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The Lancet, ISSN 0140-6736, 2008, Volume 371, Issue 9623, pp. 1505 - 1512
Journal Article
Lancet, The, ISSN 0140-6736, 2017, Volume 390, Issue 10091, pp. 267 - 275
Journal Article
PLoS Genetics, ISSN 1553-7390, 2014, Volume 10, Issue 7, pp. e1004494 - e1004494
Exome sequencing studies in complex diseases are challenged by the allelic heterogeneity, large number and modest effect sizes of associated variants on... 
PROFILE | GENE | MUTATION | DISEASE | GENETICS & HEREDITY | LEVEL | ASSOCIATION | CARDIOVASCULAR RISK | Physiological aspects | Genetic research | Genome-wide association studies | Research | Lipoprotein A | Index Medicus | Heart attacks | Disease | Genomics | Genes | Biomarkers | Medical records | Population | Grants
Journal Article
by Day, Ian and Dermitzakis, Emmanouil T and Randall, Joshua C and Weedon, Michael N and Hinney, Anke and Evans, David M and Qi, Lu and Bennett, Amanda J and Munroe, Patricia B and Herrera, Blanca and Johnson, Toby and Elliott, Katherine S and Song, Kijoung and Zeggini, Eleftheria and Cauchi, Stéphane and Teichmann, Sarah A and Lindgren, Cecilia M and Brown, Morris and Sims, Matthew A and Karpe, Fredrik and O'Rahilly, Stephen and Hattersley, Andrew T and Scherag, André and Samani, Nilesh J and Keniry, Andrew and Li, Shengxu and Beckmann, Jacques S and Cooper, Cyrus and Caulfield, Mark J and Owen, Katharine R and Luben, Robert N and McGinnis, Ralph and Ghori, Jilur and Ness, Andrew R and Bochud, Murielle and Jarvelin, Marjo-Riitta and Hebebrand, Johannes and Ong, Ken K and Freathy, Rachel M and McArdle, Wendy L and Potter, Simon and Wareham, Nicholas J and Ganz Vogel, Carla I and Mooser, Vincent and Barroso, Inês and Deloukas, Panos and Waterworth, Dawn M and Bergmann, Sven and Elliott, Paul and Gwilliam, Rhian and Tobias, Jonathan H and Jolley, Jennifer D M and Morris, Andrew D and Loos, Ruth J F and Yuan, Xin and Smith, George Davey and Palmer, Colin N A and Groves, Christopher J and Dina, Christian and Syddall, Holly E and Waeber, Gerard and Zhao, Jing Hua and Sandhu, Manjinder S and Doney, Alex S F and Hunt, Sarah E and Pouta, Anneli and Speliotes, Elizabeth K and Connell, John M and Timpson, Nicholas J and Wallace, Chris and Attwood, Antony P and Hall, Alistair S and Khaw, Kay-Tee and Meyre, David and Vollenweider, Peter and Bingham, Sheila A and Berndt, Sonja I and Hadley, David and Rayner, Nigel W and Frayling, Timothy M and Sadaf Farooqi, I and Hirschhorn, Joel N and Strachan, David P and Inouye, Michael and Papadakis, Konstantinos and Ring, Susan M and Wraight, Vicki L and Willer, Cristen J and Marchini, Jonathan and Uda, Manuela and Nica, Alexandra C and Mangino, Massimo and Soranzo, Nicole and McCarthy, Mark I and De, Subhajyoti and Neville, Matthew J and Prokopenko, Inga and Wheeler, Eleanor and Heid, Iris M and Froguel, Philippe and ... and Diabetes Genetics Initiative and SardiNIA Study and FUSION and Prostate Lung Colorectal Ovarian and KORA and Wellcome Trust Case Control Consor and Nurses' Health Study and Wellcome Trust Case Control Consortium and Prostate, Lung, Colorectal, and Ovarian (PLCO) Cancer Screening Trial and The Prostate, Lung, Colorectal, and Ovarian (PLCO) Cancer Screening Trial and The Wellcome Trust Case Control Consortium and The SardiNIA Study and Diabetes - klinisk obesitasforskning and Genomik, diabetes och endokrinologi and Lund University and Genomics, Diabetes and Endocrinology and Diabetes - Clinical Obesity and Lunds universitet
Nature Genetics, ISSN 1061-4036, 06/2008, Volume 40, Issue 6, pp. 768 - 775
To identify common variants influencing body mass index (BMI), we analyzed genome-wide association data from 16,876 individuals of European descent. After... 
