M. Berthet

发表

The genetics underlying acquired long QT syndrome: impact for genetic screening.

P. Schwartz, W. Shimizu, M. Horie, 2016, European heart journal.

Arrhythmic Risk in Long-QT Syndrome Polymorphism Acting as a Protective Modifier Against KCNQ 1 Identification of a

P. Schwartz, D. Trégouët, W. Shimizu, 2013 .

C-terminal HERG mutations: the role of hypokalemia and a KCNQ1-associated mutation in cardiac event occurrence.

P. Coumel, E. Schulze-Bahr, B. Hainque, 1999, Circulation.

Association of KCNQ1, KCNE1, KCNH2 and SCN5A polymorphisms with QTc interval length in a healthy population

Beverley Balkau, Anne Forhan, Laurence Tiret, 2005, European Journal of Human Genetics.

New KCNQ1 mutations leading to haploinsufficiency in a general population; Defective trafficking of a KvLQT1 mutant.

B. Balkau, S. Demolombe, B. Hainque, 2004, Cardiovascular research.

Electrophysiological characterization of SCN5A mutations causing long QT (E1784K) and Brugada (R1512W and R1432G) syndromes.

P. Guicheney, I. Barde, I. Denjoy, 2000, Cardiovascular research.

Electrophysiological characterization of SCN 5 A mutations causing long QT ( E 1784 K ) and Brugada ( R 1512 W and R 1432 G ) syndromes

P. Guicheney, I. Barde, I. Denjoy, 2000 .

Cardiac MR Strain: A Noninvasive Biomarker of Fibrofatty Remodeling of the Left Atrial Myocardium.

K. Clément, A. Huber, P. Leprince, 2018, Radiology.

Somatostatin cells in human somatotropic adenomas

P. Pagésy, F. Peillon, M. Berthet, 2005, Virchows Archiv A.

Cell Specific Reactivation of Epicardium at the Origin of Fibro-Fatty Remodeling of the Atrial Myocardium

D. Tregouet, M. Pucéat, B. Jagla, 2019, bioRxiv.

Defective trafficking of a KvLQT1 mutant

B. Balkau, S. Demolombe, B. Hainque, 2004 .

Novel SCN5A mutations in two families with “Brugada-like” ST elevation in the inferior leads and conduction disturbances

A. Leenhardt, P. Guicheney, I. Denjoy, 2013, Journal of Interventional Cardiac Electrophysiology.

Homozygous SCN5A Mutation in Long-QT Syndrome With Functional Two-to-One Atrioventricular Block

F Extramiana, P. Guicheney, I. Denjoy, 2001, Circulation research.

Long QT syndrome in neonates

A. Bozio, P. Guicheney, I. Denjoy, 2016 .

Identification of a KCNQ1 Polymorphism Acting as a Protective Modifier Against Arrhythmic Risk in Long-QT Syndrome

P. Schwartz, D. Trégouët, W. Shimizu, 2013, Circulation. Cardiovascular genetics.

[T wave abnormalities on Holter monitoring of congenital long QT syndrome: phenotypic marker of a mutation of LQT2 (HERG)].

P. Coumel, B. Hainque, P. Guicheney, 2001, Archives des maladies du coeur et des vaisseaux.

KVLQT1 C-terminal missense mutation causes a forme fruste long-QT syndrome.

P. Coumel, C. Cruaud, P. Guicheney, 1997, Circulation.

Effect of the slow-release formulation of somatuline (BIM 23014) on estrogen-induced hyperprolactinemia and lactotroph hyperplasia in the female rat

N. Schussler, F. Peillon, C. Rauch, 1994, Neuropeptides.

Differentiation and quantification of fibrosis, fat and fatty fibrosis in human left atrial myocardium using ex vivo MRI

P. Leprince, P. Cluzel, A. Redheuil, 2018, PloS one.

Role of common and rare variants in SCN10A: results from the Brugada syndrome QRS locus gene discovery collaborative study.

R. Redon, E. Behr, D. Roden, 2015, Cardiovascular research.

An international compendium of mutations in the SCN5A-encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testing.

J. Towbin, J. Brugada, R. Brugada, 2010, Heart rhythm.

Asymmetry of parental origin in long QT syndrome: preferential maternal transmission of KCNQ1 variants linked to channel dysfunction

S. Tezenas du Montcel, W. Shimizu, E. Schulze-Bahr, 2015, European Journal of Human Genetics.

Female predominance and transmission distortion in the long-QT syndrome.

S. Priori, M. Imboden, C. Napolitano, 2006, The New England journal of medicine.

Evidence of gonadotropin-releasing hormone mRNA in the rat anterior pituitary.

P. Pagésy, F. Peillon, M. Berthet, 1992, Molecular endocrinology.

MOG1: A New Susceptibility Gene for Brugada Syndrome

A. Leenhardt, V. Probst, J. Schott, 2011, Circulation. Cardiovascular genetics.

Confirmation of associations between ion channel gene SNPs and QTc interval duration in healthy subjects

L. Tiret, B. Balkau, V. Nicaud, 2007, European Journal of Human Genetics.

Long QT syndrome in neonates: conduction disorders associated with HERG mutations and sinus bradycardia with KCNQ1 mutations.

A. Bozio, B. Hainque, P. Guicheney, 2004, Journal of the American College of Cardiology.

Heart rate influences on repolarization duration and morphology in symptomatic versus asymptomatic KCNQ1 mutation carriers.

Fabio Badilini, Philippe Coumel, Antoine Leenhardt, 2005, The American journal of cardiology.

Reactivation of the Epicardium at the Origin of Myocardial Fibro-Fatty Infiltration During the Atrial Cardiomyopathy

D. Tregouet, M. Pucéat, B. Jagla, 2020, Circulation research.

Homozygous SCN 5 A Mutation in Long-QT Syndrome With Functional Two-toOne Atrioventricular Block

P. Guicheney, I. Denjoy, B. Cauchemez, 2001 .

Exclusion of KCNE1 (IsK) as a candidate gene for Jervell and Lange-Nielsen syndrome.

P Coumel, P. Coumel, C. Petit, 1996, Journal of molecular and cellular cardiology.

Association of Serum Cholesterol Efflux Capacity With Mortality in Patients With ST-Segment Elevation Myocardial Infarction.

G. Montalescot, M. Kerneis, J. Collet, 2018, Journal of the American College of Cardiology.

Characterization and localization of an immunoreactive growth hormone-releasing hormone precursor form in normal and tumoral human anterior pituitaries.

P. Pagésy, F. Peillon, C. Rauch, 1995, Endocrinology.

A mutation in HERG associated with notched T waves in long QT syndrome.

P. Coumel, C. Cruaud, P. Guicheney, 1996, Journal of molecular and cellular cardiology.

Notched T Waves on Holter Recordings Enhance Detection of Patients With LQT2 (HERG) Mutations

L. Demay, D. Klug, I. Denjoy, 2001, Circulation.

Response to the Letter by Kattygnarath et al

A. Leenhardt, V. Probst, J. Schott, 2011 .

R231C mutation in KCNQ1 causes long QT syndrome type 1 and familial atrial fibrillation.

Michael John Ackerman, Craig T. January, Brian P. Delisle, 2011, Heart rhythm.