Out-of-hospital cardiac arrest-the relevance of heart failure. The Maastricht Circulatory Arrest Registry by Gorgels, Anton P.M, Gijsbers, Claudia, de Vreede-Swagemakers, Jacqueline, Lousberg, Aimee, Wellens, Hein J.J

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Copy number variants in patients with short stature by van Duyvenvoorde, Hermine A, Lui, Julian C, Kant, Sarina G, Oostdijk, Wilma, Gijsbers, Antoinet C J, Hoffer, Mariëtte J V, Karperien, Marcel, Walenkamp, Marie J E, Noordam, Cees, Voorhoeve, Paul G, Mericq, Verónica, Pereira, Alberto M, Claahsen-van de Grinten, Hedi L, van Gool, Sandy A, Breuning, Martijn H, Losekoot, Monique, Baron, Jeffrey, Ruivenkamp, Claudia A L, Wit, Jan M

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A terminal 3p26.3 deletion is not associated with dysmorphic features and intellectual disability in a four-generation family by Moghadasi, Setareh, van Haeringen, Arie, Langendonck, Lieke, Gijsbers, Antoinet C. J., Ruivenkamp, Claudia A. L.

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Nine patients with a microdeletion 15q11.2 between breakpoints 1 and 2 of the Prader–Willi critical region, possibly associated with behavioural disturbances by Doornbos, Marianne, Sikkema-Raddatz, Birgit, Ruijvenkamp, Claudia A.L, Dijkhuizen, Trijnie, Bijlsma, Emilia K, Gijsbers, Antoinet C.J, Hilhorst-Hofstee, Yvonne, Hordijk, Roel, Verbruggen, Krijn T, Kerstjens-Frederikse, W.S. (Mieke), van Essen, Ton, Kok, Klaas, van Silfhout, Anneke T, Breuning, Martijn, van Ravenswaaij-Arts, Conny M.A

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Genomic and clinical characteristics of six patients with partially overlapping interstitial deletions at 10p12p11 by Wentzel, Christian, Rajcan-Separovic, Evica, Ruivenkamp, Claudia A L, Chantot-Bastaraud, Sandra, Metay, Corinne, Andrieux, Joris, Annerén, Göran, Gijsbers, Antoinet C J, Druart, Luc, Hyon, Capucine, Portnoi, Marie-France, Stattin, Eva-Lena, Vincent-Delorme, Catherine, Kant, Sarina G, Steinraths, Michelle, Marlin, Sandrine, Giurgea, Irina, Thuresson, Ann-Charlotte

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A new diagnostic workflow for patients with mental retardation and or multiple congenital abnormalities: test arrays first by Gijsbers, Antoinet CJ, Lew, Janet YK, Bosch, Cathy AJ, Schuurs-Hoeijmakers, Janneke HM, van Haeringen, Arie, den Hollander, Nicolette S, Kant, Sarina G, Bijlsma, Emilia K, Breuning, Martijn H, Bakker, Egbert, Ruivenkamp, Claudia AL

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Identification of copy number variants associated with BPES-like phenotypes by Gijsbers, Antoinet C. J., D’haene, Barbara, Hilhorst-Hofstee, Yvonne, Mannens, Marcel, Albrecht, Beate, Seidel, Joerg, Witt, David R., Maisenbacher, Melissa K., Loeys, Bart, van Essen, Ton, Bakker, Egbert, Hennekam, Raoul, Breuning, Martijn H., De Baere, Elfride, Ruivenkamp, Claudia A. L.

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miR669a and miR669q prevent skeletal muscle differentiation in postnatal cardiac progenitors by Crippa, Stefania, Cassano, Marco, Messina, Graziella, Galli, Daniela, Galvez, Beatriz G, Curk, Tomaz, Altomare, Claudia, Ronzoni, Flavio, Toelen, Jaan, Gijsbers, Rik, Debyser, Zeger, Janssens, Stefan, Zupan, Blaz, Zaza, Antonio, Cossu, Giulio, Sampaolesi, Maurilio

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Guillain-Barré syndrome after SARS-CoV-2 infection in an international prospective cohort study by Luijten, Linda W G, Leonhard, Sonja E, van der Eijk, Annemiek A, Doets, Alex Y, Appeltshauser, Luise, Arends, Samuel, Attarian, Shahram, Benedetti, Luana, Briani, Chiara, Casasnovas, Carlos, Castellani, Francesca, Dardiotis, Efthimios, Echaniz-Laguna, Andoni, Garssen, Marcel P J, Harbo, Thomas, Huizinga, Ruth, Humm, Andrea M, Jellema, Korné, van der Kooi, Anneke J, Kuitwaard, Krista, Kuntzer, Thierry, Kusunoki, Susumu, Lascano, Agustina M, Martinez-Hernandez, Eugenia, Rinaldi, Simon, Samijn, Johnny P A, Scheidegger, Olivier, Tsouni, Pinelopi, Vicino, Alex, Visser, Leo H, Walgaard, Christa, Wang, Yuzhong, Wirtz, Paul W, Ripellino, Paolo, Jacobs, Bart C

