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Matthieu Bouaziz

Researcher at University of Paris

Publications -  17
Citations -  558

Matthieu Bouaziz is an academic researcher from University of Paris. The author has contributed to research in topics: Population stratification & Sample size determination. The author has an hindex of 6, co-authored 17 publications receiving 361 citations. Previous affiliations of Matthieu Bouaziz include French Institute of Health and Medical Research & Paris Descartes University.

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Journal ArticleDOI

Tuberculosis and impaired IL-23–dependent IFN-γ immunity in humans homozygous for a common TYK2 missense variant

Stéphanie Boisson-Dupuis, +94 more
- 21 Dec 2018 - 
TL;DR: Homozygosity for the catalytically inactive P1104A missense variant of the TYK2 Janus kinase selectively disrupts the induction of IFN-γ by IL-23 and is a common monogenic etiology of tuberculosis.
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A recessive form of hyper-IgE syndrome by disruption of ZNF341-dependent STAT3 transcription and activity

Vivien Béziat, +92 more
- 15 Jun 2018 - 
TL;DR: Patients with an autosomal recessive form of HIES due to loss-of-function mutations of a previously uncharacterized gene, ZNF341 are described, revealing a Previously unappreciated layer of transcriptional regulation controlling JAK-STAT signaling.
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Inherited p40phox deficiency differs from classic chronic granulomatous disease

Annemarie van de Geer, +74 more
TL;DR: In inherited p40phox deficiency underlies a distinctive condition, resembling a mild, atypical form of CGD, which suffers from hyperinflammation and peripheral infections, but does not have any of the invasive bacterial or fungal infections seen in CGD.
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The human CIB1-EVER1-EVER2 complex governs keratinocyte-intrinsic immunity to β-papillomaviruses.

TL;DR: It is suggested that the disruption of CIB1-EVER1–EVER2-dependent keratinocyte-intrinsic immunity underlies the selective susceptibility to &bgr;-HPVs of EV patients.
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IRF4 haploinsufficiency in a family with Whipple’s disease

TL;DR: It is found that IRF4 had evolved under purifying selection, and can underlie WD by haploinsufficiency, with age-dependent incomplete penetrance.