Qing Wang

发表

KCNE1 mutations cause Jervell and Lange-Nielsen syndrome

G. Breithardt, W. Haverkamp, J. Towbin, 1997, Nature Genetics.

Genetic basis and molecular mechanism for idiopathic ventricular fibrillation

G. Breithardt, J. Towbin, J. Brugada, 1998, Nature.

SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome

Arthur J Moss, A. Moss, J. Towbin, 1995, Cell.

Spectrum of ST-T–Wave Patterns and Repolarization Parameters in Congenital Long-QT Syndrome: ECG Findings Identify Genotypes

Wojciech Zareba, Li Zhang, Carlo Napolitano, 2000, Circulation.

New Mutations in the KVLQT 1 Potassium Channel That Cause Long-QT Syndrome

S. Priori, A. Moss, P. Schwartz, 1998 .

Identification of a new SCN5A mutation, D1840G, associated with the long QT syndrome

B. Kerem, J. Blangero, J. Towbin, 1998, Human mutation.

Identification and Molecular Characterization of a de novo Supernumerary Ring Chromosome 18 in a Patient with Klippel‐Trenaunay Syndrome

S. Schwartz, D. Driscoll, Qing Wang, 2004, Annals of human genetics.

Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias

G. Landes, A. Moss, P. Schwartz, 1996, Nature Genetics.

The IPL gene on chromosome 11p15.5 is imprinted in humans and mice and is similar to TDAG51, implicated in Fas expression and apoptosis.

B. Tycko, C. Walsh, Q. Wang, 1997, Human molecular genetics.

Multiple mechanisms of Na+ channel--linked long-QT syndrome.

P. Schwartz, A. Brown, A. Brown, 1996, Circulation research.

Genomic organization of the human SCN5A gene encoding the cardiac sodium channel.

Z. Li, M. Keating, Q. Wang, 1996, Genomics.

Cardiac sodium channel mutations in patients with long QT syndrome, an inherited cardiac arrhythmia.

S. Priori, P. Schwartz, G. Vincent, 1995, Human molecular genetics.

Genetic basis and molecular mechanism for idiopathic ventricular fibrillation

G. Breithardt, J. Towbin, J. Brugada, 1998, Nature.