Sequential Regulation of the Small GTPase Rap1 in Human Platelets by Franke, Barbara, van Triest, Miranda, de Bruijn, Kim M. T., van Willigen, Gijsbert, Nieuwenhuis, H. Karel, Negrier, Claude, Akkerman, Jan-Willem N., Bos, Johannes L.

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Recent Developments in the International Restructuring Market from a Dutch Law Perspective by Gallagher, Adam, Vroom, Vincent, Bruijn, Kim De

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Investigating the efficacy of integrated cognitive behavioral therapy for adult treatment seeking substance use disorder patients with comorbid ADHD: study protocol of a randomized... by van Emmerik-van Oortmerssen, Katelijne, Vedel, Ellen, Koeter, Maarten W, de Bruijn, Kim, Dekker, Jack J M, van den Brink, Wim, Schoevers, Robert A

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The DNA-binding factor Ctcf critically controls gene expression in macrophages by Nikolic, Tatjana, Movita, Dowty, Lambers, Margaretha EH, de Almeida, Claudia Ribeiro, Biesta, Paula, Kreefft, Kim, de Bruijn, Marjolein JW, Bergen, Ingrid, Galjart, Niels, Boonstra, Andre, Hendriks, Rudi

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A novel Alzheimer disease locus located near the gene encoding tau protein by Jun, G, Ibrahim-Verbaas, C A, Vronskaya, M, Chung, J, Naj, A C, Kunkle, B W, Wang, L-S, Bis, J C, Bellenguez, C, Harold, D, Destefano, A L, Grenier-Boley, B, Sims, R, Smith, A V, Chouraki, V, Hamilton-Nelson, K L, Ikram, M A, Fievet, N, Martin, E R, Kamatani, Y, Valladares, O, Laza, A R, Zelenika, D, Choi, S-H, Boland, A, Becker, T, Kukull, W A, van der Lee, S J, Pasquier, F, Cruchaga, C, Beekly, D, Fitzpatrick, A L, Hanon, O, Gill, M, Gudnason, V, Campion, D, Love, S, Bennett, D A, Amin, N, Berr, C, Tsolaki, Magda, Buxbaum, J D, Lopez, O L, Deramecourt, V, Fox, N C, Cantwell, L B, Tárraga, L, Dufouil, C, Hardy, J, Crane, P K, Eiriksdottir, G, Hannequin, D, Clarke, R, Evans, D, Mosley, T H, Letenneur, L, Brayne, C, Maier, W, De Jager, P, Dartigues, J-F, Hampel, H, de Bruijn, R F A G, Tzourio, C, Pastor, P, Larson, E B, O'Donovan, M C, Montine, T J, Nalls, M A, Mead, S, Reiman, E M, Jonsson, P V, St George-Hyslop, P H, Boada, M, Passmore, P, Wendland, J R, Schmidt, R, Morgan, K, Powell, J F, Carasquillo, M, Jakobsdóttir, J, Kauwe, J S K, Rujescu, D, Nöthen, M M, Hofman, A, Jones, L, Haines, J L, Psaty, B M, Van Broeckhoven, C, Holmans, P, Launer, L J, Mayeux, R, Goate, A M, Escott-Price, V, Seshadri, S, Pericak-Vance, M A, Amouyel, P, Williams, J, van Duijn, C M, Schellenberg, G D, Farrer, L A

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Feasibility of whole‐genome sequencing‐based tumor diagnostics in routine pathology practice by Samsom, Kris G, Schipper, Luuk J, Roepman, Paul, Bosch, Linda JW, Lalezari, Ferry, Klompenhouwer, Elisabeth G, Langen, Adrianus J, Buffart, Tineke E, Riethorst, Immy, Schoenmaker, Lieke, Schout, Daoin, Noort, Vincent, Berg, Jose G, Bruijn, Ewart, Hoeven, Jacobus JM, Snellenberg, Hans, Kolk, Lizet E, Cuppen, Edwin, Voest, Emile E, Meijer, Gerrit A, Monkhorst, Kim

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Testing the effects of message framing, kernel state, and exercise guideline adherence on exercise intentions and resolve by de Bruijn, Gert-Jan, Out, Kim, Rhodes, Ryan E.

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Protective role of chaperone-mediated autophagy against atherosclerosis by Madrigal-Matute, Julio, de Bruijn, Jenny, van Kuijk, Kim, Riascos-Bernal, Dario F, Diaz, Antonio, Tasset, Inmaculada, Martín-Segura, Adrián, Gijbels, Marion J J, Sander, Bianca, Kaushik, Susmita, Biessen, Erik A L, Tiano, Simoni, Bourdenx, Mathieu, Krause, Gregory J, McCracken, Ian, Baker, Andrew H, Jin, Han, Sibinga, Nicholas E S, Bravo-Cordero, Jose Javier, Macian, Fernando, Singh, Rajat, Rensen, Patrick C N, Berbée, Jimmy F P, Pasterkamp, Gerard, Sluimer, Judith C, Cuervo, Ana Maria

