| In utero undernourishment perturbs the adult sperm methylome and intergenerational metabolism EJ Radford, M Ito, H Shi, JA Corish, K Yamazawa, E Isganaitis, ... Science 345 (6198), 1255903, 2014 | 677 | 2014 |
| Uniparental disomy and human disease: an overview K Yamazawa, T Ogata, AC Ferguson‐Smith American Journal of Medical Genetics Part C: Seminars in Medical Genetics …, 2010 | 199 | 2010 |
| Allele-specific binding of ZFP57 in the epigenetic regulation of imprinted and non-imprinted monoallelic expression R Strogantsev, F Krueger, K Yamazawa, H Shi, P Gould, ... Genome biology 16, 1-18, 2015 | 163 | 2015 |
| Silver-Russell syndrome in a girl born after in vitro fertilization: partial hypermethylation at the differentially methylated region of PEG1/MEST M Kagami, T Nagai, M Fukami, K Yamazawa, T Ogata Journal of assisted reproduction and genetics 24, 131-136, 2007 | 153 | 2007 |
| Molecular and clinical findings and their correlations in Silver-Russell syndrome: implications for a positive role of IGF2 in growth determination and differential imprinting … K Yamazawa, M Kagami, T Nagai, T Kondoh, K Onigata, K Maeyama, ... Journal of molecular medicine 86, 1171-1181, 2008 | 78 | 2008 |
| Molecular and clinical studies in 138 Japanese patients with Silver-Russell syndrome T Fuke, S Mizuno, T Nagai, T Hasegawa, R Horikawa, Y Miyoshi, ... PLoS one 8 (3), e60105, 2013 | 71 | 2013 |
| Parthenogenetic chimaerism/mosaicism with a Silver-Russell syndrome-like phenotype K Yamazawa, K Nakabayashi, M Kagami, T Sato, S Saitoh, R Horikawa, ... Journal of medical genetics 47 (11), 782-785, 2010 | 54 | 2010 |
| H1foo has a pivotal role in qualifying induced pluripotent stem cells A Kunitomi, S Yuasa, F Sugiyama, Y Saito, T Seki, D Kusumoto, ... Stem Cell Reports 6 (6), 825-833, 2016 | 51 | 2016 |
| Monozygotic female twins discordant for Silver–Russell syndrome and hypomethylation of the H19-DMR K Yamazawa, M Kagami, M Fukami, K Matsubara, T Ogata Journal of human genetics 53 (10), 950-955, 2008 | 51 | 2008 |
| Mutation and Polymorphism Analyses of INSL3 and LGR8/GREAT in 62 Japanese Patients with Cryptorchidism K Yamazawa, Y Wada, I Sasagawa, K Aoki, K Ueoka, T Ogata Hormone Research in Paediatrics 67 (2), 73-76, 2007 | 41 | 2007 |
| Contribution of gene mutations to Silver-Russell syndrome phenotype: multigene sequencing analysis in 92 etiology-unknown patients T Inoue, A Nakamura, M Iwahashi-Odano, K Tanase-Nakao, K Matsubara, ... Clinical Epigenetics 12, 1-14, 2020 | 40 | 2020 |
| Androgenetic/biparental mosaicism in a girl with Beckwith–Wiedemann syndrome-like and upd (14) pat-like phenotypes K Yamazawa, K Nakabayashi, K Matsuoka, K Masubara, K Hata, ... Journal of human genetics 56 (1), 91-93, 2011 | 33 | 2011 |
| Molecular and clinical analyses of two patients with UPD (16) mat detected by screening 94 patients with Silver-Russell syndrome phenotype of unknown aetiology T Inoue, H Yagasaki, J Nishioka, A Nakamura, K Matsubara, S Narumi, ... Journal of medical genetics 56 (6), 413-418, 2019 | 30 | 2019 |
| Placentomegaly in paternal uniparental disomy for human chromosome 14 M Kagami, K Yamazawa, K Matsubara, N Matsuo, T Ogata Placenta 29 (8), 760-761, 2008 | 30 | 2008 |
| Role of imprinting disorders in short children born SGA and Silver-Russell syndrome spectrum T Fuke, A Nakamura, T Inoue, S Kawashima, KI Hara, K Matsubara, ... The Journal of Clinical Endocrinology & Metabolism 106 (3), 802-813, 2021 | 23 | 2021 |
| Familial Klippel–Feil anomaly and t (5; 8)(q35. 1; p21. 1) translocation M Goto, G Nishimura, T Nagai, K Yamazawa, T Ogata American Journal of Medical Genetics Part A 140 (9), 1013-1015, 2006 | 22 | 2006 |
| Hyponatremia, hypophosphatemia, and hypouricemia in a girl with macrophage activation syndrome K Yamazawa, K Kodo, J Maeda, S Omori, M Hida, T Mori, M Awazu Pediatrics 118 (6), 2557-2560, 2006 | 18 | 2006 |
| Neonatal intestinal volvulus and preduodenal portal vein associated with situs ambiguus: report of a case T Watanabe, M Nakano, K Yamazawa, K Maeyama, M Endo Surgery today 41 (5), 726-729, 2011 | 17 | 2011 |
| Placental hypoplasia in maternal uniparental disomy for chromosome 7 K Yamazawa, M Kagami, M Ogawa, R Horikawa, T Ogata American Journal of Medical Genetics Part A 146 (4), 514-516, 2008 | 16 | 2008 |
| Dynamics of transcription-mediated conversion from euchromatin to facultative heterochromatin at the Xist promoter by Tsix T Ohhata, K Yamazawa, A Miura-Kamio, S Takahashi, S Sakai, Y Tamura, ... Cell Reports 34 (13), 2021 | 14 | 2021 |
