Browsing publications by Dr Holly Anderson

Newcastle AuthorsTitleYear
Dr Edwin Wong
Dr Holly Anderson
Rachel Challis
Dr Lisa Turnbull
Daniel Ahlert
et al.
Characterization of a Factor H Mutation That Perturbs the Alternative Pathway of Complement in a Family with Membranoproliferative GN2014
Rachel Challis
Dr Holly Anderson
Dr Edwin Wong
Dr Lisa Turnbull
Dr Kevin Marchbank
et al.
Atypical haemolytic uraemic syndrome associated with a novel hybrid CFH/CFHR3 gene2013
Dr Holly Anderson
Dr David Kavanagh
Rare variants in CFI, C3 and C9 are associated with high risk of advancedage-related macular degeneration.2013
Dr Edwin Wong
Dr Holly Anderson
Rachel Challis
Dr Kevin Marchbank
Dr David Kavanagh
et al.
Familial membranoproliferative glomerulonephritis type I associated with a functionally significant mutation in complement factor H2012
Dr David Kavanagh
Dr Holly Anderson
Interpretation of genetic variants of uncertain significance in atypical hemolytic uremic syndrome2012
Dr Holly Anderson
Dr Josephine Wardle
Dr Simon Whitehall
Silencing Mediated by the Schizosaccharomyces pombe HIRA Complex Is Dependent upon the Hpc2-Like Protein, Hip42010
Dr Holly Anderson
Dr Josephine Wardle
Heather Murton
Dr Simon Whitehall
The Fission Yeast HIRA Histone Chaperone Is Required for Promoter Silencing and the Suppression of Cryptic Antisense Transcripts2009
Dr Linda Hogarth
Dr Christopher Redfern
Professor Andy Hall
Dr Holly Anderson
Marian Case
et al.
The effect of thiopurine drugs on DNA methylation in relation to TPMT expression2008