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Results:
1-17
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Results: 17
Authors:
Massat, I
Souery, D
Del-Favero, J
Oruc, L
Jakovljevic, M
Folnegovic, V
Adolfsson, R
Kaneva, R
Papadimitriou, G
Dikeos, D
Jazin, E
Milanova, V
Van Broeckhoven, C
Mendlewicz, J
Citation: I. Massat et al., Lack of association between GABRA3 and unipolar affective disorder: a multicentre study, IN J NEUROP, 4(3), 2001, pp. 273-278
Authors:
Goossens, D
Del-Favero, J
Van Broeckhoven, C
Citation: D. Goossens et al., Trinucleotide repeat expansions: Do they contribute to bipolar disorder?, BRAIN RES B, 56(3-4), 2001, pp. 243-257
Authors:
Theuns, J
Feuk, L
Dermaut, B
Del-Favero, J
Roks, G
Van den Bossche, D
Corsmit, E
Van den Broeck, M
van Duijn, CM
Cruts, M
Brookes, AJ
Van Broeckhoven, C
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:
Souery, D
Van Gestel, S
Massat, I
Blairy, S
Adolfsson, R
Blackwood, D
Del-Favero, J
Dikeos, D
Jakovljevic, M
Kaneva, R
Lattuada, E
Lerer, B
Lilli, L
Milanova, V
Muir, W
Nothen, M
Oruc, L
Papadimitriou, G
Propping, P
Schulze, T
Serretti, A
Shapira, B
Smeraldi, E
Stefanis, C
Thomson, M
Van Broeckhoven, C
Mendlewicz, J
Citation: D. Souery et al., Tryptophan hydroxylase polymorphism and suicidality in unipolar and bipolar affective disorders: A multicenter association study, BIOL PSYCHI, 49(5), 2001, pp. 405-409
Authors:
Claes, L
Del-Favero, J
Ceulemans, B
Lagae, L
Van Broeckhoven, C
De Jonghe, P
Citation: L. Claes et al., De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy, AM J HU GEN, 68(6), 2001, pp. 1327-1332
Authors:
Goossens, D
Villafuerte, S
Tissir, F
Van Gestel, S
Claes, S
Souery, D
Massat, I
Van den Bossche, D
Van Zand, K
Mendlewicz, J
Van Broeckhoven, C
Del-Favero, J
Citation: D. Goossens et al., No evidence for the involvement of CAG/CTG repeats from within 18q21.33-q23 in bipolar disorder, EUR J HUM G, 8(5), 2000, pp. 385-388
Authors:
Theuns, J
Del-Favero, J
Dermaut, B
van Duijn, CM
Backhovens, H
Van den Broeck, M
Serneels, S
Corsmit, E
Van Broeckhoven, C
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:
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:
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:
Verheyen, GR
Del-Favero, J
Mendlewicz, J
Lindblad, K
Van Zand, K
Aalbregtse, M
Schalling, M
Souery, D
Van Roeckhoven, C
Citation: Gr. Verheyen et al., Molecular interpretation of expanded RED products in bipolar disorder by CAG/CTG repeats located at chromosomes 17q and 18q, NEUROBIOL D, 6(5), 1999, pp. 424-432
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:
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:
Mauger, C
Del-Favero, J
Ceuterick, C
Lubke, U
van Broeckhoven, C
Martin, JJ
Citation: C. Mauger et al., Identification and localization of ataxin-7 in brain and retina of a patient with cerebellar ataxia type II using anti-peptide antibody, MOL BRAIN R, 74(1-2), 1999, pp. 35-43
Authors:
Martin, JJ
Van Regemorter, N
Del-Favero, J
Lofgren, A
Van Broeckhoven, C
Citation: Jj. Martin et al., Spinocerebellar ataxia type 7 (SCA7) - correlations between phenotype and genotype in one large Belgian family, J NEUR SCI, 168(1), 1999, pp. 37-46
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