-
1
-
-
79959503826
-
The International HapMap Project
-
The International HapMap Consortium
-
The International HapMap Consortium. (2003) The International HapMap Project. Nature 426, 789-796.
-
(2003)
Nature
, vol.426
, pp. 789-796
-
-
-
2
-
-
79959524146
-
A haplotype map of the human genome
-
The International HapMap Consortium
-
The International HapMap Consortium. (2005) A haplotype map of the human genome. Nature 437, 1299-1320.
-
(2005)
Nature
, vol.437
, pp. 1299-1320
-
-
-
3
-
-
2042437650
-
-
Lander, E. S, Linton, L. M, Birren, B, Nusbaum, C, Zody, M. C, Baldwin, J, Devon, K, Dewar, K, Doyle, M, FitzHugh, W, Funke, R, Gage, D, Harris, K, Heaford, A, Howland, J, Kann, L, Lehoczky, J, LeVine, R, McEwan, P, McKernan, K, Meldrim, J, Mesirov, J. P, Miranda, C, Morris, W, Naylor, J, Raymond, C, Rosetti, M, Santos, R, Sheridan, A, Sougnez, C, Stange-Thomann, N, Stojanovic, N, Subramanian, A, Wyman, D, Rogers, J, Sulston, J, Ainscough, R, Beck, S, Bentley, D, Burton, J, Clee, C, Carter, N, Coulson, A, Deadman, R, Deloukas, P, Dunham, A, Dunham, I, Durbin, R, French, L, Grafham, D, Gregory, S, Hubbard, T, Humphray, S, Hunt, A, Jones, M, Lloyd, C, McMurray, A, Matthews, L, Mercer, S, Milne, S, Mullikin, J. C, Mungall, A, Plumb, R, Ross, M, Shownkeen, R, Sims, S, Waterston, R. H, Wilson, R. K, Hillier, L. W, McPherson, J. D, Marra, M. A, Mardis, E. R, Fulton, L. A, Chinwalla, A. T, Pepin, K. H, Gish, W. R, Chi
-
Lander, E. S., Linton, L. M., Birren, B., Nusbaum, C., Zody, M. C., Baldwin, J., Devon, K., Dewar, K., Doyle, M., FitzHugh, W., Funke, R., Gage, D., Harris, K., Heaford, A., Howland, J., Kann, L., Lehoczky, J., LeVine, R., McEwan, P., McKernan, K., Meldrim, J., Mesirov, J. P., Miranda, C., Morris, W., Naylor, J., Raymond, C., Rosetti, M., Santos, R., Sheridan, A., Sougnez, C., Stange-Thomann, N., Stojanovic, N., Subramanian, A., Wyman, D., Rogers, J., Sulston, J., Ainscough, R., Beck, S., Bentley, D., Burton, J., Clee, C., Carter, N., Coulson, A., Deadman, R., Deloukas, P., Dunham, A., Dunham, I., Durbin, R., French, L., Grafham, D., Gregory, S., Hubbard, T., Humphray, S., Hunt, A., Jones, M., Lloyd, C., McMurray, A., Matthews, L., Mercer, S., Milne, S., Mullikin, J. C., Mungall, A., Plumb, R., Ross, M., Shownkeen, R., Sims, S., Waterston, R. H., Wilson, R. K., Hillier, L. W., McPherson, J. D., Marra, M. A., Mardis, E. R., Fulton, L. A., Chinwalla, A. T., Pepin, K. H., Gish, W. R., Chissoe, S. L., Wendl, M. C., Delehaunty, K. D., Miner, T. L., Delehaunty, A., Kramer, J. B., Cook, L. L., Fulton, R. S., Johnson, D. L., Minx, P. J., Clifton, S. W., Hawkins, T., Branscomb, E., Predki, P., Richardson, P., Wenning, S., Slezak, T., Doggett, N., Cheng, J. F., Olsen, A., Lucas, S., Elkin, C., Uberbacher, E., Frazier, M., Gibbs, R. A., Muzny, D. M., Scherer, S. E., Bouck, J. B., Sodergren, E. J., Worley, K. C., Rives, C. M., Gorrell, J. H., Metzker, M. L., Naylor, S. L., Kucherlapati, R. S., Nelson, D. L., Weinstock, G. M., Sakaki, Y., Fujiyama, A., Hattori, M., Yada, T., Toyoda, A., Itoh, T., Kawagoe, C., Watanabe, H., Totoki, Y., Taylor, T., Weissenbach, J., Heilig, R., Saurin, W., Artiguenave, F., Brottier, P., Bruls, T., Pelletier, E., Robert, C., Wincker, P., Smith, D. R., Doucette-Stamm, L., Rubenfield, M., Weinstock, K., Lee, H. M., Dubois, J., Rosenthal, A., Platzer, M., Nyakatura, G., Taudien, S., Rump, A., Yang, H., Yu, J., Wang, J., Huang, G., Gu, J., Hood, L., Rowen, L., Madan, A., Qin, S., Davis, R. W., Federspiel, N. A., Abola, A. P., Proctor, M. J., Myers, R. M., Schmutz, J., Dickson, M., Grimwood, J., Cox, D. R., Olson, M. V., Kaul, R., Raymond, C., Shimizu, N., Kawasaki, K., Minoshima, S., Evans, G. A., Athanasiou, M., Schultz, R., Roe, B. A., Chen, F., Pan, H., Ramser, J., Lehrach, H., Reinhardt, R., McCombie, W. R., de la Bastide, M., Dedhia, N., Blocker, H., Hornischer, K., Nordsiek, G., Agarwala, R., Aravind, L., Bailey, J. A., Bateman, A., Batzoglou, S., Birney, E., Bork, P., Brown, D. G., Burge, C. B., Cerutti, L., Chen, H. C., Church, D., Clamp, M., Copley, R. R., Doerks, T., Eddy, S. R., Eichler, E. E., Furey, T. S., Galagan, J., Gilbert, J. G., Harmon, C., Hayashizaki, Y., Haussler, D., Hermjakob, H., Hokamp, K., Jang, W., Johnson, L. S., Jones, T. A., Kasif, S., Kaspryzk, A., Kennedy, S., Kent, W. J., Kitts, P., Koonin, E. V., Korf, I., Kulp, D., Lancet, D., Lowe, T. M., McLysaght, A., Mikkelsen, T., Moran, J. V., Mulder, N., Pollara, V. J., Ponting, C. P., Schuler, G., Schultz, J., Slater, G., Smit, A. F., Stupka, E., Szustakowski, J., Thierry-Mieg, D., Thierry-Mieg, J., Wagner, L., Wallis, J., Wheeler, R., Williams, A., Wolf, Y. I., Wolfe, K. H., Yang, S. P., Yeh, R. F., Collins, F., Guyer, M. S., Peterson, J., Felsenfeld, A., Wetterstrand, K. A., Patrinos, A., Morgan, M. J., de Jong, P., Catanese, J. J., Osoegawa, K., Shizuya, H., Choi, S. and Chen, Y. J. (2001) Initial sequencing and analysis of the human genome. Nature 409, 860-921.
-
-
-
-
4
-
-
0035895505
-
-
Venter, J. C, Adams, M. D, Myers, E. W, Li, P. W, Mural, R. J, Sutton, G. G, Smith, H. O, Yandell, M, Evans, C. A, Holt, R. A, Gocayne, J. D, Amanatides, P, Ballew, R. M, Huson, D. H, Wortman, J. R, Zhang, Q, Kodira, C. D, Zheng, X. H, Chen, L, Skupski, M, Subramanian, G, Thomas, P. D, Zhang, J, Gabor Miklos, G. L, Nelson, C, Broder, S, Clark, A. G, Nadeau, J, McKusick, V. A, Zinder, N, Levine, A. J, Roberts, R. J, Simon, M, Slayman, C, Hunkapiller, M, Bolanos, R, Delcher, A, Dew, I, Fasulo, D, Flanigan, M, Florea, L, Halpern, A, Hannenhalli, S, Kravitz, S, Levy, S, Mobarry, C, Reinert, K, Remington, K, Abu-Threideh, J, Beasley, E, Biddick, K, Bonazzi, V, Brandon, R, Cargill, M, Chandramouliswaran, I, Charlab, R, Chaturvedi, K, Deng, Z, Di Francesco, V, Dunn, P, Eilbeck, K, Evangelista, C, Gabrielian, A. E, Gan, W, Ge, W, Gong, F, Gu, Z, Guan, P, Heiman, T. J, Higgins, M. E, Ji, R. R, Ke, Z, Ketchum, K. A, Lai, Z
-
Venter, J. C., Adams, M. D., Myers, E. W., Li, P. W., Mural, R. J., Sutton, G. G., Smith, H. O., Yandell, M., Evans, C. A., Holt, R. A., Gocayne, J. D., Amanatides, P., Ballew, R. M., Huson, D. H., Wortman, J. R., Zhang, Q., Kodira, C. D., Zheng, X. H., Chen, L., Skupski, M., Subramanian, G., Thomas, P. D., Zhang, J., Gabor Miklos, G. L., Nelson, C., Broder, S., Clark, A. G., Nadeau, J., McKusick, V. A., Zinder, N., Levine, A. J., Roberts, R. J., Simon, M., Slayman, C., Hunkapiller, M., Bolanos, R., Delcher, A., Dew, I., Fasulo, D., Flanigan, M., Florea, L., Halpern, A., Hannenhalli, S., Kravitz, S., Levy, S., Mobarry, C., Reinert, K., Remington, K., Abu-Threideh, J., Beasley, E., Biddick, K., Bonazzi, V., Brandon, R., Cargill, M., Chandramouliswaran, I., Charlab, R., Chaturvedi, K., Deng, Z., Di Francesco, V., Dunn, P., Eilbeck, K., Evangelista, C., Gabrielian, A. E., Gan, W., Ge, W., Gong, F., Gu, Z., Guan, P., Heiman, T. J., Higgins, M. E., Ji, R. R., Ke, Z., Ketchum, K. A., Lai, Z., Lei, Y., Li, Z., Li, J., Liang, Y., Lin, X., Lu, F., Merkulov, G. V., Milshina, N., Moore, H. M., Naik, A. K., Narayan, V. A., Neelam, B., Nusskern, D., Rusch, D. B., Salzberg, S., Shao, W., Shue, B., Sun, J., Wang, Z., Wang, A., Wang, X., Wang, J., Wei, M., Wides, R., Xiao, C., Yan, C., Yao, A., Ye, J., Zhan, M., Zhang, W., Zhang, H., Zhao, Q., Zheng, L., Zhong, F., Zhong, W., Zhu, S., Zhao, S., Gilbert, D., Baumhueter, S., Spier, G., Carter, C., Cravchik, A., Woodage, T., Ali, F., An, H., Awe, A., Baldwin, D., Baden, H., Barnstead, M., Barrow, I., Beeson, K., Busam, D., Carver, A., Center, A., Cheng, M. L., Curry, L., Danaher, S., Davenport, L., Desilets, R., Dietz, S., Dodson, K., Doup, L., Ferriera, S., Garg, N., Gluecksmann, A., Hart, B., Haynes, J., Haynes, C., Heiner, C., Hladun, S., Hostin, D., Houck, J., Howland, T., Ibegwam, C., Johnson, J., Kalush, F., Kline, L., Koduru, S., Love, A., Mann, F., May, D., McCawley, S., McIntosh, T., McMullen, I., Moy, M., Moy, L., Murphy, B., Nelson, K., Pfannkoch, C., Pratts, E., Puri, V., Qureshi, H., Reardon, M., Rodriguez, R., Rogers, Y. H., Romblad, D., Ruhfel, B., Scott, R., Sitter, C., Smallwood, M., Stewart, E., Strong, R., Suh, E., Thomas, R., Tint, N. N., Tse, S., Vech, C., Wang, G., Wetter, J., Williams, S., Williams, M., Windsor, S., Winn-Deen, E., Wolfe, K., Zaveri, J., Zaveri, K., Abril, J. F., Guigo, R., Campbell, M. J., Sjolander, K. V., Karlak, B., Kejariwal, A., Mi, H., Lazareva, B., Hatton, T., Narechania, A., Diemer, K., Muruganujan, A., Guo, N., Sato, S., Bafna, V., Istrail, S., Lippert, R., Schwartz, R., Walenz, B., Yooseph, S., Allen, D., Basu, A., Baxendale, J., Blick, L., Caminha, M., Carnes-Stine, J., Caulk, P., Chiang, Y. H., Coyne, M., Dahlke, C., Mays, A., Dombroski, M., Donnelly, M., Ely, D., Esparham, S., Fosler, C., Gire, H., Glanowski, S., Glasser, K., Glodek, A., Gorokhov, M., Graham, K., Gropman, B., Harris, M., Heil, J., Henderson, S., Hoover, J., Jennings, D., Jordan, C., Jordan, J., Kasha, J., Kagan, L., Kraft, C., Levitsky, A., Lewis, M., Liu, X., Lopez, J., Ma, D., Majoros, W., McDaniel, J., Murphy, S., Newman, M., Nguyen, T., Nguyen, N., Nodell, M., Pan, S., Peck, J., Peterson, M., Rowe, W., Sanders, R., Scott, J., Simpson, M., Smith, T., Sprague, A., Stockwell, T., Turner, R., Venter, E., Wang, M., Wen, M., Wu, D., Wu, M., Xia, A., Zandieh, A. and Zhu, X. (2001) The sequence of the human genome. Science 291, 1304-1351.
-
-
-
-
5
-
-
33645290018
-
MHC class II proteins and disease: A structural perspective
-
Jones, E. Y., Fugger, L., Strominger, J. L. and Siebold, C. (2006) MHC class II proteins and disease: a structural perspective. Nat. Rev. Immunol. 6, 271-282.
-
(2006)
Nat. Rev. Immunol
, vol.6
, pp. 271-282
-
-
Jones, E.Y.1
Fugger, L.2
Strominger, J.L.3
Siebold, C.4
-
6
-
-
22244441834
-
PTPN22 and rheumatoid arthritis: Gratifying replication
-
Gregersen, P. K. and Batliwalla, F. (2005) PTPN22 and rheumatoid arthritis: gratifying replication. Arthritis Rheum. 52, 1952-1955.
-
(2005)
Arthritis Rheum
, vol.52
, pp. 1952-1955
-
-
Gregersen, P.K.1
Batliwalla, F.2
-
7
-
-
3242713277
-
-
Begovich, A. B., Carlton, V. E., Honigberg, L. A., Schrodi, S. J., Chokkalingam, A. P., Alexander, H. C., Ardlie, K. G., Huang, Q., Smith, A. M., Spoerke, J. M., Conn, M. T., Chang, M., Chang, S. Y., Saiki, R. K., Catanese, J. J., Leong, D. U., Garcia, V. E., McAllister, L. B., Jeffery, D. A., Lee, A. T., Batliwalla, F., Remmers, E., Criswell, L. A., Seldin, M. F., Kastner, D. L., Amos, C. I., Sninsky, J. J. and Gregersen, P. K. (2004) A missense single-nucleotide polymorphism in a gene encoding a protein tyrosine phosphatase (PTPN22) is associated with rheumatoid arthritis. Am. J. Hum. Genet. 75, 330-337.
-
Begovich, A. B., Carlton, V. E., Honigberg, L. A., Schrodi, S. J., Chokkalingam, A. P., Alexander, H. C., Ardlie, K. G., Huang, Q., Smith, A. M., Spoerke, J. M., Conn, M. T., Chang, M., Chang, S. Y., Saiki, R. K., Catanese, J. J., Leong, D. U., Garcia, V. E., McAllister, L. B., Jeffery, D. A., Lee, A. T., Batliwalla, F., Remmers, E., Criswell, L. A., Seldin, M. F., Kastner, D. L., Amos, C. I., Sninsky, J. J. and Gregersen, P. K. (2004) A missense single-nucleotide polymorphism in a gene encoding a protein tyrosine phosphatase (PTPN22) is associated with rheumatoid arthritis. Am. J. Hum. Genet. 75, 330-337.
