Professor Julian Hopkin

Rector

Medicine

Telephone: (01792) 295149

Email: j.m.hopkin@swansea.ac.uk

Room: Academic Office - 225

Second Floor

Institute of Life Science 1

Singleton Campus

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Matsuda, A. (2005). Coding SNP in tenascin-C Fn-III-D domain associates with adult asthma. Human Molecular Genetics 14(19), 2779-2786.
https://cronfa.swan.ac.uk/Record/cronfa1396 doi:10.1093/hmg/ddi311
Moller, M. Gravenor, M. Roberts, S. Sun, D. Gao, P. & Hopkin, J. (2007). Genetic haplotypes of Th-2 immune signalling link allergy to enhanced protection to parasitic worms. Human Molecular Genetics 16(15), 1828-1836.
https://cronfa.swan.ac.uk/Record/cronfa1397 doi:10.1093/hmg/ddm131
Arima, K. Umeshita-Suyama, R. Sakata, Y. Akaiwa, M. Mao, X. Enomoto, T. Dake, Y. Shimazu, S. Yamashita, T. Sugawara, N. Brodeur, S. Geha, R. Puri, R. Sayegh, M. Adra, C. Hamasaki, N. Hopkin, J. Shirakawa, T. & Izuhara, K. (2002). Upregulation of IL-13 concentration in vivo by the IL13 variant associated with bronchial asthma. Journal of Allergy and Clinical Immunology 109(6), 980-987.
https://cronfa.swan.ac.uk/Record/cronfa1398 doi:10.1067/mai.2002.124656

PMGM16 Genomics of Common and Rare Inherited Disease

This module will provide an introduction to the clinical presentation and manifestations of rare inherited and common diseases, and considers the patient and family perspective with respect to the role and impact of genomics. It reviews traditional and current strategies and techniques used to identify genes responsible for both common multifactorial and rare inherited diseases.