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.

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.

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.

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.

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.

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.

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.

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.

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.

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?.

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.

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.

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.

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.

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.

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.

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.

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

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.

Ibn Sina, Abu Ali, Carrascosa, Laura G., Korbie, Darren, Trau, Matt, Liang, Ziyu, Grewal, Yadveer S., Wardiana, Andri, Shiddiky, Muhammad J. A., Gardiner, Robert A., Samaratunga, Hemamali, Gandhi, Maher K., Scott, Rodney J.. Nature Publishing Group; 2018. Epigenetically reprogrammed methylation landscape drives the DNA self-assembly and serves as a universal cancer biomarker.

Reeves, Stuart G., Meldrum, Cliff, Groombridge, Claire, Spigelman, Allan D., Suchy, Janina, Kurzawski, Grzegorz, Lubinski, Jan, McElduff, Patrick, Scott, Rodney J.. Nature Publishing Group; 2009. MTHFR 677 C>T and 1298 A>C polymorphisms and the age of onset of colorectal cancer in hereditary nonpolyposis colorectal cancer.

Kładny, Józef, Suchy, Janina, Kłujszo-Grabowska, Ewa, Kacperski, Tomasz, Scott, Rodney J., Kurzawski, Grzegorz, Lubiński, Jan. Elsevier; 2009. Clinical characteristics of tumors derived from colorectal cancer patients who harbor the Tumor Necrosis Factor beta-1031T/T and NOD2 3020insC polymorphism.

Skerrett-Byrne, David A., Bromfield, Elizabeth G., Anderson, Amanda L., Nixon, Brett, Scott, Rodney J., Wark, Peter A. B., Dun, Matthew D., Hansbro, Philip M., Murray, Heather C., Jamaluddin, M. Fairuz B., Jarnicki, Andrew G., Fricker, Michael, Essilfie, Ama T., Jones, Bernadette, Haw, Tatt J., Hampsey, Daniel. John Wiley & Sons, Inc.; 2021. Time-resolved proteomic profiling of cigarette smoke-induced experimental chronic obstructive pulmonary disease.

Wu, Jing Qin, Green, Melissa J., Gardiner, Erin J., Tooney, Paul A., Scott, Rodney J., Carr, Vaughan J., Cairns, Murray J.. Academic Press; 2015. Altered neural signaling and immune pathways in peripheral blood mononuclear cells of schizophrenia patients with cognitive impairment: a transcriptome analysis.

Kapoor, Pooja Middha, Mavaddat, Nasim, Choudhury, Parichoy Pal, Wilcox, Amber N., Lindström, Sara, Behrens, Sabine, Michailidou, Kyriaki, Dennis, Joe, Bolla, Manjeet K., Wang, Qin, Jung, Audrey, Abu-Ful, Zomoroda, Ahearn, Thomas, Andrulis, Irene L., Anton-Culver, Hoda, Arndt, Volker, Aronson, Kristan J., Auer, Paul L., Freeman, Laura E. Beane, Becher, Heiko, Beckmann, Matthias W., Scott, Rodney J.. Oxford University Press; 2021. Combined associations of a polygenic risk score and classical risk factors with breast cancer risk.

Gandhi, Kaushal S., McKay, Fiona C., Danoy, Patrick, Stewart, Graeme J., Broadley, Simon, Moscato, Pablo, Lechner-Scott, Jeannette, Scott, Rodney J., Booth, David R., ANZgene Multiple Sclerosis Genetics Consortium, Cox, Mathew, Riveros, Carlos, Armstrong, Nicola, Heard, Robert N., Vucic, Steve, Williams, David W., Stankovich, Jim, Brown, Matthhew. Oxford University Press; 2010. The multiple sclerosis whole blood mRNA transcriptome and genetic associations indicate dysregulation of specific T cell pathways in pathogenesis.

