David C Rees

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Baba (PDB) Inusapaediatric haematologyVerified email at gstt.nhs.uk
Stephan MenzelSenior Lecturer, King's College LondonVerified email at kcl.ac.uk
Fenella Jane KirkhamProfessor of Paediatric Neurology, UCL Institute of Child HealthVerified email at ucl.ac.uk
TN WilliamsImperial College, London & KEMRI-Wellcome Trust Research Programme, KenyaVerified email at imperial.ac.uk
Dr Frédéric B. PielAssocate Professor in Spatial Epidemiology, School of Public Health, Imperial CollegeVerified email at imperial.ac.uk
Mariane de MontalembertProfesseur de Pédiatrie, Université de ParisVerified email at aphp.fr
Professor Nancy OlivieriUniversity of TorontoVerified email at hemoglobal.org
Matthew M HeeneyBoston Children’s Hospital / Harvard Medical SchoolVerified email at childrens.harvard.edu
Kate GardnerHaematology consultant, Guy's and St Thomas' NHS Foundation TrustVerified email at nhs.net
Richard PateyKent and Medway Medical SchoolVerified email at kmms.ac.uk
Mark T. GladwinUniversity of PittsburghVerified email at upmc.edu
achille iolasconAffiliazione Dept of Molecular Medicine and Medical BiotechnologyVerified email at unina.it
Martin H. SteinbergProfessor of Medicine, Boston University School of MedicineVerified email at bu.edu
Jack BartramGreat Ormond Street Hospital for Children and UCL Institute of Child HealthVerified email at ucl.ac.uk
Professor jacques RochetteUniversité de Picardie Jules VerneVerified email at usa.net
John DuleyThe University of QueenslandVerified email at pharmacy.uq.edu.au
Laurent ExcoffierInstitute of Ecology and Evolution, University of BerneVerified email at iee.unibe.ch
Søren MoestrupUniversity of AarhusVerified email at health.sdu.dk
David J RobertsUniversity of Oxford and NHS Blood and TransplantVerified email at ndcls.ox.ac.uk

David C Rees

King's College Hospital and King's College London

Verified email at kcl.ac.uk

hematology sickle cell disease


Title Sort by citations Sort by year Sort by title	Cited by Cited by	Year
Sickle-cell disease DC Rees, TN Williams, MT Gladwin The Lancet 376 (9757), 2018-2031, 2010	2675	2010
World distribution of factor V Leiden DC Rees, M Cox, JB Clegg Lancet (London, England) 346 (8983), 1133-1134, 1995	1708	1995
Sickle cell disease FB Piel, MH Steinberg, DC Rees New England Journal of Medicine 376 (16), 1561-1573, 2017	1325	2017
Geographic distribution of the 20210 G to A prothrombin variant FR Rosendaal, CJM Doggen, A Zivelin, VR Arruda, M Aiach, DS Siscovick, ... Thrombosis and haemostasis 79 (04), 706-708, 1998	1000	1998
Global distribution of the CCR5 gene 32-basepair deletion JJ Martinson, NH Chapman, DC Rees, YT Liu, JB Clegg Nature genetics 16 (1), 100-103, 1997	750	1997
Combined effect of factor V Leiden and prothrombin 20210A on the risk of venous thromboembolism J Emmerich, FR Rosendaal, M Cattaneo, M Margaglione, V De Stefano, ... Thrombosis and haemostasis 86 (09), 809-816, 2001	537	2001
Phase 3 trial of RNAi therapeutic givosiran for acute intermittent porphyria M Balwani, E Sardh, P Ventura, PA Peiró, DC Rees, U Stölzel, DM Bissell, ... New England journal of medicine 382 (24), 2289-2301, 2020	437	2020
FLT3 internal tandem duplication mutations in adult acute myeloid leukaemia define a high‐risk group FM Abu‐Duhier, AC Goodeve, GA Wilson, MA Gari, IR Peake, DC Rees, ... British journal of haematology 111 (1), 190-195, 2000	424	2000
Worldwide distribution of a common methylenetetrahydrofolate reductase mutation JA Schneider, DC Rees, YT Liu, JB Clegg The American Journal of Human Genetics 62 (5), 1258-1260, 1998	417	1998
Significant haemoglobinopathies: guidelines for screening and diagnosis. K Ryan, BJ Bain, D Worthington, J James, D Plews, A Mason, D Roper, ... British journal of haematology 149 (1), 2010	377	2010
Guidelines for the management of the acute painful crisis in sickle cell disease DC Rees, AD Olujohungbe, NE Parker, AD Stephens, P Telfer, J Wright, ... British journal of haematology 120 (5), 744-752, 2003	329	2003
Silica, silicosis and tuberculosis D Rees, J Murray Occupational Health Southern Africa 26 (5), 266-276, 2020	314	2020
Genetic basis of inosine triphosphate pyrophosphohydrolase deficiency S Sumi, AM Marinaki, M Arenas, L Fairbanks, M Shobowale-Bakre, ... Human genetics 111, 360-367, 2002	299	2002
Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis E Fotiou, S Martin-Almedina, MA Simpson, S Lin, K Gordon, G Brice, ... Nature communications 6 (1), 8085, 2015	294	2015
The spleen and sickle cell disease: the sick (led) spleen V Brousse, P Buffet, D Rees British journal of haematology 166 (2), 165-176, 2014	267	2014
Phase 1 trial of an RNA interference therapy for acute intermittent porphyria E Sardh, P Harper, M Balwani, P Stein, D Rees, DM Bissell, R Desnick, ... New England Journal of Medicine 380 (6), 549-558, 2019	247	2019
The Transfusion Alternatives Preoperatively in Sickle Cell Disease (TAPS) study: a randomised, controlled, multicentre clinical trial J Howard, M Malfroy, C Llewelyn, L Choo, R Hodge, T Johnson, S Purohit, ... The Lancet 381 (9870), 930-938, 2013	242	2013
The population genetics of factor V Leiden (Arg506Gln) DC Rees British journal of haematology 95 (4), 579-586, 1996	223	1996
Thermolabile methylenetetrahydrofolate reductase and factor V Leiden in the risk of deep-vein thrombosis LAJ Kluijtmans, M Den Heijer, PH Reitsma, SG Heil, HJ Blom, ... Thrombosis and haemostasis 79 (02), 254-258, 1998	207	1998
Risk of pregnancy-related venous thrombosis in carriers of severe inherited thrombophilia I Martinelli, C Legnani, P Bucciarelli, E Grandone, V De Stefano, ... Thrombosis and haemostasis 86 (09), 800-803, 2001	198	2001

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