Wim Mandemakers

6.0k total citations · 1 hit paper
37 papers, 3.7k citations indexed

About

Wim Mandemakers is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Neurology. According to data from OpenAlex, Wim Mandemakers has authored 37 papers receiving a total of 3.7k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Cellular and Molecular Neuroscience, 16 papers in Molecular Biology and 15 papers in Neurology. Recurrent topics in Wim Mandemakers's work include Parkinson's Disease Mechanisms and Treatments (14 papers), Neurogenesis and neuroplasticity mechanisms (13 papers) and Nerve injury and regeneration (12 papers). Wim Mandemakers is often cited by papers focused on Parkinson's Disease Mechanisms and Treatments (14 papers), Neurogenesis and neuroplasticity mechanisms (13 papers) and Nerve injury and regeneration (12 papers). Wim Mandemakers collaborates with scholars based in Netherlands, Belgium and United States. Wim Mandemakers's co-authors include Bart De Strooper, Sébastien S. Hébert, Asli Silahtaroglu, Aikaterini S. Papadopoulou, Katrien Horré, André Delacourte, Sakari Kauppinen, Vanessa A. Morais, Ben A. Barres and Kris Gevaert and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Journal of Neuroscience.

In The Last Decade

Wim Mandemakers

36 papers receiving 3.6k citations

Hit Papers

Loss of microRNA cluster miR-29a/b-1 in sporadic Alzheime... 2008 2026 2014 2020 2008 250 500 750
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

  1. Loss of microRNA cluster miR-29a/b-1 in sporadic Alzheimer's disease correlates with increased BACE1/β-secretase expression
    2008 951 citations Wim Mandemakers, Bart De Strooper et al. profile →

Peers

Wim Mandemakers
Anna Logvinova United States
Géraldine Liot France
Nicholas W. Seeds United States
Rickie Patani United Kingdom
Patrice D. Smith Canada
Jaan‐Olle Andressoo Finland
Mohamed H. Farah United States
Travis L. Unger United States
Jérôme Mertens United States
Sung Ok Yoon United States
Anna Logvinova United States
Wim Mandemakers
Citations per year, relative to Wim Mandemakers Wim Mandemakers (= 1×) peers Anna Logvinova

Countries citing papers authored by Wim Mandemakers

Since Specialization
Citations

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

Fields of papers citing papers by Wim Mandemakers

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Wim Mandemakers

This figure shows the co-authorship network connecting the top 25 collaborators of Wim Mandemakers. A scholar is included among the top collaborators of Wim Mandemakers 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 Wim Mandemakers. Wim Mandemakers 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.
Dits, Natasja F., Guido J. Breedveld, Leonie J.M. Vergouw, et al.. (2024). LRP10 and α-synuclein transmission in Lewy body diseases. Cellular and Molecular Life Sciences. 81(1). 75–75. 1 indexed citations
2.
Breedveld, Guido J., et al.. (2023). deCLUTTER2+ – a pipeline to analyze calcium traces in a stem cell model for ventral midbrain patterned astrocytes. Disease Models & Mechanisms. 16(6). 1 indexed citations
3.
4.
Jarazo, Javier, François Massart, Enrico Glaab, et al.. (2022). Generation of isogenic control DJ-1-delP GC13 for the genetic Parkinson‘s disease-patient derived iPSC line DJ-1-delP (LCSBi008-A-1). Stem Cell Research. 62. 102815–102815.
5.
Breedveld, Guido J., Hanneke Geut, Wiggert A. van Cappellen, et al.. (2021). LRP10 interacts with SORL1 in the intracellular vesicle trafficking pathway in non-neuronal brain cells and localises to Lewy bodies in Parkinson’s disease and dementia with Lewy bodies. Acta Neuropathologica. 142(1). 117–137. 14 indexed citations
6.
Chen, Rongmin, Hana Park, Nelli Mnatsakanyan, et al.. (2019). Parkinson’s disease protein DJ-1 regulates ATP synthase protein components to increase neuronal process outgrowth. Cell Death and Disease. 10(6). 469–469. 76 indexed citations
7.
Mandemakers, Wim. (2014). Retrograde Labeling of Corticospinal Motor Neurons from Early Postnatal Rodents. Cold Spring Harbor Protocols. 2014(4). pdb.prot074922–pdb.prot074922. 2 indexed citations
8.
Cornelissen, Tom, Dominik Haddad, Cindy Van Humbeeck, et al.. (2014). The deubiquitinase USP15 antagonizes Parkin-mediated mitochondrial ubiquitination and mitophagy. Human Molecular Genetics. 23(19). 5227–5242. 250 indexed citations
9.
Mandemakers, Wim. (2014). Immunopanning of Retrograde-Labeled Corticospinal Motor Neurons from Early Postnatal Rodents. Cold Spring Harbor Protocols. 2014(4). pdb.prot074930–pdb.prot074930. 3 indexed citations
10.
Kolen, Kristof Van, Wim Mandemakers, Guy Daneels, et al.. (2012). Development of an enzyme-linked immunosorbent assay for detection of cellular and in vivo LRRK2 S935 phosphorylation. Journal of Pharmaceutical and Biomedical Analysis. 76. 49–58. 19 indexed citations
11.
Humbeeck, Cindy Van, Tom Cornelissen, Wim Mandemakers, et al.. (2011). Parkin Interacts with Ambra1 to Induce Mitophagy. Journal of Neuroscience. 31(28). 10249–10261. 229 indexed citations
12.
Mandemakers, Wim, et al.. (2011). The Lipid Sulfatide Is a Novel Myelin-Associated Inhibitor of CNS Axon Outgrowth. Journal of Neuroscience. 31(17). 6481–6492. 60 indexed citations
13.
Morais, Vanessa A., Patrik Verstreken, Joél Smet, et al.. (2009). Parkinson's disease mutations in PINK1 result in decreased Complex I activity and deficient synaptic function. EMBO Molecular Medicine. 1(2). 99–111. 326 indexed citations
14.
15.
Mandemakers, Wim & Ben A. Barres. (2005). Axon Regeneration: It’s Getting Crowded at the Gates of TROY. Current Biology. 15(8). R302–R305. 24 indexed citations
16.
Karnezis, Tara, Wim Mandemakers, Jonathan L. McQualter, et al.. (2004). The neurite outgrowth inhibitor Nogo A is involved in autoimmune-mediated demyelination. Nature Neuroscience. 7(7). 736–744. 190 indexed citations
17.
Goldberg, Jeffrey L., Mauricio E. Vargas, Jack T. Wang, et al.. (2004). An Oligodendrocyte Lineage-Specific Semaphorin, Sema5A, Inhibits Axon Growth by Retinal Ganglion Cells. Journal of Neuroscience. 24(21). 4989–4999. 150 indexed citations
18.
Jaegle, Martine, Mehrnaz Ghazvini, Wim Mandemakers, et al.. (2003). The POU proteins Brn-2 and Oct-6 share important functions in Schwann cell development. Genes & Development. 17(11). 1380–1391. 218 indexed citations
19.
20.
Levavasseur, Françoise, Wim Mandemakers, Pim Visser, et al.. (1998). Comparison of sequence and function of the Oct-6 genes in zebrafish, chicken and mouse. Mechanisms of Development. 74(1-2). 89–98. 25 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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