Andrews S - Search Results

1

A maternal-effect Padi6 variant causes nuclear and cytoplasmic abnormalities in oocytes, as well as failure of epigenetic reprogramming and zygotic genome activation in embryos.

Giaccari C, Cecere F, Argenziano L, Pagano A, Galvao A, Acampora D, Rossi G, Hay Mele B, Acurzio B, Coonrod S, Cubellis MV, Cerrato F, Andrews S, Cecconi S, Kelsey G, Riccio A. Giaccari C, et al. Among authors: andrews s. Genes Dev. 2024 Mar 22;38(3-4):131-150. doi: 10.1101/gad.351238.123. Genes Dev. 2024. PMID: 38453481 Free PMC article.

2

A KHDC3L mutation resulting in recurrent hydatidiform mole causes genome-wide DNA methylation loss in oocytes and persistent imprinting defects post-fertilisation.

Demond H, Anvar Z, Jahromi BN, Sparago A, Verma A, Davari M, Calzari L, Russo S, Jahromi MA, Monk D, Andrews S, Riccio A, Kelsey G. Demond H, et al. Among authors: andrews s. Genome Med. 2019 Dec 17;11(1):84. doi: 10.1186/s13073-019-0694-y. Genome Med. 2019. PMID: 31847873 Free PMC article.

3

Dynamic CpG island methylation landscape in oocytes and preimplantation embryos.

Smallwood SA, Tomizawa S, Krueger F, Ruf N, Carli N, Segonds-Pichon A, Sato S, Hata K, Andrews SR, Kelsey G. Smallwood SA, et al. Among authors: andrews sr. Nat Genet. 2011 Jun 26;43(8):811-4. doi: 10.1038/ng.864. Nat Genet. 2011. PMID: 21706000 Free PMC article.

4

Effect of Superovulation Treatment on Oocyte's DNA Methylation.

Lopes JS, Ivanova E, Ruiz S, Andrews S, Kelsey G, Coy P. Lopes JS, et al. Among authors: andrews s. Int J Mol Sci. 2022 Dec 18;23(24):16158. doi: 10.3390/ijms232416158. Int J Mol Sci. 2022. PMID: 36555801 Free PMC article.

5

Single-cell genome-wide bisulfite sequencing for assessing epigenetic heterogeneity.

Smallwood SA, Lee HJ, Angermueller C, Krueger F, Saadeh H, Peat J, Andrews SR, Stegle O, Reik W, Kelsey G. Smallwood SA, et al. Nat Methods. 2014 Aug;11(8):817-820. doi: 10.1038/nmeth.3035. Epub 2014 Jul 20. Nat Methods. 2014. PMID: 25042786 Free PMC article.

6

Pervasive polymorphic imprinted methylation in the human placenta.

Hanna CW, Peñaherrera MS, Saadeh H, Andrews S, McFadden DE, Kelsey G, Robinson WP. Hanna CW, et al. Among authors: andrews s. Genome Res. 2016 Jun;26(6):756-67. doi: 10.1101/gr.196139.115. Epub 2016 Jan 14. Genome Res. 2016. PMID: 26769960 Free PMC article.

7

Loss of histone methyltransferase SETD1B in oogenesis results in the redistribution of genomic histone 3 lysine 4 trimethylation.

Hanna CW, Huang J, Belton C, Reinhardt S, Dahl A, Andrews S, Stewart AF, Kranz A, Kelsey G. Hanna CW, et al. Among authors: andrews s. Nucleic Acids Res. 2022 Feb 28;50(4):1993-2004. doi: 10.1093/nar/gkac051. Nucleic Acids Res. 2022. PMID: 35137160 Free PMC article.

8

Dynamic stage-specific changes in imprinted differentially methylated regions during early mammalian development and prevalence of non-CpG methylation in oocytes.

Tomizawa S, Kobayashi H, Watanabe T, Andrews S, Hata K, Kelsey G, Sasaki H. Tomizawa S, et al. Among authors: andrews s. Development. 2011 Mar;138(5):811-20. doi: 10.1242/dev.061416. Epub 2011 Jan 19. Development. 2011. PMID: 21247965 Free PMC article.

9

Multi-omics analyses demonstrate a critical role for EHMT1 methyltransferase in transcriptional repression during oogenesis.

Demond H, Hanna CW, Castillo-Fernandez J, Santos F, Papachristou EK, Segonds-Pichon A, Kishore K, Andrews S, D'Santos CS, Kelsey G. Demond H, et al. Among authors: andrews s. Genome Res. 2023 Jan;33(1):18-31. doi: 10.1101/gr.277046.122. Epub 2023 Jan 23. Genome Res. 2023. PMID: 36690445 Free PMC article.

10

DNA methylation changes during preimplantation development reveal inter-species differences and reprogramming events at imprinted genes.

Ivanova E, Canovas S, Garcia-Martínez S, Romar R, Lopes JS, Rizos D, Sanchez-Calabuig MJ, Krueger F, Andrews S, Perez-Sanz F, Kelsey G, Coy P. Ivanova E, et al. Among authors: andrews s. Clin Epigenetics. 2020 May 11;12(1):64. doi: 10.1186/s13148-020-00857-x. Clin Epigenetics. 2020. PMID: 32393379 Free PMC article.

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