Cox, Amanda J., Zhang, Ping, Evans, Tiffany J., Scott, Rodney J., Cripps, Allan W., West, Nicholas P.. Elsevier; 2018. Gene expression profiles in whole blood and associations with metabolic dysregulation in obesity.

Milne, Elizabeth, Royle, Jill A., Haber, Michelle, Thompson, Judith R., Fritschi, Lin, Marshall, Glenn M., Armstrong, Bruce K., Miller, Margaret, Bower, Carol, de Klerk , Nicholas H., Bailey, Helen D., van Bockxmeer, Frank, Attia, John, Scott, Rodney J., Norris, Murray D.. John Wiley & Sons; 2010. Maternal folate and other vitamin supplementation during pregnancy and risk of acute lymphoblastic leukemia in the offspring.

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?.

Darabi, Hatef, McCue, Karen, Dennis, Joe, Cox, A., Cross, S. S., Luben, R., Khaw, K.-T., Choi, J.-Y., Kang, D., Hartman, M., Lim, W. Y., Kabisch, M., Torres, D., Wang, Qin, Jakubowska, A., Lubinski, J., McKay, J., Sangrajrang, S., Toland, A. E., Yannoukakos, D., Shen, C.-Y., Yu, J.-C., Ziogas, A., Schoemaker, M. J., Canisius, Sander, Swerdlow, A., Borresen-Dale, A.-L., Kristensen, V., French, J. D., Edwards, S. L., Dunning, A. M., Easton, D. F., Hall, P., Chenevix-Trench, G., Scott, Christopher G., Apicella, Carmel, Hopper, John L., Southey, Melissa C., Stone, Jennifer, Broeks, Annegien, Schmidt, Marjanka K., Beesley, Jonathan, Scott, Rodney J., Lophatananon, Artitaya, Muir, Kenneth, Beckmann, Matthias W., Ekici, Arif B., Fasching, Peter A., Heusinger, Katharina, dos-Santos-Silva, Isabel, Peto, Julian, Tomlinson, Ian, Michailidou, Kyriaki, Sawyer, Elinor J., Burwinkel, Barbara, Marme, Frederik, Guénel, Pascal, Truong, Thérèse, Bojesen, Stig E., Flyger, Henrik, Benitez, Javier, González-Neira, Anna, Anton-Culver, Hoda, Nord, Silje, Neuhausen, Susan L., Arndt, Volker, Brenner, Hermann, Engel, Christoph, Meindl, Alfons, Schmutzler, Rita K., Arnold, Norbert, Brauch, Hiltrud, Hamann, Ute, Chang-Claude, Jenny, Kar, Siddhartha, Khan, Sofia, Nevanlinna, Heli, Ito, Hidemi, Matsuo, Keitaro, Bogdanova, Natalia V., Dörk, Thilo, Lindblom, Annika, Margolin, Sara, Kosma, Veli-Matti, Mannermaa, Arto, Humphreys, Keith, Tseng, Chiu-chen, Wu, Anna H., Floris, Giuseppe, Lambrechts, Diether, Rudolph, Anja, Peterlongo, Paolo, Radice, Paolo, Couch, F. J., Vachon, C., Giles, G. G., Thompson, Deborah, McLean, C., Milne, R. L., Dugué, P.-A., Haiman, C. A., Maskarinec, G., Woolcott, C., Henderson, B. E., Goldberg, M. S., Simard, J., Teo, S. H., Ghoussaini, Maya, Mariapun, S., Helland, A., Haakensen, V., Zheng, W., Beeghly-Fadiel, A., Tamimi, R., Jukkola-Vuorinen, A., Winqvist, R., Andrulis, I. L., Knight, J. A., Bolla, Manjeet K., Devilee, P., Tollenaar, R. A. E. M., Figueroa, J., García-Closas, M., Czene, K., Hooning, M. J., Tilanus-Linthorst, M., Li, J., Gao, Y.-T., Shu, X.-O.. Cell Press; 2015. Polymorphisms in a putative enhancer at the 10q21.2 breast cancer risk locus regulate NRBF2 expression.

