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by Hollingworth, P and Harold, D and Sims, R and Gerrish, A and Lambert, J.C and Carrasquillo, M.M and Abraham, R and Hamshere, M.L and Pahwa, J.S and Moskvina, V and Dowzell, K and Jones, N and Stretton, A and Thomas, C and Richards, A and Ivanov, D and Widdowson, C and Chapman, J and Lovestone, S and Powell, J and Proitsi, P and Lupton, M.K and Brayne, C and Rubinsztein, D.C and Gill, M and Lawlor, B and Lynch, A and Brown, K.S and Passmore, P.A and Craig, D and McGuinness, B and Todd, S and Holmes, C and Mann, D and Smith, A.D and Beaumont, H and Warden, D and Wilcock, G and Love, S and Kehoe, P.G and Hooper, N.M and Vardy, E.R.L.C and Hardy, J and Mead, S and Fox, N.C and Rossor, M and Collinge, J and Maier, W and Jessen, F and Ruther, E and Schurmann, B and Heun, R and Kolsch, H and van den Bussche, H and Heuser, I and Kornhuber, J and Wiltfang, J and Dichgans, M and Frolich, L and Hampel, H and Gallacher, J and Hull, M and Rujescu, D and Giegling, I and Goate, A.M and Kauwe, J.S.K and Cruchaga, C and Nowotny, P and Morris, J.C and Mayo, K and Sleegers, K and Bettens, K and Engelborghs, S and de Deyn, P.P and Van Broeckhoven, C and Livingston, G and Bass, N.J and Gurling, H and McQuillin, A and Gwilliam, R and Deloukas, P and Al-Chalabi, A and Shaw, C.E and Tsolaki, M and Singleton, A.B and Guerreiro, R and Muhleisen, T. W and Nothen, M. M and Moebus, S and Jockel, K.H and Klopp, N and Wichmann, H. E and Pankratz, V.S and Sando, S.B and Aasly, J.O and Barcikowska, M and Wszolek, Z.K and Dickson, D.W and Graff-Radford, N.R. and others and Alzheimer's Dis Neuroimaging and EADI1 Consortium and CHARGE Consortium and Alzheimer's Disease Neuroimaging Initiative and EADI1 consortium and CHARGE consortium and the Alzheimer's Disease Neuroimaging Initiative
Nature Genetics, ISSN 1061-4036, 2011, Volume 43, Issue 5, pp. 429 - 435
Journal Article
by Deloukas, Panagiotis and Hamshere, Marian L and Lovestone, Simon and Mead, Simon and Nöthen, Markus M and Gerrish, Amy and O'Donovan, Michael and Hüll, Michael and Hardy, John and Hampel, Harald and Passmore, Peter A and Engelborghs, Sebastiaan and Abraham, Richard and Thomas, Charlene and Moskvina, Valentina and Brayne, Carol and Lawlor, Brian and Bass, Nicholas J and McQuillin, Andrew and Holmans, Peter A and Jones, Nicola and Pahwa, Jaspreet Singh and Morgan, Kevin and Klopp, Norman and Schürmann, Britta and Carrasquillo, Minerva M and Jessen, Frank and Tsolaki, Magda and McGuinness, Bernadette and Van Broeckhoven, Christine and De Deyn, Peter P and Cruchaga, Carlos and Mayo, Kevin and Wichmann, H-Erich and Brown, Kristelle S and Fox, Nick and Proitsi, Petroula and Mühleisen, Thomas W and Lupton, Michelle K and Lynch, Aoibhinn and Williams, Julie and Singleton, Andrew B and Moebus, Susanne and Dowzell, Kimberley and Livingston, Gill and Powell, John and Todd, Stephen and Wiltfang, Jens and Kornhuber, Johannes and Shaw, Christopher E and Pankratz, V Shane and Owen, Michael J and Holmes, Clive and Kehoe, Patrick G and Al-Chalabi, Ammar and Morgan, Angharad R and Heuser, Isabella and Williams, Amy and Mann, David and Gurling, Hugh and Kauwe, John S K and Goate, Alison M and Frölich, Lutz and Rubinsztein, David C and Love, Seth and Rossor, Martin and Rujescu, Dan and Hollingworth, Paul and Bettens, Karolien and Younkin, Steven G and Nowotny, Petra and Dichgans, Martin and Smith, A David and Collinge, John and van den Bussche, Hendrik and Gwilliam, Rhian and Guerreiro, Rita and Jöckel, Karl-Heinz and Sims, Rebecca and Morris, John C and Gill, Michael and Craig, David and Sleegers, Kristel and Harold, Denise and Stretton, Alexandra and Maier, Wolfgang
