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Loss of DPP6 in neurodegenerative dementia: a genetic player in the dysfunction of neuronal excitability.
Cacace R, Heeman B, Van Mossevelde S, De Roeck A, Hoogmartens J, De Rijk P, Gossye H, De Vos K, De Coster W, Strazisar M, De Baets G, Schymkowitz J, Rousseau F, Geerts N, De Pooter T, Peeters K, Sieben A, Martin JJ, Engelborghs S, Salmon E, Santens P, Vandenberghe R, Cras P, P De Deyn P, C van Swieten J, M van Duijn C, van der Zee J, Sleegers K, Van Broeckhoven C; BELNEU Consortium. Cacace R, et al. Among authors: gossye h. Acta Neuropathol. 2019 Jun;137(6):901-918. doi: 10.1007/s00401-019-01976-3. Epub 2019 Mar 14. Acta Neuropathol. 2019. PMID: 30874922 Free PMC article.
Mutated ATP10B increases Parkinson's disease risk by compromising lysosomal glucosylceramide export.
Martin S, Smolders S, Van den Haute C, Heeman B, van Veen S, Crosiers D, Beletchi I, Verstraeten A, Gossye H, Gelders G, Pals P, Hamouda NN, Engelborghs S, Martin JJ, Eggermont J, De Deyn PP, Cras P, Baekelandt V, Vangheluwe P, Van Broeckhoven C; BELNEU consortium. Martin S, et al. Among authors: gossye h. Acta Neuropathol. 2020 Jun;139(6):1001-1024. doi: 10.1007/s00401-020-02145-7. Epub 2020 Mar 14. Acta Neuropathol. 2020. PMID: 32172343 Free PMC article.
No association of CpG SNP rs9357140 with onset age in Belgian C9orf72 repeat expansion carriers.
Koçoğlu C, Gossye H, Dillen L, Van Mossevelde S, De Bleecker JL, Vandenberghe R, De Deyn PP, Sleegers K, Cras P, Engelborghs S, Van Broeckhoven C, van der Zee J; BELNEU Consortium. Koçoğlu C, et al. Among authors: gossye h. Neurobiol Aging. 2021 Jan;97:145.e1-145.e4. doi: 10.1016/j.neurobiolaging.2020.07.021. Epub 2020 Aug 15. Neurobiol Aging. 2021. PMID: 32921502 Free article.
Hippocampal Sclerosis in Frontotemporal Dementia: When Vascular Pathology Meets Neurodegeneration.
Sieben A, Van Langenhove T, Vermeiren Y, Gossye H, Praet M, Vanhauwaert D, Cousaert C, Engelborghs S, Raedt R, Boon P, Santens P, De Deyn PP, Bracke KR, De Meulemeester K, Van Broeckhoven C, Martin JJ, Bjerke M. Sieben A, et al. Among authors: gossye h. J Neuropathol Exp Neurol. 2021 Mar 22;80(4):313-324. doi: 10.1093/jnen/nlab010. J Neuropathol Exp Neurol. 2021. PMID: 33638350
Family-based exome sequencing identifies RBM45 as a possible candidate gene for frontotemporal dementia and amyotrophic lateral sclerosis.
van der Zee J, Dillen L, Baradaran-Heravi Y, Gossye H, Koçoğlu C, Cuyt I, Dermaut B, Sieben A, Baets J, De Jonghe P, Vandenberghe R, De Deyn P, Cras P, Engelborghs S, Van Broeckhoven C; BELNEU Consortium. van der Zee J, et al. Among authors: gossye h. Neurobiol Dis. 2021 Aug;156:105421. doi: 10.1016/j.nbd.2021.105421. Epub 2021 Jun 9. Neurobiol Dis. 2021. PMID: 34118419 Free article.
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[No authors listed] [No authors listed] PMID: 35109291
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[No authors listed] [No authors listed] PMID: 35109374
Patients carrying the mutation p.R406W in MAPT present with non-conforming phenotypic spectrum.
Gossye H, Van Mossevelde S, Sieben A, Bjerke M, Hendrickx Van de Craen E, van der Zee J, De Deyn PP, De Bleecker J, Versijpt J, van den Ende J, Deryck O, Bourgeois P, Bier JC, Goethals M, Vandenberghe R, Engelborghs S, Van Broeckhoven C. Gossye H, et al. Brain. 2023 Apr 19;146(4):1624-1636. doi: 10.1093/brain/awac362. Brain. 2023. PMID: 36171642 Free PMC article.
13 results