Αρρυθμιογόνος καρδιομυοπάθεια (Greek Wikipedia)

Analysis of information sources in references of the Wikipedia article "Αρρυθμιογόνος καρδιομυοπάθεια" in Greek language version.

refsWebsite

Global rank Greek rank

24nih.gov

4^th place

17doi.org

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4archive.org

6^th place

5^th place

1harvard.edu

18^th place

57^th place

archive.org

«DSG2 mutations contribute to arrhythmogenic right ventricular dysplasia/cardiomyopathy». American Journal of Human Genetics 79 (1): 136–42. July 2006. doi:10.1086/504393. PMID 16773573. PMC 1474134. https://archive.org/details/sim_american-journal-of-human-genetics_2006-07_79_1/page/136.
«Mutant desmocollin-2 causes arrhythmogenic right ventricular cardiomyopathy». American Journal of Human Genetics 79 (6): 1081–8. December 2006. doi:10.1086/509044. PMID 17186466. PMC 1698714. https://archive.org/details/sim_american-journal-of-human-genetics_2006-12_79_6/page/1081.
«Arrhythmogenic right ventricular dysplasia/cardiomyopathy associated with mutations in the desmosomal gene desmocollin-2». American Journal of Human Genetics 79 (5): 978–84. November 2006. doi:10.1086/509122. PMID 17033975. PMC 1698574. https://archive.org/details/sim_american-journal-of-human-genetics_2006-11_79_5/page/978.
«A novel dominant mutation in plakoglobin causes arrhythmogenic right ventricular cardiomyopathy». American Journal of Human Genetics 81 (5): 964–73. November 2007. doi:10.1086/521633. PMID 17924338. PMC 2265660. https://archive.org/details/sim_american-journal-of-human-genetics_2007-11_81_5/page/964.

doi.org

dx.doi.org

Pilichou, Kalliopi; Thiene, Gaetano; Bauce, Barbara; Rigato, Ilaria; Lazzarini, Elisabetta; Migliore, Federico; Perazzolo Marra, Martina; Rizzo, Stefania και άλλοι. (2 April 2016). «Arrhythmogenic cardiomyopathy». Orphanet Journal of Rare Diseases 11 (1): 33. doi:10.1186/s13023-016-0407-1. PMID 27038780.
«Regulatory mutations in transforming growth factor-beta3 gene cause arrhythmogenic right ventricular cardiomyopathy type 1». Cardiovascular Research 65 (2): 366–73. February 2005. doi:10.1016/j.cardiores.2004.10.005. PMID 15639475.
«Composite polymorphisms in the ryanodine receptor 2 gene associated with arrhythmogenic right ventricular cardiomyopathy». Cardiovascular Research 71 (3): 496–505. August 2006. doi:10.1016/j.cardiores.2006.04.004. PMID 16769042.
«Arrhythmogenic right ventricular cardiomyopathy type 5 is a fully penetrant, lethal arrhythmic disorder caused by a missense mutation in the TMEM43 gene». American Journal of Human Genetics 82 (4): 809–21. April 2008. doi:10.1016/j.ajhg.2008.01.010. PMID 18313022.
«Mutation analysis and evaluation of the cardiac localization of TMEM43 in arrhythmogenic right ventricular cardiomyopathy». Clinical Genetics 80 (3): 256–64. September 2011. doi:10.1111/j.1399-0004.2011.01623.x. PMID 21214875.
«De novo desmin-mutation N116S is associated with arrhythmogenic right ventricular cardiomyopathy». Human Molecular Genetics 19 (23): 4595–607. December 2010. doi:10.1093/hmg/ddq387. PMID 20829228.
«Novel Desmin Mutation p.Glu401Asp Impairs Filament Formation, Disrupts Cell Membrane Integrity, and Causes Severe Arrhythmogenic Left Ventricular Cardiomyopathy/Dysplasia». Circulation 137 (15): 1595–1610. April 2018. doi:10.1161/CIRCULATIONAHA.117.028719. PMID 29212896.
«Clinical profile of four families with arrhythmogenic right ventricular cardiomyopathy caused by dominant desmoplakin mutations». European Heart Journal 26 (16): 1666–75. August 2005. doi:10.1093/eurheartj/ehi341. PMID 15941723.
«Mutations in the desmosomal protein plakophilin-2 are common in arrhythmogenic right ventricular cardiomyopathy». Nature Genetics 36 (11): 1162–4. November 2004. doi:10.1038/ng1461. PMID 15489853.
«Mutations in desmoglein-2 gene are associated with arrhythmogenic right ventricular cardiomyopathy». Circulation 113 (9): 1171–9. March 2006. doi:10.1161/CIRCULATIONAHA.105.583674. PMID 16505173.
«DSG2 mutations contribute to arrhythmogenic right ventricular dysplasia/cardiomyopathy». American Journal of Human Genetics 79 (1): 136–42. July 2006. doi:10.1086/504393. PMID 16773573. PMC 1474134. https://archive.org/details/sim_american-journal-of-human-genetics_2006-07_79_1/page/136.
«Mutant desmocollin-2 causes arrhythmogenic right ventricular cardiomyopathy». American Journal of Human Genetics 79 (6): 1081–8. December 2006. doi:10.1086/509044. PMID 17186466. PMC 1698714. https://archive.org/details/sim_american-journal-of-human-genetics_2006-12_79_6/page/1081.
«Arrhythmogenic right ventricular dysplasia/cardiomyopathy associated with mutations in the desmosomal gene desmocollin-2». American Journal of Human Genetics 79 (5): 978–84. November 2006. doi:10.1086/509122. PMID 17033975. PMC 1698574. https://archive.org/details/sim_american-journal-of-human-genetics_2006-11_79_5/page/978.
«Arrhythmogenic right ventricular cardiomyopathy caused by deletions in plakophilin-2 and plakoglobin (Naxos disease) in families from Greece and Cyprus: genotype-phenotype relations, diagnostic features and prognosis». European Heart Journal 27 (18): 2208–16. September 2006. doi:10.1093/eurheartj/ehl184. PMID 16893920.
«A novel dominant mutation in plakoglobin causes arrhythmogenic right ventricular cardiomyopathy». American Journal of Human Genetics 81 (5): 964–73. November 2007. doi:10.1086/521633. PMID 17924338. PMC 2265660. https://archive.org/details/sim_american-journal-of-human-genetics_2007-11_81_5/page/964.
«Mutations in ILK, encoding integrin-linked kinase, are associated with arrhythmogenic cardiomyopathy». Translational Research 208: 15–29. February 2019. doi:10.1016/j.trsl.2019.02.004. PMID 30802431.
«Clinical and functional characterization of a novel mutation in lamin a/c gene in a multigenerational family with arrhythmogenic cardiac laminopathy». PLOS ONE 10 (4): e0121723. 2015. doi:10.1371/journal.pone.0121723. PMID 25837155. Bibcode: 2015PLoSO..1021723F.

