John van Swieten

Affiliations: 
Erasmus Medical Center Rotterdam, Rotterdam, Netherlands 
Google:
"John van Swieten"
BETA: Related publications

Publications

You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect.

Wang H, Chang TS, Dombroski BA, et al. (2023) Whole-Genome Sequencing Analysis Reveals New Susceptibility Loci and Structural Variants Associated with Progressive Supranuclear Palsy. Medrxiv : the Preprint Server For Health Sciences
Le Guen Y, Luo G, Ambati A, et al. (2023) Multiancestry analysis of the HLA locus in Alzheimer's and Parkinson's diseases uncovers a shared adaptive immune response mediated by subtypes. Proceedings of the National Academy of Sciences of the United States of America. 120: e2302720120
van der Ende EL, In 't Veld SGJG, Hanskamp I, et al. (2023) CSF proteomics in autosomal dominant Alzheimer's disease highlights parallels with sporadic disease. Brain : a Journal of Neurology
Del Campo M, Peeters CFW, Johnson ECB, et al. (2022) CSF proteome profiling across the Alzheimer's disease spectrum reflects the multifactorial nature of the disease and identifies specific biomarker panels. Nature Aging. 2: 1040-1053
Finger E, Malik R, Bocchetta M, et al. (2022) Neurodevelopmental effects of genetic frontotemporal dementia in young adult mutation carriers. Brain : a Journal of Neurology
Holstege H, Hulsman M, Charbonnier C, et al. (2022) Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer's disease. Nature Genetics
Jansen IE, van der Lee SJ, Gomez-Fonseca D, et al. (2022) Genome-wide meta-analysis for Alzheimer's disease cerebrospinal fluid biomarkers. Acta Neuropathologica
Le Guen Y, Belloy ME, Grenier-Boley B, et al. (2022) Association of Rare APOE Missense Variants V236E and R251G With Risk of Alzheimer Disease. Jama Neurology
Bellenguez C, Küçükali F, Jansen IE, et al. (2022) New insights into the genetic etiology of Alzheimer's disease and related dementias. Nature Genetics
Bouzigues A, Russell LL, Peakman G, et al. (2022) Anomia is present pre-symptomatically in frontotemporal dementia due to MAPT mutations. Journal of Neurology
See more...