المؤلفون: Böger, Carsten A, Gorski, Mathias, Li, Man, Hoffmann, Michael M, Huang, Chunmei, Yang, Qiong, Teumer, Alexander, Krane, Vera, O'Seaghdha, Conall M, Kutalik, Zoltán, Wichmann, H-Erich, Haak, Thomas, Boes, Eva, Coassin, Stefan, Coresh, Josef, Kollerits, Barbara, Haun, Margot, Paulweber, Bernhard, Köttgen, Anna, Li, Guo, Shlipak, Michael G, Powe, Neil, Hwang, Shih-Jen, Dehghan, Abbas, Rivadeneira, Fernando, Uitterlinden, André, Hofman, Albert, Beckmann, Jacques S, Krämer, Bernhard K, Witteman, Jacqueline, Bochud, Murielle, Siscovick, David, Rettig, Rainer, Kronenberg, Florian, Wanner, Christoph, Thadhani, Ravi I, Heid, Iris M, Fox, Caroline S, Kao, WH, CKDGen Consortium

المصدر: PLoS genetics. 7(9)

مصطلحات موضوعية: CKDGen Consortium, Humans, Kidney Diseases, Kidney Failure, Chronic, Chronic Disease, Creatinine, Adaptor Proteins, Signal Transducing, Follow-Up Studies, Polymorphism, Single Nucleotide, Adult, Aged, Middle Aged, European Continental Ancestry Group, Female, Male, Genetic Association Studies, Uromodulin, ErbB Receptors, Kidney Disease, Genetics, Clinical Research, Renal and urogenital, Developmental Biology

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/2gp960sbTest

المؤلفون: Marketa Sjögren, Anna Maria Di Blasio, Davide Gentilini, Patricia B. Munroe, Barbara Corso, Brenda W.J.H. Penninx, Claire E. Hastie, Toby Johnson, Arjan J. Kwakernaak, Giancarlo Cesana, H.-Erich Wichmann, John M. C. Connell, Jian'an Luan, Susana Eyheramendy, Guido Grassi, Michel Burnier, Christopher Newton-Cheh, Ruth J. F. Loos, Henry Völzke, Morris Brown, Nilesh J. Samani, Maris Laan, Maria Cristina Monti, Martin W. McBride, Marc Maillard, Alberto Zanchetti, Alice Stanton, Cristiano Fava, Martina Montagnana, Harold Snieder, Peter Vollenweider, Gavin Lucas, Elisa Danese, Anna F. Dominiczak, Stewart Laing, Robert A. McDonald, Mark J. Caulfield, Peter S. Sever, Ole Torffvit, Denis C. Shields, Tim D. Spector, David P. Strachan, Wai K. Lee, Feng Zhang, Pim van der Harst, David S. Siscovick, Cristina Menni, Ilja M. Nolte, Jill P. Pell, Andrew H. Baker, Giuseppe Mancia, Murielle Bochud, Gerjan Navis, Sekar Kathiresan, Delyth Graham, Sandosh Padmanabhan, Naveed Sattar, Stuart A. Nicklin, Martin Farrall, Sverre E. Kjeldsen, Olle Melander, Christian Delles, Björn Wahlstrand, William H. Miller, Nicholas J. Wareham, Bo Hedblad, Nicole Soranzo, Paul Welsh, Alexander Teumer, Thomas Hedner, Stefano Signorini, Rainer Rettig, Pankaj Arora

المساهمون: Padmanabhan, S, Melander, O, Johnson, T, Di Blasio, A, Lee, W, Gentilini, D, Hastie, C, Menni, C, Monti, M, Delles, C, Laing, S, Corso, B, Navis, G, Kwakernaak, A, van der Harst, P, Bochud, M, Maillard, M, Burnier, M, Hedner, T, Kjeldsen, S, Wahlstrand, B, Sjögren, M, Fava, C, Montagnana, M, Danese, E, Torffvit, O, Hedblad, B, Snieder, H, Connell, J, Brown, M, Samani, N, Farrall, M, Cesana, G, Mancia, G, Signorini, S, Grassi, G, Eyheramendy, S, Wichmann, H, Laan, M, Strachan, D, Sever, P, Shields, D, Stanton, A, Vollenweider, P, Teumer, A, Völzke, H, Rettig, R, Newton Cheh, C, Arora, P, Zhang, F, Soranzo, N, Spector, T, Lucas, G, Kathiresan, S, Siscovick, D, Luan, J, Loos, R, Wareham, N, Penninx, B, Nolte, I, Mcbride, M, Miller, W, Nicklin, S, Baker, A, Graham, D, Mcdonald, R, Pell, J, Sattar, N, Welsh, P, Munroe, P, Caulfield, M, Zanchetti, A, Dominiczak, A, Global BPGen Consortium, Psychiatry, NCA - Anxiety & Depression, EMGO - Mental health, Lifestyle Medicine (LM), Groningen Kidney Center (GKC), Vascular Ageing Programme (VAP), Cardiovascular Centre (CVC), Life Course Epidemiology (LCE), Neuroscience Campus Amsterdam - Anxiety & Depression, EMGO+ - Mental Health

