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by Pattaro, Cristian and Köttgen, Anna and Teumer, Alexander and Böger, Carsten and Fuchsberger, Christian and Olden, Matthias and Chen, Ming-Huei and Li, Man and Gao, Xiaoyi and Gorski, Mathias and Yang, Qiong Fang and O'Seaghdha, Conall and Glazer, Nicole and Isaacs, Aaron and Liu, Ching-Ti and Smith, Albert Vernon and O´Connell, J.R and Struchalin, Maksim and Tanaka, Toshiko and Johnson, Anew and Feitosa, Mary Furlan and Hwang, S.J and Lohman, Kurt and Cornelis, Marilyn and Johansson, Åsa and Tönjes, Anke and Dehghan, Abbas and Chouraki, Vincent and Holliday, Elizabeth and Sorice, R and Kutalik, Zoltán and Lehtimäki, Terho and Esko, Tõnu and Ulivi, Shelia and Trompet, Stella and Imboden, Medea and Kollerits, Barbara and Pistis, Giorgio and Harris, Tamara and Launer, Lenore and Aspelund, Thor and Eiriksdottir, Gudny and Mitchell, Braxton and Boerwinkle, Eric and Schmidt, Reinhold and Cavalieri, Margherita and Hu, Frank and Demirkan, Ayşe and Oostra, Ben and Anade, Mariza and Anews, Jeanette and Koenig, Wolfgang and Illig, Thomas and Döring, Angela and Wichmann, Erich and Kolcic, Ivana and Zemunik, Tatijana and Boban, Mladen and Igl, Wilmar and Zaboli, Ghazal and Wild, Sarah and Wright, Alan and Campbell, Harry and Biffar, Reiner and Ernst, Florian and Homuth, Georg and Kroemer, Heyo and Nauck, Matthias and Kovacs, Peter and Stumvoll, Michael and Mägi, Reedik and Hofman, Albert and Uitterlinden, Ané and Rivadeneira Ramirez, Fernando and Aulchenko, Yurii and Polasek, Ozren and Hastie, Nick and Vitart, Veronique and Wang, Jie Jin and Bergmann, Sven and Kähönen, Mika and Viikari, Jorma and Province, Mike and Ketkar, Shamika and Doney, Alex and Ford, Ian and Buckley, Brendan M and Paulweber, Bernhard and Haun, Margot and Sala, Cinzia and Ciullo, M and Vollenweider, Peter and Raitakari, Olli and Metspalu, Anes and Palmer, Colin and Gasparini, Paolo and Jukema, Jan Wouter and Kronenberg, Florian and Toniolo, Daniela and Gudnason, Vilmundur and ... and CARDIoGRAM Consortium and ICBP Consortium and WTCCC2 and CARe Consortium and Wellcome Trust Case Control Consortium 2 (WTCCC2) and Medicinska fakulteten and Medicinska och farmaceutiska vetenskapsområdet and Institutionen för immunologi, genetik och patologi and Genomik and Uppsala universitet
PL o S Genetics (Online), ISSN 1553-7390, 03/2012, Volume 8, Issue 3, p. e1002584
Journal Article
PLoS ONE, ISSN 1932-6203, 10/2016, Volume 11, Issue 10, p. e0164364
Discovery and validation of genetic variants that influence disease severity in children with sickle cell anemia (SCA) could lead to early identification of... 
MICROALBUMINURIA | MULTIDISCIPLINARY SCIENCES | HYDROXYUREA TREATMENT | SALUSIN-ALPHA | RISK | ADVERSE OUTCOMES | RENAL-DISEASE | DEFICIENT MICE | APOL1 | NEPHROPATHY | CHRONIC TRANSFUSION | Albuminuria - complications | Neutrophils - cytology | Lipoproteins, HDL - genetics | Prospective Studies | Humans | Male | Anemia, Sickle Cell - drug therapy | Genetic Variation | Albuminuria - diagnosis | Apolipoproteins - genetics | Female | Leukocyte Count | Child | Leukocytes - cytology | Glomerular Filtration Rate | Anemia, Sickle Cell - complications | Risk Factors | Receptors, Cell Surface - metabolism | Genotype | Transcription Factors - genetics | Sequence Analysis, DNA | Homeodomain Proteins - genetics | Phenotype | Adolescent | Apolipoprotein L1 | Duffy Blood-Group System - metabolism | Hydroxyurea - therapeutic use | Polymorphism, Single Nucleotide | Anemia, Sickle Cell - diagnosis | Duffy Blood-Group System - genetics | Anemia, Sickle Cell - genetics | Receptors, Cell Surface - genetics | Pediatrics | Care and treatment | Sickle cell anemia | Diabetic nephropathies | African Americans | Sickle cell anemia in children | Hydroxyurea | Risk factors | Genetic polymorphisms | Diseases | Preventive health services | Genetic markers | Genetic aspects | Children | Medicine, Preventive | Blood cell count | Therapy | Clinical trials | Gene polymorphism | Blood | Gene sequencing | Duffy antigen | Rodents | Bioindicators | Sickle cell disease | Medical research | Stroke | Filtration | Risk groups | Anemia | Mortality | Diabetes mellitus | Health risks | Risk analysis | Gene expression | Glomerular filtration rate | White blood cells | Studies | CD163 antigen | Genetic variance | Biomarkers | Polymorphism | Kidney transplantation
Journal Article
PLoS ONE, ISSN 1932-6203, 03/2017, Volume 12, Issue 3, p. e0174274
