Maya Chrabieh
Overview
Explore the profile of Maya Chrabieh including associated specialties, affiliations and a list of published articles.
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Articles
37
Citations
3610
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Recent Articles
1.
Ogishi M, Kitaoka K, Good-Jacobson K, Rinchai D, Zhang B, Wang J, et al.
Immunity
. 2024 Nov;
57(12):2790-2807.e15.
PMID: 39603236
T follicular helper (Tfh) cells abundantly express the immunoreceptor programmed cell death protein 1 (PD-1), and the impact of PD-1 deficiency on antibody (Ab)-mediated immunity in mice is associated with...
2.
Ogishi M, Yang R, Rodriguez R, Golec D, Martin E, Philippot Q, et al.
J Exp Med
. 2022 Nov;
220(1).
PMID: 36326697
Inborn errors of IFN-γ immunity can underlie tuberculosis (TB). We report three patients from two kindreds without EBV viremia or disease but with severe TB and inherited complete ITK deficiency,...
3.
Ogishi M, Arias A, Yang R, Han J, Zhang P, Rinchai D, et al.
J Exp Med
. 2022 Sep;
219(10).
PMID: 36094518
Human cells homozygous for rare loss-of-expression (LOE) TYK2 alleles have impaired, but not abolished, cellular responses to IFN-α/β (underlying viral diseases in the patients) and to IL-12 and IL-23 (underlying...
4.
Spaan A, Neehus A, Laplantine E, Staels F, Ogishi M, Seeleuthner Y, et al.
Science
. 2022 May;
376(6599):eabm6380.
PMID: 35587511
The molecular basis of interindividual clinical variability upon infection with is unclear. We describe patients with haploinsufficiency for the linear deubiquitinase OTULIN, encoded by a gene on chromosome 5p. Patients...
5.
Li J, Lei W, Zhang P, Rapaport F, Seeleuthner Y, Lyu B, et al.
J Exp Med
. 2021 Sep;
218(11).
PMID: 34473196
Autosomal dominant (AD) NFKB1 deficiency is thought to be the most common genetic etiology of common variable immunodeficiency (CVID). However, the causal link between NFKB1 variants and CVID has not...
6.
Ogishi M, Yang R, Aytekin C, Langlais D, Bourgey M, Khan T, et al.
Nat Med
. 2021 Jun;
27(9):1646-1654.
PMID: 34183838
The pathophysiology of adverse events following programmed cell death protein 1 (PD-1) blockade, including tuberculosis (TB) and autoimmunity, remains poorly characterized. We studied a patient with inherited PD-1 deficiency and...
7.
Asano T, Khourieh J, Zhang P, Rapaport F, Spaan A, Li J, et al.
J Exp Med
. 2021 Jun;
218(8).
PMID: 34137790
Most patients with autosomal dominant hyper-IgE syndrome (AD-HIES) carry rare heterozygous STAT3 variants. Only six of the 135 in-frame variants reported have been experimentally shown to be dominant negative (DN),...
8.
Le Voyer T, Neehus A, Yang R, Ogishi M, Rosain J, Alroqi F, et al.
Proc Natl Acad Sci U S A
. 2021 Apr;
118(15).
PMID: 33876776
Human inborn errors of IFN-γ underlie mycobacterial disease, due to insufficient IFN-γ production by lymphoid cells, impaired myeloid cell responses to this cytokine, or both. We report four patients from...
9.
Bastard P, Michailidis E, Hoffmann H, Chbihi M, Le Voyer T, Rosain J, et al.
J Exp Med
. 2021 Feb;
218(4).
PMID: 33544838
Yellow fever virus (YFV) live attenuated vaccine can, in rare cases, cause life-threatening disease, typically in patients with no previous history of severe viral illness. Autosomal recessive (AR) complete IFNAR1...
10.
Martin-Fernandez M, Bravo Garcia-Morato M, Gruber C, Murias Loza S, Malik M, Alsohime F, et al.
Cell Rep
. 2020 May;
31(6):107633.
PMID: 32402279
Most monogenic disorders have a primary clinical presentation. Inherited ISG15 deficiency, however, has manifested with two distinct presentations to date: susceptibility to mycobacterial disease and intracranial calcifications from hypomorphic interferon-II...