Genetic Association and Gene-Gene Interaction Analyses in African American Dialysis Patients With Nondiabetic Nephropathy

Por Bostrom, Meredith A., Kao, W.H. Linda, Li, Man, Abboud, Hanna E., Adler, Sharon G., Iyengar, Sudha K., Kimmel, Paul L., Hanson, Robert L., Nicholas, Susanne B., Rasooly, Rebekah S., Sedor, John R., Coresh, Josef, Kohn, Orly F., Leehey, David J., Thornley-Brown, Denyse, Bottinger, Erwin P., Lipkowitz, Michael S., Meoni, Lucy A., Klag, Michael J., Lu, Lingyi, Hicks, Pamela J., Langefeld, Carl D., Parekh, Rulan S., Bowden, Donald W., Freedman, Barry I.
Publicado em 2011

A genome-wide admixture scan identifies MYH9 as a candidate locus associated with non-diabetic end stage renal disease in African Americans

Por Linda Kao, WH, Klag, Michael J, Meoni, Lucy A, Reich, David, Berthier-Schaad, Yvette, Li, Man, Coresh, Josef, Patterson, Nick, Tandon, Arti, Powe, Neil R, Fink, Nancy E, Sadler, John H, Weir, Matthew R, Abboud, Hanna E, Adler, Sharon, Divers, Jasmin, Iyengar, Sudha K, Freedman, Barry I, Kimmel, Paul L, Knowler, William C, Kohn, Orly F, Kramp, Kristopher, Leehey, David J, Nicholas, Susanne, Pahl, Madeleine, Schelling, Jeffrey R, Sedor, John R, Thornley-Brown, Denyse, Winkler, Cheryl A, Smith, Michael W., Parekh, Rulan S.
Publicado em 2008

Genome-Wide Association and Trans-ethnic Meta-Analysis for Advanced Diabetic Kidney Disease: Family Investigation of Nephropathy and Diabetes (FIND)

Por Iyengar, Sudha K., Sedor, John R., Freedman, Barry I., Kao, W. H. Linda, Kretzler, Matthias, Keller, Benjamin J., Abboud, Hanna E., Adler, Sharon G., Best, Lyle G., Bowden, Donald W., Burlock, Allison, Chen, Yii-Der Ida, Cole, Shelley A., Comeau, Mary E., Curtis, Jeffrey M., Divers, Jasmin, Drechsler, Christiane, Duggirala, Ravi, Elston, Robert C., Guo, Xiuqing, Huang, Huateng, Hoffmann, Michael Marcus, Howard, Barbara V., Ipp, Eli, Kimmel, Paul L., Klag, Michael J., Knowler, William C., Kohn, Orly F., Leak, Tennille S., Leehey, David J., Li, Man, Malhotra, Alka, März, Winfried, Nair, Viji, Nelson, Robert G., Nicholas, Susanne B., O’Brien, Stephen J., Pahl, Madeleine V., Parekh, Rulan S., Pezzolesi, Marcus G., Rasooly, Rebekah S., Rotimi, Charles N., Rotter, Jerome I., Schelling, Jeffrey R., Seldin, Michael F., Shah, Vallabh O., Smiles, Adam M., Smith, Michael W., Taylor, Kent D., Thameem, Farook, Thornley-Brown, Denyse P., Truitt, Barbara J., Wanner, Christoph, Weil, E. Jennifer, Winkler, Cheryl A., Zager, Philip G., Igo, Robert P., Hanson, Robert L., Langefeld, Carl D.
Publicado no PLoS Genet (2015)