Sven Asger Sørensen
University of Oklahoma(US)
Publications by Year
Research Areas
Genetic Neurodegenerative Diseases, Mitochondrial Function and Pathology, Neurofibromatosis and Schwannoma Cases, Neurological disorders and treatments, Hereditary Neurological Disorders
Most-Cited Works
- → Mutations in the endosomal ESCRTIII-complex subunit CHMP2B in frontotemporal dementia(2005)809 cited
- → Long-Term Follow-up of von Recklinghausen Neurofibromatosis(1986)624 cited
- → Familial occurrence of migraine without aura and migraine with aura(1993)106 cited
- → Trinucleotide repeat elongation in the Huntingtin gene in Huntington Disease patients from 71 Danish families(1993)87 cited
- → Reduction in mitochondrial DNA copy number in peripheral leukocytes after onset of Huntington's disease(2014)64 cited
- → Osteopenia: a common aspect of Fabry disease. Predictors of bone mineral density(2007)56 cited
- → Multiple founder effects in spinal and bulbar muscular atrophy (SBMA, Kennedy disease) around the world(2001)51 cited
- → Platelet serotonin transporters and the transporter gene in control subjects, unipolar patients and bipolar patients(2001)45 cited
- → A Study of Psychiatric Morbidity in Patients with Huntington's Disease, Their Relatives, and Controls(1993)43 cited
- → Clinical characteristics and quality of life, depression, and anxiety in adults with neurofibromatosis type 1: A nationwide study(2020)41 cited