Publications by Dr Valerie Wilson - ePrints

Browsing publications by Dr Valerie Wilson.

Newcastle Authors	Title	Year
Emily Glover Dr Kate Smith-Jackson Dr Vicky Brocklebank Dr Valerie Wilson Dr Patrick Walsh et al.	Assessing the Impact of Prophylactic Eculizumab on Renal Graft Survival in Atypical Hemolytic Uremic Syndrome	2023
Dr Vicky Brocklebank Dr Patrick Walsh Dr Kate Smith-Jackson Dr Thomas Hallam Professor Kevin Marchbank et al.	Atypical haemolytic uraemic syndrome in the era of terminal complement inhibition- An observational cohort study	2023
Dr Ruth Richardson Dr Valerie Wilson Dr Michael Wright	Further delineation of phenotypic spectrum of SCN2A-related disorder	2022
Professor Kevin Marchbank Dr Isabel Pappworth Harriet Denton Kate Cooke Grant Richardson et al.	C3 Glomerulopathy and Related Disorders in Children.	2021
Dr Valerie Wilson Professor Sir John Burn Dr Akhtar Husain Professor Neil Rajan	Detection of genetic tumour predisposition syndromes using electronic health records	2020
Dr Vicky Brocklebank Dr Kate Smith-Jackson Dr Patrick Walsh Professor Kevin Marchbank Professor Claire Harris et al.	Long-term outcomes and response to treatment in DGKE nephropathy	2020
Dr Majid Arefi Dr Valerie Wilson Dr Siobhan Muthiah Dr Simon Zwolinski Dr Dalvir Bajwa et al.	Diverse presentations of cutaneous mosaicism occur in CYLD cutaneous syndrome and may result in parent-to-child transmission	2019
Professor David Kavanagh Dr Valerie Wilson Professor Tim Goodship	Statistical Validation of Rare Complement Variants Provides Insights into the Molecular Basis of Atypical Hemolytic Uremic Syndrome and C3 Glomerulopathy	2018
Rachel Challis Dr Edwin Wong Dr Vicky Brocklebank Dr Valerie Wilson Professor Kevin Marchbank et al.	Thrombotic Microangiopathy in Inverted Formin 2-Mediated Renal Disease	2017
Rachel Challis Dr Edwin Wong Dr Holly Anderson Dr Valerie Wilson Dr Vicky Brocklebank et al.	A De Novo Deletion in the Regulators of Complement Activation Cluster Producing a Hybrid Complement Factor H/Complement Factor H–Related 3 Gene in Atypical Hemolytic Uremic Syndrome	2016
Dr Valerie Wilson Tom Cox Dr Kate Smith-Jackson Professor David Kavanagh Professor Tim Goodship et al.	Chromosomal rearrangement – a rare cause of complement factor I associated atypical haemolytic uraemic syndrome	2016
Dr Valerie Wilson Dr David Bourn Professor Neil Rajan	CYLD Genetic Testing for Brooke-Spiegler Syndrome, Familial Cylindromatosis and Multiple Familial Trichoepitheliomas	2015
Dr Valerie Wilson Professor Tim Goodship Dr Veronique Fremaux-Bacchi	Mapping interactions between complement C3 and regulators using mutations in atypical hemolytic uremic syndrome	2015
Professor Heather Cordell Dr Valerie Wilson Professor Judith Goodship Professor Tim Goodship	Factors determining penetrance in familial atypical haemolytic uraemic syndrome	2014
Dr Valerie Wilson Dr Rebecca Darlay Dr Katrina Wood Professor Claire Harris Dr Eva-Maria Hunze et al.	Genotype/Phenotype Correlations in Complement Factor H Deficiency Arising From Uniparental Isodisomy	2013
Dr Karim Bennaceur Dr Eva-Maria Hunze James Staniforth Dr Lisa Turnbull Dr Valerie Wilson et al.	MCP (CD46) autoantibodies are associated with atypical hemolytic uremic syndrome	2012
Dr Valerie Wilson Dr Iain Moore Dr Lisa Turnbull Professor Kevin Marchbank Professor Neil Sheerin et al.	Postpartum aHUS Secondary to a Genetic Abnormality in Factor H Acquired Through Liver Transplantation	2012
Dr Mauro Santibanez Koref Dr Valerie Wilson Dr Michael Cunnington Professor John Mathers Dr Ann Curtis et al.	MLH1 Differential Allelic Expression in Mutation Carriers and Controls	2010
Dr Valerie Wilson Dr John Hanley Dr Katherine Talks Dr Ann Curtis	Evaluation of a diagnostic service for haemophilia A incorporating the LightScanner high resolution melt analysis system	2009
Dr Uma Nath Dr Valerie Wilson Dr Bridget Wilkins	FIP1L1-PDGFRA positive chronic eosinophilic leukaemia and associated central nervous system involvement	2008
Dr Kate Owen James Eden Dr Claire Jennings Dr Valerie Wilson Professor Timothy Cheetham et al.	Genetic association studies of the FOXP3 gene in Graves' disease and autoimmune Addison's disease in the United Kingdom population	2006
Dr Claire Jennings Dr Kate Owen Dr Valerie Wilson Professor Simon Pearce	A haplotype of the CYP27B1 promoter is associated with autoimmune Addison's disease but not with Graves' disease in a UK population	2005
Dr Valerie Wilson Dr Mauro Santibanez Koref Dr Lisa Turnbull James Eden Dr Ann Curtis et al.	Altered allele expression in hereditary nonpolyosis colon cancer (HNPCC) patients with nonsense mutations in the Mut L homologue (MLH1) gene.	2005
Dr Claire Jennings Dr Kate Owen Dr Valerie Wilson Professor Simon Pearce	No association of the codon 55 methionine to valine polymorphism in the SUMO4 gene with Graves' disease	2005
Ravindranath Velaga Dr Claire Jennings Dr Valerie Wilson Dr Kate Owen Professor Simon Pearce et al.	Analysis of the gonadotropin-releasing hormone gene in patients with idiopathic hypogonadotrophic hypogonadism	2004
Dr Valerie Wilson	Childhood mental ability and blood pressure at midlife: Linking the Scottish Mental Survey 1932 and the Midspan studies	2004
Dr Valerie Wilson Dr Claire Jennings Dr Kate Owen Dr Peter Donaldson Dr Petros Perros et al.	Role of the CD40 locus in Graves' disease	2004
Dr Valerie Wilson Dr Claire Jennings Dr Kate Owen Susan Herington Dr Peter Donaldson et al.	The codon 620 tryptophan allele of the lymphoid tyrosine phosphatase (LYP) gene is a major determinant of Graves' disease	2004
Dr Valerie Wilson	Population sex differences in IQ at age 11: The Scottish mental survey 1932	2003
Dr Valerie Wilson Dr Alison Howard Professor Dianne Ford Emeritus Professor Barry Hirst	EGF enhanced transcription of the amino acid transporter hATB(0) in COS-7 cells	2002