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Author

Jasper Van Dongen

Observed names: Dongen, Jasper, Dongen, Jasper Van
Observed institutions: University of Antwerp, Inserm, Erasmus MC, Vlaams Instituut voor Biotechnologie, VIB-UAntwerp Center for Molecular Neurology, Institute Born-Bunge, Université de Rouen Normandie
ORCID: 0000-0001-5599-0046
Observed ORCID: 0000-0001-5599-0046
OpenAlex ID: A5081371190
New insights into the genetic etiology of Alzheimer’s disease and related dementias
2022 · Céline Bellenguez, Fahri Küçükali, et al. · Nature Genetics · 2,471
A C9orf72 promoter repeat expansion in a Flanders-Belgian cohort with disorders of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrum: a gene identification study
2011 · Ilse Gijselinck, Tim Van Langenhove, et al. · The Lancet Neurology · 633
Common variants in Alzheimer’s disease and risk stratification by polygenic risk scores
2021 · Itziar de Rojas, Sonia Moreno-Grau, et al. · Nature Communications · 322
Investigating the role of rare heterozygous TREM2 variants in Alzheimer's disease and frontotemporal dementia
2013 · Elise Cuyvers, Karolien Bettens, et al. · Neurobiology of Aging · 182
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Genome-wide meta-analysis for Alzheimer’s disease cerebrospinal fluid biomarkers
2022 · Iris E. Jansen, Sven J. van der Lee, et al. · Acta Neuropathologica · 130
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A 22‐single nucleotide polymorphism Alzheimer's disease risk score correlates with family history, onset age, and cerebrospinal fluid Aβ42
2015 · Kristel Sleegers, Karolien Bettens, et al. · Alzheimer s & Dementia · 105
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Both common variations and rare non-synonymous substitutions and small insertion/deletions in CLU are associated with increased Alzheimer risk
2012 · Karolien Bettens, Nathalie Brouwers, et al. · Molecular Neurodegeneration · 94
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An intronic VNTR affects splicing of ABCA7 and increases risk of Alzheimer’s disease
2018 · Arne De Roeck, Lena Duchateau, et al. · Acta Neuropathologica · 92
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NanoSatellite: accurate characterization of expanded tandem repeat length and sequence through whole genome long-read sequencing on PromethION
2019 · Arne De Roeck, Wouter De Coster, et al. · Genome biology · 88
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C9orf72 G4C2 repeat expansions in Alzheimer's disease and mild cognitive impairment
2013 · Rita Cacace, Caroline Van Cauwenberghe, et al. · Neurobiology of Aging · 74
Deleterious ABCA7 mutations and transcript rescue mechanisms in early onset Alzheimer’s disease
2017 · Arne De Roeck, Tobi Van den Bossche, et al. · Acta Neuropathologica · 73
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Multiancestry analysis of the HLA locus in Alzheimer’s and Parkinson’s diseases uncovers a shared adaptive immune response mediated by HLA-DRB1*04 subtypes
2023 · Yann Le Guen, Guo Luo, et al. · Proceedings of the National Academy of Sciences · 60
The SORL1 p.Y1816C variant causes impaired endosomal dimerization and autosomal dominant Alzheimer’s disease
2024 · Anne Mette G. Jensen, Jan Raska, et al. · Proceedings of the National Academy of Sciences · 25
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Complement receptor 1 coding variant p.Ser1610Thr in Alzheimer's disease and related endophenotypes
2013 · Caroline Van Cauwenberghe, Karolien Bettens, et al. · Neurobiology of Aging · 25
Dissociating effects of aging and genetic risk of sporadic Alzheimer’s disease on path integration
2023 · Lise Colmant, Anne Bierbrauer, et al. · Neurobiology of Aging · 19
Machine learning in Alzheimer’s disease genetics
2025 · Matthew Bracher-Smith, Federico Melograna, et al. · Nature Communications · 18
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Whole‐exome rare‐variant analysis of Alzheimer's disease and related biomarker traits
2022 · Fahri Küçükali, Alexander Neumann, et al. · Alzheimer s & Dementia · 16
Hypothesis-based investigation of known AD risk variants reveals the genetic underpinnings of neuropathological lesions observed in Alzheimer’s-type dementia
2024 · Celeste Laureyssen, Fahri Küçükali, et al. · Acta Neuropathologica · 7
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Scywalker: scalable end-to-end data analysis workflow for long-read single-cell transcriptome sequencing
2024 · Peter De Rijk, Tijs Watzeels, et al. · Bioinformatics · 7
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Discrepancy between Apolipoprotein E genotyping and proteotyping as a result of a nonsense mutation
2024 · Ina Vandenbroucke, Tatsushi Yuri, et al. · Alzheimer s & Dementia · 5
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ZCWPW1 loss-of-function variants in Alzheimer’s Disease
2021 · Fahri Küçükali, Katrin Nußbaumer, et al. · medRxiv · 3
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A repeat expansion in GOLGA8A is a major risk factor for atypical frontotemporal lobar degeneration with ubiquitin-positive inclusions
2026 · Wouter De Coster, Marleen Van den Broeck, et al. · Nature Genetics · 2
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Scywalker: scalable end-to-end data analysis workflow for nanopore single-cell transcriptome sequencing
2024 · Peter De Rijk, Tijs Watzeels, et al. · bioRxiv (Cold Spring Harbor Laboratory) · 2
O4‐04‐03: HIGH SCORES ON A 22‐GENE RISK SCORE FOR ALZHEIMER'S DEMENTIA CORRELATE WITH EARLIER ONSET AGE AND REDUCED CSF Aβ
2014 · Karolien Bettens, Caroline Van Cauwenberghe, et al. · Alzheimer s & Dementia · 1
Clinicopathological characteristics of Belgian SORL1 mutation carriers
2026 · Tobi Van den Bossche, Fahri Küçükali, et al. · Alzheimer s Research & Therapy
Works count: 45
Citation count: 4,453
H-index: 16
I10-index: 17
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