-
-
-
-
8
-
-
12144291502
-
A functional variant of lymphoid tyrosine phosphatase is associated with type I diabetes
-
Bottini, N., Musumeci, L., Alonso, A., Rahmouni, S., Nika, K., Rostamkhani, M., MacMurray, J., Meloni, G. F., Lucarelli, P., Pellecchia, M., Eisenbarth, G. S., Comings, D. and Mustelin, T. (2004) A functional variant of lymphoid tyrosine phosphatase is associated with type I diabetes. Nat. Genet. 36, 337-338.
-
(2004)
Nat. Genet
, vol.36
, pp. 337-338
-
-
Bottini, N.1
Musumeci, L.2
Alonso, A.3
Rahmouni, S.4
Nika, K.5
Rostamkhani, M.6
MacMurray, J.7
Meloni, G.F.8
Lucarelli, P.9
Pellecchia, M.10
Eisenbarth, G.S.11
Comings, D.12
Mustelin, T.13
-
9
-
-
33745174905
-
PTPN22: Setting thresholds for autoimmunity
-
Gregersen, P. K., Lee, H. S., Batliwalla, F. and Begovich, A. B. (2006) PTPN22: setting thresholds for autoimmunity. Semin. Immunol. 18, 214-223.
-
(2006)
Semin. Immunol
, vol.18
, pp. 214-223
-
-
Gregersen, P.K.1
Lee, H.S.2
Batliwalla, F.3
Begovich, A.B.4
-
10
-
-
28444469783
-
Autoimmune-associated lymphoid tyrosine phosphatase is a gain-of-function variant
-
Vang, T., Congia, M., Macis, M. D., Musumeci, L., Orru, V., Zavattari, P., Nika, K., Tautz, L., Tasken, K., Cucca, F., Mustelin, T. and Bottini, N. (2005) Autoimmune-associated lymphoid tyrosine phosphatase is a gain-of-function variant. Nat. Genet. 37, 1317-1319.
-
(2005)
Nat. Genet
, vol.37
, pp. 1317-1319
-
-
Vang, T.1
Congia, M.2
Macis, M.D.3
Musumeci, L.4
Orru, V.5
Zavattari, P.6
Nika, K.7
Tautz, L.8
Tasken, K.9
Cucca, F.10
Mustelin, T.11
Bottini, N.12
-
11
-
-
0037648405
-
-
Ueda, H, Howson, J. M, Esposito, L, Heward, J, Snook, H, Chamberlain, G, Rainbow, D. B, Hunter, K. M, Smith, A. N, Di Genova, G, Herr, M. H, Dahlman, I, Payne, F, Smyth, D, Lowe, C, Twells, R. C, Howlett, S, Healy, B, Nutland, S, Rance, H. E, Everett, V, Smink, L. J, Lam, A. C, Cordell, H. J, Walker, N. M, Bordin, C, Hulme, J, Motzo, C, Cucca, F, Hess, J. F, Metzker, M. L, Rogers, J, Gregory, S, Allahabadia, A, Nithiyananthan, R, Tuomilehto-Wolf, E, Tuomilehto, J, Bingley, P, Gillespie, K. M, Undlien, D. E, Ronningen, K. S, Guja, C, Ionescu-Tirgoviste, C, Savage, D. A, Maxwell, A. P, Carson, D. J, Patterson, C. C, Franklyn, J. A, Clayton, D. G, Peterson, L. B, Wicker, L. S, Todd, J. A. and Gough, S. C, 2003 Association of the T-cell regulatory gene CTLA4 with susceptibility to autoimmune disease. Nature 423, 506-511
-
Ueda, H., Howson, J. M., Esposito, L., Heward, J., Snook, H., Chamberlain, G., Rainbow, D. B., Hunter, K. M., Smith, A. N., Di Genova, G., Herr, M. H., Dahlman, I., Payne, F., Smyth, D., Lowe, C., Twells, R. C., Howlett, S., Healy, B., Nutland, S., Rance, H. E., Everett, V., Smink, L. J., Lam, A. C., Cordell, H. J., Walker, N. M., Bordin, C., Hulme, J., Motzo, C., Cucca, F., Hess, J. F., Metzker, M. L., Rogers, J., Gregory, S., Allahabadia, A., Nithiyananthan, R., Tuomilehto-Wolf, E., Tuomilehto, J., Bingley, P., Gillespie, K. M., Undlien, D. E., Ronningen, K. S., Guja, C., Ionescu-Tirgoviste, C., Savage, D. A., Maxwell, A. P., Carson, D. J., Patterson, C. C., Franklyn, J. A., Clayton, D. G., Peterson, L. B., Wicker, L. S., Todd, J. A. and Gough, S. C. (2003) Association of the T-cell regulatory gene CTLA4 with susceptibility to autoimmune disease. Nature 423, 506-511.
-
-
-
-
12
-
-
33748752137
-
Systematic review and meta-analysis of the association between complementary factor H Y402H polymorphisms and age-related macular degeneration
-
Thakkinstian, A., Han, P., McEvoy, M., Smith, W., Hoh, J., Magnusson, K., Zhang, K. and Attia, J. (2006) Systematic review and meta-analysis of the association between complementary factor H Y402H polymorphisms and age-related macular degeneration. Hum. Mol. Genet. 15, 2784-2790.
-
(2006)
Hum. Mol. Genet
, vol.15
, pp. 2784-2790
-
-
Thakkinstian, A.1
Han, P.2
McEvoy, M.3
Smith, W.4
Hoh, J.5
Magnusson, K.6
Zhang, K.7
Attia, J.8
-
13
-
-
0030823158
-
Effects of age, sex, and ethnicity on the association between apolipoprotein E genotype and Alzheimer disease: A meta-analysis. APOE and Alzheimer Disease Meta Analysis Consortium
-
Farrer, L. A., Cupples, L. A., Haines, J. L., Hyman, B., Kukull, W. A., Mayeux, R., Myers, R. H., Pericak-Vance, M. A., Risch, N. and van Duijn, C. M. (1997) Effects of age, sex, and ethnicity on the association between apolipoprotein E genotype and Alzheimer disease: a meta-analysis. APOE and Alzheimer Disease Meta Analysis Consortium. JAMA 278, 1349-1356.
-
(1997)
JAMA
, vol.278
, pp. 1349-1356
-
-
Farrer, L.A.1
Cupples, L.A.2
Haines, J.L.3
Hyman, B.4
Kukull, W.A.5
Mayeux, R.6
Myers, R.H.7
Pericak-Vance, M.A.8
Risch, N.9
van Duijn, C.M.10
-
14
-
-
23944438473
-
Large meta-analysis establishes the ACE insertion-deletion polymorphism as a marker of Alzheimer's disease
-
Lehmann, D. J., Cortina-Borja, M., Warden, D. R., Smith, A. D., Sleegers, K., Prince, J. A., van Duijn, C. M. and Kehoe, P. G. (2005) Large meta-analysis establishes the ACE insertion-deletion polymorphism as a marker of Alzheimer's disease. Am. J. Epidemiol. 162, 305-317.
-
(2005)
Am. J. Epidemiol
, vol.162
, pp. 305-317
-
-
Lehmann, D.J.1
Cortina-Borja, M.2
Warden, D.R.3
Smith, A.D.4
Sleegers, K.5
Prince, J.A.6
van Duijn, C.M.7
Kehoe, P.G.8
-
15
-
-
33845578510
-
The PTPN22 C1858T functional polymorphism and autoimmune diseases - a meta-analysis
-
Lee, Y. H., Rho, Y. H., Choi, S. J., Ji, J. D., Song, G. G., Nath, S. K. and Harley, J. B. (2007) The PTPN22 C1858T functional polymorphism and autoimmune diseases - a meta-analysis. Rheumatology 46, 49-56.
-
(2007)
Rheumatology
, vol.46
, pp. 49-56
-
-
Lee, Y.H.1
Rho, Y.H.2
Choi, S.J.3
Ji, J.D.4
Song, G.G.5
Nath, S.K.6
Harley, J.B.7
-
16
-
-
28144441356
-
Replication of putative candidate-gene associations with rheumatoid arthritis in >4,000 samples from North America and Sweden: Association of susceptibility with PTPN22, CTLA4, and PADI4
-
Plenge, R. M., Padyukov, L., Remmers, E. F., Purcell, S., Lee, A. T., Karlson, E. W., Wolfe, F., Kastner, D. L., Alfredsson, L., Altshuler, D., Gregersen, P. K., Klareskog, L. and Rioux, J. D. (2005) Replication of putative candidate-gene associations with rheumatoid arthritis in >4,000 samples from North America and Sweden: association of susceptibility with PTPN22, CTLA4, and PADI4. Am. J. Hum. Genet. 77, 1044-1060.
-
(2005)
Am. J. Hum. Genet
, vol.77
, pp. 1044-1060
-
-
Plenge, R.M.1
Padyukov, L.2
Remmers, E.F.3
Purcell, S.4
Lee, A.T.5
Karlson, E.W.6
Wolfe, F.7
Kastner, D.L.8
Alfredsson, L.9
Altshuler, D.10
Gregersen, P.K.11
Klareskog, L.12
Rioux, J.D.13
-
17
-
-
11144279151
-
Differential effects of NOD2 variants on Crohns disease risk and phenotype in diverse populations: Ametaanalysis
-
Economou, M., Trikalinos, T. A., Loizou, K. T., Tsianos, E. V. and Ioannidis, J. P. (2004) Differential effects of NOD2 variants on Crohns disease risk and phenotype in diverse populations: ametaanalysis. Am. J. Gastroenterol. 99, 2393-2404.
-
(2004)
Am. J. Gastroenterol
, vol.99
, pp. 2393-2404
-
-
Economou, M.1
Trikalinos, T.A.2
Loizou, K.T.3
Tsianos, E.V.4
Ioannidis, J.P.5
-
18
-
-
33748940263
-
CARD15 in inflammatory bowel disease and Crohns disease phenotypes: An association study and pooled analysis
-
Oostenbrug, L. E., Nolte, I. M., Oosterom, E., van der Steege, G., Te Meerman, G. J., van Dullemen, H. M., Drenth, J. P., de Jong, D. J., van der Linde, K., Jansen, P. L. and Kleibeuker, J. H. (2006) CARD15 in inflammatory bowel disease and Crohns disease phenotypes: an association study and pooled analysis. Dig. Liver Dis. 38, 834-845.
-
(2006)
Dig. Liver Dis
, vol.38
, pp. 834-845
-
-
Oostenbrug, L.E.1
Nolte, I.M.2
Oosterom, E.3
van der Steege, G.4
Te Meerman, G.J.5
van Dullemen, H.M.6
Drenth, J.P.7
de Jong, D.J.8
van der Linde, K.9
Jansen, P.L.10
Kleibeuker, J.H.11
-
19
-
-
33645825830
-
A common genetic variant is associated with adult and childhood obesity
-
Herbert, A., Gerry, N. P., McQueen, M. B., Heid, I. M., Pfeufer, A., Illig, T., Wichmann, H. E., Meitinger, T., Hunter, D., Hu, F. B., Colditz, G., Hinney, A., Hebebrand, J., Koberwitz, K., Zhu, X., Cooper, R., Ardlie, K., Lyon, H., Hirschhorn, J. N., Laird, N. M., Lenburg, M. E., Lange, C. and Christman, M. F. (2006) A common genetic variant is associated with adult and childhood obesity. Science 312, 279-283.
-
(2006)
Science
, vol.312
, pp. 279-283
-
-
Herbert, A.1
Gerry, N.P.2
McQueen, M.B.3
Heid, I.M.4
Pfeufer, A.5
Illig, T.6
Wichmann, H.E.7
Meitinger, T.8
Hunter, D.9
Hu, F.B.10
Colditz, G.11
Hinney, A.12
Hebebrand, J.13
Koberwitz, K.14
Zhu, X.15
Cooper, R.16
Ardlie, K.17
Lyon, H.18
Hirschhorn, J.N.19
Laird, N.M.20
Lenburg, M.E.21
Lange, C.22
Christman, M.F.23
more..
-
20
-
-
33745591928
-
Association between PADI4 and rheumatoid arthritis: A meta-analysis
-
Iwamoto, T., Ikari, K., Nakamura, T., Kuwahara, M., Toyama, Y., Tomatsu, T., Momohara, S. and Kamatani, N. (2006) Association between PADI4 and rheumatoid arthritis: a meta-analysis. Rheumatology 45, 804-807.
-
(2006)
Rheumatology
, vol.45
, pp. 804-807
-
-
Iwamoto, T.1
Ikari, K.2
Nakamura, T.3
Kuwahara, M.4
Toyama, Y.5
Tomatsu, T.6
Momohara, S.7
Kamatani, N.8
-
21
-
-
33646233784
-
Supportive evidence for a genetic association of the FCRL3 promoter polymorphism with rheumatoid arthritis
-
Ikari, K., Momohara, S., Nakamura, T., Hara, M., Yamanaka, H., Tomatsu, T. and Kamatani, N. (2006) Supportive evidence for a genetic association of the FCRL3 promoter polymorphism with rheumatoid arthritis. Ann. Rheum. Dis. 65, 671-673.
-
(2006)
Ann. Rheum. Dis
, vol.65
, pp. 671-673
-
-
Ikari, K.1
Momohara, S.2
Nakamura, T.3
Hara, M.4
Yamanaka, H.5
Tomatsu, T.6
Kamatani, N.7
-
22
-
-
20944434679
-
A functional variant in FCRL3, encoding Fc receptorlike 3, is associated with rheumatoid arthritis and several autoimmunities
-
Kochi, Y., Yamada, R., Suzuki, A., Harley, J. B., Shirasawa, S., Sawada, T., Bae, S. C., Tokuhiro, S., Chang, X., Sekine, A., Takahashi, A., Tsunoda, T., Ohnishi, Y., Kaufman, K. M., Kang, C. P., Kang, C., Otsubo, S., Yumura, W., Mimori, A., Koike, T., Nakamura, Y., Sasazuki, T. and Yamamoto, K. (2005) A functional variant in FCRL3, encoding Fc receptorlike 3, is associated with rheumatoid arthritis and several autoimmunities. Nat. Genet. 37, 478-485.
-
(2005)
Nat. Genet
, vol.37
, pp. 478-485
-
-
Kochi, Y.1
Yamada, R.2
Suzuki, A.3
Harley, J.B.4
Shirasawa, S.5
Sawada, T.6
Bae, S.C.7
Tokuhiro, S.8
Chang, X.9
Sekine, A.10
Takahashi, A.11
Tsunoda, T.12
Ohnishi, Y.13
Kaufman, K.M.14
Kang, C.P.15
Kang, C.16
Otsubo, S.17
Yumura, W.18
Mimori, A.19
Koike, T.20
Nakamura, Y.21
Sasazuki, T.22
Yamamoto, K.23
more..
-
23
-
-
33745616542
-
Meta-analysis shows strong positive association of the neuregulin 1 (NRG1) gene with schizophrenia
-
Li, D., Collier, D. A. and He, L. (2006) Meta-analysis shows strong positive association of the neuregulin 1 (NRG1) gene with schizophrenia. Hum. Mol. Genet. 15, 1995-2002.
-
(2006)
Hum. Mol. Genet
, vol.15
, pp. 1995-2002
-
-
Li, D.1
Collier, D.A.2
He, L.3
-
24
-
-
33646368404
-
Acommon haplotype of interferon regulatory factor 5 (IRF5) regulates splicing and expression and is associated with increased risk of systemic lupus erythematosus
-
Graham, R. R., Kozyrev, S. V., Baechler, E. C., Reddy, M. V., Plenge, R. M., Bauer, J. W., Ortmann, W. A., Koeuth, T., Gonzalez Escribano, M. F., Pons-Estel, B., Petri, M., Daly, M., Gregersen, P. K., Martin, J., Altshuler, D., Behrens, T. W. and Alarcon-Riquelme, M. E. (2006) Acommon haplotype of interferon regulatory factor 5 (IRF5) regulates splicing and expression and is associated with increased risk of systemic lupus erythematosus. Nat. Genet. 38, 550-555.
