1. 6p subtelomere deletion with congenital glaucoma, severe mental retardation, and growth impairment. Issue 3 (18th June 2013) Authors: Nakane, Takaya; Kousuke, Nakamura; Sonoko, Hata; Yuko, Kamiya; Sato, Hidenori; Kubota, Takeo; Sugita, Kanji Journal: Pediatrics international Issue: Volume 55:Issue 3(2013) Page Start: 376 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. An epigenome-wide study of cord blood DNA methylations in relation to prenatal perfluoroalkyl substance exposure: The Hokkaido study. (June 2018) Authors: Miura, Ryu; Araki, Atsuko; Miyashita, Chihiro; Kobayashi, Sumitaka; Kobayashi, Sachiko; Wang, Shu-Li; Chen, Chung-Hsing; Miyake, Kunio; Ishizuka, Mayumi; Iwasaki, Yusuke; Ito, Yoichi M.; Kubota, Takeo; Kishi, Reiko Journal: Environment international Issue: Volume 115(2018) Page Start: 21 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Combined annotation‐dependent depletion score for BRCA1/2 variants in patients with breast and/or ovarian cancer. Issue 2 (17th January 2018) Authors: Nakagomi, Hiroshi; Mochizuki, Hitoshi; Inoue, Masayuki; Hirotsu, Yosuke; Amemiya, Kenji; Sakamoto, Ikuko; Nakagomi, Satoko; Kubota, Takeo; Omata, Masao Journal: Cancer science Issue: Volume 109:Issue 2(2018) Page Start: 453 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Developmental origins of health and disease (DOHaD) : from biological basis to clinical significance /: from biological basis to clinical significance. ([2018]) Editors: Kubota, Takeo; Fukuoka, Hideoki Record Type: Book Extent: 1 online resource (vii, 95 pages), illustrations (some color) View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Epigenetics as a basis for diagnosis of neurodevelopmental disorders: challenges and opportunities. (July 2014) Authors: Kubota, Takeo; Miyake, Kunio; Hariya, Natsuyo; Mochizuki, Kazuki Journal: Expert review of molecular diagnostics Issue: Volume 14:Number 6(2014) Page Start: 685 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Epigenetics as a basis for diagnosis of neurodevelopmental disorders: challenges and opportunities. (July 2014) Authors: Kubota, Takeo; Miyake, Kunio; Hariya, Natsuyo; Mochizuki, Kazuki Journal: Expert review of molecular diagnostics Issue: Volume 14:Number 6(2014) Page Start: 685 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. GENETIC FACTORS ASSOCIATED WITH CHOROIDAL VASCULAR HYPERPERMEABILITY AND SUBFOVEAL CHOROIDAL THICKNESS IN POLYPOIDAL CHOROIDAL VASCULOPATHY. Issue 8 (August 2016) Authors: Yoneyama, Seigo; Sakurada, Yoichi; Kikushima, Wataru; Sugiyama, Atsushi; Tanabe, Naohiko; Mabuchi, Fumihiko; Kubota, Takeo; Iijima, Hiroyuki Journal: Retina Issue: Volume 36:Issue 8(2016:Aug.) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Genetic Variants in the SKIV2L Gene in Exudative Age-related Macular Degeneration in the Japanese Population. (September 2014) Authors: Yoneyama, Seigo; Sakurada, Yoichi; Mabuchi, Fumihiko; Sugiyama, Atsushi; Kubota, Takeo; Iijima, Hiroyuki Journal: Ophthalmic genetics Issue: Volume 35:Number 3(2014:Sep.) Page Start: 151 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Multicentric occurrence of multiple papillary thyroid carcinomas –HUMARA and BRAF mutation analysis. (17th April 2015) Authors: Nakazawa, Tadao; Kondo, Tetsuo; Tahara, Ippei; Kasai, Kazunari; Inoue, Tomohiro; Oishi, Naoki; Mochizuki, Kunio; Kubota, Takeo; Katoh, Ryohei Journal: Cancer medicine Issue: Volume 4:Number 8(2015:Aug.) Page Start: 1272 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Novel compound heterozygous mutations in UHRF1 are associated with atypical immunodeficiency, centromeric instability and facial anomalies syndrome with distinctive genome-wide DNA hypomethylation. Issue 9 (2nd December 2022) Authors: Unoki, Motoko; Velasco, Guillaume; Kori, Satomi; Arita, Kyohei; Daigaku, Yasukazu; Yeung, Wan Kin Au; Fujimoto, Akihiro; Ohashi, Hirofumi; Kubota, Takeo; Miyake, Kunio; Sasaki, Hiroyuki Journal: Human molecular genetics Issue: Volume 32:Issue 9(2023) Page Start: 1439 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