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Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1902 1
1958 1
1961 1
1963 1
1964 1
1965 1
1966 1
1967 1
1968 2
1969 1
1971 2
1973 4
1974 1
1975 2
1976 3
1977 1
1979 3
1980 1
1981 2
1982 3
1983 2
1985 3
1986 1
1987 5
1988 1
1989 6
1990 7
1991 2
1992 8
1993 5
1994 5
1995 6
1996 4
1997 5
1998 3
1999 6
2000 8
2001 6
2002 4
2003 10
2004 5
2005 7
2006 3
2007 6
2008 2
2009 3
2010 3
2011 3
2012 2
2013 4
2014 1
2015 1
2016 1
2017 1
2018 1
2019 2
2021 1
2022 1
2024 0

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Article type

Publication date

PubMed (OMIM) for id: 4625

172 results

Results by year

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Page 1
Oligogenic inheritance of a human heart disease involving a genetic modifier.
Gifford CA, Ranade SS, Samarakoon R, Salunga HT, de Soysa TY, Huang Y, Zhou P, Elfenbein A, Wyman SK, Bui YK, Cordes Metzler KR, Ursell P, Ivey KN, Srivastava D. Gifford CA, et al. Science. 2019 May 31;364(6443):865-870. doi: 10.1126/science.aat5056. Epub 2019 May 30. Science. 2019. PMID: 31147515 Free PMC article.
Recessive MYH7-related myopathy in two families.
Beecroft SJ, van de Locht M, de Winter JM, Ottenheijm CA, Sewry CA, Mohammed S, Ryan MM, Woodcock IR, Sanders L, Gooding R, Davis MR, Oates EC, Laing NG, Ravenscroft G, McLean CA, Jungbluth H. Beecroft SJ, et al. Neuromuscul Disord. 2019 Jun;29(6):456-467. doi: 10.1016/j.nmd.2019.04.002. Epub 2019 Apr 12. Neuromuscul Disord. 2019. PMID: 31130376
Lack of evidence for a causal role of CALR3 in monogenic cardiomyopathy.
Verhagen JMA, Veldman JH, van der Zwaag PA, von der Thüsen JH, Brosens E, Christiaans I, Dooijes D, Helderman-van den Enden ATJM, Lekanne Deprez RH, Michels M, van Mil AM, Oldenburg RA, van der Smagt JJ, van den Wijngaard A, Wessels MW, Hofstra RMW, van Slegtenhorst MA, Jongbloed JDH, van de Laar IMBH. Verhagen JMA, et al. Eur J Hum Genet. 2018 Nov;26(11):1603-1610. doi: 10.1038/s41431-018-0208-1. Epub 2018 Jul 9. Eur J Hum Genet. 2018. PMID: 29988065 Free PMC article.
Abnormal contractility in human heart myofibrils from patients with dilated cardiomyopathy due to mutations in TTN and contractile protein genes.
Vikhorev PG, Smoktunowicz N, Munster AB, Copeland O, Kostin S, Montgiraud C, Messer AE, Toliat MR, Li A, Dos Remedios CG, Lal S, Blair CA, Campbell KS, Guglin M, Richter M, Knöll R, Marston SB. Vikhorev PG, et al. Sci Rep. 2017 Nov 1;7(1):14829. doi: 10.1038/s41598-017-13675-8. Sci Rep. 2017. PMID: 29093449 Free PMC article.
172 results