-
(2006)
Nat. Genet
, vol.38
, pp. 550-555
-
-
Graham, R.R.1
Kozyrev, S.V.2
Baechler, E.C.3
Reddy, M.V.4
Plenge, R.M.5
Bauer, J.W.6
Ortmann, W.A.7
Koeuth, T.8
Gonzalez Escribano, M.F.9
Pons-Estel, B.10
Petri, M.11
Daly, M.12
Gregersen, P.K.13
Martin, J.14
Altshuler, D.15
Behrens, T.W.16
Alarcon-Riquelme, M.E.17
-
25
-
-
13844292408
-
Polymorphisms in the tyrosine kinase 2 and interferon regulatory factor 5 genes are associated with systemic lupus erythematosus
-
Sigurdsson, S., Nordmark, G., Goring, H. H., Lindroos, K., Wiman, A. C., Sturfelt, G., Jonsen, A., Rantapaa-Dahlqvist, S., Moller, B., Kere, J., Koskenmies, S., Widen, E., Eloranta, M. L., Julkunen, H., Kristjansdottir, H., Steinsson, K., Alm, G., Ronnblom, L. and Syvanen, A. C. (2005) Polymorphisms in the tyrosine kinase 2 and interferon regulatory factor 5 genes are associated with systemic lupus erythematosus. Am. J. Hum. Genet. 76, 528-537.
-
(2005)
Am. J. Hum. Genet
, vol.76
, pp. 528-537
-
-
Sigurdsson, S.1
Nordmark, G.2
Goring, H.H.3
Lindroos, K.4
Wiman, A.C.5
Sturfelt, G.6
Jonsen, A.7
Rantapaa-Dahlqvist, S.8
Moller, B.9
Kere, J.10
Koskenmies, S.11
Widen, E.12
Eloranta, M.L.13
Julkunen, H.14
Kristjansdottir, H.15
Steinsson, K.16
Alm, G.17
Ronnblom, L.18
Syvanen, A.C.19
-
26
-
-
33750889376
-
Transcription factor TCF7L2 genetic study in the french population: Expression in human {beta}-cells and adipose tissue and strong association with type 2 diabetes
-
Cauchi, S., Meyre, D., Dina, C., Choquet, H., Samson, C., Gallina, S., Balkau, B., Charpentier, G., Pattou, F., Stetsyuk, V., Scharfmann, R., Staels, B., Fruhbeck, G. and Froguel, P. (2006) Transcription factor TCF7L2 genetic study in the french population: expression in human {beta}-cells and adipose tissue and strong association with type 2 diabetes. Diabetes 55, 2903-2908.
-
(2006)
Diabetes
, vol.55
, pp. 2903-2908
-
-
Cauchi, S.1
Meyre, D.2
Dina, C.3
Choquet, H.4
Samson, C.5
Gallina, S.6
Balkau, B.7
Charpentier, G.8
Pattou, F.9
Stetsyuk, V.10
Scharfmann, R.11
Staels, B.12
Fruhbeck, G.13
Froguel, P.14
-
27
-
-
33750584981
-
Polymorphisms in the transcription factor 7-like 2 (TCF7L2) gene are associated with type 2 diabetes in the Amish: Replication and evidence for a role in both insulin secretion and insulin resistance
-
Damcott, C. M., Pollin, T. I., Reinhart, L. J., Ott, S. H., Shen, H., Silver, K. D., Mitchell, B. D. and Shuldiner, A. R. (2006) Polymorphisms in the transcription factor 7-like 2 (TCF7L2) gene are associated with type 2 diabetes in the Amish: replication and evidence for a role in both insulin secretion and insulin resistance. Diabetes 55, 2654-2659.
-
(2006)
Diabetes
, vol.55
, pp. 2654-2659
-
-
Damcott, C.M.1
Pollin, T.I.2
Reinhart, L.J.3
Ott, S.H.4
Shen, H.5
Silver, K.D.6
Mitchell, B.D.7
Shuldiner, A.R.8
-
28
-
-
33746075560
-
TCF7L2 polymorphisms and progression to diabetes in the Diabetes Prevention Program
-
Florez, J. C., Jablonski, K. A., Bayley, N., Pollin, T. I., de Bakker, P. I., Shuldiner, A. R., Knowler, W. C., Nathan, D. M. and Altshuler, D. (2006) TCF7L2 polymorphisms and progression to diabetes in the Diabetes Prevention Program. N. Engl. J. Med. 355, 241-250.
-
(2006)
N. Engl. J. Med
, vol.355
, pp. 241-250
-
-
Florez, J.C.1
Jablonski, K.A.2
Bayley, N.3
Pollin, T.I.4
de Bakker, P.I.5
Shuldiner, A.R.6
Knowler, W.C.7
Nathan, D.M.8
Altshuler, D.9
-
29
-
-
32544451924
-
-
Grant, S. F., Thorleifsson, G., Reynisdottir, I., Benediktsson, R., Manolescu, A., Sainz, J., Helgason, A., Stefansson, H., Emilsson, V., Helgadottir, A., Styrkarsdottir, U., Magnusson, K. P., Walters, G. B., Palsdottir, E., Jonsdottir, T., Gudmundsdottir, T., Gylfason, A., Saemundsdottir, J., Wilensky, R. L., Reilly, M. P., Rader, D. J., Bagger, Y., Christiansen, C., Gudnason, V., Sigurdsson, G., Thorsteinsdottir, U., Gulcher, J. R., Kong, A. and Stefansson, K. (2006) Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetes. Nat. Genet. 38, 320-323.
-
Grant, S. F., Thorleifsson, G., Reynisdottir, I., Benediktsson, R., Manolescu, A., Sainz, J., Helgason, A., Stefansson, H., Emilsson, V., Helgadottir, A., Styrkarsdottir, U., Magnusson, K. P., Walters, G. B., Palsdottir, E., Jonsdottir, T., Gudmundsdottir, T., Gylfason, A., Saemundsdottir, J., Wilensky, R. L., Reilly, M. P., Rader, D. J., Bagger, Y., Christiansen, C., Gudnason, V., Sigurdsson, G., Thorsteinsdottir, U., Gulcher, J. R., Kong, A. and Stefansson, K. (2006) Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetes. Nat. Genet. 38, 320-323.
-
-
-
-
30
-
-
33750892139
-
Common single nucleotide polymorphisms in TCF7L2 are reproducibly associated with type 2 diabetes and reduce the insulin response to glucose in nondiabetic individuals
-
Saxena, R., Gianniny, L., Burtt, N. P., Lyssenko, V., Giuducci, C., Sjogren, M., Florez, J. C., Almgren, P., Isomaa, B., Orho-Melander, M., Lindblad, U., Daly, M. J., Tuomi, T., Hirschhorn, J. N., Ardlie, K. G., Groop, L. C. and Altshuler, D. (2006) Common single nucleotide polymorphisms in TCF7L2 are reproducibly associated with type 2 diabetes and reduce the insulin response to glucose in nondiabetic individuals. Diabetes 55, 2890-2895.
-
(2006)
Diabetes
, vol.55
, pp. 2890-2895
-
-
Saxena, R.1
Gianniny, L.2
Burtt, N.P.3
Lyssenko, V.4
Giuducci, C.5
Sjogren, M.6
Florez, J.C.7
Almgren, P.8
Isomaa, B.9
Orho-Melander, M.10
Lindblad, U.11
Daly, M.J.12
Tuomi, T.13
Hirschhorn, J.N.14
Ardlie, K.G.15
Groop, L.C.16
Altshuler, D.17
-
31
-
-
33750587754
-
Association of transcription factor 7-like 2 (TCF7L2) variants with type 2 diabetes in a Finnish sample
-
Scott, L. J., Bonnycastle, L. L., Willer, C. J., Sprau, A. G., Jackson, A. U., Narisu, N., Duren, W. L., Chines, P. S., Stringham, H. M., Erdos, M. R., Valle, T. T., Tuomilehto, J., Bergman, R. N., Mohlke, K. L., Collins, F. S. and Boehnke, M. (2006) Association of transcription factor 7-like 2 (TCF7L2) variants with type 2 diabetes in a Finnish sample. Diabetes 55, 2649-2653.
-
(2006)
Diabetes
, vol.55
, pp. 2649-2653
-
-
Scott, L.J.1
Bonnycastle, L.L.2
Willer, C.J.3
Sprau, A.G.4
Jackson, A.U.5
Narisu, N.6
Duren, W.L.7
Chines, P.S.8
Stringham, H.M.9
Erdos, M.R.10
Valle, T.T.11
Tuomilehto, J.12
Bergman, R.N.13
Mohlke, K.L.14
Collins, F.S.15
Boehnke, M.16
-
32
-
-
33750594321
-
Variant of transcription factor 7-like 2 (TCF7L2) gene and the risk of type 2 diabetes in large cohorts of, U.S. women and men
-
Zhang, C., Qi, L., Hunter, D. J., Meigs, J. B., Manson, J. E., van Dam, R. M. and Hu, F. B. (2006) Variant of transcription factor 7-like 2 (TCF7L2) gene and the risk of type 2 diabetes in large cohorts of, U.S. women and men. Diabetes 55, 2645-2648.
-
(2006)
Diabetes
, vol.55
, pp. 2645-2648
-
-
Zhang, C.1
Qi, L.2
Hunter, D.J.3
Meigs, J.B.4
Manson, J.E.5
van Dam, R.M.6
Hu, F.B.7
-
33
-
-
33746943663
-
-
Tsuchiya, T., Schwarz, P. E., Bosque-Plata, L. D., Geoffrey Hayes, M., Dina, C., Froguel, P., Wayne Towers, G., Fischer, S., Temelkova-Kurktschiev, T., Rietzsch, H., Graessler, J., Vcelak, J., Palyzova, D., Selisko, T., Bendlova, B., Schulze, J., Julius, U., Hanefeld, M., Weedon, M. N., Evans, J. C., Frayling, T. M., Hattersley, A. T., Orho-Melander, M., Groop, L., Malecki, M. T., Hansen, T., Pedersen, O., Fingerlin, T. E., Boehnke, M., Hanis, C. L., Cox, N. J. and Bell, G. I. (2006) Association of the calpain-10 gene with type 2 diabetes in Europeans: results of pooled and meta-analyses. Mol. Genet. Metab. 89, 174-184.
-
Tsuchiya, T., Schwarz, P. E., Bosque-Plata, L. D., Geoffrey Hayes, M., Dina, C., Froguel, P., Wayne Towers, G., Fischer, S., Temelkova-Kurktschiev, T., Rietzsch, H., Graessler, J., Vcelak, J., Palyzova, D., Selisko, T., Bendlova, B., Schulze, J., Julius, U., Hanefeld, M., Weedon, M. N., Evans, J. C., Frayling, T. M., Hattersley, A. T., Orho-Melander, M., Groop, L., Malecki, M. T., Hansen, T., Pedersen, O., Fingerlin, T. E., Boehnke, M., Hanis, C. L., Cox, N. J. and Bell, G. I. (2006) Association of the calpain-10 gene with type 2 diabetes in Europeans: results of pooled and meta-analyses. Mol. Genet. Metab. 89, 174-184.
-
-
-
-
34
-
-
0033624575
-
The common PPARgamma Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes
-
Altshuler, D., Hirschhorn, J. N., Klannemark, M., Lindgren, C. M., Vohl, M. C., Nemesh, J., Lane, C. R., Schaffner, S. F., Bolk, S., Brewer, C., Tuomi, T., Gaudet, D., Hudson, T. J., Daly, M., Groop, L. and Lander, E. S. (2000) The common PPARgamma Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes. Nat. Genet. 26, 76-80.
-
(2000)
Nat. Genet
, vol.26
, pp. 76-80
-
-
Altshuler, D.1
Hirschhorn, J.N.2
Klannemark, M.3
Lindgren, C.M.4
Vohl, M.C.5
Nemesh, J.6
Lane, C.R.7
Schaffner, S.F.8
Bolk, S.9
Brewer, C.10
Tuomi, T.11
Gaudet, D.12
Hudson, T.J.13
Daly, M.14
Groop, L.15
Lander, E.S.16
-
35
-
-
0027933734
-
A genome-wide search for human type 1 diabetes susceptibility genes
-
Davies, J. L., Kawaguchi, Y., Bennett, S. T., Copeman, J. B., Cordell, H. J., Pritchard, L. E., Reed, P. W., Gough, S. C., Jenkins, S. C., Palmer, S. M., Balfour, K. M., Rowe, B. R., Farrall, M., Barnett, A. H., Bain, S. C. and Todd, J. (1994) A genome-wide search for human type 1 diabetes susceptibility genes. Nature 371, 130-136.
-
(1994)
Nature
, vol.371
, pp. 130-136
-
-
Davies, J.L.1
Kawaguchi, Y.2
Bennett, S.T.3
Copeman, J.B.4
Cordell, H.J.5
Pritchard, L.E.6
Reed, P.W.7
Gough, S.C.8
Jenkins, S.C.9
Palmer, S.M.10
Balfour, K.M.11
Rowe, B.R.12
Farrall, M.13
Barnett, A.H.14
Bain, S.C.15
Todd, J.16
-
36
-
-
0028070552
-
Genetic mapping of a susceptibility locus for insulin-dependent diabetes mellitus on chromosome 11q
-
Hashimoto, L., Habita, C., Beressi, J. P., Delepine, M., Besse, C., Cambon-Thomsen, A., Deschamps, I., Rotter, J. I., Djoulah, S. and James, M. R. (1994) Genetic mapping of a susceptibility locus for insulin-dependent diabetes mellitus on chromosome 11q. Nature 371, 161-164.
-
(1994)
Nature
, vol.371
, pp. 161-164
-
-
Hashimoto, L.1
Habita, C.2
Beressi, J.P.3
Delepine, M.4
Besse, C.5
Cambon-Thomsen, A.6
Deschamps, I.7
Rotter, J.I.8
Djoulah, S.9
James, M.R.10
-
37
-
-
20244380171
-
Complement factor H polymorphism in age-related macular degeneration
-
Klein, R. J., Zeiss, C., Chew, E. Y., Tsai, J. Y., Sackler, R. S., Haynes, C., Henning, A. K., SanGiovanni, J. P., Mane, S. M., Mayne, S. T., Bracken, M. B., Ferris, F. L., Ott, J., Barnstable, C. and Hoh, J. (2005) Complement factor H polymorphism in age-related macular degeneration. Science 308, 385-389.
-
(2005)
Science
, vol.308
, pp. 385-389
-
-
Klein, R.J.1
Zeiss, C.2
Chew, E.Y.3
Tsai, J.Y.4
Sackler, R.S.5
Haynes, C.6
Henning, A.K.7
SanGiovanni, J.P.8
Mane, S.M.9
Mayne, S.T.10
Bracken, M.B.11
Ferris, F.L.12
Ott, J.13
Barnstable, C.14
Hoh, J.15
-
38
-
-
27244451809
-
High-resolution wholegenome association study of Parkinson disease
-
Maraganore, D. M., de Andrade, M., Lesnick, T. G., Strain, K. J., Farrer, M. J., Rocca, W. A., Pant, P. V., Frazer, K. A., Cox, D. R. and Ballinger, D. G. (2005) High-resolution wholegenome association study of Parkinson disease. Am. J. Hum. Genet. 77, 685-693.
-
(2005)
Am. J. Hum. Genet
, vol.77
, pp. 685-693
-
-
Maraganore, D.M.1
de Andrade, M.2
Lesnick, T.G.3
Strain, K.J.4
Farrer, M.J.5
Rocca, W.A.6
Pant, P.V.7
Frazer, K.A.8
Cox, D.R.9
Ballinger, D.G.10
-
39
-
-
0028877463
-
Genetic dissection of complex traits: Guidelines for interpreting and reporting linkage results
-
Lander, E. and Kruglyak, L. (1995) Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results. Nat. Genet. 11, 241-247.
