Human Genome Epidemiology Literature Finder
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Records 1 - 22 (of 22 Records) |
| Query Trace: Kidney Diseases and EGFR[original query] |
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| Adrenergic beta-1 receptor genetic variation predicts longitudinal rate of GFR decline in hypertensive nephrosclerosis. Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2009 Dec 24 (12): 3677-86. Fung Maple M, Chen Yuqing, Lipkowitz Michael S, Salem Rany M, Bhatnagar Vibha, Mahata Manjula, Nievergelt Caroline M, Rao Fangwen, Mahata Sushil K, Schork Nicholas J, Brophy Victoria H, O'Connor Daniel T, |
| APOL1 risk variants, race, and progression of chronic kidney disease. The New England journal of medicine 2013 Dec 369 (23): 2183-96. Parsa Afshin, Kao W H Linda, Xie Dawei, Astor Brad C, Li Man, Hsu Chi-yuan, Feldman Harold I, Parekh Rulan S, Kusek John W, Greene Tom H, Fink Jeffrey C, Anderson Amanda H, Choi Michael J, Wright Jackson T, Lash James P, Freedman Barry I, Ojo Akinlolu, Winkler Cheryl A, Raj Dominic S, Kopp Jeffrey B, He Jiang, Jensvold Nancy G, Tao Kaixiang, Lipkowitz Michael S, Appel Lawrence J, , |
| Polymorphisms in the non-muscle myosin heavy chain gene (MYH9) are associated with lower glomerular filtration rate in mixed ancestry diabetic subjects from South Africa. PloS one 2012 7 (12): 12. Matsha TE, Masconi K, Yako YY, Hassan MS, Macharia M, Erasmus RT, Kengne AP |
| APOL1 G1 genotype modifies the association between HDLC and kidney function in African Americans. BMC genomics 2015 16 421. Bentley Amy R, Divers Jasmin, Shriner Daniel, Doumatey Ayo P, Gutiérrez Orlando M, Adeyemo Adebowale A, Freedman Barry I, Rotimi Charles |
| KIDNEY DISEASE GENETICS AND THE IMPORTANCE OF DIVERSITY IN PRECISION MEDICINE. Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing 2016 21 285-96. Bailey Jessica N Cooke, Wilson Sarah, Brown-Gentry Kristin, Goodloe Robert, Crawford Dana |
| Association of APOL1 With Heart Failure With Preserved Ejection Fraction in Postmenopausal African American Women. JAMA cardiology 2018 Jul . Franceschini Nora, Kopp Jeffrey B, Barac Ana, Martin Lisa W, Li Yun, Qian Huijun, Reiner Alex P, Pollak Martin, Wallace Robert B, Rosamond Wayne D, Winkler Cheryl |
| Optimal management of HIV- positive adults at risk for kidney disease in Nigeria (Renal Risk Reduction "R3" Trial): protocol and study design. Trials 2019 6 20 (1): 341. Aliyu Muktar H, Wudil Usman J, Ingles Donna J, Shepherd Bryan E, Gong Wu, Musa Baba M, Muhammad Hamza, Sani Mahmoud U, Abdu Aliyu, Nalado Aisha M, Atanda Akinfenwa, Ahonkhai Aima A, Ikizler Talat A, Winkler Cheryl A, Kopp Jeffrey B, Kimmel Paul L, Wester C Willi |
| High Serum Phosphate Level as a Risk Factor to Determine Renal Prognosis in Autosomal Dominant Polycystic Kidney Disease: A Retrospective Study. Medicines (Basel, Switzerland) 2020 3 7 (3): . Sato Masayo, Kataoka Hiroshi, Ushio Yusuke, Manabe Shun, Watanabe Saki, Akihisa Taro, Makabe Shiho, Yoshida Rie, Iwasa Naomi, Mitobe Michihiro, Hanafusa Norio, Tsuchiya Ken, Nitta Kosaku, Mochizuki Tosh |
Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline.
