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Molecular insights into genome-wide association studies of chronic kidney disease-defining traits.
Xu, Xiaoguang; Eales, James M; Akbarov, Artur; Guo, Hui; Becker, Lorenz; Talavera, David; Ashraf, Fehzan; Nawaz, Jabran; Pramanik, Sanjeev; Bowes, John; Jiang, Xiao; Dormer, John; Denniff, Matthew; Antczak, Andrzej; Szulinska, Monika; Wise, Ingrid; Prestes, Priscilla R; Glyda, Maciej; Bogdanski, Pawel; Zukowska-Szczechowska, Ewa; Berzuini, Carlo; Woolf, Adrian S; Samani, Nilesh J; Charchar, Fadi J; Tomaszewski, Maciej.
  • Xu X; Division of Cardiovascular Sciences, Faculty of Medicine, Biology and Health, University of Manchester, Manchester, M13 9PT, UK.
  • Eales JM; Division of Cardiovascular Sciences, Faculty of Medicine, Biology and Health, University of Manchester, Manchester, M13 9PT, UK.
  • Akbarov A; Division of Cardiovascular Sciences, Faculty of Medicine, Biology and Health, University of Manchester, Manchester, M13 9PT, UK.
  • Guo H; Division of Population Health, Health Services Research and Primary Care, Faculty of Medicine, Biology and Health, University of Manchester, Manchester, M13 9PL, UK.
  • Becker L; Division of Cardiovascular Sciences, Faculty of Medicine, Biology and Health, University of Manchester, Manchester, M13 9PT, UK.
  • Talavera D; Division of Cardiovascular Sciences, Faculty of Medicine, Biology and Health, University of Manchester, Manchester, M13 9PT, UK.
  • Ashraf F; Division of Cardiovascular Sciences, Faculty of Medicine, Biology and Health, University of Manchester, Manchester, M13 9PT, UK.
  • Nawaz J; Division of Cardiovascular Sciences, Faculty of Medicine, Biology and Health, University of Manchester, Manchester, M13 9PT, UK.
  • Pramanik S; Division of Cardiovascular Sciences, Faculty of Medicine, Biology and Health, University of Manchester, Manchester, M13 9PT, UK.
  • Bowes J; Division of Musculoskeletal and Dermatological Sciences, Faculty of Medicine, Biology and Health, University of Manchester, Manchester, M13 9PT, UK.
  • Jiang X; Division of Cardiovascular Sciences, Faculty of Medicine, Biology and Health, University of Manchester, Manchester, M13 9PT, UK.
  • Dormer J; University Hospitals of Leicester NHS Trust, Leicester, LE1 5WW, UK.
  • Denniff M; Department of Cardiovascular Sciences, University of Leicester, Leicester, LE3 9QP, UK.
  • Antczak A; Department of Urology and Uro-oncology, Karol Marcinkowski University of Medical Sciences, Poznan, 61-285, Poland.
  • Szulinska M; Department of Internal Medicine, Metabolic Disorders and Hypertension, Karol Marcinkowski University of Medical Sciences, Poznan, 60-569, Poland.
  • Wise I; School of Health and Life Sciences, Federation University Australia, Ballarat, 3350, VIC, Australia.
  • Prestes PR; School of Health and Life Sciences, Federation University Australia, Ballarat, 3350, VIC, Australia.
  • Glyda M; Department of Transplantology and General Surgery, District Public Hospital, University of Zielona Góra, Poznan, 65-417, Poland.
  • Bogdanski P; Department of Obesity and Metabolic Disorders Treatment and Clinical Dietetics, Karol Marcinkowski University of Medical Sciences, Poznan, 60-569, Poland.
  • Zukowska-Szczechowska E; Department of Health Care, Silesian Medical College, Katowice, 40-085, Poland.
  • Berzuini C; Division of Population Health, Health Services Research and Primary Care, Faculty of Medicine, Biology and Health, University of Manchester, Manchester, M13 9PL, UK.
  • Woolf AS; Department of Paediatric Nephrology, Royal Manchester Children's Hospital, Manchester University NHS Foundation Trust, Manchester, M13 9WL, UK.
  • Samani NJ; Department of Cardiovascular Sciences, University of Leicester, Leicester, LE3 9QP, UK.
  • Charchar FJ; NIHR Leicester Biomedical Research Centre, Glenfield Hospital, Leicester, LE3 9QP, UK.
  • Tomaszewski M; Department of Cardiovascular Sciences, University of Leicester, Leicester, LE3 9QP, UK.
Nat Commun ; 9(1): 4800, 2018 11 22.
Article en En | MEDLINE | ID: mdl-30467309
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Predisposición Genética a la Enfermedad / Polimorfismo de Nucleótido Simple / Insuficiencia Renal Crónica / Estudio de Asociación del Genoma Completo Tipo de estudio: Clinical_trials / Risk_factors_studies Límite: Humans Idioma: En Año: 2018 Tipo del documento: Article
Texto completo
Imprimir
XML
PubMed Links
Search on Google

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Predisposición Genética a la Enfermedad / Polimorfismo de Nucleótido Simple / Insuficiencia Renal Crónica / Estudio de Asociación del Genoma Completo Tipo de estudio: Clinical_trials / Risk_factors_studies Límite: Humans Idioma: En Año: 2018 Tipo del documento: Article