Cold hands, warm feet: sleep deprivation disrupts thermoregulation and its association with vigilance by Romeijn, Nico, Verweij, Ilse M, Koeleman, Anne, Mooij, Anne, Steimke, Rosa, Virkkala, Jussi, van der Werf, Ysbrand, Van Someren, Eus J W

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A prominent lack of IgG1-Fc fucosylation of platelet alloantibodies in pregnancy by Kapur, Rick, Kustiawan, Iwan, Vestrheim, Anne, Koeleman, Carolien A.M., Visser, Remco, Einarsdottir, Helga K., Porcelijn, Leendert, Jackson, Dave, Kumpel, Belinda, Deelder, André M., Blank, Dennis, Skogen, Björn, Killie, Mette Kjaer, Michaelsen, Terje E., de Haas, Masja, Rispens, Theo, van der Schoot, C. Ellen, Wuhrer, Manfred, Vidarsson, Gestur

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Afucosylated IgG characterizes enveloped viral responses and correlates with COVID-19 severity by Larsen, Mads Delbo, de Graaf, Erik L, Sonneveld, Myrthe E, Plomp, H Rosina, Nouta, Jan, Hoepel, Willianne, Chen, Hung-Jen, Linty, Federica, Visser, Remco, Brinkhaus, Maximilian, Šuštić, Tonći, de Taeye, Steven W, Bentlage, Arthur E H, Toivonen, Suvi, Koeleman, Carolien A M, Sainio, Susanna, Kootstra, Neeltje A, Brouwer, Philip J M, Geyer, Chiara Elisabeth, Derksen, Ninotska I L, Wolbink, Gertjan, de Winther, Menno, Sanders, Rogier W, van Gils, Marit J, de Bruin, Sanne, Vlaar, Alexander P J, Rispens, Theo, den Dunnen, Jeroen, Zaaijer, Hans L, Wuhrer, Manfred, Ellen van der Schoot, C, Vidarsson, Gestur

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Testing association of rare genetic variants with resistance to three common antiseizure medications by Wolking, Stefan, Moreau, Claudia, Nies, Anne T., Schaeffeler, Elke, McCormack, Mark, Auce, Pauls, Avbersek, Andreja, Becker, Felicitas, Krenn, Martin, Møller, Rikke S., Nikanorova, Marina, Weber, Yvonne G., Weckhuysen, Sarah, Cavalleri, Gianpiero L., Delanty, Norman, Depondt, Chantal, Johnson, Michael R., Koeleman, Bobby P.C., Kunz, Wolfram S., Marson, Anthony G., Sander, Josemir W., Sills, Graeme J., Striano, Pasquale, Zara, Federico, Zimprich, Fritz, Schwab, Matthias, Krause, Roland, Sisodiya, Sanjay M., Cossette, Patrick, Girard, Simon L., Lerche, Holger

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Common variation in ISL1 confers genetic susceptibility for human congenital heart disease by Stevens, Kristen N, Hakonarson, Hakon, Kim, Cecilia E, Doevendans, Pieter A, Koeleman, Bobby P C, Mital, Seema, Raue, Jennifer, Glessner, Joseph T, Coles, John G, Moreno, Victor, Granger, Anne, Gruber, Stephen B, Gruber, Peter J

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Antiepileptic Drug Teratogenicity and De Novo Genetic Variation Load by Perucca, Piero, Anderson, Alison, Jazayeri, Dana, Hitchcock, Alison, Graham, Janet, Todaro, Marian, Tomson, Torbjörn, Battino, Dina, Perucca, Emilio, Ferri, Meritxell Martinez, Rochtus, Anne, Lagae, Lieven, Canevini, Maria Paola, Zambrelli, Elena, Campbell, Ellen, Koeleman, Bobby P. C., Scheffer, Ingrid E., Berkovic, Samuel F., Kwan, Patrick, Sisodiya, Sanjay M., Goldstein, David B., Petrovski, Slavé, Craig, John, Vajda, Frank J. E., O'Brien, Terence J.

