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by Liu, Dajiang J and Peloso, Gina M and Yu, Haojie and Butterworth, Adam S and Wang, Xiao and Mahajan, Anubha and Saleheen, Danish and Emdin, Connor and Alam, Dewan and Alves, Alexessander Couto and Amouyel, Philippe and Di Angelantonio, Emanuele and Arveiler, Dominique and Assimes, Themistocles L and Auer, Paul L and Baber, Usman and Ballantyne, Christie M and Bang, Lia E and Benn, Marianne and Bis, Joshua C and Boehnke, Michael and Boerwinkle, Eric and Bork-Jensen, Jette and Bottinger, Erwin P and Brandslund, Ivan and Brown, Morris and Busonero, Fabio and Caulfield, Mark J and Chambers, John C and Chasman, Daniel I and Chen, Y Eugene and Chen, Yii-Der Ida and Chowdhury, Rajiv and Christensen, Cramer and Chu, Audrey Y and Connell, John M and Cucca, Francesco and Cupples, L Adrienne and Damrauer, Scott M and Davies, Gail and Deary, Ian J and Dedoussis, George and Denny, Joshua C and Dominiczak, Anna and Dubé, Marie-Pierre and Ebeling, Tapani and Eiriksdottir, Gudny and Esko, Tõnu and Farmaki, Aliki-Eleni and Feitosa, Mary F and Ferrario, Marco and Ferrieres, Jean and Ford, Ian and Fornage, Myriam and Franks, Paul W and Frayling, Timothy M and Frikke-Schmidt, Ruth and Fritsche, Lars G and Frossard, Philippe and Fuster, Valentin and Ganesh, Santhi K and Gao, Wei and Garcia, Melissa E and Gieger, Christian and Giulianini, Franco and Goodarzi, Mark O and Grallert, Harald and Grarup, Niels and Groop, Leif and Grove, Megan L and Gudnason, Vilmundur and Hansen, Torben and Harris, Tamara B and Hayward, Caroline and Hirschhorn, Joel N and Holmen, Oddgeir L and Huffman, Jennifer and Huo, Yong and Hveem, Kristian and Jabeen, Sehrish and Jackson, Anne U and Jakobsdottir, Johanna and Jarvelin, Marjo-Riitta and Jensen, Gorm B and Jørgensen, Marit E and Jukema, J Wouter and Justesen, Johanne M and Kamstrup, Pia R and Kanoni, Stavroula and Karpe, Fredrik and Kee, Frank and Khera, Amit V and Klarin, Derek and Koistinen, Heikki A and Kooner, Jaspal S and Kooperberg, Charles and Kuulasmaa, Kari and Kuusisto, Johanna and Laakso, Markku and Lakka, Timo and ... and VA Million Veteran Program and Charge Diabet Working Grp and EPIC-CVD Consortium and EPIC-InterAct Consortium and GOLD Consortium and Charge Diabetes Working Group and The EPIC-InterAct Consortium
Nature genetics, ISSN 1546-1718, 10/2017, Volume 49, Issue 12, pp. 1758 - 1766
Journal Article
PloS one, ISSN 1932-6203, 12/2018, Volume 13, Issue 12, pp. e0208654 - e0208654
Journal Article
Journal Article
by Traylor, Matthew and Farrall, Martin and Holliday, Elizabeth G and Sudlow, Cathie and Hopewell, Jemma C and Cheng, Yu-Ching and Fornage, Myriam and Ikram, M Arfan and Malik, Rainer and Bevan, Steve and Thorsteinsdottir, Unnur and Nalls, Mike A and Longstreth, WT and Wiggins, Kerri L and Yadav, Sunaina and Parati, Eugenio A and DeStefano, Anita L and Worrall, Bradford B and Kittner, Steven J and Khan, Muhammad Saleem and Reiner, Alex P and Helgadottir, Anna and Achterberg, Sefanja and Fernandez-Cadenas, Israel and Abboud, Sherine and Schmidt, Reinhold and Walters, Matthew and Chen, Wei-Min and Ringelstein, E Bernd and O'Donnell, Martin and Ho, Weang Kee and Pera, Joanna and Lemmens, Robin and Norrving, Bo and Higgins, Peter and Benn, Marianne and Sale, Michele and Kuhlenbäumer, Gregor and Doney, Alexander S F and Vicente, Astrid M and Delavaran, Hossein and Algra, Ale and Davies, Gail and Oliveira, Sofia A and Palmer, Colin N A and Deary, Ian and Schmidt, Helena and Pandolfo, Massimo and Montaner, Joan and Carty, Cara and de Bakker, Paul I W and Kostulas, Konstantinos and Ferro, Jose M and van Zuydam, Natalie R and Valdimarsson, Einar and Nordestgaard, Børge G and Lindgren, Arne and Thijs, Vincent and Slowik, Agnieszka and Saleheen, Danish and Paré, Guillaume and Berger, Klaus and Thorleifsson, Gudmar and Hofman, Albert and Mosley, Thomas H and Mitchell, Braxton D and Furie, Karen and Clarke, Robert and Levi, Christopher and Seshadri, Sudha and Gschwendtner, Andreas and Boncoraglio, Giorgio B and Sharma, Pankaj and Bis, Joshua C and Gretarsdottir, Solveig and Psaty, Bruce M and Rothwell, Peter M and Rosand, Jonathan and Meschia, James F and Stefansson, Kari and Dichgans, Martin and Markus, Hugh S and The Australian Stroke Genetics Collaborative, Wellcome Trust Case Control Consortium 2 (WTCCC2) and on behalf of the International Stroke Genetics Consortium and WTCCC 2 and Australian Stroke Genetics Collabo and Int Stroke Genetics Consortium and International Stroke Genetics Consortium and Australian Stroke Genetics Collaborative, Wellcome Trust Case Control Consortium 2 (WTCCC2)
