Bart Dermaut

7.9k total citations · 1 hit paper
64 papers, 3.3k citations indexed

About

Bart Dermaut is a scholar working on Molecular Biology, Physiology and Neurology. According to data from OpenAlex, Bart Dermaut has authored 64 papers receiving a total of 3.3k indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Molecular Biology, 28 papers in Physiology and 20 papers in Neurology. Recurrent topics in Bart Dermaut's work include Alzheimer's disease research and treatments (26 papers), Prion Diseases and Protein Misfolding (11 papers) and Amyotrophic Lateral Sclerosis Research (9 papers). Bart Dermaut is often cited by papers focused on Alzheimer's disease research and treatments (26 papers), Prion Diseases and Protein Misfolding (11 papers) and Amyotrophic Lateral Sclerosis Research (9 papers). Bart Dermaut collaborates with scholars based in Belgium, Netherlands and France. Bart Dermaut's co-authors include Christine Van Broeckhoven, Gert Van Goethem, Jean‐Jacques Martin, A. Löfgren, Marc Cruts, Patrick Callaerts, Rosa Rademakers, Jessie Theuns, Lies Vanden Broeck and Marleen Van den Broeck and has published in prestigious journals such as Nature Genetics, The Journal of Cell Biology and Brain.

In The Last Decade

Bart Dermaut

64 papers receiving 3.2k citations

Hit Papers

align trajectories

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.

Mutation of POLG is associated with progressive external ophthalmoplegia characterized by mtDNA deletions

