Dominguez-Valentin, Mev, Seppälä, Toni T., Sampson, Julian R., Macrae, Finlay, Winship, Ingrid, Evans, D. Gareth, Scott, Rodney J., Burn, John, Möslein, Gabriela, Bernstein, Inge, Pylvänäinen, Kirsi, Renkonen-Sinisalo, Laura, Lepistö, Anna, Lindblom, Annika, Plazzer, John-Paul, Tjandra, Douglas, Thomas, Huw, Green, Kate, Lalloo, Fiona, Crosbie, Emma J.. BioMed Central; 2019. Survival by colon cancer stage and screening interval in Lynch syndrome: a prospective Lynch syndrome database report.

Holmes, Merran, Connor, Toni, Oldmeadow, Christopher, Pockney, Peter G., Scott, Rodney J., Talseth-Palmer, Bente A.. BMC; 2018. CD36-a plausible modifier of disease phenotype in familial adenomatous polyposis.

Kho, Pik-Fang, Amant, Frederic, Annibali, Daniela, Ashton, Katie, Attia, John, Auer, Paul L., Beckmann, Matthias W., Black, Amanda, Brinton, Louise, Buchanan, Daniel D., Chanock, Stephen J., Chen, Chu, Chen, Maxine M., Cheng, Timothy H. T., Cook, Linda S., Crous-Bous, Marta, Czene, Kamila, De Vivo, Immaculata, Dennis, Joe, Döerk, Thilo, Holliday, Elizabeth G., McEvoy, Mark, Otton, Geoffrey, Proietto, Tony, Scott, Rodney J., Dowdy, Sean C., Dunning, AM, Duerst, M, Easton, DF, Ekici, AB, Fasching, PA, Fridley, BL, Friedenreich, CM, Garcia-Closas, M, Gaudet, MM, Giles, GG, Goode, EL, Gorman, M, Haiman, CA, Hall, P, Hankinson, SE, Hein, A, Hillemanns, P, Hodgson, S, Hoivik, EA, Hunter, DJ, Jones, A, Kraft, P, Krakstad, C, Lambrechts, D, Le Marchand, L, Liang, X, Lindblom, A, Lissowska, J, Long, J, Lu, L, Magliocco, AM, Martin, L, Milne, RL, Mints, M, Nassir, R, Palles, C, Pooler, L, Rebbeck, TR, Renner, SP, Risch, HA, Ruebner, M, Runnebaum, I, Sacerdote, C, Sarto, GE, Schumacher, F, Setiawan, VW, Shah, M, Sheng, X, Shu, X-O, Southey, MC, Tham, E, Tomlinson, I, Trovik, J, Turman, C, Tyrer, JP, van den Berg, D, Wang, Z, Wentzensen, N, Xia, L, Xiang, Y-B, Yang, HP, Yu, H, Zheng, W, Webb, PM, Thompson, DJ, Spurdle, AB, Glubb, DM, O'Mara, TA. John Wiley & Sons; 2020. Mendelian randomization analyses suggest a role for cholesterol in the development of endometrial cancer.

Campagna, Maria Pia, Xavier, Alexandre, Lechner-Scott, Jeannette, Maltby, Vicky, Scott, Rodney J., Butzkueven, Helmut, Jokubaitis, Vilija G., Lea, Rodney A.. BioMed Central Ltd.; 2021. Epigenome-wide association studies: current knowledge, strategies and recommendations.

Graham, Sarah E., Clarke, Shoa L., Locke, Adam E., Mollehave, LT, Thuesen, BH, Munz, M, Zeng, L, Huang, J, Yang, B, Poveda, A, Kurbasic, A, Lamina, C, Forer, L, Marouli, Eirini, Scholz, M, Galesloot, TE, Bradfield, JP, Daw, EW, Zmuda, JM, Mitchell, JS, Fuchsberger, C, Christensen, H, Brody, JA, Feitosa, MF, Hwang, Mi Yeong, Wojczynski, MK, Preuss, M, Mangino, M, Christofidou, P, Verweij, N, Benjamins, JW, Engmann, J, Kember, RL, Slieker, RC, Lo, KS, Han, Sohee, Zilhao, NR, Phuong, L, Kleber, ME, Delgado, GE, Huo, S, Ikeda, DD, Iha, H, Yang, J, Liu, J, Leonard, HL, Narita, Akira, Marten, J, Schmidt, B, Arendt, M, Smyth, LJ, Canadas-Garre, M, Wang, Carol A., Nakatochi, M, Wong, A, Hutri-Kahonen, N, Sim, X, Choudhury, Ananyo, Xia, R, Huerta-Chagoya, A, Fernandez-Lopez, JC, Lyssenko, V, Ahmed, M, Jackson, AU, Irvin, MR, Oldmeadow, Chris, Kim, H-N, Ryu, S, Bentley, Amy R., Timmers, PRHJ, Arbeeva, L, Dorajoo, R, Lange, LA, Chai, X, Prasad, G, Lores-Motta, L, Pauper, M, Long, J, Li, X, Ekoru, Kenneth, Theusch, E, Takeuchi, F, Spracklen, CN, Loukola, A, Bollepalli, S, Warner, SC, Wang, YX, Wei, WB, Nutile, T, Ruggiero, D, Verma, Anurag, Sung, YJ, Hung, Y-J, Chen, S, Liu, F, Yang, J, Kentistou, KA, Gorski, M, Brumat, M, Meidtner, K, Bielak, LF, Trivedi, Bhavi, Smith, JA, Hebbar, P, Farmaki, A-E, Hofer, E, Lin, M, Xue, C, Zhang, J, Concas, MP, Vaccargiu, S, van der Most, PJ, Wu, Kuan-Han H., Martin, HC, Pitkanen, N, Cade, BE, Lee, J, van Der Laan, SW, Chitrala, KN, Weiss, S, Zimmermann, ME, Lee, JY, Choi, HS, Nethander, M, Hunt, KA, Freitag-Wolf, S, Southam, L, Rayner, NW, Wang, CA, Lin, S-Y, Wang, J-S, Couture, C, Lyytikainen, L-P, Nikus, K, Cuellar-Partida, G, Hui, Q, Vestergaard, H, Hildalgo, B, Giannakopoulou, O, Cai, Q, Obura, MO, van Setten, J, Li, X, Schwander, K, Terzikhan, N, Shin, JH, Klarin, D, Jackson, RD, Reiner, AP, Martin, LW, Chen, Z, Li, L, Highland, HM, Young, KL, Kawaguchi, T, Thiery, J, Bis, JC, Zhu, X, Nadkarni, GN, Launer, LJ, Li, H, Nalls, MA, Raitakari, OT, Ichihara, S, Wild, SH, Nelson, CP, Campbell, H, Jager, S, Thorleifsson, G, Nabika, T, Al-Mulla, F, Niinikoski, H, Braund, PS, Kolcic, I, Kovacs, P, Giardoglou, T, Katsuya, T, Bhatti, F, de Kleijn, D, Helgadottir, A, de Borst, GJ, Kim, EK, Adams, HHH, Ikram, MA, Zhu, X, Asselbergs, FW, Kraaijeveld, AO, Beulens, JWJ, Shu, X-O, Rallidis, LS, Gudbjartsson, DF, Pedersen, O, Hansen, T, Mitchell, P, Hewitt, AW, Kahonen, M, Perusse, L, Bouchard, C, Tonjes, A, Chen, Y-DI, Pennell, Craig E., Holm, H, Mori, TA, Lieb, W, Franke, A, Ohlsson, C, Mellstrom, D, Cho, YS, Lee, H, Yuan, J-M, Koh, W-P, Rhee, SY, Olafsson, I, Woo, J-T, Heid, IM, Stark, KJ, Volzke, H, Homuth, G, Evans, MK, Zonderman, AB, Polasek, O, Pasterkamp, G, Hoefer, IE, Kanoni, Stavroula, Akiyama, M, Redline, S, Pahkala, K, Oldehinkel, AJ, Snieder, H, Biino, G, Schmidt, R, Schmidt, H, Chen, YE, Bandinelli, S, Dedoussis, G, Sakaue, S, Thanaraj, TA, Kardia, SLR, Kato, N, Schulze, MB, Girotto, G, Jung, B, Boger, CA, Joshi, PK, Bennett, DA, De Jager, PL, Terao, C, Lu, X, Mamakou, V, Brown, M, Caulfield, MJ, Munroe, PB, Guo, X, Ciullo, M, Jonas, JB, Samani, NJ, Kaprio, J, Kanai, M, Pajukanta, P, Adair, LS, Bechayda, SA, de Silva, HJ, Wickremasinghe, AR, Krauss, RM, Wu, J-Y, Zheng, W, den Hollander, A, Bharadwaj, D, Zhou, W, Correa, A, Wilson, JG, Lind, L, Heng, C-K, Nelson, AE, Golightly, YM, Wilson, JF, Penninx, B, Kim, H-L, Attia, John, Brumpton, BM, Scott, Rodney J., Rao, DC, Arnett, DK, Walker, M, Koistinen, HA, Chandak, GR, Yajnik, CS, Mercader, JM, Tusie-Luna, T, Aguilar-Salinas, CA, Rasheed, H, Villalpando, CG, Orozco, L, Fornage, M, Tai, ES, van Dam, RM, Lehtimaki, T, Chaturvedi, N, Yokota, M, Liu, J, Reilly, DF, Ruotsalainen, SE, McKnight, AJ, Kee, F, Jockel, K-H, McCarthy, M, Palmer, CNA, Vitart, V, Hayward, C, Simonsick, E, van Duijn, CM, Lu, F, Havulinna, AS, Qu, J, Hishigaki, H, Lin, X, Marz, W, Parra, EJ, Cruz, M, Gudnason, V, Tardif, J-C, Lettre, G, 't Hart, LM, Veturi, Y, Elders, PJM, Damrauer, SM, Kumari, M, Kivimaki, M, van der Harst, P, Spector, TD, Loos, RJF, Province, MA, Psaty, BM, Brandslund, I, Zajac, Greg J. M., Feng, Q, Pramstaller, PP, Christensen, K, Ripatti, S, Widen, E, Hakonarson, H, Grant, SFA, Kiemeney, LALM, de Graaf, J, Loeffler, M, Kronenberg, F, Rosenthal, EA, Gu, D, Erdmann, J, Schunkert, H, Franks, PW, Linneberg, A, Jukema, JW, Khera, A, Mannikko, M, Jarvelin, M-R, Kutalik, Z, Lingren, T, Cucca, F, Mook-Kanamori, DO, van Dijk, KW, Watkins, H, Strachan, DP, Grarup, N, Sever, P, Poulter, N, Rotter, J, Dantoft, TM, Pacheco, JA, Karpe, F, Neville, MJ, Timpson, NJ, Cheng, C-Y, Wong, T-Y, Khor, CC, Sabanayagam, C, Peters, A, Gieger, C, Hattersley, AT, Pendergrass, SA, Pedersen, NL, Magnusson, PKE, Boomsma, D, de Geus, EJC, Cupples, LA, van Meurs, JBJ, Ghanbari, M, Rsen, PG-L, Huang, W, Kim, YJ, Haessler, J, Tabara, Y, Wareham, NJ, Langenberg, C, Zeggini, E, Kuusisto, J, Laakso, M, Ingelsson, E, Abecasis, G, Chambers, JC, Kooner, JS, Giulianini, F, de Vries, PS, Morrison, AC, North, KE, Daviglus, M, Kraft, P, Martin, NG, Whitfield, JB, Abbas, S, Saleheen, D, Walters, RG, Bradford, Y, Holmes, M, Black, C, Smith, BH, Justice, AE, Baras, A, Buring, JE, Ridker, PM, Chasman, D, Kooperberg, C, Wei, W-Q, Miller, JE, Jarvik, GP, Namjou, B, Hayes, MG, Ritchie, MD, Jousilahti, P, Salomaa, V, Hveem, K, Asvold, BO, Kubo, M, Kamatani, Y, Campbell, A, Okada, Y, Murakami, Y, Thorsteinsdottir, U, Stefansson, K, Ho, Y-L, Lynch, JA, Rader, DJ, Tsao, PS, Chang, K-M, Cho, K, Ramdas, Shweta, Lin, K, O'Donnell, CJ, Gaziano, JM, Wilson, P, Rotimi, CN, Hazelhurst, S, Ramsay, M, Trembath, RC, van Heel, DA, Tamiya, G, Yamamoto, M, Millwood, IY, Kim, B-J, Mohlke, KL, Frayling, TM, Hirschhorn, JN, Kathiresan, S, Boehnke, M, Natarajan, P, Peloso, GM, Brown, CD, Morris, AP, Hindy, G, Assimes, TL, Deloukas, P, Sun, Y, Willer, CJ, Rasheed, A, Faul, JD, Zhao, W, Weir, DR, Turman, C, Huang, H, Graff, M, Surakka, Ida, Mahajan, A, Brown, MR, Zhang, W, Yu, K, Schmidt, EM, Pandit, A, Gustafsson, S, Yin, X, Luan, J, Zhao, J-H, Ntalla, Ioanna, Matsuda, F, Jang, H-M, Yoon, K, Medina-Gomez, C, Pitsillides, A, Hottenga, JJ, Willemsen, G, Wood, AR, Ji, Y, Gao, Z, Vedantam, Sailaja, Haworth, S, Mitchell, RE, Chai, JF, Aadahl, M, Yao, J, Manichaikul, A, Warren, HR, Ramirez, J, Bork-Jensen, J, Karhus, LL, Winkler, Thomas W., Goel, A, Sabater-Lleal, M, Noordam, R, Sidore, C, Fiorillo, E, McDaid, AF, Marques-Vidal, P, Wielscher, M, Trompet, S, Sattar, N. Nature Publishing Group; 2021. The power of genetic diversity in genome-wide association studies of lipids.

