Kati Donner

FinnGen provides genetic insights from a well-phenotyped isolated population

Mitja Kurki, Juha Karjalainen, Priit Palta et al. · Nature · 2023 · 3.8K citations · Full text

FinnGen: Unique genetic insights from combining isolated population and national health register data

Mitja Kurki, Juha Karjalainen, Priit Palta et al. · 2022 · 412 citations · Full text

Genetic Testing, Genetics, Genetic Epidemiology +21

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

Mutations in the β-tropomyosin (TPM2) gene – a rare cause of nemaline myopathy

Kati Donner, Miina Ollikainen, Maaret Ridanpää et al. · Neuromuscular Disorders · 2002 · 225 citations

Rare Cause, Medicine, Molecular Biology +5