Chris A. Walsh
Affiliations: | Harvard University, Cambridge, MA, United States |
Area:
Genes involved in the development and function of the cerebral cortexWebsite:
http://www.walshlab.org/Google:
"Chris Walsh"Mean distance: 12.78 (cluster 46) | S | N | B | C | P |
Parents
Sign in to add mentorRay W. Guillery | grad student | Chicago | |
Constance L. Cepko | post-doc | Harvard |
Children
Sign in to add traineeCollaborators
Sign in to add collaboratorDavid R. Beier | collaborator | Harvard Medical School | |
Anthony LaMantia | collaborator | Harvard |
BETA: Related publications
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Publications
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Shao DD, Achkar CM, Lai A, et al. (2020) Polymicrogyria is associated with pathogenic variants in PTEN. Annals of Neurology |
Schmitz-Abe K, Sanchez-Schmitz G, Doan RN, et al. (2020) Homozygous deletions implicate non-coding epigenetic marks in Autism spectrum disorder. Scientific Reports. 10: 14045 |
Kim J, Zhao B, Huang AY, et al. (2020) APP gene copy number changes reflect exogenous contamination. Nature. 584: E20-E28 |
Lim ET, Uddin M, De Rubeis S, et al. (2020) Publisher Correction: Rates, distribution and implications of postzygotic mosaic mutations in autism spectrum disorder. Nature Neuroscience |
Huang AY, Li P, Rodin RE, et al. (2020) Parallel RNA and DNA analysis after deep sequencing (PRDD-seq) reveals cell type-specific lineage patterns in human brain. Proceedings of the National Academy of Sciences of the United States of America |
Khan A, Alaamery M, Massadeh S, et al. (2020) PDCD6IP, encoding a regulator of the ESCRT complex, is mutated in microcephaly. Clinical Genetics |
Coulter ME, Musaev D, DeGennaro EM, et al. (2020) Regulation of human cerebral cortical development by EXOC7 and EXOC8, components of the exocyst complex, and roles in neural progenitor cell proliferation and survival. Genetics in Medicine : Official Journal of the American College of Medical Genetics |
Smith RS, Walsh CA. (2020) Ion Channel Functions in Early Brain Development. Trends in Neurosciences |
Dou Y, Kwon M, Rodin RE, et al. (2020) Accurate detection of mosaic variants in sequencing data without matched controls. Nature Biotechnology |
Lodato MA, Walsh CA. (2019) Corrigendum: Genome aging: somatic mutation in the brain links age-related decline with disease and nominates pathogenic mechanisms. Human Molecular Genetics |