Genome-wide association study of kidney function decline in individuals of European descent
暂无分享,去创建一个
Andrew D. Johnson | Audrey Y. Chu | F. Kronenberg | O. Franco | A. Hofman | A. Uitterlinden | T. Lehtimäki | J. O’Connell | W. Goessling | Z. Kutalik | M. Woodward | P. Ridker | D. Chasman | V. Gudnason | U. Nöthlings | P. Mitchell | Albert Vernon Smith | O. Raitakari | A. Dehghan | A. Köttgen | Qiong Yang | Shih-Jen Hwang | F. Rivadeneira | J. Coresh | C. Fox | S. Kardia | W. Lieb | I. D. de Boer | Yongmei Liu | D. Siscovick | B. Penninx | H. Snieder | C. Meisinger | S. Coassin | B. Paulweber | J. Staessen | I. Heid | J. Lambert | H. Grallert | M. Müller-Nurasyid | Jie-Jin Wang | R. Schmidt | H. Schmidt | A. Teumer | U. Völker | A. Franke | M. de Andrade | G. Eiriksdottir | E. Holliday | L. Launer | P. Vollenweider | G. Waeber | S. Kardia | T. Aspelund | V. Chouraki | I. Nolte | B. Tayo | Jingzhong Ding | S. Turner | P. van der Harst | A. Shuldiner | A. Parsa | B. Mitchell | G. McMahon | Man Li | L. Lyytikäinen | M. Bochud | E. Atkinson | Guo Li | J. Chalmers | N. Aumann | R. Rettig | P. Hamet | J. Tremblay | E. Salvi | D. Cusi | A. Chu | S. Bakker | R. Gansevoort | C. Böger | M. Gorski | C. Barlassina | B. Stengel | M. Metzger | E. Hofer | B. Krämer | C. Pattaro | Matthias Olden | A. Tin | S. Sedaghat | T. Corre | K. Endlich | H. Kramer | P. Kanetsky | M. Pietzner | M. Haun | B. Kollerits | C. Helmer | J. Stafford | S. Rosas | Maija Garnaas | T. B. Harris | P. Freudenberger | Fabiola M. Del Greco | J. Gupta | H. Kao | A. Smith | T. Harris | A. Johnson | P. van der harst | M. Olden | A. Smith | S. Turner | J. Coresh | Mathias Gorski | A. Uitterlinden | A. Hofman | S. Kardia | R. Schmidt | R. Schmidt | M. Pietzner
[1] M. Brueckner,et al. The Heterotaxy gene, GALNT11, glycosylates Notch to orchestrate cilia type and laterality , 2013, Nature.
[2] Matteo Trudu,et al. Common noncoding UMOD gene variants induce salt-sensitive hypertension and kidney damage by increasing uromodulin expression , 2013, Nature Medicine.
[3] L. Tran,et al. Integrated Systems Approach Identifies Genetic Nodes and Networks in Late-Onset Alzheimer’s Disease , 2013, Cell.
[4] J. Coresh,et al. Change in the estimated glomerular filtration rate over time and risk of all-cause mortality. , 2013, Kidney international.
[5] Brenda R. Hemmelgarn,et al. Notice , 2012, Kidney International Supplements.
[6] B. Kasiske,et al. KDIGO Clinical Practice Guideline for the Evaluation and Management of Chronic Kidney Disease Foreword , 2013 .
[7] J. Coresh,et al. Short-term change in kidney function and risk of end-stage renal disease. , 2012, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.
[8] Harold Snieder,et al. UMOD as a susceptibility gene for end-stage renal disease , 2012, BMC Medical Genetics.
[9] Benjamin J. Keller,et al. New Susceptibility Loci Associated with Kidney Disease in Type 1 Diabetes , 2012, PLoS genetics.
[10] Y. J. Kim,et al. Meta-analysis identifies multiple loci associated with kidney function–related traits in east Asian populations , 2012, Nature Genetics.
[11] M. Garrett,et al. Increased susceptibility to kidney injury by transfer of genomic segment from SHR onto Dahl S genetic background. , 2012, Physiological genomics.
[12] J. Coresh,et al. One-Year Change in Kidney Function Is Associated with an Increased Mortality Risk , 2012, American Journal of Nephrology.
