PubMed (GeneRIF) for id: 4625

Year	Number of Results
2002	4
2003	3
2004	4
2005	8
2006	6
2007	7
2008	12
2009	20
2010	16
2011	10
2012	6
2013	15
2014	17
2015	15
2016	14
2017	16
2018	11
2019	12
2020	12
2021	9
2022	8
2023	11
2024	4

1

A New Leu714Arg Variant in the Converter Domain of MYH7 is Associated with a Severe Form of Familial Hypertrophic Cardiomyopathy.

Golubenko MV, Pavlyukova EN, Salakhov RR, Makeeva OA, Puzyrev KV, Glotov OS, Puzyrev VP, Nazarenko MS. Golubenko MV, et al. Front Biosci (Schol Ed). 2024 Feb 23;16(1):1. doi: 10.31083/j.fbs1601001. Front Biosci (Schol Ed). 2024. PMID: 38538344 Free article.

2

Genetic Testing Yield and Clinical Characteristics of Hypertrophic Cardiomyopathy in Understudied Ethnic Groups: Insights From a New Zealand National Registry.

Earle NJ, Winbo A, Crawford J, Wheeler M, Stiles R, Donoghue T, Stiles MK, Hayes I, Marcondes L, Martin A, Skinner JR. Earle NJ, et al. Circ Heart Fail. 2024 Mar;17(3):e010970. doi: 10.1161/CIRCHEARTFAILURE.123.010970. Epub 2024 Mar 8. Circ Heart Fail. 2024. PMID: 38456273 Free PMC article.

3

Enhanced myofilament calcium sensitivity aggravates abnormal calcium handling and diastolic dysfunction in patient-specific induced pluripotent stem cell-derived cardiomyocytes with MYH7 mutation.

Guo G, Wang L, Li X, Fu W, Cao J, Zhang J, Liu Y, Liu M, Wang M, Zhao G, Zhao X, Zhou Y, Niu S, Liu G, Zhang Y, Dong J, Tao H, Zhao X. Guo G, et al. Cell Calcium. 2024 Jan;117:102822. doi: 10.1016/j.ceca.2023.102822. Epub 2023 Nov 8. Cell Calcium. 2024. PMID: 38101154 Free article.

4

[Clinical phenotype and genetic analysis of patients with left ventricular noncompaction caused by the biallelic mutation of MYBPC3 and MYH7].

Zhang YH, Li XY, Song BR, Wang YL, Zhang JR, Ren YL. Zhang YH, et al. Zhonghua Xin Xue Guan Bing Za Zhi. 2023 Nov 24;51(11):1160-1165. doi: 10.3760/cma.j.cn112148-20230929-00200. Zhonghua Xin Xue Guan Bing Za Zhi. 2023. PMID: 37963751 Chinese.

5

A novel heterozygous missense MYH7 mutation potentially causes an autosomal dominant form of myosin storage myopathy with dilated cardiomyopathy.

Naderi N, Mohsen-Pour N, Nilipour Y, Pourirahim M, Maleki M, Kalayinia S. Naderi N, et al. BMC Cardiovasc Disord. 2023 Oct 4;23(1):487. doi: 10.1186/s12872-023-03538-8. BMC Cardiovasc Disord. 2023. PMID: 37794383 Free PMC article.

6

Same MYH7 gene mutation but different phenotypes of cardiomyopathy in one family.

Liu T, Yao Y, Kang Y, Zhang Q. Liu T, et al. Kaohsiung J Med Sci. 2023 Oct;39(10):1052-1053. doi: 10.1002/kjm2.12741. Epub 2023 Aug 24. Kaohsiung J Med Sci. 2023. PMID: 37615266 Free article. No abstract available.

7

Penetrance and Prognosis of MYH7 Variant-Associated Cardiomyopathies: Results From a Dutch Multicenter Cohort Study.

Jansen M, de Brouwer R, Hassanzada F, Schoemaker AE, Schmidt AF, Kooijman-Reumerman MD, Bracun V, Slieker MG, Dooijes D, Vermeer AMC, Wilde AAM, Amin AS, Lekanne Deprez RH, Herkert JC, Christiaans I, de Boer RA, Jongbloed JDH, van Tintelen JP, Asselbergs FW, Baas AF. Jansen M, et al. JACC Heart Fail. 2024 Jan;12(1):134-147. doi: 10.1016/j.jchf.2023.07.007. Epub 2023 Aug 9. JACC Heart Fail. 2024. PMID: 37565978

8

Long-Term Prevalence of Systolic Dysfunction in MYBPC3 Versus MYH7-Related Hypertrophic Cardiomyopathy.

Beltrami M, Fedele E, Fumagalli C, Mazzarotto F, Girolami F, Ferrantini C, Coppini R, Tofani L, Bertaccini B, Poggesi C, Olivotto I. Beltrami M, et al. Circ Genom Precis Med. 2023 Aug;16(4):363-371. doi: 10.1161/CIRCGEN.122.003832. Epub 2023 Jul 6. Circ Genom Precis Med. 2023. PMID: 37409452 Review.

9

[Recent research on childhood hypertrophic cardiomyopathy caused by MYH7 gene mutations].

Zheng K, Liu L, Zhang YQ. Zheng K, et al. Zhongguo Dang Dai Er Ke Za Zhi. 2023 Apr 15;25(4):425-430. doi: 10.7499/j.issn.1008-8830.2211044. Zhongguo Dang Dai Er Ke Za Zhi. 2023. PMID: 37073850 Free PMC article. Chinese.

10

End-stage Hypertrophic Cardiomyopathy with Advanced Heart Failure in Patients Carrying MYH7 R453 Variants: A Case Series.

Naito S, Higo S, Kameda S, Ogawa S, Tabata T, Akazawa Y, Nakamura D, Nakamoto K, Sera F, Kuramoto Y, Asano Y, Hikoso S, Miyagawa S, Sakata Y. Naito S, et al. Intern Med. 2023 Nov 1;62(21):3167-3173. doi: 10.2169/internalmedicine.1497-22. Epub 2023 Mar 22. Intern Med. 2023. PMID: 36948619 Free PMC article.

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