Hess, Jonathan L., Tylee, Daniel S., Barve, Rahul, de Jong, Simone, Ophoff, Roel A., Kumarasinghe, Nishantha, Tooney, Paul, Schall, Ulrich, Gardiner, Erin, Beveridge, Natalie Jane, Scott, Rodney J., Yasawardene, Surangi, Perera, Antoinette, Mendis, Jayan, Carr, Vaughan, Kelly, Brian, Cairns, Murray, Neurobehavioural Genetics Unit,, Tsuang, Ming T., Glatt, Stephen J.. Elsevier; 2020. Transcriptomic abnormalities in peripheral blood in bipolar disorder, and discrimination of the major psychoses.

Moscovis, Sophia M., Hall, Sharron T., Burns, Chrstine J., Scott, Rodney J., Blackwell, C. Caroline. Sage; 2014. The male excess in sudden infant deaths.

Chen, Jinyun, Pande, Mala, Scott, Rodney J., Frazier, Marsha L., Huang, Yu-Jing, Wei, Chongjuan, Amos, Christopher I., Talseth-Palmer, Bente A., Meldrum, Cliff J., Chen, Wei V., Gorlov, Ivan P., Lynch, Patrick M.. Oxford University Press; 2013. Cell cycle-related genes as modifiers of age of onset of colorectal cancer in Lynch syndrome: a large-scale study in non-Hispanic white patients.

Loth, Daan W., Artigas, María Soler, Lee, Mi Kyeong, Scott, Rodney J., Karrasch, Stefan, Grallert, Harald, Gaddis, Nathan C., Starr, John M., Wijmenga, Cisca, Minster, Ryan L., Lederer, David J., Pekkanen, Juha, Gyllensten, Ulf, Strachan, David P., Campbell, Harry, Morris, Andrew P., Gläeser, Sven, Hammond, Christopher J., Burkart, Kristin M., Beilby, John, Kritchevsky, Stephen B., Gucinason, Vilmundur, Hancock, Dana B., Williams, O. Dale, James, Alan L., Polasek, Ozren, Zemunik, Tatijana, Kolcic, Ivana, Petrini, Marcy F., Wjst, Matthias, Kim, Woo Jin, Porteous, David J., Scotland, Generation, Smith, Blair H., Viljanen, Anne, Huffman, Jennifer E., Heliovaara, Markku, Attia, John R., Sayers, Ian, Hampel, Regina, Gieger, Christian, Deary, Ian J., Boezen, H. Marike, Newman, Anne, Jarvelin, Marjo-Riitta, Wilson, James F., Vitart, Veronique, Lind, Lars, Stricker, Bruno H., Teumer, Alexander, Spector, Timothy D., Melén, Erik, Peters, Marjolein J., Lange, Leslie A., Barr, R. Graham, Bracke, Ken R., Verhamme, Fien M., Ramasamy, Adaikalavan, Sung, Joohon, Hiemstra, Pieter S., Cassano, Patricia A., Sood, Akshay, Hayward, Caroline, Dupuis, Josée, Hall, Ian P., Brusselle, Guy G., Tobin, Martin D., London, Stephanie J., Wareham, Nicholas J., Kaprio, Jaakko, Wang, Xin-Qun, Trochet, Holly, Gharib, Sina A., Kähönen, Mika, Flexeder, Claudia, Albrecht, Eva, Lopez, Lorna M., de Jong, Kim, Thyagarajan, Bharat, Alves, Alexessander Couto, Enroth, Stefan, Omenaas, Ernst, Joshi, Peter K., Wain, Louise V., Fall, Tove, Viñuela, Ana, Launer, Lenore J., Loehr, Laura R., Fornage, Myriam, Li, Guo, Wik, Jemma B., Tang, Wenbo, Manichaikul, Ani, Lahousse, Lies, Franceschini, Nora, Harris, Tamara B., North, Kari E., Rudnicka, Alicja R., Hui, Jennie, Gu, Xiangjun, Lumley, Thomas, Wright, Alan F., Hastie, Nicholas D., Campbell, Susan, Kumar, Rajesh, Koch, Beate, Pin, Isabelle, Scott, Robert A., Pietilainen, Kirsi H., Surakka, Ida, Liu, Yongmei, Holliday, Elizabeth G., Schulz, Holger, Heinrich, Joachim, Davies, Gail, Vonk, Judith M., Pottinger, Tess D., Wojczynski, Mary, Pouta, Anneli, Johansson, Åsa, Wild, Sarah H., Ingelsson, Erik, Rivadeneira, Fernando, Vöezke, Henry, Hysi, Pirro G., Eiriksdottir, Gudny, Morrison, Alanna C., Smith, Albert Vernon, Rotter, Jerome I., Gao, Wei, Postma, Dirkje S., White, Wendy B., Rich, Stephen S., Hofman, Albert, Aspelund, Thor, Couper, David, Smith, Lewis J., Psaty, Bruce M., Duan, Qing, Lohman, Kurt, Burchard, Esteban G., Uitterlinden, André G., Garcia, Melissa, Joubert, Bonnie R., McArdle, Wendy L., Musk, A. Bill, Hansel, Nadia, Heckbert, Susan R., Zgaga, Lina, Oldmeadow, Chris, van Meurs, Joyce B. J., Navarro, Pau, Rudan, Igor, Oh, Yeon-Mok, Redline, Susan, Jarvis, Deborah L., Zhao, Jing Hua, Rantanen, Taina, O'Connor, George T., Ripatti, Samuli. Nature Publishing Group; 2014. Genome-wide association analysis identifies six new loci associated with forced vital capacity.