Nature Genetics, ISSN 1061-4036, 10/2009, Volume 41, Issue 10, pp. 1088 - 1093
Journal Article
by Fisher, Sheila A and Regueiro, Miguel D and Anderson, Carl A and Prescott, Natalie J and Mathew, Christopher G and Rutgeerts, Paul and Parkes, Miles and Steinhart, A Hillary and Drummond, Hazel and Bitton, Alain and Georges, Michel and Gut, Ivo and Jewell, Derek and Barrett, Jeffrey C and Daly, Mark J and Dewit, Olivier and Bumpstead, Suzannah and Hansoul, Sarah and Hugot, Jean-Pierre and Barmada, M Michael and Xavier, Ramnik J and Libioulle, Cécile and Tremelling, Mark and Laukens, Debby and Datta, Lisa Wu and Kistner, Emily O and Onnie, Clive M and Griffiths, Anne M and Franchimont, Denis and Lathrop, Mark and Nimmo, Elaine and Green, Todd and Mansfield, John and Zelenika, Diana and Deloukas, Panos and Taylor, Kent D and Ahmad, Tariq and de Vos, Martine and Van Gossum, André and Duerr, Richard H and Silverberg, Mark S and Nicolae, Dan L and Rotter, Jerome I and Schumm, L Philip and Cardon, Lon R and Ghori, Jilur and Heath, Simon and Dassopoulos, Themistocles and Vermeire, Severine and Sandor, Cynthia and Satsangi, Jack and Marchini, Jonathan and Gwilliam, Rhian and Louis, Edouard and Rioux, John D and Mni, Myriam and Belaiche, Jacques and Targan, Stephan R and Brant, Steven R and Murtha, Michael T and Cho, Judy H and Wellcome Trust Case Control and NIDDK IBD Genetics Consortium and Belgian-French IBD Consortium and Wellcome Trust Case Control Consortium and the NIDDK IBD Genetics Consortium and the Belgian-French IBD Consortium and the Wellcome Trust Case Control Consortium
Nature Genetics, ISSN 1061-4036, 08/2008, Volume 40, Issue 8, pp. 955 - 962
Journal Article
Nature Genetics, ISSN 1061-4036, 04/2010, Volume 42, Issue 4, pp. 295 - U42
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 | Body mass index | Obesity | Progeny | Integration | Body fat | Pedigree | Data processing | Melanocortin MC4 receptors | Single-nucleotide polymorphism | Children | Mutation | Population levels | Meta-Analysis as Topic | Biomedical research | Body Weight | Health services | Humans | Middle Aged | Male | Case-Control Studies | Genetic Variation | Proteins | Receptor, Melanocortin, Type 4 | FTO protein, human | Adiposity | Genetics | Adult | Female | Child | Body Mass Index | Medical research | Genetic Predisposition to Disease | Cross-Sectional Studies | Linkage Disequilibrium | Randomized Controlled Trials as Topic | Chromosomes, Human, Pair 18 | Adolescent | Alleles | Birth weight | Adults | Aged | Polymorphism, Single Nucleotide | Genome, Human | Quantitative Trait Loci | Cohort Studies | Alpha-Ketoglutarate-Dependent Dioxygenase FTO | Body Weight - genetics | Obesity - genetics | Receptor, Melanocortin, Type 4 - genetics | Adiposity - genetics | Obesity - pathology | Obesity - epidemiology | Chromosomes, Human, Pair 18 - genetics | Genetic variation | Physiological aspects | Genetic aspects | Diagnosis | Research | Risk factors | 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 Dupuis, Josée and Langenberg, Claudia and Prokopenko, Inga and Saxena, Richa and Soranzo, Nicole and Jackson, Anne and Wheeler, Eleanor and Glazer, Nicole and Bouatia-Naji, Nabila and Gloyn, Anna and Lindgren, Cecilia and Mägi, Reedik and Morris, Anew and Randall, Joshua and Johnson, Toby and Elliott, Paul and Rybin, Denis and Thorleifsson, Gudmar and Steinthorsdottir, Valgerdur and Henneman, Peter and Grallert, Harald and Dehghan, Abbas and JanHottenga, Jouke and Franklin, Christopher