Lorna W. Role

14.7k total citations · 5 hit papers
107 papers, 10.6k citations indexed

About

Lorna W. Role is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Cognitive Neuroscience. According to data from OpenAlex, Lorna W. Role has authored 107 papers receiving a total of 10.6k indexed citations (citations by other indexed papers that have themselves been cited), including 81 papers in Molecular Biology, 63 papers in Cellular and Molecular Neuroscience and 17 papers in Cognitive Neuroscience. Recurrent topics in Lorna W. Role's work include Nicotinic Acetylcholine Receptors Study (56 papers), Neuroscience and Neuropharmacology Research (40 papers) and Ion channel regulation and function (37 papers). Lorna W. Role is often cited by papers focused on Nicotinic Acetylcholine Receptors Study (56 papers), Neuroscience and Neuropharmacology Research (40 papers) and Ion channel regulation and function (37 papers). Lorna W. Role collaborates with scholars based in United States, Netherlands and China. Lorna W. Role's co-authors include David A. Talmage, Daniel S. McGehee, Darwin K. Berg, Young‐Hwan Jo, Steven A. Siegelbaum, Cheng‐Rong Yu, Mala Ananth, S M Schuetze, Amy B. MacDermott and Elizabeth Ballinger and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Lorna W. Role

106 papers receiving 10.4k citations

Hit Papers

Physiological Diversity of Nicotinic Acetylcholine Recept... 1995 2026 2005 2015 1995 2004 1996 2005 2016 250 500 750

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Lorna W. Role United States 48 7.1k 5.7k 1.1k 1.0k 936 107 10.6k
Julie A. Blendy United States 52 5.2k 0.7× 5.2k 0.9× 1.6k 1.5× 653 0.7× 814 0.9× 143 11.1k
William C. Wetsel United States 63 5.9k 0.8× 5.5k 1.0× 2.0k 1.8× 699 0.7× 735 0.8× 206 13.0k
Soren Impey United States 54 7.0k 1.0× 5.4k 1.0× 1.4k 1.3× 779 0.8× 1.4k 1.5× 81 13.1k
Guadalupe Mengod Spain 56 5.3k 0.7× 6.7k 1.2× 1.4k 1.3× 1.1k 1.1× 502 0.5× 177 9.9k
Emiliana Borrelli France 62 6.7k 0.9× 6.4k 1.1× 1.3k 1.2× 510 0.5× 426 0.5× 116 12.7k
Jay M. Baraban United States 60 8.4k 1.2× 7.4k 1.3× 1.7k 1.5× 577 0.6× 945 1.0× 156 14.0k
Dorit Ron United States 55 4.9k 0.7× 4.8k 0.9× 1.2k 1.1× 436 0.4× 810 0.9× 130 9.2k
Salah El Mestikawy France 51 5.7k 0.8× 8.4k 1.5× 2.0k 1.8× 613 0.6× 509 0.5× 128 11.3k
Ralf Schoepfer United Kingdom 46 6.5k 0.9× 5.7k 1.0× 976 0.9× 400 0.4× 587 0.6× 76 9.7k
Hilmar Bading Germany 52 8.1k 1.1× 8.2k 1.5× 1.4k 1.3× 654 0.7× 1.2k 1.3× 134 13.9k

Countries citing papers authored by Lorna W. Role

Since Specialization
Citations

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

Fields of papers citing papers by Lorna W. Role

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Lorna W. Role. 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 Lorna W. Role. The network helps show where Lorna W. Role may publish in the future.

