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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
Scott R.J., Cavana R.Y. and Cameron D. (2015) Client Perceptions of Reported Outcomes of Group Model Building in the New Zealand Public Sector. Group Decision and Negotiation, . doi:10.1007/s10726-015-9433-y 60   Cited 0 times in Scopus0 0
O'Gorman, C., Freeman, S., Taylor, B. V., Butzkueven, H., Australian and New Zealand MS Genetics Consortium (ANZgene), Broadley S. A., Bahlo, M., Booth, D. R., Brown, M. A., Foote, S. J., Griffiths, L. R., Kilpatrick, T. J., Lechner-Scott, J., Moscato, P., Perreau, V. M., Scott, R. J., Stankovich, J., Stewart, G. J., Chapman, C., Marriot, M., Tanner, M., Tubridy, N. and Wiley, J. (2011) Familial recurrence risks for multiple sclerosis in Australia. Journal of Neurology, Neurosurgery and Psychiatry, 82 12: 1351-1354. doi:10.1136/jnnp.2010.233064 17   5 Cited 6 times in Scopus6 0
Painter J.N., O'Mara T.A., Batra J., Cheng T., Lose F.A., Dennis J., Michailidou K., Tyrer J.P., Ahmed S., Ferguson K., Healey C.S., Kaufmann S., Hillman K.M., Walpole C., Moya L., Pollock P., Jones A., Howarth K., Martin L., Gorman M., Hodgson S., De Polanco M.M.E., Sans M., Carracedo A., Castellvi-Bel S., Rojas-Martinez A., Santos E., Teixeira M.R., Carvajal-Carmona L., Shu X.-O., Long J., Zheng W., Xiang Y.-B., Montgomery G.W., Webb P.M., Scott R.J., McEvoy M., Attia J., Holliday E., Martin N.G., Nyholt D.R., Henders A.K., Fasching P.A., Hein A., Beckmann M.W., Renner S.P., Dork T., Hillemanns P., Durst M., Runnebaum I., Lambrechts D., Coenegrachts L., Schrauwen S., Amant F., Winterhoff B., Dowdy S.C., Goode E.L., Teoman A., Salvesen H.B., Trovik J., Njolstad T.S., Werner H.M.J., Ashton K., Proietto T., Otton G., Tzortzatos G., Mints M., Tham E., Hall P., Czene K., Liu J., Li J., Hopper J.L., Southey M.C., Ekici A.B., Ruebner M., Johnson N., Peto J., Burwinkel B., Marme F., Brenner H., Dieffenbach A.K., Meindl A., Brauch H., Lindblom A., Depreeuw J., Moisse M., Chang-Claude J., Rudolph A., Couch F.J., Olson J.E., Giles G.G., Bruinsma F., Cunningham J.M., Fridley B.L., Borresen-Dale A.L., Kristensen V.N., Cox A., Swerdlow A.J., Orr N., Bolla M.K., Wang Q., Weber R.P., Chen Z., Shah M., French J.D., Pharoah P.D.P., Dunning A.M., Tomlinson I., Easton D.F., Edwards S.L., Thompson D.J. and Spurdle A.B. (2015) Fine-mapping of the HNF1B multicancer locus identifies candidate variants that mediate endometrial cancer risk. Human Molecular Genetics, 24 5: 1478-1492. doi:10.1093/hmg/ddu552 14   0 Cited 0 times in Scopus0 2
Davies, G., Armstrong, N., Bis, J. C., Bressler, J., Chouraki, V., Giddaluru, S., Hofer, E., Ibrahim-Verbaas, C. A., Kirin, M., Lahti, J., van der Lee, S. J., Le Hellard, S., Liu, T., Marioni, R. E., Oldmeadow, C., Postmus, I., Smith, A. V., Smith, J. A., Thalamuthu, A., Thomson, R., Vitart, V., Wang, J., Yu, L., Zgaga, L., Zhao, W., Boxall, R., Harris, S. E., Hill, W. D., Liewald, D. C., Luciano, M., Adams, H., Ames, D., Amin, N., Amouyel, P., Assareh, A. A., Au, R., Becker, J. T., Beiser, A., Berr, C., Bertram, L., Boerwinkle, E., Buckley, B. M., Campbell, H., Corley, J., De Jager, P. L., Dufouil, C., Eriksson, J. G., Espeseth, T., Faul, J. D., Ford, I., Gottesman, R. F., Griswold, M. E., Gudnason, V., Harris, T. B., Heiss, G., Hofman, A., Holliday, E. G., Huffman, J., Kardia, S. L. R., Kochan, N., Knopman, D. S., Kwok, J. B., Lambert, J-C, Lee, T., Li, G., Li, S-C, Loitfelder, M., Lopez, O. L., Lundervold, A. J., Lundqvist, A., Mather, K. A., Mirza, S. S., Nyberg, L., Oostra, B. A., Palotie, A., Papenberg, G., Pattie, A., Petrovic, K., Polasek, O., Psaty, B. M., Redmond, P., Reppermund, S., Rotter, J. I., Schmidt, H., Schuur, M., Schofield, P. W., Scott, R. J., Steen, V. M., Stott, D. J., Van Swieten, J. C., Taylor, K. D., Trollor, J., Trompet, S., Uitterlinden, A. G., Weinstein, G., Widen, E., Windham, B. G., Jukema, J. W., Wright, A. F., Wright, M. J., Yang, Q., Amieva, H., Attia, J. R., Bennett, D. A., Brodaty, H., de Craen, A. J. M., Hayward, C., Ikram, M. A., Lindenberger, U., Nilsson, L-G, Porteous, D. J., Raikkonen, K., Reinvang, I., Rudan, I., Sachdev, P. S., Schmidt, R., Schofield, P. R., Srikanth, V., Starr, J. M., Turner, S. T., Weir, D. R., Wilson, J. F., Van Duijn, C., Launer, L., Fitzpatrick, A. L., Seshadri, S., Jr, T. H. Mosley and Deary, I. J. (2015) Genetic contributions to variation in general cognitive function: a meta-analysis of genome-wide association studies in the CHARGE consortium (N=53‚ÄČ949). Molecular Psychiatry, 20 2: 183-192. doi:10.1038/mp.2014.188 9   0 Cited 1 times in Scopus1 127
