Genetic variants and cell-free hemoglobin processing in sickle cell nephropathy.
Haematologica
Saraf, Santosh L SL; Zhang, Xu X; Shah, Binal B; Kanias, Tamir T; Gudehithlu, Krishnamurthy P KP; Kittles, Rick R; Machado, Roberto F RF; Arruda, Jose A L JA; Gladwin, Mark T MT; Singh, Ashok K AK; Gordeuk, Victor R VR
Polymorphisms in MYH9 are associated with diabetic nephropathy in European Americans.
Nephrology, Dialysis, Transplantation : Official Publication Of The European Dialysis And Transplant Association - European Renal Association
Cooke, Jessica N JN; Bostrom, Meredith A MA; Hicks, Pamela J PJ; Ng, Maggie C Y MC; Hellwege, Jacklyn N JN; Comeau, Mary E ME; Divers, Jasmin J; Langefeld, Carl D CD; Freedman, Barry I BI; Bowden, Donald W DW
MYH9 and APOL1 are both associated with sickle cell disease nephropathy.
British Journal Of Haematology
Ashley-Koch, Allison E AE; Okocha, Emmanuel C EC; Garrett, Melanie E ME; Soldano, Karen K; De Castro, Laura M LM; Jonassaint, Jude C JC; Orringer, Eugene P EP; Eckman, James R JR; Telen, Marilyn J MJ
African ancestry allelic variation at the MYH9 gene contributes to increased susceptibility to non-diabetic end-stage kidney disease in Hispanic Americans.
Human Molecular Genetics
Behar, Doron M DM; Rosset, Saharon S; Tzur, Shay S; Selig, Sara S; Yudkovsky, Guennady G; Bercovici, Sivan S; Kopp, Jeffrey B JB; Winkler, Cheryl A CA; Nelson, George W GW; Wasser, Walter G WG; Skorecki, Karl K
Dense mapping of MYH9 localizes the strongest kidney disease associations to the region of introns 13 to 15.
Human Molecular Genetics
Nelson, George W GW; Freedman, Barry I BI; Bowden, Donald W DW; Langefeld, Carl D CD; An, Ping P; Hicks, Pamela J PJ; Bostrom, Meredith A MA; Johnson, Randall C RC; Kopp, Jeffrey B JB; Winkler, Cheryl A CA
The association of the MYH9 gene and kidney outcomes in American Indians: the Strong Heart Family Study.
Human Genetics
Franceschini, Nora N; Voruganti, V Saroja VS; Haack, Karin K; Almasy, Laura L; Laston, Sandy S; Goring, Harald H H HH; Umans, Jason G JG; Lee, Elisa T ET; Best, Lyle G LG; Fabsitz, Richard R RR; MacCluer, Jean W JW; Howard, Barbara V BV; North, Kari E KE; Cole, Shelley A SA
Non-muscle myosin heavy chain 9 gene MYH9 associations in African Americans with clinically diagnosed type 2 diabetes mellitus-associated ESRD.
Nephrology, Dialysis, Transplantation : Official Publication Of The European Dialysis And Transplant Association - European Renal Association
Freedman, Barry I BI; Hicks, Pamela J PJ; Bostrom, Meredith A MA; Comeau, Mary E ME; Divers, Jasmin J; Bleyer, Anthony J AJ; Kopp, Jeffrey B JB; Winkler, Cheryl A CA; Nelson, George W GW; Langefeld, Carl D CD; Bowden, Donald W DW
Polymorphisms in the non-muscle myosin heavy chain 9 gene (MYH9) are strongly associated with end-stage renal disease historically attributed to hypertension in African Americans.
Kidney International
Freedman, Barry I BI; Hicks, Pamela J PJ; Bostrom, Meredith A MA; Cunningham, Mary E ME; Liu, Yongmei Y; Divers, Jasmin J; Kopp, Jeffrey B JB; Winkler, Cheryl A CA; Nelson, George W GW; Langefeld, Carl D CD; Bowden, Donald W DW
MYH9 is a major-effect risk gene for focal segmental glomerulosclerosis.
Nature Genetics
Kopp, Jeffrey B JB; Smith, Michael W MW; Nelson, George W GW; Johnson, Randall C RC; Freedman, Barry I BI; Bowden, Donald W DW; Oleksyk, Taras T; McKenzie, Louise M LM; Kajiyama, Hiroshi H; Ahuja, Tejinder S TS; Berns, Jeffrey S JS; Briggs, William W; Cho, Monique E ME; Dart, Richard A RA; Kimmel, Paul L PL; Korbet, Stephen M SM; Michel, Donna M DM; Mokrzycki, Michele H MH; Schelling, Jeffrey R JR; Simon, Eric E; Trachtman, Howard H; Vlahov, David D; Winkler, Cheryl A CA