Benoit Lechat

1.0k total citations
25 papers, 666 citations indexed

About

Benoit Lechat is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Physiology. According to data from OpenAlex, Benoit Lechat has authored 25 papers receiving a total of 666 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 10 papers in Cellular and Molecular Neuroscience and 10 papers in Physiology. Recurrent topics in Benoit Lechat's work include Alzheimer's disease research and treatments (9 papers), Neuroscience and Neuropharmacology Research (9 papers) and Wnt/β-catenin signaling in development and cancer (4 papers). Benoit Lechat is often cited by papers focused on Alzheimer's disease research and treatments (9 papers), Neuroscience and Neuropharmacology Research (9 papers) and Wnt/β-catenin signaling in development and cancer (4 papers). Benoit Lechat collaborates with scholars based in Belgium, United States and Poland. Benoit Lechat's co-authors include Fred Van Leuven, Herman Devijver, Tomasz Jaworski, Peter Borghgraef, David Demedts, Sebastian Kügler, Hervé Maurin, Anton Roebroek, Leszek Kaczmarek and Fons Verheyen and has published in prestigious journals such as Nature, Nucleic Acids Research and The EMBO Journal.

In The Last Decade

Benoit Lechat

25 papers receiving 660 citations

Author Peers

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

Author Last Decade Papers Cites
Benoit Lechat 297 275 182 138 73 25 666
Courtney Lane‐Donovan 270 0.9× 383 1.4× 169 0.9× 140 1.0× 52 0.7× 17 735
Karina Hernández‐Ortega 474 1.6× 274 1.0× 136 0.7× 127 0.9× 90 1.2× 19 863
Desirée Loreth 360 1.2× 311 1.1× 210 1.2× 190 1.4× 42 0.6× 23 850
Kevin Richetin 322 1.1× 230 0.8× 235 1.3× 185 1.3× 40 0.5× 21 679
Petar Podlesniy 520 1.8× 290 1.1× 292 1.6× 143 1.0× 77 1.1× 29 922
Patrizia LoPresti 396 1.3× 349 1.3× 211 1.2× 173 1.3× 56 0.8× 19 773
Jackelien van Scheppingen 386 1.3× 233 0.8× 174 1.0× 176 1.3× 134 1.8× 23 859
Diogo Trigo 344 1.2× 141 0.5× 231 1.3× 112 0.8× 59 0.8× 18 654
Alerie Guzman de la Fuente 288 1.0× 165 0.6× 119 0.7× 322 2.3× 62 0.8× 22 808
Diana Simón 320 1.1× 266 1.0× 306 1.7× 125 0.9× 23 0.3× 22 689

