Voet T - Search Results

1

Principles guiding embryo selection following genome-wide haplotyping of preimplantation embryos.

Dimitriadou E, Melotte C, Debrock S, Esteki MZ, Dierickx K, Voet T, Devriendt K, de Ravel T, Legius E, Peeraer K, Meuleman C, Vermeesch JR. Dimitriadou E, et al. Among authors: voet t. Hum Reprod. 2017 Mar 1;32(3):687-697. doi: 10.1093/humrep/dex011. Hum Reprod. 2017. PMID: 28158716

2

Chromosome instability is common in human cleavage-stage embryos.

Vanneste E, Voet T, Le Caignec C, Ampe M, Konings P, Melotte C, Debrock S, Amyere M, Vikkula M, Schuit F, Fryns JP, Verbeke G, D'Hooghe T, Moreau Y, Vermeesch JR. Vanneste E, et al. Among authors: voet t. Nat Med. 2009 May;15(5):577-83. doi: 10.1038/nm.1924. Epub 2009 Apr 26. Nat Med. 2009. PMID: 19396175 Free article.

3

What next for preimplantation genetic screening? High mitotic chromosome instability rate provides the biological basis for the low success rate.

Vanneste E, Voet T, Melotte C, Debrock S, Sermon K, Staessen C, Liebaers I, Fryns JP, D'Hooghe T, Vermeesch JR. Vanneste E, et al. Among authors: voet t. Hum Reprod. 2009 Nov;24(11):2679-82. doi: 10.1093/humrep/dep266. Epub 2009 Jul 24. Hum Reprod. 2009. PMID: 19633308 Free PMC article.

4

Genomic rearrangements of the GREM1-FMN1 locus cause oligosyndactyly, radio-ulnar synostosis, hearing loss, renal defects syndrome and Cenani--Lenz-like non-syndromic oligosyndactyly.

Dimitrov BI, Voet T, De Smet L, Vermeesch JR, Devriendt K, Fryns JP, Debeer P. Dimitrov BI, et al. Among authors: voet t. J Med Genet. 2010 Aug;47(8):569-74. doi: 10.1136/jmg.2009.073833. Epub 2010 Jul 7. J Med Genet. 2010. PMID: 20610440

5

Somatic genomic variations in early human prenatal development.

Robberecht C, Vanneste E, Pexsters A, D'Hooghe T, Voet T, Vermeesch JR. Robberecht C, et al. Among authors: voet t. Curr Genomics. 2010 Sep;11(6):397-401. doi: 10.2174/138920210793175967. Curr Genomics. 2010. PMID: 21358983 Free PMC article.

6

Breakage-fusion-bridge cycles leading to inv dup del occur in human cleavage stage embryos.

Voet T, Vanneste E, Van der Aa N, Melotte C, Jackmaert S, Vandendael T, Declercq M, Debrock S, Fryns JP, Moreau Y, D'Hooghe T, Vermeesch JR. Voet T, et al. Hum Mutat. 2011 Jul;32(7):783-93. doi: 10.1002/humu.21502. Hum Mutat. 2011. PMID: 21412953

7

Single-cell copy number variation detection.

Cheng J, Vanneste E, Konings P, Voet T, Vermeesch JR, Moreau Y. Cheng J, et al. Among authors: voet t. Genome Biol. 2011 Aug 29;12(8):R80. doi: 10.1186/gb-2011-12-8-r80. Genome Biol. 2011. PMID: 21854607 Free PMC article.

8

Microarray analysis of copy number variation in single cells.

Konings P, Vanneste E, Jackmaert S, Ampe M, Verbeke G, Moreau Y, Vermeesch JR, Voet T. Konings P, et al. Among authors: voet t. Nat Protoc. 2012 Jan 19;7(2):281-310. doi: 10.1038/nprot.2011.426. Nat Protoc. 2012. PMID: 22262009

9

Meiotic errors followed by two parallel postzygotic trisomy rescue events are a frequent cause of constitutional segmental mosaicism.

Robberecht C, Voet T, Utine GE, Schinzel A, de Leeuw N, Fryns JP, Vermeesch J. Robberecht C, et al. Among authors: voet t. Mol Cytogenet. 2012 Apr 10;5:19. doi: 10.1186/1755-8166-5-19. Mol Cytogenet. 2012. PMID: 22490612 Free PMC article.

10

New array approaches to explore single cells genomes.

Vanneste E, Bittman L, Van der Aa N, Voet T, Vermeesch JR. Vanneste E, et al. Among authors: voet t. Front Genet. 2012 Mar 27;3:44. doi: 10.3389/fgene.2012.00044. eCollection 2012. Front Genet. 2012. PMID: 22509179 Free PMC article.

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