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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 

Fergus J. Couch

Departments of Laboratory Medicine and Pathology

Mayo Clinic

200 First Street SW

Rochester

USA

[email]@mayo.edu

Name/email consistency: high

 
 
 
 
 
 
 

Affiliation

  • Departments of Laboratory Medicine and Pathology, Mayo Clinic, 200 First Street SW, Rochester, USA. 2002 - 2012

References

  1. Common variants at the 19p13.1 and ZNF365 loci are associated with ER subtypes of breast cancer and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers. Couch, F.J., Gaudet, M.M., Antoniou, A.C., Ramus, S.J., Kuchenbaecker, K.B., Soucy, P., Beesley, J., Chen, X., Wang, X., Kirchhoff, T., McGuffog, L., Barrowdale, D., Lee, A., Healey, S., Sinilnikova, O.M., Andrulis, I.L., Ozcelik, H., Mulligan, A.M., Thomassen, M., Gerdes, A.M., Jensen, U.B., Skytte, A.B., Kruse, T.A., Caligo, M.A., von Wachenfeldt, A., Barbany-Bustinza, G., Loman, N., Soller, M., Ehrencrona, H., Karlsson, P., Nathanson, K.L., Rebbeck, T.R., Domchek, S.M., Jakubowska, A., Lubinski, J., Jaworska, K., Durda, K., Zlowocka, E., Huzarski, T., Byrski, T., Gronwald, J., Cybulski, C., Górski, B., Osorio, A., Durán, M., Tejada, M.I., Benitez, J., Hamann, U., Hogervorst, F.B., van Os, T.A., van Leeuwen, F.E., Meijers-Heijboer, H.E., Wijnen, J., Blok, M.J., Kets, M., Hooning, M.J., Oldenburg, R.A., Ausems, M.G., Peock, S., Frost, D., Ellis, S.D., Platte, R., Fineberg, E., Evans, D.G., Jacobs, C., Eeles, R.A., Adlard, J., Davidson, R., Eccles, D.M., Cole, T., Cook, J., Paterson, J., Brewer, C., Douglas, F., Hodgson, S.V., Morrison, P.J., Walker, L., Porteous, M.E., Kennedy, M.J., Side, L.E., Bove, B., Godwin, A.K., Stoppa-Lyonnet, D., Fassy-Colcombet, M., Castera, L., Cornelis, F., Mazoyer, S., Léoné, M., Boutry-Kryza, N., Bressac-de Paillerets, B., Caron, O., Pujol, P., Coupier, I., Delnatte, C., Akloul, L., Lynch, H.T., Snyder, C.L., Buys, S.S., Daly, M.B., Terry, M., Chung, W.K., John, E.M., Miron, A., Southey, M.C., Hopper, J.L., Goldgar, D.E., Singer, C.F., Rappaport, C., Tea, M.K., Fink-Retter, A., Hansen, T.V., Nielsen, F.C., Arason, A., Vijai, J., Shah, S., Sarrel, K., Robson, M.E., Piedmonte, M., Phillips, K., Basil, J., Rubinstein, W.S., Boggess, J., Wakeley, K., Ewart-Toland, A., Montagna, M., Agata, S., Imyanitov, E.N., Isaacs, C., Janavicius, R., Lazaro, C., Blanco, I., Feliubadalo, L., Brunet, J., Gayther, S.A., Pharoah, P.P., Odunsi, K.O., Karlan, B.Y., Walsh, C.S., Olah, E., Teo, S.H., Ganz, P.A., Beattie, M.S., van Rensburg, E.J., Dorfling, C.M., Diez, O., Kwong, A., Schmutzler, R.K., Wappenschmidt, B., Engel, C., Meindl, A., Ditsch, N., Arnold, N., Heidemann, S., Niederacher, D., Preisler-Adams, S., Gadzicki, D., Varon-Mateeva, R., Deissler, H., Gehrig, A., Sutter, C., Kast, K., Fiebig, B., Heinritz, W., Caldes, T., de la Hoya, M., Muranen, T.A., Nevanlinna, H., Tischkowitz, M.D., Spurdle, A.B., Neuhausen, S.L., Ding, Y.C., Lindor, N.M., Fredericksen, Z., Pankratz, V.S., Peterlongo, P., Manoukian, S., Peissel, B., Zaffaroni, D., Barile, M., Bernard, L., Viel, A., Giannini, G., Varesco, L., Radice, P., Greene, M.H., Mai, P.L., Easton, D.F., Chenevix-Trench, G., Offit, K., Simard, J. Cancer Epidemiol. Biomarkers Prev. (2012) [Pubmed]
