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Page 1
Contribution of TARDBP to Alzheimer's disease genetic etiology.
Brouwers N, Bettens K, Gijselinck I, Engelborghs S, Pickut BA, Van Miegroet H, Montoya AG, Mattheijssens M, Peeters K, De Deyn PP, Cruts M, Sleegers K, Van Broeckhoven C. Brouwers N, et al. Among authors: van miegroet h, van broeckhoven c. J Alzheimers Dis. 2010;21(2):423-30. doi: 10.3233/JAD-2010-100198. J Alzheimers Dis. 2010. PMID: 20555136
Both common variations and rare non-synonymous substitutions and small insertion/deletions in CLU are associated with increased Alzheimer risk.
Bettens K, Brouwers N, Engelborghs S, Lambert JC, Rogaeva E, Vandenberghe R, Le Bastard N, Pasquier F, Vermeulen S, Van Dongen J, Mattheijssens M, Peeters K, Mayeux R, St George-Hyslop P, Amouyel P, De Deyn PP, Sleegers K, Van Broeckhoven C. Bettens K, et al. Among authors: van dongen j, van broeckhoven c. Mol Neurodegener. 2012 Jan 16;7:3. doi: 10.1186/1750-1326-7-3. Mol Neurodegener. 2012. PMID: 22248099 Free PMC article.
Genetic insights in Alzheimer's disease.
Bettens K, Sleegers K, Van Broeckhoven C. Bettens K, et al. Among authors: van broeckhoven c. Lancet Neurol. 2013 Jan;12(1):92-104. doi: 10.1016/S1474-4422(12)70259-4. Lancet Neurol. 2013. PMID: 23237904 Review.
C9orf72 G4C2 repeat expansions in Alzheimer's disease and mild cognitive impairment.
Cacace R, Van Cauwenberghe C, Bettens K, Gijselinck I, van der Zee J, Engelborghs S, Vandenbulcke M, Van Dongen J, Bäumer V, Dillen L, Mattheijssens M, Peeters K, Cruts M, Vandenberghe R, De Deyn PP, Van Broeckhoven C, Sleegers K. Cacace R, et al. Among authors: van cauwenberghe c, van der zee j, van dongen j, van broeckhoven c. Neurobiol Aging. 2013 Jun;34(6):1712.e1-7. doi: 10.1016/j.neurobiolaging.2012.12.019. Epub 2013 Jan 24. Neurobiol Aging. 2013. PMID: 23352322
Complement receptor 1 coding variant p.Ser1610Thr in Alzheimer's disease and related endophenotypes.
Van Cauwenberghe C, Bettens K, Engelborghs S, Vandenbulcke M, Van Dongen J, Vermeulen S, Vandenberghe R, De Deyn PP, Van Broeckhoven C, Sleegers K. Van Cauwenberghe C, et al. Among authors: van dongen j, van broeckhoven c. Neurobiol Aging. 2013 Sep;34(9):2235.e1-6. doi: 10.1016/j.neurobiolaging.2013.03.008. Epub 2013 Apr 10. Neurobiol Aging. 2013. PMID: 23582656
Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration.
van der Zee J, Van Langenhove T, Kovacs GG, Dillen L, Deschamps W, Engelborghs S, Matěj R, Vandenbulcke M, Sieben A, Dermaut B, Smets K, Van Damme P, Merlin C, Laureys A, Van Den Broeck M, Mattheijssens M, Peeters K, Benussi L, Binetti G, Ghidoni R, Borroni B, Padovani A, Archetti S, Pastor P, Razquin C, Ortega-Cubero S, Hernández I, Boada M, Ruiz A, de Mendonça A, Miltenberger-Miltényi G, do Couto FS, Sorbi S, Nacmias B, Bagnoli S, Graff C, Chiang HH, Thonberg H, Perneczky R, Diehl-Schmid J, Alexopoulos P, Frisoni GB, Bonvicini C, Synofzik M, Maetzler W, vom Hagen JM, Schöls L, Haack TB, Strom TM, Prokisch H, Dols-Icardo O, Clarimón J, Lleó A, Santana I, Almeida MR, Santiago B, Heneka MT, Jessen F, Ramirez A, Sanchez-Valle R, Llado A, Gelpi E, Sarafov S, Tournev I, Jordanova A, Parobkova E, Fabrizi GM, Testi S, Salmon E, Ströbel T, Santens P, Robberecht W, De Jonghe P, Martin JJ, Cras P, Vandenberghe R, De Deyn PP, Cruts M, Sleegers K, Van Broeckhoven C. van der Zee J, et al. Among authors: van den broeck m, van langenhove t, van damme p, van broeckhoven c. Acta Neuropathol. 2014 Sep;128(3):397-410. doi: 10.1007/s00401-014-1298-7. Epub 2014 Jun 5. Acta Neuropathol. 2014. PMID: 24899140 Free PMC article.
779 results