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P. Telfer · SciRah

Researcher profile · Semantic Scholar

P. Telfer

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P. Telfer — researcher profile on SciRah

h-index: 47
Works: 191
Citations: 8,881

Most-cited papers

Controlled Trial of Transfusions for Silent Cerebral Infarcts in Sickle Cell Anemia
M. Debaun, M. Gordon, Robert C. McKinstry, M. Noetzel +34 more
2014New England Journal of Medicine493 citations Open access
Semantic Scholar
A Phase 3 Randomized Trial of Voxelotor in Sickle Cell Disease.
E. Vichinsky, C. Hoppe, K. Ataga, R. Ware +18 more
2019New England Journal of Medicine476 citations Open access
Semantic Scholar
American Society of Hematology 2020 guidelines for sickle cell disease: prevention, diagnosis, and treatment of cerebrovascular disease in children and adults.
M. Debaun, L. Jordan, A. A. King, J. Schatz +8 more
2020Blood Advances382 citations Open access
Semantic Scholar
Newborn screening for sickle cell disease in Europe: recommendations from a Pan‐European Consensus Conference
S. Lobitz, P. Telfer, E. Cela, Bichr Allaf +41 more
2018British Journal of Haematology135 citations Open access
Semantic Scholar
Pain in Sickle Cell Disease
J. Howard, P. Telfer
2015113 citations
Semantic Scholar
A phase 1/2 ascending dose study and open-label extension study of voxelotor in patients with sickle cell disease.
J. Howard, C. Hemmaway, P. Telfer, D. Layton +12 more
2019Blood103 citations Open access
Semantic Scholar
White Matter Damage Relates to Oxygen Saturation in Children With Sickle Cell Anemia Without Silent Cerebral Infarcts
J. Kawadler, F. Kirkham, J. Clayden, Matthew J. Hollocks +8 more
2015Stroke55 citations Open access
Semantic Scholar
Associations between environmental factors and hospital admissions for sickle cell disease
F. Piel, S. Tewari, V. Brousse, A. Analitis +10 more
2016Haematologica53 citations Open access
Semantic Scholar
Evaluation of the efficacy and safety of deferiprone compared with deferasirox in paediatric patients with transfusion-dependent haemoglobinopathies (DEEP-2): a multicentre, randomised, open-label, non-inferiority, phase 3 trial.
A. Maggio, A. Kattamis, M. Felisi, Giorgio Reggiardo +22 more
2020The Lancet Haematology51 citations
Semantic Scholar
Real-time national survey of COVID-19 in hemoglobinopathy and rare inherited anemia patients
P. Telfer, J. de la Fuente, M. Sohal, Rachel S. Brown +28 more
2020Haematologica50 citations Open access
Semantic Scholar
Protecting vulnerable patients with inherited anaemias from unnecessary death during the COVID‐19 pandemic
N. Roy, P. Telfer, P. Eleftheriou, J. de la Fuente +13 more
2020British Journal of Haematology47 citations Open access
Semantic Scholar
Not being heard: barriers to high quality unplanned hospital care during young people’s transition to adult services – evidence from ‘this sickle cell life’ research
A. Renedo, Sam Miles, S. Chakravorty, A. Leigh +3 more
2019BMC Health Services Research47 citations Open access
Semantic Scholar
Lack of knowledge and misperceptions about thalassaemia among college students in Bangladesh: a cross-sectional baseline study
M. S. Hossain, M. Hasan, E. Raheem, Muhammad Sougatul Islam +4 more
2020Orphanet Journal of Rare Diseases46 citations Open access
Semantic Scholar
A comparison of chronic manual and automated red blood cell exchange transfusion in sickle cell disease patients
K. Kuo, R. Ward, B. Kaya, J. Howard +1 more
2015British Journal of Haematology45 citations Open access
Semantic Scholar
Co‐morbidities and mortality associated with transfusion‐dependent beta‐thalassaemia in patients in England: a 10‐year retrospective cohort analysis
M. Jobanputra, C. Paramore, Sandra G Laird, Michael McGahan +1 more
2020British Journal of Haematology40 citations
Semantic Scholar
Management of the acute painful crisis in sickle cell disease‐ a re‐evaluation of the use of opioids in adult patients
P. Telfer, N. Bahal, A. Lo, J. Challands
2014British Journal of Haematology40 citations
Semantic Scholar
