Ellen Corsmit

2.7k total citations
21 papers, 949 citations indexed

About

Ellen Corsmit is a scholar working on Physiology, Neurology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Ellen Corsmit has authored 21 papers receiving a total of 949 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Physiology, 9 papers in Neurology and 8 papers in Cellular and Molecular Neuroscience. Recurrent topics in Ellen Corsmit's work include Alzheimer's disease research and treatments (9 papers), Parkinson's Disease Mechanisms and Treatments (8 papers) and Nuclear Receptors and Signaling (7 papers). Ellen Corsmit is often cited by papers focused on Alzheimer's disease research and treatments (9 papers), Parkinson's Disease Mechanisms and Treatments (8 papers) and Nuclear Receptors and Signaling (7 papers). Ellen Corsmit collaborates with scholars based in Belgium, Netherlands and Czechia. Ellen Corsmit's co-authors include Christine Van Broeckhoven, Jessie Theuns, Sebastiaan Engelborghs, Marc Cruts, Bart Dermaut, Samir Kumar‐Singh, Krist’l Vennekens, Kristel Sleegers, Nathalie Brouwers and Bianca Van Broeck and has published in prestigious journals such as Brain, Neurology and The American Journal of Human Genetics.

In The Last Decade

Ellen Corsmit

21 papers receiving 935 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ellen Corsmit Belgium 14 558 425 312 203 149 21 949
H. Backhovens Belgium 15 678 1.2× 608 1.4× 189 0.6× 177 0.9× 129 0.9× 27 1.1k
Sébastien Feuillette France 10 717 1.3× 572 1.3× 158 0.5× 244 1.2× 119 0.8× 11 1.2k
M. Hutton United States 10 1.1k 1.9× 546 1.3× 426 1.4× 238 1.2× 222 1.5× 16 1.4k
Guy Prihar United States 8 586 1.1× 401 0.9× 138 0.4× 161 0.8× 84 0.6× 9 755
Cynthia Zehr United States 5 454 0.8× 308 0.7× 198 0.6× 189 0.9× 91 0.6× 8 702
Pazit Bar‐On United States 9 417 0.7× 255 0.6× 423 1.4× 308 1.5× 99 0.7× 9 856
Shabnam Baig United Kingdom 9 616 1.1× 289 0.7× 85 0.3× 194 1.0× 183 1.2× 11 922
Rita Cacace Belgium 10 402 0.7× 352 0.8× 113 0.4× 122 0.6× 123 0.8× 16 787
Giuseppe Muraca Italy 8 260 0.5× 402 0.9× 153 0.5× 176 0.9× 64 0.4× 9 872
Anna Paterlini Italy 17 441 0.8× 304 0.7× 232 0.7× 94 0.5× 123 0.8× 25 784

