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Genealogy and clinical course of catecholaminergic polymorphic ventricular tachycardia caused by the ryanodine receptor type 2 P2328S mutation.
PLoS One. 2020 Dec 14;15(12):e0243649. doi: 10.1371/journal.pone.0243649. eCollection 2020.
PLoS One. 2020.
PMID: 33315912
Free PMC article.
The genetics underlying idiopathic ventricular fibrillation: A special role for catecholaminergic polymorphic ventricular tachycardia?
Leinonen JT, Crotti L, Djupsjöbacka A, Castelletti S, Junna N, Ghidoni A, Tuiskula AM, Spazzolini C, Dagradi F, Viitasalo M, Kontula K, Kotta MC, Widén E, Swan H, Schwartz PJ.
Leinonen JT, et al. Among authors: tuiskula am.
Int J Cardiol. 2018 Jan 1;250:139-145. doi: 10.1016/j.ijcard.2017.10.016. Epub 2017 Oct 5.
Int J Cardiol. 2018.
PMID: 29032884
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Clinical and molecular genetic risk determinants in adult long QT syndrome type 1 and 2 patients : Koponen et al. Follow-up of adult LQTS patients.
Koponen M, Havulinna AS, Marjamaa A, Tuiskula AM, Salomaa V, Laitinen-Forsblom PJ, Piippo K, Toivonen L, Kontula K, Viitasalo M, Swan H.
Koponen M, et al. Among authors: tuiskula am.
BMC Med Genet. 2018 Apr 5;19(1):56. doi: 10.1186/s12881-018-0574-0.
BMC Med Genet. 2018.
PMID: 29622001
Free PMC article.
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Effects of β-blockers on ventricular repolarization documented by 24-hour electrocardiography in long QT syndrome type 2.
Koponen M, Marjamaa A, Väänänen H, Tuiskula AM, Kontula K, Swan H, Viitasalo M.
Koponen M, et al. Among authors: tuiskula am.
Heart Rhythm. 2022 Sep;19(9):1491-1498. doi: 10.1016/j.hrthm.2022.04.028. Epub 2022 May 4.
Heart Rhythm. 2022.
PMID: 35525424
Free article.
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Is Symptomatic Long QT Syndrome Associated with Depression in Women and Men?
Wesołowska K, Elovainio M, Koponen M, Tuiskula AM, Hintsanen M, Keltikangas-Järvinen L, Määttänen I, Swan H, Hintsa T.
Wesołowska K, et al. Among authors: tuiskula am.
J Genet Couns. 2017 Jun;26(3):491-500. doi: 10.1007/s10897-016-0004-4. Epub 2016 Aug 23.
J Genet Couns. 2017.
PMID: 27553078
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An actionable KCNH2 Long QT Syndrome variant detected by sequence and haplotype analysis in a population research cohort.
Kerr SM, Klaric L, Halachev M, Hayward C, Boutin TS, Meynert AM, Semple CA, Tuiskula AM, Swan H, Santoyo-Lopez J, Vitart V, Haley C, Dean J, Miedzybrodzka Z, Aitman TJ, Wilson JF.
Kerr SM, et al. Among authors: tuiskula am.
Sci Rep. 2019 Jul 29;9(1):10964. doi: 10.1038/s41598-019-47436-6.
Sci Rep. 2019.
PMID: 31358886
Free PMC article.
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Replicated evidence for aminoacylase 3 and nephrin gene variations to predict antihypertensive drug responses.
Rimpelä JM, Kontula KK, Fyhrquist F, Donner KM, Tuiskula AM, Sarin AP, Mohney RP, Stirdivant SM, Hiltunen TP.
Rimpelä JM, et al. Among authors: tuiskula am.
Pharmacogenomics. 2017 Apr;18(5):445-458. doi: 10.2217/pgs-2016-0204. Epub 2017 Mar 29.
Pharmacogenomics. 2017.
PMID: 28353407
Free article.
Clinical Trial.
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