George Lawless

1.0k total citations
15 papers, 649 citations indexed

About

George Lawless is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, George Lawless has authored 15 papers receiving a total of 649 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 6 papers in Cellular and Molecular Neuroscience and 4 papers in Neurology. Recurrent topics in George Lawless's work include Pluripotent Stem Cells Research (4 papers), Nerve injury and regeneration (3 papers) and Alzheimer's disease research and treatments (2 papers). George Lawless is often cited by papers focused on Pluripotent Stem Cells Research (4 papers), Nerve injury and regeneration (3 papers) and Alzheimer's disease research and treatments (2 papers). George Lawless collaborates with scholars based in United States, Mexico and Taiwan. George Lawless's co-authors include Tzu‐Kang Sang, George R. Jackson, Shreyasi Chatterjee, George R. Jackson, Anuradha Ratnaparkhi, Felix E. Schweizer, Peyman Golshani, Allan J. Tobin, David E. Krantz and Niranjala J.K. Tillakaratne and has published in prestigious journals such as Journal of Biological Chemistry, Neuron and Journal of Neuroscience.

In The Last Decade

George Lawless

15 papers receiving 640 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
George Lawless United States 11 299 256 209 180 105 15 649
Christian Lesuisse United States 6 232 0.8× 243 0.9× 156 0.7× 168 0.9× 70 0.7× 6 550
Joanna A. Korecka Netherlands 12 273 0.9× 248 1.0× 105 0.5× 208 1.2× 52 0.5× 14 616
Liberty François‐Moutal United States 17 492 1.6× 291 1.1× 255 1.2× 198 1.1× 78 0.7× 29 801
Zhiping Shao United States 12 442 1.5× 240 0.9× 381 1.8× 91 0.5× 85 0.8× 20 852
Carina Weissmann Argentina 13 260 0.9× 201 0.8× 238 1.1× 85 0.5× 124 1.2× 26 583
Gye Sun Jeon South Korea 18 506 1.7× 241 0.9× 145 0.7× 250 1.4× 80 0.8× 47 891
Jimena Baleriola Spain 10 291 1.0× 140 0.5× 152 0.7× 45 0.3× 137 1.3× 18 551
Nguyen‐Vi Mohamed Canada 10 327 1.1× 182 0.7× 316 1.5× 73 0.4× 117 1.1× 14 584
Dongcheul Kang United States 11 753 2.5× 335 1.3× 271 1.3× 74 0.4× 98 0.9× 14 1.1k
Diana Simón Spain 14 320 1.1× 306 1.2× 266 1.3× 54 0.3× 55 0.5× 22 689

Countries citing papers authored by George Lawless

Since Specialization
Citations

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

Fields of papers citing papers by George Lawless

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by George Lawless. 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 George Lawless. The network helps show where George Lawless may publish in the future.

Co-authorship network of co-authors of George Lawless

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

All Works

15 of 15 papers shown
1.
Moser, V. Alexandra, Shaughn Bell, Eduardo Valenzuela, et al.. (2025). Human iPSC‐Derived Mononuclear Phagocytes Improve Cognition and Neural Health across Multiple Mouse Models of Aging and Alzheimer's Disease. Advanced Science. 12(41). e17848–e17848. 1 indexed citations
2.
Lall, Deepti, Michael J. Workman, Samuel Sances, et al.. (2025). An organ-chip model of sporadic ALS using iPSC-derived spinal cord motor neurons and an integrated blood-brain-like barrier. Cell stem cell. 32(7). 1139–1153.e7. 1 indexed citations
3.
Mesci, Pinar, Dwight W. Martin, George Lawless, et al.. (2024). Surface tension enables induced pluripotent stem cell culture in commercially available hardware during spaceflight. npj Microgravity. 10(1). 97–97. 3 indexed citations
4.
Laperle, Alex, Pablo Avalos, Bin Lü, et al.. (2023). Human iPSC-derived neural progenitor cells secreting GDNF provide protection in rodent models of ALS and retinal degeneration. Stem Cell Reports. 18(8). 1629–1642. 16 indexed citations
5.
Otero, María Gabriela, Shaughn Bell, Alex Laperle, et al.. (2023). Organ-Chips Enhance the Maturation of Human iPSC-Derived Dopamine Neurons. International Journal of Molecular Sciences. 24(18). 14227–14227. 3 indexed citations
6.
Akhtar, Aslam Abbasi, Genevíève Gowing, Leslie Garcia, et al.. (2018). Inducible Expression of GDNF in Transplanted iPSC-Derived Neural Progenitor Cells. Stem Cell Reports. 10(6). 1696–1704. 26 indexed citations
7.
Lawless, George, et al.. (2014). Synergistic effects on dopamine cell death in a Drosophila model of chronic toxin exposure. NeuroToxicology. 44. 344–351. 16 indexed citations
8.
Lawal, Hakeem O., Hoa A. Lam, Jin‐Young Jang, et al.. (2012). Drosophila modifier screens to identify novel neuropsychiatric drugs including aminergic agents for the possible treatment of Parkinson’s disease and depression. Molecular Psychiatry. 19(2). 235–242. 25 indexed citations
9.
Chatterjee, Shreyasi, Tzu‐Kang Sang, George Lawless, & George R. Jackson. (2008). Dissociation of tau toxicity and phosphorylation: role of GSK-3β, MARK and Cdk5 in a Drosophila model. Human Molecular Genetics. 18(1). 164–177. 130 indexed citations
10.
Ratnaparkhi, Anuradha, George Lawless, Felix E. Schweizer, Peyman Golshani, & George R. Jackson. (2008). A Drosophila Model of ALS: Human ALS-Associated Mutation in VAP33A Suggests a Dominant Negative Mechanism. PLoS ONE. 3(6). e2334–e2334. 100 indexed citations
11.
Sang, Tzu‐Kang, Hui-Yun Chang, George Lawless, et al.. (2007). A Drosophila Model of Mutant Human Parkin-Induced Toxicity Demonstrates Selective Loss of Dopaminergic Neurons and Dependence on Cellular Dopamine. Journal of Neuroscience. 27(5). 981–992. 99 indexed citations
12.
Karsten, Stanislav L., Tzu‐Kang Sang, Lauren Gehman, et al.. (2006). A Genomic Screen for Modifiers of Tauopathy Identifies Puromycin-Sensitive Aminopeptidase as an Inhibitor of Tau-Induced Neurodegeneration. Neuron. 51(5). 549–560. 112 indexed citations
13.
Srinivasan, Supriya, Christopher J. Nichols, George Lawless, Richard W. Olsen, & Allan J. Tobin. (1999). Two Invariant Tryptophans on the α1 Subunit Define Domains Necessary for GABAA Receptor Assembly. Journal of Biological Chemistry. 274(38). 26633–26638. 24 indexed citations
14.
Loza, J., et al.. (1995). Role of extracellular calcium influx in EGF-induced osteoblastic cell proliferation. Bone. 16(4). S341–S347. 26 indexed citations
15.
Segovia, José, George Lawless, Niranjala J.K. Tillakaratne, Michael Brenner, & Allan J. Tobin. (1994). Cyclic AMP Decreases the Expression of a Neuronal Marker (GAD67) and Increases the Expression of an Astroglial Marker (GFAP) in C6 Cells. Journal of Neurochemistry. 63(4). 1218–1225. 67 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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