Leigh A. Baxt

1.3k total citations
17 papers, 925 citations indexed

About

Leigh A. Baxt is a scholar working on Molecular Biology, Epidemiology and Endocrinology. According to data from OpenAlex, Leigh A. Baxt has authored 17 papers receiving a total of 925 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 5 papers in Epidemiology and 4 papers in Endocrinology. Recurrent topics in Leigh A. Baxt's work include Autophagy in Disease and Therapy (5 papers), Vibrio bacteria research studies (3 papers) and Biochemical and Molecular Research (3 papers). Leigh A. Baxt is often cited by papers focused on Autophagy in Disease and Therapy (5 papers), Vibrio bacteria research studies (3 papers) and Biochemical and Molecular Research (3 papers). Leigh A. Baxt collaborates with scholars based in United States, Australia and Netherlands. Leigh A. Baxt's co-authors include Marcia B. Goldberg, Ramnik J. Xavier, Anna Cristina Garza‐Mayers, Upinder Singh, Robert J. W. Heath, Jakob Begun, Jatin M. Vyas, Slim Sassi, Alan Huett and Rosanna P. Baker and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Leigh A. Baxt

17 papers receiving 915 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Leigh A. Baxt United States	13	382	377	183	170	169	17	925
Cristina Lourdes Vázquez Argentina	11	263 0.7×	489 1.3×	157 0.9×	123 0.7×	197 1.2×	25	901
Michal P. Wandel United Kingdom	8	743 1.9×	567 1.5×	139 0.8×	157 0.9×	462 2.7×	8	1.5k
James W. Bowman United States	7	429 1.1×	429 1.1×	72 0.4×	240 1.4×	289 1.7×	8	1.0k
Kayoko Tsuda Japan	9	463 1.2×	756 2.0×	138 0.8×	84 0.5×	259 1.5×	11	1.3k
Sangeeta Tiwari United States	17	455 1.2×	434 1.2×	95 0.5×	367 2.2×	525 3.1×	43	1.4k
Takeshi Matsuzawa Japan	18	349 0.9×	276 0.7×	64 0.3×	198 1.2×	253 1.5×	22	984
Angela van Diepen Netherlands	19	297 0.8×	193 0.5×	309 1.7×	162 1.0×	211 1.2×	52	936
Eun‐Kyung Moon South Korea	19	628 1.6×	319 0.8×	179 1.0×	121 0.7×	185 1.1×	92	1.1k
Nadia Khelef France	15	469 1.2×	355 0.9×	40 0.2×	149 0.9×	239 1.4×	18	1.3k
Aristóbolo M. Silva Brazil	20	583 1.5×	267 0.7×	104 0.6×	152 0.9×	589 3.5×	43	1.4k

Countries citing papers authored by Leigh A. Baxt

Since Specialization

Citations

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

Fields of papers citing papers by Leigh A. Baxt

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Leigh A. Baxt. 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 Leigh A. Baxt. The network helps show where Leigh A. Baxt may publish in the future.

Co-authorship network of co-authors of Leigh A. Baxt

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

All Works

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17 of 17 papers shown

1.

Ginn, John D., Tomasz Kochańczyk, Xiuju Jiang, et al.. (2024). Indazole to 2‐Cyanoindole Scaffold Progression for Mycobacterial Lipoamide Dehydrogenase Inhibitors Achieves Extended Target Residence Time and Improved Antibacterial Activity. Angewandte Chemie. 136(44). 1 indexed citations

2.

Ginn, John D., Tomasz Kochańczyk, Xiuju Jiang, et al.. (2024). Indazole to 2‐Cyanoindole Scaffold Progression for Mycobacterial Lipoamide Dehydrogenase Inhibitors Achieves Extended Target Residence Time and Improved Antibacterial Activity. Angewandte Chemie International Edition. 63(44). e202407276–e202407276. 3 indexed citations

3.

Michino, Mayako, Alexandre Beautrait, Nicholas A. Boyles, et al.. (2023). Shape-Based Virtual Screening of a Billion-Compound Library Identifies Mycobacterial Lipoamide Dehydrogenase Inhibitors. SHILAP Revista de lepidopterología. 3(6). 507–515. 7 indexed citations

4.

