An iPSC model of hereditary sensory neuropathy-1 reveals L-serine-responsive deficits in neuronal ganglioside composition and axoglial interactions by Clark, A, Kugathasan, U, Baskozos, G, Priestman, D, Fugger, N, Che, K, Blesneac, I, Platt, F, Bennett, D

Rare Nav1.7 variants associated with painful diabetic peripheral neuropathy by Blesneac, I, Themistocleous, AC, Fratter, Carl, Conrad, LJ, Ramirez, JD, Cox, JJ, Tesfaye, S, Shillo, PR, Rice, ASC, Tucker, SJ, Bennett, DLH

CACNA1H Mutations Are Associated With Different Forms of Primary Aldosteronism. by Daniil, G, Fernandes-Rosa, F, Chemin, J, Blesneac, I, Beltrand, J, Polak, M, Jeunemaitre, X, Boulkroun, S, Amar, L, Strom, T, Lory, P, Zennaro, M

Defining the Functional Role of NaV1.7 in Human Nociception by McDermott, L, Weir, G, Themistocleous, A, Segerdahl, A, Blesneac, I, Baskozos, G, Clark, A, Millar, V, Peck, L, Ebner, D, Tracey, I, Serra, J, Bennett, D

Investigating genotype–phenotype relationship of extreme neuropathic pain disorders in a UK national cohort by Themistocleous, AC, Baskozos, G, Blesneac, I, Comini, M, Megy, K, Chong, S, Deevi, SVV, Ginsberg, L, Gosal, D, Hadden, RDM, Horvath, R, Mahdi-Rogers, M, Manzur, A, Mapeta, R, Marshall, A, Matthews, E, McCarthy, MI, Reilly, MM, Renton, T, Rice, ASC, Vale, TA, van Zuydam, N, Walker, SM, Woods, CG, Bennett, DLH