PubMed (cited) for id: 214800

Year	Number of Results
1966	1
1977	1
1979	2
1981	1
1984	1
1986	3
1987	2
1988	2
1989	2
1990	3
1991	1
1992	1
1993	1
1995	1
1996	2
1997	1
1998	2
1999	1
2000	2
2001	1
2004	2
2005	6
2006	4
2007	4
2008	8
2009	3
2010	1
2011	1
2012	1
2014	1
2015	1
2024	0

1

Mouse Models for the Dissection of CHD7 Functions in Eye Development and the Molecular Basis for Ocular Defects in CHARGE Syndrome.

Gage PJ, Hurd EA, Martin DM. Gage PJ, et al. Invest Ophthalmol Vis Sci. 2015 Dec;56(13):7923-30. doi: 10.1167/iovs.15-18069. Invest Ophthalmol Vis Sci. 2015. PMID: 26670829 Free PMC article.

2

Inappropriate p53 activation during development induces features of CHARGE syndrome.

Van Nostrand JL, Brady CA, Jung H, Fuentes DR, Kozak MM, Johnson TM, Lin CY, Lin CJ, Swiderski DL, Vogel H, Bernstein JA, Attié-Bitach T, Chang CP, Wysocka J, Martin DM, Attardi LD. Van Nostrand JL, et al. Nature. 2014 Oct 9;514(7521):228-32. doi: 10.1038/nature13585. Epub 2014 Aug 3. Nature. 2014. PMID: 25119037 Free PMC article.

3

CHD7 mutations causing CHARGE syndrome are predominantly of paternal origin.

Pauli S, von Velsen N, Burfeind P, Steckel M, Mänz J, Buchholz A, Borozdin W, Kohlhase J. Pauli S, et al. Clin Genet. 2012 Mar;81(3):234-9. doi: 10.1111/j.1399-0004.2011.01701.x. Epub 2011 May 27. Clin Genet. 2012. PMID: 21554267

4

CHD7 cooperates with PBAF to control multipotent neural crest formation.

Bajpai R, Chen DA, Rada-Iglesias A, Zhang J, Xiong Y, Helms J, Chang CP, Zhao Y, Swigut T, Wysocka J. Bajpai R, et al. Nature. 2010 Feb 18;463(7283):958-62. doi: 10.1038/nature08733. Epub 2010 Feb 3. Nature. 2010. PMID: 20130577 Free PMC article.

5

Radial aplasia in CHARGE syndrome: a new association.

Wright EM, O'Connor R, Kerr BA. Wright EM, et al. Eur J Med Genet. 2009 Jul-Aug;52(4):239-41. doi: 10.1016/j.ejmg.2009.03.017. Epub 2009 Apr 16. Eur J Med Genet. 2009. PMID: 19375527

6

Defects in neural stem cell proliferation and olfaction in Chd7 deficient mice indicate a mechanism for hyposmia in human CHARGE syndrome.

Layman WS, McEwen DP, Beyer LA, Lalani SR, Fernbach SD, Oh E, Swaroop A, Hegg CC, Raphael Y, Martens JR, Martin DM. Layman WS, et al. Hum Mol Genet. 2009 Jun 1;18(11):1909-23. doi: 10.1093/hmg/ddp112. Epub 2009 Mar 11. Hum Mol Genet. 2009. PMID: 19279158 Free PMC article.

7

CHD7 mutations in patients initially diagnosed with Kallmann syndrome--the clinical overlap with CHARGE syndrome.

Jongmans MC, van Ravenswaaij-Arts CM, Pitteloud N, Ogata T, Sato N, Claahsen-van der Grinten HL, van der Donk K, Seminara S, Bergman JE, Brunner HG, Crowley WF Jr, Hoefsloot LH. Jongmans MC, et al. Clin Genet. 2009 Jan;75(1):65-71. doi: 10.1111/j.1399-0004.2008.01107.x. Epub 2008 Nov 17. Clin Genet. 2009. PMID: 19021638 Free PMC article.

8

A familial CHARGE syndrome with a CHD7 nonsense mutation and new clinical features.

Vuorela PE, Penttinen MT, Hietala MH, Laine JO, Huoponen KA, Kääriäinen HA. Vuorela PE, et al. Clin Dysmorphol. 2008 Oct;17(4):249-53. doi: 10.1097/MCD.0b013e328306a704. Clin Dysmorphol. 2008. PMID: 18978652

9

Mutations in CHD7, encoding a chromatin-remodeling protein, cause idiopathic hypogonadotropic hypogonadism and Kallmann syndrome.

Kim HG, Kurth I, Lan F, Meliciani I, Wenzel W, Eom SH, Kang GB, Rosenberger G, Tekin M, Ozata M, Bick DP, Sherins RJ, Walker SL, Shi Y, Gusella JF, Layman LC. Kim HG, et al. Am J Hum Genet. 2008 Oct;83(4):511-9. doi: 10.1016/j.ajhg.2008.09.005. Epub 2008 Oct 2. Am J Hum Genet. 2008. PMID: 18834967 Free PMC article.

10

Expanding the "E" in CHARGE.

Alazami AM, Alzahrani F, Alkuraya FS. Alazami AM, et al. Am J Med Genet A. 2008 Jul 15;146A(14):1890-2. doi: 10.1002/ajmg.a.32376. Am J Med Genet A. 2008. PMID: 18553515 No abstract available.

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