Courtney French

5PUBLICATIONS
76CO-AUTHORS
Infant and child healthGene expression (incl. microarray and other genome-wide approaches)Medical genetics (excl. cancer genetics)Neurology and neuromuscular diseasesOptical fibre communication systems and technologies
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Publications (5)

|Jan 24, 2025
Congenital Titinopathy: Comprehensive Characterization of the Most Severe End of the Disease Spectrum.

Sandra Coppens, Nicolas Deconinck, Patricia Sullivan

|Dec 02, 2024
Hospital-wide access to genomic data advanced pediatric rare disease research and clinical outcomes.

Courtney E French, Nancy C Andrews, Alan H Beggs

|Apr 28, 2022
Heterozygous frameshift variants in HNRNPA2B1 cause early-onset oculopharyngeal muscular dystrophy.

Hong Joo Kim, Payam Mohassel, Sandra Donkervoort

|Dec 15, 2021
Dual-vector gene therapy restores cochlear amplification and auditory sensitivity in a mouse model of DFNB16 hearing loss.

Olga Shubina-Oleinik, Carl Nist-Lund, Courtney French

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