Warman-Chardon, J, Diaz-Manera, J, Tasca, Giorgio, Straub, Volker. 247th ENMC International Workshop: Muscle magnetic resonance imaging - Implementing muscle MRI as a diagnostic tool for rare genetic myopathy cohorts. Hoofddorp, The Netherlands, September 2019. Elsevier Neurom Dis. Aug 2020.

Thompson, R, Spendiff S, Roos A, Bourque PR, Warman-Chardon, J, Kirschner J, Horvath R, Lochmuller, H. Diagnosing inherited neuromuscular diseases through omics and other approaches: the old ways and the new. Lancet Neurol. 2020, June; 19, 522-32

Warman Chardon J, Díaz-Manera J, Tasca G, Bönnemann CG, Gómez-Andrés D, Heerschap A, Mercuri E, Muntoni F, Pichiecchio A, Ricci E, Walter MC, Hanna M, Jungbluth H, Morrow JM, Fernández-Torrón R, Udd B, Vissing J, Yousry T, Quijano-Roy S, Straub V, Carlier RY; MYO-MRI Working Group. MYO-MRI diagnostic protocols in genetic myopathies. Neuromuscul Disord. 2019 Nov;29(11):827-841.

David Pellerin, Asli Aykanat, Benjamin Ellezam, Emily C Troiano, Jason Karamchandani, Marie-Josée Dicaire, Marc Petitclerc, Rebecca Robertson, Xavier Allard-Chamard, Denis Brunet, Chamindra G Konersman, Jean Mathieu, Jodi Warman Chardon, Vandana A Gupta, Alan H Beggs, Bernard Brais, Nicolas Chrestian. Novel Recessive TNNT1 Congenital Core-Rod Myopathy in French Canadians. Ann Neurol Apr 2020

Kernohan KD, Frésard L, Zappala Z, Hartley T, Smith KS, Wagner J, Xu H, McBride A, Bourque PR, Consortium CRC, Bennett SAL, Dyment DA, Boycott KM, Montgomery SB, Warman Chardon J. Whole-transcriptome sequencing in blood provides a diagnosis of spinal muscular atrophy with progressive myoclonic epilepsy. Hum Mutat. 2017 Jun;38(6):611-614

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