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Year Number of Results
2013 1
2014 2
2016 1
2017 1
2018 2
2019 2
2020 2
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Page 1
Prevalence and Phenotypic Correlations of Calmodulinopathy-Causative CALM1-3 Variants Detected in a Multicenter Molecular Autopsy Cohort of Sudden Unexplained Death Victims.
Clemens DJ, Gray B, Bagnall RD, Tester DJ, Giudicessi JR, Maleszewski JJ, Crotti L, Schwartz PJ, Matthews E, Semsarian C, Behr ER, Ackerman MJ. Clemens DJ, et al. Circ Genom Precis Med. 2020 Dec;13(6):e003032. doi: 10.1161/CIRCGEN.120.003032. Epub 2020 Nov 15. Circ Genom Precis Med. 2020. PMID: 33191766 Free PMC article. No abstract available.
Triadin Knockout Syndrome Is Absent in a Multi-Center Molecular Autopsy Cohort of Sudden Infant Death Syndrome and Sudden Unexplained Death in the Young and Is Extremely Rare in the General Population.
Clemens DJ, Gray B, Bagnall RD, Tester DJ, Dotzler SM, Giudicessi JR, Matthews E, Semsarian C, Behr ER, Ackerman MJ. Clemens DJ, et al. Circ Genom Precis Med. 2020 Apr;13(2):e002731. doi: 10.1161/CIRCGEN.119.002731. Epub 2020 Mar 13. Circ Genom Precis Med. 2020. PMID: 32167373
Exome-Wide Rare Variant Analyses in Sudden Infant Death Syndrome.
Tester DJ, Wong LCH, Chanana P, Gray B, Jaye A, Evans JM, Evans M, Fleming P, Jeffrey I, Cohen M, Tfelt-Hansen J, Simpson MA, Behr ER, Ackerman MJ. Tester DJ, et al. J Pediatr. 2018 Dec;203:423-428.e11. doi: 10.1016/j.jpeds.2018.08.011. Epub 2018 Sep 26. J Pediatr. 2018. PMID: 30268395 Free PMC article.
Cardiac Genetic Predisposition in Sudden Infant Death Syndrome.
Tester DJ, Wong LCH, Chanana P, Jaye A, Evans JM, FitzPatrick DR, Evans MJ, Fleming P, Jeffrey I, Cohen MC, Tfelt-Hansen J, Simpson MA, Behr ER, Ackerman MJ. Tester DJ, et al. J Am Coll Cardiol. 2018 Mar 20;71(11):1217-1227. doi: 10.1016/j.jacc.2018.01.030. J Am Coll Cardiol. 2018. PMID: 29544605 Free article.
Sudden infant death syndrome and inherited cardiac conditions.
Baruteau AE, Tester DJ, Kapplinger JD, Ackerman MJ, Behr ER. Baruteau AE, et al. Nat Rev Cardiol. 2017 Dec;14(12):715-726. doi: 10.1038/nrcardio.2017.129. Epub 2017 Sep 7. Nat Rev Cardiol. 2017. PMID: 28880023 Review.
Impact of clinical and genetic findings on the management of young patients with Brugada syndrome.
Andorin A, Behr ER, Denjoy I, Crotti L, Dagradi F, Jesel L, Sacher F, Petit B, Mabo P, Maltret A, Wong LC, Degand B, Bertaux G, Maury P, Dulac Y, Delasalle B, Gourraud JB, Babuty D, Blom NA, Schwartz PJ, Wilde AA, Probst V. Andorin A, et al. Heart Rhythm. 2016 Jun;13(6):1274-82. doi: 10.1016/j.hrthm.2016.02.013. Epub 2016 Feb 24. Heart Rhythm. 2016. PMID: 26921764
11 results