A subcutaneous infection mimicking necrotizing fasciitis due to Butyricimonas virosa von De Donder, Laura, Uyttebroek, Ortwin, Van Cleven, Stijn, Berrevoet, Frederik

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Aortic valve replacement due to granulomatosis with polyangiitis: a case series von Uijtterhaegen, Gilles, De Donder, Laura, Ameloot, Eline, Lefebvre, Kristof, Van Dorpe, Jo, De Pauw, Michel, François, Katrien

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Aortic valve replacement due to granulomatosis with polyangiitis : a case series von Uijtterhaegen, Gilles, De Donder, Laura, Ameloot, Eline, Lefebvre, Kristof, Van Dorpe, Jo, De Pauw, Michel, Francois, Katrien

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Historical consciousness and controversial statues in a postcolonial world: the case of Missionary Peerke Donders (1809-1887) von Grever, Maria

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Virtual athlete or ultimate nerd? A framing analysis of eSports in Flemish printed media von De Donder, Shauny, Robeers, Timothy, Daneels, Rowan

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Comparison of organic and palynological proxies for biomass burning and vegetation in a lacustrine sediment record (Lake Allom, Fraser Island, Australia) von Schreuder, Laura T., Donders, Timme H., Mets, Anchelique, Hopmans, Ellen C., Sinninghe Damsté, Jaap S., Schouten, Stefan

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Older Chinese migrants in coronavirus pandemic: exploring risk and protective factors to increased loneliness von Pan, Honghui, Fokkema, Tineke, Switsers, Lise, Dury, Sarah, Hoens, Sylvia, De Donder, Liesbeth

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Complement Activation Levels Are Related to Disease Stage in AMD von Heesterbeek, Thomas J, Lechanteur, Yara T E, Lorés-Motta, Laura, Schick, Tina, Daha, Mohamed R, Altay, Lebriz, Liakopoulos, Sandra, Smailhodzic, Dzenita, den Hollander, Anneke I, Hoyng, Carel B, de Jong, Eiko K, Klevering, B Jeroen

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Evaluating verbal learning and memory in patients with an at-risk mental state or first episode psychosis using structural equation modelling von Egloff, Laura, Studerus, Erich, Zimmermann, Ronan, Heitz, Ulrike, Menghini-Müller, Stephanie, Ittig, Sarah, Beck, Katharina, Andreou, Christina, Borgwardt, Stefan, Riecher-Rössler, Anita

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De Novo Truncating Variants in ASXL2 Are Associated with a Unique and Recognizable Clinical Phenotype von Pena, Loren D.M., Hempel, Maja, McLaughlin, Heather M., Cho, Megan, Stong, Nicholas, Shuss, Christine M., Burrage, Lindsay C., Dhar, Shweta U., Emrick, Lisa T., Graham, Brett H., Lalani, Seema R., Lewis, Richard A., Posey, Jennifer E., Hanchard, Neil A., Mercedes, Alejandro E., Wangler, Michael F., Muzny, Donna M., Ward, Patricia A., Ramoni, Rachel B., McCray, Alexa T., Mazur, Paul, Splinter, Kimberly, Esteves, Cecilia, Jiang, Yong-hui, Pena, Loren D.M., McConkie-Rosell, Allyn, Schoch, Kelly, Spillmann, Rebecca C., Goldstein, David B., Loscalzo, Joseph, Rodan, Lance H., Walsh, Chris A., Cooper, Cynthia M., Donnell-Fink, Laurel A., Krieg, Elizabeth L., Lincoln, Sharyn A., Worthey, Elizabeth A., Lazar, Joe, Handley, Lori H., Newberry, J. Scott, Schroeder, Molly C., Brown, Donna M., Levy, Shawn E., Dorset, Dan C., Jones, Angela L., Manolio, Teri A., Wise, Anastasia L., Eckstein, David J., Krasnewich, Donna M., Loomis, Carson R., Iglesias, Brenda, Martin, Casey, Koeller, David M., Ashley, Euan A., Zornio, Patricia A., Nelson, Stan F., Palmer, Christina G.S., Allard, Patrick, Dell Angelica, Esteban C., Lee, Hane, Papp, Jeanette C., Dorrani, Naghmeh, Draper, David D., Estwick, Tyra, Gahl, William A., Gartner, Valerie, Godfrey, Rena A., Goheen, Mitchell, Johnston, Jean M., Latham, Lea, Macnamara, Ellen F., Maduro, Valerie V., Malicdan, May V., McCarty, Alexandra J., Murphy, Jennifer L., Novacic, Donna, Pusey, Barbara N., Sadozai, Sarah, Schaffer, Katherine E., Sharma, Prashant, Soldatos, Ariane G., Tifft, Cynthia J., Tolman, Nathanial J., Toro, Camilo, Wahl, Colleen E., Weech, Alec A., Yu, Guoyun, Hamid, Rizwan, Bellet, Jane S., Keels, Martha Ann, El-Dairi, Maysantoine, Stumpel, Constance T.R.M., Klinkenberg, Sylvia, Oberndorff, Karin, Petrovski, Slavé, Kuismin, Outi, Korpi-Heikkilä, Satu, Kurki, Mitja I., Hoischen, Alexander, Goldstein, David B.

