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Fetal cell-free DNA fraction in maternal plasma is affected by fetal trisomy.
Suzumori N, Ebara T, Yamada T, Samura O, Yotsumoto J, Nishiyama M, Miura K, Sawai H, Murotsuki J, Kitagawa M, Kamei Y, Masuzaki H, Hirahara F, Saldivar JS, Dharajiya N, Sago H, Sekizawa A; Japan NIPT Consortium. Suzumori N, et al. Among authors: kamei y. J Hum Genet. 2016 Jul;61(7):647-52. doi: 10.1038/jhg.2016.25. Epub 2016 Mar 17. J Hum Genet. 2016. PMID: 26984559
Prenatal molecular diagnosis of a severe type of L1 syndrome (X-linked hydrocephalus).
Yamasaki M, Nonaka M, Suzumori N, Nakamura H, Fujita H, Namba A, Kamei Y, Yamada T, Pooh RK, Tanemura M, Sudo N, Nagasaka M, Yoshioka E, Shofuda T, Kanemura Y. Yamasaki M, et al. Among authors: kamei y. J Neurosurg Pediatr. 2011 Oct;8(4):411-6. doi: 10.3171/2011.7.PEDS10531. J Neurosurg Pediatr. 2011. PMID: 21961551
Uterine leiomyoma confounding a noninvasive prenatal test result.
Dharajiya NG, Namba A, Horiuchi I, Miyai S, Farkas DH, Almasri E, Saldivar JS, Takagi K, Kamei Y. Dharajiya NG, et al. Among authors: kamei y. Prenat Diagn. 2015 Oct;35(10):990-3. doi: 10.1002/pd.4629. Epub 2015 Jul 6. Prenat Diagn. 2015. PMID: 26058600 No abstract available.
A survey on awareness of genetic counseling for non-invasive prenatal testing: the first year experience in Japan.
Yotsumoto J, Sekizawa A, Suzumori N, Yamada T, Samura O, Nishiyama M, Miura K, Sawai H, Murotsuki J, Kitagawa M, Kamei Y, Masuzaki H, Hirahara F, Endo T, Fukushima A, Namba A, Osada H, Kasai Y, Watanabe A, Katagiri Y, Takeshita N, Ogawa M, Okai T, Izumi S, Hamanoue H, Inuzuka M, Haino K, Hamajima N, Nishizawa H, Okamoto Y, Nakamura H, Kanegawa T, Yoshimatsu J, Tairaku S, Naruse K, Masuyama H, Hyodo M, Kaji T, Maeda K, Matsubara K, Ogawa M, Yoshizato T, Ohba T, Kawano Y, Sago H; Japan NIPT Consortium. Yotsumoto J, et al. Among authors: kamei y. J Hum Genet. 2016 Dec;61(12):995-1001. doi: 10.1038/jhg.2016.96. Epub 2016 Sep 8. J Hum Genet. 2016. PMID: 27604555
Factors affecting parental decisions to terminate pregnancy in the presence of chromosome abnormalities: a Japanese multicenter study.
Nishiyama M, Sekizawa A, Ogawa K, Sawai H, Nakamura H, Samura O, Suzumori N, Nakayama S, Yamada T, Ogawa M, Katagiri Y, Murotsuki J, Okamoto Y, Namba A, Hamanoue H, Ogawa M, Miura K, Izumi S, Kamei Y, Sago H. Nishiyama M, et al. Among authors: kamei y. Prenat Diagn. 2016 Dec;36(12):1121-1126. doi: 10.1002/pd.4947. Epub 2016 Nov 21. Prenat Diagn. 2016. PMID: 27760457
Current status of non-invasive prenatal testing in Japan.
Samura O, Sekizawa A, Suzumori N, Sasaki A, Wada S, Hamanoue H, Hirahara F, Sawai H, Nakamura H, Yamada T, Miura K, Masuzaki H, Nakayama S, Okai T, Kamei Y, Namba A, Murotsuki J, Tanemoto T, Fukushima A, Haino K, Tairaku S, Matsubara K, Maeda K, Kaji T, Ogawa M, Osada H, Nishizawa H, Okamoto Y, Kanagawa T, Kakigano A, Kitagawa M, Ogawa M, Izumi S, Katagiri Y, Takeshita N, Kasai Y, Naruse K, Neki R, Masuyama H, Hyodo M, Kawano Y, Ohba T, Ichizuka K, Kido Y, Fukao T, Miharu N, Nagamatsu T, Watanabe A, Hamajima N, Hirose M, Sanui A, Shirato N, Yotsumoto J, Nishiyama M, Hirose T, Sago H. Samura O, et al. Among authors: kamei y. J Obstet Gynaecol Res. 2017 Aug;43(8):1245-1255. doi: 10.1111/jog.13373. Epub 2017 Jun 6. J Obstet Gynaecol Res. 2017. PMID: 28586143
Fetal cell-free DNA fraction in maternal plasma for the prediction of hypertensive disorders of pregnancy.
Suzumori N, Sekizawa A, Ebara T, Samura O, Sasaki A, Akaishi R, Wada S, Hamanoue H, Hirahara F, Izumi H, Sawai H, Nakamura H, Yamada T, Miura K, Masuzaki H, Yamashita T, Okai T, Kamei Y, Namba A, Murotsuki J, Tanemoto T, Fukushima A, Haino K, Tairaku S, Matsubara K, Maeda K, Kaji T, Ogawa M, Osada H, Nishizawa H, Okamoto Y, Kanagawa T, Kakigano A, Kitagawa M, Ogawa M, Izumi S, Katagiri Y, Takeshita N, Kasai Y, Naruse K, Neki R, Masuyama H, Hyodo M, Kawano Y, Ohba T, Ichizuka K, Nagamatsu T, Watanabe A, Shirato N, Yotsumoto J, Nishiyama M, Hirose T, Sago H. Suzumori N, et al. Among authors: kamei y. Eur J Obstet Gynecol Reprod Biol. 2018 May;224:165-169. doi: 10.1016/j.ejogrb.2018.03.048. Epub 2018 Mar 26. Eur J Obstet Gynecol Reprod Biol. 2018. PMID: 29605711
Maternal age-specific risk for trisomy 21 based on the clinical performance of NIPT and empirically derived NIPT age-specific positive and negative predictive values in Japan.
Yamada T, Sekizawa A, Fujii Y, Hirose T, Samura O, Suzumori N, Miura K, Sawai H, Hirahara F, Murotsuki J, Kamei Y, Sago H; Japan NIPT consortium*. Yamada T, et al. Among authors: kamei y. J Hum Genet. 2018 Oct;63(10):1035-1040. doi: 10.1038/s10038-018-0453-8. Epub 2018 May 30. J Hum Genet. 2018. PMID: 29849041 Clinical Trial.
692 results