Presence of Genetic Variants Among Young Men With Severe COVID-19 von van der Made, Caspar I, Simons, Annet, Schuurs-Hoeijmakers, Janneke, van den Heuvel, Guus, Mantere, Tuomo, Kersten, Simone, van Deuren, Rosanne C, Steehouwer, Marloes, van Reijmersdal, Simon V, Jaeger, Martin, Hofste, Tom, Astuti, Galuh, Corominas Galbany, Jordi, van der Schoot, Vyne, van der Hoeven, Hans, Hagmolen of ten Have, Wanda, Klijn, Eva, van den Meer, Catrien, Fiddelaers, Jeroen, de Mast, Quirijn, Bleeker-Rovers, Chantal P, Joosten, Leo A. B, Yntema, Helger G, Gilissen, Christian, Nelen, Marcel, van der Meer, Jos W. M, Brunner, Han G, Netea, Mihai G, van de Veerdonk, Frank L, Hoischen, Alexander

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The impact of unsolicited findings in clinical exome sequencing, a qualitative interview study von Schoot, Vyne van der, Viellevoije, Simone J, Tammer, Femke, Brunner, Han G, Arens, Yvonne, Yntema, Helger G, Oerlemans, Anke J M

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Clinical geneticists' views on and experiences with unsolicited findings in next‐generation sequencing: “A great technology creating new dilemmas” von Schoot, Vyne, Damsté, Carlijn, Yntema, Helger G., Brunner, Han G., Oerlemans, Anke J. M.

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1 in 38 individuals at risk of a dominant medically actionable disease von Haer-Wigman, Lonneke, van der Schoot, Vyne, Feenstra, Ilse, Vulto-van Silfhout, Anneke T, Gilissen, Christian, Brunner, Han G, Vissers, Lisenka E L M, Yntema, Helger G

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Ready for polygenic risk scores? An analysis of regulation of preimplantation genetic testing in European countries von Siermann, Maria, van der Schoot, Vyne, Bunnik, Eline M, Borry, Pascal

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De novo mutations in the SET nuclear proto‐oncogene, encoding a component of the inhibitor of histone acetyltransferases (INHAT) complex in patients with nonsyndromic intellectual... von Stevens, Servi J.C., der Schoot, Vyne, Leduc, Magalie S., Rinne, Tuula, Lalani, Seema R., Weiss, Marjan M., Hagen, Johanna M., Lachmeijer, Augusta M.A., Stockler‐Ipsiroglu, Sylvia G., Lehman, Anna, Brunner, Han G

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Whole exome sequencing of known eye genes reveals genetic causes for high myopia von Haarman, Annechien E G, Thiadens, Alberta A H J, van Tienhoven, Marianne, Loudon, Sjoukje E, de Klein, J E M M Annelies, Brosens, Erwin, Polling, Jan Roelof, van der Schoot, Vyne, Bouman, Arjan, Kievit, Anneke J A, Hoefsloot, Lies H, Klaver, Caroline C W, Verhoeven, Virginie J M

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Lessons learned from unsolicited findings in clinical exome sequencing of 16,482 individuals von van der Schoot, Vyne, Haer-Wigman, Lonneke, Feenstra, Ilse, Tammer, Femke, Oerlemans, Anke J M, van Koolwijk, Martine P A, van Agt, Frans, Arens, Yvonne H J M, Brunner, Han G, Vissers, Lisenka E L M, Yntema, Helger G

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Limited additional value of karyotyping cultured amniotic fluid cell colonies in addition to microarray on uncultured cells for confirmation of abnormal non-invasive prenatal testi... von Donze, Stephany H, Srebniak, Malgorzata I, Diderich, Karin E M, van den Born, Myrthe, Galjaard, Robert-Jan, Govaerts, Lutgarde C P, van der Schoot, Vyne, Knapen, Maarten F C M, Joosten, Marieke, Van Opstal, Diane

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The High Diagnostic Yield of Prenatal Exome Sequencing Followed by 3400 Gene Panel Analysis in 629 Ongoing Pregnancies With Ultrasound Anomalies von Diderich, Karin E M, Bruggenwirth, Hennie T, Joosten, Marieke, Thurik, Florentine, Mijalkovic, Jona, Polak, Marike, Kromosoeto, Joan, Somers-Bolman, Galhana M, van den Born, Myrthe, Drost, Mark, Galjaard, Robert Jan H, Galjaard, Sander, Hoefsloot, Lies H, Knapen, Maarten F C M, van Minkelen, Rick, van der Schoot, Vyne, van Slegtenhorst, Marjon A, Sleutels, Frank, Stuurman, Kyra E, Weerts, Marjolein J A, Go, Attie T J I, Wilke, Martina, Srebniak, Malgorzata I

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Perinatal follow-up of children born after preimplantation genetic diagnosis between 1995 and 2014 von Heijligers, Malou, van Montfoort, Aafke, Meijer-Hoogeveen, Madelon, Broekmans, Frank, Bouman, Katelijne, Homminga, Irene, Dreesen, Jos, Paulussen, Aimee, Engelen, John, Coonen, Edith, van der Schoot, Vyne, van Deursen-Luijten, Marieke, Muntjewerff, Nienke, Peeters, Andrea, van Golde, Ron, van der Hoeven, Mark, Arens, Yvonne, de Die-Smulders, Christine

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Exploring uncertainties regarding unsolicited findings in genetic testing von van der Schoot, Vyne, van der Meer, Eline, Hillen, Marij A., Yntema, Helger G., Brunner, Han G., Oerlemans, Anke J.M.