The parental perspective of thalassaemia in Bangladesh: lack of knowledge, regret, and barriers
M. S. Hossain, M. Mahbub Hasan, M. Petrou, P. Telfer +1 more
2021Orphanet Journal of Rare Diseases34 citations Open access
Semantic Scholar
13‐valent pneumococcal conjugate vaccine (PCV13) is immunogenic and safe in children 6‐17 years of age with sickle cell disease previously vaccinated with 23‐valent pneumococcal polysaccharide vaccine (PPSV23): Results of a phase 3 study
M. de Montalembert, M. Abboud, A. Fiquet, A. Inati +17 more
2015Pediatric Blood & Cancer34 citations
Semantic Scholar
GBT440, a Potent Anti-Sickling Hemoglobin Modifier Reduces Hemolysis, Improves Anemia and Nearly Eliminates Sickle Cells in Peripheral Blood of Patients with Sickle Cell Disease
J. Lehrer-Graiwer, J. Howard, C. Hemmaway, M. Awogbade +9 more
201530 citations
Semantic Scholar
Direct correction of haemoglobin E β-thalassaemia using base editors
M. Badat, A. Ejaz, P. Hua, S. Rice +14 more
2023Nature Communications26 citations Open access
Semantic Scholar
Routine management, healthcare resource use and patient and carer‐reported outcomes of patients with transfusion‐dependent β‐thalassaemia in the United Kingdom: A mixed methods observational study
F. Shah, P. Telfer, M. Velangi, S. Pancham +9 more
2019eJHaem25 citations Open access
Semantic Scholar
The role of haematopoietic stem cell transplantation for sickle cell disease in the era of targeted disease-modifying therapies and gene editing.
J. de la Fuente, E. Gluckman, J. Makani, P. Telfer +24 more
2020The Lancet Haematology20 citations Open access
Semantic Scholar
Impact of voxelotor (GBT440) on unconjugated bilirubin and jaundice in sickle cell disease
P. Telfer, I. Agodoa, K. Fox, L. Burke +4 more
2018Hematology Reports20 citations Open access
Semantic Scholar
Optimizing the care model for an uncomplicated acute pain episode in sickle cell disease.
P. Telfer, B. Kaya
2017Hematology. American Society of Hematology. Education Program20 citations Open access
Semantic Scholar
Deferiprone versus deferoxamine in sickle cell disease: results from a 5-year long-term Italian multi-center randomized clinical trial.
Giusi Calvaruso, A. Vitrano, R. Di Maggio, S. Ballas +7 more
2014Blood Cells, Molecules & Diseases20 citations
Semantic Scholar
Psychometric analysis of the adult sickle cell quality of life measurement information system (ACSQ-Me) in a UK population
O. Cooper, H. McBain, Sekayi Tangayi, P. Telfer +3 more
2019Health and Quality of Life Outcomes19 citations Open access
Semantic Scholar
Combination‐therapy with concurrent deferoxamine and deferiprone is effective in treating resistant cardiac iron‐loading in aceruloplasminaemia
M. Badat, B. Kaya, P. Telfer
2015British Journal of Haematology19 citations Open access
Semantic Scholar
Sickle Cell Disease in Clinical Practice
J. Howard, P. Telfer
201519 citations
Semantic Scholar
Serial prophylactic exchange blood transfusion in pregnant women with sickle cell disease (TAPS-2): study protocol for a randomised controlled feasibility trial
L. Oakley, M. Awogbade, S. Brien, A. Briley +13 more
2020Trials18 citations Open access
Semantic Scholar
Overview of Sickle Cell Disease
J. Howard, P. Telfer
201518 citations
Semantic Scholar
Precursors of Executive Function in Infants With Sickle Cell Anemia
A. Hogan, P. Telfer, F. Kirkham, M. de Haan
2013Journal of Child Neurology18 citations Open access
Semantic Scholar
Serial echocardiographic left ventricular ejection fraction measurements: a tool for detecting thalassemia major patients at risk of cardiac death.
A. Maggio, A. Vitrano, G. Calvaruso, R. Barone +18 more
2013Blood Cells, Molecules & Diseases17 citations Open access
Semantic Scholar
Extracorporeal membrane oxygenation for the treatment of adult sickle cell acute chest syndrome
K. Parhar, B. Parizkova, N. Jones, K. Valchanov +6 more
2016Perfusion16 citations
Semantic Scholar
Long-Term Dosing in Sickle Cell Disease Subjects with GBT440, a Novel HbS Polymerization Inhibitor
J. Lehrer-Graiwer, J. Howard, C. Hemmaway, M. Awogbade +11 more
