Guy M. Lenk

3.6k total citations
38 papers, 1.7k citations indexed

About

Guy M. Lenk is a scholar working on Cell Biology, Molecular Biology and Physiology. According to data from OpenAlex, Guy M. Lenk has authored 38 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Cell Biology, 12 papers in Molecular Biology and 12 papers in Physiology. Recurrent topics in Guy M. Lenk's work include Cellular transport and secretion (17 papers), Calcium signaling and nucleotide metabolism (12 papers) and Autophagy in Disease and Therapy (9 papers). Guy M. Lenk is often cited by papers focused on Cellular transport and secretion (17 papers), Calcium signaling and nucleotide metabolism (12 papers) and Autophagy in Disease and Therapy (9 papers). Guy M. Lenk collaborates with scholars based in United States, France and Japan. Guy M. Lenk's co-authors include Miriam H. Meisler, Cole Ferguson, Helena Kuivaniemi, Gerard Tromp, Roman J. Giger, Zoran Gatalica, Julie Miller Jones, Shantel Weinsheimer, Ramón Berguer and Lois S. Weisman and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Clinical Investigation and Journal of Neuroscience.

In The Last Decade

Guy M. Lenk

37 papers receiving 1.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Guy M. Lenk United States 23 620 616 351 339 287 38 1.7k
Olatz Pampliega United States 13 208 0.3× 743 1.2× 125 0.4× 161 0.5× 439 1.5× 14 1.5k
Jeong‐A Lim United States 13 305 0.5× 647 1.1× 324 0.9× 46 0.1× 711 2.5× 23 1.6k
Syed Mukhtar Ahmed United States 18 250 0.4× 742 1.2× 56 0.2× 380 1.1× 92 0.3× 24 1.4k
Owen A. Brady United States 13 327 0.5× 700 1.1× 145 0.4× 108 0.3× 489 1.7× 14 1.7k
Outi Kopra Finland 29 622 1.0× 1.0k 1.6× 187 0.5× 198 0.6× 147 0.5× 35 2.0k
Jonathan Baets Belgium 26 470 0.8× 1.1k 1.7× 51 0.1× 1.1k 3.2× 128 0.4× 80 2.2k
Françoise Levavasseur France 15 181 0.3× 533 0.9× 162 0.5× 411 1.2× 71 0.2× 21 1.3k
Lluı̈sa Vilageliu Spain 27 657 1.1× 742 1.2× 101 0.3× 98 0.3× 334 1.2× 78 1.7k
Gulab Zode United States 25 467 0.8× 1.1k 1.8× 76 0.2× 78 0.2× 110 0.4× 45 2.2k
Wanda Setlik United States 11 204 0.3× 428 0.7× 41 0.1× 362 1.1× 213 0.7× 14 1.2k

Countries citing papers authored by Guy M. Lenk

Since Specialization
Citations

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

Fields of papers citing papers by Guy M. Lenk

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Guy M. Lenk. 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 Guy M. Lenk. The network helps show where Guy M. Lenk may publish in the future.

