Courraud, Jérémie
Chater-Diehl, Eric
Durand, Benjamin
Vincent, Marie
del Mar Muniz Moreno, Maria
Boujelbene, Imene
Drouot, Nathalie
Genschik, Loréline
Schaefer, Elise
Nizon, Mathilde
Gerard, Bénédicte
Abramowicz, Marc
Cogné, Benjamin
Bronicki, Lucas
Burglen, Lydie
Barth, Magalie
Charles, Perrine
Colin, Estelle
Coubes, Christine
David, Albert
Delobel, Bruno
Demurger, Florence
Passemard, Sandrine
Denommé, Anne-Sophie
Faivre, Laurence
Feger, Claire
Fradin, Mélanie
Francannet, Christine
Genevieve, David
Goldenberg, Alice
Guerrot, Anne-Marie
Isidor, Bertrand
Johannesen, Katrine M.
Keren, Boris
Kibæk, Maria
Kuentz, Paul
Mathieu-Dramard, Michèle
Demeer, Bénédicte
Metreau, Julia
Steensbjerre Møller, Rikke
Moutton, Sébastien
Pasquier, Laurent
Pilekær Sørensen, Kristina
Perrin, Laurence
Renaud, Mathilde
Saugier, Pascale
Rio, Marlène
Svane, Joane
Thevenon, Julien
Tran Mau Them, Frédéric
Tronhjem, Cathrine Elisabeth
Vitobello, Antonio
Layet, Valérie
Auvin, Stéphane
Khachnaoui, Khaoula
Birling, Marie-Christine
Drunat, Séverine
Bayat, Allan
Dubourg, Christèle
El Chehadeh, Salima
Fagerberg, Christina
Mignot, Cyril
Guipponi, Michel
Bienvenu, Thierry
Herault, Yann
Thompson, Julie
Willems, Marjolaine
Mandel, Jean-Louis
Weksberg, Rosanna
Piton, Amélie
This article is maintained by: Elsevier
Article Title: Integrative approach to interpret DYRK1A variants, leading to a frequent neurodevelopmental disorder
Journal Title: Genetics in Medicine
CrossRef DOI link to publisher maintained version: https://doi.org/10.1038/s41436-021-01263-1
Content Type: article
Copyright: © 2021, The Author(s), under exclusive licence to the American College of Medical Genetics and Genomics