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Nature Genetics, ISSN 1061-4036, 07/2009, Volume 41, Issue 7, pp. 824 - 828
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 12/2014, Volume 95, Issue 6, pp. 729 - 735
Journal Article
by Kaiser, Frank J and Ansari, Morad and Braunholz, Diana and Concepción Gil-Roíguez, María and Decroos, Christophe and Wilde, Jonathan J and Fincher, Christopher T and Kaur, Maninder and Bando, Masashige and Amor, David J and Atwal, Paldeep S and Bahlo, Melanie and Bowman, Christine M and Bradley, Jacquelyn J and Brunner, Han G and Clark, Dinah and del Campo, Miguel and Di Donato, Nataliya and Diakumis, Peter and Dubbs, Holly and Dyment, David A and Eckhold, Juliane and Ernst, Sarah and Ferreira, Jose C and Francey, Lauren J and Gehlken, Ulrike and Guillén-Navarro, Encarna and Gyftodimou, Yolanda and Hall, Bryan D and Hennekam, Raoul and Hudgins, Louanne and Hullings, Melanie and Hunter, Jennifer M and Yntema, Helger and Innes, A. Micheil and Kline, Antonie D and Krumina, Zita and Lee, Hane and Leppig, Kathleen and Lynch, Sally Ann and Mallozzi, Mark B and Mannini, Linda and McKee, Shane and Mehta, Sarju G and Micule, Ieva and Mohammed, Shehla and Moran, Ellen and Mortier, Geert R and Moser, Joe-Ann S and Noon, Sarah E and Nozaki, Naohito and Nunes, Luis and Pappas, John G and Penney, Lynette S and Pérez-Aytés, Antonio and Petersen, Michael B and Puisac, Beatriz and Revencu, Nicole and Roeder, Elizabeth and Saitta, Sulagna and Scheuerle, Angela E and Schindeler, Karen L and Siu, Victoria M and Stark, Zornitza and Strom, Samuel P and Thiese, Heidi and Vater, Inga and Willems, Patrick and Williamson, Kathleen and Wilson, Louise C and Hakonarson, Hakon and Quintero-Rivera, Fabiola and Wierzba, Jolanta and Musio, Antonio and Gillessen-Kaesbach, Gabriele and Ramos, Feliciano J and Jackson, Laird G and Shirahige, Katsuhiko and Pié, Juan and Christianson, David W and Krantz, Ian D and Fitzpatrick, David R and Deardorff, Matthew A and Univ Washington Ctr Mendelian Geno and CareRare Canada Consortium and Care4Rare Canada Consortium and University of Washington Center for Mendelian Genomics
Human molecular genetics, ISSN 0964-6906, 2014, Volume 23, Issue 11, pp. 2888 - 2900
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 01/2008, Volume 358, Issue 3, pp. 221 - 230
Journal Article
Nature Genetics, ISSN 1061-4036, 03/2017, Volume 49, Issue 4, pp. 511 - 514
Journal Article
by Abou-Khalil, Bassel and Auce, Pauls and Avbersek, Andreja and Bahlo, Melanie and Balding, David J and Bast, Thomas and Baum, Larry and Becker, Albert J and Becker, Felicitas and Berghuis, Bianca and Berkovic, Samuel F and Boysen, Katja E and Bradfield, Jonathan P and Brody, Lawrence C and Buono, Russell J and Campbell, Ellen and Cascino, Gregory D and Catarino, Claudia B and Cavalleri, Gianpiero L and Cherny, Stacey S and Chinthapalli, Krishna and Coffey, Alison J and Compston, Alastair and Coppola, Antonietta and Cossette, Patrick and Craig, John J and de Haan, Gerrit-Jan and De Jonghe, Peter and de Kovel, Carolien G. F and Delanty, Norman and Depondt, Chantal and Devinsky, Orrin and Dlugos, Dennis J and Doherty, Colin P and Elger, Christian E and Eriksson, Johan G and Ferraro, Thomas N and Feucht, Martha and Francis, Ben and Franke, Andre and French, Jacqueline A and Freytag, Saskia and Gaus, Verena and Geller, Eric B and Gieger, Christian and Glauser, Tracy and Glynn, Simon and Goldstein, David B and Gui, Hongsheng and Guo, Youling and Haas, Kevin F and Hakonarson, Hakon and Hallmann, Kerstin and Haut, Sheryl and Heinzen, Erin L and Helbig, Ingo and Hengsbach, Christian and Hjalgrim, Helle and Iacomino, Michele and Ingason, Andrés and Jamnadas-Khoda, Jennifer and Johnson, Michael R and Kälviäinen, Reetta and Kantanen, Anne-Mari and Kasperavičiūte, Dalia and Kasteleijn-Nolst Trenite, Dorothee and Kirsch, Heidi E and Knowlton, Robert C and Koeleman, Bobby P. C and Krause, Roland and Krenn, Martin and Kunz, Wolfram S and Kuzniecky, Ruben and Kwan, Patrick and Lal, Dennis and Lau, Yu-Lung and Lehesjoki, Anna-Elina and Lerche, Holger and Leu, Costin and Lieb, Wolfgang and Lindhout, Dick and Lo, Warren D and Lopes-Cendes, Iscia and Lowenstein, Daniel H and Malovini, Alberto and Marson, Anthony G and Mayer, Thomas and McCormack, Mark and Mills, James L and Mirza, Nasir and Moerzinger, Martina and Møller, Rikke S and Molloy, Anne M and Muhle, Hiltrud and Newton, Mark and Ng, Ping-Wing and Nöthen, Markus M and Nürnberg, Peter and O’Brien, Terence J and Oliver, Karen L and ... and Int League Against Epilepsy Conso and International League Against Epilepsy Consortium on Complex Epilepsies and The International League Against Epilepsy Consortium on Complex Epilepsies
Nature Communications, ISSN 2041-1723, 12/2018, Volume 9, Issue 1, pp. 5269 - 15
The epilepsies affect around 65 million people worldwide and have a substantial missing heritability component. We report a genome-wide mega-analysis involving... 
