Dr Philip Molyneaux is a Clinical Senior Lecturer in Interstitial lung disease and an Honorary Consultant at the Royal Brompton Hospital.
Philip qualified from Guy's, King's and St Thomas' School of Medicine in 2004, where he completed an intercalated BSc. in Molecular Genetics. He undertook his SHO training at Guy’s and St Thomas’ and upon completion of the MRCP attained an NIHR Academic Clinical Fellow position in Respiratory medicine at Imperial College. He spent the next two years training at St Mary’s Hospital and working with Professors Cookson, Moffatt and Johnston studying the respiratory microbiome in COPD.
An Asmarley training fellowship allowed him to undertake a PhD examining the host response to the respiratory microbiome in Idiopathic Pulmonary Fibrosis as part of the Prospective Study of Fibrosis In the Lung Endpoints (PROFILE) study with Professors Maher, Cookson and Moffatt.
Having completed his clinical training in Respiratory and Critical Care Medicine he returned to Imperial joining the Fibrosis Research Group as a Senior Clinical Lecturer. He also holds a position as Consultant in Interstitial Lung Disease at the Royal Brompton Hospital where he has a special interest in Familial Pulmonary Fibrosis.
et al., 2019, Right ventricle to left ventricle ratio at CTPA predicts mortality in interstitial lung disease, Chest, ISSN:0012-3692
et al., Biomarkers of collagen synthesis predict progression in the PROFILE idiopathic pulmonary fibrosis cohort., Respiratory Research, Vol:20, ISSN:1465-9921, Pages:1-10
Invernizzi R, Molyneaux PL, 2019, The contribution of infection and the respiratory microbiome in acute exacerbations of idiopathic pulmonary fibrosis, European Respiratory Review, Vol:28, ISSN:0905-9180
et al., 2019, Variable utility of mosaic attenuation to distinguish fibrotic hypersensitivity pneumonitis from idiopathic pulmonary fibrosis, European Respiratory Journal, ISSN:0903-1936
et al., 2019, The transferrin receptor CD71 delineates functionally distinct airway macrophage subsets during idiopathic pulmonary fibrosis, American Journal of Respiratory and Critical Care Medicine, ISSN:1073-449X