4.5 Article

Differential methylation of lncRNA KCNQ1OT1 promoter polymorphism was associated with symptomatic cardiac long QT

Related references

Note: Only part of the references are listed.
Article Biochemistry & Molecular Biology

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

Hideki Itoh et al.

EUROPEAN JOURNAL OF HUMAN GENETICS (2016)

Article Cell Biology

KCNQ1 gene variants in the risk for type 2 diabetes and impaired renal function in the Spanish Renastur cohort

Cristina Riobello et al.

MOLECULAR AND CELLULAR ENDOCRINOLOGY (2016)

Article Cardiac & Cardiovascular Systems

Analysis for Genetic Modifiers of Disease Severity in Patients With Long-QT Syndrome Type 2

Iris C. R. M. Kolder et al.

CIRCULATION-CARDIOVASCULAR GENETICS (2015)

Article Cardiac & Cardiovascular Systems

Analysis for Genetic Modifiers of Disease Severity in Patients With Long-QT Syndrome Type 2

Iris C. R. M. Kolder et al.

CIRCULATION-CARDIOVASCULAR GENETICS (2015)

Article Cardiac & Cardiovascular Systems

Non Optical Semi-Conductor Next Generation Sequencing of the Main Cardiac QT-Interval Duration Genes in Pooled DNA Samples

Juan Gomez et al.

JOURNAL OF CARDIOVASCULAR TRANSLATIONAL RESEARCH (2014)

Article Cardiac & Cardiovascular Systems

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

Sabine Duchatelet et al.

CIRCULATION-CARDIOVASCULAR GENETICS (2013)

Article Biochemistry & Molecular Biology

Mild Beckwith-Wiedemann and severe long-QT syndrome due to deletion of the imprinting center 2 on chromosome 11p

Fiorella Gurrieri et al.

EUROPEAN JOURNAL OF HUMAN GENETICS (2013)

Article Cardiac & Cardiovascular Systems

Long Noncoding RNA: a New Player of Heart Failure?

Roberto Papait et al.

JOURNAL OF CARDIOVASCULAR TRANSLATIONAL RESEARCH (2013)

Article Cardiac & Cardiovascular Systems

Long-QT Syndrome From Genetics to Management

Peter J. Schwartz et al.

CIRCULATION-ARRHYTHMIA AND ELECTROPHYSIOLOGY (2012)

Article Cardiac & Cardiovascular Systems

Prevalence of the Congenital Long-QT Syndrome

Peter J. Schwartz et al.

CIRCULATION (2009)

Article Biochemistry & Molecular Biology

Identification of a common variant at the NOS1AP locus strongly associated to QT-interval duration

Mark Eijgelsheim et al.

HUMAN MOLECULAR GENETICS (2009)

Article Genetics & Heredity

Common variants at ten loci influence QT interval duration in the QTGEN Study

Christopher Newton-Cheh et al.

NATURE GENETICS (2009)

Article Biochemistry & Molecular Biology

Kcnq1ot1/Lit1 noncoding RNA mediates transcriptional silencing by targeting to the perinucleolar region

Faizaan Mohammad et al.

MOLECULAR AND CELLULAR BIOLOGY (2008)

Article Genetics & Heredity

Variants in KCNQ1 are associated with susceptibility to type 2 diabetes mellitus

Kazuki Yasuda et al.

NATURE GENETICS (2008)

Article Cardiac & Cardiovascular Systems

Common genetic variation in KCNH2 is associated with QT interval duration -: The framingham heart study

Christopher Newton-Cheh et al.

CIRCULATION (2007)

Article Cardiac & Cardiovascular Systems

Diagnostic miscues in congenital long-QT syndrome

Nathaniel W. Taggart et al.

CIRCULATION (2007)

Article Developmental Biology

Epigenetic dynamics of the Kcnq1 imprinted domain in the early embryo

Annabelle Lewis et al.

DEVELOPMENT (2006)

Article Biochemistry & Molecular Biology

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

L Gouas et al.

EUROPEAN JOURNAL OF HUMAN GENETICS (2005)

Article Medicine, General & Internal

Risk stratification in the long-QT syndrome

SG Priori et al.

NEW ENGLAND JOURNAL OF MEDICINE (2003)

Article Biochemistry & Molecular Biology

A differentially methylated region within the gene Kcnq1 functions as an imprinted promoter and silencer

D Mancini-DiNardo et al.

HUMAN MOLECULAR GENETICS (2003)

Article Cardiac & Cardiovascular Systems

Spectrum of mutations in long-QT syndrome genes KVLQT1, HERG, SCN5A, KCNE1, and KCNE2

I Splawski et al.

CIRCULATION (2000)