Kidney international 2020 11 99 (4): 926-939. Gorski Mathias, Jung Bettina, Li Yong, Matias-Garcia Pamela R, Wuttke Matthias, Coassin Stefan, Thio Chris H L, Kleber Marcus E, Winkler Thomas W, Wanner Veronika, Chai Jin-Fang, Chu Audrey Y, Cocca Massimiliano, Feitosa Mary F, Ghasemi Sahar, Hoppmann Anselm, Horn Katrin, Li Man, Nutile Teresa, Scholz Markus, Sieber Karsten B, Teumer Alexander, Tin Adrienne, Wang Judy, Tayo Bamidele O, Ahluwalia Tarunveer S, Almgren Peter, Bakker Stephan J L, Banas Bernhard, Bansal Nisha, Biggs Mary L, Boerwinkle Eric, Bottinger Erwin P, Brenner Hermann, Carroll Robert J, Chalmers John, Chee Miao-Li, Chee Miao-Ling, Cheng Ching-Yu, Coresh Josef, de Borst Martin H, Degenhardt Frauke, Eckardt Kai-Uwe, Endlich Karlhans, Franke Andre, Freitag-Wolf Sandra, Gampawar Piyush, Gansevoort Ron T, Ghanbari Mohsen, Gieger Christian, Hamet Pavel, Ho Kevin, Hofer Edith, Holleczek Bernd, Xian Foo Valencia Hui, Hutri-Kähönen Nina, Hwang Shih-Jen, Ikram M Arfan, Josyula Navya Shilpa, Kähönen Mika, Khor Chiea-Chuen, Koenig Wolfgang, Kramer Holly, Krämer Bernhard K, Kühnel Brigitte, Lange Leslie A, Lehtimäki Terho, Lieb Wolfgang, , , Loos Ruth J F, Lukas Mary Ann, Lyytikäinen Leo-Pekka, Meisinger Christa, Meitinger Thomas, Melander Olle, Milaneschi Yuri, Mishra Pashupati P, Mononen Nina, Mychaleckyj Josyf C, Nadkarni Girish N, Nauck Matthias, Nikus Kjell, Ning Boting, Nolte Ilja M, O'Donoghue Michelle L, Orho-Melander Marju, Pendergrass Sarah A, Penninx Brenda W J H, Preuss Michael H, Psaty Bruce M, Raffield Laura M, Raitakari Olli T, Rettig Rainer, Rheinberger Myriam, Rice Kenneth M, Rosenkranz Alexander R, Rossing Peter, Rotter Jerome I, Sabanayagam Charumathi, Schmidt Helena, Schmidt Reinhold, Schöttker Ben, Schulz Christina-Alexandra, Sedaghat Sanaz, Shaffer Christian M, Strauch Konstantin, Szymczak Silke, Taylor Kent D, Tremblay Johanne, Chaker Layal, van der Harst Pim, van der Most Peter J, Verweij Niek, Völker Uwe, Waldenberger Melanie, Wallentin Lars, Waterworth Dawn M, White Harvey D, Wilson James G, Wong Tien-Yin, Woodward Mark, Yang Qiong, Yasuda Masayuki, Yerges-Armstrong Laura M, Zhang Yan, Snieder Harold, Wanner Christoph, Böger Carsten A, Köttgen Anna, Kronenberg Florian, Pattaro Cristian, Heid Iris |
| Nephroplex: a kidney-focused NGS panel highlights the challenges of PKD1 sequencing and identifies a founder BBS4 mutation. Journal of nephrology 2021 5 34 (6): 1855-1874. Zacchia Miriam, Blanco Francesca Del Vecchio, Trepiccione Francesco, Blasio Giancarlo, Torella Annalaura, Melluso Andrea, Capolongo Giovanna, Pollastro Rosa Maria, Piluso Giulio, Di Iorio Valentina, Simonelli Francesca, Viggiano Davide, Perna Alessandra, Nigro Vincenzo, Capasso Giovambattis |
| Association Between APOL1 Genotype and Kidney Diseases and Annual Kidney Function Change: A Systematic Review and Meta-Analysis of the Prospective Studies. International journal of nephrology and renovascular disease 2021 4 14 97-104. Jagannathan Ram, Rajagopalan Kanya, Hogan Julien, Hart Allyson, Newell Kenneth A, Pastan Stephen O, Patzer Rachel |
| Genotype-phenotype correlations and nephroprotective effects of RAAS inhibition in patients with autosomal recessive Alport syndrome. Pediatric nephrology (Berlin, Germany) 2021 3 36 (9): 2719-2730. Zhang Yanqin, Böckhaus Jan, Wang Fang, Wang Suxia, Rubel Diana, Gross Oliver, Ding J |
| NR3C1 Glucocorticoid Receptor Gene Polymorphisms Are Associated with Membranous and IgA Nephropathies. Cells 2021 11 10 (11): . Pac Micha?, Krata Natalia, Moszczuk Barbara, Wycza?kowska-Tomasik Aleksandra, Kaleta Beata, Foroncewicz Bartosz, Rudnicki Witold, P?czek Leszek, Mucha Krzyszt |
