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Results: 51-75/97
A European multicenter association study of HTR2A receptor polymorphism inbipolar affective disorder
Authors:
Massat, I
Souery, D
Lipp, O
Blairy, S
Papadimitriou, G
Dikeos, D
Ackenheil, M
Fuchshuber, S
Hilger, C
Kaneva, R
Milanova, V
Verheyen, G
Raeymaekers, P
Staner, L
Oruc, L
Jakovljevic, M
Serretti, A
Macciardi, F
Van Broeckhoven, C
Mendlewicz, J
Citation: I. Massat et al., A European multicenter association study of HTR2A receptor polymorphism inbipolar affective disorder, AM J MED G, 96(2), 2000, pp. 136-140
Authors:
Leonardis, L
Zidar, J
Popovic, M
Timmerman, V
Lofgren, A
Van Broeckhoven, C
Butinar, D
Citation: L. Leonardis et al., Hereditary motor and sensory neuropathy associated with auditory neuropathy in a Gypsy family, PFLUG ARCH, 439(3), 2000, pp. R208-R210
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:
Harhangi, BS
de Rijk, MC
van Duijn, CM
Van Broeckhoven, C
Hofman, A
Breteler, MMB
Citation: Bs. Harhangi et al., APOE and the risk of PD with or without dementia in a population-based study, NEUROLOGY, 54(6), 2000, pp. 1272-1276
Authors:
Wauters, M
Considine, R
Lofgren, A
Van Broeckhoven, C
Van der Auwera, JC
De Leeuw, I
Van Gaal, L
Citation: M. Wauters et al., Associations of leptin with body fat distribution and metabolic parametersin non-insulin-dependent diabetic patients: No effect of apolipoprotein E polymorphism, METABOLISM, 49(6), 2000, pp. 724-730
Authors:
Van Goethem, G
Lofgren, A
Martin, JJ
Van Broeckhoven, C
Citation: G. Van Goethem et al., Further evidence for genetic heterogeneity of autosomal dominant disorderswith accumulation of multiple deletions of mitochondrial DNA, J MED GENET, 37(7), 2000, pp. 547-548
Authors:
Roymans, D
Willems, R
Vissenberg, K
De Jonghe, C
Grobben, B
Claes, P
Lascu, I
Van Bockstaele, D
Verbelen, JP
Van Broeckhoven, C
Slegers, H
Citation: D. Roymans et al., Nucleoside diphosphate kinase beta (Nm23-R1/NDPK beta) is associated with intermediate filaments and becomes upregulated upon cAMP-induced differentiation of rat C6 glioma, EXP CELL RE, 261(1), 2000, pp. 127-138
Authors:
Roks, G
Van Harskamp, F
De Koning, I
Cruts, M
De Jonghe, C
Kumar-Singh, S
Tibben, A
Tanghe, H
Niermeijer, MF
Hofman, A
Van Swieten, JC
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:
Van Gestel, S
Houwing-Duistermaat, JJ
Adolfsson, R
van Duijn, CM
Van Broeckhoven, C
Citation: S. Van Gestel et al., Power of selective genotyping in genetic association analyses of quantitative traits, BEHAV GENET, 30(2), 2000, pp. 141-146
Authors:
Stronach, EA
Clark, C
Bell, C
Lofgren, A
McKay, NG
Timmerman, V
Van Broeckhoven, C
Haites, NE
Citation: Ea. Stronach et al., Novel PCR-based diagnostic tools for Charcot-Marie-Tooth type 1A and hereditary neuropathy with liability to pressure palsies, J PERIPH N, 4(2), 1999, pp. 117-122
Authors:
Nelis, E
Haites, N
Van Broeckhoven, C
Citation: E. Nelis et al., Mutations in the peripheral myelin genes and associated genes in inheritedperipheral neuropathies, HUM MUTAT, 13(1), 1999, pp. 11-28
