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Sara Stuart‐Smith

Complement activation in patients with isolated antiphospholipid antibodies or primary antiphospholipid syndrome
2012 · Paul Seed, Kiran Parmar, et al. · Thrombosis and Haemostasis · 111
Protecting vulnerable patients with inherited anaemias from unnecessary death during the COVID‐19 pandemic
2020 · Noémi B. A. Roy, Paul Telfer, et al. · British Journal of Haematology · 50
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g(HbF): a genetic model of fetal hemoglobin in sickle cell disease
2018 · Kate Gardner, Tony Fulford, et al. · Blood Advances · 43
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COVID-19 in patients with sickle cell disease - a case series from a UK Tertiary Hospital
2020 · Subarna Chakravorty, Giselle Padmore-Payne, et al. · Haematologica · 38
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Resistance to annexin A5 anticoagulant activity in women with histories for obstetric antiphospholipid syndrome
2011 · Beverley J. Hunt, Xiao-Xuan Wu, et al. · American Journal of Obstetrics and Gynecology · 33
Benign ethnic neutropenia: an analysis of prevalence, timing and identification accuracy in two large inner-city NHS hospitals
2021 · Ebenezer Oloyede, Olubanke Dzahini, et al. · BMC Psychiatry · 29
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The pleiotropic effects of α‐thalassemia on HbSS and HbSC sickle cell disease: Reduced erythrocyte cation co‐transport activity, serum erythropoietin, and transfusion burden, do not translate into increased survival
2022 · John N. Brewin, Amina Nardo‐Marino, et al. · American Journal of Hematology · 15
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Males with sickle cell disease have higher risks of cerebrovascular disease, increased inflammation, and a reduced response to hydroxyurea
2023 · Margherita Di Mauro, Sara El Hoss, et al. · American Journal of Hematology · 13
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The acute pain crisis in sickle cell disease: What can be done to improve outcomes?
2024 · Paul Telfer, Kofi A. Anie, et al. · Blood Reviews · 8
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Catheter associated thromboses in patients with sickle cell anaemia and dual lumen Vortex apheresis ports are common and can be clinically asymptomatic
2020 · John N. Brewin, Maeve P. Crowley, et al. · British Journal of Haematology · 6
ACKR1 /Duffy‐null genotype testing for clozapine: A guideline developed by the UK Centre of Excellence in Regulatory Science and Innovation in Pharmacogenomics (CERSI‐PGx)
2026 · Stephen Murtough, Oriella Stellakis, et al. · British Journal of Clinical Pharmacology · 4
ACKR1 genetic testing should be offered before starting clozapine treatment
2026 · Stephen Murtough, Daisy Mills, et al. · Nature Mental Health · 2
Iron deficiency is associated with reduced levels of inflammation and haemolysis in patients with HbSS and HbSC and reduced clinical admissions in those with HbSC
2025 · Simone Villaboni, Sara Stuart‐Smith, et al. · British Journal of Haematology · 2
Dapagliflozin for treatment of sickle cell nephropathy: A multi-centre experience
2025 · Naomi Cornish, Sneha Fernandes, et al. · Blood · 2
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An Overview of Solid Organ Transplantation in Patients With Sickle Cell Disease
2022 · Claire C. Sharpe, Abid Suddle, et al. · Transplantation · 2
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Parvovirus B19-associated fat embolism syndrome in sickle cell disease: A report of two cases
2026 · Anna Corby, Jessica Lubel, et al. · Clinical Medicine · 1
Does stroke or silent infarct affect quality of life in adults with sickle cell disease?: A multi-centre study
2025 · Amy Cooper, Sheila Azouji-Benjamin, et al. · Blood
Utilising Patient-Reported Experience Measures to Drive Healthcare Improvements: The Application of Validated PREM Survey Tools in a Haemoglobinopathy Network in South London
2024 · Subarna Chakravorty, Jesufikunayomi Ifeoluwa, et al. · Blood
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Natural History and Clinical Outcomes of Patients with Sickle Cell Disease: The Burden of Avascular Necrosis in a British Cohort
2023 · Arne de Kreuk, Sara Stuart-Smith, et al. · Blood
P1436: Ageing Impacts Hydroxycarbamide Dosing in Patients With Sickle Cell Disease
2023 · Isabelle Doss, Anietie Ekong A, et al. · HemaSphere
P1422: Prevalence and Risk Factors for Retinopathy in Sickle Cell Disease
2023 · Kate Gardner, Sara Stuart-Smith, et al. · HemaSphere
S269: Male Patients With Scd Have a Higher Risk of Cerebrovascular Disease, Increased Inflammatory Markers, and Poorer Response to Hydroxyurea
2023 · Margherita DI Mauro, Amina Nardo‐marino, et al. · HemaSphere
Similar Patient-Reported Quality of Life in the US and UK in Patients with Sickle Cell: A Comparative Grndad/Cousin Study
2022 · Sophie M. Lanzkron, Jane Alison Little, et al. · Blood
S110: Acute and Chronic Pain Management in Sickle Cell Disease: Outcomes of an English National Audit.
2022 · S Lugthart, S Kotsiopoulou, et al. · HemaSphere
A Genetic Predictive Model for HbF in Sickle Cell Disease
2016 · Kate Gardner, Tony Fulford, et al. · Blood
Works count: 27
Citation count: 359
H-index: 8
I10-index: 8
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