Ebun Omoyinmi

The Royal Free Hospital — United Kingdom

Biochemistry, Genetics and Molecular Biology · Life Sciences

22h-index2.0kcitations78works1.32yr avg
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Research Topics

Inflammasome and immune disorders(36), interferon and immune responses(15), Immune Response and Inflammation(10), Neutrophil, Myeloperoxidase and Oxidative Mechanisms(9), Autoimmune and Inflammatory Disorders Research(9)

Publications75 total

Preclinical evaluation of lentiviral gene therapy for adenosine deaminase 2 deficiency (DADA2): engraftment efficiency and biodistribution in humanised NBSGW mice
Gene Therapy·2025Open Access
Somatic NLRP3 mosaicism in patients with “mutation-negative” CAPS: insights from a single centre UK cohort
Frontiers in Pediatrics·2025· 2 citedOpen Access
Mapping <scp>VEXAS</scp> ‐associated and rare <scp> <i>UBA1</i> </scp> variants in the <scp>United Kingdom</scp> : Insights from patient cohorts and the general population
British Journal of Haematology·2025· 3 citedOpen Access
OA26 The impact of next generation genetic sequencing: 10 years’ experience of the Great Ormond Street Hospital Autoinflammation Centre of Excellence (GOSH-ACE)
Lara D. Veeken·2025Open Access
Case Report: ISG15 deficiency caused by novel variants in two families and effective treatment with Janus kinase inhibition
Frontiers in Immunology·2023· 6 citedOpen Access
Genetic testing of Behçet’s disease using next-generation sequencing to identify monogenic mimics and HLA-B*51
Lara D. Veeken·2023· 11 citedOpen Access
Curation and expansion of the Human Phenotype Ontology for systemic autoinflammatory diseases improves phenotype-driven disease-matching
Frontiers in Immunology·2023· 8 citedOpen Access
Neuroinflammation, autoinflammation, splenomegaly and anemia caused by bi-allelic mutations in IRAK4
Frontiers in Immunology·2023· 11 citedOpen Access
Case report: marfan syndrome (MFS) mimicking cutaneous vasculitis
Frontiers in Pediatrics·2023Open Access
Constitutively active Lyn kinase causes a cutaneous small vessel vasculitis and liver fibrosis syndrome
Nature Communications·2023· 27 citedOpen Access
Constitutively active Lyn kinase causes a cutaneous small vessel vasculitis and liver fibrosis syndrome
2022· 2 citedOpen Access
OA28 A rare case of cardiac tumour in infancy mimicking sarcoidosis
Rheumatology Advances in Practice·2022Open Access
A rapid turnaround gene panel for severe autoinflammation: Genetic results within 48 hours
Frontiers in Immunology·2022· 3 citedOpen Access
Pericarditis and Autoinflammation: A Clinical and Genetic Analysis of Patients With Idiopathic Recurrent Pericarditis and Monogenic Autoinflammatory Diseases at a National Referral Center
Journal of the American Heart Association·2022· 48 citedOpen Access
Lentiviral Mediated ADA2 Gene Transfer Corrects the Defects Associated With Deficiency of Adenosine Deaminase Type 2
Frontiers in Immunology·2022· 15 citedOpen Access
Vasculitis in a patient with mevalonate kinase deficiency (MKD): a case report
Pediatric Rheumatology·2021· 4 citedOpen Access
Genetic analysis of NLRP3 in recurrent pericarditis
European Heart Journal·2021· 2 citedOpen Access
A case of Myhre syndrome mimicking juvenile scleroderma
Pediatric Rheumatology·2020· 8 citedOpen Access
Cerebral arteriopathy associated with heterozygous variants in the casitas B-lineage lymphoma gene
Neurology Genetics·2020· 8 citedOpen Access
TRAP1 chaperone protein mutations and autoinflammation
Life Science Alliance·2019· 16 citedOpen Access
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Frequent Co-authors

Paul Brogan(46), Despina Eleftheriou(29), Ying Hong(19), Helen J. Lachmann(15), Kimberly Gilmour(14), Ariane Standing(13), Nigel Klein(13), Sira Nanthapisal(10), Dorota Rowczenio(10), Philip N. Hawkins(10), Sónia Gomes(8), Neil J. Sebire(8), Charalampia Papadopoulou(7), Fiona Price-Kuehne(6), Barbara Jensen(6), Hadija Trojer(5), Annette Keylock(5), Bernadette Marrero(4), Adriana A. de Jesus(4), Claire Murphy(4)