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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2002 1
2004 5
2005 3
2006 5
2007 2
2008 6
2010 2
2011 3
2012 5
2013 5
2014 5
2015 7
2016 8
2017 5
2018 6
2019 4
2020 1
2021 7
2022 1
2023 1
2024 0

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Similar articles for PMID: 27177470

75 results

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Page 1
A loss-of-function variant in SUV39H2 identified in autism-spectrum disorder causes altered H3K9 trimethylation and dysregulation of protocadherin β-cluster genes in the developing brain.
Balan S, Iwayama Y, Ohnishi T, Fukuda M, Shirai A, Yamada A, Weirich S, Schuhmacher MK, Dileep KV, Endo T, Hisano Y, Kotoshiba K, Toyota T, Otowa T, Kuwabara H, Tochigi M, Watanabe A, Ohba H, Maekawa M, Toyoshima M, Sasaki T, Nakamura K, Tsujii M, Matsuzaki H, Zhang KYJ, Jeltsch A, Shinkai Y, Yoshikawa T. Balan S, et al. Mol Psychiatry. 2021 Dec;26(12):7550-7559. doi: 10.1038/s41380-021-01199-7. Epub 2021 Jul 15. Mol Psychiatry. 2021. PMID: 34262135
SUV39H2 controls trophoblast stem cell fate.
Wang L, Chakraborty D, Iqbal K, Soares MJ. Wang L, et al. Biochim Biophys Acta Gen Subj. 2021 Jun;1865(6):129867. doi: 10.1016/j.bbagen.2021.129867. Epub 2021 Feb 5. Biochim Biophys Acta Gen Subj. 2021. PMID: 33556426 Free PMC article.
75 results