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Science, ISSN 0036-8075, 2018, Volume 360, Issue 6395, pp. 1313 - 1313
Disorders of the brain can exhibit considerable epidemiological comorbidity and often share symptoms, provoking debate about their etiologic overlap. We... 
ANOREXIA-NERVOSA | POPULATION-BASED TWIN | DEFICIT HYPERACTIVITY DISORDER | LONG-TERM SURVIVAL | ALZHEIMERS-DISEASE | MULTIDISCIPLINARY SCIENCES | GENETIC CORRELATIONS | BODY-MASS INDEX | MAJOR DEPRESSIVE DISORDER | BIPOLAR DISORDER | GENOME-WIDE ASSOCIATION | Genetic Variation | Mental Disorders - genetics | Genome-Wide Association Study | Phenotype | Brain Diseases - classification | Quantitative Trait, Heritable | Brain Diseases - diagnosis | Humans | Mental Disorders - classification | Risk Factors | Brain Diseases - genetics | Mental Disorders - diagnosis | Anorexia | Disorders | Cognitive ability | Bipolar disorder | Posttraumatic stress disorder | Mental depression | Epidemiology | Risk factors | Consortia | Proteins | Ischemia | Etiology | Classification | Gilles de la Tourette syndrome | Alzheimer's disease | Neurological disorders | Neurodegenerative diseases | Comorbidity | Behavior disorders | Anorexia nervosa | Risk analysis | Patients | Neurological diseases | Correlation analysis | Heritability | Attention deficit disorder | Headache | Mental disorders | Medical services | Schizophrenia | Risk sharing | Genomes | Heterogeneity | Biological effects | Risk assessment | Stroke | Phenotypes | Migraine | Attention deficit hyperactivity disorder | Eating disorders | Personality | Genetic diversity | Statistics | Activity patterns | Crohn's Disease | Population (statistical) | Scaffolding | Diagnostic systems | Alzheimers disease | Life Sciences | Human health and pathology | Mental Disorders | Neurons and Cognition | Brain Diseases | Genetics
Journal Article
Digestive and Liver Disease, ISSN 1590-8658, 03/2018, Volume 50, Issue 2, pp. e234 - e235
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
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 and Epi25 Collaborative. Electronic address: s.berkovic@unimelb.edu.au
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
Journal Article
by Appenzeller, Silke and Balling, Rudi and Barisic, Nina and Baulac, Stéphanie and Caglayan, Hande and Craiu, Dana and De Jonghe, Peter and Depienne, Christel and Dimova, Petia and Djémié, Tania and Gormley, Padhraig and Guerrini, Renzo and Helbig, Ingo and Hjalgrim, Helle and Hoffman-Zacharska, Dorota and Jähn, Johanna and Klein, Karl Martin and Koeleman, Bobby and Komarek, Vladimir and Krause, Roland and Kuhlenbäumer, Gregor and Leguern, Eric and Lehesjoki, Anna-Elina and Lemke, Johannes R and Lerche, Holger and Linnankivi, Tarja and Marini, Carla and May, Patrick and Møller, Rikke S and Muhle, Hiltrud and Pal, Deb and Palotie, Aarno and Pendziwiat, Manuela and Robbiano, Angela and Roelens, Filip and Rosenow, Felix and Selmer, Kaja and Serratosa, Jose M and Sisodiya, Sanjay and Stephani, Ulrich and Sterbova, Katalin and Striano, Pasquale and Suls, Arvid and Talvik, Tiina and von Spiczak, Sarah and Weber, Yvonne and Weckhuysen, Sarah and Zara, Federico and Abou-Khalil, Bassel and Alldredge, Brian K and Andermann, Eva and Andermann, Frederick and Amron, Dina and Bautista, Jocelyn F and Berkovic, Samuel F and Bluvstein, Judith and Boro, Alex and Cascino, Gregory and Consalvo, Damian and Crumrine, Patricia and Devinsky, Orrin and Dlugos, Dennis and Epstein, Michael P and Fiol, Miguel and Fountain, Nathan B and French, Jacqueline and Friedman, Daniel and Geller, Eric B and Glauser, Tracy and Glynn, Simon and Haas, Kevin and Haut, Sheryl R and Hayward, Jean and Helmers, Sandra L and Joshi, Sucheta and Kanner, Andres and Kirsch, Heidi E and Knowlton, Robert C and Kossoff, Eric H and Kuperman, Rachel and Kuzniecky, Ruben and Lowenstein, Daniel H and McGuire, Shannon M and Motika, Paul V and Novotny, Edward J and Ottman, Ruth and Paolicchi, Juliann M and Parent, Jack and Park, Kristen and Poduri, Annapurna and Sadleir, Lynette and Scheffer, Ingrid E and Shellhaas, Renée A and Sherr, Elliott and Shih, Jerry J and Singh, Rani and Sirven, Joseph and Smith, Michael C and Sullivan, Joe and Thio, Liu Lin and ... and Epi4K Consortium and EuroEPINOMICS-RES Consortium and Epilepsy Phenome Genome Project and Epilepsy Phenome/Genome Project
