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In vitro fertilization does not increase the incidence of de novo copy number alterations in fetal and placental lineages.
Nat Med. 2019 Nov;25(11):1699-1705. doi: 10.1038/s41591-019-0620-2. Epub 2019 Nov 4.
Nat Med. 2019.
PMID: 31686035
rs10732516 polymorphism at the IGF2/H19 locus associates with genotype-specific effects on placental DNA methylation and birth weight of newborns conceived by assisted reproductive technology.
Marjonen H, Auvinen P, Kahila H, Tšuiko O, Kõks S, Tiirats A, Viltrop T, Tuuri T, Söderström-Anttila V, Suikkari AM, Salumets A, Tiitinen A, Kaminen-Ahola N.
Marjonen H, et al. Among authors: tiirats a.
Clin Epigenetics. 2018 Jun 18;10:80. doi: 10.1186/s13148-018-0511-2. eCollection 2018.
Clin Epigenetics. 2018.
PMID: 29946374
Free PMC article.
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Using RNA sequencing for identifying gene imprinting and random monoallelic expression in human placenta.
Metsalu T, Viltrop T, Tiirats A, Rajashekar B, Reimann E, Kõks S, Rull K, Milani L, Acharya G, Basnet P, Vilo J, Mägi R, Metspalu A, Peters M, Haller-Kikkatalo K, Salumets A.
Metsalu T, et al. Among authors: tiirats a.
Epigenetics. 2014 Oct;9(10):1397-409. doi: 10.4161/15592294.2014.970052.
Epigenetics. 2014.
PMID: 25437054
Free PMC article.
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C14orf132 gene is possibly related to extremely low birth weight.
Tiirats A, Viltrop T, Nõukas M, Reimann E, Salumets A, Kõks S.
Tiirats A, et al.
BMC Genet. 2016 Sep 22;17(1):132. doi: 10.1186/s12863-016-0439-5.
BMC Genet. 2016.
PMID: 27660052
Free PMC article.
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