Gunnarsson C - Search Results

1

Arrhythmogenic Right Ventricular Cardiomyopathy - 4 Swedish families with an associated PKP2 c.2146-1G>C variant.

Svensson A, Åström-Aneq M, Widlund KF, Fluur C, Green A, Rehnberg M, Gunnarsson C. Svensson A, et al. Among authors: gunnarsson c. Am J Cardiovasc Dis. 2016 May 18;6(2):55-65. eCollection 2016. Am J Cardiovasc Dis. 2016. PMID: 27335691 Free PMC article.

2

Osmotic-driven mass transport of water: impact on the adhesiveness of hydrophilic polymers.

Borde A, Bergstrand A, Gunnarsson C, Larsson A. Borde A, et al. Among authors: gunnarsson c. J Colloid Interface Sci. 2010 Jan 15;341(2):255-60. doi: 10.1016/j.jcis.2009.09.051. Epub 2009 Oct 1. J Colloid Interface Sci. 2010. PMID: 19880130

3

Novel L1CAM splice site mutation in a young male with L1 syndrome.

Rehnberg M, Jonasson J, Gunnarsson C. Rehnberg M, et al. Among authors: gunnarsson c. Am J Med Genet A. 2011 Feb;155A(2):439-41. doi: 10.1002/ajmg.a.33803. Epub 2010 Dec 22. Am J Med Genet A. 2011. PMID: 21271669 No abstract available.

4

Novel plakophilin2 mutation: three-generation family with arrhythmogenic right ventricular cardiomyopathy.

Aneq MÅ, Fluur C, Rehnberg M, Söderkvist P, Engvall J, Nylander E, Gunnarsson C. Aneq MÅ, et al. Among authors: gunnarsson c. Scand Cardiovasc J. 2012 Apr;46(2):72-5. doi: 10.3109/14017431.2011.636068. Epub 2011 Dec 8. Scand Cardiovasc J. 2012. PMID: 22035158 Free article.

5

Assessment of HaloPlex amplification for sequence capture and massively parallel sequencing of arrhythmogenic right ventricular cardiomyopathy-associated genes.

Gréen A, Gréen H, Rehnberg M, Svensson A, Gunnarsson C, Jonasson J. Gréen A, et al. Among authors: gunnarsson c. J Mol Diagn. 2015 Jan;17(1):31-42. doi: 10.1016/j.jmoldx.2014.09.006. Epub 2014 Oct 24. J Mol Diagn. 2015. PMID: 25445213 Free article.

6

Homozygous missense MYBPC3 Pro873His mutation associated with increased risk for heart failure development in hypertrophic cardiomyopathy.

Kissopoulou A, Trinks C, Green A, Karlsson JE, Jonasson J, Gunnarsson C. Kissopoulou A, et al. Among authors: gunnarsson c. ESC Heart Fail. 2018 Aug;5(4):716-723. doi: 10.1002/ehf2.12288. Epub 2018 Apr 16. ESC Heart Fail. 2018. PMID: 29663722 Free PMC article.

7

Novel SMAD3 p.Arg386Thr genetic variant co-segregating with thoracic aortic aneurysm and dissection.

Engström K, Vánky F, Rehnberg M, Trinks C, Jonasson J, Green A, Gunnarsson C. Engström K, et al. Among authors: gunnarsson c. Mol Genet Genomic Med. 2020 Apr;8(4):e1089. doi: 10.1002/mgg3.1089. Epub 2020 Feb 5. Mol Genet Genomic Med. 2020. PMID: 32022471 Free PMC article.

8

Monozygotic twins with myocarditis and a novel likely pathogenic desmoplakin gene variant.

Kissopoulou A, Fernlund E, Holmgren C, Isaksson E, Karlsson JE, Green H, Jonasson J, Ellegård R, Årstrand HK, Svensson A, Gunnarsson C. Kissopoulou A, et al. Among authors: gunnarsson c. ESC Heart Fail. 2020 Jun;7(3):1210-1216. doi: 10.1002/ehf2.12658. Epub 2020 Apr 17. ESC Heart Fail. 2020. PMID: 32301586 Free PMC article.

9

Technical in-depth comparison of two massive parallel DNA-sequencing methods for formalin-fixed paraffin-embedded tissue from victims of sudden cardiac death.

Adolfsson E, Qvick A, Gréen H, Kling D, Gunnarsson C, Jonasson J, Gréen A. Adolfsson E, et al. Among authors: gunnarsson c. Forensic Sci Int Genet. 2021 Jul;53:102522. doi: 10.1016/j.fsigen.2021.102522. Epub 2021 Apr 26. Forensic Sci Int Genet. 2021. PMID: 33945952 Free article.

10

Genetic Variant Score and Arrhythmogenic Right Ventricular Cardiomyopathy Phenotype in Plakophilin-2 Mutation Carriers.

Svensson A, Platonov PG, Haugaa KH, Zareba W, Jensen HK, Bundgaard H, Gilljam T, Madsen T, Hansen J, Dejgaard LA, Karlsson LO, Gréen A, Polonsky B, Edvardsen T, Svendsen JH, Gunnarsson C. Svensson A, et al. Among authors: gunnarsson c. Cardiology. 2021;146(6):763-771. doi: 10.1159/000519231. Epub 2021 Sep 1. Cardiology. 2021. PMID: 34469894 Free PMC article.

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