K08 NS062711/NS/NINDS NIH HHS/United States[Grants and Funding] - Search Results

Year	Number of Results
2008	1
2009	2
2010	4
2011	6
2012	2
2013	5
2014	1
2015	1
2016	1
2024	0

1

Ramocki MB, Tavyev YJ, Peters SU. Ramocki MB, et al. Am J Med Genet A. 2010 May;152A(5):1079-88. doi: 10.1002/ajmg.a.33184. Am J Med Genet A. 2010. PMID: 20425814 Free PMC article. Review.

2

Failure of neuronal homeostasis results in common neuropsychiatric phenotypes.

Ramocki MB, Zoghbi HY. Ramocki MB, et al. Nature. 2008 Oct 16;455(7215):912-8. doi: 10.1038/nature07457. Nature. 2008. PMID: 18923513 Free PMC article. Review.

3

Recurrent partial rhombencephalosynapsis and holoprosencephaly in siblings with a mutation of ZIC2.

Ramocki MB, Scaglia F, Stankiewicz P, Belmont JW, Jones JY, Clark GD. Ramocki MB, et al. Am J Med Genet A. 2011 Jul;155A(7):1574-80. doi: 10.1002/ajmg.a.34029. Epub 2011 Jun 2. Am J Med Genet A. 2011. PMID: 21638761 Free PMC article.

4

Bilateral in utero cerebellar infarction.

Ansari SA, Hunter JV, Nassif LM, Clark GD, Ramocki MB. Ansari SA, et al. J Child Neurol. 2011 Jul;26(7):895-9. doi: 10.1177/0883073810393961. Epub 2011 Jan 24. J Child Neurol. 2011. PMID: 21266324 Free PMC article.

5

Overexpression of methyl-CpG binding protein 2 impairs T(H)1 responses.

Yang T, Ramocki MB, Neul JL, Lu W, Roberts L, Knight J, Ward CS, Zoghbi HY, Kheradmand F, Corry DB. Yang T, et al. Sci Transl Med. 2012 Dec 5;4(163):163ra158. doi: 10.1126/scitranslmed.3004430. Sci Transl Med. 2012. PMID: 23220634 Free PMC article.

6

Replicative mechanisms for CNV formation are error prone.

Carvalho CM, Pehlivan D, Ramocki MB, Fang P, Alleva B, Franco LM, Belmont JW, Hastings PJ, Lupski JR. Carvalho CM, et al. Nat Genet. 2013 Nov;45(11):1319-26. doi: 10.1038/ng.2768. Epub 2013 Sep 22. Nat Genet. 2013. PMID: 24056715 Free PMC article.

7

MECP2 duplications in six patients with complex sex chromosome rearrangements.

Breman AM, Ramocki MB, Kang SH, Williams M, Freedenberg D, Patel A, Bader PI, Cheung SW. Breman AM, et al. Eur J Hum Genet. 2011 Apr;19(4):409-15. doi: 10.1038/ejhg.2010.195. Epub 2010 Dec 1. Eur J Hum Genet. 2011. PMID: 21119712 Free PMC article.

8

Brief report: regression timing and associated features in MECP2 duplication syndrome.

Peters SU, Hundley RJ, Wilson AK, Carvalho CM, Lupski JR, Ramocki MB. Peters SU, et al. J Autism Dev Disord. 2013 Oct;43(10):2484-90. doi: 10.1007/s10803-013-1796-9. J Autism Dev Disord. 2013. PMID: 23456562

9

Autism and other neuropsychiatric symptoms are prevalent in individuals with MeCP2 duplication syndrome.

Ramocki MB, Peters SU, Tavyev YJ, Zhang F, Carvalho CM, Schaaf CP, Richman R, Fang P, Glaze DG, Lupski JR, Zoghbi HY. Ramocki MB, et al. Ann Neurol. 2009 Dec;66(6):771-82. doi: 10.1002/ana.21715. Ann Neurol. 2009. PMID: 20035514 Free PMC article.

10

TGFBR2 deletion in a 20-month-old female with developmental delay and microcephaly.

Campbell IM, Kolodziejska KE, Quach MM, Wolf VL, Cheung SW, Lalani SR, Ramocki MB, Stankiewicz P. Campbell IM, et al. Am J Med Genet A. 2011 Jun;155A(6):1442-7. doi: 10.1002/ajmg.a.34015. Epub 2011 May 12. Am J Med Genet A. 2011. PMID: 21567932 Free PMC article.

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