A National Retrospective Cohort Study of BK Viraemia in Renal Transplant Recipients: TH-PO843 von Clince, Michelle, Sandys, Vicki K., Fitzpatrick, Fidelma, Brennan, Caoimhe, Conlon, Peter, O’kelly, Patrick, Conlon, Peter J.

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Variant renal artery anatomy in first degree relatives on MDCT angiography von Reid, Conor, Kelly, Dearbhla, Briody, Hayley, Lawless, Philip, Little, Dilly, Conlon, Peter J., Morrin, Martina

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A comparative analysis of survival of patients on dialysis and after kidney transplantation von Kaballo, Mohammed A, Canney, Mark, O'Kelly, Patrick, Williams, Yvonne, O'Seaghdha, Conall M, Conlon, Peter J

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Review of high‐risk features of cutaneous squamous cell carcinoma and discrepancies between the American Joint Committee on Cancer and NCCN Clinical Practice Guidelines In Oncology... von Skulsky, Samuel Lamarre, O'Sullivan, Barry, McArdle, Orla, Leader, Mary, Roche, Muireann, Conlon, Peter J., O'Neill, James Paul, W. Eisele, David

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C3 Glomerulopathy: Clinicopathologic Features and Predictors of Outcome von Medjeral-Thomas, Nicholas R, O'Shaughnessy, Michelle M, O'Regan, John A, Traynor, Carol, Flanagan, Michael, Wong, Limy, Teoh, Chia Wei, Awan, Atif, Waldron, Mary, Cairns, Tom, O'Kelly, Patrick, Dorman, Anthony M, Pickering, Matthew C, Conlon, Peter J, Cook, H Terence

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NPHP1 (Nephrocystin-1) Gene Deletions Cause Adult-Onset ESRD von Snoek, Rozemarijn, van Setten, Jessica, Keating, Brendan J, Israni, Ajay K, Jacobson, Pamala A, Oetting, William S, Matas, Arthur J, Mannon, Roslyn B, Zhang, Zhongyang, Zhang, Weijia, Hao, Ke, Murphy, Barbara, Reindl-Schwaighofer, Roman, Heinzl, Andreas, Oberbauer, Rainer, Viklicky, Ondrej, Conlon, Peter J, Stapleton, Caragh P, Bakker, Stephan J L, Snieder, Harold, Peters, Edith D J, van der Zwaag, Bert, Knoers, Nine V A M, de Borst, Martin H, van Eerde, Albertien M

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Adult presentation of a rare mitochondrial tRNA Val gene mutation—an expanding clinical phenotype von Joyce, Eimear, Ali, Mohib, Richard, Georgia, Kelly, Siobhan, Martin, Fiachra, Conlon, Peter J., Whelehan, Anna, Ng, Yi Shiau, Lefter, Stela

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Monoallelic IFT140 pathogenic variants are an important cause of the autosomal dominant polycystic kidney-spectrum phenotype von Senum, Sarah R., Li, Ying (Sabrina) M., Benson, Katherine A., Joli, Giancarlo, Olinger, Eric, Lavu, Sravanthi, Madsen, Charles D., Gregory, Adriana V., Neatu, Ruxandra, Kline, Timothy L., Audrézet, Marie-Pierre, Outeda, Patricia, Nau, Cherie B., Meijer, Esther, Ali, Hamad, Steinman, Theodore I., Mrug, Michal, Phelan, Paul J., Watnick, Terry J., Peters, Dorien J.M., Ong, Albert C.M., Conlon, Peter J., Perrone, Ronald D., Cornec-Le Gall, Emilie, Hogan, Marie C., Torres, Vicente E., Sayer, John A., Harris, Peter C.

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Rare hereditary COL4A3/COL4A4 variants may be mistaken for familial focal segmental glomerulosclerosis von Malone, Andrew F., Phelan, Paul J., Hall, Gentzon, Cetincelik, Umran, Homstad, Alison, Alonso, Andrea S., Jiang, Ruiji, Lindsey, Thomas B., Wu, Guanghong, Sparks, Matthew A., Smith, Stephen R., Webb, Nicholas J.A., Kalra, Philip A., Adeyemo, Adebowale A., Shaw, Andrey S., Conlon, Peter J., Charles Jennette, J., Howell, David N., Winn, Michelle P., Gbadegesin, Rasheed A.

