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by Traylor, Matthew and Farrall, Martin and Holliday, Elizabeth G and Sudlow, Cathie and Hopewell, Jemma C and Cheng, Yu-Ching and Fornage, Myriam and Ikram, M Arfan and Malik, Rainer and Bevan, Steve and Thorsteinsdottir, Unnur and Nalls, Mike A and Longstreth, WT and Wiggins, Kerri L and Yadav, Sunaina and Parati, Eugenio A and DeStefano, Anita L and Worrall, Bradford B and Kittner, Steven J and Khan, Muhammad Saleem and Reiner, Alex P and Helgadottir, Anna and Achterberg, Sefanja and Fernandez-Cadenas, Israel and Abboud, Sherine and Schmidt, Reinhold and Walters, Matthew and Chen, Wei-Min and Ringelstein, E Bernd and O'Donnell, Martin and Ho, Weang Kee and Pera, Joanna and Lemmens, Robin and Norrving, Bo and Higgins, Peter and Benn, Marianne and Sale, Michele and Kuhlenbäumer, Gregor and Doney, Alexander S F and Vicente, Astrid M and Delavaran, Hossein and Algra, Ale and Davies, Gail and Oliveira, Sofia A and Palmer, Colin N A and Deary, Ian and Schmidt, Helena and Pandolfo, Massimo and Montaner, Joan and Carty, Cara and de Bakker, Paul I W and Kostulas, Konstantinos and Ferro, Jose M and van Zuydam, Natalie R and Valdimarsson, Einar and Nordestgaard, Børge G and Lindgren, Arne and Thijs, Vincent and Slowik, Agnieszka and Saleheen, Danish and Paré, Guillaume and Berger, Klaus and Thorleifsson, Gudmar and Hofman, Albert and Mosley, Thomas H and Mitchell, Braxton D and Furie, Karen and Clarke, Robert and Levi, Christopher and Seshadri, Sudha and Gschwendtner, Andreas and Boncoraglio, Giorgio B and Sharma, Pankaj and Bis, Joshua C and Gretarsdottir, Solveig and Psaty, Bruce M and Rothwell, Peter M and Rosand, Jonathan and Meschia, James F and Stefansson, Kari and Dichgans, Martin and Markus, Hugh S and The Australian Stroke Genetics Collaborative, Wellcome Trust Case Control Consortium 2 (WTCCC2) and on behalf of the International Stroke Genetics Consortium and WTCCC 2 and Australian Stroke Genetics Collabo and Int Stroke Genetics Consortium and International Stroke Genetics Consortium and Australian Stroke Genetics Collaborative, Wellcome Trust Case Control Consortium 2 (WTCCC2)
Lancet neurology, ISSN 1474-4422, 2012, Volume 11, Issue 11, pp. 951 - 962
Journal Article
Lancet Neurology, The, ISSN 1474-4422, 2013, Volume 12, Issue 5, pp. 483 - 497
Journal Article
by Gormley, Padhraig and Anttila, Verneri and Winsvold, Bendik S and Palta, Priit and Esko, Tonu and Pers, Tune H and Farh, Kai-How and Cuenca-Leon, Ester and Muona, Mikko and Furlotte, Nicholas A and Kurth, Tobias and Ingason, Andres and McMahon, George and Ligthart, Lannie and Terwindt, Gisela M and Kallela, Mikko and Freilinger, Tobias M and Ran, Caroline and Gordon, Scott G and Stam, Anine H and Steinberg, Stacy and Borck, Guntram and Koiranen, Markku and Quaye, Lydia and Adams, Hieab H H and Lehtimäki, Terho and Sarin, Antti-Pekka and Wedenoja, Juho and Hinds, David A and Buring, Julie E and Schürks, Markus and Ridker, Paul M and Hrafnsdottir, Maria Gudlaug and Stefansson, Hreinn and Ring, Susan M and Hottenga, Jouke-Jan and Penninx, Brenda W J H and Färkkilä, Markus and Artto, Ville and Kaunisto, Mari and Vepsäläinen, Salli and Malik, Rainer and Heath, Andrew C and Madden, Pamela A F and Martin, Nicholas G and Montgomery, Grant W and Kurki, Mitja I and Kals, Mart and Mägi, Reedik and Pärn, Kalle and Hämäläinen, Eija and Huang, Hailiang and Byrnes, Andrea E and Franke, Lude and Huang, Jie and Stergiakouli, Evie and Lee, Phil H and Sandor, Cynthia and Webber, Caleb and Cader, Zameel and Muller-Myhsok, Bertram and Schreiber, Stefan and Meitinger, Thomas and Eriksson, Johan G and Salomaa, Veikko and Heikkilä, Kauko and Loehrer, Elizabeth and Uitterlinden, Andre G and Hofman, Albert and van Duijn, Cornelia M and Cherkas, Lynn and Pedersen, Linda M and Stubhaug, Audun and Nielsen, Christopher S and Männikkö, Minna and Mihailov, Evelin and Milani, Lili and