Lott, Marie T.

Mitochondrial DNA mutation associated with Leber’s hereditary optic neuropathy

Wallace, D. C., Singh, G., Lott, M. T., Hodge, J. A., Schurr, T. G., Lezza, A. M. S., Elsas, L. J., & Nikoskelainen, E. K. (1988) · Science

Mitochondrial Function and PathologyHereditary Neurological Disorders

Cited by 2,440

Mitochondrial DNA deletions in human brain: regional variability and increase with advanced age

Corral-Debrinski, M., Horton, T., Lott, M. T., Shoffner, J. M., Flint Beal, M., & Wallace, D. C. (1992) · Nature Genetics

Mitochondrial Function and PathologyGenetics, Aging, and Longevity in Model Organisms

Cited by 890

The clinical characteristics of pedigrees of Leber’s hereditary optic neuropathy with the 11778 mutation

Newman, N. J., Lott, M. T., & Wallace, D. C. (1991) · American Journal of Ophthalmology

Mitochondrial Function and PathologyGlaucoma and retinal disorders

Cited by 403

Marked changes in mitochondrial DNA deletion levels in Alzheimer brains

Corral-Debrinski, M., Horton, T., Lott, M. T., Shoffner, J. M., McKee, A. C., Beal, M. F., Graham, B. H., & Wallace, D. C. (1994) · Genomics

Mitochondrial Function and PathologyAlzheimer's disease research and treatments

Cited by 309

Mitochondrial DNA variation and cancer

Kopinski, P. K., Singh, L. N., Zhang, S., Lott, M. T., & Wallace, D. C. (2021) · Nature reviews. Cancer

Mitochondrial Function and PathologyCancer, Hypoxia, and Metabolism

Cited by 301

APOGEE 2: multi-layer machine-learning model for the interpretable prediction of mitochondrial missense variants

Bianco, S. D., Parca, L., Petrizzelli, F., Biagini, T., Giovannetti, A., Liorni, N., Napoli, A., Carella, M., Procaccio, V., Lott, M., et al. (2023) · Nature Communications

Genomics and Rare DiseasesMitochondrial Function and Pathology

Cited by 44

APOGEE 2: multi-layer machine-learning model for the interpretable prediction of mitochondrial missense variants

Bianco, S. D., Parca, L., Petrizzelli, F., Biagini, T., Giovannetti, A., Liorni, N., Napoli, A., Carella, M., Procaccio, V., Lott, M. T., et al. (2023) · Nature Communications

Genomics and Rare DiseasesMitochondrial Function and Pathology

Cited by 44