Holliday, Elizabeth G., Traylor, Matthew, Sudlow, Cathie, Rothwell, Peter M., Coresh, Josef, Hamet, Pavel, Tremblay, Johanne, Turner, Stephen T., de Andrade, Mariza, Rao, Madhumathi, Schmidt, Reinhold, Crick, Peter A., Malik, Rainer, Robino, Antonietta, Peralta, Carmen A., Jukema, J. Wouter, Mitchell, Paul, Rosas, Silvia E., Wang, Jie Jin, Scott, Rodney J., Dichgans, Martin, Mitchell, Braxton D., Kao, W. H. Linda, Bevan, Stephen, Fox, Caroline S., Levi, Christopher, Attia, John, Markus, Hugh S., , Maguire, Jane, Koblar, Simon A., Sturm, Jonathan, Hankey, Graeme J., Oldmeadow, Christopher, McEvoy, Mark. Lippincott Williams & Wilkins; 2014. Polygenic overlap between kidney function and large artery atherosclerotic stroke.

Jakubowska, Anna, Gronwald, Jacek, Eils, Roland, Lubińki, Jan, Scott, Rodney J., Hamann, Ute, Menkiszak, Janusz, Górski, Bohdan, Huzarski, Tomasz, Byrski, Tomasz, Toloczko-Grabarek, Aleksandra, Gilbert, Michael, Edler, Lutz, Zapatka, Marc. Springer; 2010. BRCA1-associated breast and ovarian cancer risks in Poland: no association with commonly studied polymorphisms.

Xavier, Alexandre, Scott, Rodney J., Talseth-Palmer, Bente. Wiley-Blackwell; 2021. Exome sequencing of familial adenomatous polyposis-like individuals identifies both known and novel causative genes.

Maltby, Vicki E., Lea, Rodney A., Burnard, Sean, Xavier, Alexandre, Van Cao, Thao, White, Nicole, Kennedy, Daniel, Groen, Kira, Sanders, Katherine A., Seeto, Rebecca, Bray, Samara, Gresle, Melissa, Laverick, Louise, Butzkueven, Helmut, Scott, Rodney J., Lechner-Scott, Jeannette. Nature Publishing Group; 2020. Epigenetic differences at the HTR2A locus in progressive multiple sclerosis patients.

Talseth, Bente A., Ashton, Katie A., Meldrum, Cliff, Suchy, Janina, Kurzawski, Grzegorz, Lubinski, Jan, Scott, Rodney J.. John Wiley & Sons; 2008. Aurora-A and Cyclin D1 polymorphisms and the age of onset of colorectal cancer in hereditary nonpolyposis colorectal cancer.

Hryhorowicz, Szymon, Kaczmarek-Rys, Marta, Zielinska, Aleksandra, Scott, Rodney J., Slomski, Ryszard, Plawski, Andrzej. Frontiers Research Foundation; 2021. Endocannabinoid System as a Promising Therapeutic Target in Inflammatory Bowel Disease – A Systematic Review.

Ritchie, Matthew E., Ruijie, Liu, Kilpatrick, Trevor J., Lechner-Scott, Jeannette, Moscato, Pablo, Perreau, Victoria M., Rubio, Justin P., Scott, Rodney J., Stankovich, Jim, Stewart, Graeme J., Taylor, Bruce V., Wiley, James, Carvalho, Benilton S., Booth, David R., Clarke, Glynnis, Cox, Mathew B., Csurhes, Peter A., Danoy, Patrick, Dickinson, Joanne L., Drysdale, Karen, Field, Judith, Greer, Judith M., Griffiths, Lyn R., Irizarry, Rafael A., Guru, Preethi, Hadler, Johanna, Hoban, Ella, McMorran, Brendan J., Jensen, Cathy J., Johnson, Laura J., McCallum, Ruth, Merriman, Marilyn, Merriman, Tony, Polanowski, Andrea, Bahlo, Melanie, Pryce, Karena, Tajouri, Lotfi, Whittock, Lucy, Wilkins, Ella J., Browning, Brian L., Browning, Sharon R., Perera, Devindri, Butzkueven, Helmut, Carroll, William M., Chapman, Caron, Booth, David R., Kermode, Allan G., Marriott, Mark, Mason, Deborah, Heard, Robert N., Pender, Michael P., Slee, Mark, Tubridy, Niall, Willoughby, Ernest, Broadley, Simon A., Brown, Matthew A., Foote, Simon J., Griffiths, Lyn R.. BioMed Central; 2011. Comparing genotyping algorithms for Illumina's Infinium whole-genome SNP BeadChips.

Köttgen, Anna, Albrecht, Eva, Yang, Qiong, Tanaka, Toshiko, Johnson, Andrew D., Kutalik, Zoltán, Smith, Albert V., Shi, Julia, Struchalin, Maksim, Middelberg, Rita P. S., Brown, Morris J., Gaffo, Angelo L., Teumer, Alexander, Oldmeadow, Christopher, Scott, Rodney J., Holliday, Elizabeth G., Attia, John, , , , , , , Vitart, Veronique, , , , , , , , , , , Krumsiek, Jan, , , , , , , , , , , Hundertmark, Claudia, , , , , , , , , , , Pistis, Giorgio, , , , , , , , , , , Ruggiero, Daniela, , , , , , , , , , , O'Seaghdha, Conall M., , , , , , , , , , , Haller, Toomas, , , , , , , , , , . Nature Publishing Group; 2013. Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.

Morten, Brianna C., Scott, Rodney J., Avery-Kiejda, Kelly A.. Public Library of Science (PLoS); 2016. Comparison of the QuantiGene 2.0 assay and real-time RT-PCR in the detection of p53 isoform mRNA expression in formalin-fixed paraffin-embedded tissues- a preliminary study.

Schache, Maria, Richardson, Andrea J., Sim, Xueling, Holliday, Elizabeth G., Attia, John, Scott, Rodney J., Baird, Paul N., Mitchell, Paul, Wang, Jie Jin, Rochtchina, Elena, Viswanathan, Anath C., Wong, Tien Y., Saw, Seang Mei, Topouzis, Fotis, Xie, Jing. Elsevier; 2013. Genetic association of refractive error and axial length with 15q14 but not 15q25 in the Blue Mountains Eye Study Cohort.

Derkacz, Róża, Marciniak, Wojciech, Jakubowska, Anna, Scott, Rodney J., Lubiński, Jan, Baszuk, Piotr, Wysokińska, Monika, Chrzanowska, Natalia, Lener, Marcin, Huzarski, Tomasz, Gronwald, Jacek, Dębniak, Tadeusz, Cybulski, Cezary. MDPI AG; 2024. Blood Cadmium Level Is a Marker of Cancer Risk in Men.

Paszkowska-Szczur, Katarzyna, Scott, Rodney J., Gapska, Paulina, Gromowski, Tomasz, Kładny, Józef, Lubiński, Jan, Dębniak, Tadeusz, Górski, Bohdan, Cybulski, Cezary, Kurzawski, Grzegorz, Dymerska, Dagmara, Gupta, Satish, van de Wetering, Thierry, Masojć, Bartłomiej, Kashyap, Aniruddh. Springer; 2015. Polymorphisms in nucleotide excision repair genes and susceptibility to colorectal cancer in the Polish population.

Milne, Elizabeth, Greenop, Kathryn R., Scott, Rodney J., Ashton, Lesley J., Cohn, Richard J., de Klerk, Nicholas H., Armstrong, Bruce K.. Wiley Blackwell Publishing; 2013. Parental smoking and risk of childhood brain tumors.

