Inferring hospital admissions from SARS-CoV-2 virus loads in wastewater in The Netherlands, August 2020 – February 2022 von Hetebrij, Wouter A., de Roda Husman, Ana Maria, Nagelkerke, Erwin, van der Beek, Rudolf F.H.J., van Iersel, Senna C.J.L., Breuning, Titus G.V., Lodder, Willemijn J., van Boven, Michiel

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Revising oversight of genetically modified plants von Huttner, S.L. (University of California, Los Angeles, CA), Arntzen, C, Beachy, R, Breuning, G, Nester, E, Qualset, C, Vidaver, A

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Mutations in SWI/SNF chromatin remodeling complex gene ARID1B cause Coffin-Siris syndrome von Santen, Gijs W E, Aten, Emmelien, Sun, Yu, Almomani, Rowida, Gilissen, Christian, Nielsen, Maartje, Kant, Sarina G, Snoeck, Irina N, Peeters, Els A J, Hilhorst-Hofstee, Yvonne, Wessels, Marja W, den Hollander, Nicolette S, Ruivenkamp, Claudia A L, van Ommen, Gert-Jan B, Breuning, Martijn H, den Dunnen, Johan T, van Haeringen, Arie, Kriek, Marjolein

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Atroposelective Synthesis of Axially Chiral Biaryl Compounds von Bringmann, Gerhard, Price Mortimer, Anne J., Keller, Paul A., Gresser, Mary J., Garner, James, Breuning, Matthias

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Craniosynostosis and Multiple Skeletal Anomalies in Humans and Zebrafish Result from a Defect in the Localized Degradation of Retinoic Acid von Laue, Kathrin, Pogoda, Hans-Martin, Daniel, Philip B., van Haeringen, Arie, Alanay, Yasemin, von Ameln, Simon, Rachwalski, Martin, Morgan, Tim, Gray, Mary J., Breuning, Martijn H., Sawyer, Gregory M., Sutherland-Smith, Andrew J., Nikkels, Peter G., Kubisch, Christian, Bloch, Wilhelm, Wollnik, Bernd, Hammerschmidt, Matthias, Robertson, Stephen P.

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Hereditary leiomyomatosis and renal cell cancer in families referred for fumarate hydratase germline mutation analysis von Smit, DL, Mensenkamp, AR, Badeloe, S, Breuning, MH, Simon, MEH, Van Spaendonck, KY, Aalfs, CM, Post, JG, Shanley, S, Krapels, IPC, Hoefsloot, LH, Van Moorselaar, RJA, Starink, TM, Bayley, J-P, Frank, J, Van Steensel, MAM, Menko, FH

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Compound inheritance of a low-frequency regulatory SNP and a rare null mutation in exon-junction complex subunit RBM8A causes TAR syndrome von Albers, Cornelis A, Paul, Dirk S, Schulze, Harald, Freson, Kathleen, Stephens, Jonathan C, Smethurst, Peter A, Jolley, Jennifer D, Cvejic, Ana, Kostadima, Myrto, Bertone, Paul, Breuning, Martijn H, Debili, Najet, Deloukas, Panos, Favier, Rémi, Fiedler, Janine, Hobbs, Catherine M, Huang, Ni, Hurles, Matthew E, Kiddle, Graham, Krapels, Ingrid, Nurden, Paquita, Ruivenkamp, Claudia A L, Sambrook, Jennifer G, Smith, Kenneth, Stemple, Derek L, Strauss, Gabriele, Thys, Chantal, van Geet, Chris, Newbury-Ecob, Ruth, Ouwehand, Willem H, Ghevaert, Cedric

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Mutations in genes encoding subunits of RNA polymerases I and III cause Treacher Collins syndrome von Dauwerse, Johannes G, Dixon, Jill, Seland, Saskia, Ruivenkamp, Claudia A L, van Haeringen, Arie, Hoefsloot, Lies H, Peters, Dorien J M, Boers, Agnes Clement-de, Daumer-Haas, Cornelia, Maiwald, Robert, Zweier, Christiane, Kerr, Bronwyn, Cobo, Ana M, Toral, Joaquín F, Hoogeboom, A Jeannette M, Lohmann, Dietmar R, Hehr, Ute, Dixon, Michael J, Breuning, Martijn H, Wieczorek, Dagmar

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Recurrent reciprocal deletions and duplications of 16p13.11: the deletion is a risk factor for MR/MCA while the duplication may be a rare benign variant von Hannes, F D, Sharp, A J, Mefford, H C, de Ravel, T, Ruivenkamp, C A, Breuning, M H, Fryns, J-P, Devriendt, K, Van Buggenhout, G, Vogels, A, Stewart, H, Hennekam, R C, Cooper, G M, Regan, R, Knight, S J L, Eichler, E E, Vermeesch, J R

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Genetic Heterogeneity in Rubinstein-Taybi Syndrome: Mutations in Both the CBP and EP300 Genes Cause Disease von Roelfsema, Jeroen H., White, Stefan J., Ariyürek, Yavuz, Bartholdi, Deborah, Niedrist, Dunja, Papadia, Francesco, Bacino, Carlos A., den Dunnen, Johan T., van Ommen, Gert-Jan B., Breuning, Martijn H., Hennekam, Raoul C., Peters, Dorien J.M.

