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by Anttila, Verneri and Winsvold, Bendik S and Gormley, Padhraig and Kurth, Tobias and Bettella, Francesco and McMahon, George and Kallela, Mikko and Malik, Rainer and de Vries, Boukje and Terwindt, Gisela and Medland, Sarah E and Todt, Unda and McArdle, Wendy L and Quaye, Lydia and Koiranen, Markku and Ikram, M. Arfan and Lehtimaki, Terho and Stam, Anine H and Ligthart, Lannie and Wedenoja, Juho and Dunham, Ian and Neale, Benjamin M and Palta, Priit and Hamalainen, Eija and Schuerks, Markus and Rose, Lynda M and Buring, Julie E and Ridker, Paul M and Steinberg, Stacy and Stefansson, Hreinn and Jakobsson, Finnbogi and Lawlor, Debbie A and Evans, David M and Ring, Susan M and Farkkila, Markus and Artto, Ville and Kaunisto, Mari A and Freilinger, Tobias and Schoenen, Jean and Frants, Rune R and Pelzer, Nadine and Weller, Claudia M and Zielman, Ronald and Heath, Anew C and Madden, Pamela A. F and Montgomery, Grant W and Martin, Nicholas G and Borck, Guntram and Goebel, Hartmut and Heinze, Axel and Heinze-Kuhn, Katja and Williams, Frances M. K and Hartikainen, Anna-Liisa and Pouta, Anneli and van den Ende, Joyce and Uitterlinden, Ane G and Hofman, Albert and Amin, Najaf and Hottenga, Jouke-Jan and Vink, Jacqueline M and Heikkila, Kauko and Alexander, Michael and Muller-Myhsok, Bertram and Schreiber, Stefan and Meitinger, Thomas and Wichmann, Heinz Erich and Aromaa, Arpo and Eriksson, Johan G and Traynor, Bryan J and Trabzuni, Daniah and Rossin, Elizabeth and Lage, Kasper and Jacobs, Suzanne B. R and Gibbs, J. Raphael and Birney, Ewan and Kaprio, Jaakko and Penninx, Brenda W and Boomsma, Dorret I and van Duijn, Cornelia and Raitakari, Olli and Jarvelin, Marjo-Riitta and Zwart, John-Anker and Cherkas, Lynn and Strachan, David P and Kubisch, Christian and Ferrari, Michel D and van den Maagdenberg, Arn M. J. M and Dichgans, Martin and Wessman, Maija and Smith, George Davey and Stefansson, Kari and Daly, Mark J and Nyholt, Dale R and Chasman, Daniel I and Palotie, Aarno and UK Brain Expression Consortium and Int Headache Genetics Consortium and North Amer Brain Expression and the International Headache Genetics Consortium and North American Brain Expression Consortium
Nature Genetics, ISSN 1061-4036, 08/2013, Volume 45, Issue 8, pp. 912 - U255
Migraine is the most common brain disorder, affecting approximately 14% of the adult population, but its molecular mechanisms are poorly understood. We report... 
PROTEIN | LEWIS(X) | GENES | GENETICS & HEREDITY | DOWN-REGULATION | TRANSFORMING-GROWTH-FACTOR | MUTATIONS | ASSOCIATION | EXPRESSION | FAMILY | Genetic susceptibility | Genetic variation | Migraine | Physiological aspects | Genetic aspects | Research | Risk factors | Studies | Proteins | Signal transduction | Headaches | Population | Genomes | Meta-analysis
Journal Article
by Anttila, Verneri and Bulik-Sullivan, Brendan and Finucane, Hilary K and Walters, Raymond K and Bras, Jose and Duncan, Laramie and Escott-Price, Valentina and Falcone, Guido J and Gormley, Padhraig and Malik, Rainer and Patsopoulos, Nikolaos A and Ripke, Stephan and Wei, Zhi and Yu, Dongmei and Lee, Phil H and Turley, Patrick and Grenier-Boley, Benjamin and Chouraki, Vincent and Kamatani, Yoichiro and Berr, Claudine and Letenneur, Luc and Hannequin, Didier and Amouyel, Philippe and Boland, Anne and Deleuze, Jean-François and Duron, Emmanuelle and Vardarajan, Badri N and Reitz, Christiane and Goate, Alison M and Huentelman, Matthew J and Ilyas Kamboh, M