An fMRI study into emotional processing in Parkinson's disease: Does increased medial prefrontal activation compensate for striatal dysfunction? by Moonen, Anja J H, Weiss, Peter H, Wiesing, Michael, Weidner, Ralph, Fink, Gereon R, Reijnders, Jennifer S A M, Weber, Wim M, Leentjens, Albert F G

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A systematic review of prevalence studies of depression in Parkinson's disease by Reijnders, Jennifer S.A.M., Ehrt, Uwe, Weber, Wim E.J., Aarsland, Dag, Leentjens, Albert F.G.

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Neuroanatomical correlates of apathy in Parkinson's disease: A magnetic resonance imaging study using voxel-based morphometry by Reijnders, Jennifer S.A.M., Scholtissen, Bart, Weber, Wim E.J., Aalten, Pauline, Verhey, Frans R.J., Leentjens, Albert F.G.

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The association between specific activity components and depression in nursing home residents: the importance of the social component by Knippenberg, Inge A. H., Reijnders, Jennifer S. A. M., Gerritsen, Debby L., Leontjevas, Ruslan

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Assessment of depression in Parkinson's disease: The contribution of somatic symptoms to the clinimetric performance of the Hamilton and Montgomery–Åsberg rating scales by Reijnders, Jennifer S.A.M, Lousberg, Richel, Leentjens, Albert F.G

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Validation of diagnostic criteria for apathy in Parkinson’s disease by Drijgers, Rosa L, Dujardin, Kathy, Reijnders, Jennifer S.A.M, Defebvre, Luc, Leentjens, Albert F.G

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"Keep your brain fit!" Effectiveness of a psychoeducational intervention on cognitive functioning in healthy adults: A randomised controlled trial by Reijnders, Jennifer S. A. M., Geusgens, Chantal A. V., Ponds, Rudolf W. H. M., van Boxtel, Martin P. J.

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Effects of a Mindfulness-Based Strengths Intervention on Adolescent Mental Health are Mediated by Changes in Negative Emotions by Kennes, Anne, Lataster, Johan J. E., Janssens, Mayke, Simons, Marianne, Reijnders, Jennifer S. A. M., Jacobs, Nele E., Peeters, Sanne C. T.

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Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt Signaling by Snijders Blok, Lot, Madsen, Erik, Juusola, Jane, Gilissen, Christian, Baralle, Diana, Reijnders, Margot R.F., Venselaar, Hanka, Helsmoortel, Céline, Cho, Megan T., Hoischen, Alexander, Vissers, Lisenka E.L.M., Koemans, Tom S., Wissink-Lindhout, Willemijn, Eichler, Evan E., Romano, Corrado, Van Esch, Hilde, Stumpel, Connie, Vreeburg, Maaike, Smeets, Eric, Oberndorff, Karin, van Bon, Bregje W.M., Shaw, Marie, Gecz, Jozef, Haan, Eric, Bienek, Melanie, Jensen, Corinna, Loeys, Bart L., Van Dijck, Anke, Innes, A. Micheil, Racher, Hilary, Vermeer, Sascha, Di Donato, Nataliya, Rump, Andreas, Tatton-Brown, Katrina, Parker, Michael J., Henderson, Alex, Lynch, Sally A., Fryer, Alan, Ross, Alison, Vasudevan, Pradeep, Kini, Usha, Newbury-Ecob, Ruth, Chandler, Kate, Male, Alison, Dijkstra, Sybe, Schieving, Jolanda, Giltay, Jacques, van Gassen, Koen L.I., Schuurs-Hoeijmakers, Janneke, Tan, Perciliz L., Pediaditakis, Igor, Haas, Stefan A., Retterer, Kyle, Reed, Patrick, Monaghan, Kristin G., Haverfield, Eden, Natowicz, Marvin, Myers, Angela, Kruer, Michael C., Stein, Quinn, Strauss, Kevin A., Brigatti, Karlla W., Keating, Katherine, Burton, Barbara K., Kim, Katherine H., Charrow, Joel, Norman, Jennifer, Foster-Barber, Audrey, Kline, Antonie D., Kimball, Amy, Zackai, Elaine, Harr, Margaret, Fox, Joyce, McLaughlin, Julie, Lindstrom, Kristin, Haude, Katrina M., van Roozendaal, Kees, Brunner, Han, Chung, Wendy K., Kooy, R. Frank, Pfundt, Rolph, Kalscheuer, Vera, Mehta, Sarju G., Katsanis, Nicholas, Kleefstra, Tjitske

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De Novo Missense Mutations in DHX30 Impair Global Translation and Cause a Neurodevelopmental Disorder by Lessel, Davor, Schob, Claudia, Küry, Sébastien, Reijnders, Margot R.F., Harel, Tamar, Eldomery, Mohammad K., Coban-Akdemir, Zeynep, Denecke, Jonas, Edvardson, Shimon, Colin, Estelle, Stegmann, Alexander P.A., Gerkes, Erica H., Tessarech, Marine, Bonneau, Dominique, Barth, Magalie, Besnard, Thomas, Cogné, Benjamin, Revah-Politi, Anya, Strom, Tim M., Rosenfeld, Jill A., Yang, Yaping, Posey, Jennifer E., Immken, LaDonna, Oundjian, Nelly, Helbig, Katherine L., Meeks, Naomi, Zegar, Kelsey, Morton, Jenny, the DDD study, Schieving, Jolanda H., Claasen, Ana, Huentelman, Matthew, Narayanan, Vinodh, Ramsey, Keri, Brunner, Han G., Elpeleg, Orly, Mercier, Sandra, Bézieau, Stéphane, Kubisch, Christian, Kleefstra, Tjitske, Kindler, Stefan, Lupski, James R., Kreienkamp, Hans-Jürgen

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Expanding the neurodevelopmental phenotype of PURA syndrome by Lee, Bo Hoon, Reijnders, Margot R. F., Abubakare, Oluwatobi, Tuttle, Emily, Lape, Brynn, Minks, Kelly Q., Stodgell, Christopher, Bennetto, Loisa, Kwon, Jennifer, Fong, Chin‐To, Gripp, Karen W., Marsh, Eric D., Smith, Wendy E., Huq, Ahm M., Coury, Stephanie A., Tan, Wen‐Hann, Solis, Orestes, Mehta, Rupal I., Leventer, Richard J., Baralle, Diana, Hunt, David, Paciorkowski, Alex R.

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Complement in Reproductive White Adipose Tissue Characterizes the Obese Preeclamptic-Like BPH/5 Mouse Prior to and During Pregnancy by Olson, Kelsey N, Reijnders, Dorien, Gomes, Viviane C.L, Hebert, R. Caitlin, Liu, Chin-Chi, Stephens, Jacqueline M, Redman, Leanne M, Douglas, Nataki C, Sones, Jennifer L

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