Peter Lavin
Peter Lavin
Trinity Health Kidney Centre, Tallaght Hospital, Trinity College, Dublin
Verified email at
Cited by
Cited by
C3 glomerulopathy: consensus report
MC Pickering, VD D'agati, CM Nester, RJ Smith, M Haas, GB Appel, ...
Kidney international 84 (6), 1079-1089, 2013
Atrasentan and renal events in patients with type 2 diabetes and chronic kidney disease (SONAR): a double-blind, randomised, placebo-controlled trial.
ZD Heerspink HJL, Parving HH, Andress DL, Bakris G, Correa-Rotter R, Hou FF ...
Lancet 393 (10184), 1937-1947, 2019
Arhgap24 inactivates Rac1 in mouse podocytes, and a mutant form is associated with familial focal segmental glomerulosclerosis
S Akilesh, H Suleiman, H Yu, MC Stander, P Lavin, R Gbadegesin, ...
The Journal of clinical investigation 121 (10), 4127-4137, 2011
Monogenic causes of chronic kidney disease in adults
DM Connaughton, C Kennedy, S Shril, N Mann, SL Murray, PA Williams, ...
Kidney international 95 (4), 914-928, 2019
Mutations in the gene that encodes the F-actin binding protein anillin cause FSGS
RA Gbadegesin, G Hall, A Adeyemo, N Hanke, I Tossidou, J Burchette, ...
Journal of the American Society of Nephrology 25 (9), 1991-2002, 2014
TRPC6 enhances angiotensin II-induced albuminuria
J Eckel, PJ Lavin, EA Finch, N Mukerji, J Burch, R Gbadegesin, G Wu, ...
Journal of the American Society of Nephrology 22 (3), 526-535, 2011
A hybrid CFHR3-1 gene causes familial C3 glomerulopathy
TH Malik, PJ Lavin, EG de Jorge, KA Vernon, KL Rose, MP Patel, ...
Journal of the American Society of Nephrology 23 (7), 1155-1160, 2012
Pathogenesis and therapy of focal segmental glomerulosclerosis: an update
R Gbadegesin, P Lavin, J Foreman, M Winn
Pediatric nephrology 26, 1001-1015, 2011
Inverted formin 2 mutations with variable expression in patients with sporadic and hereditary focal and segmental glomerulosclerosis
RA Gbadegesin, PJ Lavin, G Hall, B Bartkowiak, A Homstad, R Jiang, ...
Kidney International 81 (1), 94-99, 2011
TNXB mutations can cause vesicoureteral reflux
RA Gbadegesin, PD Brophy, A Adeyemo, G Hall, IR Gupta, D Hains, ...
Journal of the American Society of Nephrology 24 (8), 1313-1322, 2013
The Irish Kidney Gene Project-prevalence of family history in patients with kidney disease in Ireland
DM Connaughton, S Bukhari, P Conlon, E Cassidy, M O'Toole, ...
Nephron 130 (4), 293-301, 2015
Noninvasive immunohistochemical diagnosis and novel MUC1 mutations causing autosomal dominant tubulointerstitial kidney disease
M Živná, K Kidd, A Přistoupilová, V Barešová, M DeFelice, B Blumenstiel, ...
Journal of the American Society of Nephrology 29 (9), 2418-2431, 2018
A novel missense mutation of Wilms’ Tumor 1 causes autosomal dominant FSGS
G Hall, RA Gbadegesin, P Lavin, G Wu, Y Liu, EC Oh, L Wang, ...
Journal of the American Society of Nephrology 26 (4), 831-843, 2015
Hepatorenal correction in murine glycogen storage disease type I with a double-stranded adeno-associated virus vector
X Luo, G Hall, S Li, A Bird, PJ Lavin, MP Winn, AR Kemper, TT Brown, ...
Molecular therapy 19 (11), 1961-1970, 2011
Higher tacrolimus trough levels on days 2–5 post‐renal transplant are associated with reduced rates of acute rejection
CM O’Seaghdha, R McQuillan, AM Moran, P Lavin, A Dorman, P O’Kelly, ...
Clinical transplantation 23 (4), 462-468, 2009
Therapeutic targets in focal and segmental glomerulosclerosis
PJ Lavin, R Gbadegesin, TV Damodaran, MP Winn
Current opinion in nephrology and hypertension 17 (4), 386-392, 2008
Phosphodiesterase 5 inhibition ameliorates angiontensin II-induced podocyte dysmotility via the protein kinase G-mediated downregulation of TRPC6 activity
G Hall, J Rowell, F Farinelli, RA Gbadegesin, P Lavin, G Wu, A Homstad, ...
American Journal of Physiology-Renal Physiology 306 (12), F1442-F1450, 2014
Exclusion of homozygous PLCE1 (NPHS3) mutations in 69 families with idiopathic and hereditary FSGS
R Gbadegesin, B Bartkowiak, PJ Lavin, N Mukerji, G Wu, B Bowling, ...
Pediatric Nephrology 24, 281-285, 2009
Autosomal dominant tubulointerstitial kidney disease (ADTKD) in Ireland
S Cormican, DM Connaughton, C Kennedy, S Murray, M Živná, S Kmoch, ...
Renal failure 41 (1), 832-841, 2019
Utility of genomic testing after renal biopsy
SL Murray, A Dorman, KA Benson, DM Connaughton, CP Stapleton, ...
American journal of nephrology 51 (1), 43-53, 2020
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