Tracy A. Briggs
Manchester, ENG, United Kingdom
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 60 publications
Human GPR174 deficiency drives polyclonal lymphoproliferative disease via defects in T cell function.
Journal: medRxiv : the preprint server for health sciences
Published: July 30, 2026
Refining Human Phenotype Ontology (HPO) to enable better phenotype-genotype integration in systemic autoimmune rheumatic diseases.
Journal: Orphanet journal of rare diseases
Published: January 26, 2026
Recessive loss of DIAPH1 function causes a progressive neurodevelopmental syndrome with variable immunological involvement.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: May 05, 2025
Recessive Loss of DIAPH1 Function Causes a Progressive Neurodevelopmental Syndrome with Variable Immunological Involvement.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: May 05, 2025
Noonan Syndrome Spectrum Disorders Predispose to Systemic Lupus Erythematosus: Case Report and Critical Review of the Literature.
Journal: American journal of medical genetics. Part A
Published: April 04, 2025
Reverse transcriptase inhibitors in Aicardi-Goutières syndrome: A crossover clinical trial.
Journal: Developmental medicine and child neurology
Published: September 05, 2024
Multicriteria GIS-based assessment of biomass energy potentials in Nigeria.
Journal: Frontiers in bioengineering and biotechnology
Published: October 30, 2023
Type I interferon regulates interleukin-1beta and IL-18 production and secretion in human macrophages.
Journal: Life science alliance
Published: September 27, 2023
Curation and expansion of the Human Phenotype Ontology for systemic autoinflammatory diseases improves phenotype-driven disease-matching.
Journal: Frontiers in immunology
Published: May 02, 2023
Characterization of a mutant samhd1 zebrafish model implicates dysregulation of cholesterol biosynthesis in Aicardi-Goutières syndrome.
Journal: Frontiers in immunology
Published: November 17, 2022
In-depth characterisation of a cohort of individuals with missense and loss-of-function variants disrupting FOXP2.
Journal: Journal of medical genetics
Published: May 29, 2022
Last Updated: 09/26/2026