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  1. 1.   Kidney disease and APOL1
  2. Yusuf, Aminu Abba; Govender, Melanie A.; Brandenburg, Jean-Tristan; Winkler,Cheryl
  3. Human Molecular Genetics. 2021, Mar 22; 30(R1): R129-R137.
  1. 2.   APOL1 Kidney Risk Variants and Cardiovascular Disease: An Individual Participant Data Meta-Analysis
  2. Grams, Morgan E; Surapaneni, Aditya; Ballew, Shoshana H; Appel, Lawrence J; Boerwinkle, Eric; Boulware, L Ebony; Chen, Teresa K; Coresh, Josef; Cushman, Mary; Divers, Jasmin; Gutiérrez, Orlando M; Irvin, Marguerite R; Ix, Joachim H; Kopp, Jeffrey B; Kuller, Lewis H; Langefeld, Carl D; Lipkowitz, Michael S; Mukamal, Kenneth J; Musani, Solomon K; Naik, Rakhi P; Pajewski, Nicholas M; Peralta, Carmen A; Tin, Adrienne; Wassel, Christina L; Wilson, James G; Winkler,Cheryl; Young, Bessie A; Zakai, Neil A; Freedman, Barry I
  3. Journal of the American Society of Nephrology : JASN. 2019, OCT; 30(10): 2027-2036.
  1. 3.   Sickle Cell Trait and the Risk of ESRD in Blacks
  2. Naik, Rakhi P.; Irvin, Marguerite R.; Judd, Suzanne; Gutierrez, Orlando M.; Zakai, Neil A.; Derebail, Vimal K.; Peralta, Carmen; Lewis, Michael R.; Zhi, Degui; Arnett, Donna; McClellan, William; Wilson, James G.; Reiner, Alexander P.; Kopp, Jeffrey B.; Winkler, Cheryl; Cushman, Mary
  3. Journal of the American Society of Nephrology. 2017, Jul 1; 28(7): 2180-2187.
  1. 4.   APOL1 Genetic Variants in Focal Segmental Glomerulosclerosis and HIV-Associated Nephropathy
  2. Kopp, J. B.; Nelson, G. W.; Sampath, K.; Johnson, R. C.; Genovese, G.; An, P.; Friedman, D.; Briggs, W.; Dart, R.; Korbet, S.; Mokrzycki, M. H.; Kimmel, P. L.; Limou, S.; Ahuja, T. S.; Berns, J. S.; Fryc, J.; Simon, E. E.; Smith, M. C.; Trachtman, H.; Michel, D. M.; Schelling, J. R.; Vlahov, D.; Pollak, M.; Winkler, C. A.
  3. Journal of the American Society of Nephrology. 2011, Nov; 22(11): 2129-2137.
  1. 5.   The Apolipoprotein L1 (APOL1) Gene and Nondiabetic Nephropathy in African Americans
  2. Freedman, B. I.; Kopp, J. B.; Langefeld, C. D.; Genovese, G.; Friedman, D. J.; Nelson, G. W.; Winkler, C. A.; Bowden, D. W.; Pollak, M. R.
  3. Journal of the American Society of Nephrology. 2010, Sep; 21(9): 1422-1426.
  1. 6.   Association of Trypanolytic ApoL1 Variants with Kidney Disease in African Americans
  2. Genovese, G.; Friedman, D. J.; Ross, M. D.; Lecordier, L.; Uzureau, P.; Freedman, B. I.; Bowden, D. W.; Langefeld, C. D.; Oleksyk, T. K.; Knob, A. L. U.; Bernhardy, A. J.; Hicks, P. J.; Nelson, G. W.; Vanhollebeke, B.; Winkler, C. A.; Kopp, J. B.; Pays, E.; Pollak, M. R.
  3. Science. 2010, Aug; 329(5993): 841-845.
  1. 7.   MYH9 Genetic Variants Associated With Glomerular Disease: What Is the Role for Genetic Testing?
  2. Kopp, J. B.; Winkler, C. A.; Nelson, G. W.
  3. Seminars in Nephrology. 2010, Jul; 30(4): 409-417.
  1. 8.   The Non-Muscle Myosin Heavy Chain 9 Gene (MYH9) Is Not Associated with Lupus Nephritis in African Americans
  2. Freedman, B. I.; Edberg, J. C.; Comeau, M. E.; Murea, M.; Bowden, D. W.; Divers, J.; Alarcon, G. S.; Brown, E. E.; McGwin, G.; Kopp, J. B.; Winkler, C. A.; Nelson, G. W.; Illei, G.; Petri, M.; Ramsey-Goldman, R.; Reveille, J. D.; Vila, L. M.; Langefeld, C. D.; Kimberly, R. P.; Grp, P. S.
  3. American Journal of Nephrology. 2010, Jul; 32(1): 66-72.
  1. 9.   African ancestry allelic variation at the MYH9 gene contributes to increased susceptibility to non-diabetic end-stage kidney disease in Hispanic Americans
  2. Behar, D. M.; Rosset, S.; Tzur, S.; Selig, S.; Yudkovsky, G.; Bercovici, S.; Kopp, J. B.; Winkler, C. A.; Nelson, G. W.; Wasser, W. G.; Skorecki, K.
  3. Human Molecular Genetics. 2010, May; 19(9): 1816-1827.
  1. 10.   Dense mapping of MYH9 localizes the strongest kidney disease associations to the region of introns 13 to 15
  2. Nelson, G. W.; Freedman, B. I.; Bowden, D. W.; Langefeld, C. D.; An, P.; Hicks, P. J.; Bostrom, M. A.; Johnson, R. C.; Kopp, J. B.; Winkler, C. A.