المصدر: PLoS Genetics, Vol 6, Iss 10, p e1001177 (2010)
PLoS Genetics
PLOS GENETICS
Artículos CONICYT
CONICYT Chile
instacron:CONICYT
Padmanabhan, S, Melander, O, Johnson, T, Di Blasio, A M, Lee, W K, Gentilini, D, Hastie, C E, Menni, C, Monti, M C, Delles, C, Laing, S, Corso, B, Navis, G, Kwakernaak, A J, van der Harst, P, Bochud, M, Maillard, M, Burnier, M, Hedner, T, Kjeldsen, S, Wahlstrand, B, Sjogren, M, Fava, C, Montagnana, M, Danese, E, Torffvit, O, Hedblad, B, Snieder, H, Connell, J M C, Brown, M, Samani, N J, Farrall, M, Cesana, G, Mancia, G, Signorini, S, Grassi, G, Eyheramendy, S, Wichmann, H E, Laan, M, Strachan, D P, Sever, P, Shields, D C, Stanton, A, Vollenweider, P, Teumer, A, Volzke, H, Rettig, R, Newton-Cheh, C, Arora, P, Zhang, F, Soranzo, N, Spector, T D, Lucas, G, Kathiresan, S, Siscovick, D S, Luan, J A, Loos, R J F, Wareham, N J, Penninx, B W J H, Nolte, I M, McBride, M, Miller, W H, Nicklin, S A, Baker, A H, Graham, D, McDonald, R A, Pell, J P, Sattar, N, Welsh, P, Munroe, P, Caulfield, M J, Zanchetti, A & Dominiczak, A F 2010, ' Genome-Wide Association Study of Blood Pressure Extremes Identifies Variant near UMOD Associated with Hypertension ', PLoS Genetics, vol. 6, no. 10 (e1001177), pp. 1-11 . https://doi.org/10.1371/journal.pgen.1001177Test
PLoS Genetics; 6(10) (2010)
Plos Genetics, vol. 6, no. 10, pp. e1001177
PLoS Genetics, 6(10 (e1001177)), 1-11. Public Library of Science
PLoS Genetics; Vol 6
PLoS genetics, 6(10):1001177. PUBLIC LIBRARY SCIENCE
PLoS Genet. 6, 1-11:e1001177 (2010)

مصطلحات موضوعية: CHRONIC KIDNEY-DISEASE, Male, Cancer Research, URINARY-EXCRETION, Tamm–Horsfall protein, LOCI, Genome-wide association study, Blood Pressure, Genomewide Association Study, UMOD, Hypertension, 030204 cardiovascular system & hematology, 0302 clinical medicine, Gene Frequency, Risk Factors, Cardiac and Cardiovascular Systems, Multivariate Analysi, Genetics and Genomics/Genetics of Disease, Genetics (clinical), Allele, 0303 health sciences, TAMM-HORSFALL PROTEIN, Middle Aged, Colaus Study, 3. Good health, Linear Model, Female, Survival Analysi, BURDEN, Research Article, Glomerular Filtration Rate, Human, medicine.medical_specialty, FEASIBILITY, Genotype, lcsh:QH426-470, NEPHROPATHY, Locus (genetics), Genetics and Genomics/Complex Traits, Biology, Lower risk, Polymorphism, Single Nucleotide, Nephropathy, Cardiovascular Disorders/Hypertension, 03 medical and health sciences, Meta-Analysis as Topic, Internal medicine, Uromodulin, Genetics, medicine, Humans, Urology and Nephrology, Genetic Predisposition to Disease, Molecular Biology, Allele frequency, Alleles, Ecology, Evolution, Behavior and Systematics, Proportional Hazards Models, 030304 developmental biology, Aged, MUTATIONS, MORTALITY, Risk Factor, medicine.disease, Survival Analysis, lcsh:Genetics, Blood pressure, Endocrinology, Multivariate Analysis, Linear Models, biology.protein, RISK-FACTORS, Proportional Hazards Model, Chromosomes, Human, Pair 16, Genome-Wide Association Study

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5d6c6f75442d81e28bb21788402eb428Test
http://europepmc.org/articles/PMC2965757?pdf=renderTest

المؤلفون: Gudmar Thorleifsson, Hilma Holm, Gudmundur I. Eyjolfsson, Frank C H d'Ancona, Olafur S. Indridason, Thorunn Rafnar, Martin den Heijer, Unnur S. Bjornsdottir, Patrick Sulem, Femmie de Vegt, Leifur Franzson, Lambertus A. Kiemeney, Augustine Kong, Daniel F. Gudbjartsson, Kristleifur Kristjansson, Vidar O. Edvardsson, Unnur Thorsteinsdottir, Runolfur Palsson, Kari Stefansson

المصدر: Plos Genetics, 6, 7, pp. e1001039-e1001039
PLoS Genetics
Plos Genetics, 6, e1001039-e1001039
PLoS Genetics, Vol 6, Iss 7, p e1001039 (2010)

مصطلحات موضوعية: Cancer Research, Tamm–Horsfall protein, Gout, Iceland, Genome-wide association study, Comorbidity, Aetiology, screening and detection [ONCOL 5], Type 2 diabetes, chemistry.chemical_compound, Risk Factors, Urea, Genetics and Genomics/Genetics of Disease, Genetics (clinical), Netherlands, Renal disorder [IGMD 9], education.field_of_study, Age Factors, Creatinine, Genetics and Genomics/Gene Discovery, Research Article, medicine.medical_specialty, lcsh:QH426-470, Population, Biology, Polymorphism, Single Nucleotide, Molecular epidemiology [NCEBP 1], Kidney Calculi, Internal medicine, Genetics and Genomics/Population Genetics, Uromodulin, Genetics, medicine, Humans, Renal Insufficiency, Chronic, education, Molecular Biology, Ecology, Evolution, Behavior and Systematics, Hormonal regulation [IGMD 6], Genetic Variation, medicine.disease, Uric Acid, lcsh:Genetics, Endocrinology, chemistry, Evaluation of complex medical interventions [NCEBP 2], Case-Control Studies, biology.protein, Uric acid, Kidney stones, Genome-Wide Association Study, Kidney disease

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::04d8e8c77f5c1aa0a7216da69bdb05beTest
https://doi.org/10.1371/journal.pgen.1001039Test