Anderson C, Langer E, Routes T, McWilliams S, Bereslavskyy I, Kamp T, et al. Most myopathic lamin variants aggregate: a functional genomics approach for assessing variants of uncertain significance. NPJ Genom Med. 2021;6:103 pubmed publisher

Anderson C, Routes T, Eckhardt L, Delisle B, January C, Kamp T. A rapid solubility assay of protein domain misfolding for pathogenicity assessment of rare DNA sequence variants. Genet Med. 2020;: pubmed publisher

Bronshtein I, Kepten E, Kanter I, Berezin S, Lindner M, Redwood A, et al. Loss of lamin A function increases chromatin dynamics in the nuclear interior. Nat Commun. 2015;6:8044 pubmed publisher

Gilchrist S, Gilbert N, Perry P, Ostlund C, Worman H, Bickmore W. Altered protein dynamics of disease-associated lamin A mutants. BMC Cell Biol. 2004;5:46 pubmed