Loh, Po-Ro, Bhatia, Gaurav, Kendler, Kenneth S., O'Donovan, Michael, Neale, Benjamin M., Patterson, Nick, Price, Alkes L., Henskens, Frans A., Loughland, Carmel M., Michie, Patricia T., Schall, Ulrich, Scott, Rodney J., Gusev, Alexander, Tooney, Paul A., Wu, Jing Qin, Finucane, Hilary K., Bulik-Sullivan, Brendan K., Pollack, Samuela J., Schizophrenia Working Group of the Psychiatric Genomics Consortium,, de Candia, Teresa R., Lee, Sang Hong, Wray, Naomi R.. Nature Publishing; 2015. Contrasting genetic architectures of schizophrenia and other complex diseases using fast variance-components analysis.

Rush, Amanda, Christiansen, Jeffrey H., Farrell, Jake P., Goode, Susan M., Scott, Rodney J., Spring, Kevin J., Byrne, Jennifer A.. Mary Ann Liebert Publishers; 2015. Biobank classification in an Australian setting.

Pariyar, Mamta, Johns, Andrea, Thorne, Rick F., Scott, Rodney J., Avery-Kiejda, Kelly A.. Neoplasia Press; 2021. Copy number variation in triple negative breast cancer samples associated with lymph node metastasis.

Debniak, T., Scott, Rodney J., Huzarski, T., Byrski, T., Rozmiarek, A., Debniak, B., Zaluga, E., Maleszka, R., Kladny, J., Gorski, B., Cybulski, C., Gronwald, J., Kurzawski, G., Lubinski, J.. Waverly Press; 2005. CDKN2A common variants and their association with melanoma risk: A population-based study.

Liu, Xiaoman, Low, Siew-Kee, Michie, Patricia T., Catts, Stan V., Henskens, Frans, Pantelis, Christos, Loughland, Carmel, Boddy, Alan V., Tooney, Paul A., Scott, Rodney J., Carr, Vaughan J., Cairns, Murray J., Atkins, Joshua R., Wu, Jing Qin, Reay, William R., Cairns, Heath M., Green, Melissa J., Schall, Ulrich, Jablensky, Assen, Mowry, Bryan. Sage; 2020. Wnt receptor gene FZD1 was associated with schizophrenia in genome-wide SNP analysis of the Australian Schizophrenia Research Bank cohort.

Talseth-Palmer, Bente A., Bauer, Denis C., Sjursen, Wenche, Evans, Tiffany J., McPhillips, Mary, Proietto, Anthony, Otton, Geoffrey, Spigelman, Allan D., Scott, Rodney J.. John Wiley & Sons; 2016. Targeted next-generation sequencing of 22 mismatch repair genes identifies Lynch syndrome families.

The Schizophrenia Psychiatric Genome-Wide Association Study (GWAS) Consortium, Henskens, Frans A., Loughland, Carmel M., Michie, Patricia T., Schall, Ulrich, Scott, Rodney J.. Nature Publishing Group; 2011. Genome-wide association study identifies five new schizophrenia loci.

Feng, Yu Chen, Liu, Xiao Ying, Teng, Liu, Ji, Qiang, Wu, Yongyan, Li, Jin Ming, Gao, Wei, Zhang, Yuan Yuan, La, Ting, Tabatabaee, Hessam, Yan, Xu Guang, Jamaluddin, M. Fairuz B., Zhang, Didi, Guo, Su Tang, Scott, Rodney J., Liu, Tao, Thorne, Rick F., Zhang, Xu Dong, Jin, Lei. Nature Publishing Group; 2020. c-Myc inactivation of p53 through the pan-cancer lncRNA MILIP drives cancer pathogenesis.

Attia, John, Ioannidis, John P. A., Thakkinstian, Ammarin, McEvoy, Mark, Scott, Rodney J., Minelli, Cosetta, Thompson, John, Infante-Rivard, Claire, Guyatt, Gordon. American Medical Association; 2009. How to use an article about genetic association. C: what are the results and will they help me in caring for my patients?.

Cox, Mathew B., Cairns, Murray J., ANZgene Multiple Sclerosis Genetics Consortium, Gandhi, Kaushal S., Carroll, Adam P., Moscovis, Sophia, Stewart, Graeme J., Broadley, Simon, Scott, Rodney J., Booth, David R., Lechner-Scott, Jeannette. Public Library of Science; 2010. MicroRNAs miR-17 and miR-20a inhibit T cell activation genes and are under-expressed in MS whole blood.

Huckins, Laura M., Buccola, NG, Buckner, RL, Byerley, W, Cahn, W, Cai, G, Campion, D, Cantor, RM, Carr, VJ, Carrera, N, Catts, SV, Chambert, KD, Chan, RCK, Chen, RYL, Chen, EYH, Cheng, W, Cheung, EFC, Chong, SA, Cloninger, CR, Cohen, D, Cohen, N, Cormican, P, Craddock, N, Crowley, JJ, Curtis, D, Davidson, M, Davis, KL, Degenhardt, F, Del Favero, J, Demontis, D, Dikeos, D, Dinan, T, Djurovic, S, Donohoe, G, Drapeau, E, Duan, J, Dudbridge, F, Durmishi, N, Eichhammer, P, Eriksson, J, Dobbyn, Amanda, Boocock, James, Roussos, Panos, Fromer, Menachem, Kramer, Robin, Domenici, Enrico, Gamazon, Eric R., Purcell, Shaun, Johnson, Jessica S., Shah, Hardik R., Klein, Lambertus L., Ruderfer, Douglas M., Henskens, Frans A., Loughland, Carmel M., Schall, Ulrich, Michie, Patricia T., Scott, Rodney J., Gur, RE, Hahn, CG, Schadt, E, Lewis, DA, Haroutunian, V, Hoffman, Gabriel, Peters, MA, Lipska, BK, Buxbaum, JD, Hirai, K, Perumal, TM, Essioux, L, Ripke, S, Neale, BM, Corvin, A, Walters, JTR, Wang, Weiqing, Farh, KH, Holmans, PA, Lee, P, Bulik-Sullivan, B, Collier, DA, Huang, H, Pers, TH, Agartz, I, Agerbo, E, Albus, M, Pardiñas, Antonio F., Alexander, M, Amin, F, Bacanu, SA, Begemann, M, Belliveau, RA, Bene, J, Henskens, FA, Loughland, CM, Michie, PT, Schall, U, Rajagopal, Veera M., Scott, RJ, Als, Thomas D., Nguyen, Hoang T., Girdhar, Kiran. Nature Publishing Group; 2019. Gene expression imputation across multiple brain regions provides insights into schizophrenia risk.

Talseth-Palmer, Bente A., Wijnen, Juul T., Van Wezel, Tom, Vasen, Hans F. A., Scott, Rodney J., Andreassen, Eva K., Barker, Daniel, Jagmohan-Changur, Shantie, Tops, Carli M., Meldrum, Cliff, The Dutch Cancer Genetics Group, Spigelman, Allan, Hes, Frederik J.. BioMed Central; 2013. The importance of a large sample cohort for studies on modifier genes influencing disease severity in FAP patients.

Jakubowska, Anna, Menkiszak, Janusz, Gorski, Bohdan, Huzarski, Tomasz, Byrski, Tomasz, Benner, Axel, Lubinski, Jan, Scott, Rodney J., Hamann, Ute. BioMed Central; 2008. Ovarian cancer risk in Polish BRCA1 mutation carriers is not associated with the prohibitin 3' untranslated region polymorphism.

Petit, Joel, Carroll, Georgia, Gould, Tiffany, Pockney, Peter, Dun, Matthew, Scott, Rodney J.. Academic Press; 2019. Cell-free DNA as a Diagnostic Blood-Based Biomarker for Colorectal Cancer: A Systematic Review.

Grimson, Steven, Cox, Amanda J., Pringle, Kirsty G., Burns, Christine, Lumbers, Eugenie R., Blackwell, C. Caroline, Scott, Rodney J.. Wiley-Blackwell Publishing Asia; 2016. The prevalence of unique SNPs in the renin-angiotensin system highlights the need for pharmacogenetics in Indigenous Australians.

Evans, Tiffany-Jane, Milne, Elizabeth, Richardson, Ebony, Lavis, Laura, Catchpoole, Daniel, Attia, John R., Armstrong, Bruce K., Clavel, Jacqueline, Scott, Rodney J., Anderson, Denise, de Klerk, Nicholas H., Jamieson, Sarra E., Talseth-Palmer, Bente A., Bowden, Nikola A., Holliday, Elizabeth G., Rudant, Jéremié, Orsi, Laurent. Public Library of Science; 2014. Confirmation of childhood acute lymphoblastic leukemia variants, ARID5B and IKZF1, and interaction with parental environmental exposures.

Srinivasan, Saurabh, Bettella, Francesco, Mattingsdal, Morten, Wang, Yunpeng, Witoelar, Aree, Schork, Andrew J., Thompson, Wesley K., Zuber, Verena, Schizophrenia Working Group of the Psychiatric Genomics Consortium,, International Headache Genetics Consortium, Winsvold, Bendik S., Zwart, John-Anker, Collier, David A., Desikan, Rahul S., Melle, Ingrid, Werge, Thomas, Dale, Anders M., Djurovic, Srdjan, Andreassen, Ole A., Henskens, Frans A., Cairns, Murray J., Kelly, Brian J., Loughland, Carmel M., Schall, Ulrich, Tooney, Paul A., Mitchie, Patricia T., Scott, Rodney J.. Elsevier; 2016. Genetic markers of human evolution are enriched in schizophrenia.

Kho, Pik Fang, Wang, Xuemin, Cuellar-Partida, Gabriel, Dork, Thilo, Goode, Ellen L., Lambrechts, Diether, Scott, Rodney J., Spurdle, Amanda B., O'Mara, Tracy A., Glubb, Dylan M.. Nature Publishing Group; 2021. Multi-tissue transcriptome-wide association study identifies eight candidate genes and tissue-specific gene expression underlying endometrial cancer susceptibility.

Trubicka, Joanna, Grabowska-Kłujszo, Ewa, Gronwald, Jacek, Złowocka, Elżbieta, Kładny, Józef, Banaszkiewicz, Zbigniew, Wiśniowski, Rafał, Kowalska, Elżbieta, Lubinski, Jan, Scott, Rodney J., Suchy, Janina, Masojć, Bartłomiej, Serrano-Fernandez, Pablo, Kurzawski, Gregorz, Cybulski, Cezary, Górski, Bohdan, Huzarski, Tomasz, Byrski, Tomasz. Biomed Central; 2010. Variant alleles of the CYP1B1 gene are associated with colorectal cancer susceptibility.