Ashton, Katie A., Kairupan, C. F., Scott, Rodney J., Meldrum, C. J., McPhillips, M. L.. Termedia Publishing House; 2005. Frequency of the common MYH mutations (G382D and Y165C) in MMR mutation positive and negative HNPCC patients.

White, Cassandra, Kendall, Guy, Millington, Tegan, Corcoran, Bern, Paul, Christine, Scott, Rodney J., Ackland, Stephen. John Wiley & Sons; 2024. Evaluation of early fluoropyrimidine toxicity in solid organ cancer patients: a retrospective observational study in Australia.

Wu, Jing Qin, Wang, Xi, Beveridge, Natalie J., Tooney, Paul A., Scott, Rodney J., Carr, Vaughan J., Cairns, Murray J.. Public Library of Science; 2012. Transcriptome sequencing revealed significant alteration of cortical promoter usage and splicing in schizophrenia.

Avery-Kiejda, Kelly A., Braye, Stephen G., Mathe, Andrea, Forbes, John F., Scott, Rodney J.. BioMed Central; 2014. Decreased expression of key tumour suppressor microRNAs is associated with lymph node metastases in triple negative breast cancer.

Milne, Elizabeth, Greenop, Kathryn R., Scott, Rodney J., Bailey, Helen D., Attia, John, Dalla-Pozza, Luciano, de Klerk, Nicholas H., Armstrong, Bruce K.. Oxford University Press; 2012. Parental prenatal smoking and risk of childhood acute lymphoblastic leukemia.

Lee, James J., Wedow, Robbee, Okbay, Aysu, Kong, Edward, Maghzian, Omeed, Zacher, Meghan, Nguyen-Viet, Tuan Anh, Bowers, Peter, Sidorenko, Julia, Karlsson Linnér, Richard, Fontana, Mark Alan, Kundu, Tushar, Lee, Chanwook, Li, Hui, Li, Ruoxi, Royer, Rebecca, Timshel, Pascal N., Walters, Raymond K., Willoughby, Emily A., Yengo, Loïc, Agee, Michelle, Oldmeadow, Christopher, Holliday, Elizabeth G., Scott, Rodney J., Attia, John R.. Nature Publishing Group; 2018. Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals.

