E. Almqvist
Roche (Switzerland)(CH)University of Iowa(US)Harvard University(US)University of British Columbia(CA)CHDI Foundation(US)Massachusetts General Hospital(US)University College London(GB)University of Rochester(US)
Publications by Year
Research Areas
Genetic Neurodegenerative Diseases, Mitochondrial Function and Pathology, Neurological disorders and treatments, DNA Repair Mechanisms, Ubiquitin and proteasome pathways
Most-Cited Works
- Phenotypic Characterization of Individuals with 30–40 CAG Repeats in the Huntington Disease (HD) Gene Reveals HD Cases with 36 Repeats and Apparently Normal Elderly Individuals with 36–39 Repeats(1996)
- The likelihood of being affected with Huntington disease by a particular age, for a specific CAG size.(1997)
- → A Worldwide Assessment of the Frequency of Suicide, Suicide Attempts, or Psychiatric Hospitalization after Predictive Testing for Huntington Disease(1999)286 cited
- → Molecular analysis of juvenile Huntington disease: the major influence on (CAG)n repeat length is the sex of the affected parent(1993)209 cited
- → DNA haplotype analysis of Huntington disease reveals clues to the origins and mechanisms of CAG expansion and reasons for geographic variations of prevalence(1994)183 cited
- → Interaction of normal and expanded CAG repeat sizes influences age at onset of Huntington disease(2003)162 cited
- Sex-dependent mechanisms for expansions and contractions of the CAG repeat on affected Huntington disease chromosomes.(1995)