Magdalene M. Moran

6.6k total citations · 4 hit papers
18 papers, 5.0k citations indexed

About

Magdalene M. Moran is a scholar working on Sensory Systems, Cellular and Molecular Neuroscience and Molecular Biology. According to data from OpenAlex, Magdalene M. Moran has authored 18 papers receiving a total of 5.0k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Sensory Systems, 5 papers in Cellular and Molecular Neuroscience and 4 papers in Molecular Biology. Recurrent topics in Magdalene M. Moran's work include Ion Channels and Receptors (13 papers), Neurobiology and Insect Physiology Research (4 papers) and Pain Mechanisms and Treatments (3 papers). Magdalene M. Moran is often cited by papers focused on Ion Channels and Receptors (13 papers), Neurobiology and Insect Physiology Research (4 papers) and Pain Mechanisms and Treatments (3 papers). Magdalene M. Moran collaborates with scholars based in United States, Tunisia and Belgium. Magdalene M. Moran's co-authors include Jayhong A. Chong, David E. Clapham, I. Scott Ramsey, A Szállaśi, Christopher M. Fanger, Neil J. Hayward, Haoxing Xu, M. Allen McAlexander, Tamás Bı́ró and Michael Zhao and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Journal of Clinical Investigation.

In The Last Decade

Magdalene M. Moran

18 papers receiving 4.9k citations

Hit Papers

TRPA1 mediates formalin-i... 2002 2026 2010 2018 2007 2002 2011 2010 250 500 750 1000

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Magdalene M. Moran 2.8k 1.5k 1.4k 1.3k 506 18 5.0k
Jayhong A. Chong 1.7k 0.6× 2.0k 1.4× 987 0.7× 1.5k 1.1× 354 0.7× 14 4.6k
Joris Vriens 6.0k 2.2× 2.8k 1.9× 2.1k 1.5× 1.9k 1.4× 1.6k 3.1× 109 9.1k
Erika Pintér 1.8k 0.7× 1.2k 0.8× 2.0k 1.4× 1.8k 1.4× 268 0.5× 175 5.0k
Hongzhen Hu 1.8k 0.7× 1.7k 1.2× 1.2k 0.9× 1.2k 0.9× 527 1.0× 157 5.6k
Félix Viana 2.9k 1.1× 2.2k 1.5× 1.6k 1.1× 2.5k 1.9× 632 1.2× 88 6.4k
Marc Freichel 4.2k 1.5× 3.9k 2.6× 1.0k 0.7× 2.4k 1.8× 1.4k 2.7× 145 8.2k
Christopher M. Fanger 1.7k 0.6× 1.6k 1.1× 1.2k 0.8× 1.1k 0.9× 218 0.4× 18 3.7k
Zhen‐Zhong Xu 578 0.2× 1.7k 1.2× 3.8k 2.7× 2.2k 1.6× 814 1.6× 56 7.5k
Rudi Vennekens 5.4k 2.0× 3.2k 2.2× 1.2k 0.8× 1.7k 1.3× 2.0k 3.9× 106 8.0k
Connie R. Faltynek 1.4k 0.5× 2.1k 1.4× 1.8k 1.3× 1.2k 0.9× 228 0.5× 115 5.9k