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Myocardial structural alteration and systolic dysfunction in preclinical hypertrophic cardiomyopathy mutation carriers von Yiu, Kai Hang, Atsma, Douwe E, Delgado, Victoria, Ng, Arnold C T, Witkowski, Tomasz G, Ewe, See Hooi, Auger, Dominique, Holman, Eduard R, van Mil, Anneke M, Breuning, Martijn H, Tse, Hung Fat, Bax, Jeroen J, Schalij, Martin J, Marsan, Nina Ajmone

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Conclusiones Theoretico-Practicae, De Testamento Judiciali von Harpprecht, Ferdinand Christoph

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Conclusiones Theoretico-Practicae, De Testamento Judiciali von Harpprecht, Ferdinand Christoph

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Lowering of Pkd1 expression is sufficient to cause polycystic kidney disease von Leeuwen, Irma S. Lantinga-van, Dauwerse, Johannes G., Baelde, Hans J., Leonhard, Wouter N., van de Wal, Annemieke, Ward, Christopher J., Verbeek, Sjef, DeRuiter, Marco C., Breuning, Martijn H., de Heer, Emile, Peters, Dorien J.M.

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Dental models made with an intraoral scanner: A validation study von Cuperus, Anne Margreet R, Harms, Marit C, Rangel, Frits A, Bronkhorst, Ewald M, Schols, Jan G.J.H, Breuning, K. Hero

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Cancer risk in hereditary nonpolyposis colorectal cancer due to MSH6 mutations: impact on counseling and surveillance von Hendriks, Yvonne M.C., Wagner, Anja, Morreau, Hans, Menko, Fred, Stormorken, Astrid, Quehenberger, Franz, Sandkuijl, Lodewijk, Møller, Pal, Genuardi, Maurizio, van Houwelingen, Hans, Tops, Carli, van Puijenbroek, Marjo, Verkuijlen, Paul, Kenter, Gemma, van Mil, Anneke, Meijers-Heijboer, Hanne, Tan, Gita B., Breuning, Martijn H., Fodde, Riccardo, Winjen, Jull Th, Bröcker-Vriends, Annette H.J.T., Vasen, Hans

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The IGSF1 Deficiency Syndrome: Characteristics of Male and Female Patients von Joustra, S. D, Schoenmakers, N, Persani, L, Campi, I, Bonomi, M, Radetti, G, Beck-Peccoz, P, Zhu, H, Davis, T. M. E, Sun, Y, Corssmit, E. P, Appelman-Dijkstra, N. M, Heinen, C. A, Pereira, A. M, Varewijck, A. J, Janssen, J. A. M. J. L, Endert, E, Hennekam, R. C, Lombardi, M. P, Mannens, M. M. A. M, Bak, B, Bernard, D. J, Breuning, M. H, Chatterjee, K, Dattani, M. T, Oostdijk, W, Biermasz, N. R, Wit, J. M, van Trotsenburg, A. S. P

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Diagnostic exome sequencing in 266 Dutch patients with visual impairment von Haer-Wigman, Lonneke, van Zelst-Stams, Wendy Ag, Pfundt, Rolph, van den Born, L Ingeborgh, Klaver, Caroline Cw, Verheij, Joke Bgm, Hoyng, Carel B, Breuning, Martijn H, Boon, Camiel Jf, Kievit, Anneke J, Verhoeven, Virginie Jm, Pott, Jan Wr, Sallevelt, Suzanne Ceh, van Hagen, Johanna M, Plomp, Astrid S, Kroes, Hester Y, Lelieveld, Stefan H, Hehir-Kwa, Jayne Y, Castelein, Steven, Nelen, Marcel, Scheffer, Hans, Lugtenberg, Dorien, Cremers, Frans Pm, Hoefsloot, Lies, Yntema, Helger G

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Accuracy and reliability of a novel method for fusion of digital dental casts and Cone Beam Computed Tomography scans von Rangel, Frits A, Maal, Thomas J J, Bronkhorst, Ewald M, Breuning, K Hero, Schols, Jan G J H, Bergé, Stefaan J, Kuijpers-Jagtman, Anne Marie

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FACE-Q craniofacial module: Part 2 Psychometric properties of newly developed scales for children and young adults with facial conditions von Klassen, Anne F, Rae, Charlene, Riff, Wong, Denadai, Rafael, Murray, Dylan J, Bracken, Shirley, Courtemanche, Douglas J, Bulstrode, Neil, O'Hara, Justine, Butler, Daniel, Goldstein, Jesse, Tassi, Ali, Hol, Marinka LF, Johnson, David, Ganske, Ingrid M., Kölby, Lars, Benitez, Susana, Breuning, Eleonore E, Malic, Claudia C., Allen, Gregory C., Pusic, Andrea L, Cano, Stefan

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