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Simon G. Williams

Wythenshawe Hospital

48H-index
250Paper Count
8.7KCitation Count
Published Papers 111
Publication Date
Overcoming Hyperkalaemia as a Barrier to Achieving Optimal RAASi Therapy and Cardiorenal Protection in Individuals with Cardiorenal Disease: A Podcast Discussion
err2026-03-02
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errAndrew H. Frankel; Kate Bramham; Barbara Byrne; Geraldine Chiu; Ruby Chumber; Sarah Jane Davies; Ahmet Fuat; Laura Gray; Darren Green; William Priestman; Mandie Welch; Simon G. Williams; Stephen Wheatcroft
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Expert Perspectives on Managing Iron Deficiency in People with CKD and/or HF
err2026-02-27
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errSunil Bhandari; John G. F. Cleland; Fozia Z. Ahmed; Fraser J. Graham; Matt Hall; Paul R. Kalra; Philip A. Kalra; Kate I. Stevens; David C. Wheeler; Simon G. Williams; Dora. I. A. Pereira; Marco Soscia; Harry Lewis; Imogen Taylor
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Rare DCM associated variants in pre-miR-208a disrupt miRNA maturation and function
err2025-05-06
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errReckman, Yolan J.; Haas, Jan; van der Made, Ingeborg; Williams, Simon G.; Diaz, Iria Gomez; Akhtar, Mohammed; Mogensen, Jens; Rasmussen, Torsten B.; Villard, Eric; Charron, Philippe; Keavney, Bernard D.; Monserrat, Lorenzo; Pinto, Yigal M.; Meder, Benjamin; Tijsen, Anke J.
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EXAMINING THE ROLE OF RARE WHOLE-GENOME SEQUENCING VARIANTS IN ARTERIAL STIFFNESS TO ADDRESS MISSING HERITABILITY: A GWAS STUDY OF 70, 279 PARTICIPANTS IN THE UK BIOBANK
err2025-05-01
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PREAI
errSaluja, Sushant; Anderson, Simon; Williams, Simon; Cordell, Heather; Lennon, Rachel; Alawami, Mohammed; Keavney, Bernard
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Bi-allelic variants in DAP3 result in reduced assembly of the mitoribosomal small subunit with altered apoptosis and a Perrault- syndrome-spectrum phenotype
err2025-01-01
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errSmith, Thomas B.; Kopajtich, Robert; Demain, Leigh A. M.; Rea, Alessandro; Thomas, Huw B.; Schiff, Manuel; Beetz, Christian; Joss, Shelagh; Conway, Gerard S.; Shukla, Anju; Yeole, Mayuri; Radhakrishnan, Periyasamy; Azzouz, Hatem; Ben Chehida, Amel; Elmaleh-Berges, Monique; Glasgow, Ruth I. C.; Thompson, Kyle; Olahova, Monika; He, Langping; Jenkinson, Emma M.; Jahic, Amir; Belyantseva, Inna A.; Barzik, Melanie; Urquhart, Jill E.; O'Sullivan, James; Williams, Simon G.; Bhaskar, Sanjeev S.; Carrera, Samantha; Blakes, Alexander J. M.; Banka, Siddharth; Yue, Wyatt W.; Ellingford, Jamie M.; Houlden, Henry; DDD Study, D. D. D.; Munro, Kevin J.; Friedman, Thomas B.; Taylor, Robert W.; Prokisch, Holger; Keefe, Raymond T.; Newman, William G.
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The impact of COVID-19 vaccination on patients with congenital heart disease in England: a case-control study
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IF4.4
err2024-10-11
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errHarrison, Catriona; Frain, Simon; Jalalinajafabadi, Farideh; Williams, Simon G.; Keavney, Bernard
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Administration of ferric derisomaltose for iron deficiency and heart failure during hospital admission or at the clinic - insights from the IRONMAN trial
err2024-07-30
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errLee, Matthew M. Y.; Petrie, Mark C.; Cleland, John G. F.; Donnelly, Patrick; Francis, Mark; Hannah, Andrew; Japp, Alan G.; Labinjoh, Catherine; Lang, Ninian N.; Manisty, Charlotte; Petrie, Colin J.; Piper, Susan E.; Williams, Simon G.; Ford, Ian; Kalra, Paul R.
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FLT4 causes developmental disorders of the cardiovascular and lymphovascular systems via pleiotropic molecular mechanisms
err2024-05-07
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errMonaghan, Richard M.; Naylor, Richard W.; Flatman, Daisy; Kasher, Paul R.; Williams, Simon G.; Keavney, Bernard D.
