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Leukemia & Lymphoma|December 16, 2006
Haplotypic variation in MRE11, RAD50 and NBS1 and risk of non-Hodgkin's lymphomaSara Rollinson, Heather Kesby, Gareth J MorganCurrent Opinion in Neurology|November 10, 2007
The genetics of frontotemporal lobar degenerationStephen Sikkink, Sara Rollinson, Stuart M Pickering-BrownScientific Reports|March 22, 2022
C9orf72 dipeptides disrupt the nucleocytoplasmic transport machinery and cause TDP-43 mislocalisation to the cytoplasmSarah Ryan, Sara Rollinson, Eleanor Hobbs, et al.Neurobiology of Aging|November 3, 2019
CRISPR/Cas9 does not facilitate stable expression of long C9orf72 dipeptides in miceSarah Ryan, Eleanor Hobbs, Sara Rollinson, et al.The European Journal of Neuroscience|June 17, 2016
Identification of biological pathways regulated by PGRN and GRN peptide treatments using transcriptome analysisSara Rollinson, Kate Young, Janis Bennion-Callister, et al.Human Molecular Genetics|November 1, 2016
Modelling C9orf72 dipeptide repeat proteins of a physiologically relevant sizeJanis Bennion Callister, Sarah Ryan, Joan Sim, et al.Statistics in Medicine|December 8, 2004
Application of DNA pooling to large studies of diseaseGraham R Law, Sara Rollinson, Richard Feltbower, et al.British Journal of Haematology|May 25, 2002
Allele and haplotype frequency at human leucocyte antigen class I/II and immunomodulatory cytokine loci in patients with myelodysplasia and acute myeloid leukaemia: in search of an autoimmune aetiologyDuncan Gowans, Alan O'Sullivan, Sara Rollinson, et al.Neuroscience Letters|April 17, 2007
TDP-43 gene analysis in frontotemporal lobar degenerationSara Rollinson, Julie S Snowden, David Neary, et al.Neurobiology of Aging|September 3, 2014
UBQLN2 variant of unknown significance in frontotemporal lobar degenerationFrancis Ugwu, Sara Rollinson, Jenny Harris, et al.Pageof 7