Göbel, Hartmut and Esserlind, Ann-Louise and Christensen, Anne Francke and Hansen, Thomas Folkmann and Werge, Thomas and Kaprio, Jaakko and Aromaa, Arpo J and Raitakari, Olli and Ikram, M Arfan and Spector, Tim and Järvelin, Marjo-Riitta and Metspalu, Andres and Kubisch, Christian and Strachan, David P and Ferrari, Michel D and Belin, Andrea C and Dichgans, Martin and Wessman, Maija and van den Maagdenberg, Arn M J M and Zwart, John-Anker and Boomsma, Dorret I and Smith, George Davey and Stefansson, Kari and ... and International Headache Genetics Consortium and Int Headache Genetics Consortium
Nature genetics, ISSN 1546-1718, 2016, Volume 48, Issue 8, pp. 856 - 866
Journal Article
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 Lehtimäki, 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 Schürks, 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 Färkkilä, 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, Andrew C and Madden, Pamela A F and Montgomery, Grant W and Martin, Nicholas G and Borck, Guntram and Göbel, 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, Andre G and Hofman, Albert and Amin, Najaf and Hottenga, Jouke-Jan and Vink, Jacqueline M and Heikkilä, 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 UK Brain Expression Consortium and the International Headache Genetics Consortium and North American Brain Expression Consortium and Int Headache Genetics Consortium and North Amer Brain Expression
Nature genetics, ISSN 1546-1718, 2013, Volume 45, Issue 8, pp. 912 - 917
Migraine is the most common brain disorder, affecting approximately 14% of the adult population, but its molecular mechanisms are poorly understood. We report... 
POPULATION | HUMAN-DISEASE | PROTEIN | NEURITE OUTGROWTH | DOWN-REGULATION | TRANSFORMING-GROWTH-FACTOR | PROTEOLYSIS | ASSOCIATION | EXPRESSION | FAMILY | LEWIS(X) | GENES | GENETICS & HEREDITY | MUTATIONS | Genetic susceptibility | Genetic variation | Migraine | Physiological aspects | Genetic aspects | Research | Risk factors | Studies | Proteins | Signal transduction | Headaches | Population | Genomes | Meta-analysis
Journal Article
Neurology, ISSN 0028-3878, 10/2017, Volume 89, Issue 17, pp. 1829 - 1839
Journal Article
by Holliday, Elizabeth G and Maguire, Jane M and Evans, Tiffany-Jane and Koblar, Simon A and Jannes, Jim and Sturm, Jonathan W and Hankey, Graeme J and Baker, Ross and Golledge, Jonathan and Parsons, Mark W and Malik, Rainer and McEvoy, Mark and Biros, Erik and Lewis, Martin D and Lincz, Lisa F and Peel, Roseanne and Oldmeadow, Christopher and Smith, Wayne and Moscato, Pablo and Barlera, Simona and Bevan, Steve and Bis, Joshua C and Boerwinkle, Eric and Boncoraglio, Giorgio B and Brott, Thomas G and Brown, Robert D and Cheng, Yu-Ching and Cole, John W and Cotlarciuc, Ioana and Devan, William J and Fornage, Myriam and Furie, Karen L and Grétarsdóttir, Sólveig and Gschwendtner, Andreas and Ikram, M Arfan and Longstreth, W.T and Meschia, James F and Mitchell, Braxton D and Mosley, Thomas H and Nalls, Michael A and Parati, Eugenio A and Psaty, Bruce M and Sharma, Pankaj and Stefansson, Kari and Thorleifsson, Gudmar and Thorsteinsdottir, Unnur and Traylor, Matthew and Verhaaren, Benjamin F. J and Wiggins, Kerri L and Worrall, Bradford B and Sudlow, Cathie and Rothwell, Peter M and Farrall, Martin and Dichgans, Martin and Rosand, Jonathan and Markus, Hugh S and Scott, Rodney J and Levi, Christopher and Attia, John and International Stroke Genetics Cons and Wellcome Trust Case Control Consor and Australian Stroke Genetics Collabo and International Stroke Genetics Consortium and Wellcome Trust Case Control Consortium 2 and Australian Stroke Genetics Collaborative and The Wellcome Trust Case Control Consortium 2 and The Australian Stroke Genetics Collaborative and The International Stroke Genetics Consortium
Nature genetics, ISSN 1061-4036, 10/2012, Volume 44, Issue 10, pp. 1147 - 1151
Journal Article