Multi-centre evaluation of a comprehensive preimplantation genetic test through haplotyping-by-sequencing by Masset, Heleen, Zamani Esteki, Masoud, Dimitriadou, Eftychia, Dreesen, Jos, Debrock, Sophie, Derhaag, Josien, Derks, Kasper, Destouni, Aspasia, Drüsedau, Marion, Meekels, Jeroen, Melotte, Cindy, Peeraer, Karen, Tšuiko, Olga, van Uum, Chris, Allemeersch, Joke, Devogelaere, Benoit, François, Katrien Omer, Happe, Scott, Lorson, Dennis, Richards, Rebecca Louise, Theuns, Jessie, Brunner, Han, de Die-Smulders, Christine, Voet, Thierry, Paulussen, Aimée, Coonen, Edith, Vermeesch, Joris Robert

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Embryo tracking system for high-throughput sequencing-based preimplantation genetic testing by van Dijk, Wanwisa, Derks, Kasper, Drüsedau, Marion, Meekels, Jeroen, Koeck, Rebekka, Essers, Rick, Dreesen, Joseph, Coonen, Edith, de Die-Smulders, Christine, Stevens, Servi J C, Brunner, Han G, van den Wijngaard, Arthur, Paulussen, Aimée D C, Zamani Esteki, Masoud

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Mutation-specific effects in germline transmission of pathogenic mtDNA variants by Otten, Auke B C, Sallevelt, Suzanne C E H, Carling, Phillippa J, Dreesen, Joseph C F M, Drüsedau, Marion, Spierts, Sabine, Paulussen, Aimee D C, de Die-Smulders, Christine E M, Herbert, Mary, Chinnery, Patrick F, Samuels, David C, Lindsey, Patrick, Smeets, Hubert J M

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PGD for hereditary breast and ovarian cancer: the route to universal tests for BRCA1 and BRCA2 mutation carriers by Drüsedau, Marion, Dreesen, Jos C, Derks-Smeets, Inge, Coonen, Edith, van Golde, Ron, van Echten-Arends, Jannie, Kastrop, Peter M M, Blok, Marinus J, Gómez-García, Encarna, Geraedts, Joep P, Smeets, Hubert J, de Die-Smulders, Christine E, Paulussen, Aimée D

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SNP array-based copy number and genotype analyses for preimplantation genetic diagnosis of human unbalanced translocations by VAN UUM, Chris M. J, STEVENS, Servi J. C, DREESEN, Joseph C. F. M, DRÜSEDAU, Marion, SMEETS, Hubert J, HOLLANDERS-CROMBACH, Bertien, DE DIE-SMULDERS, Christine E. M, GERAEDTS, Joep Pm, ENGELEN, John J. M, COONEN, Edith

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Clinical-grade whole genome sequencing-based haplarithmisis enables all forms of preimplantation genetic testing by Janssen, Anouk E. J., Koeck, Rebekka M., Essers, Rick, Cao, Ping, van Dijk, Wanwisa, Drüsedau, Marion, Meekels, Jeroen, Yaldiz, Burcu, van de Vorst, Maartje, de Koning, Bart, Hellebrekers, Debby M. E. I., Stevens, Servi J. C., Sun, Su Ming, Heijligers, Malou, de Munnik, Sonja A., van Uum, Chris M. J., Achten, Jelle, Hamers, Lars, Naghdi, Marjan, Vissers, Lisenka E. L. M., van Golde, Ron J. T., de Wert, Guido, Dreesen, Jos C. F. M., de Die-Smulders, Christine, Coonen, Edith, Brunner, Han G., van den Wijngaard, Arthur, Paulussen, Aimee D. C., Zamani Esteki, Masoud

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PGD for the m.14487 T>C mitochondrial DNA mutation resulted in the birth of a healthy boy by Sallevelt, Suzanne C.E.H., Dreesen, Joseph C.F.M., Drüsedau, Marion, Hellebrekers, Debby M.E.I., Paulussen, Aimee D.C., Coonen, Edith, van Golde, Ronald J.T., Geraedts, Joep P.M., Gianaroli, Luca, Magli, Maria C., Zeviani, Massimo, Smeets, Hubert J.M., de Die-Smulders, Christine E.M.

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Agilent Technologies OnePGT solution: External verification on both blastomere and trophectoderm biopsies by Esteki, Masoud. Zamani, Melotte, Cindy, Coonen, Edith, Dreesen, Joseph, Paulussen, Aimee, Dumoulin, John, Van Uum, Christian, Drusedau, Marion, Engelen, John, Derks, Kasper, Van Golde, R., Dimitriadou, Eftychia, Masset, Heleen, François, Katrien O., Allemeersch, Joke, Richards, Rebecca, Moeys, Sara, Theuns, Jessie, De Die-Smulders, Christine, Vermeesch, Joris R.

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