| Authors | Title | Journal | Vol | Page | year | cited number |
| B. Vogelstein, E.R. Fearon, S.R. Hamilton, S. Kern, A.C. Presinger, M. Leppert, Y. Nakamura, R. White, L. Smets and J.L. Bos: | Genetic alterations during colorectal tumor development. | New Eng. J. Med. | 319 | 525-532 | 1988 | 4320 |
| The International HapMap Consortium: | A haplotype map of the human genome. | Nature | 437 | 1299-1320 | 2005 | 2740 |
| The International HapMap Consortium: | The International HapMap Project. | Nature | 426 | 789-796 | 2003 | 2268 |
| The International HapMap Consortium: | A second generation human haplotype map of over 3.1 million SNPs. | Nature | 449 | 851-861 | 2007 | 1758 |
| S.J. Baker, E.R. Fearon, J.M. Nigro, S.R. Hamilton, A.C. Preisinger, J.M. Jessup, P. vanTuinen, D.H. Ledbetter, D.F. Barker, Y. Nakamura, R. White and B. Vogelstein: | Chromosome 17 Deletions and p53 mutations in Colorectal Carcinomas. | Science | 244 | 217-221 | 1989 | 1647 |
| K.W. Kinzler,M.C. Nilbert, L. Su, B. Vogelstein, T.M. Bryan, D.B. Levy, K.J. Smith, A.C. Preisinger, P. Hedge, D. McKechnie, R. Finniear, A. Markham, J. Groffen, M.S. Boguski, S.F. Alschul, A. Horii, H. Ando, Y. Miyoshi, Y. Miki, I. Nishisho, Y. Nakamura: | Identification of FAP locus genes from chromosome 5q21. | Science | 253 | 661-665 | 1991 | 1579 |
| Y. Nakamura, M. Leppert, P. O'Connell, Roger Wolff, T. Holm, M. Culver, C. Martin, E. Fujimoto, M. Hoff, E. Kumlin and R. White: | Variable number of tandem repeat (VNTR) markers for human gene mapping. | Science | 235 | 1616-1622 | 1987 | 1415 |
| I. Nishisho, Y. Nakamura, Y. Miyoshi, Y. Miki, H. Ando, A. Horii, K. Koyama, J. Utsunomiya, S. Baba, P. Hedge, A. Markham, A.J. Krush, G. Petersen, S.R. Hamilton, M.C. Nilbert, D.B. Levy, T.M. Bryan, A.C. Preisinger, K.J. Smith, L. Su, K.W. Kinzler, and B. Vogelstein: | Mutations of chromosome 5q21 genes in FAP and colorectal cancer patients. | Science | 253 | 665-669 | 1991 | 1266 |
| B. Vogelstein, E.R. Fearon, S.E. Kern, S.R. Hamilton, A.C. Preisinger, Y. Nakamura and R. White: | Allelotype of colorectal carcinomas. | Science | 244 | 207-211 | 1989 | 1250 |
| C. Larsson, B. Skogseid, K. Obeg, Y. Nakamura, M. Nordenskjold: | Multiple endocrine neoplasia type 1 gene maps to chromosome 11 and is lost in insulinoma. | Nature | 332 | 85-87 | 1988 | 759 |
| K. Oda, H. Arakawa, T. Tanaka, K. Matsuda, C. Tanikawa, T. Mori, H. Nishimori, K. Tamai, T. Tokino, Y. Nakamura, and Y. Taya: | p53AIP1, a potential mediator of p53-dependent apoptosis, and its regulation by Ser-46-phosphorylated p53. | Cell | 102 | 849-862 | 2000 | 708 |
| Y. Miyoshi, H. Nagase, H. Ando, A. Horii, S. Ichii, S. Nakatsuru, T. Aoki, Y. Miki, T. Mori and Y. Nakamura: | Somatic mutation of the APC gene in colorectal tumors: mutation cluster region in the APC gene. | Human Molecular Genetics | 1 | 229-233 | 1992 | 642 |
| K.W. Kinzler, M.C. Nilbert, B. Vogelstein, T.M. Bryan, D.B. Levy, K.J. Smith, A.C. Preisinger, S.R. Hamilton, P. Hedge, A. Merkham, M. Carlson, G. Joslyn, J. Groden, R. White, Y. Miki, I. Nishisho and Y. Nakamura: | Identification of a gene located at chromosome 5q21 that is mutated in colorectal cancers. | Science | 251 | 1366-1370 | 1991 | 609 |
| S. Satoh, Y. Daigo, Y. Furukawa, T. Katoh, N. Miwa, T. Nishiwaki, T. Kawasoe, H. Ishiguro, M. Fujita, T. Tokino, Y. Sasaki, S. Imaoka, M. Murata, T. Shimano, Y. Yamaoka, and Y. Nakamura: | AXIN1 mutations in hepatocellular carcinomas, and growth suppression in cancer cells by virus-mediated transfer of AXIN1. | Nature Genetics | 24 | 245-250 | 2000 | 601 |
| M. Leppert, M. Dobbes, P. Scambler, P. O'Connell, Y. Nakamura, D. Stauffer, S. Woodward, R. Burt, J. Hughes, E. Gardner, M. Lathrop, J. Wasumuth, J.-M. Lalouel, R. White: | The gene for familial polyposis coli maps to the long arm of chromosome 5. | Science | 238 | 1411-1413 | 1987 | 562 |
| T. Sato, A. Tanigami, K. Yamakawa, F. Akiyama, F. Kasumi, G. Sakamoto and Y. Nakamura: | Allelotype of breast cancer: Cumulative allele losses promote tumor progression in primary breast cancer. | Cancer Research | 50 | 7184-7189 | 1990 | 553 |
| D. Barker, E. Wright, K. Nguyen, L. Cannon, P. Fain, D. Goldger, D. T. Bishop, J. Carey, B. Bety, H. Willard, J. S. Waye, G. Greig, L. Leinward, Y. Nakamura, P. O'Connell, M. Leppert, J.-M. Lalouel, R. White and M. Skolnick: | Gene for von Recklinghausen neurofibromatosis is in the pericentromeric region of chromosome 17. | Science | 236 | 1100-1102 | 1987 | 524 |