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De Novo Truncating Mutations in WASF1 Cause Intellectual Disability with Seizures von Duarte, Sofia T., Charles, Perinne, Pfundt, Rolph, van Bokhoven, Hans, van Ravenswaaij-Arts, Conny, Morrell, Nicholas W., Thrasher, Adrian, Fletcher, Debra, Veltman, Marijke, Davis, John, Frary, Amy, Martin, Jennifer M., Collins, Janine, Favier, Remi, Hart, Daniel, Heemskerk, Johan W.M., Liesner, Ri, Mangles, Sarah, Roughley, Catherine, Tait, R. Campbell, Thachil, Jecko, Van Geet, Chris, De Vries, Minka, Warner, Timothy Q., Furnell, Abigail, Mapeta, Rutendo, Whitehorn, Deborah, Daugherty, Louise, Deevi, Sri V.V., Hu, Fengyuan, Matser, Vera, Megy, Karyn, Tuna, Salih, von Ziegenweldt, Julie, Haimel, Matthias, Richardson, Sylvia, Rankin, Stuart, Anderson, Julie, Stock, Sophie, Armstrong, Ruth, Bitner-Glindzicz, Maria, Brady, Angie, Clement, Emma, Firth, Helen, Flinter, Frances, French, Courtney, Holder, Muriel, Hurst, Jane, Josifova, Dragana, Krishnakumar, Deepa, Kurian, Manju A., Mehta, Sarju, Moore, Anthony, Rankin, Julia, Reid, Evan, Scott, Richard, Thomas, Ellen, Wassmer, Evangeline, Creaser-Myers, Amanda, Gall, Henning, Ghataorhe, Pavandeep K., Houweling, Arjan C., in’t Veld, Anna Huis, Ross, Rob V. Mackenzie, Rhodes, Christopher J., Soubrier, Florent, Treacy, Carmen M., Vonk Noordegraaf, Anton, Antrobus, Richard, Arumugakani, Gururaj, Bibi, Shahnaz, Devlin, Lisa, Ghurye, Rohit, Grigoriadou, Sofia, Harper, Lorraine, Herwadkar, Archana, Jolles, Stephen, Kumararatne, Dinakantha, Lorenzo, Lorena, Murng, Sai, Nejentsev, Sergey, Quinti, Isabella, Samarghitean, Crina, Savic, Sinisa, Yong, Patrick, Ancliff, Phil, Layton, Mark, Mead, Adam, Roy, Noémi, Chambers, Jenny, Estiu, Cecelia, Simpson, Michael, Emmerson, Ingrid, McCarthy, Mark, Van Zuydam, Natalie, Afzal, Maryam, Colby, Elizabeth, Boycott, Kym M., Majewski, Jacek, Dyment, David

