Contribution of common and rare genetic variants in CEP72 on vincristine‐induced peripheral neuropathy in brain tumour patients

por 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, te Loo, D. Maroeska W. M., Coenen, Marieke J. H.
Publicado 2022

Genetic Variants as Predictive Markers for Ototoxicity and Nephrotoxicity in Patients with Locally Advanced Head and Neck Cancer Treated with Cisplatin-Containing Chemoradiotherapy...

por 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.
Publicado 2019

MAOA‐VNTR genotype affects structural and functional connectivity in distributed brain networks

por Harneit, Anais, Braun, Urs, Geiger, Lena S., Zang, Zhenxiang, Hakobjan, Marina, van 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
Publicado 2019

Whole Exome Sequencing in Multi-Incident Families Identifies Novel Candidate Genes for Multiple Sclerosis

por 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
Publicado 2022