Bringing Renal Biopsy Interpretation into the Molecular Age with Single Cell RNA-Sequencing

Por Malone, Andrew F., Wu, Haojia, Humphreys, Benjamin D.
Publicado no Semin Nephrol (2018)

Functional assessment of a novel COL4A5 splice region variant and immunostaining of plucked hair follicles as an alternative method of diagnosis in X-linked Alport syndrome

Por Malone, Andrew F., Funk, Steven D., Alhamad, Tarek, Miner, Jeffrey H.
Publicado no Pediatr Nephrol (2016)

Variability in phenotype induced by the podocin variant R229Q plus a single pathogenic mutation

Por Phelan, Paul J., Hall, Gentzon, Wigfall, Delbert, Foreman, John, Nagaraj, Shashi, Malone, Andrew F., Winn, Michelle P., Howell, David N., Gbadegesin, Rasheed
Publicado no Clin Kidney J (2015)

The Privilege of Induction Avoidance and Calcineurin Inhibitors Withdrawal in 2 Haplotype HLA Matched White Kidney Transplantation

Por Brifkani, Zaid, Brennan, Daniel C., Lentine, Krista L., Horwedel, Timothy A., Malone, Andrew F., Delos Santos, Rowena, Maw, Thin Thin, Alhamad, Tarek
Publicado no Transplant Direct (2017)

A Novel Missense Mutation of Wilms’ Tumor 1 Causes Autosomal Dominant FSGS

Por Hall, Gentzon, Gbadegesin, Rasheed A., Lavin, Peter, Wu, Guanghong, Liu, Yangfan, Oh, Edwin C., Wang, Liming, Spurney, Robert F., Eckel, Jason, Lindsey, Thomas, Homstad, Alison, Malone, Andrew F., Phelan, Paul J., Shaw, Andrey, Howell, David N., Conlon, Peter J., Katsanis, Nicholas, Winn, Michelle P.
Publicado no J Am Soc Nephrol (2015)

Rare hereditary COL4A3/COL4A4 variants may be mistaken for familial focal segmental glomerulosclerosis

Por Malone, Andrew F, Phelan, Paul J, Hall, Gentzon, Cetincelik, Umran, Homstad, Alison, Alonso, Andrea, Jiang, Ruiji, Lindsey, Thomas, Wu, Guanghong, Sparks, Matthew A, Smith, Stephen R, Webb, Nicholas J A, Kalra, Philip, Adeyemo, Adebowale, Shaw, Andrey S, Conlon, Peter J, Jennette, J Charles, Howell, David N, Winn, Michelle P, Gbadegesin, Rasheed A
Publicado no Kidney Int (2014)