Authors:
Theuns, J
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Dermaut, B
Del-Favero, J
Roks, G
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Citation: J. Theuns et al., The TNFRSF6 gene is not implicated in familial early-onset Alzheimer's disease, HUM GENET, 108(6), 2001, pp. 552-553
Authors:
Dermaut, B
Roks, G
Theuns, J
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van Duijn, CM
Citation: B. Dermaut et al., Variable expression of presenilin 1 is not a major determinant of risk forlate-onset Alzheimer's Disease, J NEUROL, 248(11), 2001, pp. 935-939
Authors:
Russ, C
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Zhao, JH
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Hutton, M
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Citation: C. Russ et al., The microtubule associated protein Tau gene and Alzheimer's disease - an association study and meta-analysis, NEUROSCI L, 314(1-2), 2001, pp. 92-96
Authors:
Van Everbroeck, B
Croes, EA
Pals, P
Dermaut, B
Jansen, G
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Cruts, M
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Martin, JJ
Cras, P
Citation: B. Van Everbroeck et al., Influence of the prion protein and the apolipoprotein E genotype on the Creutzfeldt-Jakob Disease phenotype, NEUROSCI L, 313(1-2), 2001, pp. 69-72
Authors:
Cruts, M
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Rademakers, R
Roks, G
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Munteanu, G
van Duijn, CM
Van Broeckhoven, CV
Citation: M. Cruts et al., Amyloid beta secretase gene (BACE) is neither mutated in nor associated with early-onset Alzheimer's disease, NEUROSCI L, 313(1-2), 2001, pp. 105-107
Authors:
Arango, D
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Torres, O
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Citation: D. Arango et al., Systematic genetic study of Alzheimer disease in Latin America: Mutation frequencies of the amyloid beta precursor protein and presenilin genes in Colombia, AM J MED G, 103(2), 2001, pp. 138-143
Authors:
Theuns, J
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Dermaut, B
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Serneels, S
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Cruts, M
Citation: J. Theuns et al., Genetic variability in the regulatory region of presenilin 1 associated with risk for Alzheimer's disease and variable expression, HUM MOL GEN, 9(3), 2000, pp. 325-331
Authors:
Kumar-Singh, S
De Jonghe, C
Cruts, M
Kleinert, R
Wang, R
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Vanderstichele, H
Lofgren, A
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Backhovens, H
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Kroisel, PM
Van Broeckhoven, C
Citation: S. Kumar-singh et al., Nonfibrillar diffuse amyloid deposition due to a gamma(42)-secretase site mutation points to an essential role for N-truncated A beta(42) in Alzheimer's disease, HUM MOL GEN, 9(18), 2000, pp. 2589-2598
Authors:
Visser, PJ
Verhey, FRJ
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Citation: Pj. Visser et al., Course of objective memory impairment in non-demented subjects attending amemory clinic and predictors of outcome, INT J GER P, 15(4), 2000, pp. 363-372
Authors:
Dermaut, B
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Sciot, R
Dom, R
Martin, JJ
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Cras, P
Citation: B. Dermaut et al., Familial Creutzfeldt-Jakob disease in a patient carrying both a presenilin1 missense substitution and a prion protein gene insertion, J NEUROL, 247(5), 2000, pp. 364-368
Authors:
Koster, MN
Dermaut, B
Cruts, M
Houwing-Duistermaat, JJ
