Kenneth Paris

The actin regulator coronin 1A is mutant in a thymic egress–deficient mouse strain and in a patient with severe combined immunodeficiency

Lawrence R. Shiow, David W. Roadcap, Kenneth Paris et al. · Nature Immunology · 2008 · 243 citations · Full text

Primary Immunodeficiency, Immunogenetics, Immunology +4

Severe combined immunodeficiency (SCID) and attention deficit hyperactivity disorder (ADHD) associated with a coronin-1A mutation and a chromosome 16p11.2 deletion

Lawrence R. Shiow, Kenneth Paris, Matthew Akana et al. · Clinical Immunology · 2008 · 146 citations · Full text

Adhd, Mendelian Disorder, Genetic Disorder +5

Hypomorphic caspase activation and recruitment domain 11 (CARD11) mutations associated with diverse immunologic phenotypes with or without atopic disease

Batsukh Dorjbal, Jeffrey R. Stinson, Chi A. et al. · Journal of Allergy and Clinical Immunology · 2018 · 142 citations

Clinical Immunology, Molecular Immunology, Immunogenetics +11

X-linked agammaglobulinemia (XLA): Phenotype, diagnosis, and therapeutic challenges around the world

Zeinab El-Sayed, Juan Carlos Aldave Becerra, Waleed Al–Herz et al. · World Allergy Organization Journal · 2019 · 112 citations · Full text

Translational Medicine, X-linked Agammaglobulinemia, Autoimmune Disease +6

Infectious vaccine-derived rubella viruses emerge, persist, and evolve in cutaneous granulomas of children with primary immunodeficiencies

Ludmila Perelygina, Min-hsin Chen, Suganthi Suppiah et al. · PLoS Pathogens · 2019 · 89 citations · Full text