Second-order stochastic differential equation model as an alternative for the ALT and CALT models von Oud, J. H. L.

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The Relationship between Mutual Family Relations and Child Psychopathology von Mathijssen, Jolanda J. J. P., Koot, Hans M., Verhulst, Frank C., De Bruyn, Eric E. J., Oud, Johan H. L.

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Continuous time state space modeling of panel data by means of SEM von OUD, J. H. L, JANSEN, R. A. R. G

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The rehabilitation process of children with motor disabilities in the Dutch therapeutic toddler class: main phases and parent involvement von HENDRIKS, A. H. C, DE MOOR, J. M. H, SAVELBERG, M. M. H. W, OUD, J. H. L

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Service needs of parents with motor or multiply disabled children in Dutch therapeutic toddler classes von Hendriks, Alexander HC, De Moor, Jan MH, Oud, Johan HL, Franken, Waltera M

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High prevalence of oncogenic MYD88 and CD79B mutations in primary testicular diffuse large B-cell lymphoma von Kraan, W, van Keimpema, M, Horlings, H M, Schilder-Tol, E J M, Oud, M E C M, Noorduyn, L A, Kluin, P M, Kersten, M J, Spaargaren, M, Pals, S T

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Enige oplossingen voor het regressie-probleem. (Some Solutions to the Problem of Regression) von OUD, J. H. L

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C14ORF179 encoding IFT43 is mutated in Sensenbrenner syndrome von Arts, Heleen H, Bongers, Ernie M H F, Mans, Dorus A, van Beersum, Sylvia E C, Oud, Machteld M, Bolat, Emine, Spruijt, Liesbeth, Cornelissen, Elisabeth A M, Schuurs-Hoeijmakers, Janneke H M, de Leeuw, Nicole, Cormier-Daire, Valérie, Brunner, Han G, Knoers, Nine V A M, Roepman, Ronald

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Exome sequencing reveals novel causes as well as new candidate genes for human globozoospermia von Oud, M S, Okutman, Ö, Hendricks, L A J, de Vries, P F, Houston, B J, Vissers, L E L M, O’Bryan, M K, Ramos, L, Chemes, H E, Viville, S, Veltman, J A

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Prolonged activation of nasal immune cell populations and development of tissue-resident SARS-CoV-2-specific CD8+ T cell responses following COVID-19 von Roukens, Anna H. E., Pothast, Cilia R., König, Marion, Huisman, Wesley, Dalebout, Tim, Tak, Tamar, Azimi, Shohreh, Kruize, Yvonne, Hagedoorn, Renate S., Zlei, Mihaela, Staal, Frank J. T., de Bie, Fenna J., van Dongen, Jacques J. M., Arbous, Sesmu M., Zhang, Jaimie L. H., Verheij, Maaike, Prins, Corine, van der Does, Anne M., Hiemstra, Pieter S., de Vries, Jutte J. C., Janse, Jacqueline J., Roestenberg, Meta, Myeni, Sebenzile K., Kikkert, Marjolein, Yazdanbakhsh, Maria, Heemskerk, Mirjam H. M., Smits, Hermelijn H., Jochems, Simon P.

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A de novo paradigm for male infertility von Oud, M. S., Smits, R. M., Smith, H. E., Mastrorosa, F. K., Holt, G. S., Houston, B. J., de Vries, P. F., Alobaidi, B. K. S., Batty, L. E., Ismail, H., Greenwood, J., Sheth, H., Mikulasova, A., Astuti, G. D. N., Gilissen, C., McEleny, K., Turner, H., Coxhead, J., Cockell, S., Braat, D. D. M., Fleischer, K., D’Hauwers, K. W. M., Schaafsma, E., Nagirnaja, L., Conrad, D. F., Friedrich, C., Kliesch, S., Aston, K. I., Riera-Escamilla, A., Krausz, C., Gonzaga-Jauregui, C., Santibanez-Koref, M., Elliott, D. J., Vissers, L. E. L. M., Tüttelmann, F., O’Bryan, M. K., Ramos, L., Xavier, M. J., van der Heijden, G. W., Veltman, J. A.

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Exome sequencing reveals variants in known and novel candidate genes for severe sperm motility disorders von Oud, M S, Houston, B J, Volozonoka, L, Mastrorosa, F K, Holt, G S, Alobaidi, B K S, deVries, P F, Astuti, G, Ramos, L, Mclachlan, R I, O'Bryan, M K, Veltman, J A, Chemes, H E, Sheth, H

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Unpacking Self-Rated Health and Quality of Life in Older Adults and Elderly in India: A Structural Equation Modelling Approach von Hirve, Siddhivinayak, Oud, Johan H. L., Sambhudas, Somnath, Juvekar, Sanjay, Blomstedt, Yulia, Tollman, Stephen, Wall, Stig, Ng, Nawi

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Awareness in children: a secondary analysis of five cohort studies von Davidson, A. J., Smith, K. R., Blussé van Oud‐Alblas, H. J., Lopez, U., Malviya, S., Bannister, C. F., Galinkin, J. L., Habre, W., Ironfield, C., Voepel‐Lewis, T., Weber, F.

