Duangrurdee Wattanasirichaigoon

Genotype-Phenotype Correlation in the Long-QT Syndrome

Peter J. Schwartz, Silvia G. Priori, Carla Spazzolini et al. · Circulation · 2001 · 1.7K citations

Mutations in the skeletal muscle α-actin gene in patients with actin myopathy and nemaline myopathy

Kristen L. Nowak, Duangrurdee Wattanasirichaigoon, Hans H. Goebel et al. · Nature Genetics · 1999 · 398 citations

Muscle Physiology, Muscle Function, Health Sciences +11

Mutations in the nebulin gene associated with autosomal recessive nemaline myopathy

Katarina Pelin, Pirta Hilpelä, Kati Donner et al. · Proceedings of the National Academy of Sciences · 1999 · 328 citations · Full text

Mutation of the Gene for <i>I</i> sK Associated With Both Jervell and Lange-Nielsen and Romano-Ward Forms of Long-QT Syndrome

Priya Duggal, Mark R. Vesely, Duangrurdee Wattanasirichaigoon et al. · Circulation · 1998 · 213 citations

De novo mutations in SMCHD1 cause Bosma arhinia microphthalmia syndrome and abrogate nasal development

Christopher T. Gordon, Shifeng Xue, Gökhan Yigit et al. · Nature Genetics · 2017 · 131 citations · Full text

Mendelian Disorder, Autoimmune Disease, Genetic Disorder +5