Lancet neurology, ISSN 1474-4422, 11/2012, Volume 11, Issue 11, pp. 951 - 962
Journal Article
The New England journal of medicine, ISSN 1533-4406, 03/2016, Volume 374, Issue 12, pp. 1134 - 1144
Journal Article
Diabetologia, ISSN 1432-0428, 12/2018, Volume 62, Issue 2, pp. 292 - 305
Journal Article
by van Zuydam, Natalie R and Ahlqvist, Emma and Sandholm, Niina and Deshmukh, Harshal and Rayner, N. William and Abdalla, Moustafa and Ladenvall, Claes and Ziemek, Daniel and Fauman, Eric and Robertson, Neil R and McKeigue, Paul M and Valo, Erkka and Forsblom, Carol and Harjutsalo, Valma and Perna, Annalisa and Rurali, Erica and Marcovecchio, M. Loredana and Igo, Robert P and Salem, Rany M and Perico, Norberto and Lajer, Maria and Käräjämäki, Annemari and Imamura, Minako and Kubo, Michiaki and Takahashi, Atsushi and Sim, Xueling and Liu, Jianjun and van Dam, Rob M and Jiang, Guozhi and Tam, Claudia H.T and Luk, Andrea O.Y and Lee, Heung Man and Lim, Cadmon K.P and Szeto, Cheuk Chun and So, Wing Yee and Chan, Juliana C.N and Ang, Su Fen and Dorajoo, Rajkumar and Wang, Ling and Clara, Tan Si Hua and McKnight, Amy-Jayne and Duffy, Seamus and Pezzolesi, Marcus G and Marre, Michel and Gyorgy, Beata and Hadjadj, Samy and Hiraki, Linda T and Ahluwalia, Tarunveer S and Almgren, Peter and Schulz, Christina-Alexandra and Orho-Melander, Marju and Linneberg, Allan and Christensen, Cramer and Witte, Daniel R and Grarup, Niels and Brandslund, Ivan and Melander, Olle and Paterson, Andrew D and Tregouet, David and Maxwell, Alexander P and Lim, Su Chi and Ma, Ronald C.W and Tai, E Shyong and Maeda, Shiro and Lyssenko, Valeriya and Tuomi, Tiinamaija and Krolewski, Andrzej S and Rich, Stephen S and Hirschhorn, Joel N and Florez, Jose C and Dunger, David and Pedersen, Oluf and Hansen, Torben and Rossing, Peter and Remuzzi, Giuseppe and Brosnan, Mary Julia and Palmer, Colin N.A and Groop, Per-Henrik and Colhoun, Helen M and Groop, Leif C and McCarthy, Mark I and Warren 3 and Genetics of Kidneys in Diabetes (GoKinD) Study Group and Hong Kong Diabetes Registry Theme-based Research Scheme Project Group and Diabetes Control and Complications Trial (DCCT)/Epidemiology of Diabetes Interventions and Complications (EDIC) Research Group and GENIE (GEnetics of Nephropathy an International Effort) Consortium and Finnish Diabetic Nephropathy Study (FinnDiane) and SUrrogate markers for Micro- and Macrovascular hard endpoints for Innovative diabetes Tools (SUMMIT) Consortium and SUrrogate Markers Micro Macrovascu and Warren 3 Genetics Kidneys Diabet and Hong Kong Diabet Registry Theme and Finnish Diabetic Nephropathy Study and Epidemiology Diabet Interventions and Diabet Control Complications Trial and GENIE GEnetics Nephropathy Int and SUMMIT Consortium and GENIE (Genetics of Nepropathy an International Effort) Consortium
Diabetes (New York, N.Y.), ISSN 1939-327X, 07/2018, Volume 67, Issue 7, pp. 1414 - 1427
Identification of sequence variants robustly associated with predisposition to diabetic kidney disease (DKD) has the potential to provide insights into the... 
Life Sciences & Biomedicine | Endocrinology & Metabolism | Science & Technology | Genetic Predisposition to Disease | Genome-Wide Association Study | Diabetes Mellitus, Type 2 - genetics | Humans | Middle Aged | Diabetic Nephropathies - genetics | Male | Renal Insufficiency, Chronic - complications | Case-Control Studies | Diabetes Mellitus, Type 2 - epidemiology | Kidney Failure, Chronic - genetics | Renal Insufficiency, Chronic - epidemiology | Kidney Failure, Chronic - epidemiology | Kidney Failure, Chronic - complications | Renal Insufficiency, Chronic - genetics | Aged, 80 and over | Adult | Female | Aged | Diabetic Nephropathies - epidemiology | Polymorphism, Single Nucleotide | Diabetes Mellitus, Type 2 - complications | Type 2 diabetes | Genome-wide association studies | Usage | Research | Diabetic nephropathies | Genotype & phenotype | Phenotypes | Kidneys | Diabetes mellitus | Replication | Genomes | Diabetes | Kidney diseases | Diabetes mellitus (non-insulin dependent) | Quantitative analysis | Glomerular filtration rate | Index Medicus | Abridged Index Medicus | Metabolomics | Genetics | 0103 | Proteomics | Medical and Health Sciences | Medicin och hälsovetenskap | Klinisk medicin | Medicinsk genetik | Medical Genetics | Endokrinologi och diabetes | Kidney Failure, Chronic/complications | Endocrinology and Diabetes | Diabetic Nephropathies/epidemiology | Basic Medicine | Renal Insufficiency, Chronic/complications | Diabetes Mellitus, Type 2/complications | Clinical Medicine | Medicinska och farmaceutiska grundvetenskaper
Journal Article