  3. Human Molecular Genetics. 2010, May; 19(9): 1805-1815.
  1. 11.   Genetics of Focal Segmental Glomerulosclerosis and Human Immunodeficiency Virus-Associated Collapsing Glomerulopathy: The Role of MYH9 Genetic Variation
  2. Winkler, C. A.; Nelson, G.; Oleksyk, T. K.; Nava, M. B.; Kopp, J. B.
  3. Seminars in Nephrology. 2010, Mar; 30(2): 111-125.
  1. 12.   Is There a Genetic Basis for Health Disparities in Human Immunodeficiency Virus Disease?
  2. Winkler, C.
  3. Mount Sinai Journal of Medicine. 2010, Mar-Apr; 77(2): 149-159.
  1. 13.   Association of APOE polymorphism with chronic kidney disease in a nationally representative sample: a Third National Health and Nutrition Examination Survey (NHANES III) Genetic Study
  2. Chu, A. Y.; Parekh, R. S.; Astor, B. C.; Coresh, J.; Berthier-Schaad, Y.; Smith, M. W.; Shuldiner, A. R.; Kao, W.
  3. BMC Medical Genetics. 2009 10 AR 108
  1. 14.   Polymorphisms in the Nonmuscle Myosin Heavy Chain 9 Gene (MYH9) Are Associated with Albuminuria in Hypertensive African Americans: The HyperGEN Study
  2. Freedman, B. I.; Kopp, J. B.; Winkler, C. A.; Nelson, G. W.; Rao, D. C.; Eckfeldt, J. H.; Leppert, M. F.; Hicks, P. J.; Divers, J.; Langefeld, C. D.; Hunt, S. C.
  3. American Journal of Nephrology. 2009 29(6): 626-632.
  1. 15.   MYH9 is a major-effect risk gene for focal segmental glomerulosclerosis
  2. Kopp, J. B.; Smith, M. W.; Nelson, G. W.; Johnson, R. C.; Freedman, B. I.; Bowden, D. W.; Oleksyk, T.; McKenzie, L. M.; Kajiyama, H.; Ahuja, T. S.; Berns, J. S.; Briggs, W.; Cho, M. E.; Dart, R. A.; Kimmel, P. L.; Korbet, S. M.; Michel, D. M.
  3. Nature Genetics. 2008 40(10): 1175-1184.
  1. 16.   NPHS2 variation in sporadic focal segmental glomerulosclerosis
  2. McKenzie, L. M.; Hendrickson, S. L.; Briggs, W. A.; Dart, R. A.; Korbet, S. M.; Mokrzycki, M. H.; Kimmel, P. L.; Ahuja, T. S.; Berns, J. S.; Simon, E. E.; Smith, M. C.; Trachtman, H.; Michel, D. M.; Schelling, J. R.; Cho, M.; Zhou, Y. C.; Binns-Roemer, E.; Kirk, G. D.; Kopp, J. B.; Winkler, C. A.
  3. Journal of the American Society of Nephrology. 2007, Nov; 18(11): 2987-2995.
  1. 17.   Genome-wide scans for diabetic nephropathy and albuntinuria in multiethnic populations - The family investigation of nephropathy and diabetes (FIND)
  2. Iyengar, S. K.; Abboud, H. E.; Goddard, K. A. B.; Saad, M. F.; Adler, S. G.; Arar, N. H.; Bowden, D. W.; Duggirala, R.; Elston, R. C.; Hanson, R. L.; Ipp, E.; Kao, W. H. L.; Kimmel, P. L.; Klag, M. J.; Knowler, W. C.; Meoni, L. A.; Nelson, R. G.; Nicholas, S. B.; Pahl, M. V.; Parekh, R. S.; Quade, S. R. E.; Rich, S. S.; Rotter, J. I.; Scavini, M.; Schelling, J. R.; Sedor, J. R.; Sehgal, A. R.; Shah, V. O.; Smith, M. W.; Taylor, K. D.; Winkler, C. A.; Zager, P. G.; Freedman, B. I.; Family Invest, N.
  3. Diabetes. 2007, Jun; 56(6): 1577-1585.
  1. 18.   Three single-nucleotide polymorphisms in LPA account for most of the increase in lipoprotein(a) level elevation in African Americans compared with European Americans
  2. Chretien, J. P.; Coresh, J.; Berthier-Schaad, Y.; Kao, W. H. L.; Fink, N. E.; Klag, M. J.; Marcovina, S. M.; Giaculli, F.; Smith, M. W.
  3. Journal of Medical Genetics. 2006, Dec; 43(12): 917-923.
  1. 19.   NPHS2 gene, nephrotic syndrome and focal segmental glomerulosclerosis: A HuGE review
  2. Franceschini, N.; North, K. E.; Kopp, J. B.; McKenzie, L.; Winkler, C.
  3. Genetics in Medicine. 2006, Feb; 8(2): 63-75.
  1. 20.   Focal Segmental Glomerulosclerosis in Primates Infected With a Simian Immunodeficiency Virus
  2. Alpers, C. E.; Tsai, C. C.; Hudkins, K. L.; Cui, Y.; Kuller, L.; Benveniste, R. E.; Ward, J. M.; Morton, W. R.
  3. Aids Research and Human Retroviruses. 1997 13(5): 413-424.
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