and Larson, Eric B and Rogaeva, Ekaterina and George-Hyslop, Peter St and Hakonarson, Hakon and Kukull, Walter A and Farrer, Lindsay A and Barnes, Lisa L and Beach, Thomas G and Yesim Demirci, F and Head, Elizabeth and Hulette, Christine M and Jicha, Gregory A and Kauwe, John S.K and Kaye, Jeffrey A and Leverenz, James B and Levey, Allan I and Lieberman, Andrew P and Pankratz, Vernon S and Poon, Wayne W and Quinn, Joseph F and Saykin, Andrew J and Schneider, Lon S and Smith, Amanda G and Sonnen, Joshua A and Stern, Robert A and Van Deerlin, Vivianna M and Van Eldik, Linda J and Harold, Denise and Russo, Giancarlo and Rubinsztein, David C and Bayer, Anthony and Tsolaki, Magda and Proitsi, Petra and Fox, Nick C and Hampel, Harald and Owen, Michael J and Mead, Simon and Passmore, Peter and Morgan, Kevin and Nöthen, Markus M and Rossor, Martin and Lupton, Michelle K and Hoffmann, Per and Kornhuber, Johannes and Lawlor, Brian and McQuillin, Andrew and Al-Chalabi, Ammar and Bis, Joshua C and Ruiz, Agustin and Boada, Mercè and Seshadri, Sudha and Beiser, Alexa and Rice, Kenneth and Van Der Lee, Sven J and De Jager, Philip L and Geschwind, Daniel H and Riemenschneider, Matthias and Riedel-Heller, Steffi and Rotter, Jerome I and Ransmayr, Gerhard and Hyman, Bradley T and Cruchaga, Carlos and Alegret, Montserrat and Winsvold, Bendik and Palta, Priit and Farh, Kai-How and Cuenca-Leon, Ester and Furlotte, Nicholas and Kurth, Tobias and ... and Brainstorm Consortium and The Brainstorm Consortium
Science, ISSN 0036-8075, 06/2018, 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
by Gormley, A.M and Stefansson, Hreinn and Winsvold, Bendik and Palta, Priit and Esko, Tõnu and Pers, Tune and Farh, Kai-How and Cuenca-Leon, E and Muona, M and Furlotte, N.A and Kurth, Karl and Ingason, Anes and Mcmahon, George and Ligthart, Lannie and Terwindt, Gisela and Todt, Unda and Müller-Myhsok, Bertram and Ran, C and Gordon, S.G and Stam, Anine and Steinberg, Stacy and Göbel, Hartmut and Koiranen, Markku and Quaye, Lydia and Adams, H.H.H and Lehtimäki, Terho and Sarin, A.-P and Wedenoja, J and Hinds, David A and Buring, J.E and Schürks, Markus and Ridker, Paul and Hrafnsdottir, M.G and Ring, Susan and Hottenga, Jouke Jan and Penninx, Brenda and Färkkilä, Markus and Artto, Ville and Hämäläinen, Eija and Lucae, Susanne and Malik, Rainer and Heath, Anew C and Madden, Pamela and Martin, Nicholas and Montgomery, Grant and Kurki, M.I and Kals, Mart and Mägi, Reedik and Pärn, K and Hamalainen, Eija and Huang, H and Byrnes, A.E and Franke, Lude and Huang, Jian and Stergiakouli, Evangelia and Lee, Phil and Sandor, C and Webber, C and Cader, Z and Müller-Myhsok, B and Schreiber, Stefan and Meitinger, Thomas and Hagen, Knut and Salomaa, Veikko and Heikkilä, Kauko and Loehrer, Elizabeth and Uitterlinden, Ané and Hofman, A and Duijn, Cornelia and Cherkas, Lynn and Pedersen, L.M and Stubhaug, A and Nielsen, C.S and Männikkö, M and Mihailov, Evelin and Milani, Lili and Esserlind, A.-L and Christensen, A.F and Hansen, T.F and Werge, Thomas and Kaprio, Jaakko and Aromaa, Arpo and Raitakari, Olli and Ikram, Arfan and Ikram, Kamran and Jarvelin, Marjo-Riitta and Metspalu, Anes and Kubisch, Christian and Strachan, David and Ferrari, Michel and Belin, A.C and Wessman, Maija and Maagdenberg, Arn and Zwart, John-Anker and Boomsma, Dorret and Smith, G.D and Stefansson, K and Eriksson, Nicholas and Daly, Mark and Neale, Benjamin and ... and Int Headache Genetics Consortium and International Headache Genetics Consortium
