Similar articles for PMID: 19668217

Year	Number of Results
1979	1
1985	1
1987	1
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1991	1
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1994	3
1999	1
2000	4
2001	2
2002	6
2003	4
2004	2
2005	5
2006	7
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2009	3
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2012	8
2013	3
2014	3
2015	4
2016	6
2017	6
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2019	5
2020	8
2021	7
2022	5
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2024	1

1

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. 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.

2

Phenotypic outcomes in Mouse and Human Foxc1 dependent Dandy-Walker cerebellar malformation suggest shared mechanisms.

Haldipur P, Dang D, Aldinger KA, Janson OK, Guimiot F, Adle-Biasette H, Dobyns WB, Siebert JR, Russo R, Millen KJ. Haldipur P, et al. Elife. 2017 Jan 16;6:e20898. doi: 10.7554/eLife.20898. Elife. 2017. PMID: 28092268 Free PMC article.

3

Pre- and postnatal phenotype of 6p25 deletions involving the FOXC1 gene.

Delahaye A, Khung-Savatovsky S, Aboura A, Guimiot F, Drunat S, Alessandri JL, Gérard M, Bitoun P, Boumendil J, Robin S, Huel C, Guilherme R, Serero S, Gressens P, Elion J, Verloes A, Benzacken B, Delezoide AL, Pipiras E. Delahaye A, et al. Am J Med Genet A. 2012 Oct;158A(10):2430-8. doi: 10.1002/ajmg.a.35548. Epub 2012 Aug 17. Am J Med Genet A. 2012. PMID: 22903608

4

Evidence of disrupted rhombic lip development in the pathogenesis of Dandy-Walker malformation.

Haldipur P, Bernardo S, Aldinger KA, Sivakumar T, Millman J, Sjoboen AH, Dang D, Dubocanin D, Deng M, Timms AE, Davis BD, Plummer JT, Mankad K, Oztekin O, Manganaro L, Guimiot F, Adle-Biassette H, Russo R, Siebert JR, Kidron D, Petrilli G, Roux N, Razavi F, Glass IA, Di Gioia C, Silvestri E, Millen KJ. Haldipur P, et al. Acta Neuropathol. 2021 Oct;142(4):761-776. doi: 10.1007/s00401-021-02355-7. Epub 2021 Aug 4. Acta Neuropathol. 2021. PMID: 34347142 Free PMC article.

5

Heterozygous deletion of the linked genes ZIC1 and ZIC4 is involved in Dandy-Walker malformation.

Grinberg I, Northrup H, Ardinger H, Prasad C, Dobyns WB, Millen KJ. Grinberg I, et al. Nat Genet. 2004 Oct;36(10):1053-5. doi: 10.1038/ng1420. Epub 2004 Aug 29. Nat Genet. 2004. PMID: 15338008

6

Three-dimensional volumetric study with VOCAL in normal and abnormal posterior fossa fetuses.

Dogan Y, Yucesoy G, Ozkan S, Yucesoy I. Dogan Y, et al. J Matern Fetal Neonatal Med. 2020 May;33(10):1647-1655. doi: 10.1080/14767058.2018.1526902. Epub 2018 Oct 29. J Matern Fetal Neonatal Med. 2020. PMID: 30231661

7

Neuroimaging of Dandy-Walker malformation: new concepts.

Correa GG, Amaral LF, Vedolin LM. Correa GG, et al. Top Magn Reson Imaging. 2011 Dec;22(6):303-12. doi: 10.1097/RMR.0b013e3182a2ca77. Top Magn Reson Imaging. 2011. PMID: 24132069 Review.

8

Posterior brain in fetuses with Dandy-Walker malformation with complete agenesis of the cerebellar vermis at 11-13 weeks: a pilot study.

Lachmann R, Sinkovskaya E, Abuhamad A. Lachmann R, et al. Prenat Diagn. 2012 Aug;32(8):765-9. doi: 10.1002/pd.3899. Epub 2012 Jun 7. Prenat Diagn. 2012. PMID: 22674727

9

Ocular developmental abnormalities and glaucoma associated with interstitial 6p25 duplications and deletions.

Lehmann OJ, Ebenezer ND, Ekong R, Ocaka L, Mungall AJ, Fraser S, McGill JI, Hitchings RA, Khaw PT, Sowden JC, Povey S, Walter MA, Bhattacharya SS, Jordan T. Lehmann OJ, et al. Invest Ophthalmol Vis Sci. 2002 Jun;43(6):1843-9. Invest Ophthalmol Vis Sci. 2002. PMID: 12036988

10

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.

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