The performance of genome sequencing as a first-tier test for neurodevelopmental disorders von van der Sanden, Bart P G H, Schobers, Gaby, Corominas Galbany, Jordi, Koolen, David A, Sinnema, Margje, van Reeuwijk, Jeroen, Stumpel, Connie T R M, Kleefstra, Tjitske, de Vries, Bert B A, Ruiterkamp-Versteeg, Martina, Leijsten, Nico, Kwint, Michael, Derks, Ronny, Swinkels, Hilde, den Ouden, Amber, Pfundt, Rolph, Rinne, Tuula, de Leeuw, Nicole, Stegmann, Alexander P, Stevens, Servi J, van den Wijngaard, Arthur, Brunner, Han G, Yntema, Helger G, Gilissen, Christian, Nelen, Marcel R, Vissers, Lisenka E L M

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Systematic analysis of short tandem repeats in 38,095 exomes provides an additional diagnostic yield von van der Sanden, Bart P.G.H., Corominas, Jordi, de Groot, Michelle, Pennings, Maartje, Meijer, Rowdy P.P., Verbeek, Nienke, van de Warrenburg, Bart, Schouten, Meyke, Yntema, Helger G., Vissers, Lisenka E. L.M., Kamsteeg, Erik-Jan, Gilissen, Christian

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Comprehensive de novo mutation discovery with HiFi long-read sequencing von Kucuk, Erdi, van der Sanden, Bart P G H, O'Gorman, Luke, Kwint, Michael, Derks, Ronny, Wenger, Aaron M, Lambert, Christine, Chakraborty, Shreyasee, Baybayan, Primo, Rowell, William J, Brunner, Han G, Vissers, Lisenka E L M, Hoischen, Alexander, Gilissen, Christian

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