Hamanoue, Haruka: search on Z-Library

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1

Distribution of PAPP-A and total hCG between 11 and 13 weeks of gestation in Japanese pregnant women

Hasegawa, Junichi, Wada, Seiji, Kasamatsu, Atsushi, Nakamura, Masamitsu, Hamanoue, Haruka, Iwata, Eriko, Murotsuki, Jun, Nagai, Ryuhei, Tateishi, Yoko, Sunami, Rei, Tajima, Atsushi, Murata, Susumu, Ma

Journal:

Journal of Maternal-Fetal and Neonatal Medicine

Year:

2018

Language:

english

File:

PDF, 854 KB

english, 2018

2

An infertile patient with Y chromosome b1/b3 deletion presenting with congenital bilateral absence of the vas deferens with normal spermatogenesis

Kuroda, Shinnosuke, Usui, Kimitsugu, Mori, Kohei, Yasuda, Kengo, Asai, Takuo, Sanjo, Hiroyuki, Yakanaka, Hiroyuki, Takeshima, Teppei, Kawahara, Takashi, Hamanoue, Haruka, Kato, Yoshitake, Miyoshi, Yas

Journal:

Clinical and Experimental Reproductive Medicine

Year:

2018

Language:

english

File:

PDF, 504 KB

english, 2018

3

Classification of factors involved in nonreportable results of noninvasive prenatal testing (NIPT) and prediction of success rate of second NIPT

Suzumori, Nobuhiro, Sekizawa, Akihiko, Takeda, Eri, Samura, Osamu, Sasaki, Aiko, Akaishi, Rina, Wada, Seiji, Hamanoue, Haruka, Hirahara, Fumiki, Kuriki, Hiroko, Sawai, Hideaki, Nakamura, Hiroaki, Yama

Journal:

Prenatal Diagnosis

Year:

2018

Language:

english

File:

PDF, 999 KB

english, 2018

4

Retrospective details of false-positive and false-negative results in non-invasive prenatal testing for fetal trisomies 21, 18 and 13

Suzumori, Nobuhiro, Sekizawa, Akihiko, Takeda, Eri, Samura, Osamu, Sasaki, Aiko, Akaishi, Rina, Wada, Seiji, Hamanoue, Haruka, Hirahara, Fumiki, Sawai, Hideaki, Nakamura, Hiroaki, Yamada, Takahiro, Mi

Journal:

European Journal of Obstetrics & Gynecology and Reproductive Biology

Year:

2020

File:

PDF, 3.10 MB

2020

5

A locus for ophthalmo-acromelic syndrome mapped to 10p11.23

Haruka Hamanoue, Andre Megarbane, Takaya Tohma, Akira Nishimura, Takeshi Mizuguchi, Hirotomo Saitsu, Haruya Sakai, Shoko Miura, Tatsushi Toda, Noriko Miyake, Norio Niikawa, Koichiro Yoshiura, Fumiki H

Journal:

American Journal of Medical Genetics Part A

Year:

2009

Language:

english

File:

PDF, 314 KB

english, 2009

6

Attitudes toward and current status of disclosure of secondary findings from next-generation sequencing: a nation-wide survey of clinical genetics professionals in Japan

Tsuchiya, Mio, Yamada, Takahiro, Akaishi, Rina, Hamanoue, Haruka, Hirasawa, Akira, Hyodo, Maki, Imoto, Issei, Kosho, Tomoki, Kurosawa, Kenji, Murakami, Hiromi, Nakatani, Kaname, Nomura, Fumio, Sasaki,

Journal:

Journal of Human Genetics

Year:

2020

File:

PDF, 821 KB

2020

7

Disrupted SOX10 regulation of GJC2 transcription causes Pelizaeus-Merzbacher-like disease

Hitoshi Osaka, Haruka Hamanoue, Ryoko Yamamoto, Atsuo Nezu, Megumi Sasaki, Hirotomo Saitsu, Kenji Kurosawa, Hiroko Shimbo, Naomichi Matsumoto, Ken Inoue

Journal:

Annals of Neurology

Year:

2010

Language:

english

File:

PDF, 282 KB

english, 2010

8

A −16C>T substitution in the 5′ UTR of thepuratrophin-1gene is prevalent in autosomal dominant cerebellar ataxia in Nagano

Takako Ohata, Kunihiro Yoshida, Haruya Sakai, Haruka Hamanoue, Takeshi Mizuguchi, Yusaku Shimizu, Tomomi Okano, Fumio Takada, Kinya Ishikawa, Hidehiro Mizusawa, Ko-ichiro Yoshiura, Yoshimitsu Fukushim

Journal:

Journal of Human Genetics

Year:

2006

Language:

english

File:

PDF, 233 KB

english, 2006

9

Complete hydatidiform mole and normal live birth following intracytoplasmic sperm injection

Haruka Hamanoue, Nobuko Umezu, Mika Okuda, Naoki Harada, Takako Ohata, Haruya Sakai, Takeshi Mizuguchi, Hiroshi Ishikawa, Tsuneo Takahashi, Kiyonori Miura, Fumiki Hirahara, Naomichi Matsumoto

Journal:

Journal of Human Genetics

Year:

2006

Language:

english

File:

