Similar articles for PMID: 30605843

Year	Number of Results
1992	3
1993	5
1994	2
1995	4
1996	5
1997	10
1998	6
1999	8
2000	1
2001	5
2002	1
2003	3
2004	3
2005	2
2006	1
2007	1
2008	3
2009	3
2010	3
2011	4
2012	2
2013	5
2014	13
2015	6
2016	4
2017	4
2018	9
2019	24
2020	9
2021	8
2022	12
2023	5
2024	1

1

Establishment of human induced pluripotent stem cell line from a patient with Angelman syndrome carrying the deletion of maternal chromosome 15q11.2-q13.

Niki T, Imamura K, Enami T, Kinoshita M, Inoue H. Niki T, et al. Stem Cell Res. 2019 Jan;34:101363. doi: 10.1016/j.scr.2018.101363. Epub 2018 Dec 10. Stem Cell Res. 2019. PMID: 30605843 Free article.

2

Generation and characterization of induced pluripotent stem cell line (IBBISTi004-A) from an Angelman syndrome patient carrying a class II deletion of the maternal chromosome 15q11.2-q13.

Maranga C, Pereira C, Raposo AC, Vieira A, Duarte S, Bekman EP, Milagre I, da Rocha ST. Maranga C, et al. Stem Cell Res. 2022 May;61:102757. doi: 10.1016/j.scr.2022.102757. Epub 2022 Mar 21. Stem Cell Res. 2022. PMID: 35339881 Free article.

3

Generation of an induced pluripotent stem cell line from a patient with Angelman syndrome carrying UBE3A mutation.

Li S, Zhu Q, Cai Y, Yang Q. Li S, et al. Stem Cell Res. 2022 Jul;62:102791. doi: 10.1016/j.scr.2022.102791. Epub 2022 Apr 25. Stem Cell Res. 2022. PMID: 35489268 Free article.

4

Angelman syndrome and severe infections in a patient with de novo 15q11.2-q13.1 deletion and maternally inherited 2q21.3 microdeletion.

Neubert G, von Au K, Drossel K, Tzschach A, Horn D, Nickel R, Kaindl AM. Neubert G, et al. Gene. 2013 Jan 10;512(2):453-5. doi: 10.1016/j.gene.2012.10.061. Epub 2012 Nov 1. Gene. 2013. PMID: 23124039

5

Somatic and germ-line mosaicism of deletion 15q11.2-q13 in a mother of dyzigotic twins with Angelman syndrome.

Sánchez J, Fernández R, Madruga M, Bernabeu-Wittel J, Antiñolo G, Borrego S. Sánchez J, et al. Am J Med Genet A. 2014 Feb;164A(2):370-6. doi: 10.1002/ajmg.a.36281. Epub 2013 Dec 5. Am J Med Genet A. 2014. PMID: 24311297

6

Gene expression analysis of human induced pluripotent stem cell-derived neurons carrying copy number variants of chromosome 15q11-q13.1.

Germain ND, Chen PF, Plocik AM, Glatt-Deeley H, Brown J, Fink JJ, Bolduc KA, Robinson TM, Levine ES, Reiter LT, Graveley BR, Lalande M, Chamberlain SJ. Germain ND, et al. Mol Autism. 2014 Aug 20;5:44. doi: 10.1186/2040-2392-5-44. eCollection 2014. Mol Autism. 2014. PMID: 25694803 Free PMC article.

7

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.

8

Distinct phenotypes distinguish the molecular classes of Angelman syndrome.

Lossie AC, Whitney MM, Amidon D, Dong HJ, Chen P, Theriaque D, Hutson A, Nicholls RD, Zori RT, Williams CA, Driscoll DJ. Lossie AC, et al. J Med Genet. 2001 Dec;38(12):834-45. doi: 10.1136/jmg.38.12.834. J Med Genet. 2001. PMID: 11748306 Free PMC article.

9

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.

10

Three lines of induced pluripotent stem cells derived from a 15q11.2-q13.1 duplication syndrome patient.

Arioka Y, Kushima I, Mori D, Ozaki N. Arioka Y, et al. Stem Cell Res. 2018 Aug;31:240-243. doi: 10.1016/j.scr.2018.08.004. Epub 2018 Aug 10. Stem Cell Res. 2018. PMID: 30144654 Free article.

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