Cited by

• Genetics and pharmacogenetics in the diagnosis and therapy of cardiovascular diseases.

  Krasi G, Precone V, Paolacci S, Stuppia L, Nodari S, Romeo F, Perrone M, Bushati V, Dautaj A, Bertelli M. Krasi G, et al. Acta Biomed. 2019 Sep 30;90(10-S):7-19. doi: 10.23750/abm.v90i10-S.8748. Acta Biomed. 2019. PMID: 31577248 Free PMC article. Review.
• Sudden cardiac death in a patient with lamin A/C mutation in the absence of dilated cardiomyopathy or conduction disease.

  Ehlermann P, Lehrke S, Papavassiliu T, Meder B, Borggrefe M, Katus HA, Schimpf R. Ehlermann P, et al. Clin Res Cardiol. 2011 Jun;100(6):547-51. doi: 10.1007/s00392-011-0289-0. Epub 2011 Feb 16. Clin Res Cardiol. 2011. PMID: 21327842 No abstract available.
• Inherited cardiac arrhythmias: diagnosis, treatment, and prevention.

  Beckmann BM, Pfeufer A, Kääb S. Beckmann BM, et al. Dtsch Arztebl Int. 2011 Sep;108(37):623-33; quiz 634. doi: 10.3238/arztebl.2011.0623. Epub 2011 Sep 16. Dtsch Arztebl Int. 2011. PMID: 21977220 Free PMC article. Review.
• Cardioprotective Role of Heat Shock Proteins in Atrial Fibrillation: From Mechanism of Action to Therapeutic and Diagnostic Target.

  van Wijk SW, Ramos KS, Brundel BJJM. van Wijk SW, et al. Int J Mol Sci. 2021 Jan 5;22(1):442. doi: 10.3390/ijms22010442. Int J Mol Sci. 2021. PMID: 33466228 Free PMC article. Review.
• Lamin A mutation impairs interaction with nucleoporin NUP155 and disrupts nucleocytoplasmic transport in atrial fibrillation.

  Han M, Zhao M, Cheng C, Huang Y, Han S, Li W, Tu X, Luo X, Yu X, Liu Y, Chen Q, Ren X, Wang QK, Ke T. Han M, et al. Hum Mutat. 2019 Mar;40(3):310-325. doi: 10.1002/humu.23691. Epub 2018 Dec 8. Hum Mutat. 2019. PMID: 30488537 Free PMC article.