Del-Favero J - Search Results

1

Trinucleotide repeat expansions: do they contribute to bipolar disorder?

Goossens D, Del-Favero J, Van Broeckhoven C. Goossens D, et al. Brain Res Bull. 2001 Oct-Nov 1;56(3-4):243-57. doi: 10.1016/s0361-9230(01)00657-8. Brain Res Bull. 2001. PMID: 11719258 Review.

2

Genetic refinement and physical mapping of a chromosome 18q candidate region for bipolar disorder.

Verheyen GR, Villafuerte SM, Del-Favero J, Souery D, Mendlewicz J, Van Broeckhoven C, Raeymaekers P. Verheyen GR, et al. Eur J Hum Genet. 1999 May-Jun;7(4):427-34. doi: 10.1038/sj.ejhg.5200318. Eur J Hum Genet. 1999. PMID: 10352933

3

Molecular interpretation of expanded RED products in bipolar disorder by CAG/CTG repeats located at chromosomes 17q and 18q.

Verheyen GR, Del-Favero J, Mendlewicz J, Lindblad K, Van Zand K, Aalbregtse M, Schalling M, Souery D, Van Broeckhoven C. Verheyen GR, et al. Neurobiol Dis. 1999 Oct;6(5):424-32. doi: 10.1006/nbdi.1999.0258. Neurobiol Dis. 1999. PMID: 10527808

4

No evidence for the involvement of CAG/CTG repeats from within 18q21.33-q23 in bipolar disorder.

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. Goossens D, et al. Eur J Hum Genet. 2000 May;8(5):385-8. doi: 10.1038/sj.ejhg.5200469. Eur J Hum Genet. 2000. PMID: 10854100

5

Isolation of CAG/CTG repeats from within the chromosome 2p21-p24 locus for autosomal dominant spastic paraplegia (SPG4) by YAC fragmentation.

Del-Favero J, Goossens D, De Jonghe P, Benson K, Michalik A, Van den Bossche D, Horwitz M, Van Broeckhoven C. Del-Favero J, et al. Hum Genet. 1999 Sep;105(3):217-25. doi: 10.1007/s004390051092. Hum Genet. 1999. PMID: 10987648

6

A novel CpG-associated brain-expressed candidate gene for chromosome 18q-linked bipolar disorder.

Goossens D, Van Gestel S, Claes S, De Rijk P, Souery D, Massat I, Van den Bossche D, Backhovens H, Mendlewicz J, Van Broeckhoven C, Del-Favero J. Goossens D, et al. Mol Psychiatry. 2003 Jan;8(1):83-9. doi: 10.1038/sj.mp.4001190. Mol Psychiatry. 2003. PMID: 12556911

7

Chromosome 10q harbors a susceptibility locus for bipolar disorder in Ashkenazi Jewish families.

Venken T, Alaerts M, Souery D, Goossens D, Sluijs S, Navon R, Van Broeckhoven C, Mendlewicz J, Del-Favero J, Claes S. Venken T, et al. Mol Psychiatry. 2008 Apr;13(4):442-50. doi: 10.1038/sj.mp.4002039. Epub 2007 Jun 19. Mol Psychiatry. 2008. PMID: 17579605

8

Molecular genetic analysis of autosomal dominant cerebellar ataxia with retinal degeneration (ADCA type II) caused by CAG triplet repeat expansion.

Del-Favero J, Krols L, Michalik A, Theuns J, Löfgren A, Goossens D, Wehnert A, Van den Bossche D, Van Zand K, Backhovens H, van Regenmorter N, Martin JJ, Van Broeckhoven C. Del-Favero J, et al. Hum Mol Genet. 1998 Feb;7(2):177-86. doi: 10.1093/hmg/7.2.177. Hum Mol Genet. 1998. PMID: 9425224

9

YAC fragmentation with repetitive and single-copy sequences: detailed physical mapping of the presenilin 1 gene on chromosome 14.

Del-Favero J, Goossens D, Van den Bossche D, Van Broeckhoven C. Del-Favero J, et al. Gene. 1999 Mar 18;229(1-2):193-201. doi: 10.1016/s0378-1119(99)00023-2. Gene. 1999. PMID: 10095119

10

Spinocerebellar ataxia type 7 (SCA7) - correlations between phenotype and genotype in one large Belgian family.

Martin J, Van Regemorter N, Del-Favero J, Löfgren A, Van Broeckhoven C. Martin J, et al. J Neurol Sci. 1999 Sep 15;168(1):37-46. doi: 10.1016/s0022-510x(99)00176-8. J Neurol Sci. 1999. PMID: 10500272

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