Walsh CA - Search Results

1

Human mutations in NDE1 cause extreme microcephaly with lissencephaly [corrected].

Alkuraya FS, Cai X, Emery C, Mochida GH, Al-Dosari MS, Felie JM, Hill RS, Barry BJ, Partlow JN, Gascon GG, Kentab A, Jan M, Shaheen R, Feng Y, Walsh CA. Alkuraya FS, et al. Among authors: walsh ca. Am J Hum Genet. 2011 May 13;88(5):536-47. doi: 10.1016/j.ajhg.2011.04.003. Epub 2011 Apr 28. Am J Hum Genet. 2011. PMID: 21529751 Free PMC article.

2

LIS1 and XLIS (DCX) mutations cause most classical lissencephaly, but different patterns of malformation.

Pilz DT, Matsumoto N, Minnerath S, Mills P, Gleeson JG, Allen KM, Walsh CA, Barkovich AJ, Dobyns WB, Ledbetter DH, Ross ME. Pilz DT, et al. Among authors: walsh ca. Hum Mol Genet. 1998 Dec;7(13):2029-37. doi: 10.1093/hmg/7.13.2029. Hum Mol Genet. 1998. PMID: 9817918

3

Molecular genetics of human microcephaly.

Mochida GH, Walsh CA. Mochida GH, et al. Among authors: walsh ca. Curr Opin Neurol. 2001 Apr;14(2):151-6. doi: 10.1097/00019052-200104000-00003. Curr Opin Neurol. 2001. PMID: 11262728 Review.

4

Protein-protein interactions, cytoskeletal regulation and neuronal migration.

Feng Y, Walsh CA. Feng Y, et al. Among authors: walsh ca. Nat Rev Neurosci. 2001 Jun;2(6):408-16. doi: 10.1038/35077559. Nat Rev Neurosci. 2001. PMID: 11389474 Review.

5

Mutations in the X-linked filamin 1 gene cause periventricular nodular heterotopia in males as well as in females.

Sheen VL, Dixon PH, Fox JW, Hong SE, Kinton L, Sisodiya SM, Duncan JS, Dubeau F, Scheffer IE, Schachter SC, Wilner A, Henchy R, Crino P, Kamuro K, DiMario F, Berg M, Kuzniecky R, Cole AJ, Bromfield E, Biber M, Schomer D, Wheless J, Silver K, Mochida GH, Berkovic SF, Andermann F, Andermann E, Dobyns WB, Wood NW, Walsh CA. Sheen VL, et al. Among authors: walsh ca. Hum Mol Genet. 2001 Aug 15;10(17):1775-83. doi: 10.1093/hmg/10.17.1775. Hum Mol Genet. 2001. PMID: 11532987

6

Filamin A and Filamin B are co-expressed within neurons during periods of neuronal migration and can physically interact.

Sheen VL, Feng Y, Graham D, Takafuta T, Shapiro SS, Walsh CA. Sheen VL, et al. Among authors: walsh ca. Hum Mol Genet. 2002 Nov 1;11(23):2845-54. doi: 10.1093/hmg/11.23.2845. Hum Mol Genet. 2002. PMID: 12393796

7

Mutations in ARFGEF2 implicate vesicle trafficking in neural progenitor proliferation and migration in the human cerebral cortex.

Sheen VL, Ganesh VS, Topcu M, Sebire G, Bodell A, Hill RS, Grant PE, Shugart YY, Imitola J, Khoury SJ, Guerrini R, Walsh CA. Sheen VL, et al. Among authors: walsh ca. Nat Genet. 2004 Jan;36(1):69-76. doi: 10.1038/ng1276. Epub 2003 Nov 30. Nat Genet. 2004. PMID: 14647276

8

Genetic basis of developmental malformations of the cerebral cortex.

Mochida GH, Walsh CA. Mochida GH, et al. Among authors: walsh ca. Arch Neurol. 2004 May;61(5):637-40. doi: 10.1001/archneur.61.5.637. Arch Neurol. 2004. PMID: 15148137 Review.

9

Abnormal cerebellar development and axonal decussation due to mutations in AHI1 in Joubert syndrome.

Ferland RJ, Eyaid W, Collura RV, Tully LD, Hill RS, Al-Nouri D, Al-Rumayyan A, Topcu M, Gascon G, Bodell A, Shugart YY, Ruvolo M, Walsh CA. Ferland RJ, et al. Among authors: walsh ca. Nat Genet. 2004 Sep;36(9):1008-13. doi: 10.1038/ng1419. Epub 2004 Aug 22. Nat Genet. 2004. PMID: 15322546

10

Mitotic spindle regulation by Nde1 controls cerebral cortical size.

Feng Y, Walsh CA. Feng Y, et al. Among authors: walsh ca. Neuron. 2004 Oct 14;44(2):279-93. doi: 10.1016/j.neuron.2004.09.023. Neuron. 2004. PMID: 15473967 Free article.

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