1. 2017
  2. CpG Methylation, a Parent-of-Origin Effect for Maternal-Biased Transmission of Congenital Myotonic Dystrophy

    Barbé, L. , Franck, S. , Spits, C. , Keymolen, K. , Seneca, S. , Sermon, K. & 16 others Lanni, S., Lopez-Castel, A., Tomé, S., Miron, I., Letourneau, J., Liang, M., Choufani, S., Weksberg, R., Wilson, M. D., Sedlacek, Z., Gagnon, C., Musova, Z., Chitayat, D., Shannon, P., Mathieu, J. & Pearson, C. E. 2 Mar 2017 In : American Journal of Human Genetics. 100, 3, p. 488-505 18 p.

    Research output: Research - peer-reviewArticle

  3. Detecting mosaicism in trophectoderm biopsies

    Sermon, K. D., Spits, C., Mertzanidou, A., Vermeesch, J. R. & Fiorentino, F. Mar 2017 In : Human Reproduction. 32, 3, p. 712-713

    Research output: Research - peer-reviewArticle

  4. Novel technologies emerging for preimplantation genetic diagnosis and preimplantation genetic testing for aneuploidy

    Sermon, K. Jan 2017 In : Expert Review of Molecular Diagnostics. 17, 1, p. 71-82 12 p.

    Research output: Research - peer-reviewArticle

  5. 2016
  6. Preimplantation genetic screening 2.0: the theory

    Geraedts, J. & Sermon, K. Aug 2016 In : Molecular Human Reproduction. 22, 8, p. 839-44 6 p., 10.1093/molehr/gaw033

    Research output: Research - peer-reviewArticle

  7. The why, the how and the when of PGS 2.0: current practices and expert opinions of fertility specialists, molecular biologists, and embryologists

    Sermon, K. , De Rycke, M. , De Vos, A. , Verpoest, W. & 28 others Capalbo, A., Cohen, J., Coonen, E., Delhanty, J., Fiorentino, F., Gleicher, N., Griesinger, G., Grifo, J., Handyside, A., Harper, J., Kokkali, G., Mastenbroek, S., Meldrum, D., Meseguer, M., Montag, M., Munné, S., Rienzi, L., Rubio, C., Scott, K., Scott, R., Simon, C., Swain, J., Treff, N., Ubaldi, F., Vassena, R., Vermeesch, J. R., Wells, D. & Geraedts, J. Aug 2016 In : Molecular Human Reproduction. 22, 8, p. 845-857 13 p., 10.1093/molehr/gaw034

    Research output: Research - peer-reviewArticle

  8. Quantification of low frequency variants of the mitochondrial DNA (mtDNA) in single cells by massive parallel sequencing (MPS)

    Zambelli, F., Daneels, D., Van Dooren, S., Caljon, B., Gianaroli, L., Van De Velde, H., Sermon, K., Seneca, S. & Spits, C. 3 Jul 2016 32nd Annual Meeting in Helsinki; ESHRE 2016.

    Research output: ResearchMeeting abstract (Book)

  9. Detection, isolation and characterization of differentiation resistant human embryonic stem cells

    Keller, A. S., Dziedzicka, D., Sermon, K. & Geens, M. Jul 2016 ESHRE 2016 Abstract Book. p. i77

    Research output: ResearchMeeting abstract (Book)

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