Filip Pattyn
Affiliations: | Center for Medical Genetics | Ghent University, Ghent, Vlaanderen, Belgium |
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"Filip Pattyn"
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| Lefever S, Rihani A, Van der Meulen J, et al. (2019) Cost-effective and robust genotyping using double-mismatch allele-specific quantitative PCR. Scientific Reports. 9: 2150 |
| Lefever S, Pattyn F, De Wilde B, et al. (2017) High-throughput PCR assay design for targeted resequencing using primerXL. Bmc Bioinformatics. 18: 400 |
| Lefever S, Pattyn F, Hellemans J, et al. (2013) Single-nucleotide polymorphisms and other mismatches reduce performance of quantitative PCR assays. Clinical Chemistry. 59: 1470-80 |
| Rihani A, Van Maerken T, Pattyn F, et al. (2013) Effective Alu repeat based RT-Qpcr normalization in cancer cell perturbation experiments. Plos One. 8: e71776 |
| Kumps C, Fieuw A, Mestdagh P, et al. (2013) Focal DNA copy number changes in neuroblastoma target MYCN regulated genes. Plos One. 8: e52321 |
| Heukamp LC, Thor T, Schramm A, et al. (2012) Targeted expression of mutated ALK induces neuroblastoma in transgenic mice. Science Translational Medicine. 4: 141ra91 |
| De Keulenaer S, Hellemans J, Lefever S, et al. (2012) Molecular diagnostics for congenital hearing loss including 15 deafness genes using a next generation sequencing platform. Bmc Medical Genomics. 5: 17 |
| Coppieters F, De Wilde B, Lefever S, et al. (2012) Massively parallel sequencing for early molecular diagnosis in Leber congenital amaurosis. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 14: 576-85 |
| Fieuw A, Kumps C, Schramm A, et al. (2012) Identification of a novel recurrent 1q42.2-1qter deletion in high risk MYCN single copy 11q deleted neuroblastomas. International Journal of Cancer. Journal International Du Cancer. 130: 2599-606 |
| De Leeneer K, De Schrijver J, Clement L, et al. (2011) Practical tools to implement massive parallel pyrosequencing of PCR products in next generation molecular diagnostics. Plos One. 6: e25531 |