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Pharmacoresponse in genetic generalized epilepsy: a genome-wide association study by Wolking, Stefan, Schulz, Herbert, Nies, Anne T, McCormack, Mark, Schaeffeler, Elke, Auce, Pauls, Avbersek, Andreja, Becker, Felicitas, Klein, Karl M, Krenn, Martin, Møller, Rikke S, Nikanorova, Marina, Weckhuysen, Sarah, Consortium, EpiPGx, Cavalleri, Gianpiero L, Delanty, Norman, Depondt, Chantal, Johnson, Michael R, Koeleman, Bobby Pc, Kunz, Wolfram S, Marson, Anthony G, Sander, Josemir W, Sills, Graeme J, Striano, Pasquale, Zara, Federico, Zimprich, Fritz, Weber, Yvonne G, Krause, Roland, Sisodiya, Sanjay, Schwab, Matthias, Sander, Thomas, Lerche, Holger

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Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies by Abou-Khalil, Bassel, Auce, Pauls, Avbersek, Andreja, Bahlo, Melanie, Balding, David J., Bast, Thomas, Baum, Larry, Becker, Albert J., Becker, Felicitas, Berghuis, Bianca, Berkovic, Samuel F., Boysen, Katja E., Bradfield, Jonathan P., Brody, Lawrence C., Buono, Russell J., Campbell, Ellen, Cascino, Gregory D., Catarino, Claudia B., Cavalleri, Gianpiero L., Cherny, Stacey S., Chinthapalli, Krishna, Coffey, Alison J., Compston, Alastair, Coppola, Antonietta, Cossette, Patrick, Craig, John J., de Haan, Gerrit-Jan, De Jonghe, Peter, de Kovel, Carolien G. F., Delanty, Norman, Depondt, Chantal, Devinsky, Orrin, Dlugos, Dennis J., Doherty, Colin P., Elger, Christian E., Eriksson, Johan G., Ferraro, Thomas N., Feucht, Martha, Francis, Ben, Franke, Andre, French, Jacqueline A., Freytag, Saskia, Gaus, Verena, Geller, Eric B., Gieger, Christian, Glauser, Tracy, Glynn, Simon, Goldstein, David B., Gui, Hongsheng, Guo, Youling, Haas, Kevin F., Hakonarson, Hakon, Hallmann, Kerstin, Haut, Sheryl, Heinzen, Erin L., Helbig, Ingo, Hengsbach, Christian, Hjalgrim, Helle, Iacomino, Michele, Ingason, Andrés, Jamnadas-Khoda, Jennifer, Johnson, Michael R., Kälviäinen, Reetta, Kantanen, Anne-Mari, Kasperavičiūte, Dalia, Kasteleijn-Nolst Trenite, Dorothee, Kirsch, Heidi E., Knowlton, Robert C., Koeleman, Bobby P. C., Krause, Roland, Krenn, Martin, Kunz, Wolfram S., Kuzniecky, Ruben, Kwan, Patrick, Lal, Dennis, Lau, Yu-Lung, Lehesjoki, Anna-Elina, Lerche, Holger, Leu, Costin, Lieb, Wolfgang, Lindhout, Dick, Lo, Warren D., Lopes-Cendes, Iscia, Lowenstein, Daniel H., Malovini, Alberto, Marson, Anthony G., Mayer, Thomas, McCormack, Mark, Mills, James L., Mirza, Nasir, Moerzinger, Martina, Møller, Rikke S., Molloy, Anne M., Muhle, Hiltrud, Newton, Mark, Ng, Ping-Wing, Nöthen, Markus M., Nürnberg, Peter, O’Brien, Terence J., Oliver, Karen L.

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Assessing the genetic association between vitamin B6 metabolism and genetic generalized epilepsy by Stevelink, Remi, Pangilinan, Faith, Jansen, Floor E., Braun, Kees P.J., Molloy, Anne M., Brody, Lawrence C., Koeleman, Bobby P.C.

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Genetic determinants of common epilepsies: a meta-analysis of genome-wide association studies by Anon

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Polygenic burden in focal and generalized epilepsies by Leu, Costin, Stevelink, Remi, Smith, Alexander W, Goleva, Slavina B, Kanai, Masahiro, Ferguson, Lisa, Campbell, Ciaran, Kamatani, Yoichiro, Okada, Yukinori, Sisodiya, Sanjay M, Cavalleri, Gianpiero L, Koeleman, Bobby P C, Lerche, Holger, Jehi, Lara, Davis, Lea K, Najm, Imad M, Palotie, Aarno, Daly, Mark J, Busch, Robyn M, Lal, Dennis

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ALT-FISH quantifies alternative lengthening of telomeres activity by imaging of single-stranded repeats by Frank, Lukas, Rademacher, Anne, Mücke, Norbert, Tirier, Stephan M, Koeleman, Emma, Knotz, Caroline, Schumacher, Sabrina, Stainczyk, Sabine A, Westermann, Frank, Fröhling, Stefan, Chudasama, Priya, Rippe, Karsten