Debniak, Tadeusz, Scott, Rodney J., Kashyap, Amiruddh, Lener, Marcin R., Malinska, Karolina, Rogoza, Emilia, Murawa, David, Rudnicka, Helena, Deptula, Jakub, Lubinski, Jan, Lea, Rodney A., Górski, Bohdan, Masojc, Bartlomiej, Cybulski, Cezary, Kram, Andrzej, Maleszka, Romuald, Gromowski, Tomasz, Paszkowska-Szczur, Katarzyna. Korean Cancer Association; 2019. Founder mutations for early onset melanoma as revealed by whole exome sequencing suggests that this is not associated with the increasing incidence of melanoma in Poland.

Griffin, Cassandra, Vilain, Ricardo, King, Simon, Nixon, Sandy, Gooley, Alisha, Bray, Samara, Lynam, James, Walker, Marjorie M., Scott, Rodney J., Paul, Christine. Sage; 2021. Mind Over Matter: Confronting Challenges in Post-Mortem Brain Biobanking for Glioblastoma Multiforme.

Green, Melissa J., Raudino, Alessandra, Cairns, Murray J., Wu, Jingqin, Tooney, Paul A., Scott, Rodney J., Carr, Vaughn J.. Elsevier; 2015. Do common genotypes of FK506 binding protein 5 (FKBP5) moderate the effects of childhood maltreatment on cognition in schizophrenia and healthy controls?.

Moir-Meyer, Gemma L., Pearson, John F., Pharoah, Paul D., Dunning, Alison M., Thompson, Deborah J., Easton, Douglas F., Spurdle, Amanda B., Walker, Logan C., Lose, Felicity, The Australian National Endometrial Cancer Study Group,, Scott, Rodney J., McEvoy, Mark, Attia, John, Holliday, Elizabeth G., The Hunter Community Study,, Studies of Epidemiology and Risk Factors in Cancer Heredity,. Springer; 2015. Rare germline copy number deletions of likely functional importance are implicated in endometrial cancer predisposition.

Baszuk, Piotr, Janasik, Beata, Grodzki, Tomasz, Wójcik, Janusz, Wojtyś, Małgorzata, Dębniak, Tadeusz, Cybulski, Cezary, Gronwald, Jacek, Kubisa, Bartosz, Wójcik, Norbert, Pieróg, Jarosław, Gajić, Darko, Pietrzak, Sandra, Scott, Rodney J., Scott, RJ, Wąsowicz, W, Jakubowska, A, Lubiński, J, Lener, MR, Marciniak, Wojciech, Reszka, Edyta, Białkowska, Katarzyna, Jabłońska, Ewa, Muszyńska, Magdalena, Lesicka, Monika, Derkacz, Róża. Springer; 2021. Lung Cancer Occurrence—Correlation with Serum Chromium Levels and Genotypes.

Scott, Rodney J., McPhillips, Mary, Meldrum, Cliff J., Fitzgerald, Patrick E., Adams, Kirsten, Spigelman, Allan D., du Sart, Desiree, Tucker, Kathy, Kirk, Judy, Hunter Family Cancer Service,. University of Chicago Press; 2001. Hereditary non polyposis colorectal cancer in 95 families: differences and similarities between mutation-positive and mutation-negative kindreds.

Schijven, Dick, Postema, Merel C., Ayesa-Arriola, Rosa, Fazio, L, Pergola, G, Bertolino, A, Díaz-Caneja, CM, Janssen, J, Lois, NG, Arango, C, Tomyshev, AS, Lebedeva, I, Cervenka, S, Ortiz-García de la Foz, Victor, Sellgren, CM, Georgiadis, F, Kirschner, M, Kaiser, S, Hajek, T, Skoch, A, Spaniel, F, Kim, M, Kwak, YB, Oh, S, Tordesillas-Gutierrez, Diana, Kwon, JS, James, A, Bakker, G, Knöchel, C, Stäblein, M, Oertel, V, Uhlmann, A, Howells, FM, Stein, DJ, Temmingh, HS, Vázquez-Bourgon, Javier, Diaz-Zuluaga, AM, Pineda-Zapata, JA, López-Jaramillo, C, Homan, S, Ji, E, Surbeck, W, Homan, P, Fisher, SE, Franke, B, Glahn, DC, Crespo-Facorro, Benedicto, Gur, RC, Hashimoto, R, Jahanshad, N, Luders, E, Medland, SE, Thompson, PM, Turner, JA, van Erp, TGM, Francks, C, Alnæs, Dag, Dahl, Andreas, Westlye, Lars T., Agartz, Ingrid, Andreassen, Ole A., Fukunaga, Masaki, Jönsson, EG, Kochunov, P, Bruggemann, JM, Catts, SV, Michie, Patricia T., Mowry, BJ, Quidé, Y, Rasser, Paul E., Schall, Ulrich, Scott, Rodney J., Matsumoto, Junya, Carr, VJ, Green, MJ, Henskens, Frans A., Loughland, Carmel M., Pantelis, C, Weickert, CS, Weickert, TW, de Haan, L, Brosch, K, Pfarr, J-K, Miura, Kenichiro, Ringwald, KG, Stein, F, Jansen, A, Kircher, TTJ, Nenadić, I, Krämer, B, Gruber, O, Satterthwaite, TD, Bustillo, J, Mathalon, DH, de Zwarte, Sonja M. C., Preda, A, Calhoun, VD, Ford, JM, Potkin, SG, Chen, J, Tan, Y, Wang, Z, Xiang, H, Fan, F, Bernardoni, F, van Haren, Neeltje E. M., Ehrlich, S, Fuentes-Claramonte, P, Garcia-Leon, MA, Guerrero-Pedraza, A, Salvador, R, Sarró, S, Pomarol-Clotet, E, Ciullo, V, Piras, F, Vecchio, D, Cahn, Wiepke, Banaj, N, Spalletta, G, Michielse, S, van Amelsvoort, T, Dickie, EW, Voineskos, AN, Sim, K, Ciufolini, S, Dazzan, P, Murray, RM, Hulshoff Pol, Hilleke E., Kim, W-S, Chung, Y-C, Andreou, C, Schmidt, A, Borgwardt, S, McIntosh, AM, Whalley, HC, Lawrie, SM, du Plessis, S, Luckhoff, HK, Kahn, Rene S., Scheffler, F, Emsley, R, Grotegerd, D, Lencer, R, Dannlowski, U, Edmond, JT, Rootes-Murdy, K, Stephen, JM, Mayer, AR, Antonucci, LA. National Academy of Sciences; 2023. Large-scale analysis of structural brain asymmetries in schizophrenia via the ENIGMA consortium.

Rhead, Brooke, Brorson, Ina S., Lea, Rodney A., Burnard, Sean, Maltby, Vicki E., Scott, Rodney J., Lechner-Scott, Jeannette, Harbo, Hanne F., Bos, Steffan D., Barcellos, Lisa F., Berge, Tone, Adams, Cameron, Quach, Hong, Moen, Stine Marit, Berg-Hansen, Pål, Celius, Elizabeth Gulowsen, Sangurdekar, Dipen P., Bronson, Paola G.. Public Library of Science; 2018. Increased DNA methylation of SLFN12 in CD4⁺ and CD8⁺ T cells from multiple sclerosis patients.

Attia, John, Ioannidis, John P. A., Thakkinstian, Ammarin, McEvoy, Mark, Scott, Rodney J., Minelli, Cosetta, Thompson, John, Infante-Rivard, Claire, Guyatt, Gordon. American Medical Association; 2009. How to use an article about genetic association. A: background concepts.

Davies, Gail, Lam, Max, Liewald, David C. M., Knopman, DS, Kochan, NA, Konte, B, Kwok, JB, Le Hellard, S, Lee, T, Lehtimaki, T, Li, S-C, Liu, T, Koini, M, Okely, Judith A., London, E, Longstreth, WT, Lopez, OL, Loukola, A, Luck, T, Lundervold, AJ, Lundquist, A, Lyytikainen, L-P, Martin, NG, Montgomery, GW, Ahola-Olli, Ari V., Murray, AD, Need, AC, Noordam, R, Nyberg, L, Ollier, W, Papenberg, G, Pattie, A, Polasek, O, Poldrack, RA, Psaty, BM, Barnes, Catriona L. K., Reppermund, S, Riedel-Heller, SG, Rose, RJ, Rotter, JI, Roussos, P, Rovio, SP, Saba, Y., Sabb, FW, Sachdev, PS, Satizabal, CL, Bertram, Lars, Schmid, M, Scott, Rodney J., Scult, MA, Simino, J, Slagboom, PE, Smyrnis, N, Soumare, A, Stefanis, NC, Stott, DJ, Straub, RE, Bis, Joshua C., Sundet, K, Taylor, AM, Taylor, KD, Tzoulaki, I, Tzourio, C, Uitterlinden, A, Vitart, V, Voineskos, AN, Kaprio, J, Wagner, M, Burdick, Katherine E., Wagner, H, Weinhold, L, Wen, KH, Widen, E, Yang, Q, Zhao, W, Adams, HHH, Arking, DE, Bilder, RM, Bitsios, P, Christoforou, Andrea, Boerwinkle, E, Chiba-Falek, O, Corvin, A, De Jager, PL, Debette, S, Donohoe, G, Elliott, P, Fitzpatrick, AL, Gill, M, Glahn, DC, DeRosse, Pamela, Hagg, S, Hansell, NK, Hariri, AR, Ikram, MK, Jukema, JW, Vuoksimaa, E, Keller, MC, Kremen, WS, Launer, L, Lindenberger, U, Djurovic, Srdjan, Palotie, A, Pedersen, NL, Pendleton, N, Porteous, DJ, Raikkonen, K, Raitakari, OT, Ramirez, A, Reinvang, I, Rudan, I, Rujescu, D, Harris, Sarah E., Espeseth, Thomas, Schmidt, R, Schmidt, H, Schofield, PW, Schofield, PR, Starr, JM, Steen, VM, Trollor, JN, Turner, ST, Van Duijn, CM, Villringer, A, Giakoumaki, Stella, Weinberger, DR, Weir, DR, Wilson, JF, Malhotra, A, McIntosh, AM, Gale, CR, Seshadri, S, Mosley, TH, Bressler, J, Lencz, T, Giddaluru, S, Deary, IJ, Gustavson, DE, Hayward, C, Hofer, E, Ikram, MA, Karlsson, R, Knowles, E, Lahti, J, Trampush, Joey W., Leber, M, Li, S, Mather, KA, Melle, I, Morris, D, Oldmeadow, Christopher, Palviainen, T, Payton, A, Pazoki, R, Petrovic, K, Luciano, Michelle, Reynolds, CA, Sargurupremraj, M, Scholz, M, Smith, JA, Smith, AV, Terzikhan, N, Thalamuthu, A, Trompet, S, van der Lee, SJ, Ware, EB, Hill, W. David, Windham, BG, Wright, MJ, Yang, J, Yu, J, Ames, D, Amin, N, Amouyel, P, Andreassen, OA, Armstrong, NJ, Assareh, AA, Hagenaars, Saskia P., Attia, John R., Attix, D, Avramopoulos, D, Bennett, DA, Boehmer, AC, Boyle, PA, Brodaty, H, Campbell, H, Cannon, TD, Cirulli, ET, Ritchie, Stuart J., Congdon, E, Conley, ED, Corley, J, Cox, SR, Dale, AM, Dehghan, A, Dick, D, Dickinson, D, Eriksson, JG, Evangelou, E, Marioni, Riccardo E., Faul, JD, Ford, I, Freimer, NA, Gao, H, Giegling, I, Gillespie, NA, Gordon, SD, Gottesman, RF, Griswold, ME, Gudnason, V, Fawns-Ritchie, Chloe, Harris, TB, Hartmann, AM, Hatzimanolis, A, Heiss, G, Holliday, Elizabeth G., Joshi, PK, Kahonen, M, Kardia, SLR, Karlsson, I, Kleineidam, L. Nature Publishing Group; 2018. Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function.

