Acikyol, B., Graham, R. M., Trinder, D., House, M. J., Olynyk, J. K., Scott, R. J., Milward, E. A., Johnstone, D. M.. Elsevier; 2013. 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.

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.. Elsevier; 2008. Common variants of DNA repair genes and malignant melanoma.

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.. Wiley-Blackwell; 2015. Cumulative effects of genetic markers and the detection of advanced colorectal neoplasias by population screening.

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.. Nature Publishing Group; 2010. IL12A, MPHOSPH9/CDK2AP1 and RGS1 are novel multiple sclerosis susceptibility loci.

Bowden, N. A., Ashton, K. A., Avery-Kiejda, K. A., Zhang, X. D., Hersey, P., Scott, R. J.. Wiley-Blackwell Publishing; 2011. Downstream effects of reduction in nucleotide excision repair in response to cisplatin treatment in melanoma.

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.. John Wiley & Sons; 2013. Xeroderma pigmentosum genes and melanoma risk.

Dudding, T., Heron, J., Thakkinstian, A., Nurk, E., Golding, J., Pembrey, M., Ring, S. M., Attia, J., Scott, R. J.. Wiley-Blackwell Publishing; 2008. Factor V Leiden is associated with pre-eclampsia but not with fetal growth restriction: a genetic association study and meta-analysis.

Xavier, M. J., Nixon, B., Roman, S. D., Scott, R. J., Drevet, J. R., Aitken, R. J.. Oxford University Press; 2019. Paternal impacts on development: identification of genomic regions vulnerable to oxidative DNA damage in human spermatozoa.

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.. Nature Publishing Group; 2012. Genetic polymorphisms and childhood acute lymphoblastic leukemia: GWAS of the ESCALE study (SFCE).

Reeves, S. G., Mossman, David, Meldrum, C. J., Kurzawski, G., Suchy, J., Lubinski, J., Scott, R. J.. Elsevier; 2008. The -149C>T SNP within the ΔDNMT3B gene, is not associated with early disease onset in hereditary non-polyposis colorectal cancer.

Weidenhofer, J., Bowden, N. A., Scott, R. J., Tooney, P. A.. John Wiley & Sons, Inc.; 2004. Gene profiling in the amygdala in schizophrenia.

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.. SciTePress; 2012. IT development and management of a live e-research system: experiences with the Australian Schizophrenia Research Bank.

Davies, G., Armstrong, N., van der Lee, S. J., , , , , , , , , , , Le Hellard, S., , , , , , , , , , , Liu, T., , , , , , , , , , Marioni, R. E., Oldmeadow, C., Postmus, I., Smith, A. V., Smith, J. A., Thalamuthu, A., Thomson, R., Bis, J. C., Holliday, E. G., Scott, R. J., Attia, J. R., Schofield, P. W., , , , , , , Bressler, J., , , , , , , , , , , Chouraki, V., , , , , , , , , , , Giddaluru, S., , , , , , , , , , , Hofer, E., , , , , , , , , , , Ibrahim-Verbaas, C. A., , , , , , , , , , , Kirin, M., , , , , , , , , , , Lahti, J., , , , , , , , , , . Nature Publishing Group; 2015. Genetic contributions to variation in general cognitive function: a meta-analysis of genome-wide association studies in the CHARGE consortium (N=53 949).

Butel-Simoes, G. I., Spigelman, A. D., Scott, R. J., Vilain, R. E.. Springer; 2019. Low-level parental mosaicism in an apparent de novo case of Peutz-Jeghers syndrome.

Wong-Brown, M. W., McPhillips, M. L., Hipwell, M., Pecenpetelovska, G., Dooley, S., Meldrum, C., Scott, R. J.. Wiley-Blackwell; 2013. cDNA analysis of the BRCA1 unclassified variant c.5194-12G > A (letter).

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.. Wiley-Blackwell; 2015. Characterizing the genetic risk for type 2 diabetes in a Malaysian multi-ethnic cohort.

Vilain, R., Braye, S. G., Ashman, L., Scott, R. J.. Wiley-Blackwell Publishing; 2011. BRAF and NRAS mutational status are prognostically important in thick and locally advanced cutaneous melanoma.

Simpson, C. J., Scott, R. J., Crawford, A. J., Meffre, S.. Taylor & Francis; 2007. Volcanology, geochemistry and structure of the Ordovician Cargo Volcanics in the Cargo-Walli region, central New South Wales.