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Whole-Exome Sequencing in Age-Related Macular Degeneration Identifies Rare Variants in COL8A1, a Component of Bruch’s Membrane von Corominas, Jordi, Colijn, Johanna M., Geerlings, Maartje J., Pauper, Marc, Bakker, Bjorn, Amin, Najaf, Lores Motta, Laura, Kersten, Eveline, Garanto, Alejandro, Verlouw, Joost A.M., van Rooij, Jeroen G.J., Kraaij, Robert, de Jong, Paulus T.V.M., Hofman, Albert, Vingerling, Johannes R., Schick, Tina, Fauser, Sascha, de Jong, Eiko K., van Duijn, Cornelia M., Hoyng, Carel B., Klaver, Caroline C.W., den Hollander, Anneke I.

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Association of Genetic Variants With Response to Anti–Vascular Endothelial Growth Factor Therapy in Age-Related Macular Degeneration von Lorés-Motta, Laura, Riaz, Moeen, Grunin, Michelle, Corominas, Jordi, van Asten, Freekje, Pauper, Marc, Leenders, Mathieu, Richardson, Andrea J, Muether, Philipp, Cree, Angela J, Griffiths, Helen L, Pham, Connie, Belanger, Marie-Claude, Meester-Smoor, Magda A, Ali, Manir, Heid, Iris M, Fritsche, Lars G, Chakravarthy, Usha, Gale, Richard, McKibbin, Martin, Inglehearn, Chris F, Schlingemann, Reinier O, Omar, Amer, Chen, John, Koenekoop, Robert K, Fauser, Sascha, Guymer, Robyn H, Hoyng, Carel B, de Jong, Eiko K, Lotery, Andrew J, Mitchell, Paul, den Hollander, Anneke I, Baird, Paul N, Chowers, Itay

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Complement C3 Associates With Incidence of Diabetes, but No Evidence of a Causal Relationship von Borné, Yan, Muhammad, Iram Faqir, Lorés-Motta, Laura, Hedblad, Bo, Nilsson, Peter M, Melander, Olle, de Jong, Eiko K, Blom, Anna M, den Hollander, Anneke I, Engström, Gunnar

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Rotating black holes, global symmetry and first order formalism von Andrianopoli, Laura, D’Auria, Riccardo, Giaccone, Paolo, Trigiante, Mario

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Genotype–phenotype correlations in neurogenetics: Lesch-Nyhan disease as a model disorder von Fu, Rong, Ceballos-Picot, Irene, Torres, Rosa J., Larovere, Laura E., Yamada, Yasukazu, Nguyen, Khue V., Hegde, Madhuri, Visser, Jasper E., Schretlen, David J., Nyhan, William L., Puig, Juan G., O’Neill, Patrick J., Jinnah, H. A.

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Analysis of task-based functional MRI data preprocessed with fMRIPrep von Esteban, Oscar, Ciric, Rastko, Finc, Karolina, Blair, Ross W., Markiewicz, Christopher J., Moodie, Craig A., Kent, James D., Goncalves, Mathias, DuPre, Elizabeth, Gomez, Daniel E. P., Ye, Zhifang, Salo, Taylor, Valabregue, Romain, Amlien, Inge K., Liem, Franziskus, Jacoby, Nir, Stojić, Hrvoje, Cieslak, Matthew, Urchs, Sebastian, Halchenko, Yaroslav O., Ghosh, Satrajit S., De La Vega, Alejandro, Yarkoni, Tal, Wright, Jessey, Thompson, William H., Poldrack, Russell A., Gorgolewski, Krzysztof J.

