James J Cox

A Gain-of-Function Mutation in TRPA1 Causes Familial Episodic Pain Syndrome

G. Bedoya, A. Ruiz-Linares, C. Woods, 2010, Neuron.

Sodium channel genes in pain-related disorders: phenotype–genotype associations and recommendations for clinical use

S. Dib-Hajj, G. Lauria, M. Gerrits, 2014, The Lancet Neurology.

Regulation of Nav1.7: A Conserved SCN9A Natural Antisense Transcript Expressed in Dorsal Root Ganglia

J. Zhao, C. Woods, A. M. Habib, 2015, PloS one.

Congenital Insensitivity to Pain: Novel SCN9A Missense and In-Frame Deletion Mutations

C. Woods, F. Reimann, E. Manor, 2010, Human mutation.

Genetic landscape of congenital insensitivity to pain and hereditary sensory and autonomic neuropathies

David L. Bennett, T. Hornemann, S. Züchner, 2023, Brain : a journal of neurology.