Désireé Schut

942 total citations
10 papers, 679 citations indexed

About

Désireé Schut is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Cell Biology. According to data from OpenAlex, Désireé Schut has authored 10 papers receiving a total of 679 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Cellular and Molecular Neuroscience, 6 papers in Molecular Biology and 6 papers in Cell Biology. Recurrent topics in Désireé Schut's work include Neuroscience and Neuropharmacology Research (5 papers), Cellular transport and secretion (4 papers) and Nerve injury and regeneration (3 papers). Désireé Schut is often cited by papers focused on Neuroscience and Neuropharmacology Research (5 papers), Cellular transport and secretion (4 papers) and Nerve injury and regeneration (3 papers). Désireé Schut collaborates with scholars based in Netherlands, Sweden and Canada. Désireé Schut's co-authors include Michael G. Fehlings, Soheila Karimi‐Abdolrezaee, Eftekhar Eftekharpour, Jian Wang, Matthijs Verhage, Jian Wang, Ruud F. Toonen, L. Niels Cornelisse, Patrick F. Sullivan and Linda Jacobsen and has published in prestigious journals such as Journal of Neuroscience, The Journal of Cell Biology and The EMBO Journal.

In The Last Decade

Désireé Schut

10 papers receiving 675 citations

Peers

Désireé Schut
Philip Duffy United States
Leung-Wah Yick Hong Kong
Theresa Connors United States
Shuxin Li United States
Aditi Falnikar United States
Angela R. Filous United States
M.B. Lowrie United Kingdom
Désireé Schut
Citations per year, relative to Désireé Schut Désireé Schut (= 1×) peers Nozomu Yoshioka

Countries citing papers authored by Désireé Schut

Since Specialization
Citations

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

Fields of papers citing papers by Désireé Schut

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Désireé Schut

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

All Works

10 of 10 papers shown
1.
Meijer, Marieke, Hanna C. A. Lammertse, Désireé Schut, et al.. (2019). A Single-Cell Model for Synaptic Transmission and Plasticity in Human iPSC-Derived Neurons. Cell Reports. 27(7). 2199–2211.e6. 67 indexed citations
2.
Kovačević, Jovana, Grégoire Maroteaux, Désireé Schut, et al.. (2018). Protein instability, haploinsufficiency, and cortical hyper-excitability underlie STXBP1 encephalopathy. Brain. 141(5). 1350–1374. 77 indexed citations
3.
Emperador-Melero, Javier, Marieke Meijer, Désireé Schut, et al.. (2017). Multi-level characterization of balanced inhibitory-excitatory cortical neuron network derived from human pluripotent stem cells. PLoS ONE. 12(6). e0178533–e0178533. 27 indexed citations
4.
Emperador-Melero, Javier, Désireé Schut, Jan R.T. van Weering, et al.. (2017). Differential Maturation of the Two Regulated Secretory Pathways in Human iPSC-Derived Neurons. Stem Cell Reports. 8(3). 659–672. 12 indexed citations
5.
Schmitz, Sabine, Christian Kortleven, Tim Kroon, et al.. (2016). Presynaptic inhibition upon CB 1 or mG lu2/3 receptor activation requires ERK / MAPK phosphorylation of Munc18‐1. The EMBO Journal. 35(11). 1236–1250. 33 indexed citations
6.
Cijsouw, Tony, Jurjen H. Broeke, Désireé Schut, et al.. (2014). Munc18-1 redistributes in nerve terminals in an activity- and PKC-dependent manner. The Journal of General Physiology. 143(4). 1434OIA9–1434OIA9. 2 indexed citations
7.
Cijsouw, Tony, Jurjen H. Broeke, Désireé Schut, et al.. (2014). Munc18-1 redistributes in nerve terminals in an activity- and PKC-dependent manner. The Journal of Cell Biology. 204(5). 759–775. 36 indexed citations
8.
Karimi‐Abdolrezaee, Soheila, Désireé Schut, Jian Wang, & Michael G. Fehlings. (2012). Chondroitinase and Growth Factors Enhance Activation and Oligodendrocyte Differentiation of Endogenous Neural Precursor Cells after Spinal Cord Injury. PLoS ONE. 7(5). e37589–e37589. 99 indexed citations
9.
Karimi‐Abdolrezaee, Soheila, Eftekhar Eftekharpour, Jian Wang, Désireé Schut, & Michael G. Fehlings. (2010). Synergistic Effects of Transplanted Adult Neural Stem/Progenitor Cells, Chondroitinase, and Growth Factors Promote Functional Repair and Plasticity of the Chronically Injured Spinal Cord. Journal of Neuroscience. 30(5). 1657–1676. 290 indexed citations
10.
Groffen, Alexander J., Linda Jacobsen, Désireé Schut, & Matthijs Verhage. (2004). Two distinct genes drive expression of seven tomosyn isoforms in the mammalian brain, sharing a conserved structure with a unique variable domain. Journal of Neurochemistry. 92(3). 554–568. 36 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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