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Deficiency of myeloid PHD proteins aggravates atherogenesis via macrophage apoptosis and paracrine fibrotic signalling by van Kuijk, Kim, Demandt, Jasper A F, Perales-Patón, Javier, Theelen, Thomas L, Kuppe, Christoph, Marsch, Elke, de Bruijn, Jenny, Jin, Han, Gijbels, Marion J, Matic, Ljubica, Mees, Barend M E, Reutelingsperger, Chris P M, Hedin, Ulf, Biessen, Erik A L, Carmeliet, Peter, Baker, Andrew H, Kramann, Rafael K, Schurgers, Leon J, Saez-Rodriguez, Julio, Sluimer, Judith C

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Sublethal consequences of urban life for wild vertebrates by Birnie-Gauvin, Kim, Peiman, Kathryn S., Gallagher, Austin J., de Bruijn, Robert, Cooke, Steven J.

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Genre Conventions of Fact-Checks: Topics, Style, and Form of Fact-Checking in Two IFCN-Certified News Media by Verhoeven, Kim, Paulussen, Steve, de Bruijn, Gert-Jan

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HLA and KIR genetic association and NK cells in anti-NMDAR encephalitis by Peris Sempere, Vicente, Luo, Guo, Muñiz-Castrillo, Sergio, Pinto, Anne-Laurie, Picard, Géraldine, Rogemond, Véronique, Titulaer, Maarten J, Finke, Carsten, Leypoldt, Frank, Kuhlenbäumer, Gregor, Jones, Hannah F, Dale, Russell C, Binks, Sophie, Irani, Sarosh R, Bastiaansen, Anna E, de Vries, Juna M, de Bruijn, Marienke A A M, Roelen, Dave L, Kim, Tae-Joon, Chu, Kon, Lee, Soon-Tae, Kanbayashi, Takamichi, Pollock, Nicholas R, Kichula, Katherine M, Mumme-Monheit, Abigail, Honnorat, Jérôme, Norman, Paul J, Mignot, Emmanuel

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ABCA4 c.6480-35A>G, a novel branchpoint variant associated with Stargardt disease by Rodríguez-Hidalgo, María, de Bruijn, Suzanne E., Corradi, Zelia, Rodenburg, Kim, Lara-López, Araceli, Valverde-Megías, Alicia, Ávila-Fernández, Almudena, Fernandez-Caballero, Lidia, Del Pozo-Valero, Marta, Corominas, Jordi, Gilissen, Christian, Irigoyen, Cristina, Cremers, Frans P. M., Ayuso, Carmen, Ruiz-Ederra, Javier, Roosing, Susanne

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Chronic exertional compartment syndrome in the differential diagnosis of peripheral artery disease in older patients with exercise-induced lower limb pain by de Bruijn, Johan A., Wijns, Kim C.A., van Kuijk, Sander M.J., Hoogeveen, Adwin R., Teijink, Joep A.W., Scheltinga, Marc R.M.

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A Comprehensive Pan-Cancer Molecular Study of Gynecologic and Breast Cancers by Berger, Ashton C., Gunaratne, Preethi H., Wang, Chen, Kuderer, Nicole M., Ojesina, Akinyemi I., Chen, Ting-Wen, Liu, Liang, Vellano, Christopher P., Caesar-Johnson, Samantha J., Demchok, John A., Kasapi, Melpomeni, Ferguson, Martin L., Yang, Liming, Gehlenborg, Nils, Noble, Michael S., Dhankani, Varsha, Knijnenburg, Theo, Liu, Yuexin, Kanchi, Rupa S., Ling, Shiyun, de Bruijn, Ino, Heins, Zachary J., Ladanyi, Marc, Sun, Yichao, Dhalla, Noreen, Mungall, Andrew J., Sipahimalani, Payal, Beroukhim, Rameen, Kucherlapati, Raju S., Danilova, Ludmila, Bootwalla, Moiz S., Maglinte, Dennis T., Fan, Cheng, Covington, Kyle, Donehower, Lawrence A., Drummond, Jennifer, Liu, Xiuping, Hess, Julian, Appelbaum, Elizabeth L., Bailey, Matthew, Fulton, Lucinda A., Kandoth, Cyriac, Mardis, Elaine R., Penny, Robert, Lichtenberg, Tara M., Zmuda, Erik, de Carvalho, Ana C., Fregnani, José H., Barnholtz-Sloan, Jill S., Eckman, John, Rabeno, Brenda, Bergeron, Alain, Desjardins, Laurence, Sastre, Xavier, Bigner, Darell, McLendon, Roger, Secord, Angeles, Brat, Daniel J., Force, Seth, Khuri, Fadlo, Zwarthoff, Ellen C., Finocchiaro, Gaetano, Perin, Alessandro, Wiznerowicz, Maciej, Baudin, Eric, Noushmehr, Houtan, Birrer, Michael, Copland, John A., Ho, Thai, Zhang, Lizhi, Meric-Bernstam, Funda, Sood, Anil, Carter, Candace, Shannon, Kerwin, Mirsaidi, Cyrus, Zaren, Howard, Hung, Nguyen Phi, Metwalli, Adam R., Tcaciuc, Diana, Rassl, Doris M., Farver, Carol, Schilero, Cathy, Manikhas, George, Janssen, Klaus-Peter, Abdel-Rahman, Mohamed H., Lehman, Norman L., Mandt, Randy, Nguyen, Phuong, Rai, Karan, Powers, James, Fehrenbach, Ashley, von Deimling, Andreas, Galbraith, Joseph, Adebamowo, Sally N., Boussioutas, Alex, Zuna, Rosemary, Rubin, Mark A., Weinstein, John N., Levine, Douglas A., Akbani, Rehan

