Gavin Monahan

5PUBLICATIONS
51CO-AUTHORS
Neurology and neuromuscular diseasesCell physiologyBiomechanical engineeringCarbon capture engineering (excl. sequestration)Optometry
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Publications (5)

|Oct 01, 2025
A novel brachydactyly type E syndrome caused by variants in helix 8 of the PTH1R.

Gavin Monahan, Jakob Höppner, Harald Jüppner

|Dec 19, 2024
Structural plasticity of the coiled-coil interactions in human SFPQ.

Heidar J Koning, Jia Y Lai, Andrew C Marshall

|Oct 17, 2024
Author Correction: A CCG expansion in ABCD3 causes oculopharyngodistal myopathy in individuals of European ancestry.

Andrea Cortese, Sarah J Beecroft, Stefano Facchini

|Jul 27, 2024
A CCG expansion in ABCD3 causes oculopharyngodistal myopathy in individuals of European ancestry.

Andrea Cortese, Sarah J Beecroft, Stefano Facchini

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