Nature Genetics, ISSN 1061-4036, 08/2016, Volume 48, Issue 8, pp. 856 - 866
Journal Article
Nature Genetics, ISSN 1061-4036, 07/2012, Volume 44, Issue 7, pp. 777 - 782
Journal Article
by Anttila, Verneri and Stefansson, Hreinn and Kallela, Mikko and Todt, Unda and Terwindt, Gisela M and Calafato, M Stella and Nyholt, Dale R and Dimas, Antigone S and Freilinger, Tobias and Müller-Myhsok, Bertram and Artto, Ville and Inouye, Michael and Alakurtti, Kirsi and Kaunisto, Mari A and Hämäläinen, Eija and De Vries, Boukje and Stam, Anine H and Weller, Claudia M and Heinze, Axel and Heinze-Kuhn, Katja and Goebel, Ingrid and Borck, Guntram and Göbel, Hartmut and Steinberg, Stacy and Wolf, Christiane and Björnsson, Asgeir and Gudmundsson, Gretar and Kirchmann, Malene and Hauge, Anne and Werge, Thomas and Schoenen, Jean and Eriksson, Johan G and Hagen, Knut and Stovner, Lars and Wichmann, H-Erich and Meitinger, Thomas and Alexander, Michael and Moebus, Susanne and Schreiber, Stefan and Aulchenko, Yurii S and Breteler, Monique M. B and Uitterlinden, Andre G and Hofman, Albert and Van Duijn, Cornelia M and Tikka-Kleemola, Päivi and Vepsäläinen, Salli and Lucae, Susanne and Tozzi, Federica and Muglia, Pierandrea and Barrett, Jeffrey and Kaprio, Jaakko and Färkkilä, Markus and Peltonen, Leena and Stefansson, Kari and Zwart, John-Anker and Ferrari, Michel D and Olesen, Jes and Daly, Mark and Wessman, Maija and Van Den Maagdenberg, Arn M.J.M and Dichgans, Martin and Kubisch, Christian and Dermitzakis, Emmanouil T and Frants, Rune R and Palotie, Aarno and Int Headache Genetics Consortium and International Headache Genetics Consortium and the International Headache Genetics Consortium
Nature Genetics, ISSN 1061-4036, 10/2010, Volume 42, Issue 10, pp. 869 - 873
Journal Article
Lancet Oncology, The, ISSN 1470-2045, 2015, Volume 16, Issue 8, pp. 949 - 956
Summary Background Diffuse-type tenosynovial giant cell tumour (dt-GCT) of the soft tissue (alternatively known as pigmented villonodular synovitis), an orphan... 
Hematology, Oncology and Palliative Medicine | PIGMENTED VILLONODULAR SYNOVITIS | DIAGNOSIS | THERAPY | EFFICACY | ONCOLOGY | PERIORBITAL EDEMA SECONDARY | MACROPHAGES | RECEPTOR | ANTIBODY | ARTHRITIS | IMATINIB MESYLATE | Receptor, Macrophage Colony-Stimulating Factor - antagonists & inhibitors | Receptor, Macrophage Colony-Stimulating Factor - immunology | Giant Cell Tumors - immunology | Humans | Middle Aged | Antibodies, Monoclonal - adverse effects | Giant Cell Tumors - pathology | Soft Tissue Neoplasms - drug therapy | Male | Antineoplastic Agents - administration & dosage | Giant Cell Tumors - metabolism | Receptor, Macrophage Colony-Stimulating Factor - metabolism | Synovitis, Pigmented Villonodular - drug therapy | Synovitis, Pigmented Villonodular - pathology | Soft Tissue Neoplasms - immunology | Young Adult | Time Factors | Antineoplastic Agents - adverse effects | Aged, 80 and over | Adult | Female | Drug Administration Schedule | Soft Tissue Neoplasms - metabolism | Synovitis, Pigmented Villonodular - metabolism | Treatment Outcome | Synovitis, Pigmented Villonodular - immunology | Giant Cell Tumors - drug therapy | Signal Transduction - drug effects | Antibodies, Monoclonal - administration & dosage | Adolescent | Soft Tissue Neoplasms - pathology | Aged | Infusions, Intravenous | Monoclonal antibodies | Macrophage colony stimulating factor | Tumors
Journal Article
Journal Article
Neurology, ISSN 0028-3878, 2015, Volume 84, Issue 21, pp. 2132 - 2145
Journal Article