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Science, ISSN 0036-8075, 9/2010, Volume 329, Issue 5999, pp. 1650 - 1653
Journal Article
Nature genetics, ISSN 1061-4036, 2012, Volume 44, Issue 12, pp. 1370 - 1374
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 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
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
PLOS Genetics, ISSN 1553-7390, 2013, Volume 9, Issue 4, p. e1003415
Journal Article
PLoS Genetics, ISSN 1553-7390, 07/2009, Volume 5, Issue 7, p. e1000559
Facioscapulohumeral dystrophy (FSHD) is an autosomal dominant muscular dystrophy in which no mutation of pathogenic gene(s) has been identified. Instead, the... 
MAMMALIAN CHROMATIN | CONTROL REGION | HP1 PROTEINS | FISSION YEAST | NIPPED-B | ICF SYNDROME | GENETICS & HEREDITY | MUSCULAR-DYSTROPHY | DE-LANGE-SYNDROME | SILENT-CHROMATIN | GENE ACTIVATION
Journal Article