Wallace, Douglas C.

The dual origin and Siberian affinities of Native American Y chromosomes

Lell, J. T., Sukernik, R. I., Starikovskaya, Y. B., Su, B., Jin, L., Schurr, T. G., Underhill, P. A., & Wallace, D. C. (2002) · The American Journal of Human Genetics

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Trans-mitochondrial coordination of cristae at regulated membrane junctions

Picard, M., McManus, M. J., Csordás, G., Várnai, P., Dorn II, G. W., Williams, D., Hajnóczky, G., & Wallace, D. C. (2015) · Nature Communications

Mitochondrial Function and PathologyAutophagy in Disease and Therapy

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Regulation of nuclear epigenome by mitochondrial DNA heteroplasmy

Kopinski, P. K., Janssen, K. A., Schaefer, P. M., Trefely, S., Perry, C. E., Potluri, P., Tintos-Hernandez, J. A., Singh, L. N., Karch, K. R., Campbell, S. L., et al. (2019) · Proceedings of the National Academy of Sciences

Mitochondrial Function and PathologyEpigenetics and DNA Methylation

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Elevated male European and female African contributions to the genomes of African American individuals

Lind, J. M., Hutcheson-Dilks, H. B., Williams, S. M., Moore, J. H., Essex, M., Ruiz-Pesini, E., Wallace, D. C., Tishkoff, S. A., O’Brien, S. J., & Smith, M. W. (2006) · Human Genetics

Forensic and Genetic ResearchRace, Genetics, and Society

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Mitochondrial dysfunction in CA1 hippocampal neurons of the UBE3A deficient mouse model for Angelman syndrome

Su, H., Fan, W., Coskun, P. E., Vesa, J., Gold, J.-A., Jiang, Y.-H., Potluri, P., Procaccio, V., Acab, A., Weiss, J. H., et al. (2011) · Neuroscience Letters

Genetic Syndromes and ImprintingMitochondrial Function and Pathology

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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

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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

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