PubMed (OMIM) for id: 55636

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	3
2001	1
2004	2
2005	6
2006	5
2007	6
2008	8
2009	4
2010	5
2011	2
2012	1
2013	1
2014	2
2015	3
2016	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

Exome sequencing identifies rare variants in multiple genes in atrioventricular septal defect.

D'Alessandro LC, Al Turki S, Manickaraj AK, Manase D, Mulder BJ, Bergin L, Rosenberg HC, Mondal T, Gordon E, Lougheed J, Smythe J, Devriendt K, Bhattacharya S, Watkins H, Bentham J, Bowdin S, Hurles ME, Mital S. D'Alessandro LC, et al. Genet Med. 2016 Feb;18(2):189-98. doi: 10.1038/gim.2015.60. Epub 2015 May 21. Genet Med. 2016. PMID: 25996639 Free PMC article.

3

Dysfunctional SEMA3E signaling underlies gonadotropin-releasing hormone neuron deficiency in Kallmann syndrome.

Cariboni A, André V, Chauvet S, Cassatella D, Davidson K, Caramello A, Fantin A, Bouloux P, Mann F, Ruhrberg C. Cariboni A, et al. J Clin Invest. 2015 Jun;125(6):2413-28. doi: 10.1172/JCI78448. Epub 2015 May 18. J Clin Invest. 2015. PMID: 25985275 Free PMC article.

4

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.

5

CHD7, the gene mutated in CHARGE syndrome, regulates genes involved in neural crest cell guidance.

Schulz Y, Wehner P, Opitz L, Salinas-Riester G, Bongers EM, van Ravenswaaij-Arts CM, Wincent J, Schoumans J, Kohlhase J, Borchers A, Pauli S. Schulz Y, et al. Hum Genet. 2014 Aug;133(8):997-1009. doi: 10.1007/s00439-014-1444-2. Epub 2014 Apr 13. Hum Genet. 2014. PMID: 24728844

6

CHD7 gene polymorphisms and familial idiopathic scoliosis.

Tilley MK, Justice CM, Swindle K, Marosy B, Wilson AF, Miller NH. Tilley MK, et al. Spine (Phila Pa 1976). 2013 Oct 15;38(22):E1432-6. doi: 10.1097/BRS.0b013e3182a51781. Spine (Phila Pa 1976). 2013. PMID: 23883829 Free PMC article.

7

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

8

Sox2 cooperates with Chd7 to regulate genes that are mutated in human syndromes.

Engelen E, Akinci U, Bryne JC, Hou J, Gontan C, Moen M, Szumska D, Kockx C, van Ijcken W, Dekkers DH, Demmers J, Rijkers EJ, Bhattacharya S, Philipsen S, Pevny LH, Grosveld FG, Rottier RJ, Lenhard B, Poot RA. Engelen E, et al. Nat Genet. 2011 Jun;43(6):607-11. doi: 10.1038/ng.825. Epub 2011 May 1. Nat Genet. 2011. PMID: 21532573

9

Kismet/CHD7 regulates axon morphology, memory and locomotion in a Drosophila model of CHARGE syndrome.

Melicharek DJ, Ramirez LC, Singh S, Thompson R, Marenda DR. Melicharek DJ, et al. Hum Mol Genet. 2010 Nov 1;19(21):4253-64. doi: 10.1093/hmg/ddq348. Epub 2010 Aug 17. Hum Mol Genet. 2010. PMID: 20716578 Free PMC article.

10

CHD7 functions in the nucleolus as a positive regulator of ribosomal RNA biogenesis.

Zentner GE, Hurd EA, Schnetz MP, Handoko L, Wang C, Wang Z, Wei C, Tesar PJ, Hatzoglou M, Martin DM, Scacheri PC. Zentner GE, et al. Hum Mol Genet. 2010 Sep 15;19(18):3491-501. doi: 10.1093/hmg/ddq265. Epub 2010 Jun 29. Hum Mol Genet. 2010. PMID: 20591827 Free PMC article.

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