Journal Article
Nature Medicine, ISSN 1078-8956, 04/2017, Volume 23, Issue 4, pp. 429 - 438
Journal Article
Arteriosclerosis, Thrombosis, and Vascular Biology, ISSN 1079-5642, 02/2016, Volume 36, Issue 2, pp. 398 - 403
Journal Article
by Teumer, Alexander and Tin, Aienne and Sorice, Rossella and Gorski, Mathias and Yeo, Nan Cher and Chu, Auey Y and Li, Man and Li, Yong and Mijatovic, Vladan and Ko, Yi-An and Taliun, Daniel and Luciani, Alessano and Chen, Ming-Huei and Yang, Qiong and Foster, Meredith C and Olden, Matthias and Hiraki, Linda T and Tayo, Bamidele O and Fuchsberger, Christian and Dieffenbach, Aida Karina and Shuldiner, Alan R and Smith, Albert V and Zappa, Allison M and Lupo, Antonio and Kollerits, Barbara and Ponte, Belen and Stengel, Bénédicte and Krämer, Bernhard K and Paulweber, Bernhard and Mitchell, Braxton D and Hayward, Caroline and Helmer, Catherine and Meisinger, Christa and Gieger, Christian and Shaffer, Christian M and Müller, Christian and Langenberg, Claudia and Ackermann, Daniel and Siscovick, David and Boerwinkle, Eric and Kronenberg, Florian and Ehret, Georg B and Homuth, Georg and Waeber, Gerard and Navis, Gerjan and Gambaro, Giovanni and Malerba, Giovanni and Eiriksdottir, Gudny and Li, Guo and Wichmann, H Erich and Grallert, Harald and Wallaschofski, Henri and Völzke, Henry and Brenner, Herrmann and Kramer, Holly and Mateo Leach, I and Rudan, Igor and Hillege, Hans L and Beckmann, Jacques S and Lambert, Jean Charles and Luan, Jian'an and Zhao, Jing Hua and Chalmers, John and Coresh, Josef and Denny, Joshua C and Butterbach, Katja and Launer, Lenore J and Ferrucci, Luigi and Kedenko, Lyudmyla and Haun, Margot and Metzger, Marie and Woodward, Mark and Hoffman, Matthew J and Nauck, Matthias and Waldenberger, Melanie and Pruijm, Menno and Bochud, Murielle and Rheinberger, Myriam and Verweij, Niek and Wareham, Nicholas J and Endlich, Nicole and Soranzo, Nicole and Polasek, Ozren and van der Harst, Pim and Pramstaller, Peter Paul and Vollenweider, Peter and Wild, Philipp S and Gansevoort, Ron T and Rettig, Rainer and Biffar, Reiner and Carroll, Robert J and Katz, Ronit and Loos, Ruth J F and Hwang, Shih-Jen and Coassin, Stefan and Bergmann, Sven and Rosas, Sylvia E and Stracke, Sylvia and Harris, Tamara B and Corre, Tanguy and ... and DCCT EDIC and DCCT/EDIC
Diabetes, ISSN 0012-1797, 03/2016, Volume 65, Issue 3, pp. 803 - 817
Journal Article
PLoS ONE, ISSN 1932-6203, 05/2012, Volume 7, Issue 5, p. e38311
Journal Article
PLoS ONE, ISSN 1932-6203, 12/2012, Volume 7, Issue 12, p. e52529
Objective: Though single nucleotide polymorphisms (SNPs) in the non-muscle myosin gene (MYH9) have been reported to explain most of the excess risk of... 
MANAGEMENT | DISPARITIES | HIV | ALBUMINURIA | MULTIDISCIPLINARY SCIENCES | RISK | AMERICANS | CHRONIC KIDNEY-DISEASE | NEPHROPATHY | STAGE RENAL-DISEASE | EPIDEMIOLOGY | Albuminuria - complications | Confidence Intervals | Gene Frequency - genetics | Kidney - pathology | Diabetes Mellitus - genetics | Humans | Middle Aged | Myosin Heavy Chains - genetics | Male | Renal Insufficiency, Chronic - complications | Molecular Motor Proteins - genetics | Albuminuria - physiopathology | Kidney - metabolism | Renal Insufficiency, Chronic - genetics | Adult | Female | Glomerular Filtration Rate - genetics | Odds Ratio | Genealogy and Heraldry | Kidney - physiopathology | Genetic Predisposition to Disease | Linear Models | Renal Insufficiency, Chronic - physiopathology | Albuminuria - genetics | Diabetes Mellitus - physiopathology | Polymorphism, Single Nucleotide - genetics | South Africa | Type 2 diabetes | Medical research | Chronic kidney failure | Genes | Myosin | Glycosylated hemoglobin | Medicine, Experimental | Genetic aspects | Research | Single nucleotide polymorphisms | Muscle proteins | End-stage renal disease | Health sciences | Nephrology | Laboratories | African Americans | Single-nucleotide polymorphism | Epidemiology | Acquired immune deficiency syndrome--AIDS | Human immunodeficiency virus--HIV | Genetics | Physiology | Public health | Chronic illnesses | Creatinine | Hypertension | Filtration | Epidermal growth factor receptors | Globalization | Diabetes mellitus | Health risks | Muscles | Metabolism | Glomerular filtration rate | Pathology | Bantu languages | Adults | Research design | Diabetes | Mutation | Kidney diseases | Kidney transplantation | Acquired immune deficiency syndrome | AIDS | Human immunodeficiency virus
Journal Article