-
(1995)
Nat. Genet
, vol.11
, pp. 241-247
-
-
Lander, E.1
Kruglyak, L.2
-
40
-
-
17344372511
-
A second-generation screen of the human genome for susceptibility to insulin-dependent diabetes mellitus
-
Concannon, P., Gogolin-Ewens, K. J., Hinds, D. A., Wapelhorst, B., Morrison, V. A., Stirling, B., Mitra, M., Farmer, J., Williams, S. R., Cox, N. J., Bell, G. I., Risch, N. and Spielman, R. S. (1998) A second-generation screen of the human genome for susceptibility to insulin-dependent diabetes mellitus. Nat. Genet. 19, 292-296.
-
(1998)
Nat. Genet
, vol.19
, pp. 292-296
-
-
Concannon, P.1
Gogolin-Ewens, K.J.2
Hinds, D.A.3
Wapelhorst, B.4
Morrison, V.A.5
Stirling, B.6
Mitra, M.7
Farmer, J.8
Williams, S.R.9
Cox, N.J.10
Bell, G.I.11
Risch, N.12
Spielman, R.S.13
-
41
-
-
0031831322
-
Sometimes it's hot, sometimes it's not
-
Lernmark, A. and Ott, J. (1998) Sometimes it's hot, sometimes it's not. Nat. Genet. 19, 213-214.
-
(1998)
Nat. Genet
, vol.19
, pp. 213-214
-
-
Lernmark, A.1
Ott, J.2
-
42
-
-
17144452354
-
A search for type 1 diabetes susceptibility genes in families from the United Kingdom
-
Mein, C. A., Esposito, L., Dunn, M. G., Johnson, G. C., Timms, A. E., Goy, J. V., Smith, A. N., Sebag-Montefiore, L., Merriman, M. E., Wilson, A. J., Pritchard, L. E., Cucca, F., Barnett, A. H., Bain, S. C. and Todd, J. A. (1998) A search for type 1 diabetes susceptibility genes in families from the United Kingdom. Nat. Genet. 19, 297-300.
-
(1998)
Nat. Genet
, vol.19
, pp. 297-300
-
-
Mein, C.A.1
Esposito, L.2
Dunn, M.G.3
Johnson, G.C.4
Timms, A.E.5
Goy, J.V.6
Smith, A.N.7
Sebag-Montefiore, L.8
Merriman, M.E.9
Wilson, A.J.10
Pritchard, L.E.11
Cucca, F.12
Barnett, A.H.13
Bain, S.C.14
Todd, J.A.15
-
43
-
-
0002710362
-
Problems of replicating linkage chlaims in psychiatry
-
Gershon, E. and Cloninger, C, Eds, pp, American Psychiatric Press, Washington DC
-
Suarez, B., Hampe, C. and Eerdewegh, P. V. (1994) Problems of replicating linkage chlaims in psychiatry. in: Genetic Approaches to Mental Disorders (Gershon, E. and Cloninger, C., Eds); pp 23-46, American Psychiatric Press, Washington DC.
-
(1994)
Genetic Approaches to Mental Disorders
, pp. 23-46
-
-
Suarez, B.1
Hampe, C.2
Eerdewegh, P.V.3
-
44
-
-
0036234398
-
A combined analysis of genomewide linkage scans for body mass index from the National Heart, Lung, and Blood Institute Family Blood Pressure Program
-
Wu, X., Cooper, R. S., Borecki, I., Hanis, C., Bray, M., Lewis, C. E., Zhu, X., Kan, D., Luke, A. and Curb, D. (2002) A combined analysis of genomewide linkage scans for body mass index from the National Heart, Lung, and Blood Institute Family Blood Pressure Program. Am. J. Hum. Genet. 70, 1247-1256.
-
(2002)
Am. J. Hum. Genet
, vol.70
, pp. 1247-1256
-
-
Wu, X.1
Cooper, R.S.2
Borecki, I.3
Hanis, C.4
Bray, M.5
Lewis, C.E.6
Zhu, X.7
Kan, D.8
Luke, A.9
Curb, D.10
-
45
-
-
20044368001
-
Genomewide linkage scans for fasting glucose, insulin, and insulin resistance in the National Heart, Lung, and Blood Institute Family Blood Pressure Program: Evidence of linkages to chromosome 7q36 and 19q13 from meta-analysis
-
An, P., Freedman, B. I., Hanis, C. L., Chen, Y. D., Weder, A. B., Schork, N. J., Boerwinkle, E., Province, M. A., Hsiung, C. A., Wu, X., Quertermous, T. and Rao, D. C. (2005) Genomewide linkage scans for fasting glucose, insulin, and insulin resistance in the National Heart, Lung, and Blood Institute Family Blood Pressure Program: evidence of linkages to chromosome 7q36 and 19q13 from meta-analysis. Diabetes 54, 909-914.
-
(2005)
Diabetes
, vol.54
, pp. 909-914
-
-
An, P.1
Freedman, B.I.2
Hanis, C.L.3
Chen, Y.D.4
Weder, A.B.5
Schork, N.J.6
Boerwinkle, E.7
Province, M.A.8
Hsiung, C.A.9
Wu, X.10
Quertermous, T.11
Rao, D.C.12
-
46
-
-
10744230909
-
A meta-analysis of four European genome screens (GIFT Consortium) shows evidence for a novel region on chromosome 17p11.2-q22 linked to type 2 Diabetes
-
Demenais, F., Kanninen, T., Lindgren, C. M., Wiltshire, S., Gaget, S., Dandrieux, C., Almgren, P., Sjogren, M., Hattersley, A., Dina, C., Tuomi, T., McCarthy, M. I., Froguel, P. and Groop, L. C. (2003) A meta-analysis of four European genome screens (GIFT Consortium) shows evidence for a novel region on chromosome 17p11.2-q22 linked to type 2 Diabetes. Hum. Mol. Genet. 12, 1865-1873.
-
(2003)
Hum. Mol. Genet
, vol.12
, pp. 1865-1873
-
-
Demenais, F.1
Kanninen, T.2
Lindgren, C.M.3
Wiltshire, S.4
Gaget, S.5
Dandrieux, C.6
Almgren, P.7
Sjogren, M.8
Hattersley, A.9
Dina, C.10
Tuomi, T.11
McCarthy, M.I.12
Froguel, P.13
Groop, L.C.14
-
47
-
-
32344446546
-
An updated meta-analysis of genome scans for hypertension and blood pressure in the NHLBI Family Blood Pressure Program (FBPP)
-
Wu, X., Kan, D., Province, M., Quertermous, T., Rao, D. C., Chang, C., Mosley, T. H., Curb, D., Boerwinkle, E. and Cooper, R. S. (2006) An updated meta-analysis of genome scans for hypertension and blood pressure in the NHLBI Family Blood Pressure Program (FBPP). Am. J. Hypertens. 19, 122-127.
-
(2006)
Am. J. Hypertens
, vol.19
, pp. 122-127
-
-
Wu, X.1
Kan, D.2
Province, M.3
Quertermous, T.4
Rao, D.C.5
Chang, C.6
Mosley, T.H.7
Curb, D.8
Boerwinkle, E.9
Cooper, R.S.10
-
48
-
-
0038003196
-
-
Lewis, C. M, Levinson, D. F, Wise, L. H, DeLisi, L. E, Straub, R. E, Hovatta, I, Williams, N. M, Schwab, S. G, Pulver, A. E, Faraone, S. V, Brzustowicz, L. M, Kaufmann, C. A, Garver, D. L, Gurling, H. M, Lindholm, E, Coon, H, Moises, H. W, Byerley, W, Shaw, S. H, Mesen, A, Sherrington, R, O'Neill, F. A, Walsh, D, Kendler, K. S, Ekelund, J, Paunio, T, Lonnqvist, J, Peltonen, L, O'Donovan, M. C, Owen, M. J, Wildenauer, D. B, Maier, W, Nestadt, G, Blouin, J. L, Antonarakis, S. E, Mowry, B. J, Silverman, J. M, Crowe, R. R, Cloninger, C. R, Tsuang, M. T, Malaspina, D, Harkavy-Friedman, J. M, Svrakic, D. M, Bassett, A. S, Holcomb, J, Kalsi, G, McQuillin, A, Brynjolfson, J, Sigmundsson, T, Petursson, H, Jazin, E, Zoega, T. and Helgason, T, 2003 Genome scan metaanalysis of schizophrenia and bipolar disorder. II. Schizophrenia. Am. J. Hum. Genet. 73, 34-48
-
Lewis, C. M., Levinson, D. F., Wise, L. H., DeLisi, L. E., Straub, R. E., Hovatta, I., Williams, N. M., Schwab, S. G., Pulver, A. E., Faraone, S. V., Brzustowicz, L. M., Kaufmann, C. A., Garver, D. L., Gurling, H. M., Lindholm, E., Coon, H., Moises, H. W., Byerley, W., Shaw, S. H., Mesen, A., Sherrington, R., O'Neill, F. A., Walsh, D., Kendler, K. S., Ekelund, J., Paunio, T., Lonnqvist, J., Peltonen, L., O'Donovan, M. C., Owen, M. J., Wildenauer, D. B., Maier, W., Nestadt, G., Blouin, J. L., Antonarakis, S. E., Mowry, B. J., Silverman, J. M., Crowe, R. R., Cloninger, C. R., Tsuang, M. T., Malaspina, D., Harkavy-Friedman, J. M., Svrakic, D. M., Bassett, A. S., Holcomb, J., Kalsi, G., McQuillin, A., Brynjolfson, J., Sigmundsson, T., Petursson, H., Jazin, E., Zoega, T. and Helgason, T. (2003) Genome scan metaanalysis of schizophrenia and bipolar disorder. II. Schizophrenia. Am. J. Hum. Genet. 73, 34-48.
-
-
-
-
49
-
-
0038341184
-
-
Segurado, R, Detera-Wadleigh, S. D, Levinson, D. F, Lewis, C. M, Gill, M, Nurnberger, J. I, Jr, Craddock, N, DePaulo, J. R, Baron, M, Gershon, E. S, Ekholm, J, Cichon, S, Turecki, G, Claes, S, Kelsoe, J. R, Schofield, P. R, Badenhop, R. F, Morissette, J, Coon, H, Blackwood, D, McInnes, L. A, Foroud, T, Edenberg, H. J, Reich, T, Rice, J. P, Goate, A, McInnis, M. G, McMahon, F. J, Badner, J. A, Goldin, L. R, Bennett, P, Willour, V. L, Zandi, P. P, Liu, J, Gilliam, C, Juo, S. H, Berrettini, W. H, Yoshikawa, T, Peltonen, L, Lonnqvist, J, Nothen, M. M, Schumacher, J, Windemuth, C, Rietschel, M, Propping, P, Maier, W, Alda, M, Grof, P, Rouleau, G. A, Del-Favero, J, Van Broeckhoven, C, Mendlewicz, J, Adolfsson, R, Spence, M. A, Luebbert, H, Adams, L. J, Donald, J. A, Mitchell, P. B, Barden, N, Shink, E, Byerley, W, Muir, W, Visscher, P. M, Macgregor, S, Gurling, H, Kalsi, G, McQuillin, A, Escamilla, M. A, Reus, V. I, Leon
-
Segurado, R., Detera-Wadleigh, S. D., Levinson, D. F., Lewis, C. M., Gill, M., Nurnberger, J. I., Jr., Craddock, N., DePaulo, J. R., Baron, M., Gershon, E. S., Ekholm, J., Cichon, S., Turecki, G., Claes, S., Kelsoe, J. R., Schofield, P. R., Badenhop, R. F., Morissette, J., Coon, H., Blackwood, D., McInnes, L. A., Foroud, T., Edenberg, H. J., Reich, T., Rice, J. P., Goate, A., McInnis, M. G., McMahon, F. J., Badner, J. A., Goldin, L. R., Bennett, P., Willour, V. L., Zandi, P. P., Liu, J., Gilliam, C., Juo, S. H., Berrettini, W. H., Yoshikawa, T., Peltonen, L., Lonnqvist, J., Nothen, M. M., Schumacher, J., Windemuth, C., Rietschel, M., Propping, P., Maier, W., Alda, M., Grof, P., Rouleau, G. A., Del-Favero, J., Van Broeckhoven, C., Mendlewicz, J., Adolfsson, R., Spence, M. A., Luebbert, H., Adams, L. J., Donald, J. A., Mitchell, P. B., Barden, N., Shink, E., Byerley, W., Muir, W., Visscher, P. M., Macgregor, S., Gurling, H., Kalsi, G., McQuillin, A., Escamilla, M. A., Reus, V. I., Leon, P., Freimer, N. B., Ewald, H., Kruse, T. A., Mors, O., Radhakrishna, U., Blouin, J. L., Antonarakis, S. E. and Akarsu, N. (2003) Genome scan metaanalysis of schizophrenia and bipolar disorder. III. Bipolar disorder. Am. J. Hum. Genet. 73, 49-62.
-
-
-
-
50
-
-
11144354272
-
Inflammatory bowel disease susceptibility loci defined by genome scan meta-analysis of 1952 affected relative pairs
-
van Heel, D. A., Fisher, S. A., Kirby, A., Daly, M. J., Rioux, J. D. and Lewis, C. M. (2004) Inflammatory bowel disease susceptibility loci defined by genome scan meta-analysis of 1952 affected relative pairs. Hum. Mol. Genet. 13, 763-770.
-
(2004)
Hum. Mol. Genet
, vol.13
, pp. 763-770
-
-
van Heel, D.A.1
Fisher, S.A.2
Kirby, A.3
Daly, M.J.4
Rioux, J.D.5
Lewis, C.M.6
-
51
-
-
33744990856
-
Meta-analysis of genome-wide linkage studies for bone mineral density
-
Lee, Y. H., Rho, Y. H., Choi, S. J., Ji, J. D. and Song, G. G. (2006) Meta-analysis of genome-wide linkage studies for bone mineral density. J. Hum. Genet. 51, 480-486.
-
(2006)
J. Hum. Genet
, vol.51
, pp. 480-486
-
-
Lee, Y.H.1
Rho, Y.H.2
Choi, S.J.3
Ji, J.D.4
Song, G.G.5
-
52
-
-
25844441709
-
Type 1 diabetes: Evidence for susceptibility loci from four genome-wide linkage scans in 1,435 multiplex families
-
Concannon, P., Erlich, H. A., Julier, C., Morahan, G., Nerup, J., Pociot, F., Todd, J. A. and Rich, S. S. (2005) Type 1 diabetes: evidence for susceptibility loci from four genome-wide linkage scans in 1,435 multiplex families. Diabetes 54, 2995-3001.
-
(2005)
Diabetes
, vol.54
, pp. 2995-3001
-
-
Concannon, P.1
Erlich, H.A.2
Julier, C.3
Morahan, G.4
Nerup, J.5
Pociot, F.6
Todd, J.A.7
Rich, S.S.8
-
53
-
-
30744456018
-
Systemic lupus erythematosus susceptibility loci defined by genome scan metaanalysis
-
Lee, Y. H. and Nath, S. K. (2005) Systemic lupus erythematosus susceptibility loci defined by genome scan metaanalysis. Hum. Genet. 118, 434-443.
-
(2005)
Hum. Genet
, vol.118
, pp. 434-443
-
-
Lee, Y.H.1
Nath, S.K.2
-
54
-
-
31544455037
-
Genome scan meta-analysis of rheumatoid arthritis
-
Choi, S. J., Rho, Y. H., Ji, J. D., Song, G. G. and Lee, Y. H. (2006) Genome scan meta-analysis of rheumatoid arthritis. Rheumatology 45, 166-170.
-
(2006)
Rheumatology
, vol.45
, pp. 166-170
-
-
Choi, S.J.1
Rho, Y.H.2
Ji, J.D.3
Song, G.G.4
Lee, Y.H.5
-
55
-
-
26944470820
-
Ankylosing spondylitis susceptibility loci defined by genome-search meta-analysis
-
Lee, Y. H., Rho, Y. H., Choi, S. J., Ji, J. D. and Song, G. G. (2005) Ankylosing spondylitis susceptibility loci defined by genome-search meta-analysis. J. Hum. Genet. 50, 453-459.
