| A Deafness-Associated Mutant Human Connexin 26 Improves the Epithelial Barrier In Vitro YKS Man, C Trolove, D Tattersall, AC Thomas, A Papakonstantinopoulou, ... Journal of Membrane Biology 218, 29-37, 2007 | 63 | 2007 |
| Maternal inheritance of a promoter variant in the imprinted PHLDA2 gene significantly increases birth weight M Ishida, D Monk, AJ Duncan, S Abu-Amero, J Chong, SM Ring, ... The American Journal of Human Genetics 90 (4), 715-719, 2012 | 57 | 2012 |
| Sphingomyelinase disables inactivation in endogenous PIEZO1 channels J Shi, AJ Hyman, D De Vecchis, J Chong, L Lichtenstein, TS Futers, ... Cell reports 33 (1), 2020 | 50 | 2020 |
| Biallelic inheritance of hypomorphic PKD1 variants is highly prevalent in very early onset polycystic kidney disease M Durkie, J Chong, MK Valluru, PC Harris, ACM Ong Genetics in Medicine 23 (4), 689-697, 2021 | 42 | 2021 |
| Modeling of full-length Piezo1 suggests importance of the proximal N-terminus for dome structure J Chong, D De Vecchis, AJ Hyman, OV Povstyan, MJ Ludlow, J Shi, ... Biophysical journal 120 (8), 1343-1356, 2021 | 28 | 2021 |
| Autosomal dominant polycystic kidney disease: recent advances in clinical management Z Mao, J Chong, ACM Ong F1000Research 5, 2016 | 25 | 2016 |
| Renal albumin excretion in healthy young adults and its association with mortality risk in the US population J Chong, J Fotheringham, C Tomson, T Ellam Nephrology Dialysis Transplantation 35 (3), 458-464, 2020 | 17 | 2020 |
| Clinical practice guideline monitoring children and young people with, or at risk of developing autosomal dominant polycystic kidney disease (ADPKD) J Dudley, P Winyard, M Marlais, O Cuthell, T Harris, J Chong, J Sayer, ... BMC nephrology 20, 1-8, 2019 | 16 | 2019 |
| Barriers and facilitators to the implementation of guidelines in rare diseases: A systematic review M Gittus, J Chong, A Sutton, ACM Ong, J Fotheringham Orphanet Journal of Rare Diseases 18 (1), 140, 2023 | 4 | 2023 |
| Regional variation in tolvaptan prescribing across England: national data and retrospective evaluation from an expert centre J Chong, T Harris, ACM Ong Clinical Kidney Journal 16 (1), 61-68, 2023 | 4 | 2023 |
| Combining genotype with height-adjusted kidney length predicts rapid progression of ADPKD EWC Chen, J Chong, MK Valluru, M Durkie, RJ Simms, PC Harris, ... Nephrology Dialysis Transplantation, gfad270, 2024 | | 2024 |
| FC029: A Multivariate Model Identifies Genotype, Hypertension and Kidney Length as Independent Baseline Predictors of Disease Progression in a Longitudinal Autosomal Dominant … W Cong Eugene Chen, A Ong, J Han Chong Nephrology Dialysis Transplantation 37 (Supplement_3), gfac101. 001, 2022 | | 2022 |
| This is a repository copy of Biallelic inheritance of hypomorphic PKD1 variants is highly prevalent in very early onset polycystic kidney disease. M Durkie, J Chong, MK Valluru | | 2020 |
| SAT-334 GENETIC TESTING OF FAMILIES WITH VERY EARLY ONSET POLYCYSTIC KIDNEY DISEASE REVEALS THE FUNCTIONAL SIGNIFICANCE OF HYPOMORPHIC VARIANTS M Durkie, J Chong, A Ong Kidney International Reports 4 (7), S148, 2019 | | 2019 |
| VERY EARLY-ONSET AUTOSOMAL DOMINANT POLYCYSTIC KIDNEY DISEASE DUE TO BI-ALLELIC MUTATIONS IN PKD1 AND PKD2 J Chong, M Durkie, A Dalton, A Ong NEPHROLOGY DIALYSIS TRANSPLANTATION 32, 94-94, 2017 | | 2017 |
| Inheritance of a copy number variant in the imprinted PHLDA2 gene promoter significantly increases fetal birth weight M Ishida, D Monk, A Duncan, S Abu-Amero, J Chong, S Ring, M Pembrey, ... GENETICS RESEARCH 93 (6), 435-435, 2011 | | 2011 |
| Reducing the risk of serious infections for children with diabetes mellitus: an audit of immunisation practice J Chong, S Bailey, A Kent, J Buck Endocrine Abstracts 27, 2011 | | 2011 |
Albert C OngUniversity of SheffieldVerified email at sheffield.ac.uk
