Cited In for PMID: 18805826

Year	Number of Results
2008	2
2009	3
2010	1
2012	2
2013	1
2015	2
2016	1
2024	0

1

Clinical experience in the evaluation of 30 patients with a prior diagnosis of FG syndrome.

Lyons MJ, Graham JM Jr, Neri G, Hunter AG, Clark RD, Rogers RC, Moscarda M, Boccuto L, Simensen R, Dodd J, Robertson S, DuPont BR, Friez MJ, Schwartz CE, Stevenson RE. Lyons MJ, et al. J Med Genet. 2009 Jan;46(1):9-13. doi: 10.1136/jmg.2008.060509. Epub 2008 Sep 19. J Med Genet. 2009. PMID: 18805826

2

A novel MED12 mutation associated with non-specific X-linked intellectual disability.

Yamamoto T, Shimojima K. Yamamoto T, et al. Hum Genome Var. 2015 Jun 18;2:15018. doi: 10.1038/hgv.2015.18. eCollection 2015. Hum Genome Var. 2015. PMID: 27081531 Free PMC article.

3

The Involvement of Neuron-Specific Factors in Dendritic Spinogenesis: Molecular Regulation and Association with Neurological Disorders.

Hu HT, Shih PY, Shih YT, Hsueh YP. Hu HT, et al. Neural Plast. 2016;2016:5136286. doi: 10.1155/2016/5136286. Epub 2015 Dec 24. Neural Plast. 2016. PMID: 26819769 Free PMC article. Review.

4

MED12 related disorders.

Graham JM Jr, Schwartz CE. Graham JM Jr, et al. Am J Med Genet A. 2013 Nov;161A(11):2734-40. doi: 10.1002/ajmg.a.36183. Epub 2013 Oct 10. Am J Med Genet A. 2013. PMID: 24123922 Free PMC article. Review.

5

Rubinstein-Taybi syndrome: Clinical profile of 11 patients and review of literature.

Kumar S, Suthar R, Panigrahi I, Marwaha RK. Kumar S, et al. Indian J Hum Genet. 2012 May;18(2):161-6. doi: 10.4103/0971-6866.100751. Indian J Hum Genet. 2012. PMID: 23162289 Free PMC article.

6

Fragile X and X-linked intellectual disability: four decades of discovery.

Lubs HA, Stevenson RE, Schwartz CE. Lubs HA, et al. Am J Hum Genet. 2012 Apr 6;90(4):579-90. doi: 10.1016/j.ajhg.2012.02.018. Am J Hum Genet. 2012. PMID: 22482801 Free PMC article. Review.

7

Behavioral features in young adults with FG syndrome (Opitz-Kaveggia syndrome).

Graham JM Jr, Clark RD, Moeschler JB, Rogers RC. Graham JM Jr, et al. Am J Med Genet C Semin Med Genet. 2010 Nov 15;154C(4):477-85. doi: 10.1002/ajmg.c.30284. Am J Med Genet C Semin Med Genet. 2010. PMID: 20981778 Free PMC article. Review.

8

FG syndrome, an X-linked multiple congenital anomaly syndrome: the clinical phenotype and an algorithm for diagnostic testing.

Clark RD, Graham JM Jr, Friez MJ, Hoo JJ, Jones KL, McKeown C, Moeschler JB, Raymond FL, Rogers RC, Schwartz CE, Battaglia A, Lyons MJ, Stevenson RE. Clark RD, et al. Genet Med. 2009 Nov;11(11):769-75. doi: 10.1097/GIM.0b013e3181bd3d90. Genet Med. 2009. PMID: 19938245 Free PMC article.

9

A missense mutation in CASK causes FG syndrome in an Italian family.

Piluso G, D'Amico F, Saccone V, Bismuto E, Rotundo IL, Di Domenico M, Aurino S, Schwartz CE, Neri G, Nigro V. Piluso G, et al. Am J Hum Genet. 2009 Feb;84(2):162-77. doi: 10.1016/j.ajhg.2008.12.018. Epub 2009 Feb 5. Am J Hum Genet. 2009. PMID: 19200522 Free PMC article.

10

Behavior of 10 patients with FG syndrome (Opitz-Kaveggia syndrome) and the p.R961W mutation in the MED12 gene.

Graham JM Jr, Visootsak J, Dykens E, Huddleston L, Clark RD, Jones KL, Moeschler JB, Opitz JM, Morford J, Simensen R, Rogers RC, Schwartz CE, Friez MJ, Stevenson RE. Graham JM Jr, et al. Am J Med Genet A. 2008 Dec 1;146A(23):3011-7. doi: 10.1002/ajmg.a.32553. Am J Med Genet A. 2008. PMID: 18973276 Free PMC article.

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