Imperial College London


Faculty of MedicineSchool of Public Health

Honorary Research Associate



ernest.turro Website




Medical SchoolSt Mary's Campus





I moved to the Computational Biology Group at the University of Cambridge in August 2011 and have since joined the Platelet Biology Group. If you are interested in my work, including methodology for microarray and RNA-seq data analysis, please visit my current personal page.



Heremans J, Garcia-Perez JE, Turro E, et al., 2018, Abnormal differentiation of B cells and megakaryocytes in patients with Roifman syndrome, Journal of Allergy and Clinical Immunology, Vol:142, ISSN:0091-6749, Pages:630-646

Tuijnenburg P, Lango Allen H, Burns SO, et al., 2018, Loss-of-function nuclear factor κB subunit 1 (NFKB1) variants are the most common monogenic cause of common variable immunodeficiency in Europeans., J Allergy Clin Immunol

Westbury SK, Canault M, Greene D, et al., 2017, Expanded repertoire of RASGRP2 variants responsible for platelet dysfunction and severe bleeding, Blood, Vol:130, ISSN:0006-4971, Pages:1026-1030

Greene D, Richardson S, Turro E, 2017, A Fast Association Test for Identifying Pathogenic Variants Involved in Rare Diseases, American Journal of Human Genetics, Vol:101, ISSN:0002-9297, Pages:104-114

Petersen R, Lambourne JJ, Javierre BM, et al., 2017, Platelet function is modified by common sequence variation in megakaryocyte super enhancers, Nature Communications, Vol:8, ISSN:2041-1723

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