PubMed for id: 105259599

Year	Number of Results
1992	1
1993	3
1996	1
1999	3
2000	5
2001	1
2002	2
2003	6
2004	4
2005	6
2006	9
2007	5
2008	14
2009	14
2010	16
2011	19
2012	19
2013	23
2014	22
2015	19
2016	2
2018	1
2019	1
2021	1
2022	1
2023	1
2024	0

1

Transient establishment of imprinted DNA methylation of transgenic human IC1 sequence in mouse during the preimplantation period.

Hirakawa K, Matsuzaki H, Tanimoto K. Hirakawa K, et al. Hum Mol Genet. 2021 Jan 21;29(22):3646-3661. doi: 10.1093/hmg/ddaa253. Hum Mol Genet. 2021. PMID: 33258474

2

Altered gene expression of H19 and IGF2 in placentas from ART pregnancies.

Sakian S, Louie K, Wong EC, Havelock J, Kashyap S, Rowe T, Taylor B, Ma S. Sakian S, et al. Placenta. 2015 Oct;36(10):1100-5. doi: 10.1016/j.placenta.2015.08.008. Epub 2015 Aug 21. Placenta. 2015. PMID: 26386650

3

Breast cancer risk and imprinting methylation in blood.

Harrison K, Hoad G, Scott P, Simpson L, Horgan GW, Smyth E, Heys SD, Haggarty P. Harrison K, et al. Clin Epigenetics. 2015 Sep 4;7(1):92. doi: 10.1186/s13148-015-0125-x. eCollection 2015. Clin Epigenetics. 2015. PMID: 26347357 Free PMC article.

4

Dynamics of DNA methylation at IGF2 in preterm and term infants during the first year of life: an observational study.

Piyasena C, Cartier J, Khulan B, French K, Menon G, Seckl JR, Reynolds RM, Drake AJ. Piyasena C, et al. Lancet. 2015 Feb 26;385 Suppl 1:S81. doi: 10.1016/S0140-6736(15)60396-8. Lancet. 2015. PMID: 26312903

5

[Impact of mobile phone radiation on the quality and DNA methylation of human sperm in vitro].

Wang D, Li B, Liu Y, Ma YF, Chen SQ, Sun HJ, Dong J, Ma XH, Zhou J, Wang XH. Wang D, et al. Zhonghua Nan Ke Xue. 2015 Jun;21(6):515-20. Zhonghua Nan Ke Xue. 2015. PMID: 26242041 Chinese.

6

Methylation-sensitive restriction enzyme nested real time PCR, a potential approach for sperm DNA identification.

Bai L, Yan P, Cao X, Jia L, Zhang C, Guo D. Bai L, et al. J Forensic Leg Med. 2015 Aug;34:34-9. doi: 10.1016/j.jflm.2015.05.001. Epub 2015 May 16. J Forensic Leg Med. 2015. PMID: 26165656

7

A prospective study validating a clinical scoring system and demonstrating phenotypical-genotypical correlations in Silver-Russell syndrome.

Azzi S, Salem J, Thibaud N, Chantot-Bastaraud S, Lieber E, Netchine I, Harbison MD. Azzi S, et al. J Med Genet. 2015 Jul;52(7):446-53. doi: 10.1136/jmedgenet-2014-102979. Epub 2015 May 7. J Med Genet. 2015. PMID: 25951829 Free PMC article.

8

(Epi)genotype-phenotype correlations in Beckwith-Wiedemann syndrome.

Mussa A, Russo S, De Crescenzo A, Freschi A, Calzari L, Maitz S, Macchiaiolo M, Molinatto C, Baldassarre G, Mariani M, Tarani L, Bedeschi MF, Milani D, Melis D, Bartuli A, Cubellis MV, Selicorni A, Cirillo Silengo M, Larizza L, Riccio A, Ferrero GB. Mussa A, et al. Eur J Hum Genet. 2016 Feb;24(2):183-90. doi: 10.1038/ejhg.2015.88. Epub 2015 Apr 22. Eur J Hum Genet. 2016. PMID: 25898929 Free PMC article.

9

The clinical course of an overgrowth syndrome, from diagnosis in infancy through adulthood: the case of Beckwith-Wiedemann syndrome.

Pappas JG. Pappas JG. Curr Probl Pediatr Adolesc Health Care. 2015 Apr;45(4):112-7. doi: 10.1016/j.cppeds.2015.03.001. Epub 2015 Apr 7. Curr Probl Pediatr Adolesc Health Care. 2015. PMID: 25861997 Review.

10

Reduced DNA methylation at the PEG3 DMR and KvDMR1 loci in children exposed to alcohol in utero: a South African Fetal Alcohol Syndrome cohort study.

Masemola ML, van der Merwe L, Lombard Z, Viljoen D, Ramsay M. Masemola ML, et al. Front Genet. 2015 Mar 10;6:85. doi: 10.3389/fgene.2015.00085. eCollection 2015. Front Genet. 2015. PMID: 25806045 Free PMC article.

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