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Family Matters: Trauma and Quality of Life in Family Members of Individuals With Prader-Willi Syndrome von Bos-Roubos, Anja, Wingbermühle, Ellen, Biert, Anneloes, Graaff, Laura de, Egger, Jos

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A Genetic Investigation of Sex Bias in the Prevalence of Attention-Deficit/Hyperactivity Disorder von Walters, Raymond K., Lee, S. Hong, Brikell, Isabell, Ghirardi, Laura, Larsson, Henrik, Lichtenstein, Paul, Bell, Robert K., Bryc, Katarzyna, Fontanillas, Pierre, Hromatka, Bethann S., Huber, Karen E., Litterman, Nadia K., McIntyre, Matthew H., Mountain, Joanna L., Pitts, Steven J., Vacic, Vladimir, Anney, Richard J.L., Vasquez, Alejandro Arias, Arranz, Maria Jesús, Banaschewski, Tobias, Banaschewski, Tobias J., Mortensen, Preben Bo, Børglum, Anders, Charach, Alice, Crosbie, Jennifer, Dalsgaard, Soeren, Demontis, Ditte, Dempfle, Astrid, Elia, Josephine, Faraone, Stephen V., Franke, Barbara, Freitag, Christine, Gelernter, Joel, Grevet, Eugenio, Haavik, Jan, Hakonarson, Hakon, Hawi, Ziarih, Hinney, Anke, Holmans, Peter, Ickowitz, Abel, Kent, Lindsey, Kittel-Schneider, Sarah, Langley, Kate, Lesch, Klaus-Peter, Loo, Sandra K., Martin, Joanna, Medland, Sarah E., Mulas, Fernando, Mulligan, Aisling, O’Donovan, Michael C., Oades, Robert D., Palmason, Haukur, Rhode, Luis, Roeyers, Herbert, Romanos, Marcel, Romanos, Jasmin, Rothenberger, Aribert, Schäfer, Helmut, Scherag, André, Schimmelmann, Benno G., Sergeant, Joseph, Smalley, Susan L., Sonuga-Barke, Edmund J.S., Steinhausen, Hans-Christoph, Sullivan, Patrick F., Todorov, Alexandre, Waldman, Irwin, Wang, Yufeng, Warnke, Andreas, Williams, Nigel, Witt, Stephanie H., Yang, Li, Agerbo, Esben, Belliveau, Rich, Børglum, Anders D., Chambert, Kimberly, Dalsgaard, Søren, Dumont, Ashley, Goldstein, Jacqueline, Grove, Jakob, Howrigan, Daniel P., Huang, Hailiang, Martin, Alicia R., Mattheisen, Manuel, Moran, Jennifer, Mors, Ole, Pallesen, Jonatan, Poterba, Timothy, Poulsen, Jesper Buchhave, Robinson, Elise B., Satterstrom, F. Kyle, Stevens, Christine, Turley, Patrick, Pedersen, Marianne Giørtz, Mors, Ole, Nordentoft, Merete, Hougaard, David M., Bybjerg-Grauholm, Jonas, Franke, Barbara, Neale, Benjamin M.

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Homozygous Truncating Variants in TBC1D23 Cause Pontocerebellar Hypoplasia and Alter Cortical Development von Ivanova, Ekaterina L., Mau-Them, Frédéric Tran, Riazuddin, Saima, Kahrizi, Kimia, Laugel, Vincent, Schaefer, Elise, de Saint Martin, Anne, Runge, Karen, Iqbal, Zafar, Spitz, Marie-Aude, Laura, Mary, Drouot, Nathalie, Gérard, Bénédicte, Deleuze, Jean-François, de Brouwer, Arjan P.M., Razzaq, Attia, Dollfus, Hélène, Assir, Muhammad Zaman, Nitchké, Patrick, Hinckelmann, Maria-Victoria, Ropers, Hilger, Riazuddin, Sheikh, Najmabadi, Hossein, van Bokhoven, Hans, Chelly, Jamel

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