| Podocyte density is reduced in kidney allografts with high-risk APOL1 genotypes at transplantation. Clinical transplantation 2021 Jan e14234. Chen Dhruti P, Zaky Ziad S, Schold Jesse D, Herlitz Leal C, El-Rifai Rasha, Drawz Paul E, Bruggeman Leslie A, Barisoni Laura, Hogan Susan L, Hu Yichun, O'Toole John F, Poggio Emilio D, Sedor John |
| Molecular Diagnosis and Identification of Novel Pathogenic Variants in a Large Cohort of Italian Patients Affected by Polycystic Kidney Diseases. Genes 2023 6 14 (6): . Ersilia Nigro, Maria Amicone, Daniela D'Arco, Gina Sellitti, Oriana De Marco, Maria Guarino, Eleonora Riccio, Antonio Pisani, Aurora Danie |
| Polygenic risk affects the penetrance of monogenic kidney disease. medRxiv : the preprint server for health sciences 2023 5 . Atlas Khan, Ning Shang, Jordan G Nestor, Chunhua Weng, George Hripcsak, Peter C Harris, Ali G Gharavi, Krzysztof Kiryl |
| Clinical and Genetic Characteristics of CKD Patients with High-risk APOL1 Genotypes. Journal of the American Society of Nephrology : JASN 2023 2 . Elliott Mark D, Marasa Maddalena, Cocchi Enrico, Vena Natalie, Zhang Jun Y, Khan Atlas, Murthy Sarath Krishna, Bheda Shiraz, Rasouly Hila Milo, Povysil Gundula, Kiryluk Krzysztof, Gharavi Ali |
| Study on Blood Pressure, e-GFR, Serum Albumin, C-reactive Protein in Normal Subjects and Patients with CKD. Mymensingh medical journal : MMJ 2023 10 32 (4): 922-926. M M Huq, A Nessa, F Rahman, T Sharmin, F Yeasmin, M Taufiq-Ul-Alam, K Dilua |
| Increased risk of kidney failure in patients with genetic kidney disorders. The Journal of clinical investigation 2024 9 134 (17): . Mark D Elliott, Natalie Vena, Maddalena Marasa, Enrico Cocchi, Shiraz Bheda, Kelsie Bogyo, Ning Shang, Francesca Zanoni, Miguel Verbitsky, Chen Wang, Victoria Kolupaeva, Gina Jin, Maayan Sofer, Rafael Gras Pena, Pietro A Canetta, Andrew S Bomback, Lisa M Guay-Woodford, Jean Hou, Brenda W Gillespie, Bruce M Robinson, Jon B Klein, Michelle N Rheault, William E Smoyer, Larry A Greenbaum, Larry B Holzman, Ronald J Falk, Afshin Parsa, Simone Sanna-Cherchi, Laura H Mariani, Matthias Kretzler, Krzysztof Kiryluk, Ali G Gharavi, |
| Renal and Extrarenal Phenotypes in Patients With HNF1B Variants and Chromosome 17q12 Microdeletions. Kidney international reports 2024 8 9 (8): 2514-2526. Bénédicte Buffin-Meyer, Juliette Richard, Vincent Guigonis, Stefanie Weber, Jens König, Laurence Heidet, Nabila Moussaoui, Jeanne-Pierrette Vu, Stanislas Faguer, Audrey Casemayou, Richa Prakash, Véronique Baudouin, Julien Hogan, Demi Alexandrou, Detlef Bockenhauer, Justine Bacchetta, Bruno Ranchin, Stepanka Pruhova, Jakub Zieg, Annie Lahoche, Christine Okorn, Violetta Antal-Kónya, Denis Morin, Francesca Becherucci, Sandra Habbig, Max C Liebau, Mathilde Mauras, Tom Nijenhuis, Brigitte Llanas, Djalila Mekahli, Julia Thumfart, Burkhard Tönshoff, Laura Massella, Philippe Eckart, Sylvie Cloarec, Alejandro Cruz, Ludwig Patzer, Gwenaelle Roussey, Isabelle Vrillon, Olivier Dunand, Lucie Bessenay, Francesca Taroni, Marcin Zaniew, Ferielle Louillet, Carsten Bergmann, Franz Schaefer, Albertien M van Eerde, Joost P Schanstra, Stéphane Decramer, |
| Exploring Adiponectin in Autosomal Dominant Kidney Disease: Insight and Implications. Genes 2024 4 15 (4): . Ersilia Nigro, Marta Mallardo, Maria Amicone, Daniela D'Arco, Eleonora Riccio, Maurizio Marra, Fabrizio Pasanisi, Antonio Pisani, Aurora Danie |
| Discovery of genomic and transcriptomic pleiotropy between kidney function and soluble receptor for advanced glycation end-products using correlated meta-analyses: The Long Life Family Study (LLFS). medRxiv : the preprint server for health sciences 2024 1 . Mary F Feitosa, Shiow J Lin, Sandeep Acharya, Bharat Thyagarajan, Mary K Wojczynski, Allison L Kuipers, Alexander Kulminski, Kaare Christensen, Joseph M Zmuda, Michael R Brent, Michael A Provin |
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