Rodolphe Dard

Poissy, France

Last Updated: 09/26/2026

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Found 32 publications

Pre-Implantation factor (PIF) restores working memory and promotes microglial ramification in the adult Dp(16)1Yey mouse model of Down syndrome.

Pre-Implantation factor (PIF) restores working memory and promotes microglial ramification in the adult Dp(16)1Yey mouse model of Down syndrome.

Journal: European journal of pharmacology

Published: September 16, 2025

Neonatal obstructive sleep apneas in a mouse model of Down syndrome.

Neonatal obstructive sleep apneas in a mouse model of Down syndrome.

Journal: Journal of neurophysiology

Published: April 11, 2025

Homozygous loss of function variant in LMNB2 gene causes major brain malformation and perinatal death.

Homozygous loss of function variant in LMNB2 gene causes major brain malformation and perinatal death.

Journal: Journal of medical genetics

Published: December 04, 2024

Use of murine models for the study of obstructive sleep apnea syndrome in Down syndrome

Use of murine models for the study of obstructive sleep apnea syndrome in Down syndrome

Journal: Revue des maladies respiratoires

Published: February 05, 2024

Prenatal treatment with preimplantation factor improves early postnatal neurogenesis and cognitive impairments in a mouse model of Down syndrome.

Prenatal treatment with preimplantation factor improves early postnatal neurogenesis and cognitive impairments in a mouse model of Down syndrome.

Journal: Cellular and molecular life sciences : CMLS

Published: January 19, 2024

The clinical value of optical genome mapping in the rapid characterization of RB1 duplication and 15q23q24.2 triplication, for more appropriate prenatal genetic counselling.

The clinical value of optical genome mapping in the rapid characterization of RB1 duplication and 15q23q24.2 triplication, for more appropriate prenatal genetic counselling.

Journal: Molecular genetics & genomic medicine

Published: January 07, 2024

X-linked transient antenatal Bartter syndrome related to MAGED2 gene: Enriching the phenotypic description and pathophysiologic investigation.

X-linked transient antenatal Bartter syndrome related to MAGED2 gene: Enriching the phenotypic description and pathophysiologic investigation.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: November 30, 2023

Prenatal exome sequencing, a powerful tool for improving the description of prenatal features associated with genetic disorders.

Prenatal exome sequencing, a powerful tool for improving the description of prenatal features associated with genetic disorders.

Journal: Prenatal diagnosis

Published: October 19, 2023

Prenatal Diagnosis of Primrose Syndrome.

Prenatal Diagnosis of Primrose Syndrome.

Journal: Journal of ultrasound in medicine : official journal of the American Institute of Ultrasound in Medicine

Published: August 30, 2023

Spermatogonial depletion and a spermatogenesis defect in the Dp(16)1Yey mouse model of Down syndrome.

Spermatogonial depletion and a spermatogenesis defect in the Dp(16)1Yey mouse model of Down syndrome.

Journal: Reproduction (Cambridge, England)

Published: August 07, 2023

Incidental and secondary findings in trio exome sequencing.

Incidental and secondary findings in trio exome sequencing.

Journal: Genes & diseases

Published: June 18, 2023

Episignatures in practice: independent evaluation of published episignatures for the molecular diagnostics of ten neurodevelopmental disorders.

Episignatures in practice: independent evaluation of published episignatures for the molecular diagnostics of ten neurodevelopmental disorders.

Journal: European journal of human genetics : EJHG

Published: May 10, 2023

Showing 1-12 of 32

Last Updated: 09/26/2026