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Toward clinical and molecular understanding of pathogenic variants in the ZBTB18 gene von Schoot, Vyne, Munnik, Sonja, Venselaar, Hanka, Elting, Mariet, Mancini, Grazia M. S., Ravenswaaij‐Arts, Conny M. A., Anderlid, Britt‐Marie, Brunner, Han G., Stevens, Servi J. C.

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Loss-of-Function Variants in CUL3 Cause a Syndromic Neurodevelopmental Disorder von Blackburn, Patrick R, Ebstein, Frédéric, Hsieh, Tzung-Chien, Motta, Marialetizia, Radio, Francesca Clementina, Herkert, Johanna C, Rinne, Tuula, Thiffault, Isabelle, Rapp, Michele, Alders, Mariel, Maas, Saskia, Gerard, Bénédicte, Smol, Thomas, Vincent-Delorme, Catherine, Cogné, Benjamin, Isidor, Bertrand, Vincent, Marie, Bachmann-Gagescu, Ruxandra, Rauch, Anita, Joset, Pascal, Ferrero, Giovanni Battista, Ciolfi, Andrea, Husson, Thomas, Guerrot, Anne-Marie, Bacino, Carlos, Macmurdo, Colleen, Thompson, Stephanie S, Rosenfeld, Jill A, Faivre, Laurence, Mau-Them, Frederic Tran, Deb, Wallid, Vignard, Virginie, Agrawal, Pankaj B, Madden, Jill A, Goldenberg, Alice, Lecoquierre, François, Zech, Michael, Prokisch, Holger, Necpál, Ján, Jech, Robert, Winkelmann, Juliane, Koprušáková, Monika Turčanová, Konstantopoulou, Vassiliki, Younce, John R, Shinawi, Marwan, Mighton, Chloe, Fung, Charlotte, Morel, Chantal F, Lerner-Ellis, Jordan, DiTroia, Stephanie, Barth, Magalie, Bonneau, Dominique, Krapels, Ingrid, Stegmann, Alexander P A, van der Schoot, Vyne, Brunet, Theresa, Bußmann, Cornelia, Mignot, Cyril, Zampino, Giuseppe, Wortmann, Saskia B, Mayr, Johannes A, Feichtinger, René G, Courtin, Thomas, Ravelli, Claudia, Keren, Boris, Ziegler, Alban, Hasadsri, Linda, Pichurin, Pavel N, Klee, Eric W, Grand, Katheryn, Sanchez-Lara, Pedro A, Krüger, Elke, Bézieau, Stéphane, Klinkhammer, Hannah, Krawitz, Peter Michael, Eichler, Evan E, Tartaglia, Marco, Küry, Sébastien, Wang, Tianyun

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The role of a multidisciplinary team in managing variants of uncertain clinical significance in prenatal genetic diagnosis von Diderich, Karin E.M., Klapwijk, Jasmijn E., van der Schoot, Vyne, van den Born, Myrthe, Wilke, Martina, Joosten, Marieke, Stuurman, Kyra E., Hoefsloot, Lies H., Van Opstal, Diane, Brüggenwirth, Hennie T., Srebniak, Malgorzata I.

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Response to the comment on Diderich et al. “The role of a multidisciplinary team in managing variants of uncertain clinical significance in prenatal genetic diagnosis” (EJMG 66(10)... von Diderich, Karin E.M., Klapwijk, Jasmijn E., van der Schoot, Vyne, van den Born, Myrthe, Wilke, Martina, Joosten, Marieke, Stuurman, Kyra E., Hoefsloot, Lies H., Van Opstal, Diane, Brüggenwirth, Hennie T., Srebniak, Malgorzata I.

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Gather'd fragments; poems von Vyne, Elwin

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Challenges and Pragmatic Solutions in Pre-Test and Post-Test Genetic Counseling for Prenatal Exome Sequencing von Diderich, Karin E M, Klapwijk, Jasmijn E, van der Schoot, Vyne, Brüggenwirth, Hennie T, Joosten, Marieke, Srebniak, Malgorzata I

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Enabling Moore's Law beyond CMOS technologies through heteroepitaxy von Thomas, S.G., Tomasini, P., Bauer, M., Vyne, B., Zhang, Y., Givens, M., Devrajan, J., Koester, S., Lauer, I.

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A study of the trimethyltin group von Sessions, William Vyne

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