Cheng, Timothy H. T., Thompson, Deborah, Hopper, John, Tomlinson, Ian, Jenkins, Mark, Lindor, Noralane M., Newcomb, Polly A., Gallinger, Steve, Conti, David, Schumacher, Fred, Casey, Graham, Giles, Graham G., Pharoah, Paul, Painter, Jodie, Peto, Julian, Cox, Angela, Swerdlow, Anthony, Couch, Fergus, Cunningham, Julie M., Goode, Ellen L., Winham, Stacey J., Lambrechts, Diether, Fasching, Peter, Burwinkel, Barbara, O'Mara, Tracy, Brenner, Hermann, Brauch, Hiltrud, Chang-Claude, Jenny, Salvesen, Helga B., Kristensen, Vessela, Darabi, Hatef, Li, Jingmei, Liu, Tao, Lindblom, Annika, Hall, Per, Gorman, Maggie, de Polanco, Magdalena Echeverry, Sans, Monica, Carracedo, Angel, Castellvi-Bel, Sergi, Rojas-Martinez, Augusto, Aguiar Jnr, Samuel, Teixeira, Manuel R., Dunning, Alison M., Dennis, Joe, Otton, Geoffrey, Martin, Lynn, Proietto, Tony, Holliday, Elizabeth, Attia, John, Ashton, Katie, Scott, Rodney J., McEvoy, Mark, Dowdy, Sean C., Fridley, Brooke L., Werner, Henrica M. J., Trovik, Jone, Palles, Claire, Njolstad, Tormund S., Tham, Emma, Mints, Miriam, Runnebaum, Ingo, Hillemanns, Peter, Dörk, Thilo, Amant, Frederic, Schrauwen, Stefanie, Hein, Alexander, Beckmann, Matthias W., Jones, Angela, Ekici, Arif, Czene, Kamila, Meindl, Alfons, Bolla, Manjeet K., Michailidou, Kyriaki, Tyrer, Jonathan P., Wang, Qin, Ahmed, Shahana, Healey, Catherine S., Shah, Mitul, Buchanan, Daniel D., Annibali, Daniela, Depreeuw, Jeroen, Al-Tassan, Nada A., Harris, Rebecca, Meyer, Brian F., Whiffin, Nicola, Hosking, Fay J., Kinnersley, Ben, Farrington, Susan M., Timofeeva, Maria, Ko Win, Aung, Tenesa, Albert, Campbell, Harry, Haile, Robert W., Hodgson, Shirley, Carvajal-Carmona, Luis, Cheadle, Jeremy P., Easton, Douglas, Dunlop, Malcolm, Houlston, Richard, Spurdle, Amanda. Nature Publishing Group; 2015. Meta-analysis of genome-wide association studies identifies common susceptibility polymorphisms for colorectal and endometrial cancer near SH2B3 and TSHZ1.

Bolton, Katherine A., Holliday, Elizabeth G., Attia, John, Bowden, Nikola A., Avery-Kiejda, Kelly A., Scott, Rodney J.. BioMed Central; 2016. A novel polymorphic repeat in the upstream regulatory region of the estrogen-induced gene EIG121 is not associated with the risk of developing breast or endometrial cancer.

Maltby, Vicki E., Graves, Moira C., Lea, Rodney A., Benton, Miles C., Sanders, Katherine A., Tajouri, Lotti, Scott, Rodney J., Lechner-Scott, Jeannette. BioMed Central; 2015. Genome-wide DNA methylation profiling of CD8+T cells shows a distinct epigenetic signature to CD4+T cells in multiple sclerosis patients.

Smith, Casey J. A., Crock, Patricia A., King, Bruce R., Meldrum, Cliff J., Scott, Rodney J.. American Diabetes Association; 2004. Phenotype-genotype correlations in a series of Wolfram syndrome families.

Xavier, Alexandre, Olsen, Maren Fridtjofsen, Lavik, Liss A., Johansen, Jostein, Singh, Ashish Kumar, Sjursen, Wenche, Scott, Rodney J., Talseth-Palmer, Bente A.. John Wiley & Sons; 2019. Comprehensive mismatch repair gene panel identifies variants in patients with Lynch-like syndrome.

Avery-Kiejda, Kelly A., Mathe, Andrea, Scott, Rodney J.. Elsevier; 2017. Genome-wide miRNA, gene and methylation analysis of triple negative breast cancer to identify changes associated with lymph node metastases.

Kiljanczyk, Adam, Matuszczak, Milena, Huzarski, Tomasz, Lener, Marcin R., Jakubowska, Anna, Cheriyan, Angela, Szwiec, Marek, Stawicka-Nielacna, Malgorzata, Godlewski, Dariusz, Prusaczyk, Artur, Jasiewicz, Andrzej, Kluz, Tomasz, Marciniak, Wojciech, Tomiczek-Szwiec, Joanna, Kilar-Kobierzycka, E, Siolek, M, Wisniowski, R, Posmyk, R, Jarkiewicz-Tretyn, J, Sun, P, Scott, Rodney J., Narod, SA, Lubinski, J, Derkacz, Roza, Stempa, Klaudia, Baszuk, Piotr, Bryskiewicz, Marta, Cybulski, Cezary, Debniak, Tadeusz, Gronwald, Jacek. MDPI AG; 2024. Blood Iodine as a Potential Marker of the Risk of Cancer in BRCA1 Carriers.

Xavier, Alexandre, Campagna, Maria Pia, Lechner-Scott, Jeannette, Ausimmune Investigator Group,, Maltby, Vicki E., Kilpatrick, Trevor, Taylor, Bruce V., Butzkueven, Helmut, Ponsonby, Anne-Louise, Scott, Rodney J., Jokubaitis, Vilija G., Lea, Rodney A.. Frontiers Research Foundation; 2023. Interferon beta treatment is a potent and targeted epigenetic modifier in multiple sclerosis.

Groen, Kira, Maltby, Vicki E., Sanders, Katherine A., Scott, Rodney J., Tajouri, Lotti, Lechner-Scott, Jeannette. Sage; 2016. Erythrocytes in multiple sclerosis - forgotten contributors to the pathophysiology?.

Rootes-Murdy, Kelly, Panta, Sandeep, Green, Melissa J., Henskens, Frans, Kiltschewskij, Dylan, Michie, Patricia T., Mowry, Bryan, Pantelis, Christos, Rasser, Paul E., Reay, William R., Schall, Ulrich, Scott, Rodney J., Kelly, Ross, Watkeys, Oliver J., Roberts, G, Mitchell, P, Fullerton, JM, Overs, BJ, Kikuchi, M, Hashimoto, R, Matsumoto, J, Fukunaga, M, Sachdev, PS, Romero, Javier, Brodaty, H, Wen, W, Jiang, J, Fani, N, Ely, TD, Lorio, A, Stevens, JS, Ressler, K, Jovanovic, T, van Rooij, SJH, Quidé, Yann, Federmann, LM, Jockwitz, C, Teumer, A, Forstner, AJ, Caspers, S, Cichon, S, Plis, SM, Sarwate, AD, Calhoun, VD, Cairns, Murray J., Loughland, Carmel, Carr, Vaughan J., Catts, Stanley V., Jablensky, Assen. Cell Press; 2024. Cortical similarities in psychiatric and mood disorders identified in federated VBM analysis via COINSTAC.

Masson, Amy L., Talseth-Palmer, Bente A., Evans, Tiffany-Jane, McElduff, Patrick, Spigelman, Allan D., Hannan, Garry N., Scott, Rodney J.. Elsevier; 2016. Copy number variants associated with 18p11.32, DCC and the promoter 1B region of APC in colorectal polyposis patients.

Rammos, Alexandros, Gonzalez, Lara A. Neira, Weinberger, Daniel R., Mitchell, Kevin J., Nicodemus, Kristin K., Ripke, Stephan, Neale, Benjamin M., Corvin, Aiden, Walters, James T. R., Farh, Kai-How, Holmans, Peter A., Lee, Phil, Bulik-Sullivan, Brendan, Collier, David, Huang, Hailiang, Pers, Tune H., Agartz, Ingrid, Agerbo, Esben, Albus, Margot, Alexander, Madeline, Amin, Farooq, Bacanu, Silviu, Begemann, Martin, Belliveau, Richard, Bene, Judit, Cairns, Murray J., Henskens, Frans A., Kelly, Brian J., Loughland, Carmel M., Michie, Patricia T., Schall, Ulrich, Scott, Rodney J., Tooney, Paul A., Wu, Jing Qin. Nature Publishing Group; 2019. The role of polygenic risk score gene-set analysis in the context of the omnigenic model of schizophrenia.

Chan, Jessica P. L., Thalamuthu, Anbupalam, Reppermund, Simone, Menant, Jasmine, Trollor, Julian N., Brodaty, Henry, Schofield, Peter R., Attia, John R., Sachdev, Perminder S., Scott, Rodney J., Mather, Karen A., Oldmeadow, Christopher, Armstrong, Nicola J., Holliday, Elizabeth G., McEvoy, Mark, Kwok, John B., Assareh, Amelia A., Peel, Rosanne, Hancock, Stephen J.. Springer; 2015. Genetics of hand grip strength in mid to late life.

Groen, Kira, Maltby, Vicki E., Lea, Rodney A., Sanders, Katherine A., Fink, J. Lynn, Scott, Rodney J., Tajouri, Lotti, Lechner-Scott, Jeannette. BioMed Central; 2018. Erythrocyte microRNA sequencing reveals differential expression in relapsing-remitting multiple sclerosis.

Xavier, Alexandre, Scott, Rodney J., Talseth-Palmer, Bente A.. Public Library of Science (PLoS); 2019. TAPES: A tool for assessment and prioritisation in exome studies.

