Letter regarding the article: “Striking phenotypic overlap between Nicolaides-Baraitser and Coffin-Siris syndromes in monozygotic twins with ARID1B intragenic deletion” von van der Sluijs, P.J. (Eline), Santen, Gijs W.E.

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Recommending revised hepatoblastoma surveillance in children with a pathogenic ARID1A variant. Reply to “Cancer in ARID1A-Coffin-Siris syndrome: Review and report of a child with h... von van der Sluijs, P.J., Vergano, S.A., Roeder, E.R., Jongmans, M.C.J., Santen, G.W.E.

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Response to Gorokhova et al von van der Sluijs, Eline (P.J.), Ruivenkamp, Claudia A. L., Santen, Gijs W. E.

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ARID1B-related disorder in 87 adults: Natural history and self-sustainability von van der Sluijs, P.J., Gösgens, M., Dingemans, A.J.M., Striano, P., Riva, A., Mignot, C., Faudet, A., Vasileiou, G., Walther, M., Schrier Vergano, S.A., Alders, M., Alkuraya, F.S., Alorainy, I., Alsaif, H.S., Anderlid, B., Bache, I., van Beek, I., Blanluet, M., van Bon, B.W., Brunet, T., Brunner, H., Carriero, M.L., Charles, P., Chatron, N., Coccia, E., Dubourg, C., Earl, R.K., Eichler, E.E., Faivre, L., Foulds, N., Graziano, C., Guerrot, A.M., Hashem, M.O., Heide, S., Heron, D., Hickey, S.E., Hopman, S.M.J., Kattentidt-Mouravieva, A., Kerkhof, J., Klein Wassink-Ruiter, J.S., Kurtz-Nelson, E.C., Kušíková, K., Kvarnung, M., Lecoquierre, F., Leszinski, G.S., Loberti, L., Magoulas, P.L., Mari, F., Maystadt, I., Merla, G., Milunsky, J.M., Moortgat, S., Nicolas, G., Leary, M.O.’, Odent, S., Ozmore, J.R., Parbhoo, K., Pfundt, R., Piccione, M., Pinto, A.M., Popp, B., Putoux, A., Rehm, H.L., Reis, A., Renieri, A., Rosenfeld, J.A., Rossi, M., Salzano, E., Saugier-Veber, P., Seri, M., Severi, G., Sonmez, F.M., Strobl-Wildemann, G., Stuurman, K.E., Uctepe, E., Van Esch, H., Vitetta, G., de Vries, B.B.A., Wahl, D., Wang, T., Zacher, P., Heitink, K.R., Ropers, F.G., Steenbeek, D., Rybak, T., Santen, G.W.E.

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Letter regarding the article: "Striking phenotypic overlap between Nicolaides-Baraitser and CoffinSiris syndromes in monozygotic twins with ARID1B intragenic deletion" von Sluijs, P.J. van der, Santen, G.W.E.

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Landscape of mSWI/SNF chromatin remodeling complex perturbations in neurodevelopmental disorders von Valencia, A.M., Sankar, A., Sluijs, P.J. van der, Satterstrom, F.K., Fu, J.C., Talkowski, M.E., Vergano, S.A.S., Santen, G.W.E., Kadoch, C.

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Prevalence of comorbidities in individuals with neurodevelopmental disorders from the aggregated phenomics data of 51,227 pediatric individuals von Dingemans, A.J.M., Jansen, S., Reeuwijk, J. van, Leeuw, N. de, Pfundt, R., Schuurs-Hoeijmakers, J., Bon, B.W. van, Marcelis, C., Ockeloen, C.W., Willemsen, M., Sluijs, P.J. van der, Santen, G.W.E., Kooy, R.F., Vulto-van Silfhout, A.T., Kleefstra, T., Koolen, D.A., Vissers, L.E.L.M., Vries, B.B.A. de

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PhenoScore quantifies phenotypic variation for rare genetic diseases by combining facial analysis with other clinical features using a machine-learning framework von Dingemans, A.J.M., Hinne, M., Truijen, K.M.G., Goltstein, L., Reeuwijk, J. van, Leeuw, N. de, Schuurs-Hoeijmakers, J., Pfundt, R., Diets, I.J., Hoed, J. den, Boer, E. de, Spek, J. van der, Jansen, S., Bon, B.W. van, Jonis, N., Ockeloen, C.W., Silfhout, A.V.V.T., Kleefstra, T., Koolen, D.A., Campeau, P.M., Palmer, E.E., Esch, H. van, Lyon, G.J., Alkuraya, F.S., Rauch, A., Marom, R., Baralle, D., Sluijs, P.J. van der, Santen, G.W.E., Kooy, R.F., Gerven, M.A.J. van, Vissers, L.E.L.M., Vries, B.B.A. de

