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3. Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19

6. Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19

7. Identification de nouveaux variants potentiellement impliqués dans la maladie de Verneuil par séquençage d’exomes

9. Inborn errors of type I IFN immunity in patients with life-threatening COVID-19

10. Auto-antibodies against type I IFNs in patients with life-threatening COVID-19

11. X-linked recessive TLR7 deficiency in similar to 1% of men under 60 years old with life-threatening COVID-19

12. Autoantibodies neutralizing type I IFNs are present in similar to 4\% of uninfected individuals over 70 years old and account for similar to 20\% of COVID-19 deaths

13. Autoantibodies neutralizing type I IFNs are present in ~4% of uninfected individuals over 70 years old and account for ~20% of COVID-19 deaths

14. X-linked recessive TLR7 deficiency in ~1% of men under 60 years old with life-threatening COVID-19

15. Erratum: Dominant-negative mutations in human IL6ST underlie hyper-IgE syndrome (J. Exp. Med. (2020) 217:6 Doi:10.1084/jem.20191804)

16. Inborn errors of type I IFN immunity in patients with life-threatening COVID-19

17. Autoantibodies against type I IFNs in patients with life-threatening COVID-19

18. Inborn errors of type I IFN immunity in patients with life-threatening COVID-19

19. Inborn errors of type I IFN immunity in patients with life-threatening COVID-19

22. Immunodeficiency, autoinflammation and amylopectinosis in humans with inherited HOIL-1 and LUBAC deficiency

23. Loss of B Cells in Patients with Heterozygous Mutations in IKAROS.

26. cpbAg1encodes an active carboxypeptidase B expressed in the midgut ofAnopheles gambiae.

27. Carboxypeptidases B of Anopheles gambiaeas Targets for a Plasmodium falciparumTransmission-Blocking Vaccine

28. Inherited ARPC5 mutations cause an actinopathy impairing cell motility and disrupting cytokine signaling

29. Serial Analysis of Gene Expression in Plasmodium berghei salivary gland sporozoites

30. X-linked recessive TLR7 deficiency in ~1% of men under 60 years old with life-threatening COVID-19

31. Human genetic and immunological determinants of critical COVID-19 pneumonia

32. The risk of COVID-19 death is much greater and age-dependent with type I IFN autoantibodies

33. Autoantibodies neutralizing type I IFNs are present in ~4% of uninfected individuals over 70 years old and account for ~20% of COVID-19 deaths

34. A combined immunodeficiency with severe infections, inflammation, and allergy caused by ARPC1B deficiency

35. Inherited DOCK2 Deficiency in Patients with Early-Onset Invasive Infections.

36. A Global Effort to Define the Human Genetics of Protective Immunity to SARS-CoV-2 Infection

37. T cell defects in patients with ARPC1B germline mutations account for their combined immunodeficiency

38. Incontinentia pigmenti underlies thymic dysplasia, autoantibodies to type I IFNs, and viral diseases.

39. Phenotypes of 126 Moroccan HIES patients according to NIH Score.

40. IL-7-dependent and -independent lineages of IL-7R-dependent human T cells.

41. Comprehensive Catalog of Variants Potentially Associated with Hidradenitis Suppurativa, Including Newly Identified Variants from a Cohort of 100 Patients.

42. Inherited human RelB deficiency impairs innate and adaptive immunity to infection.

43. Tuberculosis in otherwise healthy adults with inherited TNF deficiency.

45. A microglia clonal inflammatory disorder in Alzheimer's Disease.

46. Mechanism of neurodegeneration mediated by clonal inflammatory microglia.

47. Exclusive Characteristics of the p.E555K Dominant-Negative Variant in Autosomal Dominant E47 Deficiency.

48. ACK1 and BRK non-receptor tyrosine kinase deficiencies are associated with familial systemic lupus and involved in efferocytosis.

49. Biallelic human SHARPIN loss of function induces autoinflammation and immunodeficiency.

50. Higher COVID-19 pneumonia risk associated with anti-IFN-α than with anti-IFN-ω auto-Abs in children.

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