A novel mutation in COQ2 leading to fatal infantile multisystem disease von Jakobs, Bernadette S, van den Heuvel, Lambert P, Smeets, Roel J.P, de Vries, Maaike C, Hien, Steffen, Schaible, Thomas, Smeitink, Jan A.M, Wevers, Ron A, Wortmann, Saskia B, Rodenburg, Richard J.T

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SDHA mutations causing a multisystem mitochondrial disease: novel mutations and genetic overlap with hereditary tumors von Renkema, G Herma, Wortmann, Saskia B, Smeets, Roel J, Venselaar, Hanka, Antoine, Marion, Visser, Gepke, Ben-Omran, Tawfeg, van den Heuvel, Lambert P, Timmers, Henri J L M, Smeitink, Jan A, Rodenburg, Richard J T

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A mutation in the human CBP4 ortholog UQCC3 impairs complex III assembly, activity and cytochrome b stability von Wanschers, Bas F J, Szklarczyk, Radek, van den Brand, Mariël A M, Jonckheere, An, Suijskens, Janneke, Smeets, Roel, Rodenburg, Richard J, Stephan, Katharina, Helland, Ingrid B, Elkamil, Areej, Rootwelt, Terje, Ott, Martin, van den Heuvel, Lambert, Nijtmans, Leo G, Huynen, Martijn A

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Character Constellations : Representations of Social Groups in Present-Day Dutch Literary Fiction von Smeets, Roel

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Modeling Conflict: Representations of Social Groups in Present-Day Dutch Literature von Smeets, Roel, De Pourcq, Maarten, van den Bosch, Antal

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Branding Books Across the Ages: Strategies and Key Concepts in Literary Branding

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The Canon of Dutch Literature According to Google von Lucas van der Deijl, Antal van den Bosch, Roel Smeets

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Imagined social structures: Mirrors or alternatives? A comparison between networks of characters in contemporary Dutch literature and networks of the population in the Netherlands von Volker, Beate, Smeets, Roel

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Waar is de gender bias? von Smeets, Roel

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Mutated SUCLG1 causes mislocalization of SUCLG2 protein, morphological alterations of mitochondria and an early-onset severe neurometabolic disorder von Chinopoulos, Christos, Batzios, Spyros, van den Heuvel, Lambertus P., Rodenburg, Richard, Smeets, Roel, Waterham, Hans R., Turkenburg, Marjolein, Ruiter, Jos P., Wanders, Ronald J.A., Doczi, Judit, Horvath, Gergo, Dobolyi, Arpad, Vargiami, Euthymia, Wevers, Ron A., Zafeiriou, Dimitrios

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A novel splice site mutation in neonatal carnitine palmitoyl transferase II deficiency von Smeets, Roel J P, Smeitink, Jan A M, Semmekrot, Ben A, Scholte, Hans R, Wanders, Ronald J A, van den Heuvel, Lambert P W J

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Synergistic use of glycomics and single‐molecule molecular inversion probes for identification of congenital disorders of glycosylation type‐1 von Abu Bakar, Nurulamin, Ashikov, Angel, Brum, Jaime Moritz, Smeets, Roel, Kersten, Marjan, Huijben, Karin, Keng, Wee Teik, Speck‐Martins, Carlos Eduardo, Carvalho, Daniel Rocha, Rizzo, Isabela Maria Pinto Oliveira, Mello, Walquiria Domingues, Heiner‐Fokkema, Rebecca, Gorman, Kathleen, Grunewald, Stephanie, Michelakakis, Helen, Moraitou, Marina, Martinelli, Diego, Scherpenzeel, Monique, Janssen, Mirian, Boer, Lonneke, Heuvel, Lambertus P., Thiel, Christian, Lefeber, Dirk J.

