Vicky De Winter

1.1k citations

20 papers · 859 · h-index 16

Impact in

Cellular and Molecular Neuroscience top 5%
- Hereditary Neurological Disorders
- Genetic Neurodegenerative Diseases
Cell Biology top 5%
- Endoplasmic Reticulum Stress and Disease

Papers in

Molecular Biology 16
- Heat shock proteins research 11
- Muscle Physiology and Disorders 3
- Mitochondrial Function and Pathology 2
Cellular and Molecular Neuroscience 11
- Hereditary Neurological Disorders 11

Co-authors: Vincent Timmerman (20 shared papers)Bob Asselbergh (15 shared papers)Joy Irobi (7 shared papers)Sophie Janssens (8 shared papers)Leonardo Almeida-Souza (8 shared papers)Jean‐Pierre Timmermans (4 shared papers)Sofie Goethals (4 shared papers)Elias Adriaenssens (5 shared papers)
Journals: Human Molecular Genetics (2 papers)Brain (2 papers)Autophagy (2 papers)Acta Neuropathologica (2 papers)The Journal of Gene Medicine (1 paper)
Partner nations: Belgium Germany United Kingdom

In The Last Decade

Vicky De Winter

20 papers receiving 853 citations

Peers

Countries citing papers authored by Vicky De Winter

Since Specialization

Citations

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

Fields of papers citing papers by Vicky De Winter

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Vicky De Winter. 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 Vicky De Winter. The network helps show where Vicky De Winter may publish in the future.

