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Jakubowska, A., Rozkrut, D., Antoniou, A., Hamann, U., Scott, R. J., McGuffog, L., Healy, S., Sinilnikova, O. M., Rennert, G., Lejbkowicz, F., Flugelman, A., Andrulis, I. L., Glendon, G., Ozcelik, H., Thomassen, M., Paligo, M., Aretini, P., Kantala, J., Aroer, B., Von Wachenfeldt, A., Liljegren, A., Loman, N., Herbst, K., Kristoffersson, U., Rosenquist, R., Karlsson, P., Stenmark-Askmalm, M., Melin, B., Nathanson, K. L., Domchek, S. M., Byrski, T., Huzarski, T., Gronwald, J., Menkiszak, J., Cybulski, C., Serrano, P., Osorio, A., Cajal, T. R., Tsitlaidou, M., Benitez, J., Gilbert, M., Rookus, M., Aalfs, C. M., Kluijt, I., Boessenkool-Pape, J. L., Meijers-Heijboer, H. E. J., Oosterwijk, J. C., van Asperen, C. J., Blok, M. J., Nelen, M. R., van den Ouweland, A. M. W., Seynaeve, C., van der Luijt, R. B., Devilee, P., Easton, D. F., Peock, S., Frost, D., Platte, R., Ellis, S. D., Fineberg, E., Evans, D. G., Lalloo, F., Eeles, R., Jacobs, C., Adlard, J., Davidson, R., Eccles, D., Cole, T., Cook, J., Godwin, A., Bove, B., Stoppa-Lyonnet, D., Caux-Moncoutier, V., Belotti, M., Tirapo, C., Mazoyer, S., Barjhoux, L., Boutry-Kryza, N., Pujol, P., Coupier, I., Peyrat, J-P, Vennin, P., Muller, D., Fricker, J-P, Venat-Bouvet, L., Johannsson, OTh, Isaacs, C., Schmutzler, R., Wappenschmidt, B., Meindl, A., Arnold, N., Varon-Mateeva, R., Niederacher, D., Sutter, C., Deissler, H., Preisler-Adams, S., Simard, J., Soucy, P., Durocher, F., Chenevix-Trench, G., Beesley, J., Chen, X., Rebbeck, T., Couch, F., Wang, X., Lindor, N., Fredericksen, Z., Pankratz, V. S., Peterlongo, P., Bonanni, B., Fortuzzi, S., Peissel, B., Szabo, C., Mai, P. L., Loud, J. T. and Lubinski, J. (2012) Association of PHB 1630 C > T and MTHFR 677 C > T polymorphisms with breast and ovarian cancer risk in BRCA1/2 mutation carriers: results from a multicenter study. British Journal of Cancer, 106 12: 2016-2024. doi:10.1038/bjc.2012.160 123 1 8 Cited 9 times in Scopus9 1
Parsons, M.T., Whiley, P.J., Beesley, J., Drost, M., de Wind, N., Thompson, B.A., Marquart, L., Hopper, J.L., Jenkins, M.A., Brown, M.A., Tucker, K., Warwick, L., Buchanan, D.D. and Spurdle, A.B. (2013) Consequences of germline variation disrupting the constitutional translational initiation codon start sites of MLH1 and BRCA2: Use of potential alternative start sites and implications for predicting variant pathogenicity. Molecular Carcinogenesis, In Press . doi:10.1002/mc.22116 26   Cited 1 times in Scopus1 0
Dixon, S. C., Ibiebele, T. I., Protani, M. M., Beesley, J., deFazio, A., Crandon, A. J., Gard, G. B., Rome, R. M., Webb, P. M. and Nagle, C. M. (2014) Dietary folate and related micronutrients, folate-metabolising genes, and ovarian cancer survival. Gynecologic Oncology, 132 3: 566-572. doi:10.1016/j.ygyno.2013.12.025 29   0 Cited 0 times in Scopus0 0
