Isabelle Migeotte

Brussels, BRU, Belgium

Last Updated: 09/26/2026

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Found 31 publications

A Partial UMOD Deletion Results in Altered Uromodulin Synthesis and Autosomal-Dominant Tubulointerstitial Kidney Disease-Uromodulin.

A Partial UMOD Deletion Results in Altered Uromodulin Synthesis and Autosomal-Dominant Tubulointerstitial Kidney Disease-Uromodulin.

Journal: Kidney medicine

Published: March 09, 2026

Diagnostic yield of clinical exome sequencing in 868 children with neurodevelopmental disorders.

Diagnostic yield of clinical exome sequencing in 868 children with neurodevelopmental disorders.

Journal: European journal of medical genetics

Published: February 06, 2025

Extra-embryonic mesoderm during development and in in vitro models.

Extra-embryonic mesoderm during development and in in vitro models.

Journal: Development (Cambridge, England)

Published: June 19, 2024

Origin and flow-mediated remodeling of the murine and human extraembryonic circulation systems.

Origin and flow-mediated remodeling of the murine and human extraembryonic circulation systems.

Journal: Frontiers in physiology

Published: March 02, 2024

Non-apical mitoses contribute to cell delamination during mouse gastrulation.

Non-apical mitoses contribute to cell delamination during mouse gastrulation.

Journal: Nature communications

Published: February 20, 2024

Correction: Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19.

Correction: Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19.

Journal: Genome medicine

Published: January 06, 2024

Genetic Architecture of Ischaemic Strokes after COVID-19 Shows Similarities with Large Vessel Strokes.

Genetic Architecture of Ischaemic Strokes after COVID-19 Shows Similarities with Large Vessel Strokes.

Journal: International journal of molecular sciences

Published: July 04, 2023

Correction: Respiratory viral infections in otherwise healthy humans with inherited IRF7 deficiency.

Correction: Respiratory viral infections in otherwise healthy humans with inherited IRF7 deficiency.

Journal: The Journal of experimental medicine

Published: November 07, 2022

Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19.

Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19.

Journal: medRxiv : the preprint server for health sciences

Published: November 03, 2022

Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19.

Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19.

Journal: Genome medicine

Published: September 15, 2022

Regionally specific levels and patterns of keratin 8 expression in the mouse embryo visceral endoderm emerge upon anterior-posterior axis determination.

Regionally specific levels and patterns of keratin 8 expression in the mouse embryo visceral endoderm emerge upon anterior-posterior axis determination.

Journal: Frontiers in cell and developmental biology

Published: September 05, 2022

Natural history of Usher type 2 with the c.2299delG mutation of USH2A in a large cohort.

Natural history of Usher type 2 with the c.2299delG mutation of USH2A in a large cohort.

Journal: Ophthalmic genetics

Published: March 29, 2022

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Last Updated: 09/26/2026