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.

Issues preventing the migration of the Australian Schizophrenia Research Bank to the cloud

- Paul, D., Henskens, F. A., Mowry, B. J., Pantelis, C., Schall, U., Scott, R. J., Loughland, C. M., McCabe, K., Bridge, J., Duffy, L., Carr, V. J., Catts, S. V., Jablensky, A., Michie, P. T.

IT development and management of a live e-research system: experiences with the Australian Schizophrenia Research Bank

- Paul, D., Henskens, F. A., Pantelis, C., Schall, U., Scott, R. J., Loughland, C. M., Bridge, J., McCabe, K., Carr, V. J., Catts, S. V., Jablensky, A., Michie, P. T., Mowry, B. 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.

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.

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.

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.

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.

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.

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.