Green A - 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: green a. Am J Cardiovasc Dis. 2016 May 18;6(2):55-65. eCollection 2016. Am J Cardiovasc Dis. 2016. PMID: 27335691 Free PMC article.

2

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: green h. 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.

3

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: green a. 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.

4

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: green a. 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.

5

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: green h, green a. 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.

6

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: green a. Cardiology. 2021;146(6):763-771. doi: 10.1159/000519231. Epub 2021 Sep 1. Cardiology. 2021. PMID: 34469894 Free PMC article.

7

Whole exome sequencing of FFPE samples-expanding the horizon of forensic molecular autopsies.

Adolfsson E, Kling D, Gunnarsson C, Jonasson J, Gréen H, Gréen A. Adolfsson E, et al. Among authors: green h, green a. Int J Legal Med. 2023 Jul;137(4):1215-1234. doi: 10.1007/s00414-022-02906-x. Epub 2022 Nov 8. Int J Legal Med. 2023. PMID: 36346469 Free PMC article.

8

Ankyrin-B dysfunction predisposes to arrhythmogenic cardiomyopathy and is amenable to therapy.

Roberts JD, Murphy NP, Hamilton RM, Lubbers ER, James CA, Kline CF, Gollob MH, Krahn AD, Sturm AC, Musa H, El-Refaey M, Koenig S, Aneq MÅ, Hoorntje ET, Graw SL, Davies RW, Rafiq MA, Koopmann TT, Aafaqi S, Fatah M, Chiasson DA, Taylor MR, Simmons SL, Han M, van Opbergen CJ, Wold LE, Sinagra G, Mittal K, Tichnell C, Murray B, Codima A, Nazer B, Nguyen DT, Marcus FI, Sobriera N, Lodder EM, van den Berg MP, Spears DA, Robinson JF, Ursell PC, Green AK, Skanes AC, Tang AS, Gardner MJ, Hegele RA, van Veen TA, Wilde AA, Healey JS, Janssen PM, Mestroni L, van Tintelen JP, Calkins H, Judge DP, Hund TJ, Scheinman MM, Mohler PJ. Roberts JD, et al. Among authors: green ak. J Clin Invest. 2019 Jul 2;129(8):3171-3184. doi: 10.1172/JCI125538. eCollection 2019 Jul 2. J Clin Invest. 2019. PMID: 31264976 Free PMC article.

9

Sandestig A, Green A, Jonasson J, Vogt H, Wahlström J, Pepler A, Ellnebo K, Biskup S, Stefanova M. Sandestig A, et al. Among authors: green a. Mol Syndromol. 2019 Jan;9(5):259-265. doi: 10.1159/000492267. Epub 2018 Aug 9. Mol Syndromol. 2019. PMID: 30733661 Free PMC article.

10

A Novel DLG3 Mutation Expanding the Phenotype of X-Linked Intellectual Disability Caused by DLG3 Nonsense Variants.

Sandestig A, Green A, Aronsson J, Ellnebo K, Stefanova M. Sandestig A, et al. Among authors: green a. Mol Syndromol. 2020 Jan;10(5):281-285. doi: 10.1159/000502601. Epub 2019 Oct 9. Mol Syndromol. 2020. PMID: 32021600 Free PMC article.

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