Hannu Somer
University of Helsinki(FI)Helsinki University Hospital(FI)
Publications by Year
Research Areas
Muscle Physiology and Disorders, Genetic Neurodegenerative Diseases, Mitochondrial Function and Pathology, Cardiomyopathy and Myosin Studies, Metabolism and Genetic Disorders
Most-Cited Works
- → LDL Receptor-Related Protein 5 (LRP5) Affects Bone Accrual and Eye Development(2001)2,234 cited
- → Human mitochondrial DNA deletions associated with mutations in the gene encoding Twinkle, a phage T7 gene 4-like protein localized in mitochondria(2001)880 cited
- → Post-translational disruption of dystroglycan–ligand interactions in congenital muscular dystrophies(2002)793 cited
- → Parkinsonism, premature menopause, and mitochondrial DNA polymerase γ mutations: clinical and molecular genetic study(2004)541 cited
- LOW PREVALENCE OF HUNTINGTONS-DISEASE IN FINLAND(1900)
- Osteoporosis-pseudoglioma syndrome, a disorder affecting skeletal strength and vision, is assigned to chromosome region 11q12-13.(1996)
- → Multiple deletions of mitochondrial DNA in several tissues of a patient with severe retarded depression and familial progressive external ophthalmoplegia.(1992)242 cited