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

Year Number of Results
1995 1
2000 5
2002 2
2003 2
2004 2
2005 2
2006 6
2007 5
2008 1
2009 1
2010 1
2011 1
2012 2
2013 6
2014 5
2015 2
2016 3
2017 5
2018 4
2019 4
2020 2
2021 4
2022 3
2023 3
2024 1

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63 results

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Page 1
Placental Mesenchymal Dysplasia and Beckwith-Wiedemann Syndrome.
Soejima H, Hara S, Ohba T, Higashimoto K. Soejima H, et al. Among authors: higashimoto k. Cancers (Basel). 2022 Nov 12;14(22):5563. doi: 10.3390/cancers14225563. Cancers (Basel). 2022. PMID: 36428656 Free PMC article. Review.
Donor cord blood aging accelerates in recipients after transplantation.
Onizuka M, Imanishi T, Harada K, Aoyama Y, Amaki J, Toyosaki M, Machida S, Kikkawa E, Yamada S, Nakabayashi K, Hata K, Higashimoto K, Soejima H, Ando K. Onizuka M, et al. Among authors: higashimoto k. Sci Rep. 2023 Feb 14;13(1):2603. doi: 10.1038/s41598-023-29912-2. Sci Rep. 2023. PMID: 36788379 Free PMC article.
CTCF deletion syndrome: clinical features and epigenetic delineation.
Hori I, Kawamura R, Nakabayashi K, Watanabe H, Higashimoto K, Tomikawa J, Ieda D, Ohashi K, Negishi Y, Hattori A, Sugio Y, Wakui K, Hata K, Soejima H, Kurosawa K, Saitoh S. Hori I, et al. Among authors: higashimoto k. J Med Genet. 2017 Dec;54(12):836-842. doi: 10.1136/jmedgenet-2017-104854. Epub 2017 Aug 28. J Med Genet. 2017. PMID: 28848059
The HUS1B promoter is hypomethylated in the placentas of low-birth-weight infants.
Rumbajan JM, Yamaguchi Y, Nakabayashi K, Higashimoto K, Yatsuki H, Nishioka K, Matsuoka K, Aoki S, Toda S, Takeda S, Seki H, Hatada I, Hata K, Soejima H, Joh K. Rumbajan JM, et al. Among authors: higashimoto k. Gene. 2016 Jun 1;583(2):141-146. doi: 10.1016/j.gene.2016.02.025. Epub 2016 Feb 18. Gene. 2016. PMID: 26911255
63 results