• 1166 引用
  • 21 h指数
20062020

年単位の研究成果

Pureに変更を加えた場合、すぐここに表示されます。

研究成果

  • 1166 引用
  • 21 h指数
  • 55 Article
  • 5 Review article
  • 2 Comment/debate
  • 1 Short survey
フィルター
Article
2020

A case of a parthenogenetic 46,XX/46,XY chimera presenting ambiguous genitalia

Kawamura, R., Kato, T., Miyai, S., Suzuki, F., Naru, Y., Kato, M., Tanaka, K., Nagasaka, M., Tsutsumi, M., Inagaki, H., Ioroi, T., Yoshida, M., Nao, T., Conlin, L. K., Iijima, K., Kurahashi, H. & Taniguchi-Ikeda, M., 01-01-2020, (Accepted/In press) : : Journal of Human Genetics.

研究成果: Article

公開

Analysis of the Origin of Double Mosaic Aneuploidy in Two Cases

Kato, T., Kawai, M., Miyai, S., Suzuki, F., Tsutsumi, M., Mizuno, S., Ikeda, T. & Kurahashi, H., 01-01-2020, (Accepted/In press) : : Cytogenetic and Genome Research.

研究成果: Article

Novel mutation in the KITLG gene in familial progressive hyperpigmentation with or without hypopigmentation

Kato, M., Yagami, A., Tsukamoto, T., Shinkai, Y., Kato, T. & Kurahashi, H., 01-06-2020, : : Journal of Dermatology. 47, 6, p. 669-672 4 p.

研究成果: Article

The involvement of U-type dicentric chromosomes in the formation of terminal deletions with or without adjacent inverted duplications

Kato, T., Inagaki, H., Miyai, S., Suzuki, F., Naru, Y., Shinkai, Y., Kato, A., Kanyama, K., Mizuno, S., Muramatsu, Y., Yamamoto, T., Shinya, M., Tazaki, Y., Hiwatashi, S., Ikeda, T., Ozaki, M. & Kurahashi, H., 01-01-2020, (Accepted/In press) : : Human Genetics.

研究成果: Article

2019

A case of dihydropyrimidinase deficiency incidentally detected by urine metabolome analysis

Tsuchiya, H., Akiyama, T., Kuhara, T., Nakajima, Y., Ohse, M., Kurahashi, H., Kato, T., Maeda, Y., Yoshinaga, H. & Kobayashi, K., 03-2019, : : Brain and Development. 41, 3, p. 280-284 5 p.

研究成果: Article

A female patient with retinoblastoma and severe intellectual disability carrying an X;13 balanced translocation without rearrangement in the RB1 gene: A case report

Tsutsumi, M., Hattori, H., Akita, N., Maeda, N., Kubota, T., Horibe, K., Fujita, N., Kawai, M., Shinkai, Y., Kato, M., Kato, T., Kawamura, R., Suzuki, F. & Kurahashi, H., 05-12-2019, : : BMC Medical Genomics. 12, 1, 182.

研究成果: Article

公開
1 引用 (Scopus)

DNA methylation accumulation in gastric mucosa adjacent to cancer after Helicobacter pylori eradication

Tahara, S., Tahara, T., Horiguchi, N., Kato, T., Shinkai, Y., Yamashita, H., Yamada, H., Kawamura, T., Terada, T., Okubo, M., Nagasaka, M., Nakagawa, Y., Shibata, T., Yamada, S., Urano, M., Tsukamoto, T., Kurahashi, H., Kuroda, M. & Ohmiya, N., 01-01-2019, : : International Journal of Cancer. 144, 1, p. 80-88 9 p.

研究成果: Article

5 引用 (Scopus)
2 引用 (Scopus)

Multiplex PCR in noninvasive prenatal diagnosis for FGFR3-related disorders

Terasawa, S., Kato, A., Nishizawa, H., Kato, T., Yoshizawa, H., Noda, Y., Miyazaki, J., Ito, M., Sekiya, T., Fujii, T. & Kurahashi, H., 01-01-2019, : : Congenital anomalies. 59, 1, p. 4-10 7 p.

研究成果: Article

1 引用 (Scopus)

Obstetric complication-associated ANXA5 promoter polymorphisms may affect gene expression via DNA secondary structures

Inagaki, H., Ota, S., Nishizawa, H., Miyamura, H., Nakahira, K., Suzuki, M., Nishiyama, S., Kato, T., Yanagihara, I. & Kurahashi, H., 01-05-2019, : : Journal of Human Genetics. 64, 5, p. 459-466 8 p.

