Browsing publications by Dr David McDonald

Newcastle AuthorsTitleYear
Dr Sophie Hambleton
Dr David McDonald
Dr Helen Griffin
Angela Grainger
Dr Louise Reynard
et al.
Autosomal recessive combines immunodeficiency due to loss of function mutation in Tripeptidyl Peptidase II2012
Dr Helen Griffin
Dr David McDonald
Dr Rachel Dickinson
Angela Grainger
Dr Louise Reynard
et al.
Whole exome sequencing as a diagnostic tool in primary immunodeficiency2012
Dr Rachel Dickinson
Dr Helen Griffin
Dr Venetia Bigley
Dr Louise Reynard
Rafiqul Hussain
et al.
Exome sequencing identifies GATA-2 mutation as the cause of dendritic cell, monocyte, B and NK lymphoid deficiency2011
Dr David McDonald
Dr Helen Griffin
Angela Grainger
Dr Louise Reynard
Professor John Loughlin
et al.
Whole-exome deep sequencing identifies a novel causative mutation in primary immunodeficiency2011
Dr Sophie Hambleton
Professor Andrew Cant
Dr Andrew Gennery
Dr David McDonald
A novel human immunodeficiency disorder associated with a mutation in the T cell receptor a subunit constant gene (TRAC)2010
Dr David McDonald
Professor Heather Cordell
Dr Peter Donaldson
Professor Simon Pearce
The tryptophan 620 allele of the lymphoid tyrosine phosphatase (PTPN22 gene) predisposes to autoimmune Addison's disease2009
Dr David McDonald
Professor Simon Pearce
Thyroid peroxidase forms thionamide-sensitive homodimers: relevance for immunomodulation of thyroid autoimmunity2009
Professor Simon Pearce
Dr David McDonald
Polymorphisms in CLEC16A and CIITA at 16p13 are associated with primary adrenal insufficiency2008