R01-NS050386/NS/NINDS NIH HHS/United States[Grants and Funding] - Search Results

Year	Number of Results
2007	2
2008	2
2009	3
2010	4
2011	2
2012	2
2013	1
2014	2
2015	1
2024	0

1

Millen KJ, Gleeson JG. Millen KJ, et al. Curr Opin Neurobiol. 2008 Feb;18(1):12-9. doi: 10.1016/j.conb.2008.05.010. Epub 2008 May 29. Curr Opin Neurobiol. 2008. PMID: 18513948 Free PMC article. Review.

2

A developmental and genetic classification for midbrain-hindbrain malformations.

Barkovich AJ, Millen KJ, Dobyns WB. Barkovich AJ, et al. Brain. 2009 Dec;132(Pt 12):3199-230. doi: 10.1093/brain/awp247. Brain. 2009. PMID: 19933510 Free PMC article. Review.

3

Novel approaches to studying the genetic basis of cerebellar development.

Sajan SA, Waimey KE, Millen KJ. Sajan SA, et al. Cerebellum. 2010 Sep;9(3):272-83. doi: 10.1007/s12311-010-0169-6. Cerebellum. 2010. PMID: 20387026 Free PMC article. Review.

4

Model organisms inform the search for the genes and developmental pathology underlying malformations of the human hindbrain.

Aldinger KA, Elsen GE, Prince VE, Millen KJ. Aldinger KA, et al. Semin Pediatr Neurol. 2009 Sep;16(3):155-63. doi: 10.1016/j.spen.2009.06.003. Semin Pediatr Neurol. 2009. PMID: 19778712 Free PMC article. Review.

5

Purkinje cell compartmentalization in the cerebellum of the spontaneous mutant mouse dreher.

Sillitoe RV, George-Jones NA, Millen KJ, Hawkes R. Sillitoe RV, et al. Brain Struct Funct. 2014 Jan;219(1):35-47. doi: 10.1007/s00429-012-0482-6. Epub 2012 Nov 18. Brain Struct Funct. 2014. PMID: 23160833 Free PMC article.

6

Multiple developmental programs are altered by loss of Zic1 and Zic4 to cause Dandy-Walker malformation cerebellar pathogenesis.

Blank MC, Grinberg I, Aryee E, Laliberte C, Chizhikov VV, Henkelman RM, Millen KJ. Blank MC, et al. Development. 2011 Mar;138(6):1207-16. doi: 10.1242/dev.054114. Epub 2011 Feb 9. Development. 2011. PMID: 21307096 Free PMC article.

7

Cilia proteins control cerebellar morphogenesis by promoting expansion of the granule progenitor pool.

Chizhikov VV, Davenport J, Zhang Q, Shih EK, Cabello OA, Fuchs JL, Yoder BK, Millen KJ. Chizhikov VV, et al. J Neurosci. 2007 Sep 5;27(36):9780-9. doi: 10.1523/JNEUROSCI.5586-06.2007. J Neurosci. 2007. PMID: 17804638 Free PMC article.

8

Cerebellar hypoplasia and Cohen syndrome: a confirmed association.

Waite A, Somer M, O'Driscoll M, Millen K, Manson FD, Chandler KE. Waite A, et al. Am J Med Genet A. 2010 Sep;152A(9):2390-3. doi: 10.1002/ajmg.a.33569. Am J Med Genet A. 2010. PMID: 20683995 No abstract available.

9

Cerebellar and posterior fossa malformations in patients with autism-associated chromosome 22q13 terminal deletion.

Aldinger KA, Kogan J, Kimonis V, Fernandez B, Horn D, Klopocki E, Chung B, Toutain A, Weksberg R, Millen KJ, Barkovich AJ, Dobyns WB. Aldinger KA, et al. Am J Med Genet A. 2013 Jan;161A(1):131-6. doi: 10.1002/ajmg.a.35700. Epub 2012 Dec 7. Am J Med Genet A. 2013. PMID: 23225497 Free PMC article.

10

Zac1 plays a key role in the development of specific neuronal subsets in the mouse cerebellum.

Chung SH, Marzban H, Aldinger K, Dixit R, Millen K, Schuurmans C, Hawkes R. Chung SH, et al. Neural Dev. 2011 May 18;6:25. doi: 10.1186/1749-8104-6-25. Neural Dev. 2011. PMID: 21592321 Free PMC article.

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