1. Aberrant hypomethylation at imprinted differentially methylated regions is involved in biparental placental mesenchymal dysplasia. (October 2022) Authors: Soejima, Hidenobu; Aoki, Saori; Higashimoto, Ken; Mishima, Hiroyuki; Yoshiura, Koh-ichiro; Nakabayashi, Kazuhiko; Hata, Kenichiro; Hara, Satoshi; Ohba, Takashi; Katabuchi, Hidetaka Journal: Placenta Issue: Volume 128(2022) Page Start: 123 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Clinical manifestations of placental mesenchymal dysplasia in Japan: A multicenter case series. Issue 3 (18th January 2021) Authors: Kodera, Chisato; Aoki, Saori; Ohba, Takashi; Higashimoto, Ken; Mikami, Yoshiki; Fukunaga, Masaharu; Soejima, Hidenobu; Katabuchi, Hidetaka Journal: Journal of obstetrics and gynaecology research Issue: Volume 47:Issue 3(2021) Page Start: 1118 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Cover Image, Volume 38, Issue 6. Issue 6 (June 2017) Authors: Imagawa, Eri; Higashimoto, Ken; Sakai, Yasunari; Numakura, Chikahiko; Okamoto, Nobuhiko; Matsunaga, Satoko; Ryo, Akihide; Sato, Yoshinori; Sanefuji, Masafumi; Ihara, Kenji; Takada, Yui; Nishimura, Gen; Saitsu, Hirotomo; Mizuguchi, Takeshi; Miyatake, Satoko; Nakashima, Mitsuko; Miyake, Noriko; Soe... Journal: Human mutation Issue: Volume 38:Issue 6(2017) Page Start: i Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. CTCF deletion syndrome: clinical features and epigenetic delineation. Issue 12 (28th August 2017) Authors: Hori, Ikumi; Kawamura, Rie; Nakabayashi, Kazuhiko; Watanabe, Hidetaka; Higashimoto, Ken; Tomikawa, Junko; Ieda, Daisuke; Ohashi, Kei; Negishi, Yutaka; Hattori, Ayako; Sugio, Yoshitsugu; Wakui, Keiko; Hata, Kenichiro; Soejima, Hidenobu; Kurosawa, Kenji; Saitoh, Shinji Journal: Journal of medical genetics Issue: Volume 54:Issue 12(2017) Page Start: 836 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. DNA methylation analysis of multiple imprinted DMRs in Sotos syndrome reveals IGF2‐DMR0 as a DNA methylation‐dependent, P0 promoter‐specific enhancer. Issue 1 (28th November 2019) Authors: Watanabe, Hidetaka; Higashimoto, Ken; Miyake, Noriko; Morita, Sumiyo; Horii, Takuro; Kimura, Mika; Suzuki, Takayuki; Maeda, Toshiyuki; Hidaka, Hidenori; Aoki, Saori; Yatsuki, Hitomi; Okamoto, Nobuhiko; Uemura, Tetsuji; Hatada, Izuho; Matsumoto, Naomichi; Soejima, Hidenobu Journal: FASEB journal Issue: Volume 34:Issue 1(2020) Page Start: 960 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Fibroadenoma in Beckwith–Wiedemann syndrome with paternal uniparental disomy of chromosome 11p15.5. Issue 6 (18th December 2014) Authors: Takama, Yuichi; Kubota, Akio; Nakayama, Masahiro; Higashimoto, Ken; Jozaki, Kosuke; Soejima, Hidenobu Journal: Pediatrics international Issue: Volume 56:Issue 6(2014) Page Start: 931 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Fibroadenoma in Beckwith–Wiedemann syndrome with paternal uniparental disomy of chromosome 11p15.5. Issue 6 (December 2014) Authors: Takama, Yuichi; Kubota, Akio; Nakayama, Masahiro; Higashimoto, Ken; Jozaki, Kosuke; Soejima, Hidenobu Journal: Pediatrics international Issue: Volume 56:Issue 6(2014) Page Start: 931 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Hypomethylation of a centromeric block of ICR1 is sufficient to cause Silver-Russell syndrome. Issue 6 (23rd May 2020) Authors: Higashimoto, Ken; Watanabe, Hijiri; Tanoue, Yuka; Tonoki, Hidefumi; Tokutomi, Tomoharu; Hara, Satoshi; Yatsuki, Hitomi; Soejima, Hidenobu Journal: Journal of medical genetics Issue: Volume 58:Issue 6(2021) Page Start: 422 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Long term survival of a patient with Perlman syndrome due to novel compound heterozygous missense mutations in RNB domain of DIS3L2. Issue 4 (22nd March 2017) Authors: Soma, Noriko; Higashimoto, Ken; Imamura, Masaru; Saitoh, Akihiko; Soejima, Hidenobu; Nagasaki, Keisuke Journal: American journal of medical genetics Issue: Volume 173:Issue 4(2017) Page Start: 1077 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Molecular genetic investigation of placental mesenchymal dysplasia. Issue 10 (October 2015) Authors: Aoki, Saori; Higashimoto, Ken; Hidaka, Hidenori; Watanabe, Hidetaka; Ohtsuka, Yasufumi; Mishima, Hiroyuki; Yoshiura, Koh-ichiro; Yatsuki, Hitomi; Nishioka, Kenichi; Joh, Kei-ichiro; Ohba, Takashi; Katabuchi, Hidetaka; Soejima, Hidenobu Journal: Placenta Issue: Volume 36:Issue 10(2015:Oct.) Page Start: A2 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