Publications by Christine Hayes - ePrints

Browsing publications by Christine Hayes.

Newcastle Authors	Title	Year
Dr Richard Gallon Rachel Phelps Christine Hayes Sarah Mills Dr Gillian Borthwick et al.	A novel colorectal cancer test combining microsatellite instability and BRAF/RAS analysis: Clinical validation and impact on Lynch syndrome screening	2024
Peter Sowter Dr Richard Gallon Christine Hayes Rachel Phelps Dr Gillian Borthwick et al.	Detection of Mismatch Repair Deficiency in Endometrial Cancer: Assessment of IHC, Fragment Length Analysis, and Amplicon Sequencing Based MSI Testing	2024
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 Deficiency	2023
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 leukemia	2023
Maria Rasmussen Peter Sowter Dr Richard Gallon Christine Hayes Dr Mauro Santibanez Koref et al.	Mismatch repair deficiency testing in Lynch syndrome-associated urothelial tumors	2023
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 Assay	2022
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 strategies	2021
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 diagnostics	2020
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 leukocytes	2019
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 mice	2018
Professor Tim Goodship Dr Isabel Pappworth Dr Iain Moore Dr Eva-Maria Hunze James Staniforth et al.	Factor H autoantibodies in membranoproliferative glomerulonephritis	2012
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 Unravelled	2011
Dr Isabel Pappworth Christine Hayes Dr Andrew Knight Professor Kevin Marchbank	The role of complement in the formation of B regulatory cells	2010
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 gene	2004
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 Mutation	2004
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 cardiomyopathy	2003
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 mutation	2003
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 paraparesis	2002
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 deafness	2002
Professor Robert Taylor Dr Rajinder Singh-Kler Christine Hayes Emeritus Professor Doug Turnbull	Annals 25th anniversary	2001
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 gene	2001