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Molecular and clinical characterization of patients with a ring chromosome 11 by Hansson, Kerstin B.M, Gijsbers, Antoinet C.J, Oostdijk, Wilma, Rehbock, Jan J.B, de Snoo, Femke, Ruivenkamp, Claudia A.L, Kant, Sarina G

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Electrodiagnostic subtyping in Guillain–Barré syndrome patients in the International Guillain–Barré Outcome Study by Arends, Samuel, Drenthen, Judith, Hadden, Robert D. M., Kuwabara, Satoshi, Reisin, Ricardo C., Shahrizaila, Nortina, Ajroud‐Driss, Senda, Antonini, Giovanni, Attarian, Shahram, Balducci, Claudia, Brannagan, Thomas H., Chavada, Govind, Dillmann, Klaus‐Ulrich, Dimachkie, Mazen M., Galassi, Giuliana, Gutiérrez‐Gutiérrez, Gerardo, Islam, Badrul, Islam, Zhahirul, Katzberg, Hans, Miller, James A. L., Pardo, Julio, Rajabally, Yusuf A., Vytopil, Michal, Cornblath, David R., Badrising, Umesh A., Bateman, Kathleen, Bella, Isabelita, Bhavaraju‐Sanka, Ratna, Casasnovas, Carlos, Conti, Eugenia, Dalakas, Marinos, Damme, Philip, Davidson, Amy, Doets, Alex, Echaniz‐Laguna, Andoni, Eftimov, Filip, Faber, Karin G., Fazio, Raffaella, Fehmi, Janev, Garssen, Marcel P.J., Gijsbers, Cees J., Gilchrist, James M., Gilhuis, Job, Goldstein, Jonathan M., Gorson, Kenneth C., Gutmann, Ludwig, Holt, James K.L., Hsieh, Sung‐Tsang, Htut, Min, Hughes, Richard A.C., Kaida, Kenichi, Karafiath, Summer, Khoshnoodi, Mohammad Ali, Kiers, Lynette, Kleiweg, Ruud P., Kolb, Noah A., Kooi, Anneke J., Kramers, Hans, Kwan, Justin Y., Ladha, Shafeeq S., Lassen, Lisbeth Landschoff, Lawson, Victoria H., Cejas, Luciana Leon, Leonhard, Sonja E., Manji, Hadi, Marfia, Girolama A., Martín‐Aguilar, Lorena, Martinez‐Hernandez, Eugenia, Mataluni, Giorgia, Mattiazzi, Marcelo, Meekins, Gregg, Mohammad, Quazi Deen, Tassa, Germán Moris, Nobile‐Orazio, Eduardo, Pelouto, Farah, Pulley, Michael T., Gutiérrez, Luis Querol, Reddel, Stephen W., Rinaldi, Simon, Ripellino, Paolo, Roberts, Rhys C., Rojas‐Marcos, Iñigo, Roodbol, Joyce, Samijn, Johnny P.A., Santoro, Lucio, Tous, Maria José Sedano, Silvestri, Nicholas Joseph, Sundrup, Soeren H., Sommer, Claudia, Stein, Beth, Stino, Amro Maher, Varrato, Jay D., Vermeij, Frederique H., Verschuuren, Jan, Visser, Leo H., Walgaard, Christa, Wang, Yuzhong, Willison, Hugh J., Wirtz, Paul W., Zivkovic, Sascha A.

