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.



Freson K, Turro E, 2017, High-throughput sequencing approaches for diagnosing hereditary bleeding and platelet disorders, Journal of Thrombosis and Haemostasis, Vol:15, ISSN:1538-7933, Pages:1262-1272

Greene D, Richardson S, Turro E, 2017, ontologyX: a suite of R packages for working with ontological data, Bioinformatics, Vol:33, ISSN:1367-4803, Pages:1104-1106

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

Koehler S, Vasilevsky NA, Engelstad M, et al., 2017, The Human Phenotype Ontology in 2017, Nucleic Acids Research, Vol:45, ISSN:0305-1048, Pages:D865-D876

Morren M-A, Jaeken J, Visser G, et al., 2017, PIGO deficiency: palmoplantar keratoderma and novel mutations, Orphanet Journal of Rare Diseases, Vol:12, ISSN:1750-1172

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