[13] Liang Li,et al. Longitudinal progression trajectory of GFR among patients with CKD. , 2012, American journal of kidney diseases : the official journal of the National Kidney Foundation.
[14] Sylvia Stracke,et al. Genome-Wide Association and Functional Follow-Up Reveals New Loci for Kidney Function , 2012, PLoS genetics.
[15] C. Fox,et al. Genome-wide association studies of chronic kidney disease: what have we learned? , 2012, Nature Reviews Nephrology.
[16] Christian Fuchsberger,et al. GWAtoolbox: an R package for fast quality control and handling of genome-wide association studies meta-analysis data , 2012, Bioinform..
[17] C. Hoggart,et al. Genomewide Association Study Using a High-Density Single Nucleotide Polymorphism Array and Case-Control Design Identifies a Novel Essential Hypertension Susceptibility Locus in the Promoter Region of Endothelial NO Synthase , 2012, Hypertension.
[18] Xiwu Chen,et al. Integrin α1/Akita double knockout mice on a Balb/c background develop advanced features of human diabetic nephropathy , 2012, Kidney international.
[19] Neil Powe,et al. Association of eGFR-Related Loci Identified by GWAS with Incident CKD and ESRD , 2011, PLoS genetics.
[20] M. Nalls,et al. Genetic Association for Renal Traits among Participants of African Ancestry Reveals New Loci for Renal Function , 2011, PLoS genetics.
[21] J. Lv,et al. Polymorphisms in the nonmuscle myosin heavy chain 9 gene (MYH9) are associated with the progression of IgA nephropathy in Chinese. , 2011, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.
[22] W. Rathmann,et al. Cohort profile: the study of health in Pomerania. , 2011, International journal of epidemiology.
[23] J. Belmont,et al. Rare copy number variations in congenital heart disease patients identify unique genes in left-right patterning , 2011, Proceedings of the National Academy of Sciences.
[24] E. Lundberg,et al. Towards a knowledge-based Human Protein Atlas , 2010, Nature Biotechnology.
[25] C. Nievergelt,et al. Common Charge-Shift Mutation Glu65Lys in K+ Channel β1-Subunit KCNMB1: Pleiotropic Consequences for Glomerular Filtration Rate and Progressive Renal Disease , 2010, American Journal of Nephrology.
[26] H. Hakonarson,et al. ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data , 2010, Nucleic acids research.
[27] C. Nievergelt,et al. Progression of Chronic Kidney Disease: Adrenergic Genetic Influence on Glomerular Filtration Rate Decline in Hypertensive Nephrosclerosis , 2010, American Journal of Nephrology.
[28] Uwe Völker,et al. New loci associated with kidney function and chronic kidney disease , 2010, Nature Genetics.
[29] Mark N. Wass,et al. Genetic loci influencing kidney function and chronic kidney disease , 2010, Nature Genetics.
[30] R. Garrick. Albuminuria and Kidney Function Independently Predict Cardiovascular and Renal Outcomes in Diabetes , 2010 .
[31] C. Meisinger,et al. Effect of Chronic Kidney Disease and Comorbid Conditions on Health Care Costs: A 10-Year Observational Study in a General Population , 2009, American Journal of Nephrology.
[32] B. Astor,et al. Change in estimated GFR associates with coronary heart disease and mortality. , 2009, Journal of the American Society of Nephrology : JASN.
[33] B. Kestenbaum,et al. Rapid decline of kidney function increases cardiovascular risk in the elderly. , 2009, Journal of the American Society of Nephrology : JASN.
[34] C. Nievergelt,et al. Adrenergic beta-1 receptor genetic variation predicts longitudinal rate of GFR decline in hypertensive nephrosclerosis. , 2009, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.
[35] F. Macciardi,et al. α- and β-Adducin polymorphisms affect podocyte proteins and proteinuria in rodents and decline of renal function in human IgA nephropathy , 2009, Journal of Molecular Medicine.
[36] Nick C Fox,et al. Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease, and shows evidence for additional susceptibility genes , 2009, Nature Genetics.
[37] P. Bosco,et al. Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease , 2009, Nature Genetics.
[38] A. Köttgen,et al. Defining incident chronic kidney disease in the research setting: The ARIC Study. , 2009, American journal of epidemiology.
[39] Mark Woodward,et al. Albuminuria and kidney function independently predict cardiovascular and renal outcomes in diabetes. , 2009, Journal of the American Society of Nephrology : JASN.
