Dr Lisa Strain
Associate Lecturer
- Francis NJ, McNicholas B, Awan A, Waldron M, Reddan D, Sadlier D, Kavanagh D, Strain L, Marchbank KJ, Harris CL, Goodship THJ. Anovel hybrid CFH/CFHR3 gene generated by a microhomology-mediated deletion in familial atypical hemolytic uremic syndrome.
Blood 2012, 119(2), 591-601.
- Ermini L, Goodship THJ, Strain L, Weale ME, Sacks SH, Cordell HJ, Fremeaux-Bacchi V, Sheerin NS. Common genetic variants in complement genes other than CFH, CD46 and the CFHRs are not associated with aHUS.
Molecular Immunology 2012, 49(4), 640-648.
- Kavanagh D, Pappworth IY, Anderson H, Hayes CM, Moore I, Hunze EM, Bennaceur K, Roversi P, Lea S, Strain L, Ward R, Plant N, Nailescu C, Goodship TH, Marchbank KJ. Factor I Autoantibodies in Patients with Atypical Hemolytic Uremic Syndrome: Disease-Associated or an Epiphenomenon?.
Clinical Journal of the American Society of Nephrology 2012, (epub ahead of print).
- Ermini L, Goodship T, Strain L, Weale M, Sacks S, Cordell H, Fremeaux-Bacchi V, Sheerin N. Genetic variants in CFH and CD46 are the major susceptibility factors for aHUS-An association study of multiple complement genes.
In: Molecular Immunology: 13th European Meeting on Complement in Human Disease. 2011, Leiden, Netherlands: Pergamon.
- Wilson C, Torpey N, Jaques B, Strain L, Talbot D, Manas D, Goodship T. Successful Simultaneous Liver-Kidney Transplant in an Adult With Atypical Hemolytic Uremic Syndrome Associated With a Mutation in Complement Factor H.
American Journal of Kidney Diseases 2011, 58(1), 109-112.
- Tennant S, Strain L, Curtis A. Incidence of deletion and duplication mutations in HNPCC patients in the NE of England.
In: Journal of Medical Genetics: British Human Genetics Conference. 2004, York, UK: BMJ Group.