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Persistent DNA damage underlies tubular cell polyploidization and progression to chronic kidney disease in kidneys deficient in the DNA repair protein FAN1 von Airik, Merlin, Phua, Yu Leng, Huynh, Amy B., McCourt, Blake T., Rush, Brittney M., Tan, Roderick J., Vockley, Jerry, Murray, Susan L., Dorman, Anthony, Conlon, Peter J., Airik, Rannar

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Epigenome-wide meta-analysis identifies DNA methylation biomarkers associated with diabetic kidney disease von Smyth, Laura J., Dahlström, Emma H., Syreeni, Anna, Kerr, Katie, Kilner, Jill, Doyle, Ross, Brennan, Eoin, Nair, Viji, Fermin, Damian, Nelson, Robert G., Looker, Helen C., Wooster, Christopher, Andrews, Darrell, Anderson, Kerry, McKay, Gareth J., Cole, Joanne B., Salem, Rany M., Conlon, Peter J., Kretzler, Matthias, Hirschhorn, Joel N., Sadlier, Denise, Godson, Catherine, Florez, Jose C., Forsblom, Carol, Maxwell, Alexander P., Groop, Per-Henrik, Sandholm, Niina, McKnight, Amy Jayne

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Donor genetic burden for cerebrovascular risk and kidney transplant outcome von Collins, Kane E., Gilbert, Edmund, Mauduit, Vincent, Benson, Katherine A., Elhassan, Elhussein A. E., O’Seaghdha, Conall, Hill, Claire, McKnight, Amy Jayne, Maxwell, Alexander P., van der Most, Peter J., de Borst, Martin H., Guan, Weihua, Jacobson, Pamala A., Israni, Ajay K., Keating, Brendan J., Lord, Graham M., Markkinen, Salla, Helanterä, Ilkka, Hyvärinen, Kati, Partanen, Jukka, Madden, Stephen F., Limou, Sophie, Cavalleri, Gianpiero L., Conlon, Peter J.

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Integration of genetic and histopathology data in interpretation of kidney disease von Murray, Susan L, Fennelly, Neil K, Doyle, Brendan, Lynch, Sally Ann, Conlon, Peter J

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An Exome Sequencing Study of 10 Families with IgA Nephropathy von Stapleton, Caragh P., Kennedy, Claire, Fennelly, Neil K., Murray, Susan L., Connaughton, Dervla M., Dorman, Anthony M., Doyle, Brendan, Cavalleri, Gianpiero L., Conlon, Peter J.

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A novel missense mutation of Wilms' Tumor 1 causes autosomal dominant FSGS von 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

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Understanding What Influences the Health-Related Quality of Life of Hemodialysis Patients: A Collaborative Study in England and Ireland von Lowney, Aoife C., MRCPI, MRCPUK, Myles, Helena T., MRCPI, Bristowe, Katherine, PhD, Lowney, Eanna L., MD, Shepherd, Katie, MA, Murphy, Marie, FRCPI, O'Brien, Tony, FRCPI, Casserly, Liam, MRCPI, McQuillan, Regina, FRCPI, Plant, William D., FRCP Edin, Conlon, Peter J., PhD, Vinen, Catherine, FRCP, PhD, Eustace, Joseph A., PhD, Murtagh, Fliss E.M., FRCP, PhD

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A Rare Autosomal Dominant Variant in Regulator of Calcineurin Type 1 (RCAN1) Gene Confers Enhanced Calcineurin Activity and May Cause FSGS von Lane, Brandon M., Murray, Susan, Benson, Katherine, Bierzynska, Agnieszka, Chryst-Stangl, Megan, Wang, Liming, Wu, Guanghong, Cavalleri, Gianpiero, Doyle, Brendan, Fennelly, Neil, Dorman, Anthony, Conlon, Shane, Vega-Warner, Virginia, Fermin, Damian, Vijayan, Poornima, Qureshi, Mohammad Azfar, Shril, Shirlee, Barua, Moumita, Hildebrandt, Friedhelm, Pollak, Martin, Howell, David, Sampson, Matthew G., Saleem, Moin, Conlon, Peter J., Spurney, Robert, Gbadegesin, Rasheed

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Using omics to explore complications of kidney transplantation von Stapleton, Caragh P., Conlon, Peter J., Phelan, Paul J.

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Utility of Genomic Testing after Renal Biopsy von Murray, Susan L., Dorman, Anthony, Benson, Katherine A., Connaughton, Dervla M., Stapleton, Caragh P., Fennelly, Neil K., Kennedy, Claire, McDonnell, Ciara A., Kidd, Kendrah, Cormican, Sarah M., Ryan, Louise A., Lavin, Peter, Little, Mark A., Bleyer, Anthony J., Doyle, Brendan, Cavalleri, Gianpiero L., Hildebrandt, Friedhelm, Conlon, Peter J.

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Karyomegalic Interstitial Nephritis: Cancer Risk Following Transplantation von Murray, Susan L., Connaughton, Dervla M., Fennelly, Neil K., Kay, Elaine W., Dorman, Anthony, Doyle, Brendan, Conlon, Peter J.

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