Millen KJ - Search Results

1

Human Cerebellar Development and Transcriptomics: Implications for Neurodevelopmental Disorders.

Haldipur P, Millen KJ, Aldinger KA. Haldipur P, et al. Among authors: millen kj. Annu Rev Neurosci. 2022 Jul 8;45:515-531. doi: 10.1146/annurev-neuro-111020-091953. Epub 2022 Apr 19. Annu Rev Neurosci. 2022. PMID: 35440142 Free PMC article. Review.

2

Linkage to chromosome 2q36.1 in autosomal dominant Dandy-Walker malformation with occipital cephalocele and evidence for genetic heterogeneity.

Jalali A, Aldinger KA, Chary A, McLone DG, Bowman RM, Le LC, Jardine P, Newbury-Ecob R, Mallick A, Jafari N, Russell EJ, Curran J, Nguyen P, Ouahchi K, Lee C, Dobyns WB, Millen KJ, Pina-Neto JM, Kessler JA, Bassuk AG. Jalali A, et al. Among authors: millen kj. Hum Genet. 2008 Apr;123(3):237-45. doi: 10.1007/s00439-008-0467-y. Epub 2008 Jan 19. Hum Genet. 2008. PMID: 18204864 Free PMC article.

3

Genetic variation and population substructure in outbred CD-1 mice: implications for genome-wide association studies.

Aldinger KA, Sokoloff G, Rosenberg DM, Palmer AA, Millen KJ. Aldinger KA, et al. Among authors: millen kj. PLoS One. 2009;4(3):e4729. doi: 10.1371/journal.pone.0004729. Epub 2009 Mar 6. PLoS One. 2009. PMID: 19266100 Free PMC article.

4

FOXC1 is required for normal cerebellar development and is a major contributor to chromosome 6p25.3 Dandy-Walker malformation.

Aldinger KA, Lehmann OJ, Hudgins L, Chizhikov VV, Bassuk AG, Ades LC, Krantz ID, Dobyns WB, Millen KJ. Aldinger KA, et al. Among authors: millen kj. Nat Genet. 2009 Sep;41(9):1037-42. doi: 10.1038/ng.422. Epub 2009 Aug 9. Nat Genet. 2009. PMID: 19668217 Free PMC article.

5

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. Among authors: millen kj. 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.

6

Lmx1a regulates fates and location of cells originating from the cerebellar rhombic lip and telencephalic cortical hem.

Chizhikov VV, Lindgren AG, Mishima Y, Roberts RW, Aldinger KA, Miesegaes GR, Currle DS, Monuki ES, Millen KJ. Chizhikov VV, et al. Among authors: millen kj. Proc Natl Acad Sci U S A. 2010 Jun 8;107(23):10725-30. doi: 10.1073/pnas.0910786107. Epub 2010 May 24. Proc Natl Acad Sci U S A. 2010. PMID: 20498066 Free PMC article.

7

Phenotypic and genetic analysis of the cerebellar mutant tmgc26, a new ENU-induced ROR-alpha allele.

Swanson DJ, Steshina EY, Wakenight P, Aldinger KA, Goldowitz D, Millen KJ, Chizhikov VV. Swanson DJ, et al. Among authors: millen kj. Eur J Neurosci. 2010 Sep;32(5):707-16. doi: 10.1111/j.1460-9568.2010.07330.x. Epub 2010 Aug 16. Eur J Neurosci. 2010. PMID: 20722722 Free PMC article.

8

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.

9

Consensus paper: pathological role of the cerebellum in autism.

Fatemi SH, Aldinger KA, Ashwood P, Bauman ML, Blaha CD, Blatt GJ, Chauhan A, Chauhan V, Dager SR, Dickson PE, Estes AM, Goldowitz D, Heck DH, Kemper TL, King BH, Martin LA, Millen KJ, Mittleman G, Mosconi MW, Persico AM, Sweeney JA, Webb SJ, Welsh JP. Fatemi SH, et al. Among authors: millen kj. Cerebellum. 2012 Sep;11(3):777-807. doi: 10.1007/s12311-012-0355-9. Cerebellum. 2012. PMID: 22370873 Free PMC article. Review.

10

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. Among authors: millen kj. 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.

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