Co-authors

The 25 scholars most cited alongside Vicky De Winter, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Vicky De Winter Line = papers co-authored together Vicky De Winter links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Molecular Defects in the Motor Adaptor BICD2 Cause Proximal Spinal Muscular Atrophy with Autosomal-Dominant Inheritance The American Journal of Human Genetics ·(unknown), Ivan Litvinenko, Bob Asselbergh, Leonardo Almeida-Souza, Teodora Chamova, Thomas Geuens, Elke Ydens, (unknown), Joy Irobi, Els De Vriendt, Vicky De Winter, Tinne Ooms, Vincent Timmerman, Ivailo Tournev, Albena Jordanova	2013	96
2	Small Heat-Shock Protein HSPB1 Mutants Stabilize Microtubules in Charcot-Marie-Tooth Neuropathy Journal of Neuroscience ·Leonardo Almeida-Souza, Bob Asselbergh, Constantin d’Ydewalle, Kristof Moonens, Sofie Goethals, Vicky De Winter, Abdelkrim Azmi, Joy Irobi, Jean‐Pierre Timmermans, Kris Gevaert, Han Remaut, Ludo Van Den Bosch, Vincent Timmerman, Sophie Janssens	2011	89
3	Increased Monomerization of Mutant HSPB1 Leads to Protein Hyperactivity in Charcot-Marie-Tooth Neuropathy Journal of Biological Chemistry ·Leonardo Almeida-Souza, Sofie Goethals, Vicky De Winter, Ines Dierick, Rodrigo Gallardo, Joost Van Durme, Joy Irobi, Jan Gettemans, Frédéric Rousseau, Joost Schymkowitz, Vincent Timmerman, Sophie Janssens	2010	88
4	Mutant HSPB8 causes motor neuron-specific neurite degeneration Human Molecular Genetics ·Joy Irobi, Leonardo Almeida-Souza, Bob Asselbergh, Vicky De Winter, Sofie Goethals, Ines Dierick, Jyothsna Krishnan, Jean‐Pierre Timmermans, Wim Robberecht, Peter De Jonghe, Ludo Van Den Bosch, Sophie Janssens, Vincent Timmerman	2010	72
5	A knock-in/knock-out mouse model of HSPB8-associated distal hereditary motor neuropathy and myopathy reveals toxic gain-of-function of mutant Hspb8 Acta Neuropathologica ·Delphine Bouhy, Manisha Juneja, István Katona, A. Holmgren, Bob Asselbergh, Vicky De Winter, Tino Hochepied, Steven Goossens, Jody J. Haigh, Claude Libert, Chantal Ceuterick‐de Groote, Joy Irobi, Joachim Weis, Vincent Timmerman	2017	62
6	Neuropathy-causing mutations in HSPB1 impair autophagy by disturbing the formation of SQSTM1/p62 bodies Autophagy ·Mansour Haidar, Bob Asselbergh, Elias Adriaenssens, Vicky De Winter, Jean‐Pierre Timmermans, Michaela Auer‐Grumbach, Manisha Juneja, Vincent Timmerman	2019	59
7	Small heat shock proteins operate as molecular chaperones in the mitochondrial intermembrane space Nature Cell Biology ·Elias Adriaenssens, Bob Asselbergh, Pablo Rivera-Mejías, Sven Bervoets, Leen Vendredy, Vicky De Winter, Katrien Spaas, Riet De Rycke, Gert Van Isterdael, Francis Impens, Thomas Langer, Vincent Timmerman	2023	52
8	Nlrp6 promotes recovery after peripheral nerve injury independently of inflammasomes Journal of Neuroinflammation ·Elke Ydens, Dieter Demon, Guillaume Lornet, Vicky De Winter, Vincent Timmerman, Mohamed Lamkanfi, Sophie Janssens	2015	51
9	Charcot–Marie–Tooth causing HSPB1 mutations increase Cdk5-mediated phosphorylation of neurofilaments Acta Neuropathologica ·A. Holmgren, Delphine Bouhy, Vicky De Winter, Bob Asselbergh, Jean‐Pierre Timmermans, Joy Irobi, Vincent Timmerman	2013	43
10	Molecular Chaperones in the Pathogenesis of Amyotrophic Lateral Sclerosis: The Role of HSPB1 Human Mutation ·Simona Capponi, Thomas Geuens, Alessandro Geroldi, Paola Origone, Simonetta Verdiani, Elena Cichero, Elias Adriaenssens, Vicky De Winter, M. Poggio, Marco Barberis, Adriano Chiò, Paola Fossa, Paola Mandich, Emilia Bellone, Vincent Timmerman	2016	42
11	Induced pluripotent stem cell-derived motor neurons of CMT type 2 patients reveal progressive mitochondrial dysfunction Brain ·Jonas Van Lent, Peter Verstraelen, Bob Asselbergh, Elias Adriaenssens, Ligia Mateiu, Christophe Verbist, Vicky De Winter, Kristel Eggermont, Ludo Van Den Bosch, Winnok H. De Vos, Vincent Timmerman	2021	36
12	Sensory neuropathy-causing mutations in ATL3 affect ER–mitochondria contact sites and impair axonal mitochondrial distribution Human Molecular Genetics ·Michiel Krols, Bob Asselbergh, Riet De Rycke, Vicky De Winter, Alexandre Seyer, (unknown), Ingo Kurth, Geert Bultynck, Vincent Timmerman, Sophie Janssens	2018	32