201616 citations
Semantic Scholar
Altered Neurophysiological Processing of Auditory Attention in Preschool Children With Sickle Cell Disease
M. Downes, F. Kirkham, P. Telfer, M. de Haan
2018Journal of Pediatric Psychology15 citations Open access
Semantic Scholar
Parent reported sleep problems in preschool children with sickle cell anemia and controls in East London
M. Downes, M. de Haan, F. Kirkham, P. Telfer
2017Pediatric Blood & Cancer15 citations Open access
Semantic Scholar
Higher Hemoglobin Levels Achieved with Voxelotor Are Associated with Lower Vaso-occlusive Crisis Incidence: 72-Week Analysis from the HOPE Study
E. Vichinsky, V. Gordeuk, P. Telfer, A. Inati +4 more
202014 citations Open access
Semantic Scholar
Executive performance on the preschool executive task assessment in children with sickle cell anemia and matched controls
M. Downes, F. Kirkham, Christine Berg, P. Telfer +1 more
2018Child Neuropsychology: A Journal of Normal and Abnormal Development in Childhood and Adolescence13 citations Open access
Semantic Scholar
Effect of HBB genotype on survival in a cohort of transfusion-dependent thalassemia patients in Cyprus
P. Kountouris, K. Michailidou, S. Christou, M. Hadjigavriel +4 more
2020Haematologica12 citations Open access
Semantic Scholar
Assessment of Executive Functions in Preschool Children With Sickle Cell Anemia
M. Downes, F. Kirkham, P. Telfer, M. de Haan
2018Journal of the International Neuropsychological Society12 citations Open access
Semantic Scholar
Deferasirox for iron chelation in multitransfused children with sickle cell disease; long‐term experience in the East London clinical haemoglobinopathy network
Eva Tsouana, B. Kaya, N. Gadong, C. Hemmaway +4 more
2015European Journal of Haematology12 citations
Semantic Scholar
Efficacy, safety, and pharmacokinetics of a new, ready-to-use, liquid hydroxyurea in children with sickle cell anemia
Angela E. Rankine-Mullings, S. Chakravorty, B. Inusa, P. Telfer +7 more
2023Blood Advances7 citations Open access
Semantic Scholar
8th European Federation for Primatology Meeting
Jack D. Lester, L. Vigilant, P. Gratton, Maureen S. McCarthy +89 more
2019Folia primatologica7 citations Open access
Semantic Scholar
Are the risks of treatment to cure a child with severe sickle cell disease too high?
M. de Montalembert, V. Brousse, S. Chakravorty, A. Pagliuca +4 more
2017British medical journal7 citations
Semantic Scholar
Haploidentical BMT with a Post-Infusion of Stem Cells Cyclophosphamide Approach Is Feasible and Leads to a High Rate of Donor Engraftment in Haemoglobinopathies Allowing Universal Application of Transplantation
J. Fuente, F. O’Boyle, Yvonne Harrington, A. Bradshaw +7 more
20157 citations
Semantic Scholar
Salvage of refractory post‐transfusion hyperhaemolysis by targeting hyperinflammation and macrophage activation with tocilizumab
Frederick Chen, C. Booth, F. Barroso, S. Bennett +3 more
2021Transfusion Medicine6 citations
Semantic Scholar
Development and validation of the Satisfaction with Treatment for Pain Questionnaire (STPQ) among patients with sickle cell disease
J. Elander, Deepali Bij, R. Kapadi, Malcolm B. Schofield +4 more
2019British Journal of Haematology6 citations Open access
Semantic Scholar
Incidence of Vaso-Occlusive Crisis Does Not Increase with Achieving Higher Hemoglobin Levels on Voxelotor Treatment or after Discontinuation: Analyses of the HOPE Study
E. Vichinsky, P. Telfer, A. Inati, M. Tonda +4 more
2019Blood6 citations Open access
Semantic Scholar
The Role of Family Functioning in the Development of Executive Functions in Preschool Children with Sickle Cell Anemia
M. Downes, M. de Haan, P. Telfer, F. Kirkham
2019Developmental Neuropsychology6 citations Open access
Semantic Scholar
Optimal Manual Exchange Transfusion Protocol for Sickle Cell Disease: A Retrospective Comparison of Two Comprehensive Care Centers in the United Kingdom and Canada
H. S. Mian, R. Ward, P. Telfer, B. Kaya +1 more
2015Hemoglobin6 citations
Semantic Scholar

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