研究成果: Article

Preimplantation genetic testing for aneuploidy: A comparison of live birth rates in patients with recurrent pregnancy loss due to embryonic aneuploidy or recurrent implantation failure

Sato, T., Sugiura-Ogasawara, M., Ozawa, F., Yamamoto, T., Kato, T., Kurahashi, H., Kuroda, T., Aoyama, N., Kato, K., Kobayashi, R., Fukuda, A., Utsunomiya, T., Kuwahara, A., Saito, H., Takeshita, T. & Irahara, M., 01-12-2019, : : Human Reproduction. 34, 12, p. 2340-2349 10 p.

研究成果: Article

3 引用 (Scopus)

Prostate stem cell antigen gene polymorphism is associated with H. Pylori–related promoter DNA methylation in nonneoplastic gastric epithelium

Tahara, T., Tahara, S., Horiguchi, N., Kato, T., Shinkai, Y., Okubo, M., Terada, T., Yoshida, D., Funasaka, K., Nagasaka, M., Nakagawa, Y., Kurahashi, H., Shibata, T., Tsukamoto, T. & Ohmiya, N., 01-01-2019, : : Cancer Prevention Research. 12, 9, p. 579-584 6 p.

研究成果: Article

1 引用 (Scopus)
2018

Genomic Characterization of Chromosomal Insertions: Insights into the Mechanisms Underlying Chromothripsis

Kato, T., Ouchi, Y., Inagaki, H., Makita, Y., Mizuno, S., Kajita, M., Ikeda, T., Takeuchi, K. & Kurahashi, H., 01-01-2018, : : Cytogenetic and Genome Research. 153, 1, p. 1-9 9 p.

研究成果: Article

10 引用 (Scopus)

Lethal persistent pulmonary hypertension of the newborn in Bohring–Opitz syndrome

Kibe, M., Ibara, S., Inagaki, H., Kato, T., Kurahashi, H. & Ikeda, T., 05-2018, : : American Journal of Medical Genetics, Part A. 176, 5, p. 1245-1248 4 p.

研究成果: Article

1 引用 (Scopus)

Potential role for nectin-4 in the pathogenesis of pre-eclampsia: A molecular genetic study

Ito, M., Nishizawa, H., Tsutsumi, M., Kato, A., Sakabe, Y., Noda, Y., Ohwaki, A., Miyazaki, J., Kato, T., Shiogama, K., Sekiya, T., Kurahashi, H. & Fujii, T., 14-09-2018, : : BMC Medical Genetics. 19, 1, 166.

研究成果: Article

Prenatal diagnosis of premature chromatid separation/mosaic variegated aneuploidy (PCS/MVA) syndrome

Yamaguchi, T., Yamaguchi, M., Akeno, K., Fujisaki, M., Sumiyoshi, K., Ohashi, M., Sameshima, H., Ozaki, M., Kato, M., Kato, T., Hosoba, E. & Kurahashi, H., 01-07-2018, : : Journal of Obstetrics and Gynaecology Research. 44, 7, p. 1313-1317 5 p.

研究成果: Article

2 引用 (Scopus)

Twin pregnancy with chromosomal abnormalities mimicking a gestational trophoblastic disorder and coexistent foetus on ultrasound

Ohwaki, A., Nishizawa, H., Aida, N., Kato, T., Kambayashi, A., Miyazaki, J., Ito, M., Urano, M., Kiriyama, Y., Kuroda, M., Nakayama, M., Sonta, S. I., Suzumori, K., Sekiya, T., Kurahashi, H. & Fujii, T., 03-10-2018, : : Journal of Obstetrics and Gynaecology. 38, 7, p. 1023-1025 3 p.

研究成果: Article

2017

A Japanese case of β-ureidopropionase deficiency with dysmorphic features

Akiyama, T., Shibata, T., Yoshinaga, H., Kuhara, T., Nakajima, Y., Kato, T., Maeda, Y., Ohse, M., Oka, M., Kageyama, M. & Kobayashi, K., 01-01-2017, : : Brain and Development. 39, 1, p. 58-61 4 p.

研究成果: Article

2 引用 (Scopus)

PCS/MVA syndrome caused by an Alu insertion in the BUB1B gene

Kato, M., Kato, T., Hosoba, E., Ohashi, M., Fujisaki, M., Ozaki, M., Yamaguchi, M., Sameshima, H. & Kurahashi, H., 08-06-2017, : : Human Genome Variation. 4, 17021.

