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Browsing publications by Dr Valerie Wilson.

Newcastle AuthorsTitleYearFull text
Dr Ruth Richardson
Dr Valerie Wilson
Dr Michael Wright
Further delineation of phenotypic spectrum of SCN2A-related disorder2022
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
Dr Neil Rajan
Detection of genetic tumour predisposition syndromes using electronic health records2020
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 nephropathy2020
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 transmission2019
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 Glomerulopathy2018
Rachel Challis
Dr Edwin Wong
Dr Vicky Brocklebank
Dr Valerie Wilson
Professor Kevin Marchbank
et al.
Thrombotic Microangiopathy in Inverted Formin 2-Mediated Renal Disease2017
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 Syndrome2016
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 syndrome2016
Dr Valerie Wilson
Dr David Bourn
Dr Neil Rajan
CYLD Genetic Testing for Brooke-Spiegler Syndrome, Familial Cylindromatosis and Multiple Familial Trichoepitheliomas2015
Dr Valerie Wilson
Professor Tim Goodship
Dr Veronique Fremaux-Bacchi
Mapping interactions between complement C3 and regulators using mutations in atypical hemolytic uremic syndrome2015
Professor Heather Cordell
Dr Valerie Wilson
Professor Judith Goodship
Professor Tim Goodship
Factors determining penetrance in familial atypical haemolytic uraemic syndrome2014
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 Isodisomy2013
Dr Karim Bennaceur
Dr Eva-Maria Hunze
Scott Staniforth
Dr Lisa Turnbull
Dr Valerie Wilson
et al.
MCP (CD46) autoantibodies are associated with atypical hemolytic uremic syndrome2012
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 Transplantation2012
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 Controls2010
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 system2009
Dr Uma Nath
Dr Valerie Wilson
Dr Bridget Wilkins
FIP1L1-PDGFRA positive chronic eosinophilic leukaemia and associated central nervous system involvement2008
Dr Kate Owen
James Eden
Dr Claire Jennings
Dr Valerie Wilson
Dr Timothy Cheetham
et al.
Genetic association studies of the FOXP3 gene in Graves' disease and autoimmune Addison's disease in the United Kingdom population2006
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 population2005
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' disease2005
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 hypogonadism2004
Dr Valerie Wilson
Childhood mental ability and blood pressure at midlife: Linking the Scottish Mental Survey 1932 and the Midspan studies2004
Dr Valerie Wilson
Dr Claire Jennings
Dr Kate Owen
Dr Peter Donaldson
Dr Petros Perros
et al.
Role of the CD40 locus in Graves' disease2004
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' disease2004
Dr Valerie Wilson
Population sex differences in IQ at age 11: The Scottish mental survey 19322003
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 cells2002