harvard.edu

adsabs.harvard.edu

«Clinical and functional characterization of a novel mutation in lamin a/c gene in a multigenerational family with arrhythmogenic cardiac laminopathy». PLOS ONE 10 (4): e0121723. 2015. doi:10.1371/journal.pone.0121723. PMID 25837155. Bibcode: 2015PLoSO..1021723F.

nih.gov

ncbi.nlm.nih.gov

Pilichou, Kalliopi; Thiene, Gaetano; Bauce, Barbara; Rigato, Ilaria; Lazzarini, Elisabetta; Migliore, Federico; Perazzolo Marra, Martina; Rizzo, Stefania και άλλοι. (2 April 2016). «Arrhythmogenic cardiomyopathy». Orphanet Journal of Rare Diseases 11 (1): 33. doi:10.1186/s13023-016-0407-1. PMID 27038780.
«Regulatory mutations in transforming growth factor-beta3 gene cause arrhythmogenic right ventricular cardiomyopathy type 1». Cardiovascular Research 65 (2): 366–73. February 2005. doi:10.1016/j.cardiores.2004.10.005. PMID 15639475.
«Composite polymorphisms in the ryanodine receptor 2 gene associated with arrhythmogenic right ventricular cardiomyopathy». Cardiovascular Research 71 (3): 496–505. August 2006. doi:10.1016/j.cardiores.2006.04.004. PMID 16769042.
«Arrhythmogenic right ventricular cardiomyopathy type 5 is a fully penetrant, lethal arrhythmic disorder caused by a missense mutation in the TMEM43 gene». American Journal of Human Genetics 82 (4): 809–21. April 2008. doi:10.1016/j.ajhg.2008.01.010. PMID 18313022.
«Mutation analysis and evaluation of the cardiac localization of TMEM43 in arrhythmogenic right ventricular cardiomyopathy». Clinical Genetics 80 (3): 256–64. September 2011. doi:10.1111/j.1399-0004.2011.01623.x. PMID 21214875.
«De novo desmin-mutation N116S is associated with arrhythmogenic right ventricular cardiomyopathy». Human Molecular Genetics 19 (23): 4595–607. December 2010. doi:10.1093/hmg/ddq387. PMID 20829228.
«Novel Desmin Mutation p.Glu401Asp Impairs Filament Formation, Disrupts Cell Membrane Integrity, and Causes Severe Arrhythmogenic Left Ventricular Cardiomyopathy/Dysplasia». Circulation 137 (15): 1595–1610. April 2018. doi:10.1161/CIRCULATIONAHA.117.028719. PMID 29212896.
«Clinical profile of four families with arrhythmogenic right ventricular cardiomyopathy caused by dominant desmoplakin mutations». European Heart Journal 26 (16): 1666–75. August 2005. doi:10.1093/eurheartj/ehi341. PMID 15941723.
«Mutations in the desmosomal protein plakophilin-2 are common in arrhythmogenic right ventricular cardiomyopathy». Nature Genetics 36 (11): 1162–4. November 2004. doi:10.1038/ng1461. PMID 15489853.
«Mutations in desmoglein-2 gene are associated with arrhythmogenic right ventricular cardiomyopathy». Circulation 113 (9): 1171–9. March 2006. doi:10.1161/CIRCULATIONAHA.105.583674. PMID 16505173.
«DSG2 mutations contribute to arrhythmogenic right ventricular dysplasia/cardiomyopathy». American Journal of Human Genetics 79 (1): 136–42. July 2006. doi:10.1086/504393. PMID 16773573. PMC 1474134. https://archive.org/details/sim_american-journal-of-human-genetics_2006-07_79_1/page/136.
«Mutant desmocollin-2 causes arrhythmogenic right ventricular cardiomyopathy». American Journal of Human Genetics 79 (6): 1081–8. December 2006. doi:10.1086/509044. PMID 17186466. PMC 1698714. https://archive.org/details/sim_american-journal-of-human-genetics_2006-12_79_6/page/1081.
«Arrhythmogenic right ventricular dysplasia/cardiomyopathy associated with mutations in the desmosomal gene desmocollin-2». American Journal of Human Genetics 79 (5): 978–84. November 2006. doi:10.1086/509122. PMID 17033975. PMC 1698574. https://archive.org/details/sim_american-journal-of-human-genetics_2006-11_79_5/page/978.
«Arrhythmogenic right ventricular cardiomyopathy caused by deletions in plakophilin-2 and plakoglobin (Naxos disease) in families from Greece and Cyprus: genotype-phenotype relations, diagnostic features and prognosis». European Heart Journal 27 (18): 2208–16. September 2006. doi:10.1093/eurheartj/ehl184. PMID 16893920.
«A novel dominant mutation in plakoglobin causes arrhythmogenic right ventricular cardiomyopathy». American Journal of Human Genetics 81 (5): 964–73. November 2007. doi:10.1086/521633. PMID 17924338. PMC 2265660. https://archive.org/details/sim_american-journal-of-human-genetics_2007-11_81_5/page/964.
«Mutations in ILK, encoding integrin-linked kinase, are associated with arrhythmogenic cardiomyopathy». Translational Research 208: 15–29. February 2019. doi:10.1016/j.trsl.2019.02.004. PMID 30802431.
«Clinical and functional characterization of a novel mutation in lamin a/c gene in a multigenerational family with arrhythmogenic cardiac laminopathy». PLOS ONE 10 (4): e0121723. 2015. doi:10.1371/journal.pone.0121723. PMID 25837155. Bibcode: 2015PLoSO..1021723F.