研究成果: Article

公開
4 引用 (Scopus)

Remote intracranial recurrence of IDH mutant gliomas is associated with TP53 mutations and an 8q gain

Nakae, S., Kato, T., Murayama, K., Sasaki, H., Abe, M., Kumon, M., Kumai, T., Yamashiro, K., Inamasu, J., Hasegawa, M., Kurahashi, H. & Hirose, Y., 17-10-2017, : : Oncotarget. 8, 49, p. 84729-84742 14 p.

研究成果: Article

2016

Increased levels of soluble corin in pre-eclampsia and fetal growth restriction

Miyazaki, J., Nishizawa, H., Kambayashi, A., Ito, M., Noda, Y., Terasawa, S., Kato, T., Miyamura, H., Shiogama, K., Sekiya, T., Kurahashi, H. & Fujii, T., 01-12-2016, : : Placenta. 48, p. 20-25 6 p.

研究成果: Article

13 引用 (Scopus)

Preimplantation genetic diagnosis/screening by comprehensive molecular testing

Kurahashi, H., Kato, T., Miyazaki, J., Nishizawa, H., Nishio, E., Furukawa, H., Miyamura, H., Ito, M., Endo, T., Ouchi, Y., Inagaki, H. & Fujii, T., 01-01-2016, : : Reproductive Medicine and Biology. 15, 1, p. 13-19 7 p.

研究成果: Article

2 引用 (Scopus)
2015

Emergence and characterization of unusual DS-1-like G1P[8] rotavirus strains in children with diarrhea in Thailand

Komoto, S., Tacharoenmuang, R., Guntapong, R., Ide, T., Haga, K., Katayama, K., Kato, T., Ouchi, Y., Kurahashi, H., Tsuji, T., Sangkitporn, S. & Taniguchi, K., 05-11-2015, : : PloS one. 10, 11, e0141739.

研究成果: Article

38 引用 (Scopus)

Identification of novel FATP4 mutations in a Japanese patient with ichthyosis prematurity syndrome

Tsuge, I., Morishita, M., Kato, T., Tsutsumi, M., Inagaki, H., Mori, Y., Yamawaki, K., Inuo, C., Ieda, K., Ohye, T., Hayakawa, A. & Kurahashi, H., 12-02-2015, : : Human Genome Variation. 2, 15003.

研究成果: Article

公開
4 引用 (Scopus)

Intragenic duplication in the PHKD1 gene in autosomal recessive polycystic kidney disease

Miyazaki, J., Ito, M., Nishizawa, H., Kato, T., Minami, Y., Inagaki, H., Ohye, T., Miyata, M., Boda, H., Kiriyama, Y., Kuroda, M., Sekiya, T., Kurahashi, H. & Fujii, T., 26-10-2015, : : BMC Medical Genetics. 16, 1, 98.

研究成果: Article

2 引用 (Scopus)

Whole genomic analysis of an unusual human G6P[14] rotavirus strain isolated from a child with diarrhea in Thailand: Evidence for bovine-to-human interspecies transmission and reassortment events

Tacharoenmuang, R., Komoto, S., Guntapong, R., Ide, T., Haga, K., Katayama, K., Kato, T., Ouchi, Y., Kurahashi, H., Tsuji, T., Sangkitporn, S. & Taniguchi, K., 30-09-2015, : : PloS one. 10, 9, e0139381.

研究成果: Article

17 引用 (Scopus)
2014

Age-related decrease of meiotic cohesins in human oocytes

Tsutsumi, M., Fujiwara, R., Nishizawa, H., Ito, M., Kogo, H., Inagaki, H., Ohye, T., Kato, T., Fujii, T. & Kurahashi, H., 07-05-2014, : : PloS one. 9, 5, e96710.

研究成果: Article

72 引用 (Scopus)

Analysis of the t(3;8) of hereditary renal cell carcinoma: A palindrome-mediated translocation

Kato, T., Franconi, C. P., Sheridan, M. B., Hacker, A. M., Inagakai, H., Glover, T. W., Arlt, M. F., Drabkin, H. A., Gemmill, R. M., Kurahashi, H. & Emanuel, B. S., 04-2014, : : Cancer Genetics. 207, 4, p. 133-140 8 p.

