Lefever S - Search Results

1

Antisense Oligonucleotide-Based Downregulation of the G56R Pathogenic Variant Causing NR2E3-Associated Autosomal Dominant Retinitis Pigmentosa.

Naessens S, Ruysschaert L, Lefever S, Coppieters F, De Baere E. Naessens S, et al. Among authors: lefever s. Genes (Basel). 2019 May 10;10(5):363. doi: 10.3390/genes10050363. Genes (Basel). 2019. PMID: 31083481 Free PMC article.

2

Massively parallel sequencing for early molecular diagnosis in Leber congenital amaurosis.

Coppieters F, De Wilde B, Lefever S, De Meester E, De Rocker N, Van Cauwenbergh C, Pattyn F, Meire F, Leroy BP, Hellemans J, Vandesompele J, De Baere E. Coppieters F, et al. Among authors: lefever s. Genet Med. 2012 Jun;14(6):576-85. doi: 10.1038/gim.2011.51. Epub 2012 Jan 26. Genet Med. 2012. PMID: 22261762 Free article.

3

CEP290, a gene with many faces: mutation overview and presentation of CEP290base.

Coppieters F, Lefever S, Leroy BP, De Baere E. Coppieters F, et al. Among authors: lefever s. Hum Mutat. 2010 Oct;31(10):1097-108. doi: 10.1002/humu.21337. Hum Mutat. 2010. PMID: 20690115 Review.

4

Flexible, scalable, and efficient targeted resequencing on a benchtop sequencer for variant detection in clinical practice.

De Leeneer K, Hellemans J, Steyaert W, Lefever S, Vereecke I, Debals E, Crombez B, Baetens M, Van Heetvelde M, Coppieters F, Vandesompele J, De Jaegher A, De Baere E, Coucke P, Claes K. De Leeneer K, et al. Among authors: lefever s. Hum Mutat. 2015 Mar;36(3):379-87. doi: 10.1002/humu.22739. Hum Mutat. 2015. PMID: 25504618

5

Identity-by-descent-guided mutation analysis and exome sequencing in consanguineous families reveals unusual clinical and molecular findings in retinal dystrophy.

Coppieters F, Van Schil K, Bauwens M, Verdin H, De Jaegher A, Syx D, Sante T, Lefever S, Abdelmoula NB, Depasse F, Casteels I, de Ravel T, Meire F, Leroy BP, De Baere E. Coppieters F, et al. Among authors: lefever s. Genet Med. 2014 Sep;16(9):671-80. doi: 10.1038/gim.2014.24. Epub 2014 Mar 13. Genet Med. 2014. PMID: 24625443 Free article.

6

High-throughput PCR assay design for targeted resequencing using primerXL.

Lefever S, Pattyn F, De Wilde B, Coppieters F, De Keulenaer S, Hellemans J, Vandesompele J. Lefever S, et al. BMC Bioinformatics. 2017 Sep 6;18(1):400. doi: 10.1186/s12859-017-1809-3. BMC Bioinformatics. 2017. PMID: 28877663 Free PMC article.

7

Targeted resequencing and variant validation using pxlence PCR assays.

Coppieters F, Verniers K, De Leeneer K, Vandesompele J, Lefever S. Coppieters F, et al. Among authors: lefever s. Biomol Detect Quantif. 2015 Oct 9;6:22-6. doi: 10.1016/j.bdq.2015.09.001. eCollection 2016 Jan. Biomol Detect Quantif. 2015. PMID: 27077044 Free PMC article.

8

The development of a novel SNP genotyping assay to differentiate cacao clones.

De Wever J, Everaert H, Coppieters F, Rottiers H, Dewettinck K, Lefever S, Messens K. De Wever J, et al. Among authors: lefever s. Sci Rep. 2019 Jul 2;9(1):9512. doi: 10.1038/s41598-019-45884-8. Sci Rep. 2019. PMID: 31267023 Free PMC article.

9

Performance Evaluation of Three DNA Sample Tracking Tools in a Whole Exome Sequencing Workflow.

Wils G, Helsmoortel C, Volders PJ, Vereecke I, Milazzo M, Vandesompele J, Coppieters F, De Leeneer K, Lefever S. Wils G, et al. Among authors: lefever s. Mol Diagn Ther. 2022 Jul;26(4):411-419. doi: 10.1007/s40291-022-00585-3. Epub 2022 May 28. Mol Diagn Ther. 2022. PMID: 35633488

10

Vaccination with early ferroptotic cancer cells induces efficient antitumor immunity.

Efimova I, Catanzaro E, Van der Meeren L, Turubanova VD, Hammad H, Mishchenko TA, Vedunova MV, Fimognari C, Bachert C, Coppieters F, Lefever S, Skirtach AG, Krysko O, Krysko DV. Efimova I, et al. Among authors: lefever s. J Immunother Cancer. 2020 Nov;8(2):e001369. doi: 10.1136/jitc-2020-001369. J Immunother Cancer. 2020. PMID: 33188036 Free PMC article.

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