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by Majithia, A. R and Flannick, J and Shahinian, P and Guo, M and Bray, M.-A and Fontanillas, P and Gabriel, S. B and Rosen, E. D and Altshuler, D and Manning, A. K and Hartl, C and Agarwala, V and Green, T and Banks, E and DePristo, M and Poplin, R and Shakir, K and Fennell, T and Njolstad, P. R and Burtt, N and Gabriel, S and Fuchsberger, C and Kang, H. M and Sim, X and Ma, C and Locke, A and Blackwell, T and Jackson, A and Teslovich, T. M and Stringham, H and Chines, P and Kwan, P and Huyghe, J and Tan, A and Jun, G and Stitzel, M and Bergman, R. N and Bonnycastle, L and Tuomilehto, J and Collins, F. S and Scott, L and Mohlke, K and Abecasis, G and Boehnke, M and Strom, T and Gieger, C and Nurasyid, M. M and Grallert, H and Kriebel, J and Ried, J and Hrabe de Angelis, M and Huth, C and Meisinger, C and Peters, A and Rathmann, W and Strauch, K and Meitinger, T and Kravic, J and Algren, P and Ladenvall, C and Toumi, T and Isomaa, B and Groop, L and Gaulton, K and Moutsianas, L and Rivas, M and Pearson, R and Mahajan, A and Prokopenko, I and Kumar, A and Perry, J and Howie, B and van de Bunt, M and Small, K and Lindgren, C and Lunter, G and Robertson, N and Rayner, W and Morris, A and Buck, D and Hattersley, A and Spector, T and McVean, G and Frayling, T and Donnelly, P and McCarthy, M and Gupta, N and Taylor, H and Fox, E and Cheh, C. N and Wilson, J. G and O'Donnell, C. J and Kathiresan, S and Hirschhorn, J and Seidman, J. G and Seidman, C and Williams, A. L and Jacobs, S. B. R and Macias, H. M and Chagoya, A. H and ... and NHGRI JHS/FHS Allelic Spectrum Project and SIGMA T2D Consortium and GoT2D Consortium and T2D-GENES Consortium and NHGRI JHS-FHS Allelic Spectrum Pr
Proceedings of the National Academy of Sciences - PNAS, ISSN 1091-6490, 2014, Volume 111, Issue 36, pp. 13127 - 13132
Journal Article
by Mahajan, Anubha and Sim, Xueling and Ng, Hui Jin and Manning, Alisa and Rivas, Manuel A and Highland, Heather M and Locke, Adam E and Grarup, Niels and Im, Hae Kyung and Cingolani, Pablo and Flannick, Jason and Fontanillas, Pierre and Fuchsberger, Christian and Gaulton, Kyle J and Teslovich, Tanya M and Rayner, N. William and Robertson, Neil R and Beer, Nicola L and Rundle, Jana K and Bork-Jensen, Jette and Ladenvall, Claes and Blancher, Christine and Buck, David and Buck, Gemma and Burtt, Noël P and Gabriel, Stacey and Gjesing, Anette P and Groves, Christopher J and Hollensted, Mette and Huyghe, Jeroen R and Jackson, Anne U and Jun, Goo and Justesen, Johanne Marie and Mangino, Massimo and Murphy, Jacquelyn and Neville, Matt and Onofrio, Robert and Small, Kerrin S and Stringham, Heather M and Syvänen, Ann-Christine and Trakalo, Joseph and Abecasis, Goncalo and Bell, Graeme I and Blangero, John and Cox, Nancy J and Duggirala, Ravindranath and Hanis, Craig L and Seielstad, Mark and Wilson, James G and Christensen, Cramer and Brandslund, Ivan and Rauramaa, Rainer and Surdulescu, Gabriela L and Doney, Alex S. F and Lannfelt, Lars and Linneberg, Allan and Isomaa, Bo and Tuomi, Tiinamaija and Jørgensen, Marit E and Jørgensen, Torben and Kuusisto, Johanna and Uusitupa, Matti and Salomaa, Veikko and Spector, Timothy D and Morris, Andrew D and Palmer, Colin N. A and Collins, Francis S and Mohlke, Karen L and Bergman, Richard N and Ingelsson, Erik and Lind, Lars and Tuomilehto, Jaakko and Hansen, Torben and Watanabe, Richard M and Prokopenko, Inga and Dupuis, Josee and Karpe, Fredrik and Groop, Leif and Laakso, Markku and