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.

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.

Gene profiling in the amygdala in schizophrenia

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

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.