Bowden, N. A., Weidenhofer, J. C., Scott, R. J., Todd, J., Case, V., Schall, U., Tooney, P. A.. John Wiley & Sons, Inc.; 2004. Altered expression of brain related genes in lymphocytes in schizophrenia.

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.. Elsevier; 2017. Predicting type 2 diabetes using genetic and environmental risk factors in a multi-ethnic Malaysian cohort.

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.. IADIS Press; 2012. Issues preventing the migration of the Australian Schizophrenia Research Bank to the cloud.

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.. Karger; 2009. 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.

Ashton, K. A., Proietto, A., Otton, G., Symonds, I., McEvoy, M., Attia, J., Gilbert, M., Hamann, U., Scott, R. J.. Wiley-Blackwell; 2009. Estrogen receptor polymorphisms and the risk of endometrial cancer.

Gapska, P., Scott, R. J., Dębniak, T., Serrano-Fernandez, P., Huzarski, T., Byrski, T., Kładny, J., Gronwald, J., Górski, B., Cybulski, C., Lubinski, J.. Springer; 2009. Vitamin D receptor variants and breast cancer risk in the 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.. Wiley-Blackwell; 2017. New EPCAM founder deletion in Polish population.

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.. Elsevier; 2009. Vitamin D receptor variants and the malignant melanoma risk: a population-based study.

Milne, E., Royle, J. A., de Klerk , N. H., Blair, E., Bailey, H., Cole, C., Attia, J., Scott, R. J., Armstrong, B. K.. Oxford University Press; 2009. Fetal growth and risk of childhood acute lymphoblastic leukemia: results from an Australian case-control study.

Niu, Jun, Dorahy, Douglas J., Gu, Xinhua, Scott, R. J., Draganic, Brian, Ahmed, Nuzhat, Agrez, Michael V.. Wiley-Liss; 2002. Integrin expression in colon cancer cells is regulated by the cytoplasmic domain of the β6 integrin subunit.

Baines, K. J., Simpson, J. L., Bowden, N. A., Scott, R. J., Gibson, P. G.. European Respiratory Society; 2010. Differential gene expression and cytokine production from neutrophils in asthma phenotypes.

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.. Cambridge University Press; 2013. Schizophrenia genetic variants are not associated with intelligence.

Green, M. J., Cairns, M. J., Wu, J., Dragovic, M., Jablensky, A., Tooney, P. A., Scott, R. J., Carr, V. J.. Nature Publishing Group; 2013. Genome-wide supported variant MIR137 and severe negative symptoms predict membership of an impaired cognitive subtype of schizophrenia.

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.. BMJ Group; 2011. Familial recurrence risks for multiple sclerosis in Australia.

Barzideh, J., Scott, R. J., Aitken, R. J.. Wiley-Blackwell Verlag; 2013. Analysis of the global methylation status of human spermatozoa and its association with the tendency of these cells to enter apoptosis.

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.. Nature Publishing; 2016. GWAS for executive function and processing speed suggests involvement of the CADM2 gene.

Graves, M. C., Benton, M., Lea, R. A., Boyle, M., Tajouri, L., Macartney-Coxson, D., Scott, R. J., Lechner-Scott, J.. Sage; 2014. Methylation differences at the HLA-DRB1 locus in CD4+ T-Cells are associated with multiple sclerosis.

Petit, J., Carroll, G., Zhao, J., Roper, E., Pockney, P., Scott, R. J.. Nature Publishing Group; 2023. Evaluation of epigenetic methylation biomarkers for the detection of colorectal cancer using droplet digital PCR.

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.. Nature Publishing Group; 2018. Widespread white matter microstructural differences in schizophrenia across 4322 individuals: results from the ENIGMA Schizophrenia DTI Working Group.

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., 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., 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.. Nature Publishing Group; 2012. 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.

Gardiner, E., Beveridge, N. J., Wu, J. Q., Carr, V., Scott, R. J., Tooney, P. A., Cairns, M. J.. Nature Publishing Group; 2012. Imprinted DLK1-DIO3 region of 14q32 defines a schizophrenia-associated miRNA signature in peripheral blood mononuclear cells.

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.. Wiley-Blackwell Publishing; 2015. Characterising the genetic risk for type 2 diabetes in a Malaysian multi-ethnic cohort.