C. G. Woods

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.

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

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

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.

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

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

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.