-
(2005)
J. Hum. Genet
, vol.50
, pp. 453-459
-
-
Lee, Y.H.1
Rho, Y.H.2
Choi, S.J.3
Ji, J.D.4
Song, G.G.5
-
56
-
-
2942587072
-
Meta-analysis of genome-wide studies of psoriasis susceptibility reveals linkage to chromosomes 6p21 and 4q28-q31 in Caucasian and Chinese Hans population
-
Sagoo, G. S., Tazi-Ahnini, R., Barker, J. W., Elder, J. T., Nair, R. P., Samuelsson, L., Traupe, H., Trembath, R. C., Robinson, D. A. and Iles, M. M. (2004) Meta-analysis of genome-wide studies of psoriasis susceptibility reveals linkage to chromosomes 6p21 and 4q28-q31 in Caucasian and Chinese Hans population. J. Invest. Dermatol. 122, 1401-1405.
-
(2004)
J. Invest. Dermatol
, vol.122
, pp. 1401-1405
-
-
Sagoo, G.S.1
Tazi-Ahnini, R.2
Barker, J.W.3
Elder, J.T.4
Nair, R.P.5
Samuelsson, L.6
Traupe, H.7
Trembath, R.C.8
Robinson, D.A.9
Iles, M.M.10
-
57
-
-
0142186253
-
-
GAMES. Transatlantic Multiple Sclerosis Genetics Cooperative. (2003) A meta-analysis of whole genome linkage screens in multiple sclerosis. J. Neuroimmunol. 143, 39-46.
-
GAMES. Transatlantic Multiple Sclerosis Genetics Cooperative. (2003) A meta-analysis of whole genome linkage screens in multiple sclerosis. J. Neuroimmunol. 143, 39-46.
-
-
-
-
58
-
-
29944441305
-
Search for autism loci by combined analysis of Autism Genetic Resource Exchange and Finnish families
-
Ylisaukko-oja, T., Alarcon, M., Cantor, R. M., Auranen, M., Vanhala, R., Kempas, E., von Wendt, L., Jarvela, I., Geschwind, D. H. and Peltonen, L. (2006) Search for autism loci by combined analysis of Autism Genetic Resource Exchange and Finnish families. Ann. Neurol. 59, 145-155.
-
(2006)
Ann. Neurol
, vol.59
, pp. 145-155
-
-
Ylisaukko-oja, T.1
Alarcon, M.2
Cantor, R.M.3
Auranen, M.4
Vanhala, R.5
Kempas, E.6
von Wendt, L.7
Jarvela, I.8
Geschwind, D.H.9
Peltonen, L.10
-
59
-
-
0141919767
-
Meta-analysis of 4 coronary heart disease genome-wide linkage studies confirms a susceptibility locus on chromosome 3q
-
Chiodini, B. D. and Lewis, C. M. (2003) Meta-analysis of 4 coronary heart disease genome-wide linkage studies confirms a susceptibility locus on chromosome 3q. Arterioscler. Thromb. Vasc. Biol. 23, 1863-1868.
-
(2003)
Arterioscler. Thromb. Vasc. Biol
, vol.23
, pp. 1863-1868
-
-
Chiodini, B.D.1
Lewis, C.M.2
-
60
-
-
0035978651
-
Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease
-
Hugot, J. P., Chamaillard, M., Zouali, H., Lesage, S., Cezard, J. P., Belaiche, J., Almer, S., Tysk, C., O'Morain, C. A., Gassull, M., Binder, V., Finkel, Y., Cortot, A., Modigliani, R., Laurent-Puig, P., Gower-Rousseau, C., Macry, J., Colombel, J. F., Sahbatou, M. and Thomas, G. (2001) Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease. Nature 411, 599-603.
-
(2001)
Nature
, vol.411
, pp. 599-603
-
-
Hugot, J.P.1
Chamaillard, M.2
Zouali, H.3
Lesage, S.4
Cezard, J.P.5
Belaiche, J.6
Almer, S.7
Tysk, C.8
O'Morain, C.A.9
Gassull, M.10
Binder, V.11
Finkel, Y.12
Cortot, A.13
Modigliani, R.14
Laurent-Puig, P.15
Gower-Rousseau, C.16
Macry, J.17
Colombel, J.F.18
Sahbatou, M.19
Thomas, G.20
more..
-
61
-
-
0035978533
-
A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease
-
Ogura, Y., Bonen, D. K., Inohara, N., Nicolae, D. L., Chen, F. F., Ramos, R., Britton, H., Moran, T., Karaliuskas, R., Duerr, R. H., Achkar, J. P., Brant, S. R., Bayless, T. M., Kirschner, B. S., Hanauer, S. B., Nunez, G. and Cho, J. H. (2001) A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease. Nature 411, 603-606.
-
(2001)
Nature
, vol.411
, pp. 603-606
-
-
Ogura, Y.1
Bonen, D.K.2
Inohara, N.3
Nicolae, D.L.4
Chen, F.F.5
Ramos, R.6
Britton, H.7
Moran, T.8
Karaliuskas, R.9
Duerr, R.H.10
Achkar, J.P.11
Brant, S.R.12
Bayless, T.M.13
Kirschner, B.S.14
Hanauer, S.B.15
Nunez, G.16
Cho, J.H.17
-
62
-
-
13344259990
-
Mapping of a susceptibility locus for Crohn's disease on chromosome 16
-
Hugot, J. P., Laurent-Puig, P., Gower-Rousseau, C., Olson, J. M., Lee, J. C., Beaugerie, L., Naom, I., Dupas, J. L., Van Gossum, A., Orholm, M., Bonaiti-Pellie, C., Weissenbach, J., Mathew, C. G., Lennard-Jones, J. E., Cortot, A., Colombel, J. F. and Thomas, G. (1996) Mapping of a susceptibility locus for Crohn's disease on chromosome 16. Nature 379, 821-823.
-
(1996)
Nature
, vol.379
, pp. 821-823
-
-
Hugot, J.P.1
Laurent-Puig, P.2
Gower-Rousseau, C.3
Olson, J.M.4
Lee, J.C.5
Beaugerie, L.6
Naom, I.7
Dupas, J.L.8
Van Gossum, A.9
Orholm, M.10
Bonaiti-Pellie, C.11
Weissenbach, J.12
Mathew, C.G.13
Lennard-Jones, J.E.14
Cortot, A.15
Colombel, J.F.16
Thomas, G.17
-
63
-
-
0035066147
-
NF-kappa B may determine whether epithelial cell-microbial interactions in the intestine are hostile or friendly
-
Mahida, Y. R. and Johal, S. (2001) NF-kappa B may determine whether epithelial cell-microbial interactions in the intestine are hostile or friendly. Clin. Exp. Immunol. 123, 347-349.
-
(2001)
Clin. Exp. Immunol
, vol.123
, pp. 347-349
-
-
Mahida, Y.R.1
Johal, S.2
-
64
-
-
33646020997
-
New genes in inflammatory bowel disease: Lessons for complex diseases?
-
Gaya, D. R., Russell, R. K., Nimmo, E. R. and Satsangi, J. (2006) New genes in inflammatory bowel disease: lessons for complex diseases? Lancet 367, 1271-1284.
-
(2006)
Lancet
, vol.367
, pp. 1271-1284
-
-
Gaya, D.R.1
Russell, R.K.2
Nimmo, E.R.3
Satsangi, J.4
-
65
-
-
0033820560
-
NOD Idd5 locus controls insulitis and diabetes and overlaps the orthologous CTLA4/IDDM12 and NRAMP1 loci in humans
-
Hill, N. J., Lyons, P. A., Armitage, N., Todd, J. A., Wicker, L. S. and Peterson, L. B. (2000) NOD Idd5 locus controls insulitis and diabetes and overlaps the orthologous CTLA4/IDDM12 and NRAMP1 loci in humans. Diabetes 49, 1744-1747.
-
(2000)
Diabetes
, vol.49
, pp. 1744-1747
-
-
Hill, N.J.1
Lyons, P.A.2
Armitage, N.3
Todd, J.A.4
Wicker, L.S.5
Peterson, L.B.6
-
66
-
-
24144446703
-
Colocalization of mouse autoimmune diabetes loci Idd21.1 and Idd21.2 with IDDM6 (human) and Iddm3 (rat)
-
Hollis-Moffatt, J. E., Hook, S. M. and Merriman, T. R. (2005) Colocalization of mouse autoimmune diabetes loci Idd21.1 and Idd21.2 with IDDM6 (human) and Iddm3 (rat). Diabetes 54, 2820-2825.
-
(2005)
Diabetes
, vol.54
, pp. 2820-2825
-
-
Hollis-Moffatt, J.E.1
Hook, S.M.2
Merriman, T.R.3
-
67
-
-
0033711184
-
The NOD Idd9 genetic interval influences the pathogenicity of insulitis and contains molecular variants of Cd30, Tnfr2, and Cd137
-
Lyons, P. A., Hancock, W. W., Denny, P., Lord, C. J., Hill, N. J., Armitage, N., Siegmund, T., Todd, J. A., Phillips, M. S., Hess, J. F., Chen, S. L., Fischer, P. A., Peterson, L. B. and Wicker, L. S. (2000) The NOD Idd9 genetic interval influences the pathogenicity of insulitis and contains molecular variants of Cd30, Tnfr2, and Cd137. Immunity 13, 107-115.
-
(2000)
Immunity
, vol.13
, pp. 107-115
-
-
Lyons, P.A.1
Hancock, W.W.2
Denny, P.3
Lord, C.J.4
Hill, N.J.5
Armitage, N.6
Siegmund, T.7
Todd, J.A.8
Phillips, M.S.9
Hess, J.F.10
Chen, S.L.11
Fischer, P.A.12
Peterson, L.B.13
Wicker, L.S.14
-
68
-
-
0031571223
-
Congenic mapping of the insulin-dependent diabetes (Idd) gene, Idd10, localizes two genes mediating the Idd10 effect and eliminates the candidate Fcgr1
-
Podolin, P. L., Denny, P., Lord, C. J., Hill, N. J., Todd, J. A., Peterson, L. B., Wicker, L. S. and Lyons, P. A. (1997) Congenic mapping of the insulin-dependent diabetes (Idd) gene, Idd10, localizes two genes mediating the Idd10 effect and eliminates the candidate Fcgr1. J. Immunol. 159, 1835-1843.
-
(1997)
J. Immunol
, vol.159
, pp. 1835-1843
-
-
Podolin, P.L.1
Denny, P.2
Lord, C.J.3
Hill, N.J.4
Todd, J.A.5
Peterson, L.B.6
Wicker, L.S.7
Lyons, P.A.8
-
69
-
-
33846509234
-
Genomic DNA pooling for whole genome association scans in complex disease: Empirical demonstration of efficacy in rheumatoid arthritis
-
Steer, S., Abkevich, V., Gutin, A., Cordell, H. J., Gendall, K. L., Merriman, M. E., Rodger, R. A., Rowley, K. A., Chapman, P., Gow, P., Harrison, A. a., Highton, J., Jones, P. B. B., ODonnell, J., stamp, L., Fitzgerald, L., Iliev, D., Kouzmine, A., Tran, T., Skolnick, M. H., Timms, K. M., Lanchbury, J. S. and Merriman, T. R. (2007) Genomic DNA pooling for whole genome association scans in complex disease: empirical demonstration of efficacy in rheumatoid arthritis. Genes Immun. 8, 57-68.
-
(2007)
Genes Immun
, vol.8
, pp. 57-68
-
-
Steer, S.1
Abkevich, V.2
Gutin, A.3
Cordell, H.J.4
Gendall, K.L.5
Merriman, M.E.6
Rodger, R.A.7
Rowley, K.A.8
Chapman, P.9
Gow, P.10
Harrison, A.A.11
Highton, J.12
Jones, P.B.B.13
ODonnell, J.14
stamp, L.15
Fitzgerald, L.16
Iliev, D.17
Kouzmine, A.18
Tran, T.19
Skolnick, M.H.20
Timms, K.M.21
Lanchbury, J.S.22
Merriman, T.R.23
more..
-
70
-
-
0029741063
-
The future of genetic studies of complex human diseases
-
Risch, N. and Merikangas, K. (1996) The future of genetic studies of complex human diseases. Science 273, 1516-1517.
-
(1996)
Science
, vol.273
, pp. 1516-1517
-
-
Risch, N.1
Merikangas, K.2
-
71
-
-
33745159993
-
Whole-genome genotyping of haplotype tag single nucleotide polymorphisms
-
Gunderson, K. L., Kuhn, K. M., Steemers, F. J., Ng, P., Murray, S. S. and Shen, R. (2006) Whole-genome genotyping of haplotype tag single nucleotide polymorphisms. Pharmacogenomics 7, 641-648.
-
(2006)
Pharmacogenomics
, vol.7
, pp. 641-648
-
-
Gunderson, K.L.1
Kuhn, K.M.2
Steemers, F.J.3
Ng, P.4
Murray, S.S.5
Shen, R.6
-
72
-
-
18144425478
-
A genome-wide scalable SNP genotyping assay using microarray technology
-
Gunderson, K. L., Steemers, F. J., Lee, G., Mendoza, L. G. and Chee, M. S. (2005) A genome-wide scalable SNP genotyping assay using microarray technology. Nat. Genet. 37, 549-554.
-
(2005)
Nat. Genet
, vol.37
, pp. 549-554
-
-
Gunderson, K.L.1
Steemers, F.J.2
Lee, G.3
Mendoza, L.G.4
Chee, M.S.5
-
73
-
-
20844455582
-
-
Matsuzaki, H., Dong, S., Loi, H., Di, X., Liu, G., Hubbell, E., Law, J., Berntsen, T., Chadha, M., Hui, H., Yang, G., Kennedy, G. C., Webster, T. A., Cawley, S., Walsh, P. S., Jones, K. W., Fodor, S. P. and Mei, R. (2004) Genotyping over 100,000 SNPs on a pair of oligonucleotide arrays. Nat. Methods 1, 109-111.
-
Matsuzaki, H., Dong, S., Loi, H., Di, X., Liu, G., Hubbell, E., Law, J., Berntsen, T., Chadha, M., Hui, H., Yang, G., Kennedy, G. C., Webster, T. A., Cawley, S., Walsh, P. S., Jones, K. W., Fodor, S. P. and Mei, R. (2004) Genotyping over 100,000 SNPs on a pair of oligonucleotide arrays. Nat. Methods 1, 109-111.
-
-
-
-
74
-
-
13144306071
-
Genome-wide association studies for common diseases and complex traits
-
Hirschhorn, J. N. and Daly, M. J. (2005) Genome-wide association studies for common diseases and complex traits. Nat. Rev. Genet. 6, 95-108.
-
(2005)
Nat. Rev. Genet
, vol.6
, pp. 95-108
-
-
Hirschhorn, J.N.1
Daly, M.J.2
-
75
-
-
18444369013
-
The structure of haplotype blocks in the human genome
-
Gabriel, S. B., Schaffner, S. F., Nguyen, H., Moore, J. M., Roy, J., Blumenstiel, B., Higgins, J., DeFelice, M., Lochner, A., Faggart, M., Liu-Cordero, S. N., Rotimi, C., Adeyemo, A., Cooper, R., Ward, R., Lander, E. S., Daly, M. J. and Altshuler, D. (2002) The structure of haplotype blocks in the human genome. Science 296, 2225-2229.
-
(2002)
Science
, vol.296
, pp. 2225-2229
-
-
Gabriel, S.B.1
Schaffner, S.F.2
Nguyen, H.3
Moore, J.M.4
Roy, J.5
Blumenstiel, B.6
Higgins, J.7
DeFelice, M.8
Lochner, A.9
Faggart, M.10
Liu-Cordero, S.N.11
Rotimi, C.12
Adeyemo, A.13
Cooper, R.14
Ward, R.15
Lander, E.S.16
Daly, M.J.17
Altshuler, D.18
-
76
-
-
0034789532
-
Haplotype tagging for the identification of common disease genes
-
Johnson, G. C., Esposito, L., Barratt, B. J., Smith, A. N., Heward, J., Di Genova, G., Ueda, H., Cordell, H. J., Eaves, I. A., Dudbridge, F., Twells, R. C., Payne, F., Hughes, W., Nutland, S., Stevens, H., Carr, P., Tuomilehto-Wolf, E., Tuomilehto, J., Gough, S. C., Clayton, D. G. and Todd, J. A. (2001) Haplotype tagging for the identification of common disease genes. Nat. Genet. 29, 233-237.