[40] A. Go,et al. Chronic Renal Insufficiency Cohort (CRIC) Study: baseline characteristics and associations with kidney function. , 2009, Clinical journal of the American Society of Nephrology : CJASN.
[41] C. Nievergelt,et al. Chromogranin A regulates renal function by triggering Weibel-Palade body exocytosis. , 2009, Journal of the American Society of Nephrology : JASN.
[42] F. Kronenberg,et al. A common variant in the adiponutrin gene influences liver enzyme values , 2009, Journal of Medical Genetics.
[43] Yurii S. Aulchenko,et al. Multiple loci associated with indices of renal function and chronic kidney disease , 2009, Nature Genetics.
[44] Suzette J. Bielinski,et al. NRXN3 Is a Novel Locus for Waist Circumference: A Genome-Wide Association Study from the CHARGE Consortium , 2009, PLoS genetics.
[45] D. de Zeeuw,et al. Screening for albuminuria identifies individuals at increased renal risk. , 2009, Journal of the American Society of Nephrology : JASN.
[46] J. R. Holt,et al. A mouse model for nonsyndromic deafness (DFNB12) links hearing loss to defects in tip links of mechanosensory hair cells , 2009, Proceedings of the National Academy of Sciences.
[47] G. Curhan,et al. Genetic Polymorphisms and the Risk of Accelerated Renal Function Decline in Women , 2009, PloS one.
[48] Monique M. B. Breteler,et al. The Rotterdam Study: 2016 objectives and design update , 2015, European Journal of Epidemiology.
[49] J. Samet,et al. Mortality risks for all causes and cardiovascular diseases and reduced GFR in a middle-aged working population in Taiwan. , 2008, American journal of kidney diseases : the official journal of the National Kidney Foundation.
[50] Risto Telama,et al. Cohort profile: the cardiovascular risk in Young Finns Study. , 2008, International journal of epidemiology.
[51] D. Siscovick,et al. Rapid kidney function decline and mortality risk in older adults. , 2008, Archives of internal medicine.
[52] J. Rumberger,et al. The association of coronary artery calcification and carotid artery intima-media thickness with distinct, traditional coronary artery disease risk factors in asymptomatic adults. , 2008, American journal of epidemiology.
[53] P. Cuijpers,et al. The Netherlands Study of Depression and Anxiety (NESDA): rationale, objectives and methods , 2008, International journal of methods in psychiatric research.
[54] O. Pedersen,et al. The PPAR gamma 2 Pro12Ala variant predicts ESRD and mortality in patients with type 1 diabetes and diabetic nephropathy. , 2008, Molecular genetics and metabolism.
[55] J. O’Connell,et al. The genetic response to short-term interventions affecting cardiovascular function: rationale and design of the Heredity and Phenotype Intervention (HAPI) Heart Study. , 2008, American heart journal.
[56] J. Coresh,et al. Prevalence of chronic kidney disease in the United States. , 2007, JAMA.
[57] A. Hofman,et al. The Rotterdam Study: objectives and design update , 2007, European Journal of Epidemiology.
[58] Qiong Yang,et al. The Third Generation Cohort of the National Heart, Lung, and Blood Institute's Framingham Heart Study: design, recruitment, and initial examination. , 2007, American journal of epidemiology.
[59] B. Freedman,et al. Familial Clustering of Chronic Kidney Disease , 2007, Seminars in dialysis.
[60] V. Gudnason,et al. Age, Gene/Environment Susceptibility-Reykjavik Study: multidisciplinary applied phenomics. , 2007, American journal of epidemiology.
[62] E. Boerwinkle,et al. Influence of genomic loci on measures of chronic kidney disease in hypertensive sibships. , 2006, Journal of the American Society of Nephrology : JASN.
[63] E. Boerwinkle,et al. A comparison of serum creatinine-based methods for identifying chronic kidney disease in hypertensive individuals and their siblings. , 2006, American journal of hypertension.
[64] Michael Krawczak,et al. PopGen: Population-Based Recruitment of Patients and Controls for the Analysis of Complex Genotype-Phenotype Relationships , 2006, Public Health Genomics.
[65] F. Kronenberg,et al. Genetic architecture of the APM1 gene and its influence on adiponectin plasma levels and parameters of the metabolic syndrome in 1,727 healthy Caucasians. , 2006, Diabetes.
