Del-Favero J - Search Results

1

Multiplex Amplicon Quantification (MAQ), a fast and efficient method for the simultaneous detection of copy number alterations in neuroblastoma.

Kumps C, Van Roy N, Heyrman L, Goossens D, Del-Favero J, Noguera R, Vandesompele J, Speleman F, De Preter K. Kumps C, et al. BMC Genomics. 2010 May 12;11:298. doi: 10.1186/1471-2164-11-298. BMC Genomics. 2010. PMID: 20459859 Free PMC article.

2

Gene copy number variation in schizophrenia.

Sutrala SR, Goossens D, Williams NM, Heyrman L, Adolfsson R, Norton N, Buckland PR, Del-Favero J. Sutrala SR, et al. Schizophr Res. 2007 Nov;96(1-3):93-9. doi: 10.1016/j.schres.2007.07.029. Epub 2007 Sep 7. Schizophr Res. 2007. PMID: 17826036

3

Simultaneous mutation and copy number variation (CNV) detection by multiplex PCR-based GS-FLX sequencing.

Goossens D, Moens LN, Nelis E, Lenaerts AS, Glassee W, Kalbe A, Frey B, Kopal G, De Jonghe P, De Rijk P, Del-Favero J. Goossens D, et al. Hum Mutat. 2009 Mar;30(3):472-6. doi: 10.1002/humu.20873. Hum Mutat. 2009. PMID: 19058222

4

Rare copy number variants in neuropsychiatric disorders: Specific phenotype or not?

Van Den Bossche MJ, Johnstone M, Strazisar M, Pickard BS, Goossens D, Lenaerts AS, De Zutter S, Nordin A, Norrback KF, Mendlewicz J, Souery D, De Rijk P, Sabbe BG, Adolfsson R, Blackwood D, Del-Favero J. Van Den Bossche MJ, et al. Am J Med Genet B Neuropsychiatr Genet. 2012 Oct;159B(7):812-22. doi: 10.1002/ajmg.b.32088. Epub 2012 Aug 22. Am J Med Genet B Neuropsychiatr Genet. 2012. PMID: 22911887

5

No evidence for GNAS copy number variants in patients with features of Albright's hereditary osteodystrophy and abnormal platelet Gs activity.

Izzi B, de Zegher F, Francois I, del Favero J, Goossens D, Wittevrongel C, Thys C, Van Geet C, Freson K. Izzi B, et al. J Hum Genet. 2012 Apr;57(4):277-9. doi: 10.1038/jhg.2012.1. Epub 2012 Jan 26. J Hum Genet. 2012. PMID: 22277900

6

Copy Number Variations in DISC1 and DISC1-Interacting Partners in Major Mental Illness.

Johnstone M, Maclean A, Heyrman L, Lenaerts AS, Nordin A, Nilsson LG, De Rijk P, Goossens D, Adolfsson R, St Clair DM, Hall J, Lawrie SM, McIntosh AM, Del-Favero J, Blackwood DH, Pickard BS. Johnstone M, et al. Mol Neuropsychiatry. 2015 Oct;1(3):175-190. doi: 10.1159/000438788. Epub 2015 Oct 7. Mol Neuropsychiatry. 2015. PMID: 27239468 Free PMC article.

7

Microdeletions involving the SCN1A gene may be common in SCN1A-mutation-negative SMEI patients.

Suls A, Claeys KG, Goossens D, Harding B, Van Luijk R, Scheers S, Deprez L, Audenaert D, Van Dyck T, Beeckmans S, Smouts I, Ceulemans B, Lagae L, Buyse G, Barisic N, Misson JP, Wauters J, Del-Favero J, De Jonghe P, Claes LR. Suls A, et al. Hum Mutat. 2006 Sep;27(9):914-20. doi: 10.1002/humu.20350. Hum Mutat. 2006. PMID: 16865694

8

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. Brain. 2006 Nov;129(Pt 11):2977-83. doi: 10.1093/brain/awl203. Epub 2006 Aug 18. Brain. 2006. PMID: 16921174

9

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. 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

10

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. Hum Mutat. 2009 Jul;30(7):1054-61. doi: 10.1002/humu.21007. Hum Mutat. 2009. PMID: 19405094

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