FRONTAL-LOBE | METAANALYSIS | ILAE COMMISSION | MULTIDISCIPLINARY SCIENCES | SUSCEPTIBILITY LOCI | GENETIC ARCHITECTURE | ABSENCE | LD SCORE REGRESSION | SNP HERITABILITY | ASSOCIATION | EXPRESSION | Brain | Transcription factors | Coding | Epilepsy | Genes | Genomes | Single-nucleotide polymorphism | Heritability | Gene expression | Metabolism | Antiepileptic agents | Loci | Index Medicus
Journal Article
Nature genetics, ISSN 1061-4036, 2014, Volume 46, Issue 11, pp. 1239 - 1244
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 04/2011, Volume 88, Issue 4, pp. 508 - 515
Journal Article
by Feng, Yen-Chen Anne and Howrigan, Daniel P and Abbott, Liam E and Tashman, Katherine and Cerrato, Felecia and Singh, Tarjinder and Heyne, Henrike and Byrnes, Andrea and Churchhouse, Claire and Watts, Nick and Solomonson, Matthew and Lal, Dennis and Heinzen, Erin L and Dhindsa, Ryan S and Stanley, Kate E and Cavalleri, Gianpiero L and Hakonarson, Hakon and Helbig, Katherine L and Helbig, Ingo and Krause, Roland and May, Patrick and Weckhuysen, Sarah and Weckhuysen, Dorien and Petrovski, Slavé and Kamalakaran, Sitharthan and Sisodiya, Sanjay M and Cossette, Patrick and Cotsapas, Chris and De Jonghe, Peter and Dixon-Salazar, Tracy and Guerrini, Renzo and Kwan, Patrick and Marson, Anthony G and Stewart, Randy and Depondt, Chantal and Dlugos, Dennis J and Scheffer, Ingrid E and Striano, Pasquale and Freyer, Catharine and McKenna, Kevin and Regan, Brigid M and Bellows, Susannah T and Leu, Costin and Bennett, Caitlin A and Johns, Esther M.C and Macdonald, Alexandra and Shilling, Hannah and Burgess, Rosemary and Bahlo, Melanie and O’Brien, Terence J and Todaro, Marian and Stamberger, Hannah and Andrade, Danielle M and Sadoway, Tara R and Mo, Kelly and Krestel, Heinz and Gallati, Sabina and Papacostas, Savvas S and Kousiappa, Ioanna and Tanteles, George A and Štěrbová, Katalin and Vlčková, Markéta and Sedláčková, Lucie and Laššuthová, Petra and Klein, Karl Martin and Rosenow, Felix and Reif, Philipp S and Reif, Andreas and Knake, Susanne and Kunz, Wolfram S and Zsurka, Gábor and Elger, Christian E and Bauer, Jürgen and Rademacher, Michael and Rademacher, Annika and Pendziwiat, Manuela and Muhle, Hiltrud and van Baalen, Andreas and von Spiczak, Sarah and Stephani, Ulrich and Afawi, Zaid and Korczyn, Amos D and Kanaan, Moien and Canavati, Christina and Kurlemann, Gerhard and Müller-Schlüter, Karen and Kluger, Gerhard and Häusler, Martin and Blatt, Ilan and Lemke, Johannes R and Krey, Ilona and Weber, Yvonne G and Wolking, Stefan and Becker, Felicitas and Hengsbach, Christian and Rau, Sarah and Maisch, Ana F and Steinhoff, Bernhard J and Schulze-Bonhage, Andreas and Schubert-Bast, Susanne and ... and Epi25 Collaborative and Genomic Psychiat Cohort GPC Consor
The American Journal of Human Genetics, ISSN 0002-9297, 08/2019, Volume 105, Issue 2, pp. 267 - 282
Sequencing-based studies have identified novel risk genes associated with severe epilepsies and revealed an excess of rare deleterious variation in less-severe... 
epilepsy | seizures | exome | epileptic encephalopathy | burden analysis | sequencing | PROTEIN | METAANALYSIS | DE-NOVO MUTATIONS | VARIANTS | SUSCEPTIBILITY | GENETICS & HEREDITY | EPILEPTIC SEIZURES | GAMMA-2-SUBUNIT | GENOME | EPIDEMIOLOGY | COMMON EPILEPSIES | Psychological aspects | Genetic variation | Epilepsy | Physiological aspects | Genetic aspects | Research | Risk factors | Index Medicus
Journal Article