Blackwell, Caroline, Moscovis, Sophia, Hall, Sharron, Burns, Christine, Scott, Rodney J.. Frontiers Research Foundation; 2015. Exploring the risk factors for sudden infant deaths and their role in inflammatory responses to infection.

Hess, Jonathan L., Mattheisen, Manuel, Henskens, Frans A., Kelly, Brian J., Loughland, Carmel M., Michie, Patricia T., Schall, Ulrich, Scott, Rodney J., Tooney, Paul A., Schizophrenia Working Group of the Psychiatric Genomics Consortium,, Greenwood, Tiffany A., Tsuang, Ming T., Edenberg, Howard J., Holmans, Peter, Faraone, Stephen V., Glatt, Stephen J., Cairns, Murray J.. Wiley; 2023. A polygenic resilience score moderates the genetic risk for schizophrenia: Replication in 18,090 cases and 28,114 controls from the Psychiatric Genomics Consortium.

Wong, Michelle W., Nordfors, Cecilia, Mossman, David, Pecenpetelovska, Gordana, Avery-Kiejda, Kelly A., Talseth-Palmer, Bente, Bowden, Nikola A., Scott, Rodney J.. Springer; 2011. BRIP1, PALB2, and RAD51C mutation analysis reveals their relative importance as genetic susceptibility factors for breast cancer.

Weidenhofer, Judith, Bowden, Nikola A., Scott, Rodney J., Tooney, Paul A.. Academic Press - Elsevier; 2006. Altered gene expression in the amygdala in schizophrenia: up-regulation of genes located in the cytomatrix active zone.

Groen, Kira, Maltby, Vicki E., Scott, Rodney J., Tajouri, Lotti, Lechner-Scott, Jeannette. John Wiley & Sons; 2020. Erythrocyte microRNAs show biomarker potential and implicate multiple sclerosis susceptibility genes.

Mathe, Andrea, Wong-Brown, Michelle, Morten, Brianna, Forbes, John F., Braye, Stephen G., Avery-Kiejda, Kelly A., Scott, Rodney J.. Nature Publishing Group; 2015. Novel genes associated with lymph node metastasis in triple negative breast cancer.

Dębniak, Tadeusz, Gromowski, Tomasz, Cybulski, Cezary, Serrano-Fernandez, Pablo, Lubiński, Jan, Scott, Rodney J., Gronwald, Jacek, Huzarski, Tomasz, Byrski, Tomasz, Kurzawski, Grzegorz, Dymerska, Dagmara, Górski, Bohdan, Paszkowska-Szczur, Katarzyna. BioMed Central; 2015. Management of ovarian and endometrial cancers in women belonging to HNPCC carrier families: review of the literature and results of cancer risk assessment in Polish HNPCC families.

Cox, Mathew B., Bowden, Nikola A., Scott, Rodney J., Lechner-Scott, Jeannette. Sage; 2013. Altered expression of the plasminogen activation pathway in peripheral blood mononuclear cells in multiple sclerosis: possible pathomechanism of matrix metalloproteinase activation.

Yengo, Loïc, Vedantam, Sailaja, Miao, Jenkai, Gustafsson, S, Haessler, J, Hansen, TF, Havulinna, AS, Haworth, SJ, He, J, Heard-Costa, N, Hebbar, P, Hindy, G, Ho, Y-LA, Arias, Joshua D., Hofer, E, Holliday, Elizabeth, Horn, K, Hornsby, WE, Hottenga, J-J, Huang, H, Huang, J, Huerta-Chagoya, A, Huffman, JE, Hung, Y-J, Graham, Sarah E., Huo, S, Hwang, MY, Iha, H, Ikeda, DD, Isono, M, Jackson, AU, Jager, S, Jansen, IE, Johansson, I, Jonas, JB, Mukamel, Ronen E., Jonsson, A, Jorgensen, T, Kalafati, I-P, Kanai, M, Kanoni, S, Karhus, LL, Kasturiratne, A, Katsuya, T, Kawaguchi, T, Kember, RL, Spracklen, Cassandra N., Kentistou, KA, Kim, H-N, Kim, YJ, Kleber, ME, Knol, MJ, Kurbasic, A, Lauzon, M, Le, P, Lea, R, Lee, J-Y, Yin, Xianyong, Leonard, HL, Li, SA, Li, X, Li, X, Liang, J, Lin, H, Lin, S-Y, Liu, J, Liu, X, Lo, KS, Chen, Shyh-Huei, Long, J, Lores-Motta, L, Luan, J, Lyssenko, V, Lyytikainen, L-P, Mahajan, A, Mamakou, V, Mangino, M, Manichaikul, A, Marten, J, Ferreira, Teresa, Mattheisen, M, Mavarani, L, McDaid, AF, Meidtner, K, Melendez, TL, Mercader, JM, Milaneschi, Y, Miller, JE, Millwood, IY, Mishra, PP, Highland, Heather H., Mitchell, RE, Mollehave, LT, Morgan, A, Mucha, S, Munz, M, Nakatochi, M, Nelson, CP, Nethander, M, Nho, CW, Nielsen, AA, Ji, Yingjie, Nolte, IM, Nongmaithem, SS, Noordam, R, Ntalla, I, Nutile, T, Pandit, A, Christofidou, P, Parna, K, Pauper, M, Petersen, ERB, Marouli, Eirini, Karaderi, Tugce, Petersen, L, Pitkanen, N, Polasek, O, Poveda, A, Preuss, MH, Pyarajan, S, Raffield, LM, Rakugi, H, Ramirez, J, Rasheed, A, Lin, K, Raven, D, Rayner, NW, Riveros, Carlos, Rohde, R, Ruggiero, D, Ruotsalainen, SE, Ryan, KA, Sabater-Lleal, M, Saxena, R, Scholz, M, Lull, K, Sendamarai, A, Shen, B, Shi, J, Shin, JH, Sidore, C, Sitlani, CM, Slieker, RKC, Smit, RAJ, Smith, A, Smith, JA, Malden, DE, Smyth, LJ, Southam, LE, Steinthorsdottir, V, Sun, L, Takeuchi, F, Tallapragada, D, Taylor, KD, Tayo, BO, Tcheandjieu, C, Terzikhan, N, Medina-Gomez, C, Tesolin, P, Teumer, A, Theusch, E, Thompson, DJ, Thorleifsson, G, Timmers, PRHJ, Trompet, S, Turman, C, Vaccargiu, S, van der Laan, SW, Machado, M, van der Most, PJ, van Klinken, JB, van Setten, J, Verma, SS, Verweij, N, Veturi, Y, Wang, Carol A., Wang, C, Wang, L, Wang, Z, Moore, A, Warren, HR, Wei, WB, Wickremasinghe, AR, Wielscher, M, Wiggins, KL, Winsvold, BS, Wong, A, Wu, Y, Wuttke, M, Xia, R, Rueger, S, Xie, T, Yamamoto, K, Yang, J, Yao, J, Young, H, Yousri, NA, Yu, L, Zeng, L, Zhang, W, Zhang, X, Sim, X, Zhao, J-H, Zhao, W, Zhou, W, Zimmermann, ME, Zoledziewska, M, Adair, LS, Adams, HHH, Aguilar-Salinas, CA, Al-Mulla, F, Arnett, DK, Vrieze, S, Asselbergs, FW, Asvold, BO, Attia, John, Banas, B, Bandinelli, S, Bennett, DA, Bergler, T, Bharadwaj, D, Biino, G, Bisgaard, H, Sidorenko, Julia, Ahluwalia, TS, Boerwinkle, E, Boger, CA, Bonnelykke, K, Boomsma, D, Borglum, AD, Borja, JB, Bouchard, C, Bowden, DW, Brandslund, I, Brumpton, B, Akiyama, M, Buring, JE, Caulfield, MJ, Chambers, JC, Chandak, GR, Chanock, SJ, Chaturvedi, N, Chen, Y-DI, Chen, Z, Cheng, C-Y, Christophersen, IE, Allison, MA, Ciullo, M, Cole, JW, Collins, FS, Cooper, RS, Cruz, M, Cucca, F, Cupples, LA, Cutler, MJ, Damrauer, SM, Dantoft, TM, Alvarez, M, de Borst, GJ, de Groot, LCPGM, De Jager, PL, de Kleijn, DP, de Silva, HJ, Dedoussis, G, den Hollander, A, Du, S, Easton, DF, Elders, PJM, Andersen, MK, Eliassen, AH, Ellinor, PT, Elmstahl, S, Erdmann, J, Evans, MK, Fatkin, D, Feenstra, B, Feitosa, MF, Ferrucci, L, Ford, I, Ani, A, Fornage, M, Franke, A, Franks, PW, Freedman, B, Gasparini, P, Gieger, C, Girotto, G, Goddard, ME, Golightly, YM, Gonzalez-Villalpando, C, Appadurai, V, Gordon-Larsen, P, Grallert, H, Grant, SFA, Grarup, N, Griffiths, L, Gudnason, V, Haiman, C, Hakonarson, H, Hansen, T, Hartman, CA, Arbeeva, L, Hattersley, AT, Hayward, C, Heckbert, SR, Heng, C-K, Hengstenberg, C, Hewitt, AW, Hishigaki, H, Hoyng, CB, Huang, PL, Huang, W, Bhaskar, S, Hunt, SC, Hveem, K, Hypponen, E, Iacono, WG, Ichihara, S, Ikram, MA, Isasi, CR, Jackson, RD, Jarvelin, M-R, Jin, Z-B, Bielak, LF, Jockel, K-H, Joshi, PK, Jousilahti, P, Jukema, JW, Kahonen, M, Kamatani, Y, Kang, KD, Kaprio, J, Kardia, SLR, Karpe, F, Bartell, Eric, Bollepalli, S, Kato, N, Kee, F, Kessler, T, Khera, A, Khor, CC, Kiemeney, LALM, Kim, B-J, Kim, EK, Kim, H-L, Kirchhof, P, Bonnycastle, LL, Kivimaki, M, Koh, W-P, Koistinen, HA, Kolovou, GD, Kooner, JS, Kooperberg, C, Kottgen, A, Kovacs, P, Kraaijeveld, A, Kraft, P, Bork-Jensen, J, Krauss, RM, Kumari, M, Kutalik, Z, Laakso, M, Lange, LA, Langenberg, C, Launer, LJ, Le Marchand, L, Lee, H, Lee, NR, Bradfield, JP, Lehtimaki, T, Li, H, Li, L, Lieb, W, Lin, X, Lind, L, Linneberg, A, Liu, C-T, Liu, J, Loeffler, M, Bradford, Y, London, B, Lubitz, SA, Lye, SJ, Mackey, DA, Magi, R, Magnusson, PKE, Marcus, GM, Vidal, PM, Martin, NG, Marz, W, Braund, PS, Matsuda, F, McGarrah, RW, McGue, M, McKnight, AJ, Medland, SE, Mellstrom, D, Metspalu, A, Mitchell, BD, Mitchell, P, Mook-Kanamori, DO, Brody, JA, Morris, AD, Mucci, LA, Munroe, PB, Nalls, MA, Nazarian, S, Nelson, AE, Neville, MJ, Newton-Cheh, C, Nielsen, CS, Nothen, MM, Burgdorf, KS, Ohlsson, C, Oldehinkel, AJ, Orozco, L, Pahkala, K, Pajukanta, P, Palmer, CNA, Parra, EJ, Pattaro, C, Pedersen, O, Pennell, Craig E., Cade, BE, Penninx, BWJH, Perusse, L, Peters, A, Peyser, PA, Porteous, DJ, Posthuma, D, Power, C, Pramstaller, PP, Province, MA, Qi, Q, Cai, H, Qu, J, Rader, DJ, Raitakari, OT, Ralhan, S, Rallidis, LS, Rao, DC, Redline, S, Reilly, DF, Reiner, AP, Rhee, SY, Sakaue, Saori, Cai, Q, Ridker, PM, Rienstra, M, Ripatti, S, Ritchie, MD, Roden, DM, Rosendaal, FR, Rotter, J, Rudan, I, Rutters, F, Sabanayagam, C, Campbell, A, Saleheen, D, Salomaa, V, Samani, NJ, Sanghera, DK, Sattar, N, Schmidt, B, Schmidt, H, Schmidt, R, Schulze, MB, Schunkert, H, Canadas-Garre, M, Scott, LJ, Scott, Rodney J., Sever, P, Shiroma, EJ, Shoemaker, MB, Shu, X-O, Simonsick, EM, Sims, M, Singh, JR, Singleton, AB, Catamo, E, Sinner, MF, Smith, JG, Snieder, H, Spector, TD, Stampfer, MJ, Stark, KJ, Strachan, DP, t' Hart, LM, Tabara, Y, Tang, H, Chai, J-F, Tardif, J-C, Thanaraj, TA, Timpson, NJ, Tonjes, A, Tremblay, A, Tuomi, T, Tuomilehto, J, Tusie-Luna, M-T, Uitterlinden, AG, van Dam, RM, Chai, X, van der Harst, P, Van der Velde, N, van Duijn, CM, van Schoor, NM, Vitart, V, Volker, U, Vollenweider, P, Volzke, H, Wacher-Rodarte, NH, Walker, M, Chang, L-C, Wang, YX, Wareham, NJ, Watanabe, RM, Watkins, H, Weir, DR, Werge, TM, Widen, E, Wilkens, LR, Willemsen, G, Willett, WC, Chang, Y-C, Wilson, JF, Wong, T-Y, Woo, J-T, Wright, AF, Wu, J-Y, Xu, H, Yajnik, CS, Yokota, M, Yuan, J-M, Zeggini, E, Chen, C-H, Zemel, BS, Zheng, W, Zhu, X, Zmuda, JM, Zonderman, AB, Zwart, J-A, Chasman, D, Cho, YS, Heid, IM, McCarthy, M, Chesi, A, Ng, MCY, O'Donnell, CJ, Rivadeneira, F, Thorsteinsdottir, U, Sun, Y, Tai, ES, Boehnke, M, Deloukas, P, Justice, AE, Lindgren, CM, Graff, Marielisa, Choi, SH, Loos, RJF, Mohlke, KL, North, KE, Stefansson, K, Walters, RG, Winkler, TW, Young, KL, Loh, P-R, Yang, J, Esko, T, Chung, R-H, Assimes, TL, Auton, A, Abecasis, GR, Willer, CJ, Locke, AE, Berndt, S, Lettre, G, Frayling, TM, Okada, Y, Wood, AR, Cocca, M, Visscher, PM, Hirschhorn, JN, Concas, MP, Couture, C, Cuellar-Partida, G, Danning, R, Daw, EW, Degenhard, F, Delgado, GE, Eliasen, Anders U., Delitala, A, Demirkan, A, Deng, X, Devineni, P, Dietl, A, Dimitriou, M, Dimitrov, L, Dorajoo, R, Ekici, AB, Engmann, JE, Jiang, Yunxuan, Fairhurst-Hunter, Z, Farmaki, A-E, Faul, JD, Fernandez-Lopez, J-C, Forer, L, Francescatto, M, Freitag-Wolf, S, Fuchsberger, C, Galesloot, TE, Gao, Y, Raghavan, Sridharan, Gao, Z, Geller, F, Giannakopoulou, O, Giulianini, F, Gjesing, AP, Goel, A, Gordon, SD, Gorski, M, Grove, J, Guo, X. Nature Publishing Group; 2022. A Saturated Map of Common Genetic Variants Associated with Human Height.