-
(2001)
Nat. Genet
, vol.29
, pp. 233-237
-
-
Johnson, G.C.1
Esposito, L.2
Barratt, B.J.3
Smith, A.N.4
Heward, J.5
Di Genova, G.6
Ueda, H.7
Cordell, H.J.8
Eaves, I.A.9
Dudbridge, F.10
Twells, R.C.11
Payne, F.12
Hughes, W.13
Nutland, S.14
Stevens, H.15
Carr, P.16
Tuomilehto-Wolf, E.17
Tuomilehto, J.18
Gough, S.C.19
Clayton, D.G.20
Todd, J.A.21
more..
-
77
-
-
33745279392
-
Evaluating and improving power in whole-genome association studies using fixed marker sets
-
Pe'er, I., de Bakker, P. I., Maller, J., Yelensky, R., Altshuler, D. and Daly, M. J. (2006) Evaluating and improving power in whole-genome association studies using fixed marker sets. Nat. Genet. 38, 663-667.
-
(2006)
Nat. Genet
, vol.38
, pp. 663-667
-
-
Pe'er, I.1
de Bakker, P.I.2
Maller, J.3
Yelensky, R.4
Altshuler, D.5
Daly, M.J.6
-
78
-
-
13144265739
-
Genome-wide association studies: Theoretical and practical concerns
-
Wang, W. Y., Barratt, B. J., Clayton, D. G. and Todd, J. A. (2005) Genome-wide association studies: theoretical and practical concerns. Nat. Rev. Genet. 6, 109-118.
-
(2005)
Nat. Rev. Genet
, vol.6
, pp. 109-118
-
-
Wang, W.Y.1
Barratt, B.J.2
Clayton, D.G.3
Todd, J.A.4
-
79
-
-
21044453724
-
-
Hageman, G. S., Anderson, D. H., Johnson, L. V., Hancox, L. S., Taiber, A. J., Hardisty, L. I., Hageman, J. L., Stockman, H. A., Borchardt, J. D., Gehrs, K. M., Smith, R. J., Silvestri, G., Russell, S. R., Klaver, C. C., Barbazetto, I., Chang, S., Yannuzzi, L. A., Barile, G. R., Merriam, J. C., Smith, R. T., Olsh, A. K., Bergeron, J., Zernant, J., Merriam, J. E., Gold, B., Dean, M. and Allikmets, R. (2005) A common haplotype in the complement regulatory gene factor H (HF1/CFH) predisposes individuals to age-related macular degeneration. Proc. Natl. Acad. Sci. USA 102, 7227-7232.
-
Hageman, G. S., Anderson, D. H., Johnson, L. V., Hancox, L. S., Taiber, A. J., Hardisty, L. I., Hageman, J. L., Stockman, H. A., Borchardt, J. D., Gehrs, K. M., Smith, R. J., Silvestri, G., Russell, S. R., Klaver, C. C., Barbazetto, I., Chang, S., Yannuzzi, L. A., Barile, G. R., Merriam, J. C., Smith, R. T., Olsh, A. K., Bergeron, J., Zernant, J., Merriam, J. E., Gold, B., Dean, M. and Allikmets, R. (2005) A common haplotype in the complement regulatory gene factor H (HF1/CFH) predisposes individuals to age-related macular degeneration. Proc. Natl. Acad. Sci. USA 102, 7227-7232.
-
-
-
-
80
-
-
29944437979
-
Y402H complement factor H polymorphism associated with exudative age-related macular degeneration in the French population
-
Souied, E. H., Leveziel, N., Richard, F., Dragon-Durey, M. A., Coscas, G., Soubrane, G., Benlian, P. and Fremeaux-Bacchi, V. (2005) Y402H complement factor H polymorphism associated with exudative age-related macular degeneration in the French population. Mol. Vis. 11, 1135-1140.
-
(2005)
Mol. Vis
, vol.11
, pp. 1135-1140
-
-
Souied, E.H.1
Leveziel, N.2
Richard, F.3
Dragon-Durey, M.A.4
Coscas, G.5
Soubrane, G.6
Benlian, P.7
Fremeaux-Bacchi, V.8
-
81
-
-
33749985009
-
New pharmacologic horizons in the treatment of Parkinson disease
-
Bonuccelli, U. and Del Dotto, P. (2006) New pharmacologic horizons in the treatment of Parkinson disease. Neurology 67, S30-S38.
-
(2006)
Neurology
, vol.67
-
-
Bonuccelli, U.1
Del Dotto, P.2
-
82
-
-
33646870783
-
Conflicting results regarding the semaphorin gene (SEMA5A) and the risk for Parkinson disease
-
Clarimon, J., Scholz, S., Fung, H. C., Hardy, J., Eerola, J., Hellstrom, O., Chen, C. M., Wu, Y. R., Tienari, P. J. and Singleton, A. (2006) Conflicting results regarding the semaphorin gene (SEMA5A) and the risk for Parkinson disease. Am. J. Hum. Genet. 78, 1082-1084.
-
(2006)
Am. J. Hum. Genet
, vol.78
, pp. 1082-1084
-
-
Clarimon, J.1
Scholz, S.2
Fung, H.C.3
Hardy, J.4
Eerola, J.5
Hellstrom, O.6
Chen, C.M.7
Wu, Y.R.8
Tienari, P.J.9
Singleton, A.10
-
83
-
-
33646894113
-
Genomewide association, Parkinson disease, and PARK10
-
Farrer, M. J., Haugarvoll, K., Ross, O. A., Stone, J. T., Milkovic, N. M., Cobb, S. A., Whittle, A. J., Lincoln, S. J., Hulihan, M. M., Heckman, M. G., White, L. R., Aasly, J. O., Gibson, J. M., Gosal, D., Lynch, T., Wszolek, Z. K., Uitti, R. J. and Toft, M. (2006) Genomewide association, Parkinson disease, and PARK10. Am. J. Hum. Genet. 78, 1084-1088.
-
(2006)
Am. J. Hum. Genet
, vol.78
, pp. 1084-1088
-
-
Farrer, M.J.1
Haugarvoll, K.2
Ross, O.A.3
Stone, J.T.4
Milkovic, N.M.5
Cobb, S.A.6
Whittle, A.J.7
Lincoln, S.J.8
Hulihan, M.M.9
Heckman, M.G.10
White, L.R.11
Aasly, J.O.12
Gibson, J.M.13
Gosal, D.14
Lynch, T.15
Wszolek, Z.K.16
Uitti, R.J.17
Toft, M.18
-
84
-
-
33646891505
-
No evidence for association with Parkinson disease for 13 single-nucleotide polymorphisms identified by whole-genome association screening
-
Goris, A., Williams-Gray, C. H., Foltynie, T., Compston, D. A., Barker, R. A. and Sawcer, S. J. (2006) No evidence for association with Parkinson disease for 13 single-nucleotide polymorphisms identified by whole-genome association screening. Am. J. Hum. Genet. 78, 1088-1090.
-
(2006)
Am. J. Hum. Genet
, vol.78
, pp. 1088-1090
-
-
Goris, A.1
Williams-Gray, C.H.2
Foltynie, T.3
Compston, D.A.4
Barker, R.A.5
Sawcer, S.J.6
-
85
-
-
33646871346
-
A case-control association study of the 12 single-nucleotide polymorphisms implicated in Parkinson disease by a recent genome scan
-
Li, Y., Rowland, C., Schrodi, S., Laird, W., Tacey, K., Ross, D., Leong, D., Catanese, J., Sninsky, J. and Grupe, A. (2006) A case-control association study of the 12 single-nucleotide polymorphisms implicated in Parkinson disease by a recent genome scan. Am. J. Hum. Genet. 78, 1090-1092.
-
(2006)
Am. J. Hum. Genet
, vol.78
, pp. 1090-1092
-
-
Li, Y.1
Rowland, C.2
Schrodi, S.3
Laird, W.4
Tacey, K.5
Ross, D.6
Leong, D.7
Catanese, J.8
Sninsky, J.9
Grupe, A.10
-
86
-
-
22844449221
-
Genomic screening and replication using the same data set in family-based association testing
-
Van Steen, K., McQueen, M. B., Herbert, A., Raby, B., Lyon, H., Demeo, D. L., Murphy, A., Su, J., Datta, S., Rosenow, C., Christman, M., Silverman, E. K., Laird, N. M., Weiss, S. T. and Lange, C. (2005) Genomic screening and replication using the same data set in family-based association testing. Nat. Genet. 37, 683-691.
-
(2005)
Nat. Genet
, vol.37
, pp. 683-691
-
-
Van Steen, K.1
McQueen, M.B.2
Herbert, A.3
Raby, B.4
Lyon, H.5
Demeo, D.L.6
Murphy, A.7
Su, J.8
Datta, S.9
Rosenow, C.10
Christman, M.11
Silverman, E.K.12
Laird, N.M.13
Weiss, S.T.14
Lange, C.15
-
87
-
-
33745240931
-
A genome-wide association study of nonsynonymous SNPs identifies a type 1 diabetes locus in the interferon-induced helicase (IFIH1) region
-
Smyth, D. J., Cooper, J. D., Bailey, R., Field, S., Burren, O., Smink, L. J., Guja, C., Ionescu-Tirgoviste, C., Widmer, B., Dunger, D. B., Savage, D. A., Walker, N. M., Clayton, D. G. and Todd, J. A. (2006) A genome-wide association study of nonsynonymous SNPs identifies a type 1 diabetes locus in the interferon-induced helicase (IFIH1) region. Nat. Genet. 38, 617-619.
-
(2006)
Nat. Genet
, vol.38
, pp. 617-619
-
-
Smyth, D.J.1
Cooper, J.D.2
Bailey, R.3
Field, S.4
Burren, O.5
Smink, L.J.6
Guja, C.7
Ionescu-Tirgoviste, C.8
Widmer, B.9
Dunger, D.B.10
Savage, D.A.11
Walker, N.M.12
Clayton, D.G.13
Todd, J.A.14
-
88
-
-
31444451575
-
Environmental triggers and determinants of type 1 diabetes
-
Knip, M., Veijola, R., Virtanen, S. M., Hyoty, H., Vaarala, O. and Akerblom, H. K. (2005) Environmental triggers and determinants of type 1 diabetes. Diabetes 54 (Suppl. 2), S125-S136.
-
(2005)
Diabetes
, vol.54
, Issue.SUPPL. 2
-
-
Knip, M.1
Veijola, R.2
Virtanen, S.M.3
Hyoty, H.4
Vaarala, O.5
Akerblom, H.K.6
-
89
-
-
8544274482
-
Insulin-dependent diabetes mellitus (IDDM) is associated with CTLA4 polymorphisms inmultiple ethnic groups
-
Marron, M. P., Raffel, L. J., Garchon, H. J., Jacob, C. O., Serrano-Rios, M., Martinez Larrad, M. T., Teng, W. P., Park, Y., Zhang, Z. X., Goldstein, D. R., Tao, Y. W., Beaurain, G., Bach, J. F., Huang, H. S., Luo, D. F., Zeidler, A., Rotter, J. I., Yang, M. C., Modilevsky, T., Maclaren, N. K. and She, J. X. (1997) Insulin-dependent diabetes mellitus (IDDM) is associated with CTLA4 polymorphisms inmultiple ethnic groups. Hum. Mol. Genet. 6, 1275-1282.
-
(1997)
Hum. Mol. Genet
, vol.6
, pp. 1275-1282
-
-
Marron, M.P.1
Raffel, L.J.2
Garchon, H.J.3
Jacob, C.O.4
Serrano-Rios, M.5
Martinez Larrad, M.T.6
Teng, W.P.7
Park, Y.8
Zhang, Z.X.9
Goldstein, D.R.10
Tao, Y.W.11
Beaurain, G.12
Bach, J.F.13
Huang, H.S.14
Luo, D.F.15
Zeidler, A.16
Rotter, J.I.17
Yang, M.C.18
Modilevsky, T.19
Maclaren, N.K.20
She, J.X.21
more..
-
90
-
-
8944259914
-
The CTLA-4 gene region of chromosome 2q33 is linked to, and associated with, type 1 diabetes. Belgian Diabetes Registry
-
Nistico, L., Buzzetti, R., Pritchard, L. E., Van der Auwera, B., Giovannini, C., Bosi, E., Larrad, M. T., Rios, M. S., Chow, C. C., Cockram, C. S., Jacobs, K., Mijovic, C., Bain, S. C., Barnett, A. H., Vandewalle, C. L., Schuit, F., Gorus, F. K., Tosi, R., Pozzilli, P. and Todd, J. A. (1996) The CTLA-4 gene region of chromosome 2q33 is linked to, and associated with, type 1 diabetes. Belgian Diabetes Registry. Hum. Mol. Genet. 5, 1075-1080.
-
(1996)
Hum. Mol. Genet
, vol.5
, pp. 1075-1080
-
-
Nistico, L.1
Buzzetti, R.2
Pritchard, L.E.3
Van der Auwera, B.4
Giovannini, C.5
Bosi, E.6
Larrad, M.T.7
Rios, M.S.8
Chow, C.C.9
Cockram, C.S.10
Jacobs, K.11
Mijovic, C.12
Bain, S.C.13
Barnett, A.H.14
Vandewalle, C.L.15
Schuit, F.16
Gorus, F.K.17
Tosi, R.18
Pozzilli, P.19
Todd, J.A.20
more..
-
91
-
-
0036256007
-
Apolymorphism in the human cytotoxic T-lymphocyte antigen 4 ( CTLA4) gene (exon 1 +49) alters T-cell activation
-
Maurer, M., Loserth, S., Kolb-Maurer, A., Ponath, A., Wiese, S., Kruse, N. and Rieckmann, P. (2002) Apolymorphism in the human cytotoxic T-lymphocyte antigen 4 ( CTLA4) gene (exon 1 +49) alters T-cell activation. Immunogenetics 54, 1-8.
-
(2002)
Immunogenetics
, vol.54
, pp. 1-8
-
-
Maurer, M.1
Loserth, S.2
Kolb-Maurer, A.3
Ponath, A.4
Wiese, S.5
Kruse, N.6
Rieckmann, P.7
-
92
-
-
16844386794
-
Partners in crime
-
Daly, M. J. and Altshuler, D. (2005) Partners in crime. Nat. Genet. 37, 337-338.
-
(2005)
Nat. Genet
, vol.37
, pp. 337-338
-
-
Daly, M.J.1
Altshuler, D.2
-
93
-
-
16844366786
-
Genomewide strategies for detecting multiple loci that influence complex diseases
-
Marchini, J., Donnelly, P. and Cardon, L. R. (2005) Genomewide strategies for detecting multiple loci that influence complex diseases. Nat. Genet. 37, 413-417.
-
(2005)
Nat. Genet
, vol.37
, pp. 413-417
-
-
Marchini, J.1
Donnelly, P.2
Cardon, L.R.3
-
94
-
-
20044377204
-
The influence of CCL3L1 genecontaining segmental duplications on HIV-1/AIDS susceptibility
-
Gonzalez, E., Kulkarni, H., Bolivar, H., Mangano, A., Sanchez, R., Catano, G., Nibbs, R. J., Freedman, B. I., Quinones, M. P., Bamshad, M. J., Murthy, K. K., Rovin, B. H., Bradley, W., Clark, R. A., Anderson, S. A., O'Connell R J., Agan, B. K., Ahuja, S. S., Bologna, R., Sen, L., Dolan, M. J. and Ahuja, S. K. (2005) The influence of CCL3L1 genecontaining segmental duplications on HIV-1/AIDS susceptibility. Science 307, 1434-1440.
