Antoine Hanauer
Strasbourg, France
Last Updated: 09/26/2026
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Found 8 publications
ER proteostasis failure in HYOU1 deficiency alters B cells, neutrophils, and interferon signalling.
Journal: Journal of human immunity
Published: December 28, 2025
ER proteostasis failure in HYOU1 deficiency alters B cells, neutrophils, and interferon signalling.
Journal: Journal of human immunity
Published: December 28, 2025
A pleiotropic recurrent dominant ITPR3 variant causes a complex multisystemic disease.
Journal: Science advances
Published: September 13, 2024
Identification of driver genes for critical forms of COVID-19 in a deeply phenotyped young patient cohort.
Journal: Science translational medicine
Published: October 26, 2021
ZMIZ1 Variants Cause a Syndromic Neurodevelopmental Disorder.
Journal: American journal of human genetics
Published: December 28, 2019
Exome sequencing identifies a novel missense variant in CTSC causing nonsyndromic aggressive periodontitis.
Journal: Journal of human genetics
Published: January 17, 2019
ZMIZ1 Variants Cause a Syndromic Neurodevelopmental Disorder.
Journal: American journal of human genetics
Published: September 08, 2018
Mutations in signal recognition particle SRP54 cause syndromic neutropenia with Shwachman-Diamond-like features.
Journal: The Journal of clinical investigation
Published: January 23, 2017
Showing 1-8 of 8
Last Updated: 09/26/2026