Jess Tyson

IsK and KvLQT1: Mutation in Either of the Two Subunits of the Slow Component of the Delayed Rectifier Potassium Channel Can Cause Jervell and Lange-Nielsen Syndrome

Jess Tyson, S. Bellman, J F Taylor et al. · Human Molecular Genetics · 1997 · 313 citations · Full text

Life Sciences, Cardiology, Genetics +17

Hereditary demyelinating neuropathy of infancy. A genetically complex syndrome

Jess Tyson · Brain · 1997 · 140 citations · Full text

Medicine, Genetics, Neurology +17

Obesity, starch digestion and amylase: association between copy number variants at human salivary (AMY1) and pancreatic (AMY2) amylase genes

Danielle Carpenter, Sunil Dhar, L. M. Mitchell et al. · Human Molecular Genetics · 2015 · 136 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

Hemifacial microsomia: progress in understanding the genetic basis of a complex malformation syndrome

Daniel Kelberman, Jess Tyson, David Chandler et al. · Human Genetics · 2001 · 131 citations

Medicine, Genetics, Molecular Genetics +16

Jervell and Lange-Nielsen syndrome: A Norwegian perspective

Lisbeth Tranebj�rg, J�rn Bathen, Jess Tyson et al. · American Journal of Medical Genetics · 1999 · 87 citations

Life Sciences, Genetics, Otolaryngology +16