–825. 19 indexed citations
16.
Guo, Ling T., Theodore Friedmann, & Charles C. King. (2007). Partial characterization of the proteome of the mouse striatum. PROTEOMICS. 7(21). 3867–3869. 3 indexed citations
17.
Guo, Ling T., Wenhuan Kuang, Hong Xu, et al.. (2003). Laminin α2 deficiency and muscular dystrophy; genotype-phenotype correlation in mutant mice. Neuromuscular Disorders. 13(3). 207–215. 69 indexed citations
18.
O’Brien, Dennis P., Gayle C. Johnson, Ling T. Guo, et al.. (2001). Laminin α2 (merosin)-deficient muscular dystrophy and demyelinating neuropathy in two cats. Journal of the Neurological Sciences. 189(1-2). 37–43. 41 indexed citations
19.
Shelton, G. Diane, Ling T. Guo, Gail K. Smith, et al.. (2001). Muscular Dystrophy in female Dogs. Journal of Veterinary Internal Medicine. 15(3). 240–244. 37 indexed citations
20.
Shelton, G. Diane, Ling T. Guo, Gail K. Smith, et al.. (2001). Muscular Dystrophy in Female Dogs. Journal of Veterinary Internal Medicine. 15(3). 240–240. 40 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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