Lill, Christina M., Liu, Tian, Blaschke, Paul, Winkelmann, Alexander, Gerdes, Lisa-Ann, Luessi, Felix, Fernadez, Oscar, Izquierdo, Guillermo, Antiguedad, Alfredo, Hoffjan, Sabine, Cournu-Rebeix, Isabelle, Gromoller, Silvana, Schjeide, Brit-Maren M., Faber, Hans, Liebsch, Maria, Meissner, Esther, Chanvillard, Coralie, Touze, Emmauel, Pico, Fernando, Corcia, Philippe, Bahlo, Melanie, Booth, David R., Broadley, Simon, Roehr, Johannes T., Brown, Matthew A., Browning, Brian L., Browning, Sharon R., Butzkueven, Helmut, Carroll, William M., Cox, Mathew B., Chapman, Caron, Clarke, Glynnis, Danoy, Patrick, Drysdale, Karen, Akkad, Denis A., Field, Judith, Foote, Simon J., Greer, Judith M., Griffiths, Lyn R., Hadler, Johanna, Jensen, Cathy J., Johnson, Laura J., Kermode, Allan G., Heard, Robert N., Kilpatrick, Trevor J., Damotte, Vincent, Lechner-Scott, Jeanette, Marriott, Mark, Mason, Deborah, Moscato, Pablo, Pender, Michael P., Perreau, Victoria M., Rubio, Justin P., Scott, Rodney J., Slee, Mark, Stankovich, Jim, Alcina, Antonio, Stewart, Graeme J., Tajouri, Lofti, Taylor, Bruce V., Wiley, James, Wilkins, Ella J., Dörner, Thomas, Steinhagen-Thiessen, Elisabeth, Baeckman, Lars, Heekeren, Hauke R., Li, Shu-Chen, Ortiz, Miguel A., Lindenberger, Ulman, Chan, Andrew, Hartung, Hans-Peter, Aktas, Orhan, Lohse, Peter, Kümpfel, Tania, Kubisch, Christian, Epplen, Joerg T., Zettl, Uwe K., Fontaine, Bertrand, Arroyo, Rafa, Vandenbroeck, Koen, Matesanz, Fuencisla, Urcelay, Elena, Bertram, Lars, Zipp, Frauke, Lopez de Lapuente, Aitzkoa. BMJ Group; 2012. Closing the case of APOE in multiple sclerosis: no association with disease risk in over 29 000 subjects.

Mathers, John C., Elliott, Faye, Lindblom, Annika, Morrison, Patrick J., Rashbass, Jem, Ramesar, Raj S., Seppälä, Toni T., Thomas, Huw J. W., Sheth, Harsh J., Pylvänäinen, Kirsi, Reed, Lynn, Borthwick, Gillian M., Macrae, Finlay, Bishop, D. Timothy, Burn, J, Boussioutas, A, Brewer, C, Cook, J, Eccles, D, Ellis, A, Hodgson, SV, Lubinski, J, Maher, ER, Mecklin, Jukka-Pekka, Porteous, MEM, Sampson, J, Scott, Rodney J., Side, L, Bisgaard, ML, Chu, C, Fidalgo, P, Fidalgo, P, Gallinger, S, Homfray, T, Möslein, Gabriela, Hutter, P, Leite, J, MacKay, J, Marks, CG, Miles, A, Murday, V, Oliani, C, Olschwang, S, Segura, PP, Pichert, G, McRonald, Fiona E., Sappino, AP, Tempesta, A, Vasen, HFA, Walpole, I, Langman, C, Shand, B, Bacon, A, Bertario, Lucio, Evans, D. Gareth, Gerdes, Anne-Marie, Ho, Judy W. C.. American Association for Cancer Research; 2022. Cancer Prevention with Resistant Starch in Lynch Syndrome Patients in the CAPP2-Randomized Placebo Controlled Trial: Planned 10-Year Follow-up.

