Tim De Pooter

3.9k total citations
24 papers, 1.1k citations indexed

About

Tim De Pooter is a scholar working on Molecular Biology, Neurology and Physiology. According to data from OpenAlex, Tim De Pooter has authored 24 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 9 papers in Neurology and 6 papers in Physiology. Recurrent topics in Tim De Pooter's work include Parkinson's Disease Mechanisms and Treatments (7 papers), Alzheimer's disease research and treatments (5 papers) and Neurological diseases and metabolism (4 papers). Tim De Pooter is often cited by papers focused on Parkinson's Disease Mechanisms and Treatments (7 papers), Alzheimer's disease research and treatments (5 papers) and Neurological diseases and metabolism (4 papers). Tim De Pooter collaborates with scholars based in Belgium, Netherlands and United States. Tim De Pooter's co-authors include Christine Van Broeckhoven, Kristel Sleegers, Sebastiaan Engelborghs, Julie van der Zee, Peter De Rijk, Marleen Van den Broeck, Peter Paul De Deyn, Mojca Stražišar, Bart Dermaut and Marc Cruts and has published in prestigious journals such as Bioinformatics, Brain and Neurology.

In The Last Decade

Tim De Pooter

24 papers receiving 1.1k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Tim De Pooter Belgium 15 556 464 361 197 197 24 1.1k
Gabriela Mercado United States 14 472 0.8× 416 0.9× 233 0.6× 260 1.3× 102 0.5× 23 1.2k
Yoshito Nagano Japan 17 418 0.8× 542 1.2× 233 0.6× 212 1.1× 88 0.4× 29 1.1k
Hugo Klaassen Belgium 9 185 0.3× 216 0.5× 68 0.2× 160 0.8× 42 0.2× 17 557
Luc‐Henri Tessier France 19 94 0.2× 539 1.2× 348 1.0× 241 1.2× 37 0.2× 24 998
Thomas Rival France 15 117 0.2× 507 1.1× 210 0.6× 394 2.0× 75 0.4× 18 1.0k
Tao Feng China 19 529 1.0× 409 0.9× 191 0.5× 135 0.7× 117 0.6× 70 1.3k
Victoria L. Hewitt Australia 14 119 0.2× 520 1.1× 81 0.2× 159 0.8× 51 0.3× 17 805
Camilla Lööv Sweden 10 134 0.2× 707 1.5× 101 0.3× 106 0.5× 133 0.7× 12 972
Ana Aiastui Spain 17 406 0.7× 403 0.9× 212 0.6× 236 1.2× 72 0.4× 29 898
Aldis Krizus Canada 17 639 1.1× 458 1.0× 98 0.3× 295 1.5× 236 1.2× 26 1.2k

