Lise N. Munsie

1.6k total citations
11 papers, 761 citations indexed

About

Lise N. Munsie is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Neurology. According to data from OpenAlex, Lise N. Munsie has authored 11 papers receiving a total of 761 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Cellular and Molecular Neuroscience, 6 papers in Molecular Biology and 4 papers in Neurology. Recurrent topics in Lise N. Munsie's work include Parkinson's Disease Mechanisms and Treatments (4 papers), Genetic Neurodegenerative Diseases (4 papers) and Neuroscience and Neuropharmacology Research (3 papers). Lise N. Munsie is often cited by papers focused on Parkinson's Disease Mechanisms and Treatments (4 papers), Genetic Neurodegenerative Diseases (4 papers) and Neuroscience and Neuropharmacology Research (3 papers). Lise N. Munsie collaborates with scholars based in Canada, United States and Germany. Lise N. Munsie's co-authors include Ray Truant, Carly R. Desmond, Randy Singh Atwal, Nicholas S. Caron, Igor Tatarnikov, Matthew J. Farrer, Austen J. Milnerwood, Mattia Volta, Dayne Beccano-Kelly and Liping Cao and has published in prestigious journals such as PLoS ONE, Journal of Cell Science and Human Molecular Genetics.

In The Last Decade

Lise N. Munsie

11 papers receiving 753 citations

Peers

Lise N. Munsie

CMN

NEURO

PHYSI

Mariangela Iovino United Kingdom

Di Xia China

Aurélie Honoré France

Pietro DeCamilli United States

Daniela Sinske Germany

Silvia Rathke‐Hartlieb Germany

Séverine M. Sigoillot France

Cornelio G. Caday United States

G Fabrizi Italy

Andreas Papadopulos Australia

Mariangela Iovino United Kingdom

Lise N. Munsie

308 ×0.8

227 ×0.8

CMN

336 ×1.2

NEURO

146 ×0.7

233 ×1.8

PHYSI

Citations per year, relative to Lise N. Munsie Lise N. Munsie (= 1×) peers Mariangela Iovino

Countries citing papers authored by Lise N. Munsie

Since Specialization

Citations

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

Fields of papers citing papers by Lise N. Munsie

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Lise N. Munsie. 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 Lise N. Munsie. The network helps show where Lise N. Munsie may publish in the future.

Co-authorship network of co-authors of Lise N. Munsie

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

All Works

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11 of 11 papers shown

Follett, Jordan, Emil K. Gustavsson, Lise N. Munsie, et al.. (2019). DNAJC13 p.Asn855Ser, implicated in familial parkinsonism, alters membrane dynamics of sorting nexin 1. Neuroscience Letters. 706. 114–122. 8 indexed citations

Mair, Barbara, Jelena Tomić, Sanna N. Masud, et al.. (2019). Essential Gene Profiles for Human Pluripotent Stem Cells Identify Uncharacterized Genes and Substrate Dependencies. Cell Reports. 27(2). 599–615.e12. 80 indexed citations

Volta, Mattia, Stefano Cataldi, Dayne Beccano-Kelly, et al.. (2015). Chronic and acute LRRK2 silencing has no long-term behavioral effects, whereas wild-type and mutant LRRK2 overexpression induce motor and cognitive deficits and altered regulation of dopamine release. Parkinsonism & Related Disorders. 21(10). 1156–1163. 37 indexed citations

Nath, Siddharth, Lise N. Munsie, & Ray Truant. (2014). A huntingtin-mediated fast stress response halting endosomal trafficking is defective in Huntington's disease. Human Molecular Genetics. 24(2). 450–462. 28 indexed citations

Beccano-Kelly, Dayne, Naila Kuhlmann, Igor Tatarnikov, et al.. (2014). Synaptic function is modulated by LRRK2 and glutamate release is increased in cortical neurons of G2019S LRRK2 knock-in mice. Frontiers in Cellular Neuroscience. 8. 301–301. 86 indexed citations

Beccano-Kelly, Dayne, Mattia Volta, Lise N. Munsie, et al.. (2014). LRRK2 overexpression alters glutamatergic presynaptic plasticity, striatal dopamine tone, postsynaptic signal transduction, motor activity and memory. Human Molecular Genetics. 24(5). 1336–1349. 76 indexed citations

Munsie, Lise N., Austen J. Milnerwood, Philip Seibler, et al.. (2014). Retromer-dependent neurotransmitter receptor trafficking to synapses is altered by the Parkinson's disease VPS35 mutation p.D620N. Human Molecular Genetics. 24(6). 1691–1703. 111 indexed citations

Munsie, Lise N., Carly R. Desmond, & Ray Truant. (2012). Cofilin Nuclear-Cytoplasmic Shuttling Affects Cofilin-Actin Rod Formation During Stress. Journal of Cell Science. 125(Pt 17). 3977–88. 80 indexed citations

Caron, Nicholas S., Lise N. Munsie, Jeffrey W. Keillor, & Ray Truant. (2012). Using FLIM-FRET to Measure Conformational Changes of Transglutaminase Type 2 in Live Cells. PLoS ONE. 7(8). e44159–e44159. 66 indexed citations

10.

Munsie, Lise N., Nicholas S. Caron, Randy Singh Atwal, et al.. (2011). Mutant huntingtin causes defective actin remodeling during stress: defining a new role for transglutaminase 2 in neurodegenerative disease. Human Molecular Genetics. 20(10). 1937–1951. 103 indexed citations

11.

Truant, Ray, et al.. (2008). Huntington’s disease: revisiting the aggregation hypothesis in polyglutamine neurodegenerative diseases. FEBS Journal. 275(17). 4252–4262. 86 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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