M. Pedrazzini

发表

JAK2 Exon 14 Skipping in Patients with Primary Myelofibrosis: A Minor Splice Variant Modulated by the JAK2-V617F Allele Burden

M. Zorzetto, G. Barosi, P. Catarsi, 2015, PloS one.

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

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

KCNH2-K897T Is a Genetic Modifier of Latent Congenital Long-QT Syndrome

Dan M Roden, Alessandro Vicentini, Lia Crotti, 2005, Circulation.

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 .

MTMR4 SNVs modulate ion channel degradation and clinical severity in congenital long QT syndrome: insights in the mechanism of action of protective modifier genes

P. Sham, P. Schwartz, H. Tse, 2020, Cardiovascular research.

Running title: Genome-wide association study in long QT syndrome

T. Werge, P. Ellinor, S. Priori, 2020 .

Calmodulin Mutations Associated With Recurrent Cardiac Arrest in Infants

Thomas Meitinger, Peter J. Schwartz, Walter J. Chazin, 2013, Circulation.

Malignant Perinatal Variant of Long-QT Syndrome Caused by a Profoundly Dysfunctional Cardiac Sodium Channel

P. Schwartz, W. Shimizu, T. Ikeda, 2008, Circulation. Arrhythmia and electrophysiology.

Spectrum of Rare and Common Genetic Variants in Arrhythmogenic Cardiomyopathy Patients

V. Novelli, M. Pedrazzini, S. Mushtaq, 2022, Biomolecules.

Acute Myocarditis Associated With Desmosomal Gene Variants.

A. Keren, L. Cooper, A. Mazzanti, 2022, JACC. Heart failure.

Mutation location and IKs regulation in the arrhythmic risk of long QT syndrome type 1: the importance of the KCNQ1 S6 region.

P. Schwartz, P. Brink, P. Volders, 2021, European heart journal.

Exercise Training-Induced Repolarization Abnormalities Masquerading as Congenital Long QT Syndrome

P. Schwartz, M. Pedrazzini, L. Crotti, 2020, Circulation.

Long QT syndrome with cardiac arrest and transient short QT due to a novel KCNH2 mutation causing both loss and gain of function

P. Schwartz, A. George, M. Pedrazzini, 2005 .

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.

Common KCNH2 Polymorphism (K897T) as a genetic modifier of congenital long QT syndrome

D. Roden, P. Schwartz, Ping Yang, 2005 .

Oxidized LDL‐dependent pathway as new pathogenic trigger in arrhythmogenic cardiomyopathy

D. Andreini, W. Birchmeier, A. Dello Russo, 2021, EMBO molecular medicine.

Estimating the Posttest Probability of Long QT Syndrome Diagnosis for Rare KCNH2 Variants

D. Roden, P. Schwartz, W. Shimizu, 2021, Circulation. Genomic and precision medicine.

Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome

T. Werge, P. Ellinor, S. Priori, 2020, Circulation.

Prevalence of the Congenital Long-QT Syndrome

Fabio Mosca, Peter J. Schwartz, Marco Stramba-Badiale, 2009, Circulation.

A KCNH2 branch point mutation causing aberrant splicing contributes to an explanation of genotype-negative long QT syndrome.

P. Schwartz, A. George, F. Pagani, 2009, Heart rhythm.

Abstract 1778: Electrocardiographic and Genetic Screening for Long QT Syndrome: Results from a Prospective Study on 44,596 Neonates

P. Schwartz, P. Salice, M. Pedrazzini, 2007 .

Vagal reflexes following an exercise stress test: a simple clinical tool for gene-specific risk stratification in the long QT syndrome.

P. Schwartz, M. L. La Rovere, P. Brink, 2012, Journal of the American College of Cardiology.

Cardiac potassium channel dysfunction in sudden infant death syndrome.

Dan M Roden, Carlos G Vanoye, Lia Crotti, 2007, Journal of molecular and cellular cardiology.

Prevalence of Long-QT Syndrome Gene Variants in Sudden Infant Death Syndrome

Peter J. Schwartz, Alfred L. George, Lia Crotti, 2007, Circulation.

Cardiac Sodium Channel Dysfunction in Sudden Infant Death Syndrome

P. Schwartz, A. George, M. Pedrazzini, 2007, Circulation.

PREDESTINATION: PRimary vEntricular fibrillation and suDden dEath during a firST myocardIal iNfArcTION: Genetic basis

P. Schwartz, M. Pedrazzini, L. Crotti, 2013 .

Gene symbol: KCNQ1.

P. Schwartz, M. Pedrazzini, L. Crotti, 2007, Human genetics.

How many cases of sudden infant death syndrome are due to the long QT syndrome

P. Schwartz, M. Pedrazzini, L. Crotti, 2005 .

Transethnic genome-wide association study provides insights in the genetic architecture and heritability of long QT syndrome Running title: Genome-wide association study in long QT syndrome

T. Werge, P. Ellinor, S. Priori, 2020 .