Countries citing papers authored by Tim De Pooter

Since Specialization
Citations

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

Fields of papers citing papers by Tim De Pooter

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tim De Pooter

This figure shows the co-authorship network connecting the top 25 collaborators of Tim De Pooter. A scholar is included among the top collaborators of Tim De Pooter 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 Tim De Pooter. Tim De Pooter 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.
Rijk, Peter De, Fahri Küçükali, Jasper Van Dongen, et al.. (2024). Scywalker: scalable end-to-end data analysis workflow for long-read single-cell transcriptome sequencing. Bioinformatics. 40(9). 1 indexed citations
2.
Rombauts, Stéphane, Lisanne de Vries, Tim De Pooter, et al.. (2023). Suppression of the Arabidopsis cinnamoyl-CoA reductase 1-6 intronic T-DNA mutation by epigenetic modification. PLANT PHYSIOLOGY. 192(4). 3001–3016. 5 indexed citations
3.
Cortés-Mancera, Fabián, Janette Heegsma, Bart van de Sluis, et al.. (2023). Mitochondrial DNA methylation in metabolic associated fatty liver disease. Frontiers in Nutrition. 10. 964337–964337. 14 indexed citations
4.
Ibrahim, Joe, Ligia Mateiu, Tim De Pooter, et al.. (2023). Mitochondrial GpC and CpG DNA Hypermethylation Cause Metabolic Stress-Induced Mitophagy and Cholestophagy. International Journal of Molecular Sciences. 24(22). 16412–16412. 10 indexed citations
5.
Vriendt, Els De, et al.. (2023). Increased prime edit rates in KCNQ2 and SCN1A via single nicking all-in-one plasmids. BMC Biology. 21(1). 156–156. 7 indexed citations
6.
Valček, Adam, Tom Coenye, Tim De Pooter, et al.. (2022). Phenotypic Characterization and Heterogeneity among Modern Clinical Isolates of Acinetobacter baumannii. Microbiology Spectrum. 11(1). e0306122–e0306122. 25 indexed citations
7.
Coster, Wouter De, Peter De Rijk, Arne De Roeck, et al.. (2019). Structural variants identified by Oxford Nanopore PromethION sequencing of the human genome. Genome Research. 29(7). 1178–1187. 100 indexed citations
8.
Roeck, Arne De, Wouter De Coster, Rita Cacace, et al.. (2019). NanoSatellite: accurate characterization of expanded tandem repeat length and sequence through whole genome long-read sequencing on PromethION. Genome biology. 20(1). 239–239. 68 indexed citations
9.
Bettens, Karolien, Nathalie Brouwers, Sebastiaan Engelborghs, et al.. (2008). DNMBP is genetically associated with Alzheimer dementia in the Belgian population. Neurobiology of Aging. 30(12). 2000–2009. 9 indexed citations
10.
Nuytemans, Karen, Rosa Rademakers, Jessie Theuns, et al.. (2008). Founder mutation p.R1441C in the leucine-rich repeat kinase 2 gene in Belgian Parkinson's disease patients. European Journal of Human Genetics. 16(4). 471–479. 38 indexed citations
11.
Gijselinck, Ilse, Kristel Sleegers, Sebastiaan Engelborghs, et al.. (2008). Neuronal inclusion protein TDP-43 has no primary genetic role in FTD and ALS. Neurobiology of Aging. 30(8). 1329–1331. 72 indexed citations
12.
Sleegers, Kristel, Nathalie Brouwers, Sebastian Maurer‐Stroh, et al.. (2008). Progranulin genetic variability contributes to amyotrophic lateral sclerosis. Neurology. 71(4). 253–259. 128 indexed citations
13.
Gijselinck, Ilse, Kristel Sleegers, Sebastiaan Engelborghs, et al.. (2007). Neuronal inclusion protein TDP-43 has no primary genetic role in FTD and ALS. Ghent University Academic Bibliography (Ghent University). 3 indexed citations
14.
Zee, Julie van der, Hazel Urwin, Sebastiaan Engelborghs, et al.. (2007). CHMP2B C-truncating mutations in frontotemporal lobar degeneration are associated with an aberrant endosomal phenotype in vitro. Human Molecular Genetics. 17(2). 313–322. 121 indexed citations
15.
Zee, Julie van der, Rosa Rademakers, Sebastiaan Engelborghs, et al.. (2006). A Belgian ancestral haplotype harbours a highly prevalent mutation for 17q21-linked tau-negative FTLD. Brain. 129(4). 841–852. 60 indexed citations
16.
Theuns, Jessie, Nathalie Brouwers, Sebastiaan Engelborghs, et al.. (2006). Promoter Mutations That Increase Amyloid Precursor-Protein Expression Are Associated with Alzheimer Disease. The American Journal of Human Genetics. 78(6). 936–946. 145 indexed citations
17.
Rademakers, Rosa, Kristel Sleegers, Philippe Pals, et al.. (2006). P3–159: MAPT H1 subhaplotyping in european PD association samples implicates tau splicing in early–onset parkinson's disease susceptibility. Alzheimer s & Dementia. 2(3S_Part_14). 1 indexed citations
18.
Rademakers, Rosa, Marc Cruts, Kristel Sleegers, et al.. (2005). Linkage and Association Studies Identify a Novel Locus for Alzheimer Disease at 7q36 in a Dutch Population-Based Sample. The American Journal of Human Genetics. 77(4). 643–652. 35 indexed citations
19.
Cruts, Marc, Rosa Rademakers, Ilse Gijselinck, et al.. (2005). Genomic architecture of human 17q21 linked to frontotemporal dementia uncovers a highly homologous family of low-copy repeats in the tau region. Human Molecular Genetics. 14(13). 1753–1762. 63 indexed citations
20.
Pals, Philippe, Sarah Lincoln, Jonathan Manning, et al.. (2004). α‐Synuclein promoter confers susceptibility to Parkinson's disease. Annals of Neurology. 56(4). 591–595. 162 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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