Glioblastoma‐derived extracellular vesicles modify the phenotype of monocytic cells von de Vrij, Jeroen, Maas, S.L. Niek, Kwappenberg, Kitty M.C., Schnoor, Rosalie, Kleijn, Anne, Dekker, Lennard, Luider, Theo M., de Witte, Lot D., Litjens, Manja, van Strien, Miriam E., Hol, Elly M., Kroonen, Jerome, Robe, Pierre A., Lamfers, Martine L., Schilham, Marco W., Broekman, Marike L.D.

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Patient-specific analysis of cartilage and labrum mechanics in human hips with acetabular dysplasia von Henak, C.R, Abraham, C.L, Anderson, A.E, Maas, S.A, Ellis, B.J, Peters, C.L, Weiss, J.A

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Promote Internally or Hire Externally? The Role of Gift Exchange and Performance Measurement Precision von CHAN, ERIC W., LILL, JEREMY B., MAAS, VICTOR S.

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Spatial distribution of heavy metal concentrations in urban, suburban and agricultural soils in a Mediterranean city of Algeria von Maas, S., Scheifler, R., Benslama, M., Crini, N., Lucot, E., Brahmia, Z., Benyacoub, S., Giraudoux, P.

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Diagnostics and treatment delay in primary central nervous system lymphoma: What the neurosurgeon should know von Hasner, M. C., van Opijnen, M. P., van der Meulen, M., Verdijk, R. M., Maas, S. L. N., te Boome, L. C. J., Broekman, M. L. D.

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Validation of a personalized ligament-constraining discrete element framework for computing ankle joint contact mechanics von Peiffer, M., Duquesne, K., Van Oevelen, A., Burssens, A., De Mits, S., Maas, S.A., Atkins, P.R., Anderson, A.E., Audenaert, E.A.

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In Search of Informed Discretion: An Experimental Investigation of Fairness and Trust Reciprocity von Maas, Victor S., van Rinsum, Marcel, Towry, Kristy L.

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Genetic mutations and phenotype characteristics in peripheral vascular malformations: A systematic review von Stor, M. L. E., Horbach, S. E. R., Lokhorst, M. M., Tan, E., Maas, S. M., Noesel, C. J. M., van der Horst, C. M. A. M.

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A genome-wide DNA methylation signature for SETD1B-related syndrome von Krzyzewska, I M, Maas, S M, Henneman, P, Lip, K V D, Venema, A, Baranano, K, Chassevent, A, Aref-Eshghi, E, van Essen, A J, Fukuda, T, Ikeda, H, Jacquemont, M, Kim, H-G, Labalme, A, Lewis, S M E, Lesca, G, Madrigal, I, Mahida, S, Matsumoto, N, Rabionet, R, Rajcan-Separovic, E, Qiao, Y, Sadikovic, B, Saitsu, H, Sweetser, D A, Alders, M, Mannens, M M A M

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A comparative overview of microwave and wireless power-amplifier behavioral modeling approaches von Pedro, J.C., Maas, S.A.

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Inter-relationships of cotton plant height, canopy width, ground cover and plant nitrogen status indicators von Muharam, F.M., Bronson, K.F., Maas, S.J., Ritchie, G.L.

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Haploinsufficiency for ANKRD11-flanking genes makes the difference between KBG and 16q24.3 microdeletion syndromes: 12 new cases von Novara, Francesca, Rinaldi, Berardo, Sisodiya, Sanjay M, Coppola, Antonietta, Giglio, Sabrina, Stanzial, Franco, Benedicenti, Francesco, Donaldson, Alan, Andrieux, Joris, Stapleton, Rachel, Weber, Astrid, Reho, Paolo, van Ravenswaaij-Arts, Conny, Kerstjens-Frederikse, Wilhelmina S, Vermeesch, Joris Robert, Devriendt, Koenraad, Bacino, Carlos A, Delahaye, Andrée, Maas, S M, Iolascon, Achille, Zuffardi, Orsetta

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How CFOs Determine Management Accounting Innovation: An Examination of Direct and Indirect Effects von Naranjo-Gil, David, Maas, Victor S., Hartmann, Frank G. H.

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Genome-wide methylation profiling of Beckwith-Wiedemann syndrome patients without molecular confirmation after routine diagnostics von Krzyzewska, I M, Alders, M, Maas, S M, Bliek, J, Venema, A, Henneman, P, Rezwan, F I, Lip, K V D, Mul, A N, Mackay, D J G, Mannens, M M A M

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The association between medication use and gait in adults with intellectual disabilities von Maas, S., Festen, D. A. M., Hilgenkamp, T. I. M., Oppewal, A.

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Surgical treatment of macroglossia in patients with Beckwith–Wiedemann syndrome: a 20-year experience and review of the literature von Kadouch, D.J.M, Maas, S.M, Dubois, L, van der Horst, C.M.A.M

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The natural history and genotype–phenotype correlations of TMPRSS3 hearing loss: an international, multi-center, cohort analysis von Colbert, Brett M., Lanting, Cris, Smeal, Molly, Blanton, Susan, Dykxhoorn, Derek M., Tang, Pei-Ciao, Getchell, Richard L., Velde, Hedwig, Fehrmann, Mirthe, Thorpe, Ryan, Chapagain, Prem, Elkhaligy, Heidy, Kremer, Hannie, Yntema, Helger, Haer-Wigman, Lonneke, Redfield, Shelby, Sun, Tieqi, Bruijn, Saskia, Plomp, Astrid, Goderie, Thadé, van de Kamp, Jiddeke, Free, Rolien H., Wassink-Ruiter, Jolien Klein, Widdershoven, Josine, Vanhoutte, Els, Rotteveel, Liselotte, Kriek, Marjolein, van Dooren, Marieke, Hoefsloot, Lies, de Gier, Heriette H. W., Schaefer, Amanda, Kolbe, Diana, Azaiez, Hela, Rabie, Grace, Aburayyan, Armal, Kawas, Mariana, Kanaan, Moien, Holder, Jourdan, Usami, Shin-ichi, Chen, Zhengyi, Dai, Pu, Holt, Jeffrey, Nelson, Rick, Choi, Byung Yoon, Shearer, Eliot, Smith, Richard J. H., Pennings, Ronald, Liu, Xue Zhong

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Finding partners in crime? How transparency about managers’ behavior affects employee collusion von Maas, Victor S., Yin, Huaxiang

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Exploring the missing heritability in subjects with hearing loss, enlarged vestibular aqueducts, and a single or no pathogenic SLC26A4 variant von Smits, Jeroen J., de Bruijn, Suzanne E., Lanting, Cornelis P., Oostrik, Jaap, O’Gorman, Luke, Mantere, Tuomo, Cremers, Frans P. M., Roosing, Susanne, Yntema, Helger G., de Vrieze, Erik, Derks, Ronny, Hoischen, Alexander, Pegge, Sjoert A. H., Neveling, Kornelia, Pennings, Ronald J. E., Kremer, Hannie

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Enlarged nuchal translucency in chromosomally normal fetuses: strong association with orofacial clefts von Timmerman, E., Pajkrt, E., Maas, S. M., Bilardo, C. M.

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