Publications by Dr Edwin Wong - ePrints

Browsing publications by Dr Edwin Wong.

Newcastle Authors	Title	Year
Dr Sally Johnson Professor David Kavanagh Professor John Sayer Dr Edwin Wong Megan Bates et al.	Description and Cross-Sectional Analyses of 25,880 Adults and Children in the UK National Registry of Rare Kidney Diseases Cohort	2024
Dr Sally Johnson Dr Edwin Wong	Developing Therapies for C3 Glomerulopathy: Report of the Kidney Health Initiative C3 Glomerulopathy Trial Endpoints Work Group	2024
Dr Sally Johnson Professor David Kavanagh Professor John Sayer Dr Edwin Wong Dr Vicky Brocklebank et al.	Effects of rare kidney diseases on kidney failure: a longitudinal analysis of the UK National Registry of Rare Kidney Diseases (RaDaR) cohort	2024
Dr Edwin Wong Lee-Ann Naidoo Sarah Winn Dr Patrick Walsh Dr Vicky Brocklebank et al.	The Annual Report of the National Renal Complement Therapeutics Centre 2022/23	2024
Emily Glover Dr Kate Smith-Jackson Dr Vicky Brocklebank Dr Valerie Wilson Dr Patrick Walsh et al.	Assessing the Impact of Prophylactic Eculizumab on Renal Graft Survival in Atypical Hemolytic Uremic Syndrome	2023
Dr Vicky Brocklebank Dr Patrick Walsh Dr Kate Smith-Jackson Dr Thomas Hallam Professor Kevin Marchbank et al.	Atypical haemolytic uraemic syndrome in the era of terminal complement inhibition- An observational cohort study	2023
Dr Edwin Wong Professor David Kavanagh	Efficacy and Safety of Iptacopan in Patients With C3 Glomerulopathy	2023
Dr Ruyue Sun Dr Long Xie Rebecca Russell Dr Edwin Wong Professor Neil Sheerin et al.	Pre-eclampsia is associated with complement pathway activation in the maternal and fetal circulation, and placental tissue	2023
Dr Edwin Wong Sarah Winn Dr Michal Malina Dr Sally Johnson Professor Neil Sheerin et al.	The Annual Report of the National Renal Complement Therapeutics Centre 2021/22	2023
Dr Thomas Hallam Tom Cox Dr Kate Smith-Jackson Dr Vicky Brocklebank April Baral et al.	A novel method for real-time analysis of the complement C3b:FH:FI complex reveals dominant negative CFI variants in Age-related Macular Degeneration	2022
Emily Hunter Professor Anthony De Soyza Dr Rachel Agbeko Dr Ken Baker Dr Quentin Campbell Hewson et al.	Casirivimab and imdevimab in patients admitted to hospital with COVID-19 (RECOVERY): a randomised, controlled, open-label, platform trial	2022
Dr Alison Brown Dr Katrina Wood Dr Edwin Wong	Paraneoplastic cast nephropathy associated with malignant prolactinoma: A case report and literature review	2022
Sarah Dunn Abishek Umashankar Andrew Bryant Dr Sonya Carnell Dr Thomas Chadwick et al.	Saftey and impact of eculizumab withdrawal in patients with atypical haemolytic uraemic syndrome: protocol for a multicentre, open-label, prospective, single-arm study	2022
Dr Edwin Wong Thomas Hallam Dr Vicky Brocklebank Dr Patrick Walsh Dr Kate Smith-Jackson et al.	Functional characterisation of rare genetic variants in the N-terminus of complement factor H in aHUS, C3G and AMD	2021
Dr Edwin Wong Sarah Winn Dr Michal Malina Dr Sally Johnson Professor Neil Sheerin et al.	The Annual Report of the National Renal Complement Therapeutics Centre 2020/21	2021
Dr Edwin Wong Professor Claire Harris Professor Kevin Marchbank Dr Sally Johnson	Large scale whole-genome sequencing reveals the genetic architecture of primary membranoproliferative glomerulonephritis and C3 glomerulopathy	2020
Dr Vicky Brocklebank Dr Kate Smith-Jackson Dr Patrick Walsh Professor Kevin Marchbank Professor Claire Harris et al.	Long-term outcomes and response to treatment in DGKE nephropathy	2020
Dr Edwin Wong Lisa Batchelor Dr Michal Malina Dr Sally Johnson Professor Neil Sheerin et al.	The Annual Report of the National Renal Complement Therapeutics Centre 2019/20	2020
Dr Edwin Wong Jo Stout Jalibani Ndebele Angela Watt Lisa Batchelor et al.	The Annual Report of the National Renal Complement Therapeutics Centre 2018/19	2019
Dr Edwin Wong Professor David Kavanagh	Diseases of complement dysregulation—an overview	2018
Professor Patrick Chinnery Ingrid Emmerson Professor Rita Horvath Dr Sally Johnson Deborah Shipley et al.	Telomerecat: A ploidy-agnostic method for estimating telomere length from whole genome sequencing data	2018
Dr Edwin Wong Jo Stout Jalibani Ndebele Angela Watt Dr Michal Malina et al.	The Annual Report of the National Renal Complement Therapeutics Centre 2017/18	2018
