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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 and Medicinska fakulteten and Science for Life Laboratory, SciLifeLab and Medicinska och farmaceutiska vetenskapsområdet and Molekylär medicin and Geriatrik and Kardiovaskulär epidemiologi and Uppsala universitet and Institutionen för medicinska vetenskaper and Molekylär epidemiologi and Institutionen för folkhälso- och vårdvetenskap
PLoS Genetics, ISSN 1553-7390, 01/2015, Volume 11, Issue 1, p. e1004876
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 SF 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 NA 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 T2D-GENES, consortium and GoT2D consortium
PLoS Genetics, ISSN 1553-7390, 2015, Volume 11, Issue 1
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 9/2014, Volume 111, Issue 36, pp. 13127 - 13132
Journal Article
by Tachmazidou, I and Süveges, D and Min, JL and Ritchie, GRS and Steinberg, J and Walter, K and Iotchkova, V and Schwartzentruber, J and Huang, J and Memari, Y and McCarthy, Shane Alan and Crawford, AA and Bombieri, C and Cocca, M and Farmaki, A-E and Gaunt, TR and Jousilahti, P and Kooijman, MN and Lehne, B and Malerba, G and Männistö, S and Matchan, A and Medina-Gomez, C and Metrustry, SJ and Nag, A and Ntalla, I and Paternoster, L and Rayner, NW and Sala, C and Scott, WR and Shihab, HA and Southam, L and St Pourcain, B and Traglia, M and Trajanoska, K and Zaza, G and Zhang, W and Artigas, MS and Bansal, Narinder and Benn, M and Chen, Z and Danecek, P and Lin, W-Y and Locke, A and Luan, Jian'an and Manning, AK and Mulas, A and Sidore, C and Tybjaerg-Hansen, A and Varbo, A and Zoledziewska, M and Finan, C and Hatzikotoulas, K and Hendricks, AE and Kemp, JP and Moayyeri, A and Panoutsopoulou, K and Szpak, M and Wilson, SG and Boehnke, M and Cucca, F and Di Angelantonio, Emanuele and Langenberg, Claudia and Lindgren, C and McCarthy, MI and Morris, AP and Nordestgaard, BG and Scott, RA and Tobin, MD and Wareham, Nicholas John and SpiroMeta Consortium and GoT2D Consortium and Burton, P and Chambers, JC and Smith, GD and Dedoussis, G and Felix, JF and Franco, OH and Gambaro, G and Gasparini, P and Hammond, CJ and Hofman, A and Jaddoe, VWV and Kleber, M and Kooner, JS and Perola, M and Relton, C and Ring, SM and Rivadeneira, F and Salomaa, V and Spector, TD and Stegle, O and Toniolo, D and Uitterlinden, AG and arcOGEN Consortium and Understanding Society Scientific Group and UK10K Consortium and Barroso, Ines and Greenwood, CMT and Perry, John Richard and ...
ISSN 0002-9297, 2017
Deep sequence-based imputation can enhance the discovery power of genome-wide association studies by assessing previously unexplored variation across the... 
imputation | UK10K | anthropometry | next-generation whole-genome sequencing | DXA traits | UK Biobank | genetic association study
Journal Article
PLoS Genetics, ISSN 1553-7390, 04/2015, Volume 11, Issue 4
  Genome and exome sequencing in large cohorts enables characterization of the role of rare variation in complex diseases. Success in this endeavor, however,... 
Studies | Hypothesis testing | Datasets | Hypotheses | Disease | Genes | Statistical methods | Software | Grants | Diabetes | Charitable foundations | Experiments
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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