Improved Criteria for the Classification of Titin Variants in Inherited Skeletal MyopathiesMarco Savarese, Bjarne Udd, Sara Gibertini et al.|Journal of Neuromuscular Diseases|2020Cited by 26
An unusual ryanodine receptor 1 (RYR1) phenotypeManu Jokela, Bjarne Udd, Giorgio Tasca et al.|Neurology|2019Cited by 21
Homozygosity of a Founder Variant c.1508dupC in <i>DOK7</i> Causes Congenital Myasthenia With Variable SeverityJohanna Palmio, Bjarne Udd, Panu Kiviranta et al.|Neurology Genetics|2024Cited by 4
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G.O.1 Welander distal myopathy is caused by a mutated RNA binding proteinPeter Hackman, Bjarne Udd, J. Sarparanta et al.|Neuromuscular Disorders|2012Cited by 0