Countries citing papers authored by Magdalene M. Moran

Since Specialization
Citations

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

Fields of papers citing papers by Magdalene M. Moran

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Magdalene M. Moran

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

All Works

18 of 18 papers shown
1.
Lee, Chan, Miguel A. Gonzalez‐Lozano, Donato del Camino, et al.. (2025). DMXL1 promotes recruitment of V1-ATPase to lysosomes upon TRPML1 activation. Nature Structural & Molecular Biology. 32(10). 2060–2075. 2 indexed citations
2.
Broad, Lisa M., Jeffrey G. Suico, P. Kellie Turner, et al.. (2025). Preclinical and clinical evaluation of a novel TRPA1 antagonist LY3526318. Pain. 166(8). 1893–1908. 3 indexed citations
3.
Moran, Magdalene M.. (2017). TRP Channels as Potential Drug Targets. The Annual Review of Pharmacology and Toxicology. 58(1). 309–330. 171 indexed citations
4.
Moran, Magdalene M. & A Szállaśi. (2017). Targeting nociceptivetransient receptor potentialchannels to treat chronic pain: current state of the field. British Journal of Pharmacology. 175(12). 2185–2203. 157 indexed citations
5.
Rahaman, Shaik O., L. Grove, Sailaja Paruchuri, et al.. (2014). TRPV4 mediates myofibroblast differentiation and pulmonary fibrosis in mice. Journal of Clinical Investigation. 124(12). 5225–5238. 233 indexed citations
6.
Moran, Magdalene M., M. Allen McAlexander, Tamás Bı́ró, & A Szállaśi. (2011). Transient receptor potential channels as therapeutic targets. Nature Reviews Drug Discovery. 10(8). 601–620. 447 indexed citations breakdown →
7.
Camino, Donato del, Sarah Murphy, Lee Barrett, et al.. (2010). TRPA1 Contributes to Cold Hypersensitivity. Journal of Neuroscience. 30(45). 15165–15174. 235 indexed citations breakdown →
8.
Everaerts, Wouter, Xiao-guang Zhen, Debapriya Ghosh, et al.. (2010). Inhibition of the cation channel TRPV4 improves bladder function in mice and rats with cyclophosphamide-induced cystitis. Proceedings of the National Academy of Sciences. 107(44). 19084–19089. 321 indexed citations
9.
Caceres, Ana I., Marian Brackmann, Maxwell Elia, et al.. (2009). A sensory neuronal ion channel essential for airway inflammation and hyperreactivity in asthma. Proceedings of the National Academy of Sciences. 106(22). 9099–9104. 348 indexed citations
10.
Carlson, Anne E., Lindsey A. Burnett, Donato del Camino, et al.. (2009). Pharmacological Targeting of Native CatSper Channels Reveals a Required Role in Maintenance of Sperm Hyperactivation. PLoS ONE. 4(8). e6844–e6844. 78 indexed citations
11.
Kerstein, Patrick C., Donato del Camino, Magdalene M. Moran, & Cheryl L. Stucky. (2009). Pharmacological Blockade of TRPA1 Inhibits Mechanical Firing in Nociceptors. Molecular Pain. 5. 19–19. 132 indexed citations
12.
Qi, Huayu, Magdalene M. Moran, Betsy Navarro, et al.. (2007). All four CatSper ion channel proteins are required for male fertility and sperm cell hyperactivated motility. Proceedings of the National Academy of Sciences. 104(4). 1219–1223. 410 indexed citations
13.
Bautista, Diana M., Jan Siemens, Michael Zhao, et al.. (2007). TRPA1 mediates formalin-induced pain. Proceedings of the National Academy of Sciences. 104(33). 13525–13530. 1022 indexed citations breakdown →
14.
Ramsey, I. Scott, Magdalene M. Moran, Jayhong A. Chong, & David E. Clapham. (2006). A voltage-gated proton-selective channel lacking the pore domain. Nature. 440(7088). 1213–1216. 483 indexed citations
15.
Chong, Jayhong A., Magdalene M. Moran, Martin Teichmann, et al.. (2005). TATA-Binding Protein (TBP)-Like Factor (TLF) Is a Functional Regulator of Transcription: Reciprocal Regulation of the Neurofibromatosis Type 1 and c-fos Genes by TLF/TRF2 and TBP. Molecular and Cellular Biology. 25(7). 2632–2643. 39 indexed citations
16.
Moran, Magdalene M., Haoxing Xu, & David E. Clapham. (2004). TRP ion channels in the nervous system. Current Opinion in Neurobiology. 14(3). 362–369. 238 indexed citations
17.
Moran, Magdalene M.. (2004). TRP ion channels in the nervous system. Current Opinion in Neurobiology. 7 indexed citations
18.
Xu, Haoxing, I. Scott Ramsey, Suhas A. Kotecha, et al.. (2002). TRPV3 is a calcium-permeable temperature-sensitive cation channel. Nature. 418(6894). 181–186. 698 indexed citations breakdown →

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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