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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1998 3
1999 2
2000 3
2003 1
2010 1
2012 4
2013 2
2014 2
2015 1
2020 1
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18 results
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Page 1
Mutations in QARS, encoding glutaminyl-tRNA synthetase, cause progressive microcephaly, cerebral-cerebellar atrophy, and intractable seizures.
Zhang X, Ling J, Barcia G, Jing L, Wu J, Barry BJ, Mochida GH, Hill RS, Weimer JM, Stein Q, Poduri A, Partlow JN, Ville D, Dulac O, Yu TW, Lam AT, Servattalab S, Rodriguez J, Boddaert N, Munnich A, Colleaux L, Zon LI, Söll D, Walsh CA, Nabbout R. Zhang X, et al. Am J Hum Genet. 2014 Apr 3;94(4):547-58. doi: 10.1016/j.ajhg.2014.03.003. Epub 2014 Mar 20. Am J Hum Genet. 2014. PMID: 24656866 Free PMC article.
Potential mechanisms of mutations that affect neuronal migration in man and mouse.
Walsh CA, Goffinet AM. Walsh CA, et al. Curr Opin Genet Dev. 2000 Jun;10(3):270-4. doi: 10.1016/s0959-437x(00)00076-9. Curr Opin Genet Dev. 2000. PMID: 10826984 Review.
Genetic malformations of the human cerebral cortex.
Walsh CA. Walsh CA. Neuron. 1999 May;23(1):19-29. doi: 10.1016/s0896-6273(00)80749-7. Neuron. 1999. PMID: 10402190 Free article. Review. No abstract available.
Genetic malformations of the human frontal lobe.
Amrom D, Walsh CA. Amrom D, et al. Epilepsia. 2010 Feb;51 Suppl 1(0 1):13-6. doi: 10.1111/j.1528-1167.2009.02435.x. Epilepsia. 2010. PMID: 20331705 Free PMC article. No abstract available.
Regulation of human cerebral cortical development by EXOC7 and EXOC8, components of the exocyst complex, and roles in neural progenitor cell proliferation and survival.
Coulter ME, Musaev D, DeGennaro EM, Zhang X, Henke K, James KN, Smith RS, Hill RS, Partlow JN, Muna Al-Saffar, Kamumbu AS, Hatem N, Barkovich AJ, Aziza J, Chassaing N, Zaki MS, Sultan T, Burglen L, Rajab A, Al-Gazali L, Mochida GH, Harris MP, Gleeson JG, Walsh CA. Coulter ME, et al. Genet Med. 2020 Jun;22(6):1040-1050. doi: 10.1038/s41436-020-0758-9. Epub 2020 Feb 27. Genet Med. 2020. PMID: 32103185 Free PMC article.
Control of a neuronal morphology program by an RNA-binding zinc finger protein, Unkempt.
Murn J, Zarnack K, Yang YJ, Durak O, Murphy EA, Cheloufi S, Gonzalez DM, Teplova M, Curk T, Zuber J, Patel DJ, Ule J, Luscombe NM, Tsai LH, Walsh CA, Shi Y. Murn J, et al. Genes Dev. 2015 Mar 1;29(5):501-12. doi: 10.1101/gad.258483.115. Genes Dev. 2015. PMID: 25737280 Free PMC article.
Somatic activation of AKT3 causes hemispheric developmental brain malformations.
Poduri A, Evrony GD, Cai X, Elhosary PC, Beroukhim R, Lehtinen MK, Hills LB, Heinzen EL, Hill A, Hill RS, Barry BJ, Bourgeois BF, Riviello JJ, Barkovich AJ, Black PM, Ligon KL, Walsh CA. Poduri A, et al. Neuron. 2012 Apr 12;74(1):41-8. doi: 10.1016/j.neuron.2012.03.010. Neuron. 2012. PMID: 22500628 Free PMC article.
FLNA genomic rearrangements cause periventricular nodular heterotopia.
Clapham KR, Yu TW, Ganesh VS, Barry B, Chan Y, Mei D, Parrini E, Funalot B, Dupuis L, Nezarati MM, du Souich C, van Karnebeek C, Guerrini R, Walsh CA. Clapham KR, et al. Neurology. 2012 Jan 24;78(4):269-78. doi: 10.1212/WNL.0b013e31824365e4. Epub 2012 Jan 11. Neurology. 2012. PMID: 22238415 Free PMC article.
Posterior fossa in primary microcephaly: relationships between forebrain and mid-hindbrain size in 110 patients.
Adachi Y, Mochida G, Walsh C, Barkovich J. Adachi Y, et al. Neuropediatrics. 2014 Apr;45(2):93-101. doi: 10.1055/s-0033-1360483. Epub 2013 Nov 14. Neuropediatrics. 2014. PMID: 24234199
Location of periventricular nodular heterotopia is related to the malformation phenotype on MRI.
González G, Vedolin L, Barry B, Poduri A, Walsh C, Barkovich AJ. González G, et al. AJNR Am J Neuroradiol. 2013 Apr;34(4):877-83. doi: 10.3174/ajnr.A3312. Epub 2012 Oct 11. AJNR Am J Neuroradiol. 2013. PMID: 23064591 Free PMC article.
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