Similar articles for PMID: 33297970

Year	Number of Results
1999	1
2002	2
2003	4
2004	1
2005	1
2006	4
2007	1
2008	5
2009	5
2010	1
2011	7
2012	5
2013	6
2014	8
2015	7
2016	8
2017	12
2018	7
2019	9
2020	8
2021	4
2022	3
2023	2
2024	1

1

Genetic determinants of clinical phenotype in hypertrophic cardiomyopathy.

Velicki L, Jakovljevic DG, Preveden A, Golubovic M, Bjelobrk M, Ilic A, Stojsic S, Barlocco F, Tafelmeier M, Okwose N, Tesic M, Brennan P, Popovic D, Ristic A, MacGowan GA, Filipovic N, Maier LS, Olivotto I. Velicki L, et al. BMC Cardiovasc Disord. 2020 Dec 9;20(1):516. doi: 10.1186/s12872-020-01807-4. BMC Cardiovasc Disord. 2020. PMID: 33297970 Free PMC article.

2

Lack of Phenotypic Differences by Cardiovascular Magnetic Resonance Imaging in MYH7 (β-Myosin Heavy Chain)- Versus MYBPC3 (Myosin-Binding Protein C)-Related Hypertrophic Cardiomyopathy.

Weissler-Snir A, Hindieh W, Gruner C, Fourey D, Appelbaum E, Rowin E, Care M, Lesser JR, Haas TS, Udelson JE, Manning WJ, Olivotto I, Tomberli B, Maron BJ, Maron MS, Crean AM, Rakowski H, Chan RH. Weissler-Snir A, et al. Circ Cardiovasc Imaging. 2017 Feb;10(2):e005311. doi: 10.1161/CIRCIMAGING.116.005311. Circ Cardiovasc Imaging. 2017. PMID: 28193612

3

Prevalence and Phenotypic Expression of Mutations in the MYH7, MYBPC3 and TNNT2 Genes in Families with Hypertrophic Cardiomyopathy in the South of Brazil: A Cross-Sectional Study.

Mattos BP, Scolari FL, Torres MA, Simon L, Freitas VC, Giugliani R, Matte Ú. Mattos BP, et al. Arq Bras Cardiol. 2016 Sep;107(3):257-265. doi: 10.5935/abc.20160133. Arq Bras Cardiol. 2016. PMID: 27737317 Free PMC article.

4

Clinical features, spectrum of causal genetic mutations and outcome of hypertrophic cardiomyopathy in South Africans.

Ntusi NA, Shaboodien G, Badri M, Gumedze F, Mayosi BM. Ntusi NA, et al. Cardiovasc J Afr. 2016 May/Jun;27(3):152-158. doi: 10.5830/CVJA-2015-075. Cardiovasc J Afr. 2016. PMID: 27841901 Free PMC article.

5

[The genotype-phenotype correlation of MYH7 gene G15391A mutation and MYBPC3 gene G12101A mutation in familial hypertrophic cardiomyopathy].

WANG H, ZOU YB, WANG JZ, SONG L, SUN K, SONG XD, WANG XJ, ZHANG CN, HUI RT. WANG H, et al. Zhonghua Xin Xue Guan Bing Za Zhi. 2008 Dec;36(12):1059-62. Zhonghua Xin Xue Guan Bing Za Zhi. 2008. PMID: 19134269 Chinese.

6

Myocardial Deformation Analysis in MYBPC3 and MYH7 Related Sarcomeric Hypertrophic Cardiomyopathy-The Graz Hypertrophic Cardiomyopathy Registry.

Höller V, Seebacher H, Zach D, Schwegel N, Ablasser K, Kolesnik E, Gollmer J, Waltl G, Rainer PP, Verheyen S, Zirlik A, Verheyen N. Höller V, et al. Genes (Basel). 2021 Sep 23;12(10):1469. doi: 10.3390/genes12101469. Genes (Basel). 2021. PMID: 34680864 Free PMC article.

7

Hypertrophic cardiomyopathy clinical phenotype is independent of gene mutation and mutation dosage.

Viswanathan SK, Sanders HK, McNamara JW, Jagadeesan A, Jahangir A, Tajik AJ, Sadayappan S. Viswanathan SK, et al. PLoS One. 2017 Nov 9;12(11):e0187948. doi: 10.1371/journal.pone.0187948. eCollection 2017. PLoS One. 2017. PMID: 29121657 Free PMC article.

8

Association of variants in MYH7, MYBPC3 and TNNT2 with sudden cardiac death-related risk factors in Brazilian patients with hypertrophic cardiomyopathy.

Mori AA, Castro LR, Bortolin RH, Bastos GM, Oliveira VF, Ferreira GM, Hirata TDC, Fajardo CM, Sampaio MF, Moreira DAR, Pachón-Mateos JC, Correia EB, Sousa AGMR, Brión M, Carracedo A, Hirata RDC, Hirata MH. Mori AA, et al. Forensic Sci Int Genet. 2021 May;52:102478. doi: 10.1016/j.fsigen.2021.102478. Epub 2021 Feb 3. Forensic Sci Int Genet. 2021. PMID: 33588347

9

[Analysis of MYH7, MYBPC3 and TNNT2 gene mutations in 10 Chinese pedigrees with familial hypertrophic cardiomyopathy and the correlation between genotype and phenotype].

Liu WL, Xie WL, Hu DY, Zhu TG, Li YT, Sun YH, Li CL, Li L, Li TC, Bian H, Tong QG, Yang SN, Fan RY, Cui W. Liu WL, et al. Zhonghua Xin Xue Guan Bing Za Zhi. 2006 Mar;34(3):202-7. Zhonghua Xin Xue Guan Bing Za Zhi. 2006. PMID: 16630449 Chinese.

10

Novel deletions in MYH7 and MYBPC3 identified in Indian families with familial hypertrophic cardiomyopathy.

Waldmüller S, Sakthivel S, Saadi AV, Selignow C, Rakesh PG, Golubenko M, Joseph PK, Padmakumar R, Richard P, Schwartz K, Tharakan JM, Rajamanickam C, Vosberg HP. Waldmüller S, et al. J Mol Cell Cardiol. 2003 Jun;35(6):623-36. doi: 10.1016/s0022-2828(03)00050-6. J Mol Cell Cardiol. 2003. PMID: 12788380

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