Co-authorship network of co-authors of Guy M. Lenk

This figure shows the co-authorship network connecting the top 25 collaborators of Guy M. Lenk. A scholar is included among the top collaborators of Guy M. Lenk 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 Guy M. Lenk. Guy M. Lenk 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.
Park, Young Nyun, et al.. (2024). Protein family FAM241 in human and mouse. Mammalian Genome. 36(1). 83–92.
2.
Cao, Xu, Guy M. Lenk, & Miriam H. Meisler. (2023). Altered phenotypes due to genetic interaction between the mouse phosphoinositide biosynthesis genes Fig4 and Pip4k2c. G3 Genes Genomes Genetics. 13(8). 3 indexed citations
3.
Cao, Xu, et al.. (2023). The chloride antiporter CLCN7 is a modifier of lysosome dysfunction in FIG4 and VAC14 mutants. PLoS Genetics. 19(6). e1010800–e1010800. 8 indexed citations
4.
Presa, Maximiliano, Rachel M. Bailey, Crystal Davis, et al.. (2021). AAV9-mediated FIG4 delivery prolongs life span in Charcot-Marie-Tooth disease type 4J mouse model. Journal of Clinical Investigation. 131(11). 24 indexed citations
5.
Lenk, Guy M., Young Nyun Park, Rosemary Lemons, et al.. (2019). CRISPR knockout screen implicates three genes in lysosome function. Scientific Reports. 9(1). 9609–9609. 26 indexed citations
6.
Choy, Christopher H., Matthew Gray, Callen T. Wallace, et al.. (2018). Lysosome enlargement during inhibition of the lipid kinase PIKfyve proceeds through lysosome coalescence. Journal of Cell Science. 131(10). 96 indexed citations
7.
Lenk, Guy M., Krystyna Szymańska, Grażyna Dębska–Vielhaber, et al.. (2016). Biallelic Mutations of VAC14 in Pediatric-Onset Neurological Disease. The American Journal of Human Genetics. 99(1). 188–194. 41 indexed citations
8.
Vaccari, Ilaria, Stefano C. Previtali, Yevgeniya A. Mironova, et al.. (2014). Loss of Fig4 in both Schwann cells and motor neurons contributes to CMT4J neuropathy. Human Molecular Genetics. 24(2). 383–396. 39 indexed citations
9.
Reifler, Aaron N., Guy M. Lenk, Xingli Li, et al.. (2013). Murine Fig4 is dispensable for muscle development but required for muscle function. Skeletal Muscle. 3(1). 21–21. 5 indexed citations
10.
Campeau, Philippe M., Guy M. Lenk, Yangjin Bae, et al.. (2013). Yunis-Varón Syndrome Is Caused by Mutations in FIG4, Encoding a Phosphoinositide Phosphatase. The American Journal of Human Genetics. 92(5). 781–791. 115 indexed citations
11.
Meisler, Miriam H., Julie Miller Jones, Guy M. Lenk, et al.. (2013). C9ORF72 expansion in a family with bipolar disorder. Bipolar Disorders. 15(3). 326–332. 46 indexed citations
12.
Lenk, Guy M. & Miriam H. Meisler. (2013). Mouse Models of PI(3,5)P2 Deficiency with Impaired Lysosome Function. Methods in enzymology on CD-ROM/Methods in enzymology. 534. 245–260. 28 indexed citations
13.
Auerbach, David S., Julie Miller Jones, Brittany C. Clawson, et al.. (2013). Altered Cardiac Electrophysiology and SUDEP in a Model of Dravet Syndrome. PLoS ONE. 8(10). e77843–e77843. 117 indexed citations
14.
Ferguson, Cole, Guy M. Lenk, Julie Miller Jones, et al.. (2012). Neuronal expression of Fig4 is both necessary and sufficient to prevent spongiform neurodegeneration. Human Molecular Genetics. 21(16). 3525–3534. 48 indexed citations
15.
Ferguson, Cole, et al.. (2011). Congenital CNS Hypomyelination in theFig4Null Mouse Is Rescued by Neuronal Expression of the PI(3,5)P2PhosphataseFig4. Journal of Neuroscience. 31(48). 17736–17751. 39 indexed citations
16.
Lillvis, John H., Gerard Tromp, Guy M. Lenk, et al.. (2011). Analysis of positional candidate genes in the AAA1 susceptibility locus for abdominal aortic aneurysms on chromosome 19. BMC Medical Genetics. 12(1). 14–14. 14 indexed citations
17.
Lillvis, John H., Robert Erdman, Charles M. Schworer, et al.. (2011). Regional expression of HOXA4 along the aorta and its potential role in human abdominal aortic aneurysms. BMC Physiology. 11(1). 9–9. 28 indexed citations
18.
Ferguson, Cole, Guy M. Lenk, & Miriam H. Meisler. (2010). PtdIns(3,5)P2and autophagy in mouse models of neurodegeneration. Autophagy. 6(1). 170–171. 23 indexed citations
19.
Ferguson, Cole, Guy M. Lenk, & Miriam H. Meisler. (2009). Defective autophagy in neurons and astrocytes from mice deficient in PI(3,5)P2. Human Molecular Genetics. 18(24). 4868–4878. 163 indexed citations
20.
Lenk, Guy M., Gerard Tromp, Shantel Weinsheimer, et al.. (2007). Whole genome expression profiling reveals a significant role for immune function in human abdominal aortic aneurysms. BMC Genomics. 8(1). 237–237. 145 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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