Hata K - Search Results

1

Missense BICD2 variants in fetuses with congenital arthrogryposis and pterygia.

Masuda L, Hasegawa A, Kamura H, Hasegawa F, Yamamura M, Taniguchi K, Ito Y, Hata K, Samura O, Okamoto A. Masuda L, et al. Among authors: hata k. Hum Genome Var. 2024 Aug 26;11(1):32. doi: 10.1038/s41439-024-00290-z. Hum Genome Var. 2024. PMID: 39183348 Free PMC article.

2

Compilation of copy number variants identified in phenotypically normal and parous Japanese women.

Migita O, Maehara K, Kamura H, Miyakoshi K, Tanaka M, Morokuma S, Fukushima K, Shimamoto T, Saito S, Sago H, Nishihama K, Abe K, Nakabayashi K, Umezawa A, Okamura K, Hata K. Migita O, et al. Among authors: hata k. J Hum Genet. 2014 Jun;59(6):326-31. doi: 10.1038/jhg.2014.27. Epub 2014 May 1. J Hum Genet. 2014. PMID: 24785687

3

Increased epigenetic alterations at the promoters of transcriptional regulators following inadequate maternal gestational weight gain.

Kawai T, Yamada T, Abe K, Okamura K, Kamura H, Akaishi R, Minakami H, Nakabayashi K, Hata K. Kawai T, et al. Among authors: hata k. Sci Rep. 2015 Sep 29;5:14224. doi: 10.1038/srep14224. Sci Rep. 2015. PMID: 26415774 Free PMC article.

4

Novel Nonsense Mutation in the NLRP7 Gene Associated with Recurrent Hydatidiform Mole.

Ito Y, Maehara K, Kaneki E, Matsuoka K, Sugahara N, Miyata T, Kamura H, Yamaguchi Y, Kono A, Nakabayashi K, Migita O, Higashimoto K, Soejima H, Okamoto A, Nakamura H, Kimura T, Wake N, Taniguchi T, Hata K. Ito Y, et al. Among authors: hata k. Gynecol Obstet Invest. 2016;81(4):353-8. doi: 10.1159/000441780. Epub 2015 Nov 26. Gynecol Obstet Invest. 2016. PMID: 26606510

5

Novel TFAP2A mutation in a Japanese family with Branchio-oculo-facial syndrome.

Sato T, Samura O, Kato N, Taniguchi K, Takahashi K, Ito Y, Aoki H, Kobayashi M, Migita O, Okamoto A, Hata K. Sato T, et al. Among authors: hata k. Hum Genome Var. 2018 May 10;5:5. doi: 10.1038/s41439-018-0004-z. eCollection 2018. Hum Genome Var. 2018. PMID: 29760939 Free PMC article.

6

Placental Development and Nutritional Environment.

Taniguchi K, Kawai T, Hata K. Taniguchi K, et al. Among authors: hata k. Adv Exp Med Biol. 2018;1012:63-73. doi: 10.1007/978-981-10-5526-3_7. Adv Exp Med Biol. 2018. PMID: 29956195 Review.

7

Molecular genetic analysis reveals atypical confined placental mosaicism with a small supernumerary marker chromosome derived from chromosome 18: A clinical report of discordant results from three prenatal tests.

Sato T, Samura O, Matsuoka T, Yoshida M, Aoki H, Migita O, Okamoto A, Hata K. Sato T, et al. Among authors: hata k. Eur J Med Genet. 2019 Jun;62(6):103533. doi: 10.1016/j.ejmg.2018.08.014. Epub 2018 Aug 30. Eur J Med Genet. 2019. PMID: 30171908

8

Analysis of chromosome microstructures in products of conception associated with recurrent miscarriage.

Sato T, Migita O, Hata H, Okamoto A, Hata K. Sato T, et al. Among authors: hata k, hata h. Reprod Biomed Online. 2019 May;38(5):787-795. doi: 10.1016/j.rbmo.2018.12.010. Epub 2018 Dec 21. Reprod Biomed Online. 2019. PMID: 30926177

9

Placenta-specific epimutation at H19-DMR among common pregnancy complications: its frequency and effect on the expression patterns of H19 and IGF2.

Yamaguchi Y, Tayama C, Tomikawa J, Akaishi R, Kamura H, Matsuoka K, Wake N, Minakami H, Kato K, Yamada T, Nakabayashi K, Hata K. Yamaguchi Y, et al. Among authors: hata k. Clin Epigenetics. 2019 Aug 1;11(1):113. doi: 10.1186/s13148-019-0712-3. Clin Epigenetics. 2019. PMID: 31370882 Free PMC article.

10

Amplicon Sequencing-Based Noninvasive Fetal Genotyping for RHD-Positive D Antigen-Negative Alleles.

Takahashi K, Migita O, Sasaki A, Nasu M, Kawashima A, Sekizawa A, Sato T, Ito Y, Sago H, Okamoto A, Nakabayashi K, Hata K. Takahashi K, et al. Among authors: hata k. Clin Chem. 2019 Oct;65(10):1307-1316. doi: 10.1373/clinchem.2019.307074. Epub 2019 Sep 5. Clin Chem. 2019. PMID: 31488553

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