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Qiuyun Chen

Baylor College of Medicine

10

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2427

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Novel Roles of GATA1 in Regulation of Angiogenic Factor AGGF1 and Endothelial Cell Function

2009 Journal of Biological Chemistry
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Functional Role of Transcriptional Factor TBX5 in Pre-mRNA Splicing and Holt-Oram Syndrome via Association with SC35

2009 Journal of Biological Chemistry
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The common SCN5A mutation R1193Q causes LQTS-type electrophysiological alterations of the cardiac sodium channel

2004 Journal of Medical Genetics
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Homozygous Deletion in KVLQT1 Associated With Jervell and Lange-Nielsen Syndrome

1999 Circulation
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New Mutations in the KVLQT1 Potassium Channel That Cause Long-QT Syndrome

1998 Circulation
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Genetics, molecular mechanisms and management of long QT syndrome

1998 Annals of Medicine
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Genetic basis and molecular mechanism for idiopathic ventricular fibrillation

1998 Nature
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KCNE1 mutations cause jervell and Lange-Nielsen syndrome

1997 Nature Genetics
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Romano-Ward Long QT Syndrome: Identification of the Gene Responsible for Cardiac Arrhythmia in the First Autosomal Dominant LQT Family, the Ward Kindred • 149

1997 Pediatric Research
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