Anthony J. Oojageer
Wilmslow Road
Manchester, ENG M204BX, United Kingdom
Manchester, ENG M204BX, United Kingdom
Last Updated: 09/26/2026
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Found 9 publications
A human model to deconvolve genotype-phenotype causations in lung squamous cell carcinoma.
Journal: Nature communications
Published: February 26, 2024
Assessment of Type I Interferon Signaling in Pediatric Inflammatory Disease.
Journal: Journal of clinical immunology
Published: September 30, 2016
Unusual cutaneous features associated with a heterozygous gain-of-function mutation in IFIH1: overlap between Aicardi-Goutières and Singleton-Merten syndromes.
Journal: The British journal of dermatology
Published: August 02, 2015
Stimulator of Interferon Genes-Associated Vasculopathy With Onset in Infancy: A Mimic of Childhood Granulomatosis With Polyangiitis.
Journal: JAMA dermatology
Published: May 21, 2015
Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1.
Journal: American journal of medical genetics. Part A
Published: August 20, 2014
Mutations in CECR1 associated with a neutrophil signature in peripheral blood.
Journal: Pediatric rheumatology online journal
Published: July 25, 2014
Basal ganglia calcification in a patient with beta-propeller protein-associated neurodegeneration.
Journal: Pediatric neurology
Published: July 14, 2014
Showing 1-9 of 9
Last Updated: 09/26/2026