Noreen E. Reist

2.0k total citations
30 papers, 1.7k citations indexed

About

Noreen E. Reist is a scholar working on Molecular Biology, Cell Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Noreen E. Reist has authored 30 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Molecular Biology, 21 papers in Cell Biology and 18 papers in Cellular and Molecular Neuroscience. Recurrent topics in Noreen E. Reist's work include Cellular transport and secretion (21 papers), Lipid Membrane Structure and Behavior (14 papers) and Neurobiology and Insect Physiology Research (10 papers). Noreen E. Reist is often cited by papers focused on Cellular transport and secretion (21 papers), Lipid Membrane Structure and Behavior (14 papers) and Neurobiology and Insect Physiology Research (10 papers). Noreen E. Reist collaborates with scholars based in United States, United Kingdom and Japan. Noreen E. Reist's co-authors include U.J. McMahan, Carin A. Loewen, M. J. Werle, Stephen J Smith, James A. Drummond, Iain M. Robinson, Bruce G. Wallace, Ralph Nitkin, Justin R. Fallon and Thomas L. Schwarz and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Neuron.

In The Last Decade

Noreen E. Reist

30 papers receiving 1.6k citations

Peers

Noreen E. Reist

CMN

PHYSI

Jeong-Seop Rhee Germany

Detlev Grabs Canada

Shingo Yoshikawa Japan

Xiaofei Yang China

Lucı́a Tabares Spain

M S Perin United States

Claudia Schirra Germany

Andreas Königstorfer Germany

Karen E. Wallace United States

Stephen D. Meriney United States

Jeong-Seop Rhee Germany

Noreen E. Reist

1.5k ×1.1

1.2k ×1.2

1.0k ×1.1

CMN

156 ×0.9

PHYSI

147 ×1.0

PHYSI

Citations per year, relative to Noreen E. Reist Noreen E. Reist (= 1×) peers Jeong-Seop Rhee

Countries citing papers authored by Noreen E. Reist

Since Specialization

Citations

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

Fields of papers citing papers by Noreen E. Reist

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Noreen E. Reist. 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 Noreen E. Reist. The network helps show where Noreen E. Reist may publish in the future.

Co-authorship network of co-authors of Noreen E. Reist

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Bono, Jeremy M., et al.. (2021). The conserved alternative splicing factor caper regulates neuromuscular phenotypes during development and aging. Developmental Biology. 473. 15–32. 7 indexed citations

Reist, Noreen E., et al.. (2020). The C2A domain of synaptotagmin is an essential component of the calcium sensor for synaptic transmission. PLoS ONE. 15(2). e0228348–e0228348. 14 indexed citations

Reist, Noreen E., et al.. (2020). Synaptotagmin: Mechanisms of an electrostatic switch. Neuroscience Letters. 722. 134834–134834. 24 indexed citations

Vrailas‐Mortimer, Alysia D., et al.. (2017). Drosophila studies support a role for a presynaptic synaptotagmin mutation in a human congenital myasthenic syndrome. PLoS ONE. 12(9). e0184817–e0184817. 11 indexed citations

Vanlandingham, Phillip, et al.. (2014). AP180 Couples Protein Retrieval to Clathrin‐Mediated Endocytosis of Synaptic Vesicles. Traffic. 15(4). 433–450. 31 indexed citations

Vanlandingham, Phillip, et al.. (2013). Epsin 1 Promotes Synaptic Growth by Enhancing BMP Signal Levels in Motoneuron Nuclei. PLoS ONE. 8(6). e65997–e65997. 14 indexed citations

Biela, Laurie M., Chantell S. Evans, Zhao Wang, et al.. (2012). Calcium Binding by Synaptotagmin's C₂A Domain is an Essential Element of the Electrostatic Switch That Triggers Synchronous Synaptic Transmission. Journal of Neuroscience. 32(4). 1253–1260. 51 indexed citations

Paddock, Brie, Zhao Wang, Laurie M. Biela, et al.. (2011). Membrane Penetration by Synaptotagmin Is Required for Coupling Calcium Binding to Vesicle FusionIn Vivo. Journal of Neuroscience. 31(6). 2248–2257. 65 indexed citations

Mace, Kimberly E., et al.. (2009). Synaptotagmin I stabilizes synaptic vesicles via its C₂A polylysine motif. genesis. 47(5). 337–345. 11 indexed citations

10.

Bao, Hong, Noreen E. Reist, & Bing Zhang. (2008). The Drosophila Epsin 1 is Required for Ubiquitin‐Dependent Synaptic Growth and Function but Not for Synaptic Vesicle Recycling. Traffic. 9(12). 2190–2205. 15 indexed citations

11.

Paddock, Brie, et al.. (2008). Ca²⁺-Dependent, Phospholipid-Binding Residues of Synaptotagmin Are Critical for Excitation–Secretion CouplingIn Vivo. Journal of Neuroscience. 28(30). 7458–7466. 39 indexed citations

12.

Loewen, Carin A., et al.. (2006). C₂B Polylysine Motif of Synaptotagmin Facilitates a Ca²⁺-independent Stage of Synaptic Vesicle Priming In Vivo. Molecular Biology of the Cell. 17(12). 5211–5226. 47 indexed citations

13.

Tamura, Takuya, et al.. (2006). Nerve-Evoked Synchronous Release and High K⁺-Induced Quantal Events Are Regulated Separately by Synaptotagmin I at Drosophila Neuromuscular Junctions. Journal of Neurophysiology. 97(1). 540–549. 9 indexed citations

14.

Loewen, Carin A., Suzanne M. Royer, & Noreen E. Reist. (2006). Drosophila synaptotagmin Inull mutants show severe alterations in vesicle populations but calcium-binding motif mutants do not. The Journal of Comparative Neurology. 496(1). 1–12. 10 indexed citations

15.

Drummond, James A., et al.. (2002). The C2B Ca2+-binding motif of synaptotagmin is required for synaptic transmission in vivo. Nature. 418(6895). 340–344. 264 indexed citations

16.

Loewen, Carin A., et al.. (2001). Drosophila synaptotagmin I null mutants survive to early adulthood. genesis. 31(1). 30–36. 36 indexed citations

17.

Parfitt, Karen D., Noreen E. Reist, Jingtao Li, et al.. (1995). Drosophila Genetics and the Functions of Synaptic Proteins. Cold Spring Harbor Symposia on Quantitative Biology. 60(0). 371–377. 16 indexed citations

18.

Reist, Noreen E., M. J. Werle, & U.J. McMahan. (1992). Agrin released by motor neurons induces the aggregation of acetylcholine receptors at neuromuscular junctions. Neuron. 8(5). 865–868. 203 indexed citations

19.

Smith, Martin A., et al.. (1987). Identification of Agrin in Electric Organ Extracts and Localization of Agrin-Like Molecules in Muscle and Central Nervous System. Journal of Experimental Biology. 132(1). 223–230. 24 indexed citations

20.

Reist, Noreen E., et al.. (1986). Molecules antigenically similar to agrin are highly concentrated in the synaptic basal lamina of skeletal muscles. The Society for Neuroscience Abstracts. 12(1). 189. 4 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.

Explore authors with similar magnitude of impact