Godelieve Morel

University Of Reunion Island
Saint-pierre-les-bois, France

Last Updated: 09/26/2026

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Found 30 publications

Expanding phenotypic and genotypic spectrum of PDE6C-associated retinal disorders.

Expanding phenotypic and genotypic spectrum of PDE6C-associated retinal disorders.

Journal: Eye (London, England)

Published: April 02, 2026

Clinical and Genotypic Spectrum of Twinkle-Related Disorders: Insights From a Multinational Cohort Study.

Clinical and Genotypic Spectrum of Twinkle-Related Disorders: Insights From a Multinational Cohort Study.

Journal: Neurology

Published: January 15, 2026

DNA methylation signature and clinical delineation of PACS1-related disorder in 24 unreported individuals.

DNA methylation signature and clinical delineation of PACS1-related disorder in 24 unreported individuals.

Journal: European journal of human genetics : EJHG

Published: September 19, 2025

Systematic analysis of snRNA genes reveals frequent RNU2-2 variants in dominant and recessive developmental and epileptic encephalopathies.

Systematic analysis of snRNA genes reveals frequent RNU2-2 variants in dominant and recessive developmental and epileptic encephalopathies.

Journal: medRxiv : the preprint server for health sciences

Published: September 15, 2025

Systematic analysis of snRNA genes reveals frequent RNU2-2 variants in dominant and recessive developmental and epileptic encephalopathies.

Systematic analysis of snRNA genes reveals frequent RNU2-2 variants in dominant and recessive developmental and epileptic encephalopathies.

Journal: Nature genetics

Published: September 02, 2025

Genetic analyses using chromosomal microarray and exome sequencing in fetuses and women with Müllerian duct anomalies.

Genetic analyses using chromosomal microarray and exome sequencing in fetuses and women with Müllerian duct anomalies.

Journal: Journal of assisted reproduction and genetics

Published: April 29, 2025

Rare features in Feingold syndrome type 1.

Rare features in Feingold syndrome type 1.

Journal: European journal of medical genetics

Published: November 19, 2024

First Description of a Large Clinical Series of Fetal Alcohol Spectrum Disorders Children and Adolescents in Reunion Island, France.

First Description of a Large Clinical Series of Fetal Alcohol Spectrum Disorders Children and Adolescents in Reunion Island, France.

Journal: Children (Basel, Switzerland)

Published: July 12, 2024

Reanalysis of unsolved prenatal exome sequencing for structural defects: diagnostic yield and contribution of postnatal/postmortem features.

Reanalysis of unsolved prenatal exome sequencing for structural defects: diagnostic yield and contribution of postnatal/postmortem features.

Journal: European journal of human genetics : EJHG

Published: July 03, 2024

Clinical and genetic characterization of a progressive RBL2-associated neurodevelopmental disorder.

Clinical and genetic characterization of a progressive RBL2-associated neurodevelopmental disorder.

Journal: Brain : a journal of neurology

Published: May 16, 2024

Clinical and neurogenetic characterisation of autosomal recessive RBL2-associated progressive neurodevelopmental disorder.

Clinical and neurogenetic characterisation of autosomal recessive RBL2-associated progressive neurodevelopmental disorder.

Journal: medRxiv : the preprint server for health sciences

Published: May 15, 2024

Prenatal and neonatal phenotype of Larsen of La Réunion Island syndrome (B4GALT7-linkeropathy).

Prenatal and neonatal phenotype of Larsen of La Réunion Island syndrome (B4GALT7-linkeropathy).

Journal: European journal of medical genetics

Published: November 20, 2023

Showing 1-12 of 30

Last Updated: 09/26/2026