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Prognostic Value of Fractional Flow Reserve: Linking Physiologic Severity to Clinical Outcomes von JOHNSON, Nils P, TOTH, Gábor G, DI SERAFINO, Luigi, DOMINGUEZ-FRANCO, Antonio J, DUPOUY, Patrick, ESEN, Ali M, ESEN, Özlem B, HAMILOS, Michalis, IWASAKI, Kohichiro, JENSEN, Lisette O, JIMENEZ-NAVARRO, Manuel F, KATRITSIS, Demosthenes G, DEJIAN LAI, KOCAMAN, Sinan A, KOO, Bon-Kwon, LOPEZ-PALOP, Ramón, LORIN, Jeffrey D, MILLER, Louis H, MULLER, Olivier, NAM, Chang-Wook, OUD, Niels, PUYMIRAT, Etienne, RIEBER, Johannes, HONGJIAN ZHU, RIOUFOL, Gilles, RODES-CABAU, Josep, SEDLIS, Steven P, TAKEISHI, Yasuchika, TONINO, Pim A. L, VAN BELLE, Eric, VERNA, Edoardo, WERNER, Gerald S, FEARON, William F, PIJLS, Nico H. J, ACAR, Göksel, DE BRUYNE, Bernard, GOULD, K. Lance, AGOSTONI, Pierfrancesco, APPELMAN, Yolande, ARSLAN, Fatih, BARBATO, Emanuele, CHEN, Shao-Liang

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Mutations in the Gene Encoding IFT Dynein Complex Component WDR34 Cause Jeune Asphyxiating Thoracic Dystrophy von Schmidts, Miriam, Vodopiutz, Julia, Christou-Savina, Sonia, Cortés, Claudio R., McInerney-Leo, Aideen M., Emes, Richard D., Arts, Heleen H., Tüysüz, Beyhan, D’Silva, Jason, Leo, Paul J., Giles, Tom C., Oud, Machteld M., Harris, Jessica A., Koopmans, Marije, Marshall, Mhairi, Elçioglu, Nursel, Kuechler, Alma, Bockenhauer, Detlef, Moore, Anthony T., Wilson, Louise C., Janecke, Andreas R., Hurles, Matthew E., Emmet, Warren, Gardiner, Brooke, Streubel, Berthold, Dopita, Belinda, Zankl, Andreas, Kayserili, Hülya, Scambler, Peter J., Brown, Matthew A., Beales, Philip L., Wicking, Carol, Duncan, Emma L., Mitchison, Hannah M.

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An organelle-specific protein landscape identifies novel diseases and molecular mechanisms von Boldt, Karsten, van Reeuwijk, Jeroen, Lu, Qianhao, Koutroumpas, Konstantinos, Nguyen, Thanh-Minh T., Texier, Yves, van Beersum, Sylvia E. C., Horn, Nicola, Willer, Jason R., Mans, Dorus A., Dougherty, Gerard, Lamers, Ideke J. C., Coene, Karlien L. M., Arts, Heleen H., Betts, Matthew J., Beyer, Tina, Bolat, Emine, Gloeckner, Christian Johannes, Haidari, Khatera, Hetterschijt, Lisette, Iaconis, Daniela, Jenkins, Dagan, Klose, Franziska, Knapp, Barbara, Latour, Brooke, Letteboer, Stef J. F., Marcelis, Carlo L., Mitic, Dragana, Morleo, Manuela, Oud, Machteld M., Riemersma, Moniek, Rix, Susan, Terhal, Paulien A., Toedt, Grischa, van Dam, Teunis J. P., de Vrieze, Erik, Wissinger, Yasmin, Wu, Ka Man, Apic, Gordana, Beales, Philip L., Blacque, Oliver E., Gibson, Toby J., Huynen, Martijn A., Katsanis, Nicholas, Kremer, Hannie, Omran, Heymut, van Wijk, Erwin, Wolfrum, Uwe, Kepes, François, Davis, Erica E., Franco, Brunella, Giles, Rachel H., Ueffing, Marius, Russell, Robert B., Roepman, Ronald

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Nationwide variations in the execution of minimally invasive right hemicolectomy and short-term outcomes: first phase of the RIGHT study von Grüter, Alexander A J, Jongsma, Willemijn A, Leone, Nicola, Barai, Hasti, Toorenvliet, Boudewijn R, Tanis, Pieter J, Tuynman, Jurriaan B

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Meta-analysis of Parkinson's Disease: Identification of a novel locus, RIT2 von Pankratz, Nathan, Beecham, Gary W., DeStefano, Anita L., Dawson, Ted M., Doheny, Kimberly F., Factor, Stewart A., Hamza, Taye H., Hung, Albert Y., Hyman, Bradley T., Ivinson, Adrian J., Krainc, Dmitri, Latourelle, Jeanne C., Clark, Lorraine N., Marder, Karen, Martin, Eden R., Mayeux, Richard, Ross, Owen A., Scherzer, Clemens R., Simon, David K., Tanner, Caroline, Vance, Jeffery M., Wszolek, Zbigniew K., Zabetian, Cyrus P., Myers, Richard H., Payami, Haydeh, Scott, William K., Foroud, Tatiana

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ADH1B is associated with alcohol dependence and alcohol consumption in populations of European and African ancestry von Bierut, L J, Goate, A M, Breslau, N, Johnson, E O, Bertelsen, S, Fox, L, Agrawal, A, Bucholz, K K, Grucza, R, Hesselbrock, V, Kramer, J, Kuperman, S, Nurnberger, J, Porjesz, B, Saccone, N L, Schuckit, M, Tischfield, J, Wang, J C, Foroud, T, Rice, J P, Edenberg, H J

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