Liang, Rui, Daisuke Tomita, Yusuke Sasaki, et al.. (2022). A Chemical Strategy toward Novel Brain-Penetrant EZH2 Inhibitors. ACS Medicinal Chemistry Letters. 13(3). 377–387. 4 indexed citations

5.

Kastan, Nathaniel R., Leigh A. Baxt, Robert W. Myers, et al.. (2022). Development of an improved inhibitor of Lats kinases to promote regeneration of mammalian organs. Proceedings of the National Academy of Sciences. 119(28). e2206113119–e2206113119. 29 indexed citations

6.

Khor, Bernard, Kara L. Conway, Moshe Biton, et al.. (2019). Distinct Tissue-Specific Roles for the Disease-Associated Autophagy Genes ATG16L2 and ATG16L1. The Journal of Immunology. 203(7). 1820–1829. 19 indexed citations

7.

Heath, Robert J. W., Gautam Goel, Leigh A. Baxt, et al.. (2016). RNF166 Determines Recruitment of Adaptor Proteins during Antibacterial Autophagy. Cell Reports. 17(9). 2183–2194. 77 indexed citations

8.

Lassen, Kara G., Craig I. McKenzie, Muriel Mari, et al.. (2016). Genetic Coding Variant in GPR65 Alters Lysosomal pH and Links Lysosomal Dysfunction with Colitis Risk. Immunity. 44(6). 1392–1405. 97 indexed citations

9.

Russo, Brian C., Luisa M. Stamm, Matthijs Raaben, et al.. (2016). Intermediate filaments enable pathogen docking to trigger type 3 effector translocation. Nature Microbiology. 1(4). 16025–16025. 39 indexed citations

10.

Baxt, Leigh A. & Ramnik J. Xavier. (2015). Role of Autophagy in the Maintenance of Intestinal Homeostasis. Gastroenterology. 149(3). 553–562. 77 indexed citations

11.

Allen, John E., Brian C. Russo, Soo Young Lee, et al.. (2014). Systematic Analysis of Bacterial Effector-Postsynaptic Density 95/Disc Large/Zonula Occludens-1 (PDZ) Domain Interactions Demonstrates Shigella OspE Protein Promotes Protein Kinase C Activation via PDLIM Proteins. Journal of Biological Chemistry. 289(43). 30101–30113. 14 indexed citations

12.

Baxt, Leigh A. & Marcia B. Goldberg. (2014). Host and Bacterial Proteins That Repress Recruitment of LC3 to Shigella Early during Infection. PLoS ONE. 9(4). e94653–e94653. 51 indexed citations

13.

Baxt, Leigh A., Anna Cristina Garza‐Mayers, & Marcia B. Goldberg. (2013). Bacterial Subversion of Host Innate Immune Pathways. Science. 340(6133). 697–701. 163 indexed citations

14.

Huett, Alan, Robert J. W. Heath, Jakob Begun, et al.. (2012). The LRR and RING Domain Protein LRSAM1 Is an E3 Ligase Crucial for Ubiquitin-Dependent Autophagy of Intracellular Salmonella Typhimurium. Cell Host & Microbe. 12(6). 778–790. 175 indexed citations

15.

Baxt, Leigh A., et al.. (2010). Downregulation of an Entamoeba histolytica Rhomboid Protease Reveals Roles in Regulating Parasite Adhesion and Phagocytosis. Eukaryotic Cell. 9(8). 1283–1293. 49 indexed citations

16.

Baxt, Leigh A., Rosanna P. Baker, Upinder Singh, & Siniša Urban. (2008). An Entamoeba histolytica rhomboid protease with atypical specificity cleaves a surface lectin involved in phagocytosis and immune evasion. Genes & Development. 22(12). 1636–1646. 71 indexed citations

17.

Baxt, Leigh A. & Upinder Singh. (2008). New insights into Entamoeba histolytica pathogenesis. Current Opinion in Infectious Diseases. 21(5). 489–494. 49 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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