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Inactivating PAPSS2 Mutations in a Patient with Premature Pubarche von Noordam, Cees, Dhir, Vivek, McNelis, Joanne C, Schlereth, Florian, Hanley, Neil A, Krone, Nils, Smeitink, Jan A, Smeets, Roel, Sweep, Fred C.G.J, Grinten, Hedi L. Claahsen-van der, Arlt, Wiebke

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Clonal expansion of mutated mitochondrial DNA is associated with tumor formation and complex I deficiency in the benign renal oncocytoma von Gasparre, Giuseppe, Hervouet, Eric, de Laplanche, Elodie, Demont, Jocelyne, Pennisi, Lucia Fiammetta, Colombel, Marc, Mège-Lechevallier, Florence, Scoazec, Jean-Yves, Bonora, Elena, Smeets, Roel, Smeitink, Jan, Lazar, Vladimir, Lespinasse, James, Giraud, Sophie, Godinot, Catherine, Romeo, Giovanni, Simonnet, Hélène

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Mutated SUCLG1 causes mislocalization of SUCLG2 protein, morphological alterations of mitochondria and an early-onset severe neurometabolic disorder von Chinopoulos, Christos, Batzios, Spyros, van den Heuvel, Lambertus P, Rodenburg, Richard, Smeets, Roel, Waterham, Hans R, Turkenburg, Marjolein, Ruiter, Jos P, Wanders, Ronald J.A, Doczi, Judit, Horvath, Gergo, Dobolyi, Arpad, Vargiami, Euthymia, Weverse, Ron A, Zafeiriou, Dimitrios

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Integrating glycomics and genomics uncovers SLC10A7 as essential factor for bone mineralization by regulating post-Golgi protein transport and glycosylation von Ashikov, Angel, Abu Bakar, Nurulamin, Wen, Xiao-Yan, Niemeijer, Marco, Osorio, Glentino Rodrigues Pinto, Brand-Arzamendi, Koroboshka, Hasadsri, Linda, Hansikova, Hana, Raymond, Kimiyo, Vicogne, Dorothee, Ondruskova, Nina, Simon, Marleen E.H, Pfundt, Rolph, Timal, Sharita, Beumers, Roel, Biot, Christophe, Smeets, Roel, Kersten, Marjan, Huijben, Karin, Linders, Peter T.A, van den Bogaart, Geert, van Hijum, Sacha A.F.T, Rodenburg, Richard, van den Heuvel, Lambertus P, van Spronsen, Francjan, Honzik, Tomas, Foulquier, Francois, van Scherpenzeel, Monique, Lefeber, Dirk J

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X-linked NDUFA1 gene mutations associated with mitochondrial encephalomyopathy von Fernandez-Moreira, Daniel, Ugalde, Cristina, Smeets, Roel, Rodenburg, Richard J. T., Lopez-Laso, Eduardo, Ruiz-Falco, Maria L., Briones, Paz, Martin, Miguel A., Smeitink, Jan A. M., Arenas, Joaquín

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Iron refractory iron deficiency anemia: a heterogeneous disease that is not always iron refractory von Donker, Albertine E., Schaap, Charlotte C.M., Novotny, Vera M. J., Smeets, Roel, Peters, Tessa M. A., van den Heuvel, Bert L. P., Raphael, Martine F., Rijneveld, Anita W., Appel, Inge M., Vlot, Andre J., Versluijs, A. Birgitta, van Gelder, Michel, Granzen, Bernd, Janssen, Mirian C.H., Rennings, Alexander J.M., van de Veerdonk, Frank L., Brons, Paul P.T., Bakkeren, Dirk L., Nijziel, Marten R., Vlasveld, L. Thom, Swinkels, Dorine W.

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Mapping the Demographic Landscape of Characters in Recent Dutch Prose: A Quantitative Approach to Literary Representation von van der Deijl, Lucas, Pieterse, S.A, Prinse, Marion, Smeets, Roel

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Mutations in the complex I NDUFS2 gene of patients with cardiomyopathy and encephalomyopathy von Loeffen, Jan, Elpeleg, Orly, Smeitink, Jan, Smeets, Roel, Stöckler-Ipsiroglu, Sylvia, Mandel, Hanna, Sengers, Rob, Trijbels, Frans, Van Den Heuvel, Lambert

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