Rokas Navickas
Dr Helen Griffin
Dr Manisha Ahuja
Angela Grainger
Professor Mary Slatter
et al. | A de novo TLR7 gain-of-function mutation causing severe monogenic lupus in an infant | 2024 |
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Dr Florian Gothe
Catherine Hatton
Angela Grainger
Dr Venetia Bigley
Dr Joanna Perthen
et al. | A Novel Case of Homozygous Interferon Alpha/Beta Receptor Alpha Chain (IFNAR1) Deficiency With Hemophagocytic Lymphohistiocytosis | 2022 |
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Dr Ina Schim van der Loeff
Dr Mario Abinun
Angela Grainger
Dr Karin Engelhardt
Professor Sophie Hambleton
| Defective neutrophil development and specific granule deficiency caused by a homozygous splice-site mutation in SMARCD2 | 2021 |
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Dr Florian Gothe
Emeritus Professor Drew Rowan
Angela Grainger
Professor Andrew Cant
Professor Mary Slatter
et al. | Novel Gain-of-Function Mutation in Stat1 Sumoylation Site Leads to CMC/CID Phenotype Responsive to Ruxolitinib | 2019 |
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Dr Christopher Duncan
Angela Grainger
Andrew Skelton
Raf Hussain
Dr Joe Willet
et al. | Early-onset autoimmune disease due to a heterozygous loss-of-function mutation in TNFAIP3 (A20) | 2018 |
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Dr Meghan Acres
Dr Florian Gothe
Angela Grainger
Andrew Skelton
Dr David Swan
et al. | STAT5B deficiency due to a novel missense mutation in the coiled-coil domain | 2018 |
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Dr Karin Engelhardt
Dr Yaobo Xu
Angela Grainger
Dr David Swan
Dr Joe Willet
et al. | Identification of Heterozygous Single- and Multi-exon Deletions in IL7R by Whole Exome Sequencing | 2017 |
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Dr Karin Engelhardt
Yaobo Xu
Angela Grainger
Dr David Swan
Dr Joe Willet
et al. | Identification Of Heterozygous Single- And Multi-exon Deletions In IL7R By Whole Exome Sequencing | 2015 |
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Professor 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 II | 2012 |
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Dr Emily Mavin
Angela Grainger
Dr Xiao Wang
Professor Andrew Gennery
| Regulatory T cell subsets, T cell receptor repertoire, and autoantibodies in RAG1-deficient Omenn syndrome | 2012 |
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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 immunodeficiency | 2012 |
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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 immunodeficiency | 2011 |
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Dr Alan Fenton
Dr Jennifer Toomey
Angela Grainger
Professor Andrew Gennery
| Immunogenicity of a Heptavalent Conjugate Pneumococcal Vaccine Administered Concurrently with a Combination Diphtheria, Tetanus, Five-Component Acellular Pertussis, Inactivated Polio, and Haemophilus influenzae Type b Vaccine and a Meningococcal Group C Conjugate Vaccine at 2, 3, and 4 Months of Age | 2010 |
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Dr Alan Fenton
Dr Jennifer Toomey
Angela Grainger
Professor Andrew Gennery
| Responses to a Conjugate Pneumococcal Vaccine in Preterm Infants Immunized at 2, 3, and 4 Months of Age | 2010 |
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Angela Grainger
S Papastefanou
Charles Greenough
| Juvenile spondylolysis: a comparative analysis of CT, SPECT and MRI | 2005 |
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