Human Genome Epidemiology Literature Finder
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Records 1 - 12 (of 12 Records) |
| Query Trace: Albuminuria and CUBN[original query] |
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CUBN is a gene locus for albuminuria.
Journal of the American Society of Nephrology : JASN 2011 Mar 22 (3): 555-70. Böger Carsten A, Chen Ming-Huei, Tin Adrienne, Olden Matthias, Köttgen Anna, de Boer Ian H, Fuchsberger Christian, O'Seaghdha Conall M, Pattaro Cristian, Teumer Alexander, Liu Ching-Ti, Glazer Nicole L, Li Man, O'Connell Jeffrey R, Tanaka Toshiko, Peralta Carmen A, Kutalik Zoltán, Luan Jian'an, Zhao Jing Hua, Hwang Shih-Jen, Akylbekova Ermeg, Kramer Holly, van der Harst Pim, Smith Albert V, Lohman Kurt, de Andrade Mariza, Hayward Caroline, Kollerits Barbara, Tönjes Anke, Aspelund Thor, Ingelsson Erik, Eiriksdottir Gudny, Launer Lenore J, Harris Tamara B, Shuldiner Alan R, Mitchell Braxton D, Arking Dan E, Franceschini Nora, Boerwinkle Eric, Egan Josephine, Hernandez Dena, Reilly Muredach, Townsend Raymond R, Lumley Thomas, Siscovick David S, Psaty Bruce M, Kestenbaum Bryan, Haritunians Talin, Bergmann Sven, Vollenweider Peter, Waeber Gerard, Mooser Vincent, Waterworth Dawn, Johnson Andrew D, Florez Jose C, Meigs James B, Lu Xiaoning, Turner Stephen T, Atkinson Elizabeth J, Leak Tennille S, Aasarød Knut, Skorpen Frank, Syvänen Ann-Christine, Illig Thomas, Baumert Jens, Koenig Wolfgang, Krämer Bernhard K, Devuyst Olivier, Mychaleckyj Josyf C, Minelli Cosetta, Bakker Stephan J L, Kedenko Lyudmyla, Paulweber Bernhard, Coassin Stefan, Endlich Karlhans, Kroemer Heyo K, Biffar Reiner, Stracke Sylvia, Völzke Henry, Stumvoll Michael, Mägi Reedik, Campbell Harry, Vitart Veronique, Hastie Nicholas D, Gudnason Vilmundur, Kardia Sharon L R, Liu Yongmei, Polasek Ozren, Curhan Gary, Kronenberg Florian, Prokopenko Inga, Rudan Igor, Arnlöv Johan, Hallan Stein, Navis Gerjan, , Parsa Afshin, Ferrucci Luigi, Coresh Josef, Shlipak Michael G, Bull Shelley B, Paterson Nicholas J, Wichmann H-Erich, Wareham Nicholas J, Loos Ruth J F, Rotter Jerome I, Pramstaller Peter P, Cupples L Adrienne, Beckmann Jacques S, Yang Qiong, Heid Iris M, Rettig Rainer, Dreisbach Albert W, Bochud Murielle, Fox Caroline S, Kao W H |
| The association of a single-nucleotide polymorphism in CUBN and the risk of albuminuria and cardiovascular disease. Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2014 Feb 29 (2): 342-7. McMahon Gearoid M, O'Seaghdha Conall M, Hwang Shih-Jen, Meigs James B, Fox Caroline |
| The association between vitamin B12, albuminuria and reduced kidney function: an observational cohort study. BMC nephrology 2015 16 7. McMahon Gearoid M, Hwang Shih-Jen, Tanner Rikki M, Jacques Paul F, Selhub Jacob, Muntner Paul, Fox Caroline |
| Genome-wide Association Studies Identify Genetic Loci Associated With Albuminuria in Diabetes.
Diabetes 2015 Dec . Teumer Alexander, Tin Adrienne, Sorice Rossella, Gorski Mathias, Yeo Nan Cher, Chu Audrey Y, Li Man, Li Yong, Mijatovic Vladan, Ko Yi-An, Taliun Daniel, Luciani Alessandro, Chen Ming-Huei, Yang Qiong, Foster Meredith C, Olden Matthias, Hiraki Linda T, Tayo Bamidele O, Fuchsberger Christian, Dieffenbach Aida Karina, Shuldiner Alan R, Smith Albert V, Zappa Allison M, Lupo Antonio, Kollerits Barbara, Ponte Belen, Stengel Bénédicte, Krämer Bernhard K, Paulweber Bernhard, Mitchell Braxton D, Hayward Caroline, Helmer Catherine, Meisinger Christa, Gieger Christian, Shaffer Christian M, Müller Christian, Langenberg Claudia, Ackermann Daniel, Siscovick David, , Boerwinkle Eric, Kronenberg Florian, Ehret Georg B, Homuth Georg, Waeber Gerard, Navis Gerjan, Gambaro Giovanni, Malerba Giovanni, Eiriksdottir Gudny, Li Guo, Wichmann H Erich, Grallert Harald, Wallaschofski Henri, Völzke Henry, Brenner Herrmann, Kramer Holly, Leach I Mateo, Rudan Igor, Hillege J L, Beckmann Jacques S, Lambert Jean Charles, Luan Jian'an, Zhao Jing Hua, Chalmers John, Coresh Josef, Denny Joshua C, Butterbach Katja, Launer Lenore J, Ferrucci Luigi, Kedenko Lyudmyla, Haun Margot, Metzger Marie, Woodward Mark, Hoffman Matthew J, Nauck Matthias, Waldenberger Melanie, Pruijm Menno, Bochud Murielle, Rheinberger Myriam, Verweij N, Wareham Nicholas J, Endlich Nicole, Soranzo Nicole, Polasek Ozren, van der Harst P, Pramstaller Peter Paul, Vollenweider Peter, Wild Philipp S, Gansevoort R T, Rettig Rainer, Biffar Reiner, Carroll Robert J, Katz Ronit, Loos Ruth J F, Hwang Shih-Jen, Coassin Stefan, Bergmann Sven, Rosas Sylvia E, Stracke Sylvia, Harris Tamara B, Corre Tanguy, Zeller Tanja, Illig Thomas, Aspelund Thor, Tanaka Toshiko, Lendeckel Uwe, Völker Uwe, Gudnason Vilmundur, Chouraki Vincent, Koenig Wolfgang, Kutalik Zoltan, O'Connell Jeffrey R, Parsa Afshin, Heid Iris M, Paterson Andrew D, de Boer Ian H, Devuyst Olivier, Lazar Jozef, Endlich Karlhans, Susztak Katalin, Tremblay Johanne, Hamet Pavel, Jacob Howard J, Böger Carsten A, Fox Caroline S, Pattaro Cristian, Köttgen An |
