Bart Dermaut

8.1k citations

73 papers · 3.8k · h-index 35

Impact in

Clinical Biochemistry top 0.5%
- Metabolism and Genetic Disorders
Neurology top 1%
- Amyotrophic Lateral Sclerosis Research
- Neurological diseases and metabolism

Papers in

Physiology 34
- Alzheimer's disease research and treatments 32
Neurology 19
- Neurological diseases and metabolism 10
- Amyotrophic Lateral Sclerosis Research 9

Co-authors: Christine Van Broeckhoven (47 shared papers)Gert Van Goethem (2 shared papers)Jean‐Jacques Martin (3 shared papers)Marc Cruts (35 shared papers)Ann Löfgren (1 shared paper)Patrick Callaerts (7 shared papers)Rosa Rademakers (14 shared papers)Marleen Van den Broeck (16 shared papers)
Journals: Neurobiology of Aging (11 papers)The American Journal of Human Genetics (6 papers)Human Molecular Genetics (4 papers)Neurology (4 papers)Brain (3 papers)
Partner nations: Belgium Netherlands United States

In The Last Decade

Bart Dermaut

71 papers receiving 3.7k citations

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-authors

The 25 scholars most cited alongside Bart Dermaut, 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 Bart Dermaut Line = papers co-authored together Bart Dermaut links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 73 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Mutation of POLG is associated with progressive external ophthalmoplegia characterized by mtDNA deletions Nature Genetics ·Gert Van Goethem, Bart Dermaut, Ann Löfgren, Jean‐Jacques Martin, Christine Van Broeckhoven	2001	664
2	Mean age-of-onset of familial alzheimer disease caused by presenilin mutations correlates with both increased Aβ42 and decreased Aβ40 Human Mutation ·Samir Kumar‐Singh, Jessie Theuns, Bianca Van Broeck, Daniel Nicolae Pirici, Krist’l Vennekens, Ellen Corsmit, Marc Cruts, Bart Dermaut, Rong Wang, Christine Van Broeckhoven	2006	268
3	Recessive POLG mutations presenting with sensory and ataxic neuropathy in compound heterozygote patients with progressive external ophthalmoplegia Neuromuscular Disorders ·G. Van Goethem, J.J. Martin, Bart Dermaut, Ann Löfgren, Alain Wibail, D Ververken, Peter I. Tack, I. Dehaene, Michel Van Zandijcke, M Moonen, C. Ceuterick, Peter De Jonghe, Christine Van Broeckhoven	2003	202
4	A novel presenilin 1 mutation associated with Pick's disease but not β‐amyloid plaques Annals of Neurology ·Bart Dermaut, Samir Kumar‐Singh, Sebastian Engelborghs, Jessie Theuns, Rosa Rademakers, Jos Saerens, Barbara Anne Pickut, Karin Peeters, Marleen Van den Broeck, Krist’l Vennekens, Stephan J. Claes, Marc Cruts, Patrick P Cras, Jean‐Jacques Martin, Christine Van Broeckhoven, Peter Paul De Deyn	2004	170
5	Involvement of GATOR complex genes in familial focal epilepsies and focal cortical dysplasia Epilepsia ·Sarah Weckhuysen, Elise Marsan, Virginie Lambrecq, Cécile Marchal, Mélanie Morin‐Brureau, Isabelle An-Gourfinkel, Michel Baulac, Martine Fohlen, Christine Kallay Zetchi, Margitta Seeck, Pierre de la Grange, Bart Dermaut, Alfred Meurs, P. Thomas, Francine Chassoux, Éric Leguern, Fabienne Picard, Stéphanie Baulac	2016	137
6	CHMP2B C-truncating mutations in frontotemporal lobar degeneration are associated with an aberrant endosomal phenotype in vitro Human Molecular Genetics ·Julie van der Zee, Hazel Urwin, S. Engelborghs, Marc Bruyland, Rik R. Vandenberghe, Bart Dermaut, Tim De Pooter, Karin Peeters, Patrick Santens, Peter Paul De Deyn, Elizabeth Fisher, John Collinge, Adrian M. Isaacs, Christine Van Broeckhoven	2007	133
7	Novel POLG mutations in progressive external ophthalmoplegia mimicking mitochondrial neurogastrointestinal encephalomyopathy European Journal of Human Genetics ·Gert Van Goethem, Marianne Schwartz, Ann Löfgren, Bart Dermaut, Christine Van Broeckhoven, J. Vissing	2003	131
8	Aberrant lysosomal carbohydrate storage accompanies endocytic defects and neurodegeneration inDrosophila benchwarmer The Journal of Cell Biology ·Bart Dermaut, Koen Norga, Artur Kania, Patrik Verstreken, Hongling Pan, Yi Zhou, Patrick Callaerts, Hugo Jozef Bellen	2005	118
9	Loss and gain of Drosophila TDP-43 impair synaptic efficacy and motor control leading to age-related neurodegeneration by loss-of-function phenotypes Human Molecular Genetics ·Danielle C. Diaper, Yoshitsugu Adachi, Ben Sutcliffe, Dickon M. Humphrey, Christopher J. H. Elliott, Alan Stepto, Zoe N. Ludlow, Lies Vanden Broeck, Patrick Callaerts, Bart Dermaut, Ammar Al‐Chalabi, Christopher E. Shaw, Iain Martin Robinson, Frank Hirth	2013	111
10	TDP-43-mediated neurodegeneration: towards a loss-of-function hypothesis? Trends in Molecular Medicine ·Lies Vanden Broeck, Patrick Callaerts, Bart Dermaut	2013	104
11	PRNP Val129 homozygosity increases risk for early‐onset Alzheimer's disease Annals of Neurology ·Bart Dermaut, Esther A. Croes, Rosa Rademakers, Marleen Van den Broeck, Marc Cruts, Albert Hofman, Cornelia M. van Duijn, Christine Van Broeckhoven	2003	88
12	Tau negative frontal lobe dementia at 17q21: significant finemapping of the candidate region to a 4.8 cM interval Molecular Psychiatry ·Roos Rademakers, Marc Cruts, Bart Dermaut, Kristel Sleegers, S. Rosso, Marleen Van den Broeck, H. Backhovens, John Cornelis Van Swieten, C M van Duijn, Christine Van Broeckhoven	2002	88
13	Functional screening of Alzheimer risk loci identifies PTK2B as an in vivo modulator and early marker of Tau pathology Molecular Psychiatry ·Pierre Dourlen, Francisco-José Fernández-Gómez, Clément Dupont, Benjamin Grenier‐Boley, Céline Bellenguez, Hélène Obriot, Raphaëlle Caillierez, Yoann Sottejeau, Julien Chapuis, Alexis Bretteville, Farida Abdelfettah, Cyril Delay, Nicolas Malmanche, Hilkka S. Soininen, Mikko O. Hiltunen, (unknown), Philippe Amouyel, Nicolas Sergeant, Luc Buée, (unknown), Bart Dermaut	2016	85
14	Neuronal inclusion protein TDP-43 has no primary genetic role in FTD and ALS Neurobiology of Aging ·Ilse Gijselinck, Kristel Sleegers, S. Engelborghs, Wim Robberecht, Jean‐Jacques Martin, Rik R. Vandenberghe, Raf Sciot, Bart Dermaut, Dirk 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	2008	77
15	Aberrant Splicing in the Presenilin-1 Intron 4 Mutation Causes Presenile Alzheimer's Disease by Increased A 42 Secretion Human Molecular Genetics ·Chris De Jonghe, MarcCruts, E. A. Rogaeva, Carolyn J. Tysoe, Andrew Singleton, Hugo Vanderstichele, Wendy S. Meschino, Bart Dermaut, Inge Vanderhoeven, H. Backhovens, Eugeen Vanmechelen, Christopher M. Morris, John Hardy, D. C. Rubinsztein, Peter St George‐Hyslop, Christine Van Broeckhoven	1999	72
16	Cerebral amyloid angiopathy is a pathogenic lesion in Alzheimer's disease due to a novel presenilin 1 mutation Brain ·Bart Dermaut	2001	70
17	Moyamoya disease emerging as an immune-related angiopathy Trends in Molecular Medicine ·Caroline Asselman, Dimitri Hemelsoet, Denzel Eggermont, Bart Dermaut, Francis Impens	2022	69
18	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 ·Marc Cruts, Rosa Rademakers, Ilse Gijselinck, Julie van der Zee, Bart Dermaut, Tim De Pooter, Peter De Rijk, Jurgen Del‐Favero, Christine Van Broeckhoven	2005	67
19	Tau phosphorylation regulates the interaction between BIN1’s SH3 domain and Tau’s proline-rich domain Acta Neuropathologica Communications ·Yoann Sottejeau, Alexis Bretteville, François‐Xavier Cantrelle, Nicolas Malmanche, Florie Demiaute, Tiago Mendes, Charlotte Delay, Harmony Alves dos Alves, Amandine Flaig, Peter R.T. Davies, Pierre Dourlen, Bart Dermaut, Jocelyn Laporte, Philippe Amouyel, Guy M. Lippens, Julien Chapuis, Isabelle Landrieu, Jean‐Charles Lambert	2015	66
20	A Belgian ancestral haplotype harbours a highly prevalent mutation for 17q21-linked tau-negative FTLD Brain ·Julie van der Zee, Rosa Rademakers, S. Engelborghs, Ilse Gijselinck, Veerle Bogaerts, Rik R. Vandenberghe, Patrick Santens, Jo Caekebeke, Tim De Pooter, Karin Peeters, Ursula Lübke, Marleen Van den Broeck, Jean‐Jacques Martin, Marc Cruts, Peter Paul De Deyn, Christine Van Broeckhoven, Bart Dermaut	2006	65