研究成果: Article

13 引用 (Scopus)

Breakpoint analysis of the recurrent constitutional t(8;22)(q24.13;q11.21) translocation

Mishra, D., Kato, T., Inagaki, H., Kosho, T., Wakui, K., Kido, Y., Sakazume, S., Taniguchi-Ikeda, M., Morisada, N., Iijima, K., Fukushima, Y., Emanuel, B. S. & Kurahashi, H., 13-08-2014, : : Molecular Cytogenetics. 7, 1, 55.

研究成果: Article

5 引用 (Scopus)
2013

Two sequential cleavage reactions on cruciform DNA structures cause palindrome-mediated chromosomal translocations

Inagaki, H., Ohye, T., Kogo, H., Tsutsumi, M., Kato, T., Tong, M., Emanuel, B. S. & Kurahashi, H., 10-04-2013, : : Nature Communications. 4, 1592.

研究成果: Article

25 引用 (Scopus)
2011

A rare synaptonemal complex protein 3 gene variant in unexplained female infertility

Nishiyama, S., Kishi, T., Kato, T., Suzuki, M., Bolor, H., Nishizawa, H., Iwata, N., Udagawa, Y. & Kurahashi, H., 01-04-2011, : : Molecular Human Reproduction. 17, 4, p. 266-271 6 p.

研究成果: Article

6 引用 (Scopus)
77 引用 (Scopus)

DNA secondary structure is influenced by genetic variation and alters susceptibility to de novo translocation

Kato, T., Inagaki, H., Tong, M., Kogo, H., Ohye, T., Yamada, K., Tsutsumi, M., Emanuel, B. S. & Kurahashi, H., 14-09-2011, : : Molecular Cytogenetics. 4, 1, 18.

研究成果: Article

6 引用 (Scopus)

Lack of association between orexin receptor gene polymorphisms and obstructive sleep apnea syndrome in Japanese

Ahmed, W. A., Mori, T., Nishimura, Y., Nakata, S., Kato, T., Abdelhamid, W., Kurahashi, H. & Suzuki, K., 01-04-2011, : : Sleep and Biological Rhythms. 9, 2, p. 73-77 5 p.

研究成果: Article

Polymorphisms in the annexin A5 gene promoter in Japanese women with recurrent pregnancy loss

Miyamura, H., Nishizawa, H., Ota, S., Suzuki, M., Inagaki, A., Egusa, H., Nishiyama, S., Kato, T., Pryor-Koishi, K., Nakanishi, I., Fujita, T., Imayoshi, Y., Markoff, A., Yanagihara, I., Udagawa, Y. & Kurahashi, H., 01-07-2011, : : Molecular Human Reproduction. 17, 7, p. 447-452 6 p., gar008.

研究成果: Article

43 引用 (Scopus)
2010

A palindrome-mediated recurrent translocation with 3:1 meiotic nondisjunction: The t(8;22)(q24.13;q11.21)

Sheridan, M. B., Kato, T., Haldeman-Englert, C., Jalali, G. R., Milunsky, J. M., Zou, Y., Klaes, R., Gimelli, G., Gimelli, S., Gemmill, R. M., Drabkin, H. A., Hacker, A. M., Brown, J., Tomkins, D., Shaikh, T. H., Kurahashi, H., Zackai, E. H. & Emanuel, B. S., 13-08-2010, : : American Journal of Human Genetics. 87, 2, p. 209-218 10 p.

研究成果: Article

31 引用 (Scopus)

CD9 gene variations are not associated with female infertility in humans

Nishiyama, S., Kishi, T., Kato, T., Suzuki, M., Nishizawa, H., Pryor-Koishi, K., Sawada, T., Nishiyama, Y., Iwata, N., Udagawa, Y. & Kurahashi, H., 01-03-2010, : : Gynecologic and Obstetric Investigation. 69, 2, p. 116-121 6 p.

研究成果: Article

3 引用 (Scopus)

Genetic Variation in the Indoleamine 2,3-Dioxygenase Gene in Pre-eclampsia

Nishizawa, H., Kato, T., Ota, S., Nishiyama, S., Pryor-Koishi, K., Suzuki, M., Tsutsumi, M., Inagaki, H., Kurahashi, H. & Udagawa, Y., 01-07-2010, : : American Journal of Reproductive Immunology. 64, 1, p. 68-76 9 p.

