Wada T - Search Results

1

Association of ALPL variants with serum alkaline phosphatase and bone traits in the general Japanese population: The Nagahama Study.

Nagata M, Setoh K, Takahashi M, Higasa K, Kawaguchi T, Kawasaki H, Wada T, Watanabe A, Sawai H, Tabara Y, Yamada T, Matsuda F, Kosugi S. Nagata M, et al. Among authors: wada t. J Hum Genet. 2020 Mar;65(3):337-343. doi: 10.1038/s10038-019-0712-3. Epub 2019 Dec 20. J Hum Genet. 2020. PMID: 31857675

2

The short-term mortality and morbidity of very low birth weight infants with trisomy 18 or trisomy 13 in Japan.

Kawasaki H, Yamada T, Takahashi Y, Nakayama T, Wada T, Kosugi S; Neonatal Research Network of Japan. Kawasaki H, et al. Among authors: wada t. J Hum Genet. 2021 Mar;66(3):273-285. doi: 10.1038/s10038-020-00825-6. Epub 2020 Sep 17. J Hum Genet. 2021. PMID: 32943740

3

Mortality and morbidity of infants with trisomy 21, weighing 1500 grams or less, in Japan.

Kawasaki H, Yamada T, Takahashi Y, Nakayama T, Wada T, Kosugi S; Neonatal Research Network of Japan. Kawasaki H, et al. Among authors: wada t. J Hum Genet. 2022 Nov;67(11):623-628. doi: 10.1038/s10038-022-01061-w. Epub 2022 Jul 5. J Hum Genet. 2022. PMID: 35787654

4

Current status and legal/ethical problems in the research use of the tissues of aborted human fetuses in Japan.

Kawasaki H, Yamada T, Wada T, Kosugi S. Kawasaki H, et al. Among authors: wada t. Congenit Anom (Kyoto). 2020 Nov;60(6):166-174. doi: 10.1111/cga.12381. Epub 2020 Aug 14. Congenit Anom (Kyoto). 2020. PMID: 32572995 Free article.

5

Epidemiology of Birth Defects in Very Low Birth Weight Infants in Japan.

Kawasaki H, Yamada T, Takahashi Y, Nakayama T, Wada T, Kosugi S; Neonatal Research Network of Japan. Kawasaki H, et al. Among authors: wada t. J Pediatr. 2020 Nov;226:106-111.e10. doi: 10.1016/j.jpeds.2020.07.012. Epub 2020 Jul 5. J Pediatr. 2020. PMID: 32634406

6

Analysis of triptan use during pregnancy in Japan: A case series.

Yamaguchi Y, Yamada T, Goto M, Kawasaki H, Wada T, Ikeda-Sakai Y, Saito Y, Hayashi M, Tanaka S, Takahashi R, Nakayama T, Murashima A, Kosugi S. Yamaguchi Y, et al. Among authors: wada t. Congenit Anom (Kyoto). 2022 Mar;62(2):78-81. doi: 10.1111/cga.12456. Epub 2022 Jan 13. Congenit Anom (Kyoto). 2022. PMID: 34981573

7

Complex hereditary spastic paraplegia associated with episodic visual loss caused by ACO2 variants.

Tozawa T, Nishimura A, Ueno T, Shikata A, Taura Y, Yoshida T, Nakagawa N, Wada T, Kosugi S, Uehara T, Takenouchi T, Kosaki K, Chiyonobu T. Tozawa T, et al. Among authors: wada t. Hum Genome Var. 2021 Jan 26;8(1):4. doi: 10.1038/s41439-021-00136-y. Hum Genome Var. 2021. PMID: 33500398 Free PMC article.

8

A case report of two brothers with ATR-X syndrome due to low maternal frequency of somatic mosaicism for an intragenic deletion in the ATRX.

Shimbo H, Ninomiya S, Kurosawa K, Wada T. Shimbo H, et al. Among authors: wada t. J Hum Genet. 2014 Jul;59(7):408-10. doi: 10.1038/jhg.2014.45. Epub 2014 Jun 5. J Hum Genet. 2014. PMID: 24898829

9

Breakpoint determination of X;autosome balanced translocations in four patients with premature ovarian failure.

Nishimura-Tadaki A, Wada T, Bano G, Gough K, Warner J, Kosho T, Ando N, Hamanoue H, Sakakibara H, Nishimura G, Tsurusaki Y, Doi H, Miyake N, Wakui K, Saitsu H, Fukushima Y, Hirahara F, Matsumoto N. Nishimura-Tadaki A, et al. Among authors: wada t. J Hum Genet. 2011 Feb;56(2):156-60. doi: 10.1038/jhg.2010.155. Epub 2010 Dec 9. J Hum Genet. 2011. PMID: 21150920

10

Nationwide survey on predictive genetic testing for late-onset, incurable neurological diseases in Japan.

Yoshida K, Wada T, Sakurai A, Wakui K, Ikeda SI, Fukushima Y. Yoshida K, et al. Among authors: wada t. J Hum Genet. 2007;52(8):675-679. doi: 10.1007/s10038-007-0170-1. Epub 2007 Jul 5. J Hum Genet. 2007. PMID: 17611709

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