  2. Association of mitotic regulation pathway polymorphisms with pancreatic cancer risk and outcome. Couch, F.J., Wang, X., Bamlet, W.R., de Andrade, M., Petersen, G.M., McWilliams, R.R. Cancer Epidemiol. Biomarkers Prev. (2010) [Pubmed]
  3. Association of breast cancer susceptibility variants with risk of pancreatic cancer. Couch, F.J., Wang, X., McWilliams, R.R., Bamlet, W.R., de Andrade, M., Petersen, G.M. Cancer Epidemiol. Biomarkers Prev. (2009) [Pubmed]
  4. Assessment of functional effects of unclassified genetic variants. Couch, F.J., Rasmussen, L.J., Hofstra, R., Monteiro, A.N., Greenblatt, M.S., de Wind, N. Hum. Mutat. (2008) [Pubmed]
  5. AURKA F31I polymorphism and breast cancer risk in BRCA1 and BRCA2 mutation carriers: a consortium of investigators of modifiers of BRCA1/2 study. Couch, F.J., Sinilnikova, O., Vierkant, R.A., Pankratz, V.S., Fredericksen, Z.S., Stoppa-Lyonnet, D., Coupier, I., Hughes, D., Hardouin, A., Berthet, P., Peock, S., Cook, M., Baynes, C., Hodgson, S., Morrison, P.J., Porteous, M.E., Jakubowska, A., Lubinski, J., Gronwald, J., Spurdle, A.B., Schmutzler, R., Versmold, B., Engel, C., Meindl, A., Sutter, C., Horst, J., Schaefer, D., Offit, K., Kirchhoff, T., Andrulis, I.L., Ilyushik, E., Glendon, G., Devilee, P., Vreeswijk, M.P., Vasen, H.F., Borg, A., Backenhorn, K., Struewing, J.P., Greene, M.H., Neuhausen, S.L., Rebbeck, T.R., Nathanson, K., Domchek, S., Wagner, T., Garber, J.E., Szabo, C., Zikan, M., Foretova, L., Olson, J.E., Sellers, T.A., Lindor, N., Nevanlinna, H., Tommiska, J., Aittomaki, K., Hamann, U., Rashid, M.U., Torres, D., Simard, J., Durocher, F., Guenard, F., Lynch, H.T., Isaacs, C., Weitzel, J., Olopade, O.I., Narod, S., Daly, M.B., Godwin, A.K., Tomlinson, G., Easton, D.F., Chenevix-Trench, G., Antoniou, A.C. Cancer Epidemiol. Biomarkers Prev. (2007) [Pubmed]
  6. The prevalence of BRCA2 mutations in familial pancreatic cancer. Couch, F.J., Johnson, M.R., Rabe, K.G., Brune, K., de Andrade, M., Goggins, M., Rothenmund, H., Gallinger, S., Klein, A., Petersen, G.M., Hruban, R.H. Cancer Epidemiol. Biomarkers Prev. (2007) [Pubmed]
  7. Germ line Fanconi anemia complementation group C mutations and pancreatic cancer. Couch, F.J., Johnson, M.R., Rabe, K., Boardman, L., McWilliams, R., de Andrade, M., Petersen, G. Cancer Res. (2005) [Pubmed]
  8. Genetic epidemiology of BRCA1. Couch, F.J. Cancer Biol. Ther. (2004) [Pubmed]
  9. Is BRCA1 associated with familial breast cancer in India?. Couch, F.J. Cancer Biol. Ther. (2002) [Pubmed]
 
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