-
(2005)
Science
, vol.307
, pp. 1434-1440
-
-
Gonzalez, E.1
Kulkarni, H.2
Bolivar, H.3
Mangano, A.4
Sanchez, R.5
Catano, G.6
Nibbs, R.J.7
Freedman, B.I.8
Quinones, M.P.9
Bamshad, M.J.10
Murthy, K.K.11
Rovin, B.H.12
Bradley, W.13
Clark, R.A.14
Anderson, S.A.15
O'Connell, R.J.16
Agan, B.K.17
Ahuja, S.S.18
Bologna, R.19
Sen, L.20
Dolan, M.J.21
Ahuja, S.K.22
more..
-
95
-
-
34247133431
-
-
Dean, M., Carrington, M., Winkler, C., Huttley, G. A., Smith, M. W., Allikmets, R., Goedert, J. J., Buchbinder, S. P., Vittinghoff, E., Gomperts, E., Donfield, S., Vlahov, D., Kaslow, R., Saah, A., Rinaldo, C., Detels, R. and O'Brien, S. J. (1996) Genetic restriction of HIV-1 infection and progression to AIDS by a deletion allele of the CKR5 structural gene. Hemophilia Growth and Development Study, Multicenter AIDS Cohort Study, Multicenter Hemophilia Cohort Study, San Francisco City Cohort, ALIVE Study. Science 273, 1856-1862.
-
Dean, M., Carrington, M., Winkler, C., Huttley, G. A., Smith, M. W., Allikmets, R., Goedert, J. J., Buchbinder, S. P., Vittinghoff, E., Gomperts, E., Donfield, S., Vlahov, D., Kaslow, R., Saah, A., Rinaldo, C., Detels, R. and O'Brien, S. J. (1996) Genetic restriction of HIV-1 infection and progression to
-
-
-
-
96
-
-
0036591666
-
Molecular-evolutionary mechanisms for genomic disorders
-
Stankiewicz, P. and Lupski, J. R. (2002) Molecular-evolutionary mechanisms for genomic disorders. Curr. Opin. Genet. Dev. 12, 312-319.
-
(2002)
Curr. Opin. Genet. Dev
, vol.12
, pp. 312-319
-
-
Stankiewicz, P.1
Lupski, J.R.2
-
97
-
-
0031731487
-
Genomic disorders: Structural features of the genome can lead to DNA rearrangements and human disease traits
-
Lupski, J. R. (1998) Genomic disorders: structural features of the genome can lead to DNA rearrangements and human disease traits. Trends. Genet. 14, 417-422.
-
(1998)
Trends. Genet
, vol.14
, pp. 417-422
-
-
Lupski, J.R.1
-
98
-
-
0041386350
-
Polymorphically duplicated genes: Their relevance to phenotypic variation in humans
-
Buckland, P. R. (2003) Polymorphically duplicated genes: their relevance to phenotypic variation in humans. Ann. Med. 35, 308-315.
-
(2003)
Ann. Med
, vol.35
, pp. 308-315
-
-
Buckland, P.R.1
-
99
-
-
4444291843
-
Detection of large-scale variation in the human genome
-
Iafrate, A. J., Feuk, L., Rivera, M. N., Listewnik, M. L., Donahoe, P. K., Qi, Y., Scherer, S. W. and Lee, C. (2004) Detection of large-scale variation in the human genome. Nat. Genet. 36, 949-951.
-
(2004)
Nat. Genet
, vol.36
, pp. 949-951
-
-
Iafrate, A.J.1
Feuk, L.2
Rivera, M.N.3
Listewnik, M.L.4
Donahoe, P.K.5
Qi, Y.6
Scherer, S.W.7
Lee, C.8
-
100
-
-
3242808027
-
Large-scale copy number polymorphism in the human genome
-
Sebat, J., Lakshmi, B., Troge, J., Alexander, J., Young, J., Lundin, P., Maner, S., Massa, H., Walker, M., Chi, M., Navin, N., Lucito, R., Healy, J., Hicks, J., Ye, K., Reiner, A., Gilliam, T. C., Trask, B., Patterson, N., Zetterberg, A. and Wigler, M. (2004) Large-scale copy number polymorphism in the human genome. Science 305, 525-528.
-
(2004)
Science
, vol.305
, pp. 525-528
-
-
Sebat, J.1
Lakshmi, B.2
Troge, J.3
Alexander, J.4
Young, J.5
Lundin, P.6
Maner, S.7
Massa, H.8
Walker, M.9
Chi, M.10
Navin, N.11
Lucito, R.12
Healy, J.13
Hicks, J.14
Ye, K.15
Reiner, A.16
Gilliam, T.C.17
Trask, B.18
Patterson, N.19
Zetterberg, A.20
Wigler, M.21
more..
-
101
-
-
20544462642
-
Segmental duplications and copynumber variation in the human genome
-
Sharp, A. J., Locke, D. P., McGrath, S. D., Cheng, Z., Bailey, J. A., Vallente, R. U., Pertz, L. M., Clark, R. A., Schwartz, S., Segraves, R., Oseroff, V. V., Albertson, D. G., Pinkel, D. and Eichler, E. E. (2005) Segmental duplications and copynumber variation in the human genome. Am. J. Hum. Genet. 77, 78-88.
-
(2005)
Am. J. Hum. Genet
, vol.77
, pp. 78-88
-
-
Sharp, A.J.1
Locke, D.P.2
McGrath, S.D.3
Cheng, Z.4
Bailey, J.A.5
Vallente, R.U.6
Pertz, L.M.7
Clark, R.A.8
Schwartz, S.9
Segraves, R.10
Oseroff, V.V.11
Albertson, D.G.12
Pinkel, D.13
Eichler, E.E.14
-
102
-
-
29444441336
-
A high-resolution survey of deletion polymorphism in the human genome
-
Conrad, D. F., Andrews, T. D., Carter, N. P., Hurles, M. E. and Pritchard, J. K. (2006) A high-resolution survey of deletion polymorphism in the human genome. Nat. Genet. 38, 75-81.
-
(2006)
Nat. Genet
, vol.38
, pp. 75-81
-
-
Conrad, D.F.1
Andrews, T.D.2
Carter, N.P.3
Hurles, M.E.4
Pritchard, J.K.5
-
103
-
-
0025303121
-
Two inflammatory mediator cytokine genes are closely linked and variably amplified on chromosome 17q
-
Irving, S. G., Zipfel, P. F., Balke, J., McBride, O. W., Morton, C. C., Burd, P. R., Siebenlist, U. and Kelly, K. (1990) Two inflammatory mediator cytokine genes are closely linked and variably amplified on chromosome 17q. Nucleic Acids Res. 18, 3261-3270.
-
(1990)
Nucleic Acids Res
, vol.18
, pp. 3261-3270
-
-
Irving, S.G.1
Zipfel, P.F.2
Balke, J.3
McBride, O.W.4
Morton, C.C.5
Burd, P.R.6
Siebenlist, U.7
Kelly, K.8
-
104
-
-
0036772531
-
Gene copy number regulates the production of the human chemokine CCL3-L1
-
Townson, J. R., Barcellos, L. F. and Nibbs, R. J. (2002) Gene copy number regulates the production of the human chemokine CCL3-L1. Eur. J. Immunol. 32, 3016-3026.
-
(2002)
Eur. J. Immunol
, vol.32
, pp. 3016-3026
-
-
Townson, J.R.1
Barcellos, L.F.2
Nibbs, R.J.3
-
105
-
-
22244433460
-
Genetic variations in the receptor-ligand pair CCR5 and CCL3L1 are important determinants of susceptibility to Kawasaki disease
-
Burns, J. C., Shimizu, C., Gonzalez, E., Kulkarni, H., Patel, S., Shike, H., Sundel, R. S., Newburger, J. W. and Ahuja, S. K. (2005) Genetic variations in the receptor-ligand pair CCR5 and CCL3L1 are important determinants of susceptibility to Kawasaki disease. J. Infect. Dis. 192, 344-349.
-
(2005)
J. Infect. Dis
, vol.192
, pp. 344-349
-
-
Burns, J.C.1
Shimizu, C.2
Gonzalez, E.3
Kulkarni, H.4
Patel, S.5
Shike, H.6
Sundel, R.S.7
Newburger, J.W.8
Ahuja, S.K.9
-
106
-
-
13844269028
-
No evidence of association or interaction between the IL4RA, IL4, and IL13 genes in type 1 Diabetes
-
Maier, L. M., Chapman, J., Howson, J. M., Clayton, D. G., Pask, R., Strachan, D. P., McArdle, W. L., Twells, R. C. and Todd, J. A. (2005) No evidence of association or interaction between the IL4RA, IL4, and IL13 genes in type 1 Diabetes. Am. J. Hum. Genet. 76, 517-521.
-
(2005)
Am. J. Hum. Genet
, vol.76
, pp. 517-521
-
-
Maier, L.M.1
Chapman, J.2
Howson, J.M.3
Clayton, D.G.4
Pask, R.5
Strachan, D.P.6
McArdle, W.L.7
Twells, R.C.8
Todd, J.A.9
-
107
-
-
31444446832
-
-
Maier, L. M., Cooper, J. D., Walker, N., Smyth, D. J. and Todd, J. A. (2005) Comment to: Biason-Lauber A, Boehm B, Lang-Muritano M et al. (2005) association of childhood type 1 diabetes mellitus with a variant of PAX4: possible link to beta cell regenerative capacity. Diabetologia 48:900-905, 2180-2182.
-
Maier, L. M., Cooper, J. D., Walker, N., Smyth, D. J. and Todd, J. A. (2005) Comment to: Biason-Lauber A, Boehm B, Lang-Muritano M et al. (2005) association of childhood type 1 diabetes mellitus with a variant of PAX4: possible link to beta cell regenerative capacity. Diabetologia 48:900-905, 2180-2182.
-
-
-
-
108
-
-
4644246531
-
Analysis of the vitamin D receptor gene sequence variants in type 1 diabetes
-
Nejentsev, S., Cooper, J. D., Godfrey, L., Howson, J. M., Rance, H., Nutland, S., Walker, N. M., Guja, C., Ionescu-Tirgoviste, C., Savage, D. A., Undlien, D. E., Ronningen, K. S., Tuomilehto-Wolf, E., Tuomilehto, J., Gillespie, K. M., Ring, S. M., Strachan, D. P., Widmer, B., Dunger, D. and Todd, J. A. (2004) Analysis of the vitamin D receptor gene sequence variants in type 1 diabetes. Diabetes 53, 2709-2712.
-
(2004)
Diabetes
, vol.53
, pp. 2709-2712
-
-
Nejentsev, S.1
Cooper, J.D.2
Godfrey, L.3
Howson, J.M.4
Rance, H.5
Nutland, S.6
Walker, N.M.7
Guja, C.8
Ionescu-Tirgoviste, C.9
Savage, D.A.10
Undlien, D.E.11
Ronningen, K.S.12
Tuomilehto-Wolf, E.13
Tuomilehto, J.14
Gillespie, K.M.15
Ring, S.M.16
Strachan, D.P.17
Widmer, B.18
Dunger, D.19
Todd, J.A.20
more..
-
109
-
-
33748994275
-
No evidence for amajor effect of two common polymorphisms of the catalase gene in type 1 diabetes susceptibility
-
Pask, R., Cooper, J. D., Walker, N. M., Nutland, S., Hutchings, J., Dunger, D. B., Nejentsev, S. and Todd, J. A. (2006) No evidence for amajor effect of two common polymorphisms of the catalase gene in type 1 diabetes susceptibility. Diabetes Metab. Res. Rev. 22, 356-360.
-
(2006)
Diabetes Metab. Res. Rev
, vol.22
, pp. 356-360
-
-
Pask, R.1
Cooper, J.D.2
Walker, N.M.3
Nutland, S.4
Hutchings, J.5
Dunger, D.B.6
Nejentsev, S.7
Todd, J.A.8
-
110
-
-
20944437768
-
No evidence for association of the TATA-box binding protein glutamine repeat sequence or the flanking chromosome 6q27 region with type 1 diabetes
-
Payne, F., Smyth, D. J., Pask, R., Cooper, J. D., Masters, J., Wang, W. Y., Godfrey, L. M., Bowden, G., Szeszko, J., Smink, L. J., Lam, A. C., Burren, O., Walker, N. M., Nutland, S., Rance, H., Undlien, D. E., Ronningen, K. S., Guja, C., Ionescu-Tirgoviste, C., Todd, J. A. and Twells, R. C. (2005) No evidence for association of the TATA-box binding protein glutamine repeat sequence or the flanking chromosome 6q27 region with type 1 diabetes. Biochem. Biophys. Res. Commun. 331, 435-441.
-
(2005)
Biochem. Biophys. Res. Commun
, vol.331
, pp. 435-441
-
-
Payne, F.1
Smyth, D.J.2
Pask, R.3
Cooper, J.D.4
Masters, J.5
Wang, W.Y.6
Godfrey, L.M.7
Bowden, G.8
Szeszko, J.9
Smink, L.J.10
Lam, A.C.11
Burren, O.12
Walker, N.M.13
Nutland, S.14
Rance, H.15
Undlien, D.E.16
Ronningen, K.S.17
Guja, C.18
Ionescu-Tirgoviste, C.19
Todd, J.A.20
Twells, R.C.21
more..
-
111
-
-
33745292629
-
No evidence for association of OAS1 with type 1 diabetes in unaffected siblings or type 1 diabetic cases
-
Smyth, D. J., Cooper, J. D., Lowe, C. E., Nutland, S., Walker, N. M., Clayton, D. G. and Todd, J. A. (2006) No evidence for association of OAS1 with type 1 diabetes in unaffected siblings or type 1 diabetic cases. Diabetes 55, 1525-1528.
-
(2006)
Diabetes
, vol.55
, pp. 1525-1528
-
-
Smyth, D.J.1
Cooper, J.D.2
Lowe, C.E.3
Nutland, S.4
Walker, N.M.5
Clayton, D.G.6
Todd, J.A.7
-
112
-
-
33644769241
-
Analysis of polymorphisms of the interleukin-18 gene in type 1 diabetes and Hardy-Weinberg equilibrium testing
-
Szeszko, J. S., Howson, J. M., Cooper, J. D., Walker, N. M., Twells, R. C., Stevens, H. E., Nutland, S. L. and Todd, J. A. (2006) Analysis of polymorphisms of the interleukin-18 gene in type 1 diabetes and Hardy-Weinberg equilibrium testing. Diabetes 55, 559-562.
-
(2006)
Diabetes
, vol.55
, pp. 559-562
-
-
Szeszko, J.S.1
Howson, J.M.2
Cooper, J.D.3
Walker, N.M.4
Twells, R.C.5
Stevens, H.E.6
Nutland, S.L.7
Todd, J.A.8
-
113
-
-
12144290500
-
Lack of association of the Ala(45)Thr polymorphism and other common variants of the NeuroD gene with type 1 diabetes
-
Vella, A., Howson, J. M., Barratt, B. J., Twells, R. C., Rance, H. E., Nutland, S., Tuomilehto-Wolf, E., Tuomilehto, J., Undlien, D. E., Ronningen, K. S., Guja, C., Ionescu-Tirgoviste, C., Savage, D. A. and Todd, J. A. (2004) Lack of association of the Ala(45)Thr polymorphism and other common variants of the NeuroD gene with type 1 diabetes. Diabetes 53, 1158-1161.
-
(2004)
Diabetes
, vol.53
, pp. 1158-1161
-
-
Vella, A.1
Howson, J.M.2
Barratt, B.J.3
Twells, R.C.4
Rance, H.E.5
Nutland, S.6
Tuomilehto-Wolf, E.7
Tuomilehto, J.8
Undlien, D.E.9
Ronningen, K.S.10
Guja, C.11
Ionescu-Tirgoviste, C.12
Savage, D.A.13
Todd, J.A.14
-
114
-
-
0035179971
-
Replication validity of genetic association studies
-
Ioannidis, J. P., Ntzani, E. E., Trikalinos, T. A. and Contopoulos-Ioannidis, D. G. (2001) Replication validity of genetic association studies. Nat. Genet. 29, 306-309.