Shen H., Fridley B.L., Song H., Lawrenson K., Cunningham J.M., Ramus S.J., Cicek M.S., Tyrer J., Stram D., Larson M.C., Kobel M., Ziogas A., Zheng W., Yang H.P., Wu A.H., Wozniak E.L., Ling Woo Y., Winterhoff B., Wik E., Whittemore A.S., Wentzensen N., Palmieri Weber R., Vitonis A.F., Vincent D., Vierkant R.A., Vergote I., Van Den Berg D., Van Altena A.M., Tworoger S.S., Thompson P.J., Tessier D.C., Terry K.L., Teo S.-H., Templeman C., Stram D.O., Southey M.C., Sieh W., Siddiqui N., Shvetsov Y.B., Shu X.-O., Shridhar V., Wang-Gohrke S., Severi G., Schwaab I., Salvesen H.B., Rzepecka I.K., Runnebaum I.B., Anne Rossing M., Rodriguez-Rodriguez L., Risch H.A., Renner S.P., Poole E.M., Pike M.C., Phelan C.M., Pelttari L.M., Pejovic T., Paul J., Orlow I., Zawiah Omar S., Olson S.H., Odunsi K., Nickels S., Nevanlinna H., Ness R.B., Narod S.A., Nakanishi T., Moysich K.B., Monteiro A.N.A., Moes-Sosnowska J., Modugno F., Menon U., McLaughlin J.R., McGuire V., Matsuo K., Mat Adenan N.A., Massuger L.F.A.G., Lurie G., Lundvall L., Lubinski J., Lissowska J., Levine D.A., Leminen A., Lee A.W., Le N.D., Lambrechts S., Lambrechts D., Kupryjanczyk J., Krakstad C., Konecny G.E., Kruger Kjaer S., Kiemeney L.A., Kelemen L.E., Keeney G.L., Karlan B.Y., Karevan R., Kalli K.R., Kajiyama H., Ji B.-T., Jensen A., Jakubowska A., Iversen E., Hosono S., Hogdall C.K., Hogdall E., Hoatlin M., Hillemanns P., Heitz F., Hein R., Harter P., Halle M.K., Hall P., Gronwald J., Gore M., Goodman M.T., Giles G.G., Gentry-Maharaj A., Garcia-Closas M., Flanagan J.M., Fasching P.A., Ekici A.B., Edwards R., Eccles D., Easton D.F., Durst M., Du Bois A., Dork T., Doherty J.A., Despierre E., Dansonka-Mieszkowska A., Cybulski C., Cramer D.W., Cook L.S., Chen X., Charbonneau B., Chang-Claude J., Campbell I., Butzow R., Bunker C.H., Brueggmann D., Brown R., Brooks-Wilson A., Brinton L.A., Bogdanova N., Block M.S., Benjamin E., Beesley J., Beckmann M.W., Bandera E.V., Baglietto L., Bacot F., Armasu S.M., Antonenkova N., Anton-Culver H., Aben K.K., Liang D., Wu X., Lu K., Hildebrandt M.A.T., Schildkraut J.M., Sellers T.A., Huntsman D., Berchuck A., Chenevix-Trench G., Gayther S.A., Pharoah P.D.P., Laird P.W., Goode E.L. and Leigh Pearce C. (2013) Epigenetic analysis leads to identification of HNF1B as a subtype-specific susceptibility gene for ovarian cancer. Nature Communications, 4 Article number: 1628: 1-10. doi:10.1038/ncomms2629 25   33 Cited 29 times in Scopus29 130
Barnes, D.R., Barrowdale, D., Beesley, J., Chen, X., James, P.A., Hopper, J.L., Goldgar, D., Chenevix-Trench, G., Antoniou, A.C. and Mitchell, G. (2013) Estimating single nucleotide polymorphism associations using pedigree data: Applications to breast cancer. British Journal of Cancer, 108 12: 2610-2622. doi:10.1038/bjc.2013.277 23 2 3 Cited 3 times in Scopus3 0