Gaddis, Nathan, Mathur, Ravi, Jeffries, Paul W., Martin, Nicholas G., Degenhardt, Louisa, Montgomery, Grant W., Wetherill, Leah, Lai, Dongbing, Bucholz, Kathleen, Foroud, Tatiana, Porjesz, Bernice, Runarsdottir, Valgerdur, Marks, Jesse, Holliday, Elizabeth G., McEvoy, Mark, Scott, Rodney J., Webb, BT, Crist, RC, Kranzler, HR, Sherva, R, Zhou, H, Hulse, G, Wildenauer, D, Zhou, Linran, Kelty, E, Attia, J, Holliday, EG, McEvoy, M, Scott, RJ, Schwab, SG, Maher, BS, Gruza, R, Kreek, MJ, Nelson, EC, Quach, Bryan, Thorgeirsson, T, Stefansson, K, Berrettini, WH, Gelernter, J, Edenberg, HJ, Bierut, L, Hancock, DB, Johnson, EO, Waldrop, Alex, Levran, Orna, Agrawal, Arpana, Randesi, Matthew, Adelson, Miriam. Nature Publishing Group; 2022. Multi-trait genome-wide association study of opioid addiction: OPRM1 and beyond.

Dymerska, Dagmara, Serrano-Fernandez, Pablo, Huzarski, Tomasz, Lubinski, Jan, Kurzawski, Grzegorz, Suchy, Janina, Plawski, Andrzej, Slomski, Ryrszard, Kaklewski, Krzysztof, Scott, Rodney J., Gronwald, Jacek, Kladny, Jozef, Byrski, Tomasz. Elsevier; 2010. Combined iPLEX and TaqMan assays to screen for 45 common mutations in Lynch Syndrome and FAP patients.

Holliday, Elizabeth G., Traylor, Matthew, Boncoraglio, Giorgio B., Clarke, Robert, Cole, John W., Fornage, Myriam, Furie, Karen L., Ikram, M. Arfan, Jannes, Jim, Kittner, Steven J., Lincz, Lisa F., Maguire, Jane M., Malik, Rainer, Oldmeadow, Christopher, Scott, Rodney J., Levi, Christopher, Attia, John, , , , , , , Bevan, Steve, , , , , , , , , , , Falcone, Guido, , Hopewell, Jemma C., Cheng, Yu-Ching, Cotlarciuc, Ioana, Bis, Joshua C., Boerwinkle, Eric. Lippincott Williams & Wilkins; 2015. Genetic overlap between diagnostic subtypes of ischemic stroke.

Bulik-Sullivan, Brendan K., Albus, M, Alexander, M, Amin, F, Bacanu, SA, Begemann, M, Belliveau, RA, Bene, J, Bergen, SE, Bruggeman, R, Bevilacqua, E, Bigdeli, TB, Black, DW, Buccola, NG, Buckner, RL, Byerley, W, Cahn, W, Cai, G, Cairns, MJ, Campion, D, Cantor, RM, Carr, VJ, Carrera, N, Catts, SV, Chambert, KD, Chan, RCK, Chen, RYL, Cohen, D, Chen, EYH, Cheng, W, Cheung, EFC, Chong, SA, Cloninger, CR, Cohen, N, Cormican, P, Craddock, N, Crespo-Facorro, B, Crowley, JJ, Curtis, D, Davidson, M, Davis, KL, Degenhardt, F, Del Favero, J, Loh, Po-Ru, Michie, Patricia T., Schall, Ulrich, Scott, Rodney J., Tooney, Paul A., Wu, Jing Qin, Patterson, Nick, Daly, Mark J., Price, Alkes L., Neale, Benjamin M., Finucane, Hilary K., Ripke, Stephan, Yang, Jian, Schizophrenia Working Group of the Psychiatric Genomics Consortium,, Cairns, Murray J., Henskens, Frans A., Kelly, Brian J., Loughland, Carmel M.. Nature Publishing Group; 2015. LD score regression distinguishes confounding from polygenicity in genome-wide association studies.