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.

Widespread white matter microstructural differences in schizophrenia across 4322 individuals: results from the ENIGMA Schizophrenia DTI Working Group

- Kelly, S., Jahanshad, N., Bousman, C. A., Brouwer, R. M., Bruggemann, J., Bustillo, J., Cahn, W., Calhoun, V., Cannon, D., Carr, V., Catts, S., Chen, J., Zalesky, A., Henskens, F. A., Michie, P. T., Piras, F., Scott, R. J., Kochunov, P., Agartz, I., Alloza, C., Andreassen, O. A., Arango, C., Banaj, N., Bouix, S.

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.

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.

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.

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.

Schizophrenia genetic variants are not associated with intelligence

- Terwisscha van Scheltinga, A. F., Bakker, S. C., Kendler, K. S., Kirov, G. K., Konnerth, H., Konte, B., Krabbendam, L., Krasucki, R., Lasseter, V. K., Laurent, C., Lawrence, J., Lencz, T., Lerer, F. B., Levinson, D. F., Liang, K.-Y., Lichtenstein, P., Lieberman, J. A., Linszen, D. H., Lönnqvist, J., Loughland, C. M., Maclean, A. W., Maher, B. S., Maier, W., Mallet, J., Sklar, P., Malloy, P., Mattheisen, M., Mattingsdal, M., McGhee, K. A., McGrath, J. J., McIntosh, A., McLean, D. E., McQuillin, A., Melle, I., Michie, P. T., Holmans, P. A., Milanova, V., Morris, D. W., Mors, O., Mortensen, P. B., Moskvina, V., Muglia, P., Myin-Germeys, I., Nertney, D. A., Nestadt, G., Nielsen, J., Lin, D.-Y., Nikolov, I., Nordentoft, M., Norton, N., Nöthen, M. M., O'Dushlaine, C. T., Olincy, A., Olsen, L., O'Neill, F. A., Ørntoft, T. F., Owen, M. J., Duan, J., Pantelis, C., Papadimitriou, G., Pato, M. T., Peltonen, L., Petursson, H., Pickard, B., Pimm, J., Pulver, A. E., Puri, V., Quested, D., Andreassen, O. A., Quinn, E. M., Rasmussen, H. B., Réthelyi, J. M., Ribble, R., Rietschel, M., Riley, B. P., Ruggeri, M., Schall, U., Schulze, T. G., Schwab, S. G., Scolnick, E., Scott, R. J., Shi, J., Sigurdsson, E., Silverman, J. M., Spencer, C. C. A., Stefansson, K., Strange, A., Strengman, E., Stroup, T. S., Suvisaari, J., Cichon, S., Terenius, L., Thirumalai, S., Thygesen, J. H., Timm, S., Toncheva, D., Van Den Oord, E., Van Os, J., Van Winkel, R., Veldink, J., Walsh, D., St Clair, D., Wang, A. G., Wiersma, D., Wildenauer, D. B., Williams, H. J., Williams, N. M., Wormley, B., Zammit, S., Sullivan, P. F., O'Donovan, M. C., Daly, M. J., van Haren, N. E. M., Corvin, A., Gejman, P. V., Gurling, H., Werge, T., Rujescu, D., Blackwood, D. H. R., Pato, C. N., Malhotra, A. K., Purcell, S., Dudbridge, F., Neale, B. M., Derks, E. M., Rossin, L., Visscher, P. M., Posthuma, D., Ruderfer, D. M., Fanous, A., Stefansson, H., Steinberg, S., Mowry, B. J., Golimbet, V., De Hert, M., Buizer-Voskamp, J. E., Jönsson, E. G.., Bitter, I., Pietiläinen, O. P. H., Collier, D. A., Tosato, S., Agartz, I., Albus, M., Alexander, M., Amdur, R. L., Amin, F., Cahn, W., Bass, N., Bergen, S. E., Black, D. W., Børglum, A. D., Brown, M. A., Bruggeman, R., Buccola, N. G., Byerley, W. F., Cantor, R. M., Carr, V. J., Ripke, S., Catts, S. V., Choudhury, K., Cloninger, C. R., Cormican, P., Craddock, N., Danoy, P. A., Datta, S., De Haan, L., Demontis, D., Dikeos, D., Ophoff, R. A., Djurovic, S., Donnelly, P., Donohoe, G., Duong, L., Dwyer, S., Fink-Jensen, A., Freedman, R., Freimer, N. B., Friedl, M., Georgieva, L., Kahn, R. S., Giegling, I., Gill, M., Glenthøj, B., Godard, S., Hamshere, M, Hansen, M., Hansen, T., Hartmann, A. M., Henskens, F. A., Hougaard, D. M., Sanders, A. R., Hultman, C. M., Ingason, A., Jablensky, A. V., Jakobsen, K. D., Jay, M., Jürgens, G., Keller, M. C., Kenis, G., Kenny, E., Kim, Y.

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.

Paternal impacts on development: identification of genomic regions vulnerable to oxidative DNA damage in human spermatozoa

- Xavier, M. J., Nixon, B., Roman, S. D., Scott, R. J., Drevet, J. R., Aitken, R. J.

New EPCAM founder deletion in Polish population

- Dymerska, D., Gołębiewska, K., Szwiec, M., Kilar, E., Huzarski, T., Byrski, T., Lubiński, J., Kurzawski, G., Kuświk, M., Rudnicka, H., Scott, R. J., Billings, R., Pławski, A., Boruń, P., Siołek, M., Kozak-Klonowska, B.

Methylation differences at the HLA-DRB1 locus in CD4+ T-Cells are associated with multiple sclerosis

- Graves, M. C., Benton, M., Lea, R. A., Boyle, M., Tajouri, L., Macartney-Coxson, D., Scott, R. J., Lechner-Scott, J.

Low-level parental mosaicism in an apparent de novo case of Peutz-Jeghers syndrome

- Butel-Simoes, G. I., Spigelman, A. D., Scott, R. J., Vilain, R. E.

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.

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.

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.

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.

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.

GWAS for executive function and processing speed suggests involvement of the CADM2 gene

- Ibrahim-Verbaas, C. A., Bressler, J., Chibnik, L. B., Liu, Y., Vitart, V., Kirin, M., Petrovic, K., Polasek, O., Zgaga, L., Fawns-Ritchie, C., Hoffmann, P., Karjalainen, J., Debette, S., Oldmeadow, C., Holliday, E. G., Scott, R. J., Attia, J. R., Schofield, P. W., Schuur, M., Smith, A. V., Bis, J. C., Davies, G., Trompet, S., Smith, J. A., Wolf, C.

Genome-wide supported variant MIR137 and severe negative symptoms predict membership of an impaired cognitive subtype of schizophrenia

- Green, M. J., Cairns, M. J., Wu, J., Dragovic, M., Jablensky, A., Tooney, P. A., Scott, R. J., Carr, V. 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.