Integrin expression in colon cancer cells is regulated by the cytoplasmic domain of the β6 integrin subunit

- Niu, Jun, Dorahy, Douglas J., Gu, Xinhua, Scott, R. J., Draganic, Brian, Ahmed, Nuzhat, Agrez, Michael V.

Altered expression of brain related genes in lymphocytes in schizophrenia

- Bowden, N. A., Weidenhofer, J. C., Scott, R. J., Todd, J., Case, V., Schall, U., Tooney, P. A.

Gene profiling in the amygdala in schizophrenia

- Weidenhofer, J., Bowden, N. A., Scott, R. J., Tooney, P. A.

Volcanology, geochemistry and structure of the Ordovician Cargo Volcanics in the Cargo-Walli region, central New South Wales

- Simpson, C. J., Scott, R. J., Crawford, A. J., Meffre, S.

Common variants of DNA repair genes and malignant melanoma

- Debniak, T., Scott, R. J., Kowalska, E., Jakubowska, A., Gronwald, J., Wokolorczyk, D., Maleszka, R., Kładny, J., Lubinski, J., Gorski, B., Cybulskia, C., van de Wetering, T., Serrano-Fernandez, P., Huzarski, T., Byrski, T., Nagay, L., Dębniak, B.

Factor V Leiden is associated with pre-eclampsia but not with fetal growth restriction: a genetic association study and meta-analysis

- Dudding, T., Heron, J., Thakkinstian, A., Nurk, E., Golding, J., Pembrey, M., Ring, S. M., Attia, J., Scott, R. J.

The -149C>T SNP within the ΔDNMT3B gene, is not associated with early disease onset in hereditary non-polyposis colorectal cancer

- Reeves, S. G., Mossman, David, Meldrum, C. J., Kurzawski, G., Suchy, J., Lubinski, J., Scott, R. J.

A 1q44 deletion, paternal UPD of chromosome 2 and a deletion due to a complex translocation detected in children with abnormal phenotypes using new SNP array technology

- Talseth-Palmer, B. A., Bowden, N. A., Scott, R. J., Meldrum, C., Nicholl, J., Thompson, E., Friend, K., Liebelt, J., Bratkovic, D., Haan, E., Yu, S.

Estrogen receptor polymorphisms and the risk of endometrial cancer

- Ashton, K. A., Proietto, A., Otton, G., Symonds, I., McEvoy, M., Attia, J., Gilbert, M., Hamann, U., Scott, R. J.

Fetal growth and risk of childhood acute lymphoblastic leukemia: results from an Australian case-control study

- Milne, E., Royle, J. A., de Klerk , N. H., Blair, E., Bailey, H., Cole, C., Attia, J., Scott, R. J., Armstrong, B. K.

Vitamin D receptor variants and breast cancer risk in the Polish population

- Gapska, P., Scott, R. J., Dębniak, T., Serrano-Fernandez, P., Huzarski, T., Byrski, T., Kładny, J., Gronwald, J., Górski, B., Cybulski, C., Lubinski, J.

Vitamin D receptor variants and the malignant melanoma risk: a population-based study

- Gapska, P., Scott, R. J., Maleszka, R., Sulikowski, M., Lubinski, J., Debniak, T., Serrano-Fernandez, P., Mirecka, A., Rassoud, I., Gorski, B., Cybulski, C., Huzarski, T., Byrski, T., Nagay, L.

Differential gene expression and cytokine production from neutrophils in asthma phenotypes

- Baines, K. J., Simpson, J. L., Bowden, N. A., Scott, R. J., Gibson, P. G.

IL12A, MPHOSPH9/CDK2AP1 and RGS1 are novel multiple sclerosis susceptibility loci

- The International Multiple Sclerosis Genetics Consortium, Esposito, F., Patsopoulos, N. A., Lechner-Scott, J., Goris, A., Dobosi, R., Dubois, B., Rioux, J. D., Oturai, A. B., Sondergaard, H. B., Sellebjerg, F., Sorensen, P. S., Reunanen, M., Cepok, S., Koivisto, K., Cournu-Rebeix, I., Fontaine, B., Winkelmann, J., Gieger, C., Infante-Duarte, C., Zipp, F., Bergamaschi, L., Leone, M., Bergamaschi, R., Kockum, I., Cavalla, P., Lorentzen, A. R., Mero, I. L., Celius, E. G., Harbo, H. F., Spurkland, A., Comabella, M., Brynedal, B., Alfredsson, L., Bernardinelli, L., Leppa, V., Robertson, N. P., Hawkins, C. P., Barcellos, L. F., Beecham, G., Bush, W., Cree, B. A. C., Daly, M. J., Ivinson, A. J., Aubin, C., Compston, A., Booth, D. R., D'Alfonso, S., Haines, J. L., Hauser, S. L., Hemmer, B., Hillert, J., McCauley, J. L., Oksenberg, J., Olsson, T., Palotie, A., Peltonen, L., Heard, R. N., Pericak-Vance, M. A., Saarela, J., Sawcer, S. J., Stranger, B., Boneschi, F. M., Comi, G., Hafler, D. A., de Bakker, P. I. W., De Jager, P. L., Stewart, G. J., Cox, M., Scott, R. J.

BRAF and NRAS mutational status are prognostically important in thick and locally advanced cutaneous melanoma

- Vilain, R., Braye, S. G., Ashman, L., Scott, R. J.

Downstream effects of reduction in nucleotide excision repair in response to cisplatin treatment in melanoma

- Bowden, N. A., Ashton, K. A., Avery-Kiejda, K. A., Zhang, X. D., Hersey, P., Scott, R. J.

Familial recurrence risks for multiple sclerosis in Australia

- O'Gorman, C., Freeman, S., 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., Taylor, B. V., Tubridy, N., Wiley, J., Butzkueven, H., Broadley, S. A., Bahlo, M., Booth, D. R., Brown, M. A., Foote, S. J., Griffiths, L. R.

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

- van der Luijt, B., Devilee, P., EMBRACE,, 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., GEMO Study Collaborators,, Stoppa-Lyonnet, D., Caux-Moncoutier, V., Coupier, I., Peyrat, J.-P., Vennin, P., Muller, D., Fricker, J. P., Venat-Bouvet, L., Johannsson, O. Th., 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., ConFab, K., 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., Lubinski, J., 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.

Genetic polymorphisms and childhood acute lymphoblastic leukemia: GWAS of the ESCALE study (SFCE)

- Orsi, L., Rudant, J., Michel, G., Sirvent, N., Chastagner, P., Ducassou, S., Rialland, X., Hémon, D., Milne, E., Scott, R. J., Baruchel, A., Clavel, J., Bonaventure, A., Goujon-Bellec, S., Corda, E., Evans, T. J., Petit, A., Bertrand, Y., Nelken, B., Robert, A.

Imprinted DLK1-DIO3 region of 14q32 defines a schizophrenia-associated miRNA signature in peripheral blood mononuclear cells

- Gardiner, E., Beveridge, N. J., Wu, J. Q., Carr, V., Scott, R. J., Tooney, P. A., Cairns, M. J.