FTO GENE | GENETICS & HEREDITY | MELANOCORTIN-4 RECEPTOR GENE | EARLY-ONSET OBESITY | FRAMESHIFT MUTATION | DOMINANT | ADULT OBESITY | EXPRESSION | CHILDHOOD | DEFICIENCY | GENOME-WIDE ASSOCIATION | Meta-Analysis as Topic | Humans | Middle Aged | Alpha-Ketoglutarate-Dependent Dioxygenase FTO | Male | Body Weight - genetics | Obesity - genetics | Case-Control Studies | Genetic Variation | Proteins | Adult | Female | Child | Body Mass Index | Genetic Predisposition to Disease | Cross-Sectional Studies | Receptor, Melanocortin, Type 4 - genetics | Adiposity - genetics | Linkage Disequilibrium | Obesity - pathology | Randomized Controlled Trials as Topic | Obesity - epidemiology | Adolescent | Alleles | Aged | Polymorphism, Single Nucleotide | Chromosomes, Human, Pair 18 - genetics | Genome, Human | Quantitative Trait Loci | Cohort Studies | Obesity | Body mass index | Genetic variation | Physiological aspects | Genetic aspects | Diagnosis | Research | Risk factors | Medical research | Biomedical research | Body fat | Health services | Genetics | Birth weight | Adults | Progeny | Integration | Pedigree | Data processing | Melanocortin MC4 receptors | Single-nucleotide polymorphism | Children | Mutation | Population levels | Index Medicus | Clinical Medicine | Näringslära | Hälsovetenskap | Endokrinologi och diabetes | Medical and Health Sciences | Medicin och hälsovetenskap | Klinisk medicin | Nutrition and Dietetics | Endocrinology and Diabetes | Health Sciences
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
by Prokopenko, I and Langenberg, C and Florez, J.C and Saxena, R and Soranzo, N and Thorleifsson, G and Loos, R.J.F and Manning, A.K and Jackson, A.U and Aulchenko, Y.S and Potter, S.C and Erdos, M.R and Sanna, S and Hottenga, J.J and Wheeler, E and Kaakinen, M and Lyssenko, V and Chen, W.-M and Ahmadi, K and Beckmann, J.S and Bergman, R.N and Bochud, M and Bonnycastle, L.L and Buchanan, T.A and Cao, A and Cervin, A and Coin, L and Collins, F.S and Crisponi, L and de Geus, E.J.C and Dehghan, A and Deloukas, P and Doney, A.S.F and Elliott, P and Freimer, N.B and Gateva, V and Herder, C and Hofman, A and Hughes, T.E and Hunt, S and Illig, T and Inouye, M and Isomaa, B and Johnson, T and Kong, A and Krestyaninova, M and Kuusisto, J and Laaks, M and Lim, N and Lindblad, U and Lindgren, C.M and McCann, O.T and Mohlke, K.L and Morris, A.D and Naitza, S and Orrù, M and Palmer, C.N.A and Pouta, A and Randall, J and Rathmann, W and Saramies, J and Scheet, P and Scott, L.J and Scuteri, A and Sharp, S and Sijbrands, E.J.G and Smit, J.H and Song, K and Steinthorsdottir, V and Stringham, H.M and Tuomi, T and Tuomilehto, J and Uitterlinden, A.G and Voight, B.F and Waterworth, D and Wichmann, H.-E and Willemsen, G and Witteman, J.C.M and Yuan, X and Zha, J.H and Zeggini, E and Schlessinger, D and Sandhu, M and Boomsma, D.I and Uda, M and Spector, T.D and Penninx, B.W.J.H and Altshuler, D and Vollenweider, P and Jarvelin, M.-R and Lakatta, E and Waeber, G and Fox, C.S and Peltonen, L and Groop, L.C and Mooser, V and Cupples, L.A and Thorsteinsdottir, U and Abecasis, G.R and Institutionen för medicin, avdelningen för samhällsmedicin och folkhälsa and Sahlgrenska akademin and Göteborgs universitet and Gothenburg University and Sahlgrenska Academy and Institute of Medicine, Department of Public Health and Community Medicine
Nature Genetics, ISSN 1061-4036, 2009, Volume 41, Issue 1, pp. 77 - 81
Journal Article