Imperial College London

DrCarolynMillar

Faculty of MedicineFaculty of Medicine Centre

Honorary Clinical Senior Lecturer
 
 
 
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Contact

 

+44 (0)20 3313 2153c.millar

 
 
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Location

 

Commonwealth BuildingHammersmith Campus

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Summary

 

Summary

Carolyn Millar is a Senior Lecturer in the department of haematology and a Consultant Haematologist specialising in haemostasis and thrombosis. She is the clinical lead in haemophilia at the Hammersmith hospital. Dr Millar completed undergraduate medical training at the University of Newcastle-upon-Tyne, graduating with honours. She undertook postgraduate medical training at University College London, the National Hospital for Neurology & Neurosurgery, Queen Square, and St George’s Hospital, Tooting. Dr Millar’s haematology training was largely undertaken at the Hammersmith, Great Ormond Street and Royal Free hospitals, where her doctoral thesis investigated the role of glycans in von Willebrand factor clearance and their relation to von Willebrand disease. Dr Millar has continued to study the configuration, function and kinetics of von Willebrand factor since being awarded a HEFCE clinical senior lectureship to start her position at Imperial College in December 2008 . As well as von Willebrand disease, her clinical interests include obstetric haemostasis, rare bleeding disorders, haemophilia and anticoagulant therapy. Dr Millar has led on the UK surveillance of vCJD in patients with bleeding disorders since 2002.

Dr Millar supervises postdoctoral research fellows and MSc., BSc., MD and PhD students and holds a variety of leadership and senior teaching positions at Imperial College. Between 2012 and 2019 she was course co-director of the intercalated BSc programme in haematology and is now head of assessment. Dr Millar is haematology lead for Phase I of the new curriculum and personal tutor to MBBS students in years 3-6.. Dr Millar obtained a diploma in undergraduate teaching in 2012 and in 2013 was awarded an Imperial College Teaching Excellence award

Publications

Journals

Bury L, Megy K, Stephens JC, et al., 2019, Next-generation sequencing for the diagnosis of MYH9-RD: Predicting pathogenic variants, Human Mutation, ISSN:1059-7794

Shovlin C, Millar C, Droege F, et al., 2019, Safety of direct oral anticoagulants in patients with hereditary hemorrhagic telangiectasia, Orphanet Journal of Rare Diseases, Vol:14, ISSN:1750-1172

van Oorschot R, Marneth AE, Bergevoet SM, et al., 2019, Inherited missense variants that affect GFI1B function do not necessarily cause bleeding diatheses, Haematologica, Vol:104, ISSN:0390-6078, Pages:E260-E264

Wei W, Tuna S, Keogh MJ, et al., 2019, Germline selection shapes human mitochondrial DNA diversity, Science, Vol:364, ISSN:0036-8075

Ito Y, Carss KJ, Duarte ST, et al., 2018, De Novo truncating mutations in WASF1 cause intellectual disability with seizures, American Journal of Human Genetics, Vol:103, ISSN:0002-9297, Pages:144-153

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