Olivier Monestier

Gosselies, WAL, Belgium

Last Updated: 09/26/2026

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Found 19 publications

Insights in the underlying pathophysiology of brain malformations associated with VRK1-related syndrome derived from fetal neuropathology.

Insights in the underlying pathophysiology of brain malformations associated with VRK1-related syndrome derived from fetal neuropathology.

Journal: Journal of neuropathology and experimental neurology

Published: March 06, 2025

K acetyltransferase 2B (KAT2B) variants can be responsible for early onset steroid-resistant nephrotic syndrome.

K acetyltransferase 2B (KAT2B) variants can be responsible for early onset steroid-resistant nephrotic syndrome.

Journal: Journal of medical genetics

Published: May 22, 2024

An unusual presentation of de novo RAC3 variation in prenatal diagnosis.

An unusual presentation of de novo RAC3 variation in prenatal diagnosis.

Journal: Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery

Published: December 05, 2023

A new case of sodium-dependent multivitamin transporter defect occurring as a life-threatening condition responsive to early vitamin supplementation and literature review.

A new case of sodium-dependent multivitamin transporter defect occurring as a life-threatening condition responsive to early vitamin supplementation and literature review.

Journal: Molecular genetics & genomic medicine

Published: October 10, 2023

Dual targeting of MAPK and PI3K pathways unlocks redifferentiation of Braf-mutated thyroid cancer organoids.

Dual targeting of MAPK and PI3K pathways unlocks redifferentiation of Braf-mutated thyroid cancer organoids.

Journal: Oncogene

Published: May 10, 2023

Episignature analysis of moderate effects and mosaics.

Episignature analysis of moderate effects and mosaics.

Journal: European journal of human genetics : EJHG

Published: January 30, 2023

Case Report: Inactivating PTH/PTHrP Signaling Disorder Type 1 Presenting With PTH Resistance.

Case Report: Inactivating PTH/PTHrP Signaling Disorder Type 1 Presenting With PTH Resistance.

Journal: Frontiers in endocrinology

Published: April 25, 2022

Functional and clinical studies reveal pathophysiological complexity of CLCN4-related neurodevelopmental condition.

Functional and clinical studies reveal pathophysiological complexity of CLCN4-related neurodevelopmental condition.

Journal: Molecular psychiatry

Published: April 05, 2022

Transplantable human thyroid organoids generated from embryonic stem cells to rescue hypothyroidism.

Transplantable human thyroid organoids generated from embryonic stem cells to rescue hypothyroidism.

Journal: Nature communications

Published: November 03, 2021

Trout myomaker contains 14 minisatellites and two sequence extensions but retains fusogenic function.

Trout myomaker contains 14 minisatellites and two sequence extensions but retains fusogenic function.

Journal: The Journal of biological chemistry

Published: October 02, 2018

Naa15 knockdown enhances c2c12 myoblast fusion and induces defects in zebrafish myotome morphogenesis.

Naa15 knockdown enhances c2c12 myoblast fusion and induces defects in zebrafish myotome morphogenesis.

Journal: Comparative biochemistry and physiology. Part B, Biochemistry & molecular biology

Published: September 19, 2018

WFIKKN1 and WFIKKN2: "Companion" proteins regulating TGFB activity.

WFIKKN1 and WFIKKN2: "Companion" proteins regulating TGFB activity.

Journal: Cytokine & growth factor reviews

Published: May 10, 2016

Showing 1-12 of 19

Last Updated: 09/26/2026