Walsh CA - Search Results

1

Somatic mutations in single human cardiomyocytes reveal age-associated DNA damage and widespread oxidative genotoxicity.

Choudhury S, Huang AY, Kim J, Zhou Z, Morillo K, Maury EA, Tsai JW, Miller MB, Lodato MA, Araten S, Hilal N, Lee EA, Chen MH, Walsh CA. Choudhury S, et al. Among authors: walsh ca. Nat Aging. 2022 Aug;2(8):714-725. doi: 10.1038/s43587-022-00261-5. Epub 2022 Aug 11. Nat Aging. 2022. PMID: 36051457 Free PMC article.

2

Filamin A (FLNA) is required for cell-cell contact in vascular development and cardiac morphogenesis.

Feng Y, Chen MH, Moskowitz IP, Mendonza AM, Vidali L, Nakamura F, Kwiatkowski DJ, Walsh CA. Feng Y, et al. Among authors: walsh ca. Proc Natl Acad Sci U S A. 2006 Dec 26;103(52):19836-41. doi: 10.1073/pnas.0609628104. Epub 2006 Dec 15. Proc Natl Acad Sci U S A. 2006. PMID: 17172441 Free PMC article.

3

Single-neuron sequencing analysis of L1 retrotransposition and somatic mutation in the human brain.

Evrony GD, Cai X, Lee E, Hills LB, Elhosary PC, Lehmann HS, Parker JJ, Atabay KD, Gilmore EC, Poduri A, Park PJ, Walsh CA. Evrony GD, et al. Among authors: walsh ca. Cell. 2012 Oct 26;151(3):483-96. doi: 10.1016/j.cell.2012.09.035. Cell. 2012. PMID: 23101622 Free PMC article.

4

Cell lineage analysis in human brain using endogenous retroelements.

Evrony GD, Lee E, Mehta BK, Benjamini Y, Johnson RM, Cai X, Yang L, Haseley P, Lehmann HS, Park PJ, Walsh CA. Evrony GD, et al. Among authors: walsh ca. Neuron. 2015 Jan 7;85(1):49-59. doi: 10.1016/j.neuron.2014.12.028. Neuron. 2015. PMID: 25569347 Free PMC article.

5

Somatic mutation in single human neurons tracks developmental and transcriptional history.

Lodato MA, Woodworth MB, Lee S, Evrony GD, Mehta BK, Karger A, Lee S, Chittenden TW, D'Gama AM, Cai X, Luquette LJ, Lee E, Park PJ, Walsh CA. Lodato MA, et al. Among authors: walsh ca. Science. 2015 Oct 2;350(6256):94-98. doi: 10.1126/science.aab1785. Science. 2015. PMID: 26430121 Free PMC article.

6

Resolving rates of mutation in the brain using single-neuron genomics.

Evrony GD, Lee E, Park PJ, Walsh CA. Evrony GD, et al. Among authors: walsh ca. Elife. 2016 Feb 22;5:e12966. doi: 10.7554/eLife.12966. Elife. 2016. PMID: 26901440 Free PMC article.

7

Cell-Type-Specific Alternative Splicing Governs Cell Fate in the Developing Cerebral Cortex.

Zhang X, Chen MH, Wu X, Kodani A, Fan J, Doan R, Ozawa M, Ma J, Yoshida N, Reiter JF, Black DL, Kharchenko PV, Sharp PA, Walsh CA. Zhang X, et al. Among authors: walsh ca. Cell. 2016 Aug 25;166(5):1147-1162.e15. doi: 10.1016/j.cell.2016.07.025. Cell. 2016. PMID: 27565344 Free PMC article.

8

PaSD-qc: quality control for single cell whole-genome sequencing data using power spectral density estimation.

Sherman MA, Barton AR, Lodato MA, Vitzthum C, Coulter ME, Walsh CA, Park PJ. Sherman MA, et al. Among authors: walsh ca. Nucleic Acids Res. 2018 Feb 28;46(4):e20. doi: 10.1093/nar/gkx1195. Nucleic Acids Res. 2018. PMID: 29186545 Free PMC article.

9

Aging and neurodegeneration are associated with increased mutations in single human neurons.

Lodato MA, Rodin RE, Bohrson CL, Coulter ME, Barton AR, Kwon M, Sherman MA, Vitzthum CM, Luquette LJ, Yandava CN, Yang P, Chittenden TW, Hatem NE, Ryu SC, Woodworth MB, Park PJ, Walsh CA. Lodato MA, et al. Among authors: walsh ca. Science. 2018 Feb 2;359(6375):555-559. doi: 10.1126/science.aao4426. Epub 2017 Dec 7. Science. 2018. PMID: 29217584 Free PMC article.

10

Thoracic aortic aneurysm in patients with loss of function Filamin A mutations: Clinical characterization, genetics, and recommendations.

Chen MH, Choudhury S, Hirata M, Khalsa S, Chang B, Walsh CA. Chen MH, et al. Among authors: walsh ca. Am J Med Genet A. 2018 Feb;176(2):337-350. doi: 10.1002/ajmg.a.38580. Am J Med Genet A. 2018. PMID: 29334594 Free PMC article.

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