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References

  • Barrett, J. C., Fry, B., Maller, J. & Daly, M. J. (2005) Haploview: analysis and visualization of LD and haplotype maps. Bioinformatics 21, 263265.
  • Cupples, L. A., Arruda, H. T., Benjamin, E. J., D’agostino, R. B., Sr., Demissie, S., Destefano, A. L., Dupuis, J., Falls, K. M., Fox, C. S., Gottlieb, D. J., Govindaraju, D. R., Guo, C. Y., Heard-Costa, N. L., Hwang, S. J., Kathiresan, S., Kiel, D. P., Laramie, J. M., Larson, M. G., Levy, D., Liu, C. Y., Lunetta, K. L., Mailman, M. D., Manning, A. K., Meigs, J. B., Murabito, J. M., Newton-Cheh, C., O’connor, G. T., O’donnell, C. J., Pandey, M., Seshadri, S., Vasan, R. S., Wang, Z. Y., Wilk, J. B., Wolf, P. A., Yang, Q. & Atwood, L. D. (2007) The Framingham Heart Study 100K SNP genome-wide association study resource: overview of 17 phenotype working group reports. BMC Med Genet 8(Suppl 1), S1.
  • Davey Smith, G., Hart, C., Upton, M., Hole, D., Gillis, C., Watt, G. & Hawthorne, V. (2000) Height and risk of death among men and women: aetiological implications of associations with cardiorespiratory disease and cancer mortality. J Epidemiol Community Health 54, 97103.
  • Dawber, T. R., Kannel, W. B. & Lyell, L. P. (1963) An approach to longitudinal studies in a community: the Framingham Study. Ann N Y Acad Sci 107, 539556.
  • Dawber, T. R., Meadors, G. F. & Moore, F. E., Jr. (1951) Epidemiological approaches to heart disease: the Framingham Study. Am J Public Health Nations Health 41, 279281.
  • Gunnell, D., Okasha, M., Smith, G. D., Oliver, S. E., Sandhu, J. & Holly, J. M. (2001) Height, leg length, and cancer risk: a systematic review. Epidemiol Rev 23, 313342.
  • Hemenway, D., Feskanich, D. & Colditz, G. A. (1995) Body height and hip fracture: a cohort study of 90,000 women. Int J Epidemiol 24, 783786.
  • Lettre, G., Jackson, A. U., Gieger, C., Schumacher, F. R., Berndt, S. I., Sanna, S., Eyheramendy, S., Voight, B. F., Butler, J. L., Guiducci, C., Illig, T., Hackett, R., Heid, I. M., Jacobs, K. B., Lyssenko, V., Uda, M., Boehnke, M., Chanock, S. J., Groop, L. C., Hu, F. B., Isomaa, B., Kraft, P., Peltonen, L., Salomaa, V., Schlessinger, D., Hunter, D. J., Hayes, R. B., Abecasis, G. R., Wichmann, H. E., Mohlke, K. L. & Hirschhorn, J. N. (2008) Identification of ten loci associated with height highlights new biological pathways in human growth. Nat Genet 40, 584591.
  • Ligon, A. H., Moore, S. D., Parisi, M. A., Mealiffe, M. E., Harris, D. J., Ferguson, H. L., Quade, B. J. & Morton, C. C. (2005) Constitutional rearrangement of the architectural factor HMGA2: a novel human phenotype including overgrowth and lipomas. Am J Hum Genet 76, 340348.
  • Liu, Y. J., Liu, X. G., Wang, L., Dina, C., Yan, H., Liu, J. F., Levy, S., Papasian, C. J., Drees, B. M., Hamilton, J. J., Meyre, D., Delplanque, J., Pei, Y. F., Zhang, L., Recker, R. R., Froguel, P. & Deng, H. W. (2008) Genome-wide association scans identified CTNNBL1 as a novel gene for obesity. Hum Mol Genet 17, 18031813.
  • Macgregor, S., Cornes, B. K., Martin, N. G. & Visscher, P. M. (2006) Bias, precision and heritability of self-reported and clinically measured height in Australian twins. Hum Genet 120, 571580.