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Principles of regulatory information conservation between mouse and human by Cheng, Yong, Ma, Zhihai, Kim, Bong-Hyun, Wu, Weisheng, Cayting, Philip, Boyle, Alan P., Sundaram, Vasavi, Xing, Xiaoyun, Dogan, Nergiz, Li, Jingjing, Euskirchen, Ghia, Lin, Shin, Lin, Yiing, Visel, Axel, Kawli, Trupti, Yang, Xinqiong, Patacsil, Dorrelyn, Keller, Cheryl A., Giardine, Belinda, The Mouse ENCODE Consortium, Kundaje, Anshul, Wang, Ting, Pennacchio, Len A., Weng, Zhiping, Hardison, Ross C., Snyder, Michael P.

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Next-generation sequencing to genetically diagnose a diverse range of inherited eye disorders in 15 consanguineous families from Pakistan by Basharat, Rabia, de Bruijn, Suzanne E., Zahid, Muhammad, Rodenburg, Kim, Hitti-Malin, Rebekkah J., Rodríguez-Hidalgo, María, Boonen, Erica G.M., Jarral, Afeefa, Mahmood, Arif, Corominas, Jordi, Khalil, Sharqa, Zai, Jawaid Ahmed, Ali, Ghazanfar, Ruiz-Ederra, Javier, Gilissen, Christian, Cremers, Frans P.M., Ansar, Muhammad, Panneman, Daan M., Roosing, Susanne

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CARMN Loss Regulates Smooth Muscle Cells and Accelerates Atherosclerosis in Mice by Vacante, Francesca, Rodor, Julie, Lalwani, Mukesh K., Mahmoud, Amira D., Bennett, Matthew, De Pace, Azzurra L., Miller, Eileen, Van Kuijk, Kim, de Bruijn, Jenny, Gijbels, Marion, Williams, Thomas C., Clark, Michael B., Scanlon, Jessica P., Doran, Amanda C., Montgomery, Rusty, Newby, David E., Giacca, Mauro, O’Carroll, Dónal, Hadoke, Patrick W.F., Denby, Laura, Sluimer, Judith C., Baker, Andrew H.

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Pre- and perinatal complications in relation to Tourette syndrome and co-occurring obsessive-compulsive disorder and attention-deficit/hyperactivity disorder by Abdulkadir, Mohamed, Tischfield, Jay A, King, Robert A, Fernandez, Thomas V, Brown, Lawrence W, Cheon, Keun-Ah, Coffey, Barbara J, de Bruijn, Sebastian F.T.M, Elzerman, Lonneke, Garcia-Delgar, Blanca, Gilbert, Donald L, Grice, Dorothy E, Hagstrøm, Julie, Hedderly, Tammy, Heyman, Isobel, Hong, Hyun Ju, Huyser, Chaim, Ibanez-Gomez, Laura, Kim, Young Key, Kim, Young-Shin, Koh, Yun-Joo, Kook, Sodahm, Kuperman, Samuel, Lamerz, Andreas, Leventhal, Bennett, Ludolph, Andrea G, Madruga-Garrido, Marcos, Maras, Athanasios, Messchendorp, Marieke D, Mir, Pablo, Morer, Astrid, Münchau, Alexander, Murphy, Tara L, Openneer, Thaïra J.C, Plessen, Kerstin J, Rath, Judith J.G, Roessner, Veit, Fründt, Odette, Shin, Eun-Young, Sival, Deborah A, Song, Dong-Ho, Song, Jungeun, Stolte, Anne-Marie, Tübing, Jennifer, van den Ban, Els, Visscher, Frank, Wanderer, Sina, Woods, Martin, Zinner, Samuel H, State, Matthew W, Heiman, Gary A, Hoekstra, Pieter J, Dietrich, Andrea

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Whole genome sequencing identifies elusive variants in genetically unsolved Italian inherited retinal disease patients by Zeuli, Roberta, Karali, Marianthi, de Bruijn, Suzanne E., Rodenburg, Kim, Scarpato, Margherita, Capasso, Dalila, Astuti, Galuh D.N., Gilissen, Christian, Rodríguez-Hidalgo, María, Ruiz-Ederra, Javier, Testa, Francesco, Simonelli, Francesca, Cremers, Frans P.M., Banfi, Sandro, Roosing, Susanne

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