Pedersen, Oluf and Florez, Jose C and Morris, Andrew P and Altshuler, David and Meigs, James B and Boehnke, Michael and McCarthy, Mark I and Lindgren, Cecilia M and Gloyn, Anna L and Abboud, Hanna E and Afzal, Uzma and Aguilar, David and Arya, Rector and Atzmon, Gil and Aung, Tin and Banks, Eric and Barroso, Inês and Barzilai, Nir and Below, Jennifer E and Bharadwaj, Dwaipayan and Blackwell, Thomas W and ... and Go T2D Consortium and T2D-GENES Consortium and T2D-GENES consortium and GoT2D consortium and On Behalf of the T2D-GENES consortium and GoT2D consortium
PLoS genetics, ISSN 1553-7390, 01/2015, Volume 11, Issue 1, p. e1004876
Journal Article
Journal Article
PLoS genetics, ISSN 1553-7404, 2018, Volume 14, Issue 5, p. e1007329
Journal Article
BMC MEDICAL GENOMICS, ISSN 1755-8794, 07/2019, Volume 12, Issue Suppl 5, pp. 102 - 15
BackgroundIn genome-wide association studies (GWASs), meta-analysis has been widely used to improve statistical power by combining the results of different... 
Rare variant analysis | Meta-Qtest | ASSOCIATION | Exome sequencing | GENETICS & HEREDITY | Meta-analysis | Medical research | Usage | Genome-wide association studies | Genetic variation | Analysis | Medicine, Experimental
Journal Article
by Anubha Mahajan and Xueling Sim and Hui Jin Ng and Alisa Manning and Manuel A Rivas and Heather M Highland and Adam E Locke and Niels Grarup and Hae Kyung Im and Pablo Cingolani and Jason Flannick and Pierre Fontanillas and Christian Fuchsberger and Kyle J Gaulton and Tanya M Teslovich and N William Rayner and Neil R Robertson and Nicola L Beer and Jana K Rundle and Jette Bork-Jensen and Claes Ladenvall and Christine Blancher and David Buck and Gemma Buck and Noël P Burtt and Stacey Gabriel and Anette P Gjesing and Christopher J Groves and Mette Hollensted and Jeroen R Huyghe and Anne U Jackson and Goo Jun and Johanne Marie Justesen and Massimo Mangino and Jacquelyn Murphy and Matt Neville and Robert Onofrio and Kerrin S Small and Heather M Stringham and Ann-Christine Syvänen and Joseph Trakalo and Goncalo Abecasis and Graeme I Bell and John Blangero and Nancy J Cox and Ravindranath Duggirala and Craig L Hanis and Mark Seielstad and James G Wilson and Cramer Christensen and Ivan Brandslund and Rainer Rauramaa and Gabriela L Surdulescu and Alex S F Doney and Lars Lannfelt and Allan Linneberg and Bo Isomaa and Tiinamaija Tuomi and Marit E Jørgensen and Torben Jørgensen and Johanna Kuusisto and Matti Uusitupa and Veikko Salomaa and Timothy D Spector and Andrew D Morris and Colin N A Palmer and Francis S Collins and Karen L Mohlke and Richard N Bergman and Erik Ingelsson and Lars Lind and Jaakko Tuomilehto and Torben Hansen and Richard M Watanabe and Inga Prokopenko and Josee Dupuis and Fredrik Karpe and Leif Groop and Markku Laakso and Oluf Pedersen and Jose C Florez and Andrew P Morris and David Altshuler and James B Meigs and Michael Boehnke and Mark I McCarthy and Cecilia M Lindgren and Anna L Gloyn and of the T2D-GENES consortium and GoT2D consortium
PLoS genetics, ISSN 1553-7390, 01/2015, Volume 11, Issue 1
Genome wide association studies (GWAS) for fasting glucose (FG) and insulin (FI) have identified common variant signals which explain 4.8% and 1.2% of trait... 
Medical research | Biomedical research | Genomics | Science | Genomes | Grants | Glucose | Epidemiology | Medicine | Studies | Hospitals | Diabetes | Informatics | Public health | Endocrinology | Metabolic disorders
Journal Article
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