  • Perola, M., Sammalisto, S., Hiekkalinna, T., Martin, N. G., Visscher, P. M., Montgomery, G. W., Benyamin, B., Harris, J. R., Boomsma, D., Willemsen, G., Hottenga, J. J., Christensen, K., Kyvik, K. O., Sorensen, T. I., Pedersen, N. L., Magnusson, P. K., Spector, T. D., Widen, E., Silventoinen, K., Kaprio, J., Palotie, A. & Peltonen, L. (2007) Combined genome scans for body stature in 6,602 European twins: evidence for common Caucasian loci. PLoS Genet 3, e97.
  • Purcell, S., Neale, B., Todd-Brown, K., Thomas, L., Ferreira, M. A., Bender, D., Maller, J., Sklar, P., De Bakker, P. I., Daly, M. J. & Sham, P. C. (2007) PLINK: a tool set for whole-genome association and population-based linkage analyses. Am J Hum Genet 81, 559575.
  • Rosenthal, R. (1991) Meta-analytic procedures for social research. Beverly Hills , CA : Sage.
  • Silventoinen, K., Kaprio, J., Lahelma, E. & Koskenvuo, M. (2000) Relative effect of genetic and environmental factors on body height: differences across birth cohorts among Finnish men and women. Am J Public Health 90, 627630.
  • Silventoinen, K., Sammalisto, S., Perola, M., Boomsma, D. I., Cornes, B. K., Davis, C., Dunkel, L., De Lange, M., Harris, J. R., Hjelmborg, J. V., Luciano, M., Martin, N. G., Mortensen, J., Nistico, L., Pedersen, N. L., Skytthe, A., Spector, T. D., Stazi, M. A., Willemsen, G. & Kaprio, J. (2003) Heritability of adult body height: a comparative study of twin cohorts in eight countries. Twin Res 6, 399408.
  • Weedon, M. N., Lango, H., Lindgren, C. M., Wallace, C., Evans, D. M., Mangino, M., Freathy, R. M., Perry, J. R., Stevens, S., Hall, A. S., Samani, N. J., Shields, B., Prokopenko, I., Farrall, M., Dominiczak, A., Johnson, T., Bergmann, S., Beckmann, J. S., Vollenweider, P., Waterworth, D. M., Mooser, V., Palmer, C. N., Morris, A. D., Ouwehand, W. H., Zhao, J. H., Li, S., Loos, R. J., Barroso, I., Deloukas, P., Sandhu, M. S., Wheeler, E., Soranzo, N., Inouye, M., Wareham, N. J., Caulfield, M., Munroe, P. B., Hattersley, A. T., Mccarthy, M. I. & Frayling, T. M. (2008) Genome-wide association analysis identifies 20 loci that influence adult height. Nat Genet 40, 575583.
  • Weedon, M. N., Lettre, G., Freathy, R. M., Lindgren, C. M., Voight, B. F., Perry, J. R., Elliott, K. S., Hackett, R., Guiducci, C., Shields, B., Zeggini, E., Lango, H., Lyssenko, V., Timpson, N. J., Burtt, N. P., Rayner, N. W., Saxena, R., Ardlie, K., Tobias, J. H., Ness, A. R., Ring, S. M., Palmer, C. N., Morris, A. D., Peltonen, L., Salomaa, V., Davey Smith, G., Groop, L. C., Hattersley, A. T., Mccarthy, M. I., Hirschhorn, J. N. & Frayling, T. M. (2007) A common variant of HMGA2 is associated with adult and childhood height in the general population. Nat Genet 39, 12451250.
  • Yang, T. L., Chen, X. D., Guo, Y., Lei, S. F., Wang, J. T., Zhou, Q., Pan, F., Chen, Y., Zhang, Z. X., Dong, S. S., Xu, X. H., Yan, H., Liu, X., Qiu, C., Zhu, X. Z., Chen, T., Li, M., Zhang, H., Zhang, L., Drees, B. M., Hamilton, J. J., Papasian, C. J., Recker, R. R., Song, X. P., Cheng, J. & Deng, H. W. (2008) Genome-wide copy-number-variation study identified a susceptibility gene, UGT2B17, for osteoporosis. Am J Hum Genet 83, 633674.
  • Zhou, X., Benson, K. F., Ashar, H. R. & Chada, K. (1995) Mutation responsible for the mouse pygmy phenotype in the developmentally regulated factor HMGI-C. Nature 376, 771774.