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Rare coding variants in genes encoding GABA A receptors in genetic generalised epilepsies: an exome-based case-control study by May, Patrick, Girard, Simon, Harrer, Merle, Bobbili, Dheeraj R, Schubert, Julian, Wolking, Stefan, Becker, Felicitas, Lachance-Touchette, Pamela, Meloche, Caroline, Gravel, Micheline, Niturad, Cristina E, Knaus, Julia, De Kovel, Carolien, Toliat, Mohamad, Polvi, Anne, Iacomino, Michele, Guerrero-López, Rosa, Baulac, Stéphanie, Marini, Carla, Thiele, Holger, Altmüller, Janine, Jabbari, Kamel, Ruppert, Ann-Kathrin, Jurkowski, Wiktor, Lal, Dennis, Rusconi, Raffaella, Cestèle, Sandrine, Terragni, Benedetta, Coombs, Ian D, Reid, Christopher A, Striano, Pasquale, Caglayan, Hande, Siren, Auli, Everett, Kate, Møller, Rikke S, Hjalgrim, Helle, Muhle, Hiltrud, Helbig, Ingo, Kunz, Wolfram S, Weber, Yvonne G, Weckhuysen, Sarah, Jonghe, Peter De, Sisodiya, Sanjay M, Nabbout, Rima, Franceschetti, Silvana, Coppola, Antonietta, Vari, Maria S, Kasteleijn-Nolst Trenité, Dorothée, Baykan, Betul, Ozbek, Ugur, Bebek, Nerses, Klein, Karl M, Rosenow, Felix, Nguyen, Dang K, Dubeau, François, Carmant, Lionel, Lortie, Anne, Desbiens, Richard, Clément, Jean-François, Cieuta-Walti, Cécile, Sills, Graeme J, Auce, Pauls, Francis, Ben, Johnson, Michael R, Marson, Anthony G, Berghuis, Bianca, Sander, Josemir W, Avbersek, Andreja, McCormack, Mark, Cavalleri, Gianpiero L, Delanty, Norman, Depondt, Chantal, Krenn, Martin, Zimprich, Fritz, Peter, Sarah, Nikanorova, Marina, Kraaij, Robert, van Rooij, Jeroen, Balling, Rudi, Ikram, M Arfan, Uitterlinden, André G, Avanzini, Giuliano, Schorge, Stephanie, Petrou, Steven, Mantegazza, Massimo, Sander, Thomas, LeGuern, Eric, Serratosa, Jose M, Koeleman, Bobby P C, Palotie, Aarno, Lehesjoki, Anna-Elina, Nothnagel, Michael, Nürnberg, Peter, Maljevic, Snezana, Zara, Federico, Cossette, Patrick, Krause, Roland, Lerche, Holger

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A Genome-wide Association Study Identifies Risk Alleles in Plasminogen and P4HA2 Associated with Giant Cell Arteritis by Vaglio, Augusto, Mackie, Sarah L., Hernández-Rodríguez, José, Monach, Paul A., Castañeda, Santos, Solans, Roser, Morado, Inmaculada C., Narváez, Javier, Pease, Colin T., Dasgupta, Bhaskar, Watts, Richard, Khalidi, Nader, Ytterberg, Steven, Boiardi, Luigi, Beretta, Lorenzo, Govoni, Marcello, Bonatti, Francesco, Witte, Torsten, Schönau, Verena, Papo, Thomas, Haroche, Julien, Mahr, Alfred, Molberg, Øyvind, Voskuyl, Alexandre, Brouwer, Elisabeth, Daikeler, Thomas, Berger, Christoph T., Molloy, Eamonn S., Blockmans, Daniel, Lie, Benedicte A., Mclaren, Paul, Wijmenga, Cisca, Allanore, Yannick, Koeleman, Bobby P.C., Callejas, José Luis, Caminal-Montero, Luis, Corbera-Bellalta, Marc, de Miguel, Eugenio, López, J. Bernardino Díaz, Gómez-Vaquero, Carmen, Guijarro-Rojas, Mercedes, Hidalgo-Conde, Ana, Marí-Alfonso, Begoña, Berriochoa, Agustín Martínez, Zapico, Aleida Martínez, Miranda-Filloy, José A., Monfort, Jordi, Ortego-Centeno, Norberto, Pérez-Conesa, Mercedes, Prieto-González, Sergio, Fernández, Raquel Ríos, Sánchez-Martín, Julio, Sopeña, Bernardo, Unzurrunzaga, Ainhoa, Gough, Andrew, Isaacs, John D., McHugh, Neil, Hordon, Lesley, Kamath, Sanjeet, Patel, Yusuf, Yee, Cee-Seng, Nandi, Pradip, Nandagudi, Anupama, Jarrett, Stephen, Levy, Sarah, Mollan, Susan, Salih, Abdel, Wordsworth, Oliver, Sanders, Emma, Gill, Anne, Carr, Lisa, Routledge, Christine, Culfear, Karen, James, Lynne, Spimpolo, Jenny, Kempa, Andy, Masqood, Zahira, Wood, Rose, Rashid, Lubna Haroon, Robinson, James I., Morgan, Mike, Sorensen, Louise, Taylor, John, Carette, Simon, Chung, Sharon, Cuthbertson, David, Forbess, Lindsy J., Gewurz-Singer, Ora, Hoffman, Gary S., Maksimowicz-McKinnon, Kathleen M., Pagnoux, Christian, Seo, Philip, Specks, Ulrich, Spiera, Robert F., Sreih, Antoine, Barrett, Jennifer H., Merkel, Peter A., Morgan, Ann W., González-Gay, Miguel A., Martín, Javier

