-
Little, MH, Quinlan, C.
Advances in our understanding of genetic kidney disease using kidney organoids..
Pediatr Nephrol
35(6)
:
915 -926
2020
view publication
-
Quinlan, C.
CUBN variants uncouple proteinuria from kidney function..
Nat Rev Nephrol
16(3)
:
135 -136
2020
view publication
-
De Rechter, S, Bockenhauer, D, Guay-Woodford, LM, Liu, I, Mallett, AJ, Soliman, NA, Sylvestre, LC, Schaefer, F, Liebau, MC, Mekahli, D, et al.
ADPedKD: A Global Online Platform on the Management of Children With ADPKD..
Kidney Int Rep
4(9)
:
1271 -1284
2019
view publication
-
Jayasinghe, K, White, SM, Kerr, PG, MacGregor, D, Stark, Z, Wilkins, E, Simons, C, Mallett, A, Quinlan, C.
Isolated proteinuria due to CUBN homozygous mutation - challenging the investigative paradigm..
BMC Nephrol
20(1)
:
330
2019
view publication
-
Jayasinghe, K, Stark, Z, Patel, C, Mallawaarachchi, A, McCarthy, H, Faull, R, Chakera, A, Sundaram, M, Jose, M, Kerr, P, et al.
Comprehensive evaluation of a prospective Australian patient cohort with suspected genetic kidney disease undergoing clinical genomic testing: a study protocol..
BMJ Open
9(8)
:
e029541
2019
view publication