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Satoshi Okada
Affiliation : Rockefeller University
- 6Publications (affiliation in the United States)
- 356Total publications
- 18889Citations
- 58h-index
Research profile
Satoshi Okada has 6 indexed publications (2013–2016). Their work appears mainly in “Blood”, “Proceedings of the National Academy of Sciences” and “Journal of Allergy and Clinical Immunology”. Their most cited article, “Heterozygous STAT1 gain-of-function mutations underlie an unexpectedly broad clinical phenotype” (2016), has been cited 577 times. 4 of these publications date from the last three years of activity. Their work is co-authored with at least 12 researchers, including institutions in France, Colombia.
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Create my free profile Add my publicationsResearch areas
- Immunodeficiency and Autoimmune Disorders
- T-cell and B-cell Immunology
- interferon and immune responses
- Cytokine Signaling Pathways and Interactions
- Blood disorders and treatments
Publications (6)
- Heterozygous STAT1 gain-of-function mutations underlie an unexpectedly broad clinical phenotype
- Genetic, immunological, and clinical features of patients with bacterial and fungal infections due to inherited IL-17RA deficiency
- Alanine-scanning mutagenesis of human signal transducer and activator of transcription 1 to estimate loss- or gain-of-function variants
- Human TYK2 deficiency: Mycobacterial and viral infections without hyper-IgE syndrome
- A Novel Homozygous p.R1105X Mutation of the AP4E1 Gene in Twins with Hereditary Spastic Paraplegia and Mycobacterial Disease
- IL-17 T Cells’ Defective Differentiation In Vitro Despite Normal Range Ex Vivo in Chronic Mucocutaneous Candidiasis Due to STAT1 Mutation
Publication venues
- Blood × 1
- Proceedings of the National Academy of Sciences × 1
- Journal of Allergy and Clinical Immunology × 1
- The Journal of Experimental Medicine × 1
- PLoS ONE × 1
- Journal of Investigative Dermatology × 1
Publications per year
- 20163
- 20151
- 20132
Collaborations
Partner institutions : Inserm · Institut des Maladies Génétiques Imagine · Human Genetic of Infectious Diseases · Université Paris Descartes · Hôpital Necker-Enfants Malades
Co-authors’ countries : France · Colombia
Co-authors
- Jean‐Laurent Casanova
- Stéphanie Boisson‐Dupuis
- Yuval Itan
- Anne Puel
- Xiao‐Fei Kong
- Laurent Abel
- Jacinta C. Bustamante
- Sergio D. Rosenzweig
- Xiaoxia Li
- Jennifer L. Stoddard
- Dusan Bogunovic
- Rubén Martínez‐Barricarte
Bibliographic data from OpenAlex (open database).
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