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Identification of heart failure hospitalization from NHS Digital data: comparison with expert adjudication
err2024-01-17
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errSoltani, Fardad; Bradley, Joshua; Bonandi, Antonio; Black, Nicholas; Farrant, John P.; Pailing, Adam; Orsborne, Christopher; Williams, Simon G.; Schelbert, Erik B.; Dodd, Susanna; Williams, Richard; Peek, Niels; Schmitt, Matthias; McDonagh, Theresa; Miller, Christopher A.
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Remote myocardial fibrosis predicts adverse outcome in patients with myocardial infarction on clinical cardiovascular magnetic resonance imaging
err2024-01-01
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errBlack, Nicholas; Bradley, Joshua; Schelbert, Erik B.; Bonnett, Laura J.; Lewis, Gavin A.; Lagan, Jakub; Orsborne, Christopher; Brown, Pamela F.; Soltani, Fardad; Frojdh, Fredrika; Ugander, Martin; Wong, Timothy C.; Fukui, Miho; Cavalcante, Joao L.; Naish, Josephine H.; Williams, Simon G.; McDonagh, Theresa; Schmitt, Matthias; Miller, Christopher A.
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Diagnostic Yield of Whole Genome Sequencing in Congenital Heart Disease: Data From the UK 100,000 Genomes Project
err2023-11-07
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PREAI
errBaross, Stephanie L.; Williams, Simon G.; Hentges, Kathryn E.; Keavney, Bernard D.
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Growth differentiation factor-15 in patients with or at risk of heart failure but before first hospitalisation
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IF4.4
err2023-08-11
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errBradley, Joshua; Schelbert, Erik B.; Bonnett, Laura J.; Lewis, Gavin A.; Lagan, Jakub; Orsborne, Christopher; Brown, Pamela Frances; Black, Nicholas; Naish, Josephine H.; Williams, Simon G.; McDonagh, Theresa; Schmitt, Matthias; Miller, Christopher A.
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Treatment Adherence in a Randomized Controlled Trial of Pirfenidone in HFpEF: Determinants and Impact on Efficacy
err2023-07-01
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errSoltani, Fardad; Lewis, Gavin A.; Rosala-Hallas, Anna; Dodd, Susanna; Schelbert, Erik B.; Williams, Simon G.; Cunnington, Colin; Mcdonagh, Theresa; Miller, Christopher A.
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Significantly increased risk of chronic obstructive pulmonary disease amongst adults with predominantly mild congenital heart disease
err2022-11-04
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errByrne, Dominic J. F.; Williams, Simon G.; Nakev, Apostol; Frain, Simon; Baross, Stephanie L.; Vestbo, Jorgen; Keavney, Bernard D.; Talavera, David
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Characteristics Associated With Growth Differentiation Factor 15 in Heart Failure With Preserved Ejection Fraction and the Impact of Pirfenidone
err2022-07-19
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errLewis, Gavin A.; Rosala-Hallas, Anna; Dodd, Susanna; Schelbert, Erik B.; Williams, Simon G.; Cunnington, Colin; McDonagh, Theresa; Miller, Christopher A.
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INCREASING THE DIAGNOSTIC YIELD OF THE 100,000 GENOMES PROJECT FOR PARTICIPANTS WITH CONGENITAL HEART DISEASE
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IF4.4
err2022-06-06
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errBaross, Stephanie; Williams, Simon; Hentges, Kathryn; Keavney, Bernard
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Predicting hospitalisation for heart failure and death in patients with, or at risk of, heart failure before first hospitalisation: a retrospective model development and external validation study
err2022-06-01
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errBradley, Joshua; Schelbert, Erik B.; Bonnett, Laura J.; Lewis, Gavin A.; Lagan, Jakub; Orsborne, Christopher; Brown, Pamela F.; Naish, Josephine H.; Williams, Simon G.; McDonagh, Theresa; Schmitt, Matthias; Miller, Christopher A.
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Bi-allelic mutation of CTNNB1 causes a severe form of syndromic microphthalmia, persistent foetal vasculature and vitreoretinal dysplasia
err2022-03-04
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errTaylor, Rachel L.; Soriano, Carla Sanjuro; Williams, Simon; Dzulova, Denisa; Ashworth, Jane; Hall, Georgina; Gale, Theodora; Lloyd, I. Christopher; Inglehearn, Chris F.; Toomes, Carmel; Douzgou, Sofia; Black, Graeme C.
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