Walsh, Christopher A.
Broad Institute · Boston Children's Hospital · Howard Hughes Medical Institute · Harvard University · Manton Center for Orphan Disease Research · Massachusetts Institute of Technology
56 papers on CoChatORCID 0000-0002-0156-2238
Most cited papers
- Verified
Rates and Patterns of Clonal Oncogenic Mutations in the Normal Human Brain
Ganz, J., Maury, E. A., Becerra, B., Bizzotto, S., Doan, R. N., Kenny, C. J., Shin, T., Kim, J., Zhou, Z., Ligon, K. L., et al. (2022) · Cancer Discovery
Cancer Genomics and DiagnosticsGlioma Diagnosis and Treatment
Cited by 48
- Verified
Delineation of the Clinical, Molecular and Cellular Aspects of Novel JAM 3 Mutations Underlying the Autosomal Recessive Hemorrhagic Destruction of the Brain, Subependymal Calcification, and Congenital Cataracts
Akawi, N. A., Canpolat, F. E., White, S. M., Quilis‐Esquerra, J., Morales Sanchez, M., Gamundi, M. J., Mochida, G. H., Walsh, C. A., Ali, B. R., & Al‐Gazali, L. (2013) · Human Mutation
Barrier Structure and Function StudiesGenomics and Rare Diseases
Cited by 47
- Verified
Single-cell, genome-wide sequencing identifies clonal somatic copy-number variation in the human brain
Cai, X., Evrony, G. D., Lehmann, H. S., Elhosary, P. C., Mehta, B. K., Poduri, A., & Walsh, C. A. (2015) · Cell Reports
Genomic variations and chromosomal abnormalitiesCancer Genomics and Diagnostics
Cited by 42
- Verified
PSMD12 haploinsufficiency in a neurodevelopmental disorder with autistic features
Khalil, R., Kenny, C., Hill, R. S., Mochida, G. H., Nasir, R., Partlow, J. N., Barry, B. J., Al‐Saffar, M., Egan, C., Stevens, C. R., et al. (2018) · American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
Genetics and Neurodevelopmental DisordersAutism Spectrum Disorder Research
Cited by 39
- Verified
Exome Sequencing and the Identification of New Genes and Shared Mechanisms in Polymicrogyria
Akula, S. K., Chen, A. Y., Neil, J. E., Shao, D. D., Mo, A., Hylton, N. K., DiTroia, S., Ganesh, V. S., Smith, R. S., O’Kane, K., et al. (2023) · JAMA Neurology
Fetal and Pediatric Neurological DisordersGenomics and Rare Diseases
Cited by 37
- Verified
Somatic cancer driver mutations are enriched and associated with inflammatory states in Alzheimer’s disease microglia
Huang, A. Y., Zhou, Z., Talukdar, M., Miller, M. B., Chhouk, B., Enyenihi, L., Rosen, I., Stronge, E., Zhao, B., Kim, D., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory)
Alzheimer's disease research and treatmentsNeuroinflammation and Neurodegeneration Mechanisms
Cited by 16
- Verified
Somatic cancer variants enriched in Alzheimer’s disease microglia-like cells drive inflammatory and proliferative states
Huang, A. Y., Zhou, Z., Talukdar, M., Enyenihi, L., Miller, M. B., Chhouk, B., Rosen, I., Zheng, M., Zhou, M., Yang, A., et al. (2026) · Cell
Neuroinflammation and Neurodegeneration MechanismsAlzheimer's disease research and treatments
Cited by 15
- Verified
Clonal Hematopoiesis Mutations Increase Risk of Alzheimer’s Disease with APOE ε3/ε3 Genotype
Choi, J., Park, K. S., Le Guen, Y., Park, J.-H., Zhou, Z., Enyenihi, L., Rosen, I., Choi, Y.-H., Walsh, C. A., Kim, J.-W., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory)
Alzheimer's disease research and treatmentsDementia and Cognitive Impairment Research
Cited by 5
Go further with a free account
Verify every reference, keep papers in a library, and ask questions across them.
Sign up - it is free