Megana K. Prasad
Strasbourg, France
Last Updated: 09/26/2026
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Found 17 publications
Spatial transcriptomics and single-nucleus RNA sequencing reveal rAAV2- and rAAV9-specific transduction signatures in the mouse liver.
Journal: Gene therapy
Published: April 16, 2025
Angelman syndrome patient-derived neuron screen leads to clinical ASO rugonersen targeting UBE3A-ATS with long-lasting effect in monkeys.
Journal: Nucleic acids research
Published: February 10, 2025
Bi-allelic PRMT9 loss-of-function variants cause a syndromic form of intellectual disability.
Journal: American journal of human genetics
Published: July 22, 2024
Beyond the promise: evaluating and mitigating off-target effects in CRISPR gene editing for safer therapeutics.
Journal: Frontiers in bioengineering and biotechnology
Published: November 15, 2023
A Simple, Quick, and Partially Automated Protocol for the Isolation of Single Nuclei from Frozen Mammalian Tissues for Single Nucleus Sequencing.
Journal: Journal of visualized experiments : JoVE
Published: August 14, 2023
Alzheimer's Risk Gene TREM2 Determines Functional Properties of New Type of Human iPSC-Derived Microglia.
Journal: Frontiers in immunology
Published: October 15, 2020
BCL11B-related disorder in two canadian children: Expanding the clinical phenotype.
Journal: European journal of medical genetics
Published: December 21, 2019
Protocol GenoDENT: Implementation of a New NGS Panel for Molecular Diagnosis of Genetic Disorders with Orodental Involvement.
Journal: Methods in molecular biology (Clifton, N.J.)
Published: March 07, 2019
Insights into Ciliary Genes and Evolution from Multi-Level Phylogenetic Profiling.
Journal: Molecular biology and evolution
Published: May 02, 2017
Expanding phenotype of hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis caused by FAM111B mutations: Report of an additional family raising the question of cancer predisposition and a short review of early-onset poikiloderma.
Journal: JAAD case reports
Published: March 29, 2017
Evolutionary Analysis Predicts Sensitive Positions of MMP20 and Validates Newly- and Previously-Identified MMP20 Mutations Causing Amelogenesis Imperfecta.
Journal: Frontiers in physiology
Published: March 10, 2017
Last Updated: 09/26/2026