Human Genome Epidemiology Literature Finder
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Records 1 - 8 (of 8 Records) |
| Query Trace: Cardiomyopathies and RYR2[original query] |
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| Genetic investigations of sudden unexpected deaths in infancy using next-generation sequencing of 100 genes associated with cardiac diseases. European journal of human genetics : EJHG 2015 Sep . Hertz Christin Loeth, Christiansen Sofie Lindgren, Larsen Maiken Kudahl, Dahl Morten, Ferrero-Miliani Laura, Weeke Peter Ejvind, Pedersen Oluf, Hansen Torben, Grarup Niels, Ottesen Gyda Lolk, Frank-Hansen Rune, Banner Jytte, Morling Nie |
| Identification of pathogenic variants in genes related to channelopathy and cardiomyopathy in Korean sudden cardiac arrest survivors. Journal of human genetics 2017 Jun 62 (6): 615-620. Song Ju Sun, Kang Jong-Sun, Kim Young-Eun, Park Seung-Jung, Park Kyoung-Min, Huh June, Kim June Soo, Cho Hana, Ki Chang-Seok, On Young Ke |
| The genetics underlying idiopathic ventricular fibrillation: A special role for catecholaminergic polymorphic ventricular tachycardia? International journal of cardiology 2017 10 250 139-145. Leinonen Jaakko T, Crotti Lia, Djupsjöbacka Aurora, Castelletti Silvia, Junna Nella, Ghidoni Alice, Tuiskula Annukka M, Spazzolini Carla, Dagradi Federica, Viitasalo Matti, Kontula Kimmo, Kotta Maria-Christina, Widén Elisabeth, Swan Heikki, Schwartz Peter |
| Genetic basis of channelopathies and cardiomyopathies in Hong Kong Chinese patients: a 10-year regional laboratory experience. Hong Kong medical journal = Xianggang yi xue za zhi 2018 3 24 (4): 340-349. Mak C M, Chen S Pl, Mok N S, Siu W K, Lee H Hc, Ching C K, Tsui P T, Fong N C, Yuen Y P, Poon W T, Law C Y, Chong Y K, Chan Y W, Yung T C, Fan K Yy, Lam C |
| Targeted panel sequencing in adult patients with left ventricular non-compaction reveals a large genetic heterogeneity. Clinical genetics 2018 11 95 (3): 356-367. Richard Pascale, Ader Flavie, Roux Maguelonne, Donal Erwan, Eicher Jean-Christophe, Aoutil Nadia, Huttin Olivier, Selton-Suty Christine, Coisne Damien, Jondeau Guillaume, Damy Thibaud, Mansencal Nicolas, Casalta Anne-Claire, Michel Nicolas, Haentjens Julie, Faivre Laurence, Lavoute Cecile, Nguyen Karine, Tregouët David-Alexandre, Habib Gilbert, Charron Philip |
| Systematic large-scale assessment of the genetic architecture of left ventricular noncompaction reveals diverse etiologies. Genetics in medicine : official journal of the American College of Medical Genetics 2021 Jan . Mazzarotto Francesco, Hawley Megan H, Beltrami Matteo, Beekman Leander, de Marvao Antonio, McGurk Kathryn A, Statton Ben, Boschi Beatrice, Girolami Francesca, Roberts Angharad M, Lodder Elisabeth M, Allouba Mona, Romeih Soha, Aguib Yasmine, Baksi A John, Pantazis Antonis, Prasad Sanjay K, Cerbai Elisabetta, Yacoub Magdi H, O'Regan Declan P, Cook Stuart A, Ware James S, Funke Birgit, Olivotto Iacopo, Bezzina Connie R, Barton Paul J R, Walsh Rod |
| Genetic screening of relatives of decedents experiencing sudden unexpected death: medical examiner's office referrals to a multi-disciplinary cardiogenetics program. Journal of community genetics 2022 10 13 (6): 629-639. Siskind Tamar, Williams Nori, Sebastin Monisha, Marion Robert, McDonald Thomas V, Walsh Christine, Sampson Barbara, Tang Yingying, Clark Bradley |
| Genetic Variants Associated With Sudden Cardiac Death in Victims With Single Vessel Coronary Artery Disease and Left Ventricular Hypertrophy With or Without Fibrosis. Frontiers in cardiovascular medicine 2021 8 755062. Vähätalo Juha H, Holmström Lauri T A, Pylkäs Katri, Skarp Sini, Porvari Katja, Pakanen Lasse, Kaikkonen Kari S, Perkiömäki Juha S, Kerkelä Risto, Huikuri Heikki V, Myerburg Robert J, Junttila M Juha |
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