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  1. Neyroud, Nathalie; Denjoy, Isabelle; Donger, Claire; Gary, Françoise; Villain, Elisabeth; Leenhardt, Antoine; Benali, Karim; Schwartz, Ketty; Coumel, Philippe; Guicheney, Pascale

    Heterozygous mutation in the pore of potassium channel gene KvLQT1 causes an apparently normal phenotype in long QT syndrome

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    Springer Science and Business Media LLC, 1998

    Published in: European Journal of Human Genetics

  2. Badilini, Fabio; Fayn, Jocelyne; Maison‐Blanche, Pierre; Leenhardt, Antoine; Forlini, Marie Claire; Denjoy, Isabelle; Coumel, Philippe; Rubel, Paul

    Quantitative Aspects of Ventricular Repolarization : Relationship Between Three‐Dimensional T Wave Loop Morphology and Scalar QT Dispersion : Relationship Between Three‐Dimensional T Wave Loop Morphology and Scalar QT Dispersion

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    Wiley, 1997

    Published in: Annals of Noninvasive Electrocardiology

  3. Leclercq, Jean-Frangois; Coumel, Philippe; Denjoy, Isabelle; Maisonblanche, Pierre; Cauchemez, Bruno; Chouty, Fabrice; Leenhardt, Antoine; Slama, Robert

    Long-term follow-up after sustained monomorphic ventricular tachycardia: Causes, pump failure, and empiric antiarrhythmic therapy that modify survival

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    Elsevier BV, 1991

    Published in: American Heart Journal

  4. Clatot, Jérôme; Ziyadeh-Isleem, Azza; Maugenre, Svetlana; Denjoy, Isabelle; Liu, Haiyan; Dilanian, Gilles; Hatem, Stéphane N.; Deschênes, Isabelle; Coulombe, Alain; Guicheney, Pascale; Neyroud, Nathalie

    Dominant-negative effect of SCN5A N-terminal mutations through the interaction of Nav1.5 α-subunits

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    Oxford University Press (OUP), 2012

    Published in: Cardiovascular Research

  5. Roux-Buisson, Nathalie; Rendu, John; Denjoy, Isabelle; Guicheney, Pascale; Goldenberg, Alice; David, Nadine; Faivre, Laurence; Barthez, Olivier; Danieli, Gian Antonio; Marty, Isabelle; Lunardi, Joel; Fauré, Julien

    Functional analysis reveals splicing mutations of the CASQ2 gene in patients with CPVT: implication for genetic counselling and clinical management

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    Hindawi Limited, 2011

    Published in: Human Mutation

  6. Morgat, Charles; Denjoy, Isabelle; Fressart, Veronique; Neyroud, Nathalie; Messali, Anne; Temmar, Yassine; Porretta, Alessandra Pia; Algalarrondo, vincent; Surget, Elodie; Leenhardt, Antoine; Extramiana, Fabrice

    Abstract 17871: Heterozygous Carriers of KCNQ1 Variants Associated With the Jervell-Lange-Nielsen Syndrome Have a Better Outcome When Compared to Other Type 1 LQTS Patients

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    Ovid Technologies (Wolters Kluwer Health), 2023

    Published in: Circulation

  7. Kato, Koichi; Isbell, Holly M.; Fressart, Véronique; Denjoy, Isabelle; Debbiche, Amal; Itoh, Hideki; Poinsot, Jacques; George, Alfred L.; Coulombe, Alain; Shea, Madeline A.; Guicheney, Pascale

    Novel CALM3 Variant Causing Calmodulinopathy With Variable Expressivity in a 4-Generation Family

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    Ovid Technologies (Wolters Kluwer Health), 2022

    Published in: Circulation: Arrhythmia and Electrophysiology

  8. Plumereau, Quentin; Theriault, Olivier; Pouliot, Valérie; Moreau, Adrien; Morel, Elodie; Fressart, Véronique; Denjoy, Isabelle; Delinière, Antoine; Bessière, Francis; Chevalier, Philippe; Gamal El-Din, Tamer M.; Chahine, Mohamed

    Novel G1481V and Q1491H SCN5A Mutations Linked to Long QT Syndrome Destabilize the Nav1.5 Inactivation State

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    Elsevier BV, 2021

    Published in: CJC Open

  9. Jourdain, Jean-Rene; Landon, Geraldine; Clero, Enora; Doroshchenko, Vladimir; Silenok, Aleksandr; Kurnosova, Irina; Butsenin, Andrei; Denjoy, Isabelle; Franck, Didier; Heuze, Jean-Pierre; Gourmelon, Patrick

    Is exposure to ionising radiation associated with childhood cardiac arrhythmia in the Russian territories contaminated by the Chernobyl fallout? A cross-sectional population-based study

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    BMJ, 2018

    Published in: BMJ Open

  10. Itoh, Hideki; Dochi, Kenichi; Shimizu, Wataru; Denjoy, Isabelle; Ohno, Seiko; Aiba, Takeshi; Kimura, Hiromi; Kato, Koichi; Fukuyama, Megumi; Hasagawa, Kanae; Schulze-Bahr, Eric; Guicheney, Pascale; Horie, Minoru

    A Common Mutation of Long QT Syndrome Type 1 in Japan

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    Japanese Circulation Society, 2015

    Published in: Circulation Journal