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Meta-analysis of the clinical performance of commercial SARS-CoV-2 nucleic acid and antibody tests up to 22 August 2020 by Van Walle, Ivo, Leitmeyer, Katrin, Broberg, Eeva K

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Using common genetic variants to find drugs for common epilepsies by Mirza, Nasir, Stevelink, Remi, Taweel, Basel, Koeleman, Bobby P C, Marson, Anthony G

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Exon‐disrupting deletions of NRXN1 in idiopathic generalized epilepsy by Møller, Rikke S., Weber, Yvonne G., Klitten, Laura L., Trucks, Holger, Muhle, Hiltrud, Kunz, Wolfram S., Mefford, Heather C., Franke, Andre, Kautza, Monika, Wolf, Peter, Dennig, Dieter, Schreiber, Stefan, Rückert, Ina‐Maria, Wichmann, H.‐Erich, Ernst, Jan P., Schurmann, Claudia, Grabe, Hans J., Tommerup, Niels, Stephani, Ulrich, Lerche, Holger, Hjalgrim, Helle, Helbig, Ingo, Sander, Thomas

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Painful knees and hearing-loss: a rare presentation of meningococcal disease by Kahlmann, Vivienne, Alves, Celina, Coleman, Johannes, Korswagen, Lindy-Anne

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Complement component C4 structural variation and quantitative traits contribute to sex-biased vulnerability in systemic sclerosis by Kerick, Martin, Acosta-Herrera, Marialbert, Simeón-Aznar, Carmen Pilar, Callejas, José Luis, Assassi, Shervin, Proudman, Susanna M., Nikpour, Mandana, Hunzelmann, Nicolas, Moroncini, Gianluca, de Vries-Bouwstra, Jeska K., Orozco, Gisela, Barton, Anne, Herrick, Ariane L., Terao, Chikashi, Allanore, Yannick, Fonseca, Carmen, Alarcón-Riquelme, Marta Eugenia, Radstake, Timothy R. D. J., Beretta, Lorenzo, Denton, Christopher P., Mayes, Maureen D., Martin, Javier

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Genome-wide linkage meta-analysis identifies susceptibility loci at 2q34 and 13q31.3 for genetic generalized epilepsies by Leu, Costin, de Kovel, Carolien G.F., Zara, Federico, Striano, Pasquale, Pezzella, Marianna, Robbiano, Angela, Bianchi, Amedeo, Bisulli, Francesca, Coppola, Antonietta, Giallonardo, Anna Teresa, Beccaria, Francesca, Trenité, Dorothée Kasteleijn-Nolst, Lindhout, Dick, Gaus, Verena, Schmitz, Bettina, Janz, Dieter, Weber, Yvonne G., Becker, Felicitas, Lerche, Holger, Kleefuß-Lie, Ailing A., Hallman, Kerstin, Kunz, Wolfram S., Elger, Christian E., Muhle, Hiltrud, Stephani, Ulrich, Møller, Rikke S., Hjalgrim, Helle, Mullen, Saul, Scheffer, Ingrid E., Berkovic, Samuel F., Everett, Kate V., Gardiner, Mark R., Marini, Carla, Guerrini, Renzo, Lehesjoki, Anna-Elina, Siren, Auli, Nabbout, Rima, Baulac, Stephanie, Leguern, Eric, Serratosa, Jose M., Rosenow, Felix, Feucht, Martha, Unterberger, Iris, Covanis, Athanasios, Suls, Arvid, Weckhuysen, Sarah, Kaneva, Radka, Caglayan, Hande, Turkdogan, Dilsad, Baykan, Betul, Bebek, Nerses, Ozbek, Ugur, Hempelmann, Anne, Schulz, Herbert, Rüschendorf, Franz, Trucks, Holger, Nürnberg, Peter, Avanzini, Giuliano, Koeleman, Bobby P.C., Sander, Thomas

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