研究成果: Article

8 引用 (Scopus)

Paternal origin of the de novo constitutional t(11;22)(q23;q11)

Ohye, T., Inagaki, H., Kogo, H., Tsutsumi, M., Kato, T., Tong, M., MacVille, M. V. E., Medne, L., Zackai, E. H., Emanuel, B. S. & Kurahashi, H., 01-07-2010, : : European Journal of Human Genetics. 18, 7, p. 783-787 5 p.

研究成果: Article

21 引用 (Scopus)

Polymorphisms of the 22q11.2 breakpoint region influence the frequency of de novo constitutional t(11;22)s in sperm

Tong, M., Kato, T., Yamada, K., Inagaki, H., Kogo, H., Ohye, T., Tsutsumi, M., Wang, J., Emanuel, B. S. & Kurahashi, H., 13-04-2010, : : Human molecular genetics. 19, 13, p. 2630-2637 8 p., ddq150.

研究成果: Article

15 引用 (Scopus)
2009

Analysis of nitric oxide metabolism as a placental or maternal factor underlying the etiology of pre-eclampsia

Nishizawa, H., Pryor-Koishi, K., Suzuki, M., Kato, T., Sekiya, T., Tada, S., Kurahashi, H. & Udagawa, Y., 01-11-2009, : : Gynecologic and Obstetric Investigation. 68, 4, p. 239-247 9 p.

研究成果: Article

13 引用 (Scopus)

Chromosomal instability mediated by non-B DNA: Cruciform conformation and not DNA sequence is responsible for recurrent translocation in humans

Inagaki, H., Ohye, T., Kogo, H., Kato, T., Bolor, H., Taniguchi, M., Shaikh, T. H., Emanuel, B. S. & Kurahashi, H., 01-02-2009, : : Genome Research. 19, 2, p. 191-198 8 p.

研究成果: Article

54 引用 (Scopus)

Impaired DNA replication prompts deletions within palindromic sequences, but does not induce translocations in human cells

Kurahashi, H., Inagaki, H., Kato, T., Hosoba, E., Kogo, H., Ohye, T., Tsutsumi, M., Bolor, H., Tong, M. & Emanuel, B. S., 04-09-2009, : : Human molecular genetics. 18, 18, p. 3397-3406 10 p.

研究成果: Article

14 引用 (Scopus)

Mutations of the SYCP3 Gene in Women with Recurrent Pregnancy Loss

Bolor, H., Mori, T., Nishiyama, S., Ito, Y., Hosoba, E., Inagaki, H., Kogo, H., Ohye, T., Tsutsumi, M., Kato, T., Tong, M., Nishizawa, H., Pryor-Koishi, K., Kitaoka, E., Sawada, T., Nishiyama, Y., Udagawa, Y. & Kurahashi, H., 09-01-2009, : : American Journal of Human Genetics. 84, 1, p. 14-20 7 p.

研究成果: Article

56 引用 (Scopus)
2008

Increased levels of pregnancy-associated plasma protein-A2 in the serum of pre-eclamptic patients

Nishizawa, H., Pryor-Koishi, K., Suzuki, M., Kato, T., Kogo, H., Sekiya, T., Kurahashi, H. & Udagawa, Y., 01-12-2008, : : Molecular Human Reproduction. 14, 10, p. 595-602 8 p.

研究成果: Article

39 引用 (Scopus)
20 引用 (Scopus)

Two different forms of palindrome resolution in the human genome: Deletion or translocation

Kato, T., Inagaki, H., Kogo, H., Ohye, T., Yamada, K., Emanuel, B. S. & Kurahashi, H., 15-04-2008, : : Human molecular genetics. 17, 8, p. 1184-1191 8 p.

研究成果: Article

15 引用 (Scopus)
2007

Age has no effect on de novo constitutional t(11;22) translocation frequency in sperm

Kato, T., Yamada, K., Inagaki, H., Kogo, H., Ohye, T., Emanuel, B. S. & Kurahashi, H., 01-11-2007, : : Fertility and Sterility. 88, 5, p. 1446-1448 3 p.

研究成果: Article

14 引用 (Scopus)

Cruciform extrusion propensity of human translocation-mediating palindromic AT-rich repeats

Kogo, H., Inagaki, H., Ohye, T., Kato, T., Emanuel, B. S. & Kurahashi, H., 01-02-2007, : : Nucleic Acids Research. 35, 4, p. 1198-1208 11 p.

研究成果: Article

26 引用 (Scopus)
113 引用 (Scopus)