M Weigell-Weber
University of Zurich(CH)Kantonsspital Aarau(CH)Zentrum für Labormedizin(CH)
Publications by Year
Research Areas
Genetic Neurodegenerative Diseases, Mitochondrial Function and Pathology, Retinal Diseases and Treatments, Retinal Development and Disorders, Neurological disorders and treatments
Most-Cited Works
- → Striatal glucose metabolism and dopamine D2 receptor binding in asymptomatic gene carriers and patients with Huntington's disease(1996)320 cited
- → Mcleod syndrome: A novel mutation, predominant psychiatric manifestations, and distinct striatal imaging findings(2001)102 cited
- → DNA analysis of Huntington’s disease(1999)81 cited
- → Psychiatric symptoms and CAG expansion in Huntington's disease(1996)55 cited
- → Codons 837 and 838 in the Retinal Guanylate Cyclase Gene on Chromosome 17p: Hot Spots for Mutations in Autosomal Dominant Cone-Rod Dystrophy?(2000)35 cited
- → Genomewide Homozygosity Mapping and Molecular Analysis of a Candidate Gene Located on 22q13 (Fibulin-1) in a Previously Undescribed Vitreoretinal Dystrophy(2003)24 cited
- → Genetic heterogeneity in autosomal dominant pattern dystrophy of the retina.(1996)10 cited
- → A NOVEL COMPLEX MUTATION EVENT IN THE PERIPHERIN/RDS GENE IN A FAMILY WITH RETINAL PATTERN DYSTROPHY(2006)4 cited
- [Hereditary hearing loss due to mutations in the connexin-26 gene].(2000)