and Navarro, Pau and Song, Kijoung and Goel, Anuj and Perry, John and Egan, Josephine and Lajunen, Taina and Grarup, Niels and Sparsø, Thomas and Doney, Alex and Voight, Benjamin and Stringham, Heather and Li, Man and Kanoni, Stavroula and Shrader, Peter and Cavalcanti-Proença, Christine and Kumari, Meena and Qi, Lu and Timpson, Nicholas and Gieger, Christian and Zabena, Carina and Rocheleau, Ghislain and Ingelsson, Erik and An, Ping and O´Connell, J.R and Luan, J and McCarroll, Steven and Payne, Felicity and Roccasecca, R.M and Pattou, François and Sethupathy, Praveen and Ardlie, Kristin and Ariyurek, Yavuz and Balkau, Beverley and Barter, Phil and Beilby, John and Ben-Shlomo, Y and Benediktsson, Rafn and Bennett, Amanda and Bergmann, Sven and Bochud, Murielle and Boerwinkle, Eric and Bonnefond, Amélie and Bonnycastle, Lori and Borch-Johnsen, K and Böttcher, Yvonne and Brunner, Eric and Bumpstead, Suzannah and Charpentier, Guillaume and IdaChen, Yii and Chines, Peter and Clarke, R and McOin, Lachlan and Cooper, Matthew and Cornelis, Marilyn and Crawford, Gabe and Crisponi, Laura and Day, Ian and Geus, Eco and Delplanque, Jerome and Dina, Christian and Erdos, Michael and Fedson, Annette and Fischer-Rosinsky, Antje and Forouhi, Nita and Fox, Caroline and Frants, Rune and GraziaFranzosi, Maria and Galan, Pilar and Goodarzi, Mark and Graessler, Jürgen and Groves, Christopher and Grundy, Scott and Gwilliam, Rhian and Gyllensten, Ulf and Hadjadj, Samy and Hallmans, Göran and ... and DIAGRAM Consortium and Global BPgen Consortium and Anders Hamsten Procardis Consortiu and GIANT Consortium and MAGIC Investigators and Anders Hamsten on behalf of Procardis Consortium and MAGIC investigators and the MAGIC investigators and Medicinska fakulteten and Institutionen för folkhälsa och klinisk medicin and Allmänmedicin and Näringsforskning and Umeå universitet and Medicin
Nature Genetics, ISSN 1061-4036, 02/2010, Volume 42, Issue 2, pp. 105 - 116
textabstractLevels of circulating glucose are tightly regulated. To identify new loci influencing glycemic traits, we performed meta-analyses of 21 genome-wide... 
CIRCADIAN CLOCK | COMMON VARIANTS | DISEASE RISK | TRIGLYCERIDE LEVELS | INSULIN-SECRETION | GENETICS & HEREDITY | BETA-CELL DYSFUNCTION | PLASMA-GLUCOSE | MODEL ASSESSMENT | GENOME-WIDE ASSOCIATION | ESSENTIAL COMPONENTS | Circadian rhythms | Cell proliferation | Signal transduction | Reviews | Fasting | Insulin-like growth factor I | Diabetes mellitus | Development | Homeostasis | Glucose | Insulin | Meta-Analysis as Topic | Sample size | Humans | Databases, Genetic | Genetic Loci | DNA Copy Number Variations | Hyperglycemia | Adult | Diabetes Mellitus, Type 2 | Child | Genetic Predisposition to Disease | Genome-Wide Association Study | Reproducibility of Results | Quantitative Trait, Heritable | Gene Expression Regulation | Blood Glucose | Meta-analysis | Studies | Adolescent | Alleles | Polymorphism, Single Nucleotide | Diabetes | Quantitative Trait Loci | Diabetes Mellitus, Type 2 - genetics | Genetic Loci - genetics | DNA Copy Number Variations - genetics | Fasting - blood | Polymorphism, Single Nucleotide - genetics | Blood Glucose - genetics | Blood Glucose - metabolism | Homeostasis - genetics | Quantitative Trait Loci - genetics | Type 2 diabetes | Physiological aspects | Genetic aspects | Research | Health aspects | Risk factors | Index Medicus | Clinical Medicine | Medical and Health Sciences | Endokrinologi och diabetes | Klinisk medicin | Medicin och hälsovetenskap | Endocrinology and Diabetes
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