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Shenghan Chen

Cleveland Clinic Lerner College of Medicine

4

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Genome-Wide Linkage Scan Identifies Two Novel Genetic Loci for Coronary Artery Disease: In GeneQuest Families

2014 PLOS ONE
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Protective effect of KCNH2 single nucleotide polymorphism K897T in LQTS families and identification of novel KCNQ1 and KCNH2 mutations

2008 BMC Medical Genetics
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Mutation in Nuclear Pore Component NUP155 Leads to Atrial Fibrillation and Early Sudden Cardiac Death

2008 Cell
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Genomewide linkage scan identifies a novel susceptibility locus for restless legs syndrome on chromosome 9p.

2004 American Journal of Human Genetics
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