The American Journal of Human Genetics, ISSN 0002-9297, 10/2014, Volume 95, Issue 4, pp. 360 - 370
Journal Article
by Anney, Richard J.L and Avbersek, Andreja and Balding, David and Baum, Larry and Becker, Felicitas and Berkovic, Samuel F and Bradfi, Jonathan P and Brody, Lawrence C and Buono, Russell J and Catarino, Claudia B and Cavalleri, Gianpiero L and Cherny, Stacey S and Chinthapalli, Krishna and Coffey, Alison J and Compston, Alastair and Cossette, Patrick and De Haan, Gerrit-Jan and De Jonghe, Peter and De Kovel, Carolien G. F and Delanty, Norman and Depondt, Chantal and Dlugos, Dennis J and Doherty, Colin P and Elger, Christian E and Ferraro, Thomas N and Feucht, Martha and Franke, Andre and French, Jacqueline and Gaus, Verena and Goldstein, David B and Gui, Hongsheng and Guo, Youling and Hakonarson, Hakon and Hallmann, Kerstin and Heinzen, Erin L and Helbig, Ingo and Hjalgrim, Helle and Jackson, Margaret and Jamnadas-Khoda, Jennifer and Janz, Dieter and Johnson, Michael R and Kalviainen, Reetta and Kantanen, Anne-Mari and Kasperaviciute, Dalia and Trenite, Dorothee Kasteleijn-Nolst and Koeleman, Bobby P.C and Kunz, Wolfram S and Kwan, Patrick and Lau, Yu Lung and Lehesjoki, Anna-Elina and Lerche, Holger and Leu, Costin and Lieb, Wolfgang and Lindhout, Dick and Lo, Warren and Lowenstein, Daniel H and Malovini, Alberto and Marson, Anthony G and McCormack, Mark and Mills, James L and Moerzinger, Martina and Moller, Rikke S and Molloy, Anne M and Muhle, Hiltrud and Newton, Mark and Ng, Ping-Wing and Nothen, Markus M and Nurnberg, Peter and OBrien, Terence J and Oliver, Karen L and Palotie, Aarno and Pangilinan, Faith and Pernhorst, Katharina and Petrovski, Slave and Privitera, Michael and Radtke, Rodney and Reif, Philipp S and Rosenow, Felix and Ruppert, Ann-Kathrin and Sander, Thomas and Scattergood, Theresa and Schachter, Steven and Schankin, Christoph and Scheffer, Ingrid E and Schmitz, Bettina and Schoch, Susanne and Sham, Pak C and Sisodiya, Sanjay and Smith, David F and Smith, Philip E and Speed, Doug and Sperling, Michael R and Steffens, Michael and Stephani, Ulrich and Striano, Pasquale and Stroink, Hans and Surges, Rainer and Tan, K Meng and Thomas, G Neil and Todaro, Marian and ... and KORA Study Grp and Int League Epilepsy Consortium Com and International League Against Epilepsy Consortium on Complex Epilepsies. Electronic address: epilepsy-austin@unimelb.edu.au
Lancet Neurology, The, ISSN 1474-4422, 2014, Volume 13, Issue 9, pp. 893 - 903
Journal Article
by Kasperavičiūtė, Dalia and Catarino, Claudia B and Matarin, Mar and Leu, Costin and Novy, Jan and Tostevin, Anna and Leal, Bárbara and Hessel, Ellen V. S and Hallmann, Kerstin and Hildebrand, Michael S and Dahl, Hans-Henrik M and Ryten, Mina and Trabzuni, Daniah and Ramasamy, Adaikalavan and Alhusaini, Saud and Doherty, Colin P and Dorn, Thomas and Hansen, Jörg and Krämer, Günter and Steinhoff, Bernhard J and Zumsteg, Dominik and Duncan, Susan and Kälviäinen, Reetta K and Eriksson, Kai J and Kantanen, Anne-Mari and Pandolfo, Massimo and Gruber-Sedlmayr, Ursula and Schlachter, Kurt and Reinthaler, Eva M and Stogmann, Elisabeth and Zimprich, Fritz and Théâtre, Emilie and Smith, Colin and O’Brien, Terence J and Meng Tan, K and Petrovski, Slave and Robbiano, Angela and Paravidino, Roberta and Zara, Federico and Striano, Pasquale and Sperling, Michael R and Buono, Russell J and Hakonarson, Hakon and Chaves, João and Costa, Paulo P and Silva, Berta M and da Silva, António M and de Graan, Pierre N. E and Koeleman, Bobby P. C and Becker, Albert and Schoch, Susanne and von Lehe, Marec and Reif, Philipp S and Rosenow, Felix and Becker, Felicitas and Weber, Yvonne and Lerche, Holger and Rössler, Karl and Buchfelder, Michael and Hamer, Hajo M and Kobow, Katja and Coras, Roland and Blumcke, Ingmar and Scheffer, Ingrid E and Berkovic, Samuel F and Weale, Michael E and Delanty, Norman and Depondt, Chantal and Cavalleri, Gianpiero L and Kunz, Wolfram S and Sisodiya, Sanjay M and UK Brain Expression Consortium
Brain, ISSN 0006-8950, 10/2013, Volume 136, Issue 10, pp. 3140 - 3150
Journal Article