J Wilde

Whole exome sequencing identifies genetic variants in inherited thrombocytopenia with secondary qualitative function defects

Benjamin C. Johnson, Gillian Lowe, Jane Wong Fütterer et al. · Haematologica · 2016 · 142 citations · Full text

Medicine, Genetics, Hematology +16

Prevalence of the factor V Leiden mutation in hepatic and portal vein thrombosis.

Abeer E. Mahmoud, Elwyn Elias, N Beauchamp et al. · Gut · 1997 · 141 citations · Full text

Medicine, Genetics, Hematology +17

Clinical spectrum, investigations and treatment of Budd-Chiari syndrome

Abeer E. Mahmoud, Abdul-Wahed Nasir Meshikhes, Simon Olliff et al. · QJM · 1996 · 114 citations · Full text

Medicine, Radiology, Surgery +9

Consensus protocol for the use of recombinant activated factor VII [eptacog alfa (activated); NovoSeven^®] in elective orthopaedic surgery in haemophilic patients with inhibitors

Paul Giangrande, J Wilde, B. Madan et al. · Haemophilia · 2009 · 81 citations · Full text

Medicine, Orthopaedic Surgery, Surgery +15

Evaluation of individual and ensemble probabilistic forecasts of COVID-19 mortality in the US

Estee Y. Cramer, Evan L Ray, Velma K. Lopez et al. · medRxiv · 2021 · 77 citations · Full text

Business, Health Sciences, Epidemiology +16