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1
Genetics of syndromic and non-syndromic mitral valve prolapse
Genetics of syndromic and non-syndromic mitral valve prolapse
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Genetics of syndromic and non-syndromic mitral valve prolapse

Le Tourneau, Thierry ; Mérot, Jean ; Rimbert, Antoine ; Le Scouarnec, Solena ; Probst, Vincent ; Le Marec, Hervé ; Levine, Robert A ; Schott, Jean-Jacques

Heart (British Cardiac Society), 2018-06, Vol.104 (12), p.978-984 [Periódico revisado por pares]

England: BMJ Publishing Group LTD

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2
SCN5A Mutations and the Role of Genetic Background in the Pathophysiology of Brugada Syndrome
SCN5A Mutations and the Role of Genetic Background in the Pathophysiology of Brugada Syndrome
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SCN5A Mutations and the Role of Genetic Background in the Pathophysiology of Brugada Syndrome

Probst, Vincent ; Wilde, Arthur A.M ; Barc, Julien ; Sacher, Frederic ; Babuty, Dominique ; Mabo, Philippe ; Mansourati, Jacques ; Le Scouarnec, Solena ; Kyndt, Florence ; Le Caignec, Cedric ; Guicheney, Pascale ; Gouas, Laetitia ; Albuisson, Juliette ; Meregalli, Paola G ; Le Marec, Herve ; Tan, Hanno L ; Schott, Jean-Jacques

Circulation. Cardiovascular genetics, 2009-12, Vol.2 (6), p.552-557 [Periódico revisado por pares]

United States: American Heart Association, Inc

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3
TRPM4 non-selective cation channel variants in long QT syndrome
TRPM4 non-selective cation channel variants in long QT syndrome
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TRPM4 non-selective cation channel variants in long QT syndrome

Hof, Thomas ; Liu, Hui ; Sallé, Laurent ; Schott, Jean-Jacques ; Ducreux, Corinne ; Millat, Gilles ; Chevalier, Philippe ; Probst, Vincent ; Guinamard, Romain ; Bouvagnet, Patrice

BMC medical genetics, 2017-03, Vol.18 (1), p.31-31, Article 31 [Periódico revisado por pares]

England: BioMed Central Ltd

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4
Dysfunction in ankyrin-B-dependent ion channel and transporter targeting causes human sinus node disease
Dysfunction in ankyrin-B-dependent ion channel and transporter targeting causes human sinus node disease
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Dysfunction in ankyrin-B-dependent ion channel and transporter targeting causes human sinus node disease

Le Scouarnec, Solena ; Bhasin, Naina ; Vieyres, Claude ; Hund, Thomas J ; Cunha, Shane R ; Koval, Olha ; Marionneau, Celine ; Chen, Biyi ; Wu, Yuejin ; Demolombe, Sophie ; Song, Long-Sheng ; Le Marec, Hervé ; Probst, Vincent ; Schott, Jean-Jacques ; Anderson, Mark E ; Mohler, Peter J

Proceedings of the National Academy of Sciences - PNAS, 2008-10, Vol.105 (40), p.15617-15622 [Periódico revisado por pares]

United States: National Academy of Sciences

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5
Identification of a strong genetic background for progressive cardiac conduction defect by epidemiological approach
Identification of a strong genetic background for progressive cardiac conduction defect by epidemiological approach
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Identification of a strong genetic background for progressive cardiac conduction defect by epidemiological approach

Gourraud, Jean Baptiste ; Kyndt, Florence ; Fouchard, Swanny ; Rendu, Eric ; Jaafar, Philippe ; Gully, Claude ; Gacem, Karim ; Dupuis, Jean Marc ; Longueville, Aurelie ; Baron, Estelle ; Karakachoff, Matilde ; Cebron, Jean Pierre ; Chatel, Stephanie ; Schott, Jean Jacques ; Le Marec, Hervé ; Probst, Vincent

Heart (British Cardiac Society), 2012-09, Vol.98 (17), p.1305-1310 [Periódico revisado por pares]

London: BMJ Publishing Group Ltd and British Cardiovascular Society

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6
Mapping of X-Linked Myxomatous Valvular Dystrophy to Chromosome Xq28
Mapping of X-Linked Myxomatous Valvular Dystrophy to Chromosome Xq28
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Mapping of X-Linked Myxomatous Valvular Dystrophy to Chromosome Xq28

Kyndt, Florence ; Schott, Jean-Jacques ; Trochu, Jean-Noël ; Baranger, Florence ; Herbert, Odile ; Scott, Valérie ; Fressinaud, Edith ; David, Albert ; Moisan, Jean-Paul ; Bouhour, Jean-Brieuc ; Le Marec, Hervé ; Bénichou, Bernard

American journal of human genetics, 1998-03, Vol.62 (3), p.627-632 [Periódico revisado por pares]

Chicago, IL: Elsevier Inc

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7
Genetic Risk in Early Repolarization Syndrome
Genetic Risk in Early Repolarization Syndrome
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Genetic Risk in Early Repolarization Syndrome

Schott, Jean-Jacques ; Gourraud, Jean-Baptiste ; Portero, Vincent ; Le Scouarnec, Solena ; Chavernac, Pascal ; Mabo, Philippe ; Sacher, Frederic ; Haïssaguerre, Michel ; Le Marec, Herve

Journal of arrhythmia, 2011, Vol.27 (Supplement), p.SY10_3 [Periódico revisado por pares]

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8
SY10-3 Genetic Risk in Early Repolarization Syndrome
SY10-3 Genetic Risk in Early Repolarization Syndrome
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SY10-3 Genetic Risk in Early Repolarization Syndrome

Jean-Jacques Schott ; Jean-Baptiste Gourraud ; Vincent Portero ; Solena Le Scouarnec ; Pascal Chavernac ; Philippe Mabo ; Frederic Sacher ; Michel Haissaguerre ; Herve Le Marec

Journal of Arrhythmia, 2011-09, Vol.27 (suppl), p.329-329 [Periódico revisado por pares]

Japanese Heart Rhythm Society

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9
心フ-1. 家族性進行性心臓伝導障害に同定されたconnexin40遺伝子GJA5変異の機能異常
心フ-1. 家族性進行性心臓伝導障害に同定されたconnexin40遺伝子GJA5変異の機能異常
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心フ-1. 家族性進行性心臓伝導障害に同定されたconnexin40遺伝子GJA5変異の機能異常

蒔田直昌 ; 住友直方 ; 関明子 ; 萩原誠久 ; 渡部裕 ; 福原茂朋 ; 望月直樹 ; 牧山武 ; 堀江稔 ; Jean-Jacques Schott

Journal of Arrhythmia, 2009, Vol.25 (suppl), p.235-235 [Periódico revisado por pares]

日本不整脈学会

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10
Mapping of quantitative trait loci for blood pressure and cardiac mass in the rat by genome scanning of recombinant inbred strains
Mapping of quantitative trait loci for blood pressure and cardiac mass in the rat by genome scanning of recombinant inbred strains
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Mapping of quantitative trait loci for blood pressure and cardiac mass in the rat by genome scanning of recombinant inbred strains

Pravenec, M ; Gauguier, D ; Schott, J J ; Buard, J ; Kren, V ; Bila, V ; Szpirer, C ; Szpirer, J ; Wang, J M ; Huang, H

The Journal of clinical investigation, 1995-10, Vol.96 (4), p.1973-1978 [Periódico revisado por pares]

United States

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