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Elucidating the clinical and molecular spectrum of SMARCC2-associated NDD in a cohort of 65 affected individuals von Bosch, E., Popp, B., Güse, E., Skinner, C., Sluijs, P.J. van der, Maystadt, I., Pinto, A.M., Renieri, A., Bruno, L.P., Granata, S., Marcelis, C., Baysal, Ö., Hartwich, D., Holthöfer, L., Isidor, B., Cogne, B., Wieczorek, D., Capra, V., Scala, M., Marco, P. de, Ognibene, M., Abou Jamra, R., Platzer, K., Carter, L.B., Kuismin, O., Haeringen, A. van, Maroofian, R., Valenzuela, I., Cuscó, I., Martinez-Agosto, J.A., Rabani, A.M., Mefford, H.C., Pereira, E.M., Close, C., Anyane-Yeboa, K., Wagner, M., Hannibal, M.C., Zacher, P., Thiffault, I., Beunders, G., Umair, M., Bhola, P.T., Mcginnis, E., Millichap, J., Kamp, J.M. van de, Prijoles, E.J., Dobson, A., Shillington, A., Graham, B.H., Garcia, E.J., Galindo, M.K., Ropers, F.G., Nibbeling, E.A.R., Hubbard, G., Karimov, C., Goj, G., Bend, R., Rath, J., Morrow, M.M., Millan, F., Salpietro, V., Torella, A., Nigro, V., Kurki, M., Stevenson, R.E., Santen, G.W.E., Zweier, M., Campeau, P.M., Severino, M., Reis, A., Accogli, A., Vasileiou, G.

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Discovering a new part of the phenotypic spectrum of Coffin-Siris syndrome in a fetal cohort von Sluijs, P.J. van der, Joosten, M., Alby, C., Gilmore, K., Dubourg, C., Fradin, M., Wang, T.Y., Kurtz-Nelson, E.C., Ahlers, K.P., Arts, P., Barnett, C.P., Ashfaq, M., Baban, A., Born, M. van den, Borrie, S., Busa, T., Byrne, A., Carriero, M., Cesario, C., Chong, K., Dempsey, J.C., Cueto-Gonzalez, A.M., Diderich, K.E.M., Doherty, D., Farholt, S., Gerkes, E.H., Gorokhova, S., Govaerts, L.C.P., Gregersen, P.A., Hickey, S.E., Lefebvre, M., Mari, F., Martinovic, J., Northrup, H., O'Leary, M., Parbhoo, K., Patrier, S., Popp, B., Santos-Simarro, F., Stoltenburg, C., Thauvin-Robinet, C., Thompson, E., Vulto-van Silfhout, A.T., Zahir, F.R., Scott, H.S., Earl, R.K., Eichler, E.E., Vora, N.L., Wilnai, Y., Giordano, J.L., Wapner, R.J., Rosenfeld, J.A., Haak, M.C., Santen, G.W.E.

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A Case Series of Familial ARID1B Variants Illustrating Variable Expression and Suggestions to Update the ACMG Criteria von Sluijs, P.J. van der, Alders, M., Dingemans, A.J.M., Parbhoo, K., Bon, B.W. van, Dempsey, J.C., Doherty, D., Dunnen, J.T. den, Gerkes, E.H., Milller, I.M., Moortgat, S., Regier, D.S., Ruivenkamp, C.A.L., Schmalz, B., Smol, T., Stuurman, K.E., Vincent-Delorme, C., Vries, B.B.A. de, Sadikovic, B., Hickey, S.E., Rosenfeld, J.A., Maystadt, I., Santen, G.W.E.

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Functional correlation of genome-wide DNA methylation profiles in genetic neurodevelopmental disorders von Levy, M.A., Relator, R., McConkey, H., Pranckeviciene, E., Kerkhof, J., Barat-Houari, M., Bargiacchi, S., Biamino, E., Bralo, M.P., Cappuccio, G., Ciolfi, A., Clarke, A., DuPont, B.R., Elting, M.W., Faivre, L., Fee, T., Ferilli, M., Fletcher, R.S., Cherick, F., Foroutan, A., Friez, M.J., Gervasini, C., Haghshenas, S., Hilton, B.A., Jenkins, Z., Kaur, S., Lewis, S., Louie, R.J., Maitz, S., Milani, D., Morgan, A.T., Oegema, R., Ostergaard, E., Pallares, N.R., Piccione, M., Plomp, A.S., Poulton, C., Reilly, J., Rius, R., Robertson, S., Rooney, K., Rousseau, J., Santen, G.W.E., Santos-Simarro, F., Schijns, J., Squeo, G.M., St John, M., Thauvin-Robinet, C., Traficante, G., Sluijs, P.J. van der, Vergano, S.A., Vos, N., Walden, K.K., Azmanov, D., Balci, T.B., Banka, S., Gecz, J., Henneman, P., Lee, J.A., Mannens, M.M.A.M., Roscioli, T., Siu, V., Amor, D.J., Baynam, G., Bend, E.G., Boycott, K., Brunetti-Pierri, N., Campeau, P.M., Campion, D., Christodoulou, J., Dyment, D., Esber, N., Fahrner, J.A., Fleming, M.D., Genevieve, D., Heron, D., Husson, T., Kernohan, K.D., McNeill, A., Menke, L.A., Merla, G., Prontera, P., Rockman-Greenberg, C., Schwartz, C., Skinner, S.A., Stevenson, R.E., Vincent, M., Vitobello, A., Tartaglia, M., Alders, M., Tedder, M.L., Sadikovic, B.