pubmedcentral.nih.gov

Pilichou, Kalliopi; Thiene, Gaetano; Bauce, Barbara; Rigato, Ilaria; Lazzarini, Elisabetta; Migliore, Federico; Perazzolo Marra, Martina; Rizzo, Stefania και άλλοι. (2 April 2016). «Arrhythmogenic cardiomyopathy». Orphanet Journal of Rare Diseases 11 (1): 33. doi:10.1186/s13023-016-0407-1. PMID 27038780.
«Arrhythmogenic right ventricular cardiomyopathy type 5 is a fully penetrant, lethal arrhythmic disorder caused by a missense mutation in the TMEM43 gene». American Journal of Human Genetics 82 (4): 809–21. April 2008. doi:10.1016/j.ajhg.2008.01.010. PMID 18313022.
«DSG2 mutations contribute to arrhythmogenic right ventricular dysplasia/cardiomyopathy». American Journal of Human Genetics 79 (1): 136–42. July 2006. doi:10.1086/504393. PMID 16773573. PMC 1474134. https://archive.org/details/sim_american-journal-of-human-genetics_2006-07_79_1/page/136.
«Mutant desmocollin-2 causes arrhythmogenic right ventricular cardiomyopathy». American Journal of Human Genetics 79 (6): 1081–8. December 2006. doi:10.1086/509044. PMID 17186466. PMC 1698714. https://archive.org/details/sim_american-journal-of-human-genetics_2006-12_79_6/page/1081.
«Arrhythmogenic right ventricular dysplasia/cardiomyopathy associated with mutations in the desmosomal gene desmocollin-2». American Journal of Human Genetics 79 (5): 978–84. November 2006. doi:10.1086/509122. PMID 17033975. PMC 1698574. https://archive.org/details/sim_american-journal-of-human-genetics_2006-11_79_5/page/978.
«A novel dominant mutation in plakoglobin causes arrhythmogenic right ventricular cardiomyopathy». American Journal of Human Genetics 81 (5): 964–73. November 2007. doi:10.1086/521633. PMID 17924338. PMC 2265660. https://archive.org/details/sim_american-journal-of-human-genetics_2007-11_81_5/page/964.
«Clinical and functional characterization of a novel mutation in lamin a/c gene in a multigenerational family with arrhythmogenic cardiac laminopathy». PLOS ONE 10 (4): e0121723. 2015. doi:10.1371/journal.pone.0121723. PMID 25837155. Bibcode: 2015PLoSO..1021723F.