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180 results

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Page 1
Forensic massively parallel sequencing data analysis tool: Implementation of MyFLq as a standalone web- and Illumina BaseSpace(®)-application.
Van Neste C, Gansemans Y, De Coninck D, Van Hoofstat D, Van Criekinge W, Deforce D, Van Nieuwerburgh F. Van Neste C, et al. Among authors: van hoofstat d, van criekinge w, van nieuwerburgh f. Forensic Sci Int Genet. 2015 Mar;15:2-7. doi: 10.1016/j.fsigen.2014.10.006. Epub 2014 Oct 14. Forensic Sci Int Genet. 2015. PMID: 25457631 Free article.
Analysing 454 amplicon resequencing experiments using the modular and database oriented Variant Identification Pipeline.
De Schrijver JM, De Leeneer K, Lefever S, Sabbe N, Pattyn F, Van Nieuwerburgh F, Coucke P, Deforce D, Vandesompele J, Bekaert S, Hellemans J, Van Criekinge W. De Schrijver JM, et al. Among authors: van nieuwerburgh f, van criekinge w. BMC Bioinformatics. 2010 May 20;11:269. doi: 10.1186/1471-2105-11-269. BMC Bioinformatics. 2010. PMID: 20487544 Free PMC article.
Practical tools to implement massive parallel pyrosequencing of PCR products in next generation molecular diagnostics.
De Leeneer K, De Schrijver J, Clement L, Baetens M, Lefever S, De Keulenaer S, Van Criekinge W, Deforce D, Van Nieuwerburgh F, Bekaert S, Pattyn F, De Wilde B, Coucke P, Vandesompele J, Claes K, Hellemans J. De Leeneer K, et al. Among authors: van criekinge w, van nieuwerburgh f. PLoS One. 2011;6(9):e25531. doi: 10.1371/journal.pone.0025531. Epub 2011 Sep 30. PLoS One. 2011. PMID: 21980484 Free PMC article.
Molecular diagnostics for congenital hearing loss including 15 deafness genes using a next generation sequencing platform.
De Keulenaer S, Hellemans J, Lefever S, Renard JP, De Schrijver J, Van de Voorde H, Tabatabaiefar MA, Van Nieuwerburgh F, Flamez D, Pattyn F, Scharlaken B, Deforce D, Bekaert S, Van Criekinge W, Vandesompele J, Van Camp G, Coucke P. De Keulenaer S, et al. Among authors: van nieuwerburgh f, van criekinge w, van de voorde h, van camp g. BMC Med Genomics. 2012 May 18;5:17. doi: 10.1186/1755-8794-5-17. BMC Med Genomics. 2012. PMID: 22607986 Free PMC article.
Illumina sequencing of 15 deafness genes using fragmented amplicons.
Van Nieuwerburgh F, De Keulenaer S, De Schrijver J, Vandesompele J, Van Criekinge W, Coucke PJ, Deforce D. Van Nieuwerburgh F, et al. Among authors: van criekinge w. BMC Res Notes. 2014 Aug 9;7:509. doi: 10.1186/1756-0500-7-509. BMC Res Notes. 2014. PMID: 25106482 Free PMC article.
BMP-SMAD Signaling Regulates Lineage Priming, but Is Dispensable for Self-Renewal in Mouse Embryonic Stem Cells.
Gomes Fernandes M, Dries R, Roost MS, Semrau S, de Melo Bernardo A, Davis RP, Ramakrishnan R, Szuhai K, Maas E, Umans L, Abon Escalona V, Salvatori D, Deforce D, Van Criekinge W, Huylebroeck D, Mummery C, Zwijsen A, de Sousa Lopes SM. Gomes Fernandes M, et al. Among authors: van criekinge w. Stem Cell Reports. 2016 Jan 12;6(1):85-94. doi: 10.1016/j.stemcr.2015.11.012. Epub 2015 Dec 17. Stem Cell Reports. 2016. PMID: 26711875 Free PMC article.
Dynamic epigenetic changes to VHL occur with sunitinib in metastatic clear cell renal cancer.
Stewart GD, Powles T, Van Neste C, Meynert A, O'Mahony F, Laird A, Deforce D, Van Nieuwerburgh F, Trooskens G, Van Criekinge W, De Meyer T, Harrison DJ. Stewart GD, et al. Among authors: van nieuwerburgh f, van criekinge w, van neste c. Oncotarget. 2016 May 3;7(18):25241-50. doi: 10.18632/oncotarget.8308. Oncotarget. 2016. PMID: 27029034 Free PMC article. Clinical Trial.
180 results