Osorio, A., Milne, R. L., Alonso, R., Pita, G., Peterlongo, P., Teule, A., Nathanson, K. L., Domchek, S. M., Rebbeck, T., Lasa, A., Konstantopoulou, I., Hogervorst, F. B., Verhoef, S., van Dooren, M. F., Jager, A., Ausems, M. G. E. M., Aalfs, C. M., van Asperen, C. J., Vreeswijk, M., Waisfisz, Q., Van Roozendaal, C. E., Ligtenberg, M. J., Easton, D. F., Peock, S., Cook, M., Oliver, C. T., Frost, D., Curzon, B., Evans, D. G., Lalloo, F., Eeles, R., Izatt, L., Davidson, R., Adlard, J., Eccles, D., Ong, K-R, Douglas, F., Downing, S., Brewer, C., Walker, L., Nevanlinna, H., Aittomaki, K., Couch, F. J., Fredericksen, Z., Lindor, N. M., Godwin, A., Isaacs, C., Caligo, M. A., Loman, N., Jernstrom, H., Barbany-Bustinza, G., Liljegren, A., Ehrencrona, H., Stenmark-Askmalm, M., Feliubadalo, L., Manoukian, S., Peissel, B., Zaffaroni, D., Bonanni, B., Fortuzzi, S., Johannsson, O. T., Chenevix-Trench, G., Chen, X-C, Beesley, J., Spurdle, A. B., Sinilnikova, O. M., Healey, S., McGuffog, L., Antoniou, A. C., Brunet, J., Radice, P. and Benitez, J. (2011) Evaluation of the XRCC1 gene as a phenotypic modifier in BRCA1/2 mutation carriers. Results from the consortium of investigators of modifiers of BRCA1/BRCA2. British Journal of Cancer, 104 8: 1356-1361. doi:10.1038/bjc.2011.91 93   3 Cited 3 times in Scopus3 0
Webb, P.M., Ibiebele, T.I., Hughes, M.C., Beesley, J., van der Pols, J.C., Chen, X., Nagle, C.M., Bain, C.J. and Chenevix-Trench, G. (2011) Folate and related micronutrients, folate-metabolising genes and risk of ovarian cancer. European Journal of Clinical Nutrition, 65 10: 1133-1140. doi:10.1038/ejcn.2011.99 70   12 Cited 11 times in Scopus11 1
Amankwah, E.K., Kelemen, L.E., Wang, Q., Song, H., Chenevix-Trench, G., Beesley, J., Webb, P.M., Pearce, C.L., Wu, A.H., Pike, M.C., Stram, D.O., Chang-Claude, J., Wang-Gohrke, S., Ness, R.B., Goode, E.L., Cunningham, J.M., Fridley, B.L., Vierkant, R.A., Tworoger, S.S., Whittemore, A.S., McGuire, V., Sieh, W., Gayther, S.A., Gentry-Maharaj, A., Menon, U., Ramus, S.J., Rossing, M.A., Doherty, J.A., Goodman, M.T., Carney, M.E., Lurie, G., Wilkens, L.R., Kjær, S.K., Høgdall, E., Cramer, D.W., Terry, K.L., Garcia-Closas, M., Yang, H., Lissowska, J., Anton-Culver, H., Ziogas, A., Schildkraut, J.M., Berchuck, A. and Pharoah, P.D.P. (2011) Prostate cancer susceptibility polymorphism rs2660753 is not associated with invasive ovarian cancer. Cancer Epidemiology Biomarkers and Prevention, 20 5: 1028-1031. doi:10.1158/1055-9965.EPI-11-0053 46   0 Cited 0 times in Scopus0 1
Rothnagel, J. A., Beesley, J. M., Ross, I. L. and Wang, X. Q. (2002). Regulation of alternative splicing of GL11 in normal tissues and in cancer. In: ComBio 2002. ComBio 2002, Sydney, ((Abstract)). 29 September - 3 October, 2002. 46  
Dowty, J. G., Lose, F., Jenkins, M. A., Chang, J. H., Chen, X. Q., Beesley, J., Dite, G. S., Southey, M. C., Byrnes, G. B., Tesoriero, A., Giles, G. G., ConFab Investigators, Australian Breast Cancer Family Study, Hooper, J. L. and Spurdle, A. B. (2008) The RAD51D E233G variant and breast cancer risk: population-based and clinic based family studies of Australian women. Breast Cancer Research and Treatment, 112 1: 35-39. doi:10.1007/s10549-007-9832-0 54   6 Cited 5 times in Scopus5 0