About Bart Dermaut

Bart Dermaut is a scholar working on Physiology, Neurology, Neurology, Molecular Biology and Pharmacology, having authored 73 papers that have together received 3.8k indexed citations. Recurring topics across this work include Alzheimer's disease research and treatments (32 papers), Prion Diseases and Protein Misfolding (15 papers), Neurological diseases and metabolism (10 papers), Cholinesterase and Neurodegenerative Diseases (10 papers), Amyotrophic Lateral Sclerosis Research (9 papers), Mitochondrial Function and Pathology (5 papers), Dementia and Cognitive Impairment Research (4 papers) and Amyloidosis: Diagnosis, Treatment, Outcomes (4 papers). The work is most often cited by research in Clinical Biochemistry (548 citations), Neurology (910 citations), Physiology (1.5k citations), Neurology (464 citations) and Cellular and Molecular Neuroscience (586 citations). Bart Dermaut has collaborated with scholars based in Belgium, Netherlands and United States. Frequent co-authors include Christine Van Broeckhoven, Gert Van Goethem, Jean‐Jacques Martin, Marc Cruts, Ann Löfgren, Patrick Callaerts, Rosa Rademakers, Marleen Van den Broeck, Jessie Theuns and Cornelia M. van Duijn. Their work appears in journals such as Neurobiology of Aging, The American Journal of Human Genetics, Human Molecular Genetics, Neurology and Brain.

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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Bart Dermaut

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