Postmortem genetic screening of SNPs in RyR2 gene in sudden unexplained nocturnal death syndrome in the southern Chinese Han population

Mutations in the Cardiac Ryanodine Receptor Gene ( <i>hRyR2</i> ) Underlie Catecholaminergic Polymorphic Ventricular Tachycardia

Silvia G. Priori, Carlo Napolitano, Natascia Tiso et al. · Circulation · 2001 · 1.4K citations · Full text

Medicine, Cardiology, Genetics +16

Synonymous mutations in the human dopamine receptor D2 (DRD2) affect mRNA stability and synthesis of the receptor

Jubao Duan · Human Molecular Genetics · 2003 · 924 citations

Life Sciences, Genetics, Molecular Genetics +13

Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2)

Natascia Tiso · Human Molecular Genetics · 2001 · 806 citations · Full text

Medicine, Genetics, Molecular Genetics +17

FKBP12.6 Deficiency and Defective Calcium Release Channel (Ryanodine Receptor) Function Linked to Exercise-Induced Sudden Cardiac Death

Xander H.T. Wehrens, Stephan E. Lehnart, Fannie Huang et al. · Cell · 2003 · 755 citations · Full text

Medicine, Cardiology, Physiology +17

Arrhythmogenic Marker for the Sudden Unexplained Death Syndrome in Thai Men

Koonlawee Nademanee, Gumpanart Veerakul, S Nimmannit et al. · Circulation · 1997 · 537 citations

Medicine, Cardiology, Internal Medicine +15