Sherrington, R.
5 papers on CoChat
Most cited papers
- Verified
Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease
Sherrington, R., Rogaev, E. I., Liang, Y., Rogaeva, E. A., Levesque, G., Ikeda, M., Chi, H., Lin, C., Li, G., Holman, K., et al. (1995) · Nature
Alzheimer's disease research and treatmentsDementia and Cognitive Impairment Research
Cited by 4,051
- Verified
Familial Alzheimer's disease in kindreds with missense mutations in a gene on chromosome 1 related to the Alzheimer's disease type 3 gene
Rogaev, E. I., Sherrington, R., Rogaeva, E. A., Levesque, G., Ikeda, M., Liang, Y., Chi, H., Lin, C., Holman, K., Tsuda, T., et al. (1995) · Nature
Alzheimer's disease research and treatmentsDementia and Cognitive Impairment Research
Cited by 2,052
- Verified
Mutant presenilins of Alzheimer's disease increase production of 42-residue amyloid β-protein in both transfected cells and transgenic mice
Citron, M., Westaway, D., Xia, W., Carlson, G., Diehl, T., Levesque, G., Johnson-wood, K., Lee, M., Seubert, P., Davis, A., et al. (1997) · Nature Medicine
Alzheimer's disease research and treatmentsDementia and Cognitive Impairment Research
Cited by 1,271
- Verified
A genome-wide scan points to a susceptibility locus for bipolar disorder on chromosome 12
Shink, E., Morissette, J., Sherrington, R., & Barden, N. (2005) · Molecular Psychiatry
Bipolar Disorder and TreatmentGenetic Associations and Epidemiology
Cited by 79
- Verified
The Clinical phenotype of two missense mutations in the presenilin I gene in Japanese patients
Ikeda, M., Sharma, V., Mark Sumi, S., Rogaeva, E. A., Poorkaj, P., Sherrington, R., Nee, L., Tsuda, T., Oda, N., Watanabe, M., et al. (1996) · Annals of Neurology
Alzheimer's disease research and treatmentsDementia and Cognitive Impairment Research
Cited by 60
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