Duangrurdee Wattanasirichaigoon

Genotype-Phenotype Correlation in the Long-QT Syndrome

Peter J. Schwartz, Silvia G. Priori, Carla Spazzolini et al. · Circulation · 2001 · 1.8K citations

Life Sciences, Cardiology, Genetics +10

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

Duangrurdee Wattanasirichaigoon, Hans H. Goebel, Matthew C. J. Wilce et al. · Nature Genetics · 1999 · 401 citations

Medicine, Genetics, Molecular Genetics +13

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 · 332 citations

Medicine, Genetics, Molecular Genetics +11

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

Life Sciences, Cardiology, Genetics +17

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 · 135 citations · Full text

Life Sciences, Genetics, Molecular Genetics +8