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Electrodiagnosis of Guillain-Barre syndrome in the International GBS Outcome Study: Differences in methods and reference values by Drenthen, Judith, Franssen, Hessel, Hadden, Robert D.M., Kuwabara, Satoshi, Antonini, Giovanni, Attarian, Shahram, Balducci, Claudia, Barroso, Fabio, Bertorini, Tulio, Binda, Davide, Fulgenzi, Ernesto A., Galassi, Giuliana, Harbo, Thomas, Hartung, Hans-Peter, Hsieh, Sung-Tsang, Kiers, Lynette, Lehmann, Helmar C., Manganelli, Fiore, Pardo, Julio, Rajabally, Yusuf A., Santoro, Lucio, Stein, Beth, Stettner, Mark, Verhamme, Camiel, Jacobs, Bart C., Addington, J.M., Ajroud-Driss, S., Antonini, G., Attarian, S., Badrising, U.A., Bateman, K., van den Bergh, P., Bhavaraju-Sanka, R., Bianco, M., Brannagan, T.H., Briani, C., Buerrmann, Busby, M., Casasnovas, C., Chavada, G., Cornblath, D.R., Dalakas, M.C., Dardiotis, E., Derejko, M.A., van Dijk, G.W., Dimachkie, M.M., van Doorn, P.A., Faber, C.G., Feasby, T.E., Galassi, G., Garcia-Sobrino, T., Gijsbers, C.J., Gorson, K.C., Gutiérrez-Gutiérrez, Hadden, R.D.M., Holt, J.K.L., Htut, M., Fehmi, J., Jellema, K., Jerico Pascual, I., Karafiath, S., Khoshnoodi, M.A., Kimpinski, K., Kleyweg, R.P., Kokubun, N., van Koningsveld, R., Kuwabara, S., Kwan, J.Y., Lawson, V., Manji, H., Marfia, G.A., Martin-Aguilar, L., Mataluni, G., McDermott, C.J., Meekins, G.D., Miller, J.A.L., Moris de la Tassa, G., Nascimbene, C., Nowak, R.J., Pulley, M.T., Reddel, S.W., van der Ree, T., Roberts, R.C., Rojas-Marcos, I., Samijn, J.P.A., Schenone, A., Shahrizaila, N., Sheikh, K.A., Silvestri, N.J., Stein, B., Song, Y., Stino, A.M., Tankisi, H., Vélez-Santamaria, P.V., Varrato, J.D., Visser, L.H., Vytopil, M.V., Wang, Y.Z., Willison, H.J., Zivkovic, S.A.

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Additional cryptic CNVs in mentally retarded patients with apparently balanced karyotypes by Gijsbers, Antoinet C.J, Bosch, Cathy A.J, Dauwerse, Johannes G, Giromus, Osdilly, Hansson, Kerstin, Hilhorst-Hofstee, Yvonne, Kriek, Marjolein, van Haeringen, Arie, Bijlsma, Emilia K, Bakker, Egbert, Breuning, Martijn H, Ruivenkamp, Claudia A.L

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Three new cases with a mosaicism involving a normal cell line and a cryptic unbalanced autosomal reciprocal translocation by Gijsbers, Antoinet C.J, Dauwerse, Johannes G, Bosch, Cathy A.J, Boon, Elles M.J, van den Ende, Wilco, Kant, Sarina G, Hansson, Kerstin M.B, Breuning, Martijn H, Bakker, Egbert, Ruivenkamp, Claudia A.L

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A 797 kb de novo deletion of 18q21.31 in a patient with speech delay, mental retardation, sleeping problems, facial dysmorphism, and feet anomalies by van Diepen, Mireille M.L, Gijsbers, Antoinet C.J, Bosch, Cathy A.J, Oudesluys-Murphy, Anne Marie, Ruivenkamp, Claudia A.L, Bijlsma, Emilia K

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A 400 kb duplication, 2.4 Mb triplication and 130 kb duplication of 9q34.3 in a patient with severe mental retardation by Gijsbers, Antoinet C.J, Bijlsma, Emilia K, Weiss, Marjan M, Bakker, Egbert, Breuning, Martijn H, Hoffer, Mariëtte J.V, Ruivenkamp, Claudia A.L

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Interstitial duplication in the proximal long arm of chromosome 16 by Hansson, Kerstin, Dauwerse, Hans, Gijsbers, Antoinet, van Diepen, Mireille, Ruivenkamp, Claudia, Kant, Sarina

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A 400kb duplication, 2.4Mb triplication and 130kbduplication of 9q34.3 in a patient with severe mental retardation by Gijsbers, Antoinet C.J., Bijlsma, Emilia K., Weiss, Marjan M., Bakker, Egbert, Breuning, Martijn H., Hoffer, Mariëtte J.V., Ruivenkamp, Claudia A.L.

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A 400kb duplication, 2.4Mb triplication and 130kb duplication of 9q34.3 in a patient with severe mental retardation by Gijsbers, Antoinet C J, Bijlsma, Emilia K, Weiss, Marjan M, Bakker, Egbert, Breuning, Martijn H, Hoffer, Mariëtte J V, Ruivenkamp, Claudia A L

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Nine patients with a microdeletion 15q11.2 between breakpoints 1 and 2 of the Prader―Willi critical region, possibly associated with behavioural disturbances: Emerging Microdeletio... by DOORNBOS, Marianne, SIKKEMA-RADDATZ, Birgit, VAN ESSEN, Ton, KOK, Klaas, VAN SILFHOUT, Anneke T, BREUNING, Martijn, VAN RAVENSWAAIJ-ARTS, Conny M. A, RUIJVENKAMP, Claudia A. L, DIJKHUIZEN, Trijnie, BIJLSMA, Emilia K, GIJSBERS, Antoinet C. J, HILHORST-HOFSTEE, Yvonne, HORDIJK, Roel, VERBRUGGEN, Krijn T, KERSTJENS-FREDERIKSE, W. S

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