-
(2001)
Nat. Genet
, vol.29
, pp. 306-309
-
-
Ioannidis, J.P.1
Ntzani, E.E.2
Trikalinos, T.A.3
Contopoulos-Ioannidis, D.G.4
-
115
-
-
0037312921
-
Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease
-
Lohmueller, K. E., Pearce, C. L., Pike, M., Lander, E. S. and Hirschhorn, J. N. (2003) Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease. Nat. Genet. 33, 177-182.
-
(2003)
Nat. Genet
, vol.33
, pp. 177-182
-
-
Lohmueller, K.E.1
Pearce, C.L.2
Pike, M.3
Lander, E.S.4
Hirschhorn, J.N.5
-
116
-
-
20244373351
-
Localization of a type 1 diabetes locus in the IL2RA/CD25 region by use of tag single-nucleotide polymorphisms
-
Vella, A., Cooper, J. D., Lowe, C. E., Walker, N., Nutland, S., Widmer, B., Jones, R., Ring, S. M., McArdle, W., Pembrey, M. E., Strachan, D. P., Dunger, D. B., Twells, R. C., Clayton, D. G. and Todd, J. A. (2005) Localization of a type 1 diabetes locus in the IL2RA/CD25 region by use of tag single-nucleotide polymorphisms. Am. J. Hum. Genet. 76, 773-779.
-
(2005)
Am. J. Hum. Genet
, vol.76
, pp. 773-779
-
-
Vella, A.1
Cooper, J.D.2
Lowe, C.E.3
Walker, N.4
Nutland, S.5
Widmer, B.6
Jones, R.7
Ring, S.M.8
McArdle, W.9
Pembrey, M.E.10
Strachan, D.P.11
Dunger, D.B.12
Twells, R.C.13
Clayton, D.G.14
Todd, J.A.15
-
117
-
-
30044440451
-
Genotyping errors: Causes, consequences and solutions
-
Pompanon, F., Bonin, A., Bellemain, E. and Taberlet, P. (2005) Genotyping errors: causes, consequences and solutions. Nat. Rev. Genet. 6, 847-859.
-
(2005)
Nat. Rev. Genet
, vol.6
, pp. 847-859
-
-
Pompanon, F.1
Bonin, A.2
Bellemain, E.3
Taberlet, P.4
-
118
-
-
17444409580
-
Association of childhood type 1 diabetes mellitus with a variant of PAX4: Possible link to beta cell regenerative capacity
-
Biason-Lauber, A., Boehm, B., Lang-Muritano, M., Gauthier, B. R., Brun, T., Wollheim, C. B. and Schoenle, E. J. (2005) Association of childhood type 1 diabetes mellitus with a variant of PAX4: possible link to beta cell regenerative capacity. Diabetologia 48, 900-905.
-
(2005)
Diabetologia
, vol.48
, pp. 900-905
-
-
Biason-Lauber, A.1
Boehm, B.2
Lang-Muritano, M.3
Gauthier, B.R.4
Brun, T.5
Wollheim, C.B.6
Schoenle, E.J.7
-
119
-
-
23644440522
-
TNFR2 is not associated with rheumatoid arthritis susceptibility in a Caucasian population
-
Potter, C., Worthington, J., Silman, A. and Barton, A. (2005) TNFR2 is not associated with rheumatoid arthritis susceptibility in a Caucasian population. Arthritis Rheum. 52, 2579-2581.
-
(2005)
Arthritis Rheum
, vol.52
, pp. 2579-2581
-
-
Potter, C.1
Worthington, J.2
Silman, A.3
Barton, A.4
-
120
-
-
21744448518
-
Hardy-Weinberg equilibrium in genetic association studies: An empirical evaluation of reporting, deviations, and power
-
Salanti, G., Amountza, G., Ntzani, E. E. and Ioannidis, J. P. (2005) Hardy-Weinberg equilibrium in genetic association studies: an empirical evaluation of reporting, deviations, and power. Eur. J. Hum. Genet. 13, 840-848.
-
(2005)
Eur. J. Hum. Genet
, vol.13
, pp. 840-848
-
-
Salanti, G.1
Amountza, G.2
Ntzani, E.E.3
Ioannidis, J.P.4
-
121
-
-
0042667153
-
Functional haplotypes of PADI4, encoding citrullinating enzyme peptidylarginine deiminase 4, are associated with rheumatoid arthritis
-
Suzuki, A., Yamada, R., Chang, X., Tokuhiro, S., Sawada, T., Suzuki, M., Nagasaki, M., Nakayama-Hamada, M., Kawaida, R., Ono, M., Ohtsuki, M., Furukawa, H., Yoshino, S., Yukioka, M., Tohma, S., Matsubara, T., Wakitani, S., Teshima, R., Nishioka, Y., Sekine, A., Iida, A., Takahashi, A., Tsunoda, T., Nakamura, Y. and Yamamoto, K. (2003) Functional haplotypes of PADI4, encoding citrullinating enzyme peptidylarginine deiminase 4, are associated with rheumatoid arthritis. Nat. Genet. 34, 395-402.
-
(2003)
Nat. Genet
, vol.34
, pp. 395-402
-
-
Suzuki, A.1
Yamada, R.2
Chang, X.3
Tokuhiro, S.4
Sawada, T.5
Suzuki, M.6
Nagasaki, M.7
Nakayama-Hamada, M.8
Kawaida, R.9
Ono, M.10
Ohtsuki, M.11
Furukawa, H.12
Yoshino, S.13
Yukioka, M.14
Tohma, S.15
Matsubara, T.16
Wakitani, S.17
Teshima, R.18
Nishioka, Y.19
Sekine, A.20
Iida, A.21
Takahashi, A.22
Tsunoda, T.23
Nakamura, Y.24
Yamamoto, K.25
more..
-
122
-
-
26844480664
-
Association between PADI4 and rheumatoid arthritis: A replication study
-
Ikari, K., Kuwahara, M., Nakamura, T., Momohara, S., Hara, M., Yamanaka, H., Tomatsu, T. and Kamatani, N. (2005) Association between PADI4 and rheumatoid arthritis: a replication study. Arthritis Rheum. 52, 3054-3057.
-
(2005)
Arthritis Rheum
, vol.52
, pp. 3054-3057
-
-
Ikari, K.1
Kuwahara, M.2
Nakamura, T.3
Momohara, S.4
Hara, M.5
Yamanaka, H.6
Tomatsu, T.7
Kamatani, N.8
-
123
-
-
1842733194
-
A functional haplotype of the PADI4 gene associated with rheumatoid arthritis in a Japanese population is not associated in a United Kingdom population
-
Barton, A., Bowes, J., Eyre, S., Spreckley, K., Hinks, A., John, S. and Worthington, J. (2004) A functional haplotype of the PADI4 gene associated with rheumatoid arthritis in a Japanese population is not associated in a United Kingdom population. Arthritis Rheum. 50, 1117-1121.
-
(2004)
Arthritis Rheum
, vol.50
, pp. 1117-1121
-
-
Barton, A.1
Bowes, J.2
Eyre, S.3
Spreckley, K.4
Hinks, A.5
John, S.6
Worthington, J.7
-
124
-
-
22844452701
-
Genetic and genomic studies of PADI4 in rheumatoid arthritis
-
Harney, S. M., Meisel, C., Sims, A. M., Woon, P. Y., Wordsworth, B. P. and Brown, M. A. (2005) Genetic and genomic studies of PADI4 in rheumatoid arthritis. Rheumatology 44, 869-872.
-
(2005)
Rheumatology
, vol.44
, pp. 869-872
-
-
Harney, S.M.1
Meisel, C.2
Sims, A.M.3
Woon, P.Y.4
Wordsworth, B.P.5
Brown, M.A.6
-
125
-
-
27144488150
-
PADI4 polymorphisms are not associated with rheumatoid arthritis in the Spanish population
-
Martinez, A., Valdivia, A., Pascual-Salcedo, D., Lamas, J. R., Fernandez-Arquero, M., Balsa, A., Fernandez-Gutierrez, B., de la Concha, E. G. and Urcelay, E. (2005) PADI4 polymorphisms are not associated with rheumatoid arthritis in the Spanish population. Rheumatology 44, 1263-1266.
-
(2005)
Rheumatology
, vol.44
, pp. 1263-1266
-
-
Martinez, A.1
Valdivia, A.2
Pascual-Salcedo, D.3
Lamas, J.R.4
Fernandez-Arquero, M.5
Balsa, A.6
Fernandez-Gutierrez, B.7
de la Concha, E.G.8
Urcelay, E.9
-
126
-
-
21544436852
-
Ethnic differences in allele frequency of autoimmune-disease-associated SNPs
-
Mori, M., Yamada, R., Kobayashi, K., Kawaida, R. and Yamamoto, K. (2005) Ethnic differences in allele frequency of autoimmune-disease-associated SNPs. J. Hum. Genet. 50, 264-266.
-
(2005)
J. Hum. Genet
, vol.50
, pp. 264-266
-
-
Mori, M.1
Yamada, R.2
Kobayashi, K.3
Kawaida, R.4
Yamamoto, K.5
-
127
-
-
0024510601
-
Identification of susceptibility loci for insulin-dependent diabetes mellitus by trans-racial gene mapping
-
Todd, J. A., Mijovic, C., Fletcher, J., Jenkins, D., Bradwell, A. R. and Barnett, A. H. (1989) Identification of susceptibility loci for insulin-dependent diabetes mellitus by trans-racial gene mapping. Nature 338, 587-589.
-
(1989)
Nature
, vol.338
, pp. 587-589
-
-
Todd, J.A.1
Mijovic, C.2
Fletcher, J.3
Jenkins, D.4
Bradwell, A.R.5
Barnett, A.H.6
-
128
-
-
22244475440
-
Association of the PTPN22 locus with rheumatoid arthritis in a New Zealand Caucasian cohort
-
Simkins, H. M., Merriman, M. E., Highton, J., Chapman, P. T., ODonnell, J. L., Jones, P. B., Gow, P. J., McLean, L., Pokorny, V., Harrison, A. A. and Merriman, T. R. (2005) Association of the PTPN22 locus with rheumatoid arthritis in a New Zealand Caucasian cohort. Arthritis Rheum. 52, 2222-2225.
-
(2005)
Arthritis Rheum
, vol.52
, pp. 2222-2225
-
-
Simkins, H.M.1
Merriman, M.E.2
Highton, J.3
Chapman, P.T.4
ODonnell, J.L.5
Jones, P.B.6
Gow, P.J.7
McLean, L.8
Pokorny, V.9
Harrison, A.A.10
Merriman, T.R.11
-
129
-
-
0031710646
-
HLA-DR binding analysis of peptides from islet antigens in IDDM
-
Geluk, A., van Meijgaarden, K. E., Schloot, N. C., Drijfhout, J. W., Ottenhoff, T. H. and Roep, B. O. (1998) HLA-DR binding analysis of peptides from islet antigens in IDDM. Diabetes 47, 1594-1601.
-
(1998)
Diabetes
, vol.47
, pp. 1594-1601
-
-
Geluk, A.1
van Meijgaarden, K.E.2
Schloot, N.C.3
Drijfhout, J.W.4
Ottenhoff, T.H.5
Roep, B.O.6
-
130
-
-
0031018819
-
Insulin expression in human thymus is modulated by INS VNTR alleles at the IDDM2 locus
-
Vafiadis, P., Bennett, S. T., Todd, J. A., Nadeau, J., Grabs, R., Goodyer, C. G., Wickramasinghe, S., Colle, E. and Polychronakos, C. (1997) Insulin expression in human thymus is modulated by INS VNTR alleles at the IDDM2 locus. Nat. Genet. 15, 289-292.
-
(1997)
Nat. Genet
, vol.15
, pp. 289-292
-
-
Vafiadis, P.1
Bennett, S.T.2
Todd, J.A.3
Nadeau, J.4
Grabs, R.5
Goodyer, C.G.6
Wickramasinghe, S.7
Colle, E.8
Polychronakos, C.9
-
131
-
-
3042698329
-
Remapping the insulin gene/IDDM2 locus in type 1 diabetes
-
Barratt, B. J., Payne, F., Lowe, C. E., Hermann, R., Healy, B. C., Harold, D., Concannon, P., Gharani, N., McCarthy, M. I., Olavesen, M. G., McCormack, R., Guja, C., Ionescu-Tirgoviste, C., Undlien, D. E., Ronningen, K. S., Gillespie, K. M., Tuomilehto-Wolf, E., Tuomilehto, J., Bennett, S. T., Clayton, D. G., Cordell, H. J. and Todd, J. A. (2004) Remapping the insulin gene/IDDM2 locus in type 1 diabetes. Diabetes 53, 1884-1889.
-
(2004)
Diabetes
, vol.53
, pp. 1884-1889
-
-
Barratt, B.J.1
Payne, F.2
Lowe, C.E.3
Hermann, R.4
Healy, B.C.5
Harold, D.6
Concannon, P.7
Gharani, N.8
McCarthy, M.I.9
Olavesen, M.G.10
McCormack, R.11
Guja, C.12
Ionescu-Tirgoviste, C.13
Undlien, D.E.14
Ronningen, K.S.15
Gillespie, K.M.16
Tuomilehto-Wolf, E.17
Tuomilehto, J.18
Bennett, S.T.19
Clayton, D.G.20
Cordell, H.J.21
Todd, J.A.22
more..
-
132
-
-
33746835005
-
-
Durinovic-Bello, I., Rosinger, S., Olson, J. A., Congia, M., Ahmad, R. C., Rickert, M., Hampl, J., Kalbacher, H., Drijfhout, J. W., Mellins, E. D., Al Dahouk, S., Kamradt, T., Maeurer, M. J., Nhan, C., Roep, B. O., Boehm, B. O., Polychronakos, C., Nepom, G. T., Karges, W., McDevitt, H. O. and Sonderstrup, G. (2006) DRB1*0401-restricted human T cell clone specific for the major proinsulin73 - 90 epitope expresses a down-regulatory Thelper 2 phenotype. Proc. Natl. Acad. Sci. USA 103, 11683-11688.
-
Durinovic-Bello, I., Rosinger, S., Olson, J. A., Congia, M., Ahmad, R. C., Rickert, M., Hampl, J., Kalbacher, H., Drijfhout, J. W., Mellins, E. D., Al Dahouk, S., Kamradt, T., Maeurer, M. J., Nhan, C., Roep, B. O., Boehm, B. O., Polychronakos, C., Nepom, G. T., Karges, W., McDevitt, H. O. and Sonderstrup, G. (2006) DRB1*0401-restricted human T cell clone specific for the major proinsulin73 - 90 epitope expresses a down-regulatory Thelper 2 phenotype. Proc. Natl. Acad. Sci. USA 103, 11683-11688.
-
-
-
-
133
-
-
33646269938
-
Tesaglitazar: A promising approach in type 2 diabetes
-
Cox, S. L. (2006) Tesaglitazar: a promising approach in type 2 diabetes Drugs Today (Barc.). 42, 139-146.
-
(2006)
Drugs Today (Barc.)
, vol.42
, pp. 139-146
-
-
Cox, S.L.1
-
134
-
-
21644468434
-
The evolving clinical profile of abatacept (CTLA4-Ig): A novel co-stimulatory modulator for the treatment of rheumatoid arthritis
-
Ruderman, E. M. and Pope, R. M. (2005)The evolving clinical profile of abatacept (CTLA4-Ig): a novel co-stimulatory modulator for the treatment of rheumatoid arthritis. Arthritis Res. Ther. 7 (Suppl. 2), S21-S25.
-
(2005)
Arthritis Res. Ther
, vol.7
, Issue.SUPPL. 2
-
-
Ruderman, E.M.1
Pope, R.M.2
-
135
-
-
24944540240
-
Progress in targeting HIV-1 entry
-
Ryser, H. J. and Fluckiger, R. (2005) Progress in targeting HIV-1 entry. Drug Discov. Today 10, 1085-1094.
-
(2005)
Drug Discov. Today
, vol.10
, pp. 1085-1094
-
-
Ryser, H.J.1
Fluckiger, R.2
|