[66] P. Mitchell,et al. Low hemoglobin, chronic kidney disease, and risk for coronary heart disease-related death: the Blue Mountains Eye Study. , 2005, Journal of the American Society of Nephrology : JASN.
[67] Gudmundur A. Thorisson,et al. The International HapMap Project Web site. , 2005, Genome research.
[68] I. Drummond,et al. Organization of the pronephric filtration apparatus in zebrafish requires Nephrin, Podocin and the FERM domain protein Mosaic eyes. , 2005, Developmental biology.
[69] C. Gieger,et al. KORA-gen - Resource for Population Genetics, Controls and a Broad Spectrum of Disease Phenotypes , 2005 .
[70] A. Bello,et al. Chronic kidney disease: the global challenge , 2005, The Lancet.
[71] U. John,et al. Study of Health in Pomerania (SHIP): A health examination survey in an east German region: Objectives and design , 2005, Sozial- und Präventivmedizin.
[72] E. Boerwinkle,et al. Familial aggregation of hypertension treatment and control in the Genetic Epidemiology Network of Arteriopathy (GENOA) study. , 2004, The American journal of medicine.
[73] Daniel Levy,et al. Predictors of new-onset kidney disease in a community-based population. , 2004, JAMA.
[74] A. Hofman,et al. Determinants of disease and disability in the elderly: The Rotterdam elderly study , 1991, European Journal of Epidemiology.
[75] R. Holman,et al. Vascular Factors and Risk of Dementia: Design of the Three-City Study and Baseline Characteristics of the Study Population , 2003, Neuroepidemiology.
[76] S. Rubin,et al. Inflammatory markers and cardiovascular disease (The Health, Aging and Body Composition [Health ABC] Study). , 2003, The American journal of cardiology.
[77] R. Kronmal,et al. Multi-Ethnic Study of Atherosclerosis: objectives and design. , 2002, American journal of epidemiology.
[78] Ulrich Müller,et al. The Usher syndrome proteins cadherin 23 and harmonin form a complex by means of PDZ-domain interactions , 2002, Proceedings of the National Academy of Sciences of the United States of America.
[79] Tom Greene,et al. Calibration and random variation of the serum creatinine assay as critical elements of using equations to estimate glomerular filtration rate. , 2002, American journal of kidney diseases : the official journal of the National Kidney Foundation.
[80] M. Bitner-Glindzicz,et al. Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23. , 2001, American journal of human genetics.
[81] M. Seeliger,et al. Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D , 2001, Nature genetics.
[82] K. Steel,et al. Mutations in Cdh23, encoding a new type of cadherin, cause stereocilia disorganization in waltzer, the mouse model for Usher syndrome type 1D , 2001, Nature Genetics.
[83] K. Roeder,et al. Genomic Control for Association Studies , 1999, Biometrics.
[84] F. Fazekas,et al. MRI white matter hyperintensities , 1999, Neurology.
[85] A. Schier,et al. Early development of the zebrafish pronephros and analysis of mutations affecting pronephric function. , 1998, Development.
[86] L. Almasy,et al. Multipoint quantitative-trait linkage analysis in general pedigrees. , 1998, American journal of human genetics.
[87] P. Mitchell,et al. Visual acuity and the causes of visual loss in Australia. The Blue Mountains Eye Study. , 1996, Ophthalmology.
[88] J. J. Wang,et al. Prevalence of age-related maculopathy in Australia. The Blue Mountains Eye Study. , 1995, Ophthalmology.
[89] F. Fazekas,et al. Assessment of cerebrovascular risk profiles in healthy persons: definition of research goals and the Austrian Stroke Prevention Study (ASPS). , 1994, Neuroepidemiology.
[90] R. Kronmal,et al. The Cardiovascular Health Study: design and rationale. , 1991, Annals of epidemiology.
[91] A. Folsom,et al. The Atherosclerosis Risk in Communities (ARIC) Study: design and objectives. The ARIC investigators. , 1989, American journal of epidemiology.
[92] W. Kannel,et al. An investigation of coronary heart disease in families. The Framingham offspring study. , 1979, American journal of epidemiology.
[93] W. Kannel,et al. The Framingham Offspring Study. Design and preliminary data. , 1975, Preventive medicine.