Countries citing papers authored by Ellen Corsmit

Since Specialization
Citations

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

Fields of papers citing papers by Ellen Corsmit

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ellen Corsmit

This figure shows the co-authorship network connecting the top 25 collaborators of Ellen Corsmit. A scholar is included among the top collaborators of Ellen Corsmit 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 Ellen Corsmit. Ellen Corsmit 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.
Verstraeten, Aline, David Crosiers, Bram Meeus, et al.. (2012). Contribution of VPS35 genetic variability to LBD in the Flanders-Belgian population. Neurobiology of Aging. 33(8). 1844.e11–1844.e13. 16 indexed citations
2.
Theuns, Jessie, David Crosiers, Luc Debaene, et al.. (2012). Guanosine triphosphate cyclohydrolase 1 promoter deletion causes dopa‐responsive dystonia. Movement Disorders. 27(11). 1451–1456. 8 indexed citations
3.
Meeus, Bram, Aline Verstraeten, David Crosiers, et al.. (2011). DLB and PDD: a role for mutations in dementia and Parkinson disease genes?. Neurobiology of Aging. 33(3). 629.e5–629.e18. 57 indexed citations
4.
Meeus, Bram, Aline Verstraeten, Karen Nuytemans, et al.. (2010). Dementia with Lewy Bodies: A Role for Dementia and Parkinson's Disease Genes?. Movement Disorders. 25. 1 indexed citations
5.
Meeus, Bram, Karen Nuytemans, David Crosiers, et al.. (2010). Comprehensive Genetic and Mutation Analysis of Familial Dementia with Lewy Bodies Linked to 2q35-q36. Journal of Alzheimer s Disease. 20(1). 197–205. 9 indexed citations
6.
Meeus, Bram, Karen Nuytemans, David Crosiers, et al.. (2009). GIGYF2 has no major role in Parkinson genetic etiology in a Belgian population. Neurobiology of Aging. 32(2). 308–312. 19 indexed citations
7.
Nuytemans, Karen, Bram Meeus, David Crosiers, et al.. (2009). Relative contribution of simple mutations vs. copy number variations in five Parkinson disease genes in the Belgian population. Human Mutation. 30(7). 1054–1061. 46 indexed citations
8.
Bogaerts, Veerle, Karen Nuytemans, Joke Reumers, et al.. (2008). Genetic variability in the mitochondrial serine proteaseHTRA2contributes to risk for Parkinson disease. Human Mutation. 29(6). 832–840. 78 indexed citations
9.
Nuytemans, Karen, P. Pals, Kristel Sleegers, et al.. (2008). Progranulin variability has no major role in Parkinson disease genetic etiology. Neurology. 71(15). 1147–1151. 15 indexed citations
10.
Dierick, Ines, Joy Irobi, Sophie Janssens, et al.. (2007). Genetic variant in theHSPB1 promoter region impairs the HSP27 stress response. Human Mutation. 28(8). 830–830. 31 indexed citations
11.
Gijselinck, Ilse, Julie van der Zee, Sebastiaan Engelborghs, et al.. (2007). Progranulin locus deletion in frontotemporal dementia. Human Mutation. 29(1). 53–58. 73 indexed citations
12.
Brouwers, Nathalie, Kristel Sleegers, Sebastiaan Engelborghs, et al.. (2006). Genetic risk and transcriptional variability of amyloid precursor protein in Alzheimer's disease. Brain. 129(11). 2984–2991. 65 indexed citations
13.
Kumar‐Singh, Samir, Jessie Theuns, Bianca Van Broeck, et al.. (2006). Mean age-of-onset of familial alzheimer disease caused by presenilin mutations correlates with both increased Aβ42 and decreased Aβ40. Human Mutation. 27(7). 686–695. 252 indexed citations
14.
Theuns, Jessie, Mathieu Vandenbulcke, Koen Van Laere, et al.. (2006). Alzheimer dementia caused by a novel mutation located in the APP C-terminal intracytosolic fragment. Human Mutation. 27(9). 888–896. 53 indexed citations
15.
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
16.
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
17.
Dermaut, Bart, Jessie Theuns, Marleen Van den Broeck, et al.. (2002). Nicastrin significantly modifies risk for familial early-onset Alzheimer's disease in a Dutch population based sample. Ghent University Academic Bibliography (Ghent University). 1 indexed citations
18.
Theuns, Jessie, Samir Kumar‐Singh, Bart Dermaut, et al.. (2002). In vitro analysis of Alzheimer's disease-related presenilin 1 and 2 mutations: effect on beta-amyloid processing. Neurobiology of Aging. 23(1). 1 indexed citations
19.
Dermaut, Bart, Jessie Theuns, Kristel Sleegers, et al.. (2002). The Gene Encoding Nicastrin, a Major γ-Secretase Component, Modifies Risk for Familial Early-Onset Alzheimer Disease in a Dutch Population-Based Sample. The American Journal of Human Genetics. 70(6). 1568–1574. 35 indexed citations
20.
Theuns, Jessie, Lars Feuk, Bart Dermaut, et al.. (2001). TheTNFRSF6 gene is not implicated in familial early-onset Alzheimer's disease. Human Genetics. 108(6). 552–553. 7 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by H. Backhovens Breakdown of academic impact, for papers by Sébastien Feuillette Breakdown of academic impact, for papers by M. Hutton Breakdown of academic impact, for papers by Guy Prihar Breakdown of academic impact, for papers by Cynthia Zehr Breakdown of academic impact, for papers by Pazit Bar‐On Breakdown of academic impact, for papers by Shabnam Baig Breakdown of academic impact, for papers by Rita Cacace Breakdown of academic impact, for papers by Giuseppe Muraca Breakdown of academic impact, for papers by Anna Paterlini
Rankless by CCL
2026