Goossens D - 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

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

3

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. Among authors: goossens d. Hum Genet. 1999 Sep;105(3):217-25. doi: 10.1007/s004390051092. Hum Genet. 1999. PMID: 10987648

4

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

5

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. Among authors: goossens d. Mol Psychiatry. 2008 Apr;13(4):442-50. doi: 10.1038/sj.mp.4002039. Epub 2007 Jun 19. Mol Psychiatry. 2008. PMID: 17579605

6

APP duplication is sufficient to cause early onset Alzheimer's dementia with cerebral amyloid angiopathy.

Sleegers K, Brouwers N, Gijselinck I, Theuns J, Goossens D, Wauters J, Del-Favero J, Cruts M, van Duijn CM, Van Broeckhoven C. Sleegers K, et al. Among authors: goossens d. Brain. 2006 Nov;129(Pt 11):2977-83. doi: 10.1093/brain/awl203. Epub 2006 Aug 18. Brain. 2006. PMID: 16921174

7

A novel locus for dementia with Lewy bodies: a clinically and genetically heterogeneous disorder.

Bogaerts V, Engelborghs S, Kumar-Singh S, Goossens D, Pickut B, van der Zee J, Sleegers K, Peeters K, Martin JJ, Del-Favero J, Gasser T, Dickson DW, Wszolek ZK, De Deyn PP, Theuns J, Van Broeckhoven C. Bogaerts V, et al. Among authors: goossens d. Brain. 2007 Sep;130(Pt 9):2277-91. doi: 10.1093/brain/awm167. Epub 2007 Aug 6. Brain. 2007. PMID: 17681982

8

Detailed analysis of the serotonin transporter gene (SLC6A4) shows no association with bipolar disorder in the Northern Swedish population.

Alaerts M, Ceulemans S, Forero D, Moens LN, De Zutter S, Heyrman L, Lenaerts AS, Norrback KF, Goossens D, De Rijk P, Nilsson LG, Adolfsson R, Del-Favero J. Alaerts M, et al. Among authors: goossens d. Am J Med Genet B Neuropsychiatr Genet. 2009 Jun 5;150B(4):585-92. doi: 10.1002/ajmg.b.30853. Am J Med Genet B Neuropsychiatr Genet. 2009. PMID: 18792946

9

Relative contribution of simple mutations vs. copy number variations in five Parkinson disease genes in the Belgian population.

Nuytemans K, Meeus B, Crosiers D, Brouwers N, Goossens D, Engelborghs S, Pals P, Pickut B, Van den Broeck M, Corsmit E, Cras P, De Deyn PP, Del-Favero J, Van Broeckhoven C, Theuns J. Nuytemans K, et al. Among authors: goossens d. Hum Mutat. 2009 Jul;30(7):1054-61. doi: 10.1002/humu.21007. Hum Mutat. 2009. PMID: 19405094

10

Identification of a CACNA2D4 deletion in late onset bipolar disorder patients and implications for the involvement of voltage-dependent calcium channels in psychiatric disorders.

Van Den Bossche MJ, Strazisar M, De Bruyne S, Bervoets C, Lenaerts AS, De Zutter S, Nordin A, Norrback KF, Goossens D, De Rijk P, Green EK, Grozeva D, Mendlewicz J, Craddock N, Sabbe BG, Adolfsson R, Souery D, Del-Favero J. Van Den Bossche MJ, et al. Among authors: goossens d. Am J Med Genet B Neuropsychiatr Genet. 2012 Jun;159B(4):465-75. doi: 10.1002/ajmg.b.32053. Epub 2012 Apr 9. Am J Med Genet B Neuropsychiatr Genet. 2012. PMID: 22488967

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