K. Ricker

Myotonic Dystrophy Type 2 Caused by a CCTG Expansion in Intron 1 of <i>ZNF9</i>

Christina L. Liquori, K. Ricker, Melinda L. Moseley et al. · Science · 2001 · 1.2K citations

Life Sciences, Genetics, Molecular Genetics +9

The Skeletal Muscle Chloride Channel in Dominant and Recessive Human Myotonia

Manuela C. Koch, Klaus Steinmeyer, C Lorenz et al. · Science · 1992 · 712 citations

Life Sciences, Genetics, Molecular Genetics +17

Myotonic dystrophy type 2

John Day, K. Ricker, Jennifer F. Jacobsen et al. · Neurology · 2003 · 462 citations

Life Sciences, Genetics, Molecular Genetics +12

Proximal myotonic myopathy

K. Ricker, Manuela C. Koch, F. Lehmann‐Horn et al. · Neurology · 1994 · 254 citations

Medicine, Neurology, Human Genetics +9

Adynamia episodica hereditaria with myotonia: A non‐inactivating sodium current and the effect of extracellular pH

Frank Lehmann‐Horn, G. Küther, K. Ricker et al. · Muscle & Nerve · 1987 · 239 citations · Full text

Life Sciences, Neurology, Physiology +16