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.

Predicting type 2 diabetes using genetic and environmental risk factors in a multi-ethnic Malaysian cohort

- Abdullah, N., Abdul Murad, N. A., Jamal, R., Scott, R. J., Holliday, E. G., Mohd Haniff, E. A., Syafruddin, S. E., Attia, J., Oldmeadow, C., Kamaruddin, M. A., Abd Jalal, N., Ismail, N., Ishak, M.

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.

Xeroderma pigmentosum genes and melanoma risk

- Paszkowska-Szczur, K., Scott, R. J., Lubinski, J., Debniak, T., Serrano-Fernandez, P., Mirecka, A., Gapska, P., Górski, B., Cybulski, C., Maleszka, R., Sulikowski, M., Nagay, L.

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.

Characterising the genetic risk for type 2 diabetes in a Malaysian multi-ethnic cohort

- Abdullah, N., Abdul Murad, N., Scott, R. J., Holliday, E. G., Attia, J., Oldmeadow, C., Mohd Haniff, E. A., Syafruddin, S. E., Abd Jalal, N., Ismail, N., Ishak, M., Jamal, R.

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.

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.

Characterizing the genetic risk for type 2 diabetes in a Malaysian multi-ethnic cohort

- Abdullah, N., Abdul Murad, N. A., Scott, R. J., Holliday, E. G., Attia, J., Oldmeadow, C., Mohd Haniff, E. A., Syafruddin, S. E., Abd Jalal, N., Ismail, N., Ishak, M., Jamal, R.

Cumulative effects of genetic markers and the detection of advanced colorectal neoplasias by population screening

- Kurlapska, A., Serrano-Fernández, P., Rogoza-Mateja, W., Scott, R. J., Lubiński, J., Baszuk, P., Gupta, S., Starzyńska, T., Małecka-Panas, E., Dabrowski, A., Dębniak, T., Kurzawski, G., Suchy, J.

Gene profiling in the amygdala in schizophrenia

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

Brain transcriptome perturbations in the transferrin receptor 2 mutant mouse support the case for brain changes in iron loading disorders, including effects relating to long-term depression and long-term potentiation

- Acikyol, B., Graham, R. M., Trinder, D., House, M. J., Olynyk, J. K., Scott, R. J., Milward, E. A., Johnstone, D. M.

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.

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.

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.

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.

cDNA analysis of the BRCA1 unclassified variant c.5194-12G > A (letter)

- Wong-Brown, M. W., McPhillips, M. L., Hipwell, M., Pecenpetelovska, G., Dooley, S., Meldrum, C., Scott, R. J.

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.

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.

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.