| Contribution of intragenic DNA methylation in mouse gametic DNA methylomes to establish oocyte-specific heritable marks H Kobayashi, T Sakurai, M Imai, N Takahashi, A Fukuda, O Yayoi, S Sato, ... PLoS genetics 8 (1), e1002440, 2012 | 595 | 2012 |
| Disruption of a long-range cis-acting regulator for Shh causes preaxial polydactyly LA Lettice, T Horikoshi, SJH Heaney, MJ van Baren, HC van der Linde, ... Proceedings of the national academy of sciences 99 (11), 7548-7553, 2002 | 565 | 2002 |
| Targeted DNA demethylation in vivo using dCas9–peptide repeat and scFv–TET1 catalytic domain fusions S Morita, H Noguchi, T Horii, K Nakabayashi, M Kimura, K Okamura, ... Nature biotechnology 34 (10), 1060-1065, 2016 | 509 | 2016 |
| The transcriptional network that controls growth arrest and differentiation in a human myeloid leukemia cell line Nature genetics 41 (5), 553-562, 2009 | 422 | 2009 |
| Human genetic variation database, a reference database of genetic variations in the Japanese population K Higasa, N Miyake, J Yoshimura, K Okamura, T Niihori, H Saitsu, ... Journal of human genetics 61 (6), 547-553, 2016 | 304 | 2016 |
| Genome-wide parent-of-origin DNA methylation analysis reveals the intricacies of human imprinting and suggests a germline methylation-independent mechanism of establishment C Tayama, V Romanelli, A Martin-Trujillo, I Iglesias-Platas, K Okamura, ... Genome research 24 (4), 554-569, 2014 | 284 | 2014 |
| Human chromosome 7: DNA sequence and biology SW Scherer, J Cheung, JR MacDonald, LR Osborne, K Nakabayashi, ... Science 300 (5620), 767-772, 2003 | 275 | 2003 |
| Absence of a paternally inherited FOXP2 gene in developmental verbal dyspraxia L Feuk, A Kalervo, M Lipsanen-Nyman, J Skaug, K Nakabayashi, ... The American Journal of Human Genetics 79 (5), 965-972, 2006 | 249 | 2006 |
| ZNF384-related fusion genes define a subgroup of childhood B-cell precursor acute lymphoblastic leukemia with a characteristic immunotype S Hirabayashi, K Ohki, K Nakabayashi, H Ichikawa, Y Momozawa, ... haematologica 102 (1), 118, 2017 | 218 | 2017 |
| 5-Bromodeoxyuridine induces senescence-like phenomena in mammalian cells regardless of cell type or species M Eriko, K Nakabayashi, T Suzuki, SC Kaul, H Ogino, M Fujii, Y Mitsui, ... The journal of biochemistry 126 (6), 1052-1059, 1999 | 193 | 1999 |
| Offspring production with sperm grown in vitro from cryopreserved testis tissues T Yokonishi, T Sato, M Komeya, K Katagiri, Y Kubota, K Nakabayashi, ... Nature communications 5 (1), 4320, 2014 | 173 | 2014 |
| Histone methylation is mechanistically linked to DNA methylation at imprinting control regions in mammals A Henckel, K Nakabayashi, LA Sanz, R Feil, K Hata, P Arnaud Human molecular genetics 18 (18), 3375-3383, 2009 | 167 | 2009 |
| Post-transcriptional regulation of endothelial nitric-oxide synthase by an overlapping antisense mRNA transcript GB Robb, AR Carson, SC Tai, JE Fish, S Singh, T Yamada, SW Scherer, ... Journal of Biological Chemistry 279 (36), 37982-37996, 2004 | 165 | 2004 |
| Endothelial nitric-oxide synthase antisense (NOS3AS) gene encodes an autophagy-related protein (APG9-like2) highly expressed in trophoblast T Yamada, AR Carson, I Caniggia, K Umebayashi, T Yoshimori, ... Journal of Biological Chemistry 280 (18), 18283-18290, 2005 | 149 | 2005 |
| Release of telomeric DNA from chromosomes in immortal human cells lacking telomerase activity H Ogino, K Nakabayashi, M Suzuki, E Takahashi, M Fujii, T Suzuki, ... Biochemical and biophysical research communications 248 (2), 223-227, 1998 | 127 | 1998 |
| Mutations in SERPINB7, encoding a member of the serine protease inhibitor superfamily, cause Nagashima-type palmoplantar keratosis A Kubo, A Shiohama, T Sasaki, K Nakabayashi, H Kawasaki, T Atsugi, ... The American Journal of Human Genetics 93 (5), 945-956, 2013 | 126 | 2013 |
| Identification of the Imprinted KLF14 Transcription Factor Undergoing Human-Specific Accelerated Evolution L Parker-Katiraee, AR Carson, T Yamada, P Arnaud, R Feil, ... PLoS genetics 3 (5), e65, 2007 | 111 | 2007 |
| Identification of C7orf11 (TTDN1) gene mutations and genetic heterogeneity in nonphotosensitive trichothiodystrophy K Nakabayashi, D Amann, Y Ren, U Saarialho-Kere, N Avidan, S Gentles, ... The American Journal of Human Genetics 76 (3), 510-516, 2005 | 107 | 2005 |
| Human oocyte-derived methylation differences persist in the placenta revealing widespread transient imprinting M Sanchez-Delgado, F Court, E Vidal, J Medrano, ... PLoS genetics 12 (11), e1006427, 2016 | 104 | 2016 |
| Absence of Maternal Methylation in Biparental Hydatidiform Moles from Women with NLRP7 Maternal-Effect Mutations Reveals Widespread Placenta-Specific … M Sanchez-Delgado, A Martin-Trujillo, C Tayama, E Vidal, M Esteller, ... PLoS genetics 11 (11), e1005644, 2015 | 103 | 2015 |