Co-authorship network of co-authors of Lorna W. Role

This figure shows the co-authorship network connecting the top 25 collaborators of Lorna W. Role. A scholar is included among the top collaborators of Lorna W. Role 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 Lorna W. Role. Lorna W. Role 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.
Rajebhosale, Prithviraj, et al.. (2024). Neuregulin1 Nuclear Signaling Influences Adult Neurogenesis and Regulates a Schizophrenia Susceptibility Gene Network within the Mouse Dentate Gyrus. Journal of Neuroscience. 44(43). e0063242024–e0063242024. 1 indexed citations
2.
Rajebhosale, Prithviraj, Mala Ananth, Ronald Kim, et al.. (2024). Functionally refined encoding of threat memory by distinct populations of basal forebrain cholinergic projection neurons. eLife. 13. 4 indexed citations
3.
Kim, Ronald, Mala Ananth, Niraj S. Desai, Lorna W. Role, & David A. Talmage. (2024). Distinct subpopulations of ventral pallidal cholinergic projection neurons encode valence of olfactory stimuli. Cell Reports. 43(4). 114009–114009. 5 indexed citations
4.
Ananth, Mala, Prithviraj Rajebhosale, Ronald Kim, David A. Talmage, & Lorna W. Role. (2023). Basal forebrain cholinergic signalling: development, connectivity and roles in cognition. Nature reviews. Neuroscience. 24(4). 233–251. 61 indexed citations
5.
Ananth, Mala, et al.. (2021). NeuroConstruct: 3D Reconstruction and Visualization of Neurites in Optical Microscopy Brain Images. IEEE Transactions on Visualization and Computer Graphics. 28(12). 4951–4965. 12 indexed citations
6.
Crouse, Richard B., Kristen K.O. Kim, Hannah M. Batchelor, et al.. (2020). Acetylcholine is released in the basolateral amygdala in response to predictors of reward and enhances the learning of cue-reward contingency. eLife. 9. 57 indexed citations
7.
Ballinger, Elizabeth, Christian P. Schaaf, Akash J. Patel, et al.. (2019). Mecp2Deletion from Cholinergic Neurons Selectively Impairs Recognition Memory and Disrupts Cholinergic Modulation of the Perirhinal Cortex. eNeuro. 6(6). ENEURO.0134–19.2019. 16 indexed citations
8.
Záborszky, László, Péter Gombkötő, Matthew R. Gielow, et al.. (2018). Specific Basal Forebrain–Cortical Cholinergic Circuits Coordinate Cognitive Operations. Journal of Neuroscience. 38(44). 9446–9458. 134 indexed citations
9.
López‐Hernández, Gretchen Y., Mala Ananth, Li Jiang, et al.. (2017). Electrophysiological properties of basal forebrain cholinergic neurons identified by genetic and optogenetic tagging. Journal of Neurochemistry. 142(S2). 103–110. 14 indexed citations
10.
Akmentin, Wendy, et al.. (2017). Axonal Type III Nrg1 Controls Glutamate Synapse Formation and GluA2 Trafficking in Hippocampal-Accumbens Connections. eNeuro. 4(1). ENEURO.0232–16.2017. 11 indexed citations
11.
Jiang, Li, Srikanya Kundu, Gretchen Y. López‐Hernández, et al.. (2016). Cholinergic Signaling Controls Conditioned Fear Behaviors and Enhances Plasticity of Cortical-Amygdala Circuits. Neuron. 90(5). 1057–1070. 133 indexed citations
12.
Talmage, David A., et al.. (2013). Type III Neuregulin 1 Is Required for Multiple Forms of Excitatory Synaptic Plasticity of Mouse Cortico-Amygdala Circuits. Journal of Neuroscience. 33(23). 9655–9666. 30 indexed citations
13.
Johnson, Matthew A., Michael D. Lieberman, Rose E. Goodchild, et al.. (2008). Type III Neuregulin-1 Is Required for Normal Sensorimotor Gating, Memory-Related Behaviors, and Corticostriatal Circuit Components. Journal of Neuroscience. 28(27). 6872–6883. 149 indexed citations
14.
Role, Lorna W. & Eric R. Kandel. (2008). Nicotinic Acetylcholine Receptors: From Molecular Biology to Cognition. Neuron. 58(6). 847–849. 2 indexed citations
15.
Berman, Joshua A., David A. Talmage, & Lorna W. Role. (2007). Cholinergic Circuits and Signaling in the Pathophysiology of Schizophrenia. International review of neurobiology. 78. 193–223. 36 indexed citations
16.
Michailov, G., Michael W. Sereda, Bastian G. Brinkmann, et al.. (2004). Axonal Neuregulin-1 Regulates Myelin Sheath Thickness. Science. 304(5671). 700–703. 730 indexed citations breakdown →
17.
Bao, Jianxin, David A. Talmage, Lorna W. Role, & Jean Gautier. (2000). Regulation of neurogenesis by interactions between HEN1 and neuronal LMO proteins. Development. 127(2). 425–435. 43 indexed citations
18.
Brussaard, Arjen B., Xia Yang, Joseph Doyle, Sigismund Huck, & Lorna W. Role. (1994). Developmental regulation of multiple nicotinic AChR channel subtypes in embryonic chick habenula neurons: contributions of both theα2 andα4 subunit genes. Pflügers Archiv - European Journal of Physiology. 429(1). 27–43. 30 indexed citations
19.
Role, Lorna W.. (1992). Diversity in structure and function of neuronal nicotinic acetycholine receptor channels. Current Biology. 2(6). 291–291. 2 indexed citations
20.
Gardette, Robert, et al.. (1991). Developmental changes in transmitter sensitivity and synaptic transmission in embryonic chicken sympathetic neurons innervated in Vitro. Developmental Biology. 147(1). 83–95. 31 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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