Authors:
Meuleman, J
Kuhlenbaumer, G
Schirmacher, A
Wehnert, M
De Jonghe, P
De Vriendt, E
Young, P
Airaksinen, E
Pou-Serradell, A
Prats, JM
Ringelstein, B
Stogbauer, F
Van Broeckhoven, C
Timmerman, V
Citation: J. Meuleman et al., Genetic refinement of the hereditary neuralgic amyotrophy (HNA) locus at chromosome 17q25, EUR J HUM G, 7(8), 1999, pp. 920-927
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:
Verheyen, GR
Villafuerte, SM
Del-Favero, J
Souery, D
Mendlewicz, J
Van Broeckhoven, C
Raeymaekers, P
Citation: Gr. Verheyen et al., Genetic refinement and physical mapping of a chromosome 18q candidate region for bipolar disorder, EUR J HUM G, 7(4), 1999, pp. 427-434
Authors:
Van Gassen, G
De Jonghe, C
Pype, S
Van Criekinge, W
Julliams, A
Vanderhoeven, I
Woodrow, S
Beyaert, R
Huylebroeck, D
Van Broeckhoven, C
Citation: G. Van Gassen et al., Alzheimer's disease associated presenilin 1 interacts with HC5 and ZETA, subunits of the catalytic 20S proteasome, NEUROBIOL D, 6(5), 1999, pp. 376-391
Authors:
De Jonghe, C
Cras, P
Vanderstichele, H
Cruts, M
Vanderhoeven, I
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:
Kuhlenbaumer, G
Schirmacher, A
Meuleman, J
Tissir, F
Del-Favero, J
Stogbauer, F
Young, P
Ringelstein, B
Van Broeckhoven, C
Timmerman, V
Citation: G. Kuhlenbaumer et al., A sequence-ready BAC/PAC contig and partial transcript map of approximately 1.5 Mb in human chromosome 17q25 comprising multiple disease genes, GENOMICS, 62(2), 1999, pp. 242-250
Authors:
Liehr, T
Kuhlenbaumer, G
Wulf, P
Taylor, V
Suter, U
Van Broeckhoven, C
Lupski, JR
Claussen, U
Rautenstrauss, B
Citation: T. Liehr et al., Regional localization of the human epithelial membrane protein genes 1, 2,and 3 (EMP1, EMP2, EMP3) to 12p12.3, 16p13.2, and 19q13.3, GENOMICS, 58(1), 1999, pp. 106-108
Authors:
Del-Favero, J
Goossens, D
Van den Bossche, D
Van Broeckhoven, C
Citation: J. Del-favero et al., YAC fragmentation with repetitive and single-copy sequences: detailed physical mapping of the presenilin 1 gene on chromosome 14, GENE, 229(1-2), 1999, pp. 193-201
Authors:
Michalik, A
Del-Favero, J
Mauger, C
Lofgren, A
Van Broeckhoven, C
Citation: A. Michalik et al., Genomic organisation of the spinocerebellar ataxia type 7 (SCA7) gene responsible for autosomal dominant cerebellar ataxia with retinal degeneration, HUM GENET, 105(5), 1999, pp. 410-417
Authors:
Del-Favero, J
Goossens, D
De Jonghe, P
Benson, K
Michalik, A
Van den Bossche, D
Horwitz, M
Van Broeckhoven, C
Citation: J. Del-favero et al., Isolation of CAG/CTG repeat from within the chromosome 2p21-p24 locus for autosomal dominant spastic paraplegia (SPC4) by YAC fragmentation, HUM GENET, 105(3), 1999, pp. 217-225
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:
Roks, G
Dermaut, B
Heutink, P
Julliams, A
Backhovens, H
Van de Broeck, M
Serneels, S
Hofman, A
Van Broeckhoven, C
van Duijn, CM
Cruts, M
Citation: G. Roks et al., Mutation screening of the tau gene in patients with early-onset Alzheimer's disease, NEUROSCI L, 277(2), 1999, pp. 137-139