| The DNA sequence of human chromosome 22 I Dunham, AR Hunt, JE Collins, R Bruskiewich, DM Beare, M Clamp, ... Nature 402 (6761), 489-495, 1999 | 1476 | 1999 |
| Chromosome 22-specific low copy repeats and the 22q11. 2 deletion syndrome: genomic organization and deletion endpoint analysis TH Shaikh, H Kurahashi, SC Saitta, AM O’Hare, P Hu, BA Roe, ... Human molecular genetics 9 (4), 489-501, 2000 | 650 | 2000 |
| CDH1 is a specific marker for undifferentiated spermatogonia in mouse testes M Tokuda, Y Kadokawa, H Kurahashi, T Marunouchi Biology of reproduction 76 (1), 130-141, 2007 | 294 | 2007 |
| Increased water intake decreases progression of polycystic kidney disease in the PCK rat S Nagao, K Nishii, M Katsuyama, H Kurahashi, T Marunouchi, ... Journal of the American Society of Nephrology 17 (8), 2220-2227, 2006 | 281 | 2006 |
| Human herpesvirus 6 (HHV‐6) is transmitted from parent to child in an integrated form and characterization of cases with chromosomally integrated HHV‐6 DNA K Tanaka‐Taya, J Sashihara, H Kurahashi, K Amo, H Miyagawa, K Kondo, ... Journal of medical virology 73 (3), 465-473, 2004 | 275 | 2004 |
| Identification of the gene responsible for gelatinous drop-like corneal dystrophy M Tsujikawa, H Kurahashi, T Tanaka, K Nishida, Y Shimomura, Y Tano, ... Nature genetics 21 (4), 420-423, 1999 | 201 | 1999 |
| Microarray analysis of differentially expressed fetal genes in placental tissue derived from early and late onset severe pre-eclampsia H Nishizawa, K Pryor-Koishi, T Kato, H Kowa, H Kurahashi, Y Udagawa Placenta 28 (5-6), 487-497, 2007 | 200 | 2007 |
| Pathogenic exon-trapping by SVA retrotransposon and rescue in Fukuyama muscular dystrophy M Taniguchi-Ikeda, K Kobayashi, M Kanagawa, C Yu, K Mori, T Oda, ... Nature 478 (7367), 127-131, 2011 | 199 | 2011 |
| Long AT-rich palindromes and the constitutional t (11; 22) breakpoint H Kurahashi, BS Emanuel Human molecular genetics 10 (23), 2605-2617, 2001 | 180 | 2001 |
| Comparative gene expression profiling of placentas from patients with severe pre-eclampsia and unexplained fetal growth restriction H Nishizawa, S Ota, M Suzuki, T Kato, T Sekiya, H Kurahashi, Y Udagawa Reproductive Biology and Endocrinology 9, 1-12, 2011 | 175 | 2011 |
| 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 | 165 | 2014 |
| Evolutionarily conserved low copy repeats (LCRs) in 22q11 mediate deletions, duplications, translocations, and genomic instability: an update and literature review TH Shaikh, H Kurahashi, BS Emanuel Genetics in Medicine 3 (1), 6-13, 2001 | 161 | 2001 |
| Regions of genomic instability on 22q11 and 11q23 as the etiology for the recurrent constitutional t (11; 22) H Kurahashi, TH Shaikh, P Hu, BA Roe, BS Emanuel, ML Budarf Human Molecular Genetics 9 (11), 1665-1670, 2000 | 161 | 2000 |
| Molecular and virological evidence of viral activation from chromosomally integrated human herpesvirus 6A in a patient with X-linked severe combined immunodeficiency A Endo, K Watanabe, T Ohye, K Suzuki, T Matsubara, N Shimizu, ... Clinical Infectious Diseases 59 (4), 545-548, 2014 | 152 | 2014 |
| The constitutional t (17; 22): another translocation mediated by palindromic AT-rich repeats H Kurahashi, T Shaikh, M Takata, T Toda, BS Emanuel The American Journal of Human Genetics 72 (3), 733-738, 2003 | 137 | 2003 |
| Preimplantation genetic testing for aneuploidy: a comparison of live birth rates in patients with recurrent pregnancy loss due to embryonic aneuploidy or recurrent implantation … T Sato, M Sugiura-Ogasawara, F Ozawa, T Yamamoto, T Kato, ... Human Reproduction 34 (12), 2340-2348, 2019 | 134 | 2019 |
| Cruciform DNA structure underlies the etiology for palindrome-mediated human chromosomal translocations H Kurahashi, H Inagaki, K Yamada, T Ohye, M Taniguchi, BS Emanuel, ... Journal of Biological Chemistry 279 (34), 35377-35383, 2004 | 132 | 2004 |
| Fukutin is required for maintenance of muscle integrity, cortical histiogenesis and normal eye development S Takeda, M Kondo, J Sasaki, H Kurahashi, H Kano, K Arai, K Misaki, ... Human molecular genetics 12 (12), 1449-1459, 2003 | 131 | 2003 |
| A kerato-epithelin (βig-h3) mutation in lattice corneal dystrophy type IIIA S Yamamoto, M Okada, M Tsujikawa, Y Shimomura, K Nishida, Y Inoue, ... The American Journal of Human Genetics 62 (3), 719-722, 1998 | 129 | 1998 |
| Biallelic Inactivation of the APC Gene in Hepatoblastoma H Kurahashi, K Takami, T Oue, T Kusafuka, A Okada, A Tawa, S Okada, ... Cancer research 55 (21), 5007-5011, 1995 | 124 | 1995 |
