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Browsing publications by Christine Hayes.

Newcastle AuthorsTitleYearFull text
Dr Richard Gallon
Rachel Phelps
Christine Hayes
Annabel Kunzemann Martinez
Dr Gillian Borthwick
et al.
Constitutional Microsatellite Instability, Genotype, and Phenotype Correlations in Constitutional Mismatch Repair Deficiency2023
Maria Rasmussen
Peter Sowter
Dr Richard Gallon
Christine Hayes
Dr Mauro Santibanez Koref
et al.
Mismatch repair deficiency testing in Lynch syndrome-associated urothelial tumors2023
Dr Richard Gallon
Rachel Phelps
Christine Hayes
Dr Dino Masic
Professor Julie Irving
et al.
Detection of constitutional mismatch repair deficiency in children and adolescents with acute lymphoblastic leukemia2022
Rachel Phelps
Dr Richard Gallon
Christine Hayes
Dr Tom Lee
Professor Rakesh Heer
et al.
Detection of Microsatellite Instability in Colonoscopic Biopsies and Postal Urine Samples from Lynch Syndrome Cancer Patients Using a Multiplex PCR Assay2022
Dr Richard Gallon
Peter Sowter
Rachel Phelps
Christine Hayes
Dr Gillian Borthwick
et al.
How should we test for Lynch syndrome? A review of current guidelines and future strategies2021
Dr Richard Gallon
Dr Harsh Sheth
Christine Hayes
Lisa Redford
Dr Ghanim Alhilal
et al.
Sequencing‐based microsatellite instability testing using as few as six markers for high‐throughput clinical diagnostics2020
Dr Richard Gallon
Dr Harsh Sheth
Christine Hayes
Dr Gillian Borthwick
Professor Sir John Burn
et al.
A sensitive and scalable microsatellite instability assay to diagnose constitutional mismatch repair deficiency by sequencing of peripheral blood leukocytes2019
Yonggang He
Joshua Paulin
Tarry Mavimba
Christine Hayes
Dr Andrew Knight
et al.
A novel C3d-containing oligomeric vaccine provides insight into the viability of testing human C3d-based vaccines in mice2018
Professor Tim Goodship
Dr Isabel Pappworth
Dr Iain Moore
Dr Eva-Maria Hunze
James Staniforth
et al.
Factor H autoantibodies in membranoproliferative glomerulonephritis2012
Professor David Kavanagh
Dr Isabel Pappworth
Christine Hayes
Dr Iain Moore
Dr Eva-Maria Hunze
et al.
Factor I Autoantibodies in Patients with Atypical Hemolytic Uremic Syndrome: Disease-Associated or an Epiphenomenon?2012
Christine Hayes
Dr Sonia Bussey
Podiatric Medicine Unravelled2011
Dr Isabel Pappworth
Christine Hayes
Dr Andrew Knight
Professor Kevin Marchbank
The role of complement in the formation of B regulatory cells2010
Professor Robert Taylor
Dr Andrew Schaefer
Christine Hayes
Professor Bobby McFarland
Emeritus Professor Doug Turnbull
et al.
Catastrophic presentation of mitochondrial disease due to a mutation in the tRNAHis gene2004
Professor Bobby McFarland
Dr Andrew Schaefer
Dr Julie Murphy
Dr Stephen Lynn
Christine Hayes
et al.
Familial Myopathy: New Insights into the T14709C Mitochondrial tRNA Mutation2004
Professor Robert Taylor
Dr Hugh Bain
Christine Hayes
Dr Martin Barron
Professor Robert Lightowlers
et al.
A homoplasmic mitochondrial transfer ribonucleic acid mutation as a cause of maternally inherited hypertrophic cardiomyopathy2003
Dr Andrew Schaefer
Professor Bobby McFarland
Dr Julie Murphy
Dr Stephen Lynn
Christine Hayes
et al.
Familial mitochondrial myopathy: New insights into the T14709C mitochondrial tRNA mutation2003
Professor Robert Taylor
Christine Hayes
Emerita Professor Katherine Bushby
Emeritus Professor Doug Turnbull
Professor Pamela Shaw
et al.
Investigation of mitochondrial function in hereditary spastic paraparesis2002
Professor Robert Taylor
Christine Hayes
Emeritus Professor Doug Turnbull
Molecular and functional effects of the T14709C point mutation in the mitochondrial DNA of a patient with maternally inherited diabetes and deafness2002
Professor Robert Taylor
Dr Rajinder Singh-Kler
Christine Hayes
Emeritus Professor Doug Turnbull
Annals 25th anniversary2001
Professor Robert Taylor
Dr Rajinder Singh-Kler
Christine Hayes
Emeritus Professor Doug Turnbull
Progressive mitochondrial disease resulting from a novel missense mutation in the mitochondrial DNA ND3 gene2001