D’Gama, Alissa M.
4 papers on CoChatORCID 0000-0002-2482-5328
Most cited papers
- Verified
Somatic mutation in single human neurons tracks developmental and transcriptional history
Lodato, M. A., Woodworth, M. B., Lee, S., Evrony, G. D., Mehta, B. K., Karger, A., Lee, S., Chittenden, T. W., D’Gama, A. M., Cai, X., et al. (2015) · Science
Single-cell and spatial transcriptomicsCancer Genomics and Diagnostics
Cited by 570
- Verified
Using Whole-Exome Sequencing to Identify Inherited Causes of Autism
Yu, T. W., Chahrour, M. H., Coulter, M. E., Jiralerspong, S., Okamura-Ikeda, K., Ataman, B., Schmitz-Abe, K., Harmin, D. A., Adli, M., Malik, A. N., et al. (2013) · Neuron
Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders
Cited by 442
- Verified
Somatic mutations in cerebral cortical malformations
Jamuar, S. S., Lam, A.-T. N., Kircher, M., D’Gama, A. M., Wang, J., Barry, B. J., Zhang, X., Hill, R. S., Partlow, J. N., Rozzo, A., et al. (2014) · New England Journal of Medicine
Fetal and Pediatric Neurological DisordersGenomics and Rare Diseases
Cited by 392
- Verified
Intersection of diverse neuronal genomes and neuropsychiatric disease: The Brain Somatic Mosaicism Network
McConnell, M. J., Moran, J. V., Abyzov, A., Akbarian, S., Bae, T., Cortes-Ciriano, I., Erwin, J. A., Fasching, L., Flasch, D. A., Freed, D., et al. (2017) · Science
Genomic variations and chromosomal abnormalitiesGenetics and Neurodevelopmental Disorders
Cited by 262
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