Walsh CA - Search Results

1

Genomic data resources of the Brain Somatic Mosaicism Network for neuropsychiatric diseases.

Garrison MA, Jang Y, Bae T, Cherskov A, Emery SB, Fasching L, Jones A, Moldovan JB, Molitor C, Pochareddy S, Peters MA, Shin JH, Wang Y, Yang X, Akbarian S, Chess A, Gage FH, Gleeson JG, Kidd JM, McConnell M, Mills RE, Moran JV, Park PJ, Sestan N, Urban AE, Vaccarino FM, Walsh CA, Weinberger DR, Wheelan SJ, Abyzov A; BSMN Consortium. Garrison MA, et al. Among authors: walsh ca. Sci Data. 2023 Nov 20;10(1):813. doi: 10.1038/s41597-023-02645-7. Sci Data. 2023. PMID: 37985666 Free PMC article.

2

A YAC contig in Xq22.3-q23, from DXS287 to DXS8088, spanning the brain-specific genes doublecortin (DCX) and PAK3.

Allen KM, Gleeson JG, Shoup SM, Walsh CA. Allen KM, et al. Among authors: walsh ca. Genomics. 1998 Sep 1;52(2):214-8. doi: 10.1006/geno.1998.5424. Genomics. 1998. PMID: 9782089

3

Doublecortin is a microtubule-associated protein and is expressed widely by migrating neurons.

Gleeson JG, Lin PT, Flanagan LA, Walsh CA. Gleeson JG, et al. Among authors: walsh ca. Neuron. 1999 Jun;23(2):257-71. doi: 10.1016/s0896-6273(00)80778-3. Neuron. 1999. PMID: 10399933 Free article.

4

Neuronal migration disorders: from genetic diseases to developmental mechanisms.

Gleeson JG, Walsh CA. Gleeson JG, et al. Among authors: walsh ca. Trends Neurosci. 2000 Aug;23(8):352-9. doi: 10.1016/s0166-2236(00)01607-6. Trends Neurosci. 2000. PMID: 10906798 Review.

5

Somatic and germline mosaic mutations in the doublecortin gene are associated with variable phenotypes.

Gleeson JG, Minnerath S, Kuzniecky RI, Dobyns WB, Young ID, Ross ME, Walsh CA. Gleeson JG, et al. Among authors: walsh ca. Am J Hum Genet. 2000 Sep;67(3):574-81. doi: 10.1086/303043. Epub 2000 Jul 27. Am J Hum Genet. 2000. PMID: 10915612 Free PMC article.

6

Patient mutations in doublecortin define a repeated tubulin-binding domain.

Taylor KR, Holzer AK, Bazan JF, Walsh CA, Gleeson JG. Taylor KR, et al. Among authors: walsh ca. J Biol Chem. 2000 Nov 3;275(44):34442-50. doi: 10.1074/jbc.M007078200. J Biol Chem. 2000. PMID: 10946000 Free article.

7

Molecular insights into human brain evolution.

Hill RS, Walsh CA. Hill RS, et al. Among authors: walsh ca. Nature. 2005 Sep 1;437(7055):64-7. doi: 10.1038/nature04103. Nature. 2005. PMID: 16136130

8

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.

9

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.

10

Mammalian target of rapamycin pathway mutations cause hemimegalencephaly and focal cortical dysplasia.

D'Gama AM, Geng Y, Couto JA, Martin B, Boyle EA, LaCoursiere CM, Hossain A, Hatem NE, Barry BJ, Kwiatkowski DJ, Vinters HV, Barkovich AJ, Shendure J, Mathern GW, Walsh CA, Poduri A. D'Gama AM, et al. Among authors: walsh ca. Ann Neurol. 2015 Apr;77(4):720-5. doi: 10.1002/ana.24357. Epub 2015 Feb 26. Ann Neurol. 2015. PMID: 25599672 Free PMC article.

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