Similar articles for PMID: 18835857

Year	Number of Results
1990	1
1991	1
1992	2
1993	7
1994	5
1995	3
1996	3
1997	12
1998	9
1999	16
2000	6
2001	9
2002	7
2003	8
2004	9
2005	11
2006	9
2007	11
2008	10
2009	9
2010	11
2011	10
2012	12
2013	14
2014	6
2015	9
2016	16
2017	6
2018	9
2019	13
2020	11
2021	11
2022	7
2023	5
2024	1

1

Chromosome 15q11-13 duplication syndrome brain reveals epigenetic alterations in gene expression not predicted from copy number.

Hogart A, Leung KN, Wang NJ, Wu DJ, Driscoll J, Vallero RO, Schanen NC, LaSalle JM. Hogart A, et al. J Med Genet. 2009 Feb;46(2):86-93. doi: 10.1136/jmg.2008.061580. Epub 2008 Oct 7. J Med Genet. 2009. PMID: 18835857 Free PMC article.

2

Prader-Willi, Angelman, and 15q11-q13 Duplication Syndromes.

Kalsner L, Chamberlain SJ. Kalsner L, et al. Pediatr Clin North Am. 2015 Jun;62(3):587-606. doi: 10.1016/j.pcl.2015.03.004. Epub 2015 Apr 22. Pediatr Clin North Am. 2015. PMID: 26022164 Free PMC article. Review.

3

15q11-13 GABAA receptor genes are normally biallelically expressed in brain yet are subject to epigenetic dysregulation in autism-spectrum disorders.

Hogart A, Nagarajan RP, Patzel KA, Yasui DH, Lasalle JM. Hogart A, et al. Hum Mol Genet. 2007 Mar 15;16(6):691-703. doi: 10.1093/hmg/ddm014. Epub 2007 Mar 5. Hum Mol Genet. 2007. PMID: 17339270 Free PMC article.

4

Screening for genomic rearrangements and methylation abnormalities of the 15q11-q13 region in autism spectrum disorders.

Depienne C, Moreno-De-Luca D, Heron D, Bouteiller D, Gennetier A, Delorme R, Chaste P, Siffroi JP, Chantot-Bastaraud S, Benyahia B, Trouillard O, Nygren G, Kopp S, Johansson M, Rastam M, Burglen L, Leguern E, Verloes A, Leboyer M, Brice A, Gillberg C, Betancur C. Depienne C, et al. Biol Psychiatry. 2009 Aug 15;66(4):349-59. doi: 10.1016/j.biopsych.2009.01.025. Epub 2009 Mar 17. Biol Psychiatry. 2009. PMID: 19278672 Free article.

5

Genomic imprinting: potential function and mechanisms revealed by the Prader-Willi and Angelman syndromes.

Glenn CC, Driscoll DJ, Yang TP, Nicholls RD. Glenn CC, et al. Mol Hum Reprod. 1997 Apr;3(4):321-32. doi: 10.1093/molehr/3.4.321. Mol Hum Reprod. 1997. PMID: 9237260 Review.

6

Increased copy number for methylated maternal 15q duplications leads to changes in gene and protein expression in human cortical samples.

Scoles HA, Urraca N, Chadwick SW, Reiter LT, Lasalle JM. Scoles HA, et al. Mol Autism. 2011 Dec 12;2(1):19. doi: 10.1186/2040-2392-2-19. Mol Autism. 2011. PMID: 22152151 Free PMC article.

7

Parental Origin of Interstitial Duplications at 15q11.2-q13.3 in Schizophrenia and Neurodevelopmental Disorders.

Isles AR, Ingason A, Lowther C, Walters J, Gawlick M, Stöber G, Rees E, Martin J, Little RB, Potter H, Georgieva L, Pizzo L, Ozaki N, Aleksic B, Kushima I, Ikeda M, Iwata N, Levinson DF, Gejman PV, Shi J, Sanders AR, Duan J, Willis J, Sisodiya S, Costain G, Werge TM, Degenhardt F, Giegling I, Rujescu D, Hreidarsson SJ, Saemundsen E, Ahn JW, Ogilvie C, Girirajan SD, Stefansson H, Stefansson K, O'Donovan MC, Owen MJ, Bassett A, Kirov G. Isles AR, et al. PLoS Genet. 2016 May 6;12(5):e1005993. doi: 10.1371/journal.pgen.1005993. eCollection 2016 May. PLoS Genet. 2016. PMID: 27153221 Free PMC article.

8

Does parent of origin matter? Methylation studies should be performed on patients with multiple copies of the Prader-Willi/Angelman syndrome critical region.

Aypar U, Brodersen PR, Lundquist PA, Dawson DB, Thorland EC, Hoppman N. Aypar U, et al. Am J Med Genet A. 2014 Oct;164A(10):2514-20. doi: 10.1002/ajmg.a.36663. Epub 2014 Jun 26. Am J Med Genet A. 2014. PMID: 24975781

9

Identification of novel imprinted transcripts in the Prader-Willi syndrome and Angelman syndrome deletion region: further evidence for regional imprinting control.

Lee S, Wevrick R. Lee S, et al. Am J Hum Genet. 2000 Mar;66(3):848-58. doi: 10.1086/302817. Am J Hum Genet. 2000. PMID: 10712201 Free PMC article.

10

Mechanisms of imprinting of the Prader-Willi/Angelman region.

Horsthemke B, Wagstaff J. Horsthemke B, et al. Am J Med Genet A. 2008 Aug 15;146A(16):2041-52. doi: 10.1002/ajmg.a.32364. Am J Med Genet A. 2008. PMID: 18627066 Review.

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