Kiltschewskij, Dylan J., Reay, William R., Cairns, Murray J., Geaghan, Michael P., Atkins, Joshua R., Xavier, Alexandre, Zhang, Xiajie, Watkeys, Oliver J., Carr, Vaughan J., Scott, Rodney J., Green, Melissa J.. Elsevier; 2024. Alteration of DNA Methylation and Epigenetic Scores Associated with Features of Schizophrenia and Common Variant Genetic Risk.

Reeves, Stuart G., Rich, Dominique, Meldrum, Cliff J., Colyvas, Kim, Kurzawski, Grzegorz, Suchy, Janina, Lubinski, Jan, Scott, Rodney J.. John Wiley & Sons, Inc.; 2008. IGF1 is a modifier of disease risk in hereditary non-polyposis colorectal cancer.

Jaworowska, Ewa, Trubicka, Joanna, Grodzki, Tomasz, Serwatowski, Piotr, Nej-Wołosiak, Katarzyna, Tołoczko-Grabarek, Aleksandra, Sikorski, Andrzej, Słojewski, Marcin, Jakubowska, Anna, Cybulski, Cezary, Lubiński, Jan, Scott, Rodney J., Lener, Marcin R., Masojć, Bartłomiej, Złowocka-Perłowska, Elżbieta, McKay, James D., Renard, Hélène, Oszutowska, Dorota, Wokołorczyk, Dominika, Lubiński, Jakub. Public Library Of Science; 2011. Smoking related cancers and loci at chromosomes 15q25, 5p15, 6p22.1 and 6p21.33 in the Polish population.

Berry, Nadine K., Scott, Rodney J., Sutton, Rosemary, Law, Tamara, Trahair, Toby N., Dalla-Pozza, Luce, Ritchie, Petra, Barbaric, Draga, Enjeti, Anoop K.. Elsevier; 2020. Enrichment of atypical hyperdiploidy and IKZF1 deletions detected by SNP-microarray in high-risk Australian AIEOP-BFM B-cell acute lymphoblastic leukaemia cohort.

Milne, Elizabeth, Royle, Jill A., Armstrong, Bruce K., Bennett, Lisa C., De Klerk, Nicholas H., Bailey, Helen D., Bower, Carol, Miller, Margaret, Attia, John, Scott, Rodney J., Kirby, Maria. Springer; 2011. Maternal consumption of coffee and tea during pregnancy and risk of childhood ALL: results from an Australian case-control study.

Bowden, Nikola A., Scott, Rodney J., Tooney, Paul A.. BioMed Central; 2008. Altered gene expression in the superior temporal gyrus in schizophrenia.

Lener, Marcin R., Scott, Rodney J., Soluch, Agnieszka, Jakubowska, Anna, Lubiński, Jan, Kluźniak, Wojciech, Baszuk, Piotr, Cybulski, Cezary, Wiechowska-Kozłowska, Anna, Huzarski, Tomasz, Byrski, Tomasz, Kładny, Józef, Pietrzak, Sandra. John Wiley & Sons; 2016. Do founder mutations characteristic of some cancer sites also predispose to pancreatic cancer?.

Marshall, Christian R., , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Howrigan, Daniel P., Gujral, Madhusudan, Brandler, William M., Malhotra, Dheeraj, Wang, Zhouzhi, Fuentes Fajarado, Karin V., Maile, Michelle S., Ripke, Stephan, Agartz, Ingrud, Albus, Margot, Alexander, Madeline, Merico, Daniele, Atkins, Joshua, Cairns, Murray J., Carr, Vaughan J., Henskens, Frans A., Kelly, Brian J., Loughland, Carmel L., Michie, Patricia T., Schall, Ulrich, Scott, Rodney J., Tooney, Paul A., Thiruvahindrapuram, Bhooma, Wu, Jing Qin, Wu, Wenting, Greer, Douglas S., Antaki, Douglas, Shetty, Aniket, Holmans, Peter A., Pinto, Dalila. Nature Publishing Group; 2017. Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects.

Zlowocka, Elzbieta, Cybulski, Cezary, Scott, Rodney J., Lubinski, Jan, Gorski, Bohdan, Debniak, Tadeusz, Slojewski, Marcin, Wokolorczyk, Dominika, Serrano-Fernandez, Pablo, Matyjasik, Joanna, van de Wetering, Thierry, Sikorski, Andrzej. John Wiley & Sons; 2008. Germline mutations in the CHEK2 kinase gene are associated with an increased risk of bladder cancer.

Ma, Gerry Z. M., Stankovich, Jim, Browning, Sharon R., Butzkueven, Helmut, Carroll, William M., Danoy, Patrick, Foote, Simon J., Griffiths, Lyn, Heard, Robert N., Kermode, Allan G., Lechner-Scott, Jeannette, Moscato, Pablo, Kilpatrick, Trevor J., Perreau, Victoria M., Scott, Rodney J., Slee, Mark, Stewart, Graeme J., Taylor, Bruce V., Wiley, James, Stankovich, Jim, Binder, Michele D., Field, Judith, Bahlo, Melanie, Booth, David R., Broadley, Simon, Brown, Matthew A., Browning, Brian L.. Public Library of Science; 2011. Polymorphisms in the receptor tyrosine kinase MERTK gene are associated with multiple sclerosis susceptibility.

Rogoza-Janiszewska, Emilia, Malinska, Karolina, Górski, Bohdan, Scott, Rodney J., Cybulski, Cezary, Kluzniak, Wojciech, Lener, Marcin, Jakubowska, Anna, Gronwald, Jacek, Huzarski, Tomasz, Lubinski, Jan, Debniak, Tadeusz. Springer; 2021. Prevalence of germline TP53 variants among early-onset breast cancer patients from Polish population.

