| Age-related decrease of meiotic cohesins in human oocytes M Tsutsumi, R Fujiwara, H Nishizawa, M Ito, H Kogo, H Inagaki, T Ohye, ... PloS one 9 (5), e96710, 2014 | 166 | 2014 |
| Mutations of the SYCP3 gene in women with recurrent pregnancy loss H Bolor, T Mori, S Nishiyama, Y Ito, E Hosoba, H Inagaki, H Kogo, T Ohye, ... The American Journal of Human Genetics 84 (1), 14-20, 2009 | 119 | 2009 |
| In vivo visual reporter system for detection of estrogen-like substances by transgenic medaka K Kurauchi, Y Nakaguchi, M Tsutsumi, H Hori, R Kurihara, S Hashimoto, ... Environmental science & technology 39 (8), 2762-2768, 2005 | 91 | 2005 |
| HORMAD 2 is essential for synapsis surveillance during meiotic prophase via the recruitment of ATR activity H Kogo, M Tsutsumi, H Inagaki, T Ohye, H Kiyonari, H Kurahashi Genes to Cells 17 (11), 897-912, 2012 | 76 | 2012 |
| HORMAD1‐dependent checkpoint/surveillance mechanism eliminates asynaptic oocytes H Kogo, M Tsutsumi, T Ohye, H Inagaki, T Abe, H Kurahashi Genes to Cells 17 (6), 439-454, 2012 | 71 | 2012 |
| Structural and functional evolution of three cardiac natriuretic peptides K Inoue, T Sakamoto, S Yuge, H Iwatani, S Yamagami, M Tsutsumi, ... Molecular biology and evolution 22 (12), 2428-2434, 2005 | 69 | 2005 |
| The constitutional t (11; 22): implications for a novel mechanism responsible for gross chromosomal rearrangements H Kurahashi, H Inagaki, T Ohye, H Kogo, M Tsutsumi, T Kato, M Tong, ... Clinical genetics 78 (4), 299-309, 2010 | 65 | 2010 |
| Molecular basis of maternal age‐related increase in oocyte aneuploidy H Kurahashi, M Tsutsumi, S Nishiyama, H Kogo, H Inagaki, T Ohye Congenital Anomalies 52 (1), 8-15, 2012 | 55 | 2012 |
| Mutant analyses reveal different functions of fgfr1 in medaka and zebrafish despite conserved ligand–receptor relationships H Yokoi, A Shimada, M Carl, S Takashima, D Kobayashi, T Narita, T Jindo, ... Developmental biology 304 (1), 326-337, 2007 | 45 | 2007 |
| Zebrafish Dmrta2 regulates neurogenesis in the telencephalon A Yoshizawa, Y Nakahara, T Izawa, T Ishitani, M Tsutsumi, A Kuroiwa, ... Genes to Cells 16 (11), 1097-1109, 2011 | 44 | 2011 |
| Two sequential cleavage reactions on cruciform DNA structures cause palindrome-mediated chromosomal translocations H Inagaki, T Ohye, H Kogo, M Tsutsumi, T Kato, M Tong, BS Emanuel, ... Nature communications 4 (1), 1592, 2013 | 43 | 2013 |
| FAK-mediated extracellular signals are essential for interkinetic nuclear migration and planar divisions in the neuroepithelium S Tsuda, T Kitagawa, S Takashima, S Asakawa, N Shimizu, H Mitani, ... Journal of cell science 123 (3), 484-496, 2010 | 43 | 2010 |
| Failure of homologous synapsis and sex-specific reproduction problems H Kurahashi, H Kogo, M Tsutsumi, H Inagaki, T Ohye Frontiers in genetics 3, 112, 2012 | 38 | 2012 |
| Paternal origin of the de novo constitutional t (11; 22)(q23; q11) T Ohye, H Inagaki, H Kogo, M Tsutsumi, T Kato, M Tong, MVE Macville, ... European journal of human genetics 18 (7), 783-787, 2010 | 38 | 2010 |
| Recent advance in our understanding of the molecular nature of chromosomal abnormalities H Kurahashi, H Bolor, T Kato, H Kogo, M Tsutsumi, H Inagaki, T Ohye Journal of human genetics 54 (5), 253-260, 2009 | 37 | 2009 |
| Amino acid sequence of a putative transposase protein of the medaka fish transposable element Tol2 deduced from mRNA nucleotide sequences A Koga, M Suzuki, Y Maruyama, M Tsutsumi, H Hori FEBS letters 461 (3), 295-298, 1999 | 37 | 1999 |
| Biallelic variants in LIG3 cause a novel mitochondrial neurogastrointestinal encephalomyopathy E Bonora, S Chakrabarty, G Kellaris, M Tsutsumi, F Bianco, C Bergamini, ... Brain 144 (5), 1451-1466, 2021 | 35 | 2021 |
| Effectiveness of an oral health promotion programme at the workplace M Morishita, M Sakemi, M Tsutsumi, S Gake Journal of oral rehabilitation 30 (4), 414-417, 2003 | 33 | 2003 |
| Palindrome-mediated translocations in humans: a new mechanistic model for gross chromosomal rearrangements H Inagaki, T Kato, M Tsutsumi, Y Ouchi, T Ohye, H Kurahashi Frontiers in genetics 7, 125, 2016 | 30 | 2016 |
| TUBA1A mutation can cause a hydranencephaly-like severe form of cortical dysgenesis S Yokoi, N Ishihara, F Miya, M Tsutsumi, I Yanagihara, N Fujita, ... Scientific reports 5 (1), 15165, 2015 | 30 | 2015 |
