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Nature reviews. Genetics, ISSN 1471-0064, 2010, Volume 11, Issue 7, pp. 499 - 511
Journal Article
by Wray, Naomi R and Ripke, Stephan and Mattheisen, Manuel and Trzaskowski, Maciej and Byrne, Enda M and Abdellaoui, Abdel and Adams, Mark J and Agerbo, Esben and Air, Tracy M and Andlauer, Till M. F and Bacanu, Silviu-Alin and Bækvad-Hansen, Marie and Beekman, Aartjan F. T and Bigdeli, Tim B and Binder, Elisabeth B and Blackwood, Douglas R. H and Bryois, Julien and Buttenschøn, Henriette N and Bybjerg-Grauholm, Jonas and Cai, Na and Castelao, Enrique and Christensen, Jane Hvarregaard and Clarke, Toni-Kim and Coleman, Jonathan I. R and Colodro-Conde, Lucía and Couvy-Duchesne, Baptiste and Craddock, Nick and Crawford, Gregory E and Crowley, Cheynna A and Dashti, Hassan S and Davies, Gail and Deary, Ian J and Degenhardt, Franziska and Derks, Eske M and Direk, Nese and Dolan, Conor V and Dunn, Erin C and Eley, Thalia C and Eriksson, Nicholas and Escott-Price, Valentina and Kiadeh, Farnush Hassan Farhadi and Finucane, Hilary K and Forstner, Andreas J and Frank, Josef and Gaspar, Héléna A and Gill, Michael and Giusti-Rodríguez, Paola and Goes, Fernando S and Gordon, Scott D and Grove, Jakob and Hall, Lynsey S and Hannon, Eilis and Hansen, Christine Søholm and Hansen, Thomas F and Herms, Stefan and Hickie, Ian B and Hoffmann, Per and Homuth, Georg and Horn, Carsten and Hottenga, Jouke-Jan and Hougaard, David M and Hu, Ming and Hyde, Craig L and Ising, Marcus and Jansen, Rick and Jin, Fulai and Jorgenson, Eric and Knowles, James A and Kohane, Isaac S and Kraft, Julia and Kretzschmar, Warren W and Krogh, Jesper and Kutalik, Zoltán and Lane, Jacqueline M and Li, Yihan and Li, Yun and Lind, Penelope A and Liu, Xiaoxiao and Lu, Leina and MacIntyre, Donald J and MacKinnon, Dean F and Maier, Robert M and Maier, Wolfgang and Marchini, Jonathan and Mbarek, Hamdi and McGrath, Patrick and McGuffin, Peter and Medland, Sarah E and Mehta, Divya and Middeldorp, Christel M and Mihailov, Evelin and Milaneschi, Yuri and Milani, Lili and Mill, Jonathan and Mondimore, Francis M and Montgomery, Grant W and Mostafavi, Sara and Mullins, Niamh and Nauck, Matthias and Ng, Bernard and ... and eQTLGen and 23andMe and the Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium and Major Depressive Disorder Working and EQTLGEN and Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium
Nature genetics, ISSN 1546-1718, 2018, Volume 50, Issue 5, pp. 668 - 681
Journal Article
PLoS genetics, ISSN 1553-7404, 2009, Volume 5, Issue 6, p. e1000529
Journal Article
Nature genetics, ISSN 1546-1718, 2012, Volume 44, Issue 8, pp. 955 - 959
Journal Article
by Loos, Ruth J F and Lindgren, Cecilia M and Li, Shengxu and Wheeler, Eleanor and Zhao, Jing Hua and Prokopenko, Inga and Inouye, Michael and Freathy, Rachel M and Attwood, Antony P and Beckmann, Jacques S and Berndt, Sonja I and Bergmann, Sven and Bennett, Amanda J and Bingham, Sheila A and Bochud, Murielle and Brown, Morris and Cauchi, Stéphane and Connell, John M and Cooper, Cyrus and Smith, George Davey and Day, Ian and Dina, Christian and De, Subhajyoti and Dermitzakis, Emmanouil T and Doney, Alex S F and Elliott, Katherine S and Elliott, Paul and Evans, David M and Sadaf Farooqi, I and Froguel, Philippe and Ghori, Jilur and Groves, Christopher J and Gwilliam, Rhian and Hadley, David and Hall, Alistair S and Hattersley, Andrew T and Hebebrand, Johannes and Heid, Iris M and Herrera, Blanca and Hinney, Anke and Hunt, Sarah E and Jarvelin, Marjo-Riitta and Johnson, Toby and Jolley, Jennifer D M and Karpe, Fredrik and Keniry, Andrew and Khaw, Kay-Tee and Luben, Robert N and Mangino, Massimo and Marchini, Jonathan and McArdle, Wendy L and McGinnis, Ralph and Meyre, David and Munroe, Patricia B and Morris, Andrew D and Ness, Andrew R and Neville, Matthew J and Nica, Alexandra C and Ong, Ken K and O'Rahilly, Stephen and Owen, Katharine R and Palmer, Colin N A and Papadakis, Konstantinos and Potter, Simon and Pouta, Anneli and Qi, Lu and Randall, Joshua C and Rayner, Nigel W and Ring, Susan M and Sandhu, Manjinder S and Scherag, André and Sims, Matthew A and Song, Kijoung and Soranzo, Nicole and Speliotes, Elizabeth K and Syddall, Holly E and Teichmann, Sarah A and Timpson, Nicholas J and Tobias, Jonathan H and Uda, Manuela and Ganz Vogel, Carla I and Wallace, Chris and Waterworth, Dawn M and Weedon, Michael N and Willer, Cristen J and Wraight, Vicki L and Yuan, Xin and Zeggini, Eleftheria and Hirschhorn, Joel N and Strachan, David P and Ouwehand, Willem H and Caulfield, Mark J and Samani, Nilesh J and Frayling, Timothy M and Vollenweider, Peter and Waeber, Gerard and Mooser, Vincent and Deloukas, Panos and McCarthy, Mark I and Wareham, Nicholas J and ... and Diabetes Genetics Initiative and The Prostate, Lung, Colorectal, and Ovarian (PLCO) Cancer Screening Trial and FUSION and The Wellcome Trust Case Control Consortium and KORA and The SardiNIA Study and Nurses' Health Study and SardiNIA Study and Prostate Lung Colorectal Ovarian and Wellcome Trust Case Control Consor and Wellcome Trust Case Control Consortium and Prostate, Lung, Colorectal, and Ovarian (PLCO) Cancer Screening Trial
Nature genetics, ISSN 1546-1718, 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 | 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
Nature communications, ISSN 2041-1723, 2014, Volume 5, Issue 1, p. 3934
... 1000 Genomes Project haplotype reference panel Olivier Delaneau1, Jonathan Marchini1,2 & The 1000 Genomes Project Consortium* A major use of the 1000 Genomes... 
INDIVIDUALS | GENOTYPE IMPUTATION | MULTIDISCIPLINARY SCIENCES | FRAMEWORK | INFERENCE | ASSOCIATION | READS | DISCOVERY | Haplotypes | Genome-Wide Association Study | Algorithms | Gene Frequency | Humans | Alleles | Polymorphism, Single Nucleotide | Genome, Human | Microarray Analysis - statistics & numerical data
Journal Article
Nature genetics, ISSN 1546-1718, 2006, Volume 38, Issue 10, pp. 1166 - 1172
Journal Article