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

Year Number of Results
2009 1
2010 1
2012 1
2013 1
2014 2
2015 3
2016 3
2017 1
2018 3
2019 2
2020 4
2021 4
2023 1
2024 0

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Page 1
De novo mutations in FLNC leading to early-onset restrictive cardiomyopathy and congenital myopathy.
Kiselev A, Vaz R, Knyazeva A, Khudiakov A, Tarnovskaya S, Liu J, Sergushichev A, Kazakov S, Frishman D, Smolina N, Pervunina T, Jorholt J, Sjoberg G, Vershinina T, Rudenko D, Arner A, Sejersen T, Lindstrand A, Kostareva A. Kiselev A, et al. Among authors: smolina n. Hum Mutat. 2018 Sep;39(9):1161-1172. doi: 10.1002/humu.23559. Epub 2018 Jun 17. Hum Mutat. 2018. PMID: 29858533
Truncating Variant in Myof Gene Is Associated With Limb-Girdle Type Muscular Dystrophy and Cardiomyopathy.
Kiselev A, Vaz R, Knyazeva A, Sergushichev A, Dmitrieva R, Khudiakov A, Jorholt J, Smolina N, Sukhareva K, Fomicheva Y, Mikhaylov E, Mitrofanova L, Predeus A, Sjoberg G, Rudenko D, Sejersen T, Lindstrand A, Kostareva A. Kiselev A, et al. Among authors: smolina n. Front Genet. 2019 Jun 26;10:608. doi: 10.3389/fgene.2019.00608. eCollection 2019. Front Genet. 2019. PMID: 31297131 Free PMC article.
Variants in the NOTCH1 gene in patients with aortic coarctation.
Freylikhman O, Tatarinova T, Smolina N, Zhuk S, Klyushina A, Kiselev A, Moiseeva O, Sjoberg G, Malashicheva A, Kostareva A. Freylikhman O, et al. Among authors: smolina n. Congenit Heart Dis. 2014 Sep-Oct;9(5):391-6. doi: 10.1111/chd.12157. Epub 2014 Jan 12. Congenit Heart Dis. 2014. PMID: 24418111
Infantile restrictive cardiomyopathy: cTnI-R170G/W impair the interplay of sarcomeric proteins and the integrity of thin filaments.
Cimiotti D, Fujita-Becker S, Möhner D, Smolina N, Budde H, Wies A, Morgenstern L, Gudkova A, Sejersen T, Sjöberg G, Mügge A, Nowaczyk MM, Reusch P, Pfitzer G, Stehle R, Schröder RR, Mannherz HG, Kostareva A, Jaquet K. Cimiotti D, et al. Among authors: smolina n. PLoS One. 2020 Mar 17;15(3):e0229227. doi: 10.1371/journal.pone.0229227. eCollection 2020. PLoS One. 2020. PMID: 32182250 Free PMC article.
24 results