Christopher T Gordon
20PUBLICATIONS
68CO-AUTHORS
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Publications (20)
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|Feb 22, 2024
TREX tetramer disruption alters RNA processing necessary for corticogenesis in THOC6 Intellectual Disability Syndrome.Elizabeth A Werren, Geneva R LaForce, Anshika Srivastava
|Sep 18, 2023
Mechanisms of mRNA processing defects in inherited THOC6 intellectual disability syndrome.Elizabeth Werren, Geneva LaForce, Anshika Srivastava
|Sep 04, 2023
Biallelic truncating variants in VGLL2 cause syngnathia in humans.Valeria Agostini, Aude Tessier, Nabila Djaziri
|Jul 27, 2023
Heterozygous rare variants in NR2F2 cause a recognizable multiple congenital anomaly syndrome with developmental delays.Mythily Ganapathi, Leticia S Matsuoka, Michael March
|Dec 14, 2021
Discovery of a genetic module essential for assigning left-right asymmetry in humans and ancestral vertebrates.Emmanuelle Szenker-Ravi, Tim Ott, Muznah Khatoo
|Feb 06, 2021
Impaired eIF5A function causes a Mendelian disorder that is partially rescued in model systems by spermidine.Víctor Faundes, Martin D Jennings, Siobhan Crilly
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Frequent Collaborators
3 joint publications
Bruno Reversade
3 joint publications
Tania Attié-Bitach
2 joint publications
Emmanuelle Szenker-Ravi
2 joint publications
Katta M Girisha
2 joint publications
Stephanie L Bielas
2 joint publications
Ashleigh Schaffer
2 joint publications
Vydianathan Ravi
2 joint publications
Guillaume Louvel
2 joint publications
Anja Beckers
2 joint publications
William G Newman