| Association Analysis of the Cubilin (CUBN) and Megalin (LRP2) Genes with ESRD in African Americans. Clinical journal of the American Society of Nephrology : CJASN 2016 May . Ma Jun, Guan Meijian, Bowden Donald W, Ng Maggie C Y, Hicks Pamela J, Lea Janice P, Ma Lijun, Gao Chuan, Palmer Nicholette D, Freedman Barry |
| Genetic Modifiers of White Blood Cell Count, Albuminuria and Glomerular Filtration Rate in Children with Sickle Cell Anemia. PloS one 2016 11 (10): e0164364. Schaefer Beverly A, Flanagan Jonathan M, Alvarez Ofelia A, Nelson Stephen C, Aygun Banu, Nottage Kerri A, George Alex, Roberts Carla W, Piccone Connie M, Howard Thad A, Davis Barry R, Ware Russell |
| A novel rare CUBN variant and three additional genes identified in Europeans with and without diabetes: results from an exome-wide association study of albuminuria.
Diabetologia 2019 02 62 (2): 292-305. Ahluwalia Tarunveer S, Schulz Christina-Alexandra, Waage Johannes, Skaaby Tea, Sandholm Niina, van Zuydam Natalie, Charmet Romain, Bork-Jensen Jette, Almgren Peter, Thuesen Betina H, Bedin Mathilda, Brandslund Ivan, Christensen Cramer K, Linneberg Allan, Ahlqvist Emma, Groop Per-Henrik, Hadjadj Samy, Tregouet David-Alexandre, Jørgensen Marit E, Grarup Niels, Pedersen Oluf, Simons Matias, Groop Leif, Orho-Melander Marju, McCarthy Mark I, Melander Olle, Rossing Peter, Kilpeläinen Tuomas O, Hansen Torb |
| Not all proteinuria is created equal. The Journal of clinical investigation 2019 12 130 (1): 74-76. Beenken Andrew, Barasch Jonathan M, Gharavi Ali |
| Human C-terminal CUBN variants associate with chronic proteinuria and normal renal function. The Journal of clinical investigation 2019 10 130 (1): 335-344. Bedin Mathilda, Boyer Olivia, Servais Aude, Li Yong, Villoing-Gaudé Laure, Tête Marie-Josephe, Cambier Alexandra, Hogan Julien, Baudouin Veronique, Krid Saoussen, Bensman Albert, Lammens Florie, Louillet Ferielle, Ranchin Bruno, Vigneau Cecile, Bouteau Iseline, Isnard-Bagnis Corinne, Mache Christoph J, Schäfer Tobias, Pape Lars, Gödel Markus, Huber Tobias B, Benz Marcus, Klaus Günter, Hansen Matthias, Latta Kay, Gribouval Olivier, Morinière Vincent, Tournant Carole, Grohmann Maik, Kuhn Elisa, Wagner Timo, Bole-Feysot Christine, Jabot-Hanin Fabienne, Nitschké Patrick, Ahluwalia Tarunveer S, Köttgen Anna, Andersen Christian Brix Folsted, Bergmann Carsten, Antignac Corinne, Simons Mati |
| Albuminuria-Related Genetic Biomarkers: Replication and Predictive Evaluation in Individuals with and without Diabetes from the UK Biobank. International journal of molecular sciences 2023 7 24 (13): . Marisa Cañadas-Garre, Andrew T Kunzmann, Kerry Anderson, Eoin P Brennan, Ross Doyle, Christopher C Patterson, Catherine Godson, Alexander P Maxwell, Amy Jayne McKnig |
| Four missense genetic variants in CUBN are associated with higher levels of eGFR in non-diabetes but not in diabetes mellitus or its subtypes: A genetic association study in Europeans. Frontiers in endocrinology 2023 3 14 1081741. Uglebjerg Nicoline, Ahmadizar Fariba, Aly Dina M, Cañadas-Garre Marisa, Hill Claire, Naber Annemieke, Oddsson Asmundur, Singh Sunny S, Smyth Laura, Trégouët David-Alexandre, Chaker Layal, Ghanbari Mohsen, Steinthorsdottir Valgerdur, Ahlqvist Emma, Hadjadj Samy, Van Hoek Mandy, Kavousi Maryam, McKnight Amy Jayne, Sijbrands Eric J, Stefansson Kari, Simons Matias, Rossing Peter, Ahluwalia Tarunveer |
| Systematic Review of Genetic Modifiers Associated with the Development and/or Progression of Nephropathy in Patients with Sickle Cell Disease. International journal of molecular sciences 2024 5 25 (10): . Veerle Labarque, Emmanuel Chide Okocha, |
- Page last reviewed:Feb 1, 2024
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