Scott, Rodney J., Fox, Stephen B., Byron, Keith, Rudzki, Barney, Waring, Paul, Iacopetta, Barry, Desai, Jayesh, Grieu, Fabienne, Amanuel, Benhur, Garrett, Kerryn, Harraway, James, Cheetham, Glenice, Pattle, Neville, Haddad, Afaf. Wiley-Blackwell Publishing; 2014. KRAS mutation testing of metastatic colorectal cancer in Australia: where are we at?.

Mirecka, Aneta, Paszkowska-Szczur, Katarzyna, Gupta, Satish, Gołąb, Adam, Słojewski, Marcin, Sikorski, Andrzej, Lubiński, Jan, Dębniak, Tadeusz, Scott, Rodney J., Górski, Bohdan, van de Wetering, Thierry, Wokołorczyk, Dominika, Gromowski, Tomasz, Serrano-Fernandez, Pablo, Cybulski, Cezary, Kashyap, Aniruddh. Elsevier BV; 2014. Common variants of xeroderma pigmentosum genes and prostate cancer risk.

Johnstone, Daniel M., Riveros, Carlos, Heidari, Moones, Graham, Ross M., Trinder, Debbie, Berretta, Regina, Olynyk, John K., Scott, Rodney J., Moscato, Pablo, Milward, Elizabeth A.. MDPI AG; 2013. Evaluation of different normalization and analysis procedures for Illumina gene expression microarray data involving small changes.

Avery-Kiejda, Kelly A., Wong, Michelle W., Scott, Rodney J.. Universiti Putra Malaysia; 2011. Genetic markers in breast cancer - how far have we come from BRCA1?.

Debniak, Tadeusz, Scott, Rodney J., Malinska, Karolina, Kiedrowicz, Magdalena, Rogoza-Janiszewska, Emilia, Rudnicka, Helena, Deptula, Jakub, Domagala, Paweo, Kluzniak, Wojciech, Lener, Marcin R., Lubinski, Jan, Górski, Bohdan, Masojc, Bartoomiej, Kram, Andrzej, Maleszka, Romuald, Cybulski, Cezary, Paszkowska-Szczur, Katarzyna, Kashyap, Aniruddh, Murawa, Dawid. Public Library of Science; 2018. BRCA1/2 mutations are not a common cause of malignant melanoma in the Polish population.

Shu, Xiang, Wu, Lang, Schmidt, Marjanka K., Hopper, JL, Howell, A, Huang, G, Jakubowska, A, Janni, W, John, EM, Johnson, N, Jones, K, Jung, A, Kaaks, R, Pharoah, Paul D. P., Kabisch, M, Kerin, MJ, Khusnutdinova, E, Kitahara, CM, Kosma, V-M, Koutros, S, Kraft, P, Kristensen, VN, Lambrechts, D, Le Marchand, L, Andrulis, Irene L., Lindstrom, S, Linet, MS, Lissowska, J, Loibl, S, Lubinski, J, Luccarini, C, Lux, MP, Maishman, T, Kostovska, IM, Mannermaa, A, Hunter, David J., Manoukian, S, Manson, JE, Margolin, S, Mavroudis, D, Meijers-Heijboer, H, Meindl, A, Menon, U, Meyer, J, Mulligan, AM, Neuhausen, SL, Simard, Jacques, Nevanlinna, H, Neven, P, Newman, WT, Nielsen, SF, Nordestgaard, BG, Olopade, OI, Olshan, AF, Olson, JE, Olsson, H, Olswol, C, Easton, Douglas F., Orr, N, Perou, CM, Peto, J, Plaseska-Karanfilska, D, Prentice, R, Presneau, N, Pylkas, K, Rack, B, Radice, P, Rahman, N, Zheng, Wei, Rennert, G, Rennert, HS, Romero, A, Romm, J, Saloustros, E, Sandler, DP, Sawyer, EJ, Schmutzler, RK, Schneeweiss, A, Scott, Rodney J., Alicia, Beeghly-Fadiel J., Scott, C, Seal, S, Seynaeve, C, Smeets, A, Southey, MC, Spinelli, JJ, Stone, J, Surowy, H, Swerdlow, AJ, Tamimi, R, Anton-Culver, Hoda, Tapper, W, Taylor, JA, Terry, MB, Tessier, DC, Thone, K, Tollenaar, RAEM, Torres, D, Troester, MA, Truong, T, Untch, M, Antonenkova, Natalia N., Vachon, C, Van Den Berg, D, van den Ouweland, AMW, van Veen, EM, Vincent, D, Waisfisz, Q, Weinberg, CR, Wendt, C, Whittemore, AS, Wildiers, H, Khankari, Nikhil K., Arndt, Volker, Winqvist, R, Wolk, A, Xia, L, Yang, XR, Ziogas, A, Ziv, E, Aronson, KJ, Auer, PL, Barrdahl, M, Baynes, C, Freeman, LEB, Beckmann, MW, Behrens, S, Benitez, J, Bermisheva, M, Shu, Xiao-Ou, Blomqvist, C, Bogdanova, NV, Bojesen, SE, Brauch, H, Brenner, H, Brinton, L, Broberg, P, Brucker, SY, Bruning, T, Burwinkel, B, Wang, Thomas J., Cai, Q, Caldes, T, Canzian, F, Carter, BD, Castelao, JE, Chang-Claude, J, Chenevix-Trench, G, Cheng, T-YD, Clarke, CL, Conroy, DM, Michailidou, Kyriaki, Couch, FJ, Cox, DG, Cox, A, Cross, SS, Cunningham, JM, Czene, K, Daly, MB, Doheny, KF, Dork, T, dos-Santos-Silva, I, Bolla, Manjeet K., Dumont, M, Dunning, AM, Dwek, M, Earp, HS, Eccles, DM, Eliassen, AH, Engel, C, Eriksson, M, Evans, DG, Fachal, L, Wang, Qin, Fasching, PA, Figueroa, J, Fletcher, O, Flyger, H, Fritschi, L, Gabrielson, M, Gago-Dominguez, M, Gapstur, SM, Garcia-Closas, M, Gaudet, MM, Dennis, Joe, Ghoussaini, M, Giles, GG, Goldberg, MS, Goldgar, DE, Gonzalez-Neira, A, Guenel, P, Hahnen, E, Haiman, CA, Hakansson, N, Hall, P, Milne, Roger L, Hallberg, E, Hamann, U, Harrington, P, He, W, Hein, A, Hicks, B, Hillemanns, P, Hogervorst, FB, Hollestelle, A, Hoover, RN. Oxford University Press; 2019. Associations of obesity and circulating insulin and glucose with breast cancer risk: a Mendelian randomization analysis.

Stambolian, Dwight, Wojciechowski, Robert, Wong, Tien Y., Simpson, Claire L., Klaver, Caroline C. W., van Duijn, Cornelia M., Verhoeven, Virginie J. M., Baird, Paul N., Vitart, Veronique, Paterson, Andrew D., Mitchell, Paul, Saw, Seang Mei, Oexle, Konrad, Holliday, Elizabeth G., Attia, John, Scott, Rodney J., , , , , , , , Pirastu, Mario, , , , , , , , , , , Li, Xiaohui, , , , , , , , , , , Raffel, Leslie J., , , , , , , , , , , Cotch, Mary Frances, , , Chew, Emily Y., Klein, Barbara, Klein, Ronald. Oxford University Press; 2013. Meta-analysis of genome-wide association studies in five cohorts reveals common variants in RBFOX1, a regulator of tissue-specific splicing, associated with refractive error.

Mossman, David, Scott, Rodney J.. Public Library of Science; 2011. Long term transcriptional reactivation of epigenetically silenced genes in colorectal cancer cells requires DNA hypomethylation and histone acetylation.

Bailey, Helen D., Miller, Margaret, Langridge, Amanda, de Klerk, Nicholas H., van Bockxmeer, Frank M., Attia, John, Scott, Rodney J., Armstrong, Bruce K., Milne, Elizabeth. Routledge; 2012. Maternal dietary intake of folate and vitamins B6 and B12 during pregnancy and the risk of childhood acute lymphoblastic leukemia.

Walker, Marjorie M., Keely, Simon J., Scott, Rodney J., Talley, Nicholas J.. Nature Publishing Group; 2016. Genetics, mucosal inflammation, and the environment in post-infectious chronic gut syndromes.

Hungate, Eric A., Vora, Sapana R., Rudant, Jéremie, Orsi, Laurent, Clavel, Jacqueline, Milne, Elizabeth, Scott, Rodney J., Pui, Ching-Hon, Cox, Nancy J., Loh, Mignon L., Yang, Jun J., Skol, Andrew D., Gamazon, Eric R., Onel, Kenan, Moriyama, Takaya, Best, Timothy, Hulur, Imge, Lee, Younghee, Evans, Tiffany-Jane, Ellinghaus, Eva, Stanulla, Martin. Nature Publishing Group; 2016. A variant at 9p21.3 functionally implicates CDKN2B in paediatric B-cell precursor acute lymphoblastic leukaemia aetiology..

Petit, Joel, Carroll, Georgia, Williams, Henry, Pockney, Peter, Scott, Rodney J.. MDPI AG; 2023. Evaluation of a Multi-Gene Methylation Blood-Test for the Detection of Colorectal Cancer.

Out, Astrid A., Tops, Carli M. J., Fostira, Florentia, Franken, Patrick F., Gaustadnes, Mette, Heinimann, Karl, Hodgson, Shirley V., Hogervorst, Frans B. L., Holinski-Feder, Elke, Lagerstedt-Robinson, Kristina, Olschwang, Sylviane, van den Ouweland , Ans M. W., Nielsen, Maartje, Scott, Rodney J., Weiss, Marjan M., van Minderhout, Ivonne J. H. M., Fokkema, Ivo F. A. C., Buisine, Marie-Pierre, Claes, Kathleen, Colas, Chrystelle, Fodde, Riccardo. John Wiley & Sons; 2010. Leiden Open Variation Database of the MUTYH gene.

Talseth-Palmer, Bente A., Scott, Rodney J.. Master Publishing Group; 2011. Genetic variation and its role in malignancy.

Milne, Elizabeth, Greenop, Kathryn R., Bower, Carol, Miller, Margaret, van Bockxmeer, Frank M., Scott, Rodney J., de Klerk, Nicholas H., Ashton, Lesley J., Gottardo, Nicholas G., Armstrong, Bruce K.. American Association for Cancer Research; 2012. Maternal use of folic acid and other supplements and risk of childhood brain tumors.

Greenop, Kathryn R., Peters, Susan, Milne, Elizabeth, Fritschi, Lin, Glass, Deborah C., Ashton, Lesley J., Bailey, Helen D., Scott, Rodney J., Daubenton, John, de Klerk, Nicholas H., Armstrong, Bruce K.. Springer; 2014. Exposure to household painting and floor treatments, and parental occupational paint exposure and risk of childhood brain tumors: results from an Australian case-control study.

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