Brunner syndrome associated MAOA mutations result in NMDAR hyperfunction and increased network activity in human dopaminergic neurons von van Rhijn, Jon-Ruben, Shi, Yan, Bormann, Maren, Mossink, Britt, Frega, Monica, Recaioglu, Hatice, Hakobjan, Marina, Klein Gunnewiek, Teun, Schoenmaker, Chantal, Palmer, Elizabeth, Faivre, Laurence, Kittel-Schneider, Sarah, Schubert, Dirk, Brunner, Han, Franke, Barbara, Nadif Kasri, Nael

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Whole Exome Sequencing in Multi-Incident Families Identifies Novel Candidate Genes for Multiple Sclerosis von Horjus, Julia, van Mourik-Banda, Tineke, Heerings, Marco A. P., Hakobjan, Marina, De Witte, Ward, Heersema, Dorothea J., Jansen, Anne J., Strijbis, Eva M. M., de Jong, Brigit A., Slettenaar, Astrid E. J., Zeinstra, Esther M. P. E., Hoogervorst, Erwin L. J., Franke, Barbara, Kruijer, Wiebe, Jongen, Peter J., Visser, Leo J., Poelmans, Geert

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Replication of a genetic variant in ACYP2 associated with cisplatin-induced hearing loss in patients with osteosarcoma von Vos, Hanneke I, Guchelaar, Henk-Jan, Gelderblom, Hans, de Bont, Eveline S.J.M, Kremer, Leontien C.M, Naber, Anne Marlies, Hakobjan, Marina H, van der Graaf, Winette T.A, Coenen, Marieke J.H, te Loo, Dunja Maroeska W.M

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Genetic Variants as Predictive Markers for Ototoxicity and Nephrotoxicity in Patients with Locally Advanced Head and Neck Cancer Treated with Cisplatin-Containing Chemoradiotherapy... von Driessen, Chantal M, Ham, Janneke C, Te Loo, Maroeska, van Meerten, Esther, van Lamoen, Maurits, Hakobjan, Marina H, Takes, Robert P, van der Graaf, Winette T, Kaanders, Johannes H, Coenen, Marieke J H, van Herpen, Carla M

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DNA methylation associated with persistent ADHD suggests TARBP1 as novel candidate von Weiß, Annika L., Meijer, Mandy, Budeus, Bettina, Pauper, Marc, Hakobjan, Marina, Groothuismink, Johanne, Shi, Yan, Neveling, Kornelia, Buitelaar, Jan K., Hoogman, Martine, Franke, Barbara, Klein, Marieke

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Brunner syndrome associated MAOA mutations result in NMDAR hyperfunction and increased network activity in human dopaminergic neurons von Van Rhijn, Jon-Ruben, Shi, Yan, Bormann, Maren, Mossink, Britt, Frega, Monica, Recaioglu, Hatice, Hakobjan, Marina, Gunnewiek, Teun Klein, Schoenmaker, Chantal, Palmer, Elizabeth, Faivre, Laurence, Kittel-Schneider, Sarah, Schubert, Dirk, Brunner, Han, Franke, Barbara, Kasri, Nael Nadif

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Contribution of common and rare genetic variants in CEP72 on vincristine‐induced peripheral neuropathy in brain tumour patients von Klumpers, Marije J., Brand, Annouk C. A. M., Hakobjan, Marina, Gattuso, Giovanna, Schiavello, Elisabetta, Terenziani, Monica, Massimino, Maura, Gidding, Corrie E. M., Guchelaar, Henk‐Jan, Loo, D. Maroeska W. M., Coenen, Marieke J. H.

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MAOA‐VNTR genotype affects structural and functional connectivity in distributed brain networks von Harneit, Anais, Braun, Urs, Geiger, Lena S., Zang, Zhenxiang, Hakobjan, Marina, Donkelaar, Marjolein M. J., Schweiger, Janina I., Schwarz, Kristina, Gan, Gabriela, Erk, Susanne, Heinz, Andreas, Romanczuk‐Seiferth, Nina, Witt, Stephanie, Rietschel, Marcella, Walter, Henrik, Franke, Barbara, Meyer‐Lindenberg, Andreas, Tost, Heike

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BDNF polymorphism associates with decline in set shifting in Parkinson's disease von van der Kolk, Nicolien M, Speelman, Arlene D, van Nimwegen, Marlies, Kessels, Roy P.C, IntHout, Joanna, Hakobjan, Marina, Munneke, Marten, Bloem, Bastiaan R, van de Warrenburg, Bart P

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F12AGGRESSION IN A DISH: A HUMAN MODEL FOR BRUNNER SYNDROME REVEALS INCREASED NEURONAL NETWORK ACTIVITY OF DOPAMINERGIC NEURONS von Shi, Yan, van Rhijn, Jon-Ruben, Bormann, Maren, Mossink, Britt, Frega, Monica, Hakobjan, Marina, Kittel-Schneider, Sarah, Keller, Jason, Schubert, Dirk, Brunner, Han, Franke, Barbara, Kasri, Nael Nadif

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Female‐specific association of NOS 1 genotype with white matter microstructure in ADHD patients and controls von van Ewijk, Hanneke, Bralten, Janita, van Duin, Esther D.A., Hakobjan, Marina, Buitelaar, Jan K., Heslenfeld, Dirk J., Hoekstra, Pieter J., Hartman, Catharina, Hoogman, Martine, Oosterlaan, Jaap, Franke, Barbara

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Female‐specific association of NOS1 genotype with white matter microstructure in ADHD patients and controls von Ewijk, Hanneke, Bralten, Janita, Duin, Esther D.A., Hakobjan, Marina, Buitelaar, Jan K., Heslenfeld, Dirk J., Hoekstra, Pieter J., Hartman, Catharina, Hoogman, Martine, Oosterlaan, Jaap, Franke, Barbara

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Exploration of Shared Genetic Architecture Between Subcortical Brain Volumes and Anorexia Nervosa von Walton, E., Hibar, D., Yilmaz, Z., Jahanshad, N., Cheung, J., Batury, V.-L., Seitz, J., Bulik, C. M., Thompson, P. M., Ehrlich, Stefan

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Sequencing of the DKK1 gene in patients with anorectal malformations and hypospadias von van de Putte, Romy, Wijers, Charlotte H. W., de Blaauw, Ivo, Feitz, Wout F. J., Marcelis, Carlo L. M., Hakobjan, Marina, Sloots, Cornelius E. J., van Bever, Yolande, Brunner, Han G., Roeleveld, Nel, van Rooij, Iris A. L. M., van der Zanden, Loes F. M.

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Genetic Variation in Ataxia Gene ATXN7 Influences Cerebellar Grey Matter Volume in Healthy Adults von van der Heijden, Charlotte D. C. C., Rijpkema, Mark, Arias-Vásquez, Alejandro, Hakobjan, Marina, Scheffer, Hans, Fernandez, Guillen, Franke, Barbara, van de Warrenburg, Bart P.

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