PDF, 216 KB

english, 2006

10

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

Nishimura-Tadaki, Akira, Wada, Takahito, Bano, Gul, Gough, Karen, Warner, Janet, Kosho, Tomoki, Ando, Noriko, Hamanoue, Haruka, Sakakibara, Hideya, Nishimura, Gen, Tsurusaki, Yoshinori, Doi, Hiroshi,

Journal:

Journal of Human Genetics

Year:

2011

Language:

english

File:

PDF, 598 KB

english, 2011

11

Attitudes of clinical geneticists and certified genetic counselors to genome editing and its clinical applications: A nation-wide questionnaire survey in Japan

Taguchi, Iku, Yamada, Takahiro, Akaishi, Rina, Imoto, Issei, Kurosawa, Kenji, Nakatani, Kaname, Nomura, Fumio, Hamanoue, Haruka, Hyodo, Maki, Murakami, Hiromi, Yoshihashi, Hiroshi, Yotsumoto, Junko, K

Journal:

Journal of Human Genetics

Year:

2019

Language:

english

File:

PDF, 707 KB

english, 2019

12

Clinical features of Birt-Hogg-Dubé syndrome: A Japanese case with pulmonary cysts, fibrofolliculomas and renal cell carcinoma

Tanegashima, Tomohiko, Yamaguchi, Yukie, Hamanoue, Haruka, Yao, Masahiro, Furuya, Mitsuko, Aihara, Michiko

Journal:

The Journal of Dermatology

Year:

2016

Language:

english

File:

PDF, 292 KB

english, 2016

13

SMOC1 Is Essential for Ocular and Limb Development in Humans and Mice

Ippei Okada, Haruka Hamanoue, Koji Terada, Takaya Tohma, Andre Megarbane, Eliane Chouery, Joelle Abou-Ghoch, Nadine Jalkh, Ozgur Cogulu, Ferda Ozkinay, Kyoji Horie, Junji Takeda, Tatsuya Furuichi, Shi

Journal:

The American Journal of Human Genetics

Year:

2011

Language:

english

File:

PDF, 1.94 MB

english, 2011

14

Whole-exome sequencing identified a homozygous FNBP4 mutation in a family with a condition similar to microphthalmia with limb anomalies

Kondo, Yukiko, Koshimizu, Eriko, Megarbane, Andre, Hamanoue, Haruka, Okada, Ippei, Nishiyama, Kiyomi, Kodera, Hirofumi, Miyatake, Satoko, Tsurusaki, Yoshinori, Nakashima, Mitsuko, Doi, Hiroshi, Miyake

Journal:

American Journal of Medical Genetics Part A

Year:

2013

Language:

english

File:

PDF, 716 KB

english, 2013

15

Current status of non-invasive prenatal testing in Japan

Samura, Osamu, Sekizawa, Akihiko, Suzumori, Nobuhiro, Sasaki, Aiko, Wada, Seiji, Hamanoue, Haruka, Hirahara, Fumiki, Sawai, Hideaki, Nakamura, Hiroaki, Yamada, Takahiro, Miura, Kiyonori, Masuzaki, Hid

Journal:

Journal of Obstetrics and Gynaecology Research

Year:

2017

File:

PDF, 254 KB

2017

16

Genetic screening of 104 patients with congenitally malformed hearts revealed a fresh mutation of GATA4 in those with atrial septal defects

Hamanoue, Haruka, Rahayuningsih, Sri Endah, Hirahara, Yuya, Itoh, Junko, Yokoyama, Utako, Mizuguchi, Takeshi, Saitsu, Hirotomo, Miyake, Noriko, Hirahara, Fumiki, Matsumoto, Naomichi

Journal:

Cardiology in the Young

Year:

2009

Language:

english

File:

PDF, 120 KB

english, 2009

17

Preconceptional folic acid supplementation in Japan

Hirahara, Fumiki, Hamanoue, Haruka, Kurasawa, Kentaro

Journal:

Congenital Anomalies

Year:

2017

Language:

english

File:

PDF, 163 KB

english, 2017

18

Fetal cell-free DNA fraction in maternal plasma for the prediction of hypertensive disorders of pregnancy

Suzumori, Nobuhiro, Sekizawa, Akihiko, Ebara, Takeshi, Samura, Osamu, Sasaki, Aiko, Akaishi, Rina, Wada, Seiji, Hamanoue, Haruka, Hirahara, Fumiki, Izumi, Haruna, Sawai, Hideaki, Nakamura, Hiroaki, Ya

Journal:

European Journal of Obstetrics & Gynecology and Reproductive Biology

Year:

2018

Language:

english

File:

PDF, 635 KB

english, 2018

19

Multicenter experience with large panel next-generation sequencing in patients with advanced solid cancers in Japan

Kato, Shingo, Hayashi, Takuo, Suehara, Yoshiyuki, Hamanoue, Haruka, Yamanaka, Shoji, Ichikawa, Yasushi, Higurashi, Takuma, Ohashi, Kenichi, Yamaguchi, Shigeo, Nozaki, Yumi, Terao, Yasuhisa, Saito, Tsu

Journal:

Japanese Journal of Clinical Oncology

Year:

2018

Language:

english

File:

PDF, 1006 KB

english, 2018

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