Del-Favero J - Search Results

1

Optimized filtering reduces the error rate in detecting genomic variants by short-read sequencing.

Reumers J, De Rijk P, Zhao H, Liekens A, Smeets D, Cleary J, Van Loo P, Van Den Bossche M, Catthoor K, Sabbe B, Despierre E, Vergote I, Hilbush B, Lambrechts D, Del-Favero J. Reumers J, et al. Nat Biotechnol. 2011 Dec 18;30(1):61-8. doi: 10.1038/nbt.2053. Nat Biotechnol. 2011. PMID: 22178994

2

Sequencing of DISC1 pathway genes reveals increased burden of rare missense variants in schizophrenia patients from a northern Swedish population.

Moens LN, De Rijk P, Reumers J, Van den Bossche MJ, Glassee W, De Zutter S, Lenaerts AS, Nordin A, Nilsson LG, Medina Castello I, Norrback KF, Goossens D, Van Steen K, Adolfsson R, Del-Favero J. Moens LN, et al. PLoS One. 2011;6(8):e23450. doi: 10.1371/journal.pone.0023450. Epub 2011 Aug 11. PLoS One. 2011. PMID: 21853134 Free PMC article.

3

Less cognitive and neurological deficits in schizophrenia patients carrying risk variant in ZNF804A.

Van Den Bossche MJ, Docx L, Morrens M, Cammaerts S, Strazisar M, Bervoets C, Smolders S, Depreeuw V, Lenaerts AS, De Rijk P, Del-Favero J, Sabbe BG. Van Den Bossche MJ, et al. Neuropsychobiology. 2012;66(3):158-66. doi: 10.1159/000339731. Epub 2012 Aug 29. Neuropsychobiology. 2012. PMID: 22948380

4

Identification of rare copy number variants in high burden schizophrenia families.

Van Den Bossche MJ, Strazisar M, Cammaerts S, Liekens AM, Vandeweyer G, Depreeuw V, Mattheijssens M, Lenaerts AS, De Zutter S, De Rijk P, Sabbe B, Del-Favero J. Van Den Bossche MJ, et al. Am J Med Genet B Neuropsychiatr Genet. 2013 Apr;162B(3):273-82. doi: 10.1002/ajmg.b.32146. Epub 2013 Mar 15. Am J Med Genet B Neuropsychiatr Genet. 2013. PMID: 23505263

5

miRVaS: a tool to predict the impact of genetic variants on miRNAs.

Cammaerts S, Strazisar M, Dierckx J, Del Favero J, De Rijk P. Cammaerts S, et al. Nucleic Acids Res. 2016 Feb 18;44(3):e23. doi: 10.1093/nar/gkv921. Epub 2015 Sep 17. Nucleic Acids Res. 2016. PMID: 26384425 Free PMC article.

6

SSHSuite: an integrated software package for analysis of large-scale suppression subtractive hybridization data.

Weckx S, De Rijk P, Van Broeckhoven C, Del-Favero J. Weckx S, et al. Biotechniques. 2004 Jun;36(6):1043-5. doi: 10.2144/04366BC02. Biotechniques. 2004. PMID: 15211756 Free article.

7

SNPbox: web-based high-throughput primer design from gene to genome.

Weckx S, De Rijk P, Van Broeckhoven C, Del-Favero J. Weckx S, et al. Nucleic Acids Res. 2004 Jul 1;32(Web Server issue):W170-2. doi: 10.1093/nar/gkh369. Nucleic Acids Res. 2004. PMID: 15215373 Free PMC article.

8

SNPbox: a modular software package for large-scale primer design.

Weckx S, De Rijk P, Van Broeckhoven C, Del-Favero J. Weckx S, et al. Bioinformatics. 2005 Feb 1;21(3):385-7. doi: 10.1093/bioinformatics/bti006. Epub 2004 Sep 3. Bioinformatics. 2005. PMID: 15347573

9

SNPbox: web-based high-throughput primer design with an eye for repetitive sequences.

Weckx S, De Rijk P, Glassee W, Van Broeckhoven C, Del-Favero J. Weckx S, et al. Methods Mol Biol. 2007;402:179-200. doi: 10.1007/978-1-59745-528-2_9. Methods Mol Biol. 2007. PMID: 17951796 Review.

10

BioGraph: unsupervised biomedical knowledge discovery via automated hypothesis generation.

Liekens AM, De Knijf J, Daelemans W, Goethals B, De Rijk P, Del-Favero J. Liekens AM, et al. Genome Biol. 2011 Jun 22;12(6):R57. doi: 10.1186/gb-2011-12-6-r57. Genome Biol. 2011. PMID: 21696594 Free PMC article.

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