Dr Edwin Wong Dr Yi Yang Professor Kevin Marchbank Professor David Kavanagh	Disease-linked mutations in factor H reveal pivotal role of cofactor activity in self surface-selective regulation of complement activation	2017
Dr Vicky Brocklebank Dr Sally Johnson Dr Patrick Walsh Dr Edwin Wong Dr Larissa Kerecuk et al.	Factor H autoantibody is associated with atypical hemolytic uremic syndrome in children in the United Kingdom and Ireland	2017
Professor David Kavanagh Dr Edwin Wong Dr Vicky Brocklebank	Hemolytic Uremic Syndrome in Pregnancy and Post-Partum	2017
Dr Edwin Wong Dr Sally Johnson Professor Neil Sheerin Professor David Kavanagh	The Annual Report of the National Renal Complement Therapeutics Centre 2016/2017	2017
Rachel Challis Dr Edwin Wong Dr Vicky Brocklebank Dr Valerie Wilson Professor Kevin Marchbank et al.	Thrombotic Microangiopathy in Inverted Formin 2-Mediated Renal Disease	2017
Rachel Challis Dr Edwin Wong Dr Holly Anderson Dr Valerie Wilson Dr Vicky Brocklebank et al.	A De Novo Deletion in the Regulators of Complement Activation Cluster Producing a Hybrid Complement Factor H/Complement Factor H–Related 3 Gene in Atypical Hemolytic Uremic Syndrome	2016
Dr Vicky Brocklebank Dr Edwin Wong Professor Kevin Marchbank Professor Tim Goodship Professor David Kavanagh et al.	The role of ADAMTS-13 activity and complement mutational analysis in differentiating acute thrombotic microangiopathies	2016
Dr Isabel Pappworth Dr Edwin Wong Professor Neil Sheerin Professor Kevin Marchbank	An extended mini-complement factor H molecule ameliorates experimental C3 glomerulopathy	2015
Dr Edwin Wong Professor David Kavanagh	Anticomplement C5 therapy with eculizumab for the treatment of paroxysmal nocturnal hemoglobinuria and atypical hemolytic uremic syndrome	2015
Dr Edwin Wong Dr Vicky Brocklebank Professor Tim Goodship Professor David Kavanagh Dr Anna Richards et al.	Characterisation of a C3 Mutation with Increased Resistance to Complement Regulation in an Individual with Recurrent C3GN in a Renel Transplant	2015
Dr Edwin Wong Dr Jeremy Palmer Professor Neil Sheerin Dr Isabel Pappworth	FH1-5^(18-20) ameliorates experimental C3 glomerulopathy; generation and testing of a murine version for further pre-clinical experiments	2015
Dr Edwin Wong Rachel Challis Professor Neil Sheerin Dr Sally Johnson Professor David Kavanagh et al.	Patient stratification and therapy in atypical haemolytic uraemic syndrome (aHUS)	2015
Dr Edwin Wong Dr Isabel Pappworth Professor Claire Harris Professor Tim Goodship Dr Sally Johnson et al.	The national study of membranoproliferative glomerulonephrtis and C3 glomerulopathy - characterisation of the paediatric cohort	2015
Dr Vicky Brocklebank Dr Edwin Wong Professor Tim Goodship Professor David Kavanagh	Atypical haemolytic uraemic syndrome associated with a CD46 mutation triggered by Shigella flexneri	2014
Dr Edwin Wong Dr Holly Anderson Rachel Challis Dr Lisa Turnbull Gladys - et al.	Characterization of a Factor H Mutation That Perturbs the Alternative Pathway of Complement in a Family with Membranoproliferative GN	2014
Dr Sally Johnson Dr Edwin Wong	Making sense of the spectrum of glomerular disease associated with complement dysregulation	2014
Dr Edwin Wong Professor John Sayer	Sarcoidosis presenting with hypercalcaemia following withdrawal of long-term immunosuppression in renal transplantation	2014
Dr Edwin Wong Professor David Kavanagh	Whole-exome sequencing identifies rare, functional CFH variants in families with macular degeneration	2014
Rachel Challis Dr Holly Anderson Dr Edwin Wong Dr Lisa Turnbull Professor Kevin Marchbank et al.	Atypical haemolytic uraemic syndrome associated with a novel hybrid CFH/CFHR3 gene	2013
Dr Edwin Wong Professor Tim Goodship Professor David Kavanagh	Complement therapy in atypical haemolytic uraemic syndrome (aHUS)	2013
Dr Edwin Wong Mark Brady Professor Neil Sheerin	Severe intestinal oedema due to nephrotic syndrome	2013
Dr Edwin Wong Dr Holly Anderson Rachel Challis Professor Kevin Marchbank Professor David Kavanagh et al.	Familial membranoproliferative glomerulonephritis type I associated with a functionally significant mutation in complement factor H	2012
Dr Edwin Wong	Successful management of bilateral emphysematous pyelonephritis in end-stage polycystic kidneys: bilateral native nephrectomies and preservation of functioning renal transplant	2011