Heritable risk for severe anaphylaxis associated with increased α-tryptase–encoding germline copy number at TPSAB1

Cited by (231)

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4. Hereditary alpha-tryptasemia – a potential cause of severe anaphylactic reactions and a modifier of mast cell diseases
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8. Identifying Genetic Variants in Patients With Cefaclor‐Induced Anaphylaxis Using Human Leukocyte Antigen Typing and Whole‐Exome Sequencing
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11. Elevated Tryptase and Hereditary Alpha Tryptasemia in Drug Hypersensitivity and Desensitization
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12. A Single‐Nucleotide Polymorphism as a Surrogate Marker for Hereditary Alpha‐Tryptasemia: Are We There Yet?
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13. Aggiornamenti sull'utilizzo della triptasi alla luce delle nuove conoscenze dell'alfa-triptasemia ereditaria
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14. Soluble FcεRI is increased in advanced mastocytosis and acts as a negative regulator of mast cell expansion and activation
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15. Hereditary Alpha-Tryptasemia and Mastocytosis: What We Know and What We Need To Learn
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16. Emerging Insights into Hereditary Alpha-Tryptasemia in the Context of Mast Cell Disorders: A Greek Case Series
    Fotios Koliofotis, Natalia Katrachoura, Niki Papapostolou, Styliani Τaka, Maria Martinou, Anthi Bouchla, Sotirios G. Papageorgiou, Michael P. Makris · 2026 · Journal of Personalized Medicine
17. Hereditary Alpha-Tryptasemia (HαT) as a Risk Modifier for Severe Anaphylaxis
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18. Hereditary alpha-tryptasemia demonstrates relative basophil enrichment without signs of cellular hyperreactivity
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19. Mast Cell Activation Syndrome and Mimickers
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21. Hereditary α-tryptasemia; a review of mechanisms linking α-tryptase gene dosage to intestinal homeostasis and immunopathology
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24. Only specific combinations of findings indicate mastocytosis, hereditary α-tryptasemia, histamine intolerance, or mast cell activation syndrome
    Knut Brockow, Tobias Michael Franz, Magdalena Saak, Hannah Lorenz, Julia Plötz, Leonhard Stark, Alexander Schäbitz, Görkem Aydin, Svenja Rupp, Johannes Untch et al. · 2026 · Allergo Journal International
25. Nur spezifische Befundkonstellationen indizieren eine Abklärung auf Mastozytose, hereditäre α-Tryptasämie, Histaminintoleranz oder ein Mastzellaktivierungssyndrom
    Knut Brockow, Tobias Michael Franz, Magdalena Saak, Hannah Lorenz, Julia Plötz, Leonhard Stark, Alexander Schäbitz, Görkem Aydin, Svenja Rupp, Johannes Untch et al. · 2026 · Allergo Journal
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28. Understanding Tryptase Physiology, Clinical Significance, and Diagnostic Applications: Where Do We Stand?
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29. Tryptase Locus Variation Contributes to Normal‐Range Basal Serum Tryptase Variability and Is Associated With Anaphylaxis
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30. Editorial: Hereditary alpha-tryptasemia: 10 years on
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31. Hereditary α-tryptasemia is associated with response to omalizumab in severe allergic asthma
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