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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
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 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
PLoS genetics, ISSN 1553-7390, 05/2018, Volume 14, Issue 5, p. e1007329
Journal Article
Journal Article
Nature Genetics, ISSN 1061-4036, 03/2017, Volume 49, Issue 3, pp. 403 - 415
Elevated blood pressure is the leading heritable risk factor for cardiovascular disease worldwide. We report genetic association of blood pressure (systolic,... 
Journal Article | genome-wide association studies | hypertension | Medical and Health Sciences | Medicin och hälsovetenskap
Journal Article
by Liu, Chunyu and Kraja, Aldi T and Smith, Jennifer A and Brody, Jennifer A and Franceschini, Nora and Bis, Joshua C and Rice, Kenneth and Morrison, Alanna C and Lu, Yingchang and Weiss, Stefan and Guo, Xiuqing and Palmas, Walter and Martin, Lisa W and Chen, Yii-Der Ida and Surendran, Praveen and Drenos, Fotios and Cook, James P and Auer, Paul L and Chu, Audrey Y and Giri, Ayush and Zhao, Wei and Jakobsdottir, Johanna and Lin, Li-An and Stafford, Jeanette M and Amin, Najaf and Mei, Hao and Yao, Jie and Voorman, Arend and CHD Exome+ Consortium and ExomeBP Consortium and GoT2DGenes Consortium and T2D-GENES Consortium and Larson, Martin G and Grove, Megan L and Smith, Albert V and Hwang, Shih-Jen and Chen, Han and Huan, Tianxiao and Kosova, Gulum and Stitziel, Nathan O and Kathiresan, Sekar and Samani, Nilesh and Schunkert, Heribert and Deloukas, Panos and Myocardial Infarction Genetics and CARDIoGRAM Exome Consortia and Li, Man and Fuchsberger, Christian and Pattaro, Cristian and Gorski, Mathias and CKDGen Consortium and Kooperberg, Charles and Papanicolaou, George J and Rossouw, Jacques E and Faul, Jessica D and Kardia, Sharon LR and Bouchard, Claude and Raffel, Leslie J and Uitterlinden, André G and Franco, Oscar H and Vasan, Ramachandran S and O'Donnell, Christopher J and Taylor, Kent D and Liu, Kiang and Bottinger, Erwin P and Gottesman, Omri and Daw, E Warwick and Giulianini, Franco and Ganesh, Santhi and Salfati, Elias and Harris, Tamara B and Launer, Lenore J and Dörr, Marcus and Felix, Stephan B and Rettig, Rainer and Völzke, Henry and Kim, Eric and Lee, Wen-Jane and Lee, I-Te and Sheu, Wayne H-H and Tsosie, Krystal S and Edwards, Digna R Velez and Liu, Yongmei and Correa, Adolfo and Weir, David R and Völker, Uwe and Ridker, Paul M and Boerwinkle, Eric and Gudnason, Vilmundur and Reiner, Alexander P and van Duijn, Cornelia M and Borecki, Ingrid B and Edwards, Todd L and Chakravarti, Aravinda and Rotter, Jerome I and Psaty, Bruce M and Loos, Ruth JF and Fornage, Myriam and Ehret, Georg B and Newton-Cheh, Christopher and Levy, Daniel and ...
ISSN 1061-4036, 2016
Journal Article
ISSN 0964-6906, 2016
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
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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