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Novel diagnostic DNA methylation episignatures expand and refine the epigenetic landscapes of Mendelian disorders von Levy, M.A., McConkey, H., Kerkhof, J., Barat-Houari, M., Bargiacchi, S., Biamino, E., Cappuccio, G., Ciolfi, A., Clarke, A., DuPont, B.R., Elting, M.W., Faivre, L., Fee, T., Fletcher, R.S., Cherik, F., Foroutan, A., Friez, M.J., Gervasini, C., Haghshenas, S., Hilton, B.A., Jenkins, Z., Kaur, S., Lewis, S., Louie, R.J., Maitz, S., Milani, D., Morgan, A.T., Oegema, R., Ostergaard, E., Pallares, N.R., Piccione, M., Pizzi, S., Plomp, A.S., Poulton, C., Reilly, J., Relator, R., Rius, R., Robertson, S., Rooney, K., Rousseau, J., Santen, G.W.E., Santos-Simarro, F., Schijns, J., Squeo, G.M., St John, M., Thauvin-Robinet, C., Traficante, G., Sluijs, P.J. van der, Vergano, S.A., Vos, N., Walden, K.K., Azmanov, D., Balci, T., Banka, S., Gecz, J., Henneman, P., Lee, J.A., Mannens, M.M.A.M., Roscioli, T., Siu, V., Amor, D.J., Baynam, G., Bend, E.G., Boycott, K., Brunetti-Pierri, N., Campeau, P.M., Christodoulou, J., Dyment, D., Esber, N., Fahrner, J.A., Fleming, M.D., Genevieve, D., Kerrnohan, K.D., McNeill, A., Menke, L.A., Merla, G., Prontera, P., Rockman-Greenberg, C., Schwartz, C., Skinner, S.A., Stevenson, R.E., Vitobello, A., Tartaglia, M., Alders, M., Tedder, M.L., Sadikovic, B.

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Ventilator-induced Lung Injury Is Mediated by the NLRP3 Inflammasome von KUIPERS, Maria T, ASLAMI, Hamid, BRESSER, Paul, LEEMANS, Jaklien C, DER POLL, Tom Van, SCHULTZ, Marcus J, WIELAND, Catharina W, JANCZY, John R, DER SLUIJS, Koenraad F. Van, VLAAR, Alexander P. J, WOLTHUIS, Esther K, CHOI, Goda, ROELOFS, Joris J. T. H, FLAVELL, Richard A, SUTTERWALA, Fayyaz S

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ICU capacity management during the COVID-19 pandemic using a process simulation von Alban, Andres, Chick, Stephen E., Dongelmans, Dave A., Vlaar, Alexander P. J., Sent, Danielle

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The impact of changes in intensive care organization on patient outcome and cost-effectiveness-a narrative review von van der Sluijs, Alexander F, van Slobbe-Bijlsma, Eline R, Chick, Stephen E, Vroom, Margreeth B, Dongelmans, Dave A, Vlaar, Alexander P J

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Ervaringsgerichte acceptatie bij de behandeling van complexe somatisch-symptoomstoornis von Herremans, P.J, van Eck van der Sluijs, J, Geenen, R, Houtveen, J

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Adaptation to climate change-related risks in Dutch urban areas: stimuli and barriers von Runhaar, Hens, Mees, Heleen, Wardekker, Arjan, van der Sluijs, Jeroen, Driessen, Peter P. J.

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Reducing errors in the administration of medication with infusion pumps in the intensive care department: A lean approach von van der Sluijs, Alexander F, van Slobbe-Bijlsma, Eline R, Goossens, Astrid, Vlaar, Alexander PJ, Dongelmans, Dave A

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The prognostic value of the head-shaft angle on hip displacement in children with cerebral palsy von van der List, J. P. J., Witbreuk, M. M., Buizer, A. I., van der Sluijs, J. A.

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