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Nature genetics, ISSN 1546-1718, 2012, Volume 44, Issue 3, pp. 269 - 276
Journal Article
Science (American Association for the Advancement of Science), ISSN 1095-9203, 2007, Volume 316, Issue 5823, pp. 445 - 449
Journal Article
Journal Article
Diabetes care, ISSN 1935-5548, 2012, Volume 35, Issue 8, pp. 1749 - 1756
Journal Article
Journal Article
Journal of the American College of Cardiology, ISSN 0735-1097, 2016, Volume 67, Issue 10, pp. 1200 - 1210
Abstract Background Statins are first-line therapy for cardiovascular disease prevention, but their systemic effects across lipoprotein subclasses, fatty... 
Cardiovascular | Internal Medicine | drug development | Mendelian randomization | metabolomics | cholesterol lowering | lipoproteins | COHORT PROFILE | CARDIAC & CARDIOVASCULAR SYSTEMS | BIOMARKER | VARIANTS | FATTY-ACID-COMPOSITION | RISK | TRIGLYCERIDES | LDL CHOLESTEROL | CORONARY-HEART-DISEASE | ASSOCIATION | EPIDEMIOLOGY | Hydroxymethylglutaryl CoA Reductases - drug effects | Mendelian Randomization Analysis - methods | Magnetic Resonance Spectroscopy - methods | Cardiovascular Diseases - prevention & control | Humans | Middle Aged | Male | United Kingdom | Cardiovascular Diseases - genetics | Forecasting | Metabolomics - methods | Hydroxymethylglutaryl-CoA Reductase Inhibitors - therapeutic use | Finland | Cardiovascular Diseases - blood | Adult | Female | Retrospective Studies | Hydroxymethylglutaryl CoA Reductases - blood | Hydroxymethylglutaryl CoA Reductases - genetics | Medical colleges | Metabolites | Pharmacy | Genomics | Genetic research | Drugstores | Fatty acids | Epidemiology | Statins | Public health | Cardiovascular agents | Lipids | Cholesterol | LDL-C, low-density lipoprotein cholesterol | CVD, cardiovascular disease | IDL, intermediate-density lipoprotein | VLDL, very-low-density lipoprotein | HMGCR, HMG-CoA reductase | NMR, nuclear magnetic resonance | HDL, high-density lipoprotein | Original Investigation
Journal Article
Journal Article
PLoS genetics, ISSN 1553-7404, 2014, Volume 10, Issue 7, p. e1004494
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