13	NCAM1 and GDF15 are biomarkers of Charcot-Marie-Tooth disease in patients and mice Brain ·(unknown), Alexia Kagiava, Leen Vendredy, Emily L. Spaulding, Marina Stavrou, Denisa Hathazi, Anika Grüneboom, Vicky De Winter, Burkhard Gess, Ulrike Schara, Oksana Pogoryelova, Hanns Lochmüller, Christoph H. Borchers, Andreas Roos, Robert W. Burgess, Vincent Timmerman, Kleopas A. Kleopa, Rita Horváth	2022	28
14	Sensory-Neuropathy-Causing Mutations in ATL3 Cause Aberrant ER Membrane Tethering Cell Reports ·Michiel Krols, Sammy Detry, Bob Asselbergh, Leonardo Almeida-Souza, (unknown), Saskia Lippens, Riet De Rycke, Vicky De Winter, (unknown), Ingo Kurth, Harvey T. McMahon, Savvas N. Savvides, Vincent Timmerman, Sophie Janssens	2018	28
15	Mutant HSPB8 causes protein aggregates and a reduced mitochondrial membrane potential in dermal fibroblasts from distal hereditary motor neuropathy patients Neuromuscular Disorders ·Joy Irobi, A. Holmgren, Vicky De Winter, Bob Asselbergh, Jan Gettemans, Dirk Adriaensen, Chantal Ceuterick‐de Groote, Rudy Van Coster, Peter De Jonghe, Vincent Timmerman	2012	28
16	Mutant HSPB1 causes loss of translational repression by binding to PCBP1, an RNA binding protein with a possible role in neurodegenerative disease Acta Neuropathologica Communications ·Thomas Geuens, Vicky De Winter, Nicholas Rajan, Tilmann Achsel, Ligia Mateiu, Leonardo Almeida-Souza, Bob Asselbergh, Delphine Bouhy, Michaela Auer‐Grumbach, Claudia Bagni, Vincent Timmerman	2017	24
17	HSPB1 Facilitates the Formation of Non-Centrosomal Microtubules PLoS ONE ·Leonardo Almeida-Souza, Bob Asselbergh, Vicky De Winter, Sofie Goethals, Vincent Timmerman, Sophie Janssens	2013	14
18	Characterization of New Transgenic Mouse Models for Two Charcot-Marie-Tooth-Causing HspB1 Mutations using the Rosa26 Locus Journal of Neuromuscular Diseases ·Delphine Bouhy, Thomas Geuens, Vicky De Winter, Leonardo Almeida-Souza, István Katona, Joachim Weis, Tino Hochepied, Steven Goossens, Jody J. Haigh, Sophie Janssens, Vincent Timmerman	2016	10
19	Autophagy induction by piplartine ameliorates axonal degeneration caused by mutant HSPB1 and HSPB8 in Charcot-Marie-Tooth type 2 neuropathies Autophagy ·Angela Sisto, Tamira van Wermeskerken, Michael Pancher, Pamela Gatto, Bob Asselbergh, Ágata Sofia Assunção Carreira, Vicky De Winter, Valentina Adami, Alessandro Provenzani, Vincent Timmerman	2024	4
20	RNA Interference Targeting Small Heat Shock Protein B8 Failed to Improve Distal Hereditary Motor Neuropathy in the Mouse Model The Journal of Gene Medicine ·Leen Vendredy, Vicky De Winter, Jonas Van Lent, Jasmien Orije, Tatiana Da Silva Authier, István Katona, Bob Asselbergh, Elias Adriaenssens, Joachim Weis, Marleen Verhoye, Vincent Timmerman	2025	1

About Vicky De Winter

Vicky De Winter is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience, Cell Biology, Psychiatry and Mental health and Epidemiology, having authored 20 papers that have together received 859 indexed citations. Recurring topics across this work include Heat shock proteins research (11 papers), Hereditary Neurological Disorders (11 papers), Endoplasmic Reticulum Stress and Disease (5 papers), Muscle Physiology and Disorders (3 papers), Fibromyalgia and Chronic Fatigue Syndrome Research (3 papers), Mitochondrial Function and Pathology (2 papers), Autophagy in Disease and Therapy (2 papers) and Cellular Mechanics and Interactions (2 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (338 citations), Cell Biology (294 citations), Aging (30 citations), Neurology (82 citations) and Molecular Biology (553 citations). Vicky De Winter has collaborated with scholars based in Belgium, Germany and United Kingdom. Frequent co-authors include Vincent Timmerman, Bob Asselbergh, Joy Irobi, Sophie Janssens, Leonardo Almeida-Souza, Jean‐Pierre Timmermans, Sofie Goethals, Elias Adriaenssens, Ludo Van Den Bosch and Elke Ydens. Their work appears in journals such as Human Molecular Genetics, Brain, Autophagy, Acta Neuropathologica and The Journal of Gene Medicine.

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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