Countries citing papers authored by Benoit Lechat

Since Specialization
Citations

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

Fields of papers citing papers by Benoit Lechat

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Benoit Lechat

This figure shows the co-authorship network connecting the top 25 collaborators of Benoit Lechat. A scholar is included among the top collaborators of Benoit Lechat 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 Benoit Lechat. Benoit Lechat 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.
Steklov, Mikhail, Hyunbum Jang, Raj Nayan Sewduth, et al.. (2024). K128 ubiquitination constrains RAS activity by expanding its binding interface with GAP proteins. The EMBO Journal. 43(14). 2862–2877. 8 indexed citations
2.
Sewduth, Raj Nayan, Paolo Carai, Mingzhen Zhang, et al.. (2023). Spatial Mechano‐Signaling Regulation of GTPases through Non‐Degradative Ubiquitination. Advanced Science. 10(36). e2303367–e2303367. 13 indexed citations
3.
Najm, Paul, Mikhail Steklov, Raj Nayan Sewduth, et al.. (2021). Loss-of-Function Mutations in TRAF7 and KLF4 Cooperatively Activate RAS-Like GTPase Signaling and Promote Meningioma Development. Cancer Research. 81(16). 4218–4229. 16 indexed citations
4.
Kashyap, Rudra, Benoit Lechat, Antonio Luis Egea-Jiménez, et al.. (2021). Syntenin-knock out reduces exosome turnover and viral transduction. Scientific Reports. 11(1). 4083–4083. 21 indexed citations
5.
Sewduth, Raj Nayan, Silvia Pandolfi, Mikhail Steklov, et al.. (2020). The Noonan Syndrome Gene Lztr1 Controls Cardiovascular Function by Regulating Vesicular Trafficking. Circulation Research. 126(10). 1379–1393. 20 indexed citations
6.
Detrez, Jan R., Hervé Maurin, Kristof Van Kolen, et al.. (2019). Regional vulnerability and spreading of hyperphosphorylated tau in seeded mouse brain. Neurobiology of Disease. 127. 398–409. 30 indexed citations
7.
Storck, Steffen E., Benoit Lechat, Philip L.S.M. Gordts, et al.. (2019). LRP1 Has a Predominant Role in Production over Clearance of Aβ in a Mouse Model of Alzheimer’s Disease. Molecular Neurobiology. 56(10). 7234–7245. 82 indexed citations
8.
Urbańska, Małgorzata, Paulina Kaźmierska, Tomasz Kowalczyk, et al.. (2018). GSK3β activity alleviates epileptogenesis and limits GluA1 phosphorylation. EBioMedicine. 39. 377–387. 26 indexed citations
9.
Schreurs, An, Benoit Lechat, Jesper Mogensen, et al.. (2018). Single mild traumatic brain injury results in transiently impaired spatial long-term memory and altered search strategies. Behavioural Brain Research. 365. 222–230. 14 indexed citations
10.
Lechat, Benoit, Tom Struys, Peter Borghgraef, et al.. (2018). Longitudinal assessment of cerebral perfusion and vascular response to hypoventilation in a bigenic mouse model of Alzheimer's disease with amyloid and tau pathology. NMR in Biomedicine. 32(2). e4037–e4037. 11 indexed citations
11.
Urbańska, Małgorzata, Agata Góźdź, Matylda Macias, et al.. (2017). GSK3β Controls mTOR and Prosurvival Signaling in Neurons. Molecular Neurobiology. 55(7). 6050–6062. 20 indexed citations
12.
Kondratiuk, Ilona, Szymon Łęski, Małgorzata Urbańska, et al.. (2016). GSK-3β and MMP-9 Cooperate in the Control of Dendritic Spine Morphology. Molecular Neurobiology. 54(1). 200–211. 40 indexed citations
13.
Maurin, Hervé, Seon‐Ah Chong, Igor Kraev, et al.. (2014). Early Structural and Functional Defects in Synapses and Myelinated Axons in Stratum Lacunosum Moleculare in Two Preclinical Models for Tauopathy. PLoS ONE. 9(2). e87605–e87605. 31 indexed citations
14.
Kondratiuk, Ilona, Herman Devijver, Benoit Lechat, et al.. (2013). Glycogen synthase kinase-3beta affects size of dentate gyrus and species-typical behavioral tasks in transgenic and knockout mice. Behavioural Brain Research. 248. 46–50. 22 indexed citations
15.
Maurin, Hervé, Benoit Lechat, Peter Borghgraef, et al.. (2013). Tauopathy Differentially Affects Cell Adhesion Molecules in Mouse Brain: Early Down-Regulation of Nectin-3 in Stratum Lacunosum Moleculare. PLoS ONE. 8(5). e63589–e63589. 18 indexed citations
16.
Maurin, Hervé, Benoit Lechat, Ilse Dewachter, et al.. (2013). Neurological characterization of mice deficient in GSK3α highlight pleiotropic physiological functions in cognition and pathological activity as Tau kinase. Molecular Brain. 6(1). 27–27. 36 indexed citations
17.
Meléndez‐Ferro, Miguel, Gautam N. Bijur, Fred Van Leuven, et al.. (2013). Glycogen synthase kinase‐3β (GSK3β) expression in a mouse model of Alzheimer's disease: A light and electron microscopy study. Synapse. 67(6). 313–327. 20 indexed citations
18.
Jaworski, Tomasz, Ilse Dewachter, Benoit Lechat, et al.. (2011). GSK-3 alpha/beta kinases and amyloid production in vivo. Nature. 480(7376). 4 indexed citations
19.
Jaworski, Tomasz, Benoit Lechat, David Demedts, et al.. (2011). Dendritic Degeneration, Neurovascular Defects, and Inflammation Precede Neuronal Loss in a Mouse Model for Tau-Mediated Neurodegeneration. American Journal Of Pathology. 179(4). 2001–2015. 99 indexed citations
20.
Jaworski, Tomasz, Ilse Dewachter, Benoit Lechat, et al.. (2009). AAV-Tau Mediates Pyramidal Neurodegeneration by Cell-Cycle Re-Entry without Neurofibrillary Tangle Formation in Wild-Type Mice. PLoS ONE. 4(10). e7280–e7280. 69 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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