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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 - 102
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 | Hypertension | Information management | Genomics
Journal Article
Journal Article
by Turcot, Valérie and Lu, Yingchang and Highland, Heather M and Schurmann, Claudia and Justice, Anne E and Fine, Rebecca S and Bradfield, Jonathan P and Esko, Tõnu and Giri, Ayush and Graff, Mariaelisa and Guo, Xiuqing and Hendricks, Audrey E and Karaderi, Tugce and Lempradl, Adelheid and Locke, Adam E and Mahajan, Anubha and Marouli, Eirini and Sivapalaratnam, Suthesh and Young, Kristin L and Alfred, Tamuno and Feitosa, Mary F and Masca, Nicholas GD and Manning, Alisa K and Medina-Gomez, Carolina and Mudgal, Poorva and Ng, Maggie CY and Reiner, Alex P and Vedantam, Sailaja and Willems, Sara M and Winkler, Thomas W and Abecasis, Gonçalo and Aben, Katja K and Alam, Dewan S and Alharthi, Sameer E and Allison, Matthew and Amouyel, Philippe and Asselbergs, Folkert W and Auer, Paul L and Balkau, Beverley and Bang, Lia E and Barroso, Ines and Bastarache, Lisa and Benn, Marianne and Bergmann, Sven and Bielak, Lawrence F and Blüher, Matthias and Boehnke, Michael and Boeing, Heiner and Boerwinkle, Eric and Böger, Carsten A and Bork-Jensen, Jette and Bots, Michiel L and Bottinger, Erwin P and Bowden, Donald W and Brandslund, Ivan and Breen, Gerome and Brilliant, Murray H and Broer, Linda and Brumat, Marco and Burt, Amber A and Butterworth, Adam Stuart and Campbell, Peter T and Cappellani, Stefania and Carey, David J and Catamo, Eulalia and Caulfield, Mark J and Chambers, John C and Chasman, Daniel I and Chen, Yii-Der I and Chowdhury, Rajiv and Christensen, Cramer and Chu, Audrey Y and Cocca, Massimiliano and Collins, Francis S and Cook, James P and Corley, Janie and Corominas Galbany, Jordi and Cox, Amanda J and Crosslin, David S and Cuellar-Partida, Gabriel and D'Eustacchio, Angela and Danesh, John and Davies, Gail and Bakker, Paul IW and Groot, Mark CH and Mutsert, Renée and Deary, Ian J and Dedoussis, George and Demerath, Ellen W and Heijer, Martin and Hollander, Anneke I and Ruijter, Hester M and Dennis, Joe G and Denny, Josh C and Di Angelantonio, Emanuele and Drenos, Fotios and Du, Mengmeng and Dubé, Marie-Pierre and Dunning, Alison Margaret and Easton, Douglas Frederick and ... and Medicinska fakulteten and Science for Life Laboratory, SciLifeLab and Medicinska och farmaceutiska vetenskapsområdet and Kardiologi and Medicinska och farmaceutiska vetenskapsområdet, centrumbildningar mm and Geriatrik and Kardiovaskulär epidemiologi and Uppsala universitet and Institutionen för medicinska vetenskaper and Molekylär epidemiologi and Institutionen för folkhälso- och vårdvetenskap and Uppsala kliniska forskningscentrum (UCR)
Nature Genetics, ISSN 1061-4036, 2018, Volume 50, Issue 1, p. 26
Journal Article
by Warren, Helen R and Evangelou, Evangelos and Cabrera, Claudia P and Gao, He and Ren, Meixia and Mifsud, Borbala and Ntalla, Ioanna and Surenan, Praveen and Liu, Chunyu and Cook, James P and Kraja, Aldi T and nos, Fotios and Loh, Marie and Verweij, Niek and Marten, Jonathan and Karaman, Ibrahim and Lepe, Marcelo P. Segura and O'Reilly, Paul F and Knight, Joanne and Snieder, Harold and Kato, Norihiro and He, Jiang and Tai, E. Shyong and Said, M. Abdullah and Porteous, David and Alver, Maris and Poulter, Neil and Farrall, Martin and Gansevoort, Ron T and Padmanabhan, Sandosh and Magi, Reedik and Stanton, Alice and Connell, John and Bakker, Stephan J. L and Metspalu, Anes and Shields, Denis C and Thom, Simon and Brown, Morris and Sever, Peter and Esko, Tonu and Hayward, Caroline and van der Harst, Pim and Saleheen, Danish and Chowdhury, Rajiv and Chambers, John C and Chasman, Daniel I and Chakravarti, Aravinda and Newton-Cheh, Christopher and Lindgren, Cecilia M and Levy, Daniel and Kooner, Jaspal S and Keavney, Bernard and Tomaszewski, Maciej and Samani, Nilesh J and Howson, Joanna M. M and Tobin, Martin D and Munroe, Patricia B and Ehret, Georg B and Wain, Louise V and Barnes, Michael R and Tzoulaki, Joanna and Caulfield, Mark J and Elliott, Paul and Vaez, Ahmad and Jansen, Rick and Joehanes, Roby and van der Most, Peter J and Erzurumluoglu, A. Mesut and O'Reilly, Paul and Rose, Lynda M and Verwoert, Germaine C and Hottenga, Jouke-Jan and Strawbridge, Rona J and Arking, Dan E and Hwang, Shih-Jen and Guo, Xiuqing and Kutalik, Zoltan and Trompet, Stella and Shrine, Nick and Teumer, Alexander and Ried, Janina S and Bis, Joshua C and Smith, Albert V and Amin, Najaf and Nolte, Ilja M and Lyytikainen, Leo-Pekka and Mahajan, Anubha and Wareham, Nicholas J and Hofer, Edith and Joshi, Peter K and Kristiansson, Kati and Traglia, Michela and Havulinna, Aki S and Goel, Anuj and Nalls, Mike A and Sober, Siim and Vuckovic, gana and Luan, Jian'an and Del Greco M, Fabiola and Ayers, Kristin L and ... and Medicinska fakulteten and Science for Life Laboratory, SciLifeLab and Medicinska och farmaceutiska vetenskapsområdet and Institutionen för immunologi, genetik och patologi and Medicinsk genetik och genomik and Geriatrik and Kardiovaskulär epidemiologi and Uppsala universitet and Institutionen för medicinska vetenskaper and Molekylär epidemiologi and Institutionen för folkhälso- och vårdvetenskap
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,... 
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 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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