Roks, G
Tol, J
Ott, A
Hofman, A
Munteanu, G
Breteler, MMB
van Duijn, CM
Van Broeckhoven, C
Citation: Mn. Koster et al., The alpha 2-macroglobulin gene in AD - A population-based study and meta-analysis, NEUROLOGY, 55(5), 2000, pp. 678-684
Authors:
Singleton, AB
Hall, R
Ballard, CG
Perry, RH
Xuereb, JH
Rubinsztein, DC
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Kumar-Singh, S
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Morris, CM
Citation: Ab. Singleton et al., Pathology of early-onset Alzheimer's disease cases bearing the Thr113-114ins presenilin-1 mutation, BRAIN, 123, 2000, pp. 2467-2474
Authors:
Roks, G
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Cruts, M
De Jonghe, C
Kumar-Singh, S
Tibben, A
Tanghe, H
Niermeijer, MF
Hofman, A
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Van Broeckhoven, C
Van Duijn, CM
Citation: G. Roks et al., Presentation of amyloidosis in carriers of the codon 692 mutation in the amyloid precursor protein gene (APP692), BRAIN, 123, 2000, pp. 2130-2140
Authors:
Wang, SY
Cruts, M
Del-Favero, J
Zhang, Y
Tissir, F
Potier, MC
Patterson, D
Nizetic, D
Bosch, A
Chen, HM
Bennett, L
Estivill, X
Kessling, A
Antonarakis, SE
van Broeckhoven, C
Citation: Sy. Wang et al., A high-resolution physical map of human chromosome 21p using yeast artificial chromosomes, GENOME RES, 9(11), 1999, pp. 1059-1073
Authors:
van Duijn, CM
Cruts, M
Theuns, J
Van Gassen, G
Backhovens, H
van den Broeck, M
Wehnert, A
Serneels, S
Hofman, A
Van Broeckhoven, C
Citation: Cm. Van Duijn et al., Genetic association of the presenilin-1 regulatory region with early-onsetAlzheimer's disease in a population-based sample, EUR J HUM G, 7(7), 1999, pp. 801-806
Authors:
De Jonghe, C
Cras, P
Vanderstichele, H
Cruts, M
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Smouts, I
Vanmechelen, E
Martin, JJ
Hendriks, L
Van Broeckhoven, C
Citation: C. De Jonghe et al., Evidence that A beta 42 plasma levels in presenilin-1 mutation carriers donot allow for prediction of their clinical phenotype, NEUROBIOL D, 6(4), 1999, pp. 280-287
Authors:
De Jonghe, C
Cruts, M
Rogaeva, EA
Tysoe, C
Singleton, A
Vanderstichele, H
Meschino, W
Dermaut, D
Vanderhoeven, I
Backhovens, H
Vanmechelen, E
Morris, CM
Hardy, J
Rubinsztein, DC
St George-Hyslop, PH
Van Broeckhoven, C
Citation: C. De Jonghe et al., Aberrant splicing in the presenilin-1 intron 4 mutation causes presenile Alzheimer's disease by increased A beta 42 secretion, HUM MOL GEN, 8(8), 1999, pp. 1529-1540
Authors:
Theuns, J
Cruts, M
Del-Favero, J
Goossens, D
Dauwerse, H
Wehnert, A
den Dunnen, JT
Van Broeckhoven, C
Citation: J. Theuns et al., Determination of the genomic organization of human presenilin 1 by fiber-FISH analysis and restriction mapping of cloned DNA, MAMM GENOME, 10(4), 1999, pp. 410-414
Authors:
Slooter, AJC
Houwing-Duistermaat, JJ
van Harskamp, F
Cruts, M
Van Broeckhoven, C
Breteler, MMB
Hofman, A
Stijnen, T
van Duijn, CM
Citation: Ajc. Slooter et al., Apolipoprotein E genotype and progression of Alzheimer's disease: the Rotterdam study, J NEUROL, 246(4), 1999, pp. 304-308
Authors:
Slooter, AJC
Cruts, M
Ott, A
Bots, ML
Witteman, JCM
Hofman, A
Van Broeckhoven, C
Breteler, MMB
van Duijn, CM
Citation: Ajc. Slooter et al., The effect of APOE on dementia is not through atherosclerosis: The Rotterdam Study, NEUROLOGY, 53(7), 1999, pp. 1593-1595
Authors:
Dermaut, B
Cruts, M
Slooter, AJC
Van Gestel, S
De Jonghe, C
Vanderstichele, H
Vanmechelen, E
Breteler, MM
Hofman, A
van Duijn, CM
Van Broeckhoven, C
Citation: B. Dermaut et al., The Glu318Gly substitution in presenilin 1 is not causally related to Alzheimer disease, AM J HU GEN, 64(1), 1999, pp. 290-292