Anna Vihola
University of Helsinki(FI)
Publications by Year
Research Areas
Muscle Physiology and Disorders, Cardiomyopathy and Myosin Studies, Neurogenetic and Muscular Disorders Research, Genetic Neurodegenerative Diseases, RNA Research and Splicing
Most-Cited Works
- → The Kinase Domain of Titin Controls Muscle Gene Expression and Protein Turnover(2005)586 cited
- → Tibial Muscular Dystrophy Is a Titinopathy Caused by Mutations in TTN, the Gene Encoding the Giant Skeletal-Muscle Protein Titin(2002)482 cited
- → Mutations affecting the cytoplasmic functions of the co-chaperone DNAJB6 cause limb-girdle muscular dystrophy(2012)274 cited
- → Interactions with titin and myomesin target obscurin and obscurin-like 1 to the M-band – implications for hereditary myopathies(2008)193 cited
- → Recessive TTN truncating mutations define novel forms of core myopathy with heart disease(2013)189 cited
- → Secondary calpain3 deficiency in 2q-linked muscular dystrophy(2001)174 cited
- → Histopathological differences of myotonic dystrophy type 1 (DM1) and PROMM/DM2(2003)172 cited
- → Increasing Role of Titin Mutations in Neuromuscular Disorders(2016)163 cited
- → Welander distal myopathy is caused by a mutation in the RNA‐binding protein TIA1(2012)155 cited
- → Zaspopathy in a large classic late-onset distal myopathy family(2007)139 cited