Leen Moens

7PUBLICATIONS

147CO-AUTHORS

Gene and molecular therapyDevelopmental genetics (incl. sex determination)Innate immunityMedical biochemistry - proteins and peptides (incl. medical proteomics)Infant and child health

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Publications (7)

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|Jul 01, 2026

Two novel kindreds with autosomal recessive STAT2 deficiency.

|Aug 27, 2025

Dominant negative ADA2 mutations cause ADA2 deficiency in heterozygous carriers.

Marjon Wouters, Lisa Ehlers, Wout Van Eynde

|Dec 23, 2024

Dominant negative <i>ADA2</i> mutations cause ADA2 deficiency in heterozygous carriers.

Marjon Wouters, Lisa Ehlers, Wout Van Eynde

|Mar 07, 2023

Humans with inherited MyD88 and IRAK-4 deficiencies are predisposed to hypoxemic COVID-19 pneumonia.

Ana García-García, Rebeca Pérez de Diego, Carlos Flores

|Feb 23, 2023

PERK recruits E-Syt1 at ER-mitochondria contacts for mitochondrial lipid transport and respiration.

Maria Livia Sassano, Alexander R van Vliet, Ellen Vervoort

|Jun 16, 2022

Recessive inborn errors of type I IFN immunity in children with COVID-19 pneumonia.

Qian Zhang, Daniela Matuozzo, Jérémie Le Pen

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Frequent Collaborators

7 joint publications

Isabelle Meyts

6 joint publications

Giorgia Bucciol

4 joint publications

Jean-Laurent Casanova

Paul Bastard

Laurent Abel

Selket Delafontaine

Qian Zhang

Aurélie Cobat

Lucy Bizien

Şemsi Nur Karabela

Frequent Collaborators

7 joint publications

Isabelle Meyts

6 joint publications

Giorgia Bucciol

4 joint publications

Jean-Laurent Casanova

4 joint publications

Paul Bastard