2001 610 citations Bart Dermaut, Christine Van Broeckhoven et al. profile →

Peers

Countries citing papers authored by Bart Dermaut

Since Specialization

Citations

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

Fields of papers citing papers by Bart Dermaut

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Bart Dermaut

This figure shows the co-authorship network connecting the top 25 collaborators of Bart Dermaut. A scholar is included among the top collaborators of Bart Dermaut 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 Bart Dermaut. Bart Dermaut is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Pooled analysis of patients with inherited prion disease caused by two- to twelve-octapeptide repeat insertions in the prion protein gene (PRNP) 2023 ·Journal of Neurology ·(unknown), (unknown), (unknown), Hannah Verdin, (unknown), Anne Sieben, Bart Dermaut, Dimitri Hemelsoet	2
2	Contribution of homozygous and compound heterozygous missense mutations in VWA2 to Alzheimer’s disease 2020 ·Neurobiology of Aging ·(unknown), (unknown), Sebastiaan Engelborghs, Rik Vandenberghe, (unknown), Rita Cacace, Christine Van Broeckhoven, Patrick Cras, Johan Goeman, R Crols, Jan De Bleecker, Tim Van Langenhove, Anne Sieben, Bart Dermaut, Olivier Deryck, Bruno Bergmans, Jan Versijpt	8
3	Loss and gain of Drosophila TDP-43 impair synaptic efficacy and motor control leading to age-related neurodegeneration by loss-of-function phenotypes 2013 ·Human Molecular Genetics ·Danielle C. Diaper, Yoshitsugu Adachi, Ben Sutcliffe, Dickon M. Humphrey, Christopher Elliott, (unknown), (unknown), Lies Vanden Broeck, Patrick Callaerts, Bart Dermaut, Ammar Al‐Chalabi, Christopher E. Shaw, Iain M. Robinson, Frank Hirth	104
4	DrosophilaModels of Tauopathies: What Have We Learned? 2012 ·International Journal of Alzheimer s Disease ·Marc Gistelinck, Jean‐Charles Lambert, Patrick Callaerts, Bart Dermaut, Pierre Dourlen	45
5	Progressive myoclonic epilepsy as an adult-onset manifestation of Leigh syndrome due to m.14487T>C 2009 ·Journal of Neurology Neurosurgery & Psychiatry ·Bart Dermaut, Sara Seneca, Lina Dom, Kaat Smets, (unknown), Joél Smet, Boél De Paepe, Simon Tousseyn, Sarah Weckhuysen, Marc Gewillig, P. Pals, Paul M. Parizel, Jan De Bleecker, Paul Boon, Linda De Meırleır, Peter De Jonghe, Rudy Van Coster, Wim Van Paesschen, Patrick Santens	27
6	Neuronal inclusion protein TDP-43 has no primary genetic role in FTD and ALS 2007 ·Ghent University Academic Bibliography (Ghent University) ·Ilse Gijselinck, Kristel Sleegers, Sebastiaan Engelborghs, Wim Robberecht, Jean‐Jacques Martin, Rik Vandenberghe, Raf Sciot, Bart Dermaut, D. Goossens, Julie van der Zee, Tim De Pooter, Jurgen Del‐Favero, Patrick Santens, Peter De Jonghe, Peter P. De Deyn, Christine Van Broeckhoven, Marc Cruts	3
7	CHMP2B C-truncating mutations in frontotemporal lobar degeneration are associated with an aberrant endosomal phenotype in vitro 2007 ·Human Molecular Genetics ·Julie van der Zee, Hazel Urwin, Sebastiaan Engelborghs, M. Bruyland, Rik Vandenberghe, Bart Dermaut, Tim De Pooter, Karin Peeters, Patrick Santens, Peter Paul De Deyn, Elizabeth Fisher, John Collinge, Adrian M. Isaacs, Christine Van Broeckhoven	121
8	Mean age-of-onset of familial alzheimer disease caused by presenilin mutations correlates with both increased Aβ42 and decreased Aβ40 2006 ·Human Mutation ·Samir Kumar‐Singh, Jessie Theuns, Bianca Van Broeck, Daniel Pirici, Krist’l Vennekens, Ellen Corsmit, Marc Cruts, Bart Dermaut, Rong Wang, Christine Van Broeckhoven	252
9	The UBQLN1 polymorphism, UBQ-8i, at 9q22 is not associated with Alzheimer's disease with onset before 70 years 2005 ·Neuroscience Letters ·Nathalie Brouwers, Kristel Sleegers, Sebastiaan Engelborghs, Veerle Bogaerts, Cornelia M. van Duijn, Peter Paul De Deyn, Christine Van Broeckhoven, Bart Dermaut	26
10	Dose dependent effect of APOE ɛ4 on behavioral symptoms in frontal lobe dementia 2005 ·Neurobiology of Aging ·Sebastiaan Engelborghs, Bart Dermaut, Peter Mariën, R. C. Andrew Symons, Ellen Vloeberghs, Kirsten Maertens, Nore Somers, (unknown), Rosa Rademakers, (unknown)	51
11	The molecular genetics of early-onset Alzheimer's disease 2004 ·Ghent University Academic Bibliography (Ghent University) ·Christine Van Broeckhoven, R. Rademakers, Bart Dermaut, Samir Kumar‐Singh, (unknown), Marc Cruts	2
12	A novel presenilin 1 mutation associated with Pick's disease but not β‐amyloid plaques 2004 ·Annals of Neurology ·Bart Dermaut, Samir Kumar‐Singh, S. Engelborghs, Jessie Theuns, Rosa Rademakers, J. Saerens, Barbara Pickut, Karin Peeters, Marleen Van den Broeck, Krist’l Vennekens, Stephan Claes, Marc Cruts, Patrick Cras, Jean‐Jacques Martin, Christine Van Broeckhoven, Peter Paul De Deyn	147
13	Nicastrin significantly modifies risk for familial early-onset Alzheimer's disease in a Dutch population based sample 2002 ·Ghent University Academic Bibliography (Ghent University) ·Bart Dermaut, Jessie Theuns, Marleen Van den Broeck, Kristel M. Vennekens, Ellen Corsmit, Marc Cruts, Christine Van Broeckhoven, Kristel Sleegers, (unknown), Hikaru Hasegawa, Peter St George‐Hyslop	1
14	Novel German APP V715A mutation associated with presenile Alzheimer's disease 2002 ·Neurobiology of Aging ·Marc Cruts, Bart Dermaut, Samir Kumar‐Singh, R. Rademakers, Marleen Van den Broeck, Christine Van Broeckhoven, Florian Stögbauer	5
15	In vitro analysis of Alzheimer's disease-related presenilin 1 and 2 mutations: effect on beta-amyloid processing 2002 ·Neurobiology of Aging ·Jessie Theuns, Samir Kumar‐Singh, Bart Dermaut, Kristel M. Vennekens, Ellen Corsmit, Marc Cruts, Christine Van Broeckhoven, (unknown)	1
16	Tau negative frontal lobe dementia at 17q21: Significant finemapping of the candidate region to a 4.8 cm interval 2002 ·Neurobiology of Aging ·R. Rademakers, Marc Cruts, Bart Dermaut, Marleen Van den Broeck, H. Backhovens, Christine Van Broeckhoven, Kristel Sleegers, Cornelia M. van Duijn, (unknown), (unknown)	17
17	Amyloid beta-secretase gene (BACE) is neither mutated nor associated with early-onset Alzheimers disease 2001 ·Ghent University Academic Bibliography (Ghent University) ·Marc Cruts, Bart Dermaut, R. Rademakers, Gerwin Roks, Marleen Van den Broeck, (unknown), (unknown), Christine Van Broeckhoven	1
18	Cerebral amyloid angiopathy is a pathogenic lesion in Alzheimer's disease due to a novel presenilin 1 mutation 2001 ·Brain ·Bart Dermaut	64
19	Variable expression of presenilin 1 is not a major determinant of risk for late-onset Alzheimer's Disease 2001 ·Journal of Neurology ·Bart Dermaut, Gerwin Roks, Jessie Theuns, Rosa Rademakers, Jeanine J. Houwing‐Duistermaat, Sally Serneels, Albert Hofman, Monique M.B. Breteler, Marc Cruts, Christine Van Broeckhoven, Cornelia M. van Duijn	13
20	Aberrant splicing in the presenilin-1 intron 4 mutation causes presenile Alzheimers disease by increased a beta 42 secretion 1999 ·The American Journal of Human Genetics ·Marc Cruts, C. De Jonghe, (unknown), Carolyn Tysoe, Andrew Singleton, Hugo Vanderstichele, Wendy S. Meschino, Bart Dermaut, (unknown), H. Backhovens, Eugeen Vanmechelen, Christopher M. Morris, John Hardy, (unknown), (unknown), Christine Van Broeckhoven	10

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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