Sim X., Jensen R.A., Ikram M.K., Cotch M.F., Li X., MacGregor S., Xie J., Smith A.V., Boerwinkle E., Mitchell P., Klein R., Klein B.E.K., Glazer N.L., Lumley T., McKnight B., Psaty B.M., de Jong P.T.V.M., Hofman A., Rivadeneira F., Uitterlinden A.G., van Duijn C.M., Aspelund T., Eiriksdottir G., Harris T.B., Jonasson F., Launer L.J., Attia J., Baird P.N., Harrap S., Holliday E.G., Inouye M., Rochtchina E., Scott R.J., Viswanathan A., Li G., Smith N.L., Wiggins K.L., Kuo J.Z., Taylor K.D., Hewitt A.W., Martin N.G., Montgomery G.W., Sun C., Young T.L., Mackey D.A., van Zuydam N.R., Doney A.S.F., Palmer C.N.A., Morris A.D., Rotter J.I., Tai E.S., Gudnason V., Vingerling J.R., Siscovick D.S., Wang J.J. and Wong T.Y. (2013) Genetic Loci for Retinal Arteriolar Microcirculation. PLoS ONE, 8 6: e65804.1-e65804.12. doi:10.1371/journal.pone.0065804 31   2 Cited 2 times in Scopus2 0
Stankovich, J., Butzkueven, H., Marriott, M., Chapman, C., Tubridy, N., Tait, B.D., Varney, M.D., Taylor, B.V., Foote, S.J., Booth, D.R., Broadley, S., Greer, J.M., Griffiths, L.R., Heard, R.N., Lechner-Scott, M.J., Pender, M.J., Scott, R.J. and Stewart, G.J. (2009) HLA-DRB1 associations with disease susceptibility and clinical course in australians with multiple sclerosis. Tissue Antigens, 74 1: 17-21. doi:10.1111/j.1399-0039.2009.01262.x 60   22 Cited 25 times in Scopus25 0
Paul, D., Henskens, F. A., Loughland, C. M., Bridge, J., McCabe, K., Carr, V. J., Catts, S. V., Jablensky, A., Michie, P. T., Mowry, B. J., Pantelis, C., Schall, U. and Scott, R. J. (2012). It development and management of a live e-research system: Experiences with the Australian Schizophrenia Research Bank. In: HEALTHINF 2012 - Proceedings of the International Conference on Health Informatics. HEALTHINF 2012 - International Conference on Health Informatics, Vilamoura, Algarve, (125-130). 1 - 4 February 2012. 28 6 Cited 0 times in Scopus0
Henskens, F. A., Loughland, C. A., Aphale, M. S., Paul, D., Richards, J. A., Rasser, P., Carr, V. J., Catts, S. V., Jablensky, A., Michie, P. T., Mowry, B. J., Pantelis, C., Schall, U. and Scott, R. J. (2009). IT support for the Australian Schizophrenia Research Bank. In: Healthinf 2009: Proceedings of the International Conference On Health Informatics. 2nd International Conference on Health Informatics (HEALTHINF 2009), Oporto, Portugal, (405-410). 14-17 January 2009. 17   0 Cited 0 times in Scopus0
Breast Cancer Linkage Consortium*, Lakhani, Sunil R., Easton, Douglas F., Stratton, Michael R., Anderson, Thomas J., Farid, Linda M., Gusterson, B. A., Jaquemier, J., Sloane, J. P., Venter, D., VandeVijver, M. J., Bishop, D. T., Barkardottir, R. B., Bignon, Y. J., Cornelisse, C., ChangClaude, J., Daly, P. A., Devilee, P., Egilsson, V., Ford, D., Goldgar, D., Haites, N., Hamann, U., Klijn, J. G. M., Lasset, C., Lenoir, G., McManus, R., Neuhausen, S., Ormiston, W., Ponder, B. A. J., Peto, J., Steel, C. M., StoppaLyonnet, D., Smyth, E., Sobol, H., Spurr, N. K., Scott, R. J., Scherneck, S., Streuwing, J. P. and Vasen, H. (1997) Pathology of familial breast cancer: differences between breast cancers in carriers of BRCA1 or BRCA2 mutations and sporadic cases. Lancet, 349 9064: 1505-1510. 52   380
Loughland, Carmel Maree, Richards, J., Aphale, M., Henskens, F., Carr, V. J., Catts, S. V., Jablensky, A., Michie, P., Mowrey, B. J., Pantelis, C., Schall, U., Scott, R. J. and Lewin, T. J. (2009). The Australian Schizophrenia Research Bank (Asrb): the Development of An Electronically Delivered Clinical Assessment Battery. In: Schizophrenia Bulletin. 12th International Congress on Schizophrenia Research, San Diego Ca, (4-5). Mar 28-Apr 01, 2009. 16   0
Cox, M. B., Scott, R. J., Stankovich, J., Kermode, A., Cortes, A., Brown, M., Lechner-Scott, J., Wiley, J. and ANZgene (2012). The P2X7 receptor: Interaction with a HLA Class II allele which modulates the autoantibody response in Multiple Sclerosis. In: Multiple Sclerosis Journal. 17th Annual Conference on RIMS, Hamburg Germany, (702-703). May 31-Jun 02, 2012. 51   0