Follow
Dr Andrew Mumford
Dr Andrew Mumford
Professor of Haematology, University of Bristol
Verified email at bristol.ac.uk
Title
Cited by
Cited by
Year
Colchicine in patients admitted to hospital with COVID-19 (RECOVERY): a randomised, controlled, open-label, platform trial
RC Group
The Lancet Respiratory Medicine 9 (12), 1419-1426, 2021
1403*2021
The Human Phenotype Ontology project: linking molecular biology and disease through phenotype data
S Köhler, SC Doelken, CJ Mungall, S Bauer, HV Firth, I Bailleul-Forestier, ...
Nucleic acids research 42 (D1), D966-D974, 2014
9112014
The rare coagulation disorders–review with guidelines for management from the United Kingdom Haemophilia Centre Doctors' Organisation
PHB Bolton‐Maggs, DJ Perry, EA Chalmers, LA Parapia, JT Wilde, ...
Haemophilia 10 (5), 593-628, 2004
6462004
Guidelines for the laboratory investigation of heritable disorders of platelet function
P Harrison, I Mackie, A Mumford, C Briggs, R Liesner, M Winter, S Machin, ...
British journal of haematology 155 (1), 30-44, 2011
4742011
Guidelines for the use of platelet transfusions
L Estcourt, J Birchall, S Allard, S Bassey, P Hersey, J Kerr, A Mumford, ...
British journal of haematology 176 (3), 2016
4682016
A review of inherited platelet disorders with guidelines for their management on behalf of the UKHCDO
PHB Bolton‐Maggs, EA Chalmers, PW Collins, P Harrison, S Kitchen, ...
British journal of haematology 135 (5), 603-633, 2006
4512006
Whole-genome sequencing of patients with rare diseases in a national health system
E Turro, WJ Astle, K Megy, S Gräf, D Greene, O Shamardina, HL Allen, ...
Nature 583 (7814), 96-102, 2020
3922020
Tocilizumab in patients admitted to hospital with COVID-19 (RECOVERY): a randomised, controlled, open-label, platform trial
O Abani, A Abbas, F Abbas, M Abbas, S Abbasi, H Abbass, A Abbott, ...
The Lancet 397 (10285), 1637-1645, 2021
3772021
100,000 genomes pilot on rare-disease diagnosis in health care—preliminary report
100,000 Genomes Project Pilot Investigators
New England Journal of Medicine 385 (20), 1868-1880, 2021
3622021
Guideline for the diagnosis and management of the rare coagulation disorders: a United Kingdom Haemophilia Centre Doctors' Organization guideline on behalf of the British …
AD Mumford, S Ackroyd, R Alikhan, L Bowles, P Chowdary, J Grainger, ...
British journal of haematology 167 (3), 304-326, 2014
3512014
Transcriptional diversity during lineage commitment of human blood progenitors
L Chen, M Kostadima, JHA Martens, G Canu, SP Garcia, E Turro, ...
Science 345 (6204), 1251033, 2014
3242014
Azithromycin in patients admitted to hospital with COVID-19 (RECOVERY): a randomised, controlled, open-label, platform trial
E Abaleke, M Abbas, S Abbasi, A Abbott, A Abdelaziz, S Abdelbadiee, ...
The Lancet 397 (10274), 605-612, 2021
3162021
Guideline on the management of bleeding in patients on antithrombotic agents.
M Makris, JJ Van Veen, CR Tait, AD Mumford, M Laffan
British journal of haematology 160 (1), 35-46, 2012
2762012
Elevation of FVIII: C in venous thromboembolism is persistent and independent of the acute phase response
J O’Donnell, AD Mumford, RA Manning, M Laffan
Thrombosis and haemostasis 83 (01), 10-13, 2000
2732000
Bleeding symptoms and coagulation abnormalities in 337 patients with AL‐amyloidosis
AD Mumford, J O'donnell, JD Gillmore, RA Manning, PN Hawkins, ...
British journal of haematology 110 (2), 454-460, 2000
2612000
Purpura fulminans: recognition, diagnosis and management
E Chalmers, P Cooper, K Forman, C Grimley, K Khair, A Minford, ...
Archives of Disease in Childhood 96 (11), 1066-1071, 2011
2402011
Factor VII deficiency and the FVII mutation database
JH McVey, E Boswell, AD Mumford, G Kemball‐Cook, EGD Tuddenham
Human mutation 17 (1), 3-17, 2001
2312001
Diagnosis of inherited platelet function disorders: guidance from the SSC of the ISTH
P Gresele, P Harrison, C Gachet, C Hayward, D Kenny, D Mezzano, ...
Journal of Thrombosis and Haemostasis 13 (2), 314-322, 2015
2232015
Baricitinib in patients admitted to hospital with COVID-19 (RECOVERY): a randomised, controlled, open-label, platform trial and updated meta-analysis
O Abani, A Abbas, F Abbas, J Abbas, K Abbas, M Abbas, S Abbasi, ...
The Lancet 400 (10349), 359-368, 2022
2132022
A high-throughput sequencing test for diagnosing inherited bleeding, thrombotic, and platelet disorders
I Simeoni, JC Stephens, F Hu, SVV Deevi, K Megy, TK Bariana, ...
Blood, The Journal of the American Society of Hematology 127 (23), 2791-2803, 2016
1892016
The system can't perform the operation now. Try again later.
Articles 1–20