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.

Avery-Kiejda, Kelly A., Braye, Stephen G., Forbes, John F., Scott, Rodney J.. BioMed Central; 2014. The expression of Dicer and Drosha in matched normal tissues, tumours and lymph node metastases in triple negative breast cancer.

Wong-Brown, Michelle W., Avery-Kiejda, Kelly A., Bowden, Nikola A., Scott, Rodney J.. John Wiley & Sons; 2014. Low prevalence of germline PALB2 mutations in Australian triple-negative breast cancer.

Ingason, A., Giegling, I., Collier, D. A., O'Donovan, M. C., Mirnics, K., Rujescu, D., Henskens, Frans A., Cairns, Murray J., Kelly, Brian J., Loughland, Carmel M., Schall, Ulrich, Scott, Rodney J., Hartmann, A. M., Tooney, Paul A., Michie, Patricia T., Wu, Jing Qin, Genius, J., Konte, B., Friedl, M., Schizophrenia Working Group of the Psychiatric Genomics Consortium (PGC),, Ripke, S., Sullivan, P. F., St. Clair, D.. Nature Publishing; 2015. Expression analysis in a rat psychosis model identifies novel candidate genes validated in a large case-control sample of schizophrenia.

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.

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.

Revelas, Mary, Thalamuthu, Anbupalam, Attia, John R., Mather, Karen A., Oldmeadow, Christopher, Evans, Tiffany-Jane, Armstrong, Nicola J., Kwok, John B., Brodaty, Henry, Schofield, Peter R., Scott, Rodney J., Sachdev, Perminder S.. Elsevier; 2018. Review and meta-analysis of genetic polymorphisms associated with exceptional human longevity.

Cheng, Timothy H. T., Thompson, Deborah J., Gorman, Maggie, Martin, Lynn, National Study of Endometrial Cancer Genetics Group (NSECG),, Hodgson, Shirley, Webb, Penelope M., Australian National Endometrial Cancer Study Group (ANECS),, Attia, John, Holliday, Elizabeth G., McEvoy, Mark, Scott, Rodney J., O'Mara, Tracy A., Dowdy, Sean C., Ashton, Katie, Otton, Geoffrey, Proietto, Tony, , , , , , , Painter, Jodie N., , , , , , , , , , , Glubb, Dylan M., , , , , , , , , , , Flach, Susanne, , , , , , , , , , , Lewis, Annabelle, , , , , , , , , , , French, Juliet D., , , , , , , , , , , Freeman-Mills, Luke, , , , , , , , , , , Church, David, , . Nature Publishing Group; 2016. Five endometrial cancer risk loci identified through genome-wide association analysis.

Thompson, Bryony A., Spurdle, Amanda B., du Sart, Desiree, Fabre, Aurelie, Farrell, Michael P., Farrington, Susan M., Frayling, Ian M., Frebourg, Thierry, Goldgar, David E., Heinen, Christopher D., Holinski-Feder, Elke, Kohonen-Corish, Maija, Plazzer, John-Paul, Robinson, Kristina Lagerstedt, Leung, Suet Yi, Martins, Alexandra, Moller, Pat, Morak, Monika, Nystrom, Minna, Peltomaki, Paivi, Pineda, Marta, Qi, Ming, Ramesar, Rajkumar, Greenblatt, Marc S., Rasmussen, Lene Juel, Royer-Pokora, Brigitte, Scott, Rodney J., Sijmons, Rolf, Tavtigian, Sean V., Tops, Carli M., Weber, Thomas, Wijnen, Juul, Woods, Michael O., Macrae, Finlay, Akagi, Kiwamu, Genuardi, Maurizio, Al-Mulla, Fahd, Bapat, Bharati, Bernstein, Inge, Capellá, Gabriel, den Dunnen, John T.. Nature Publishing Group; 2014. Application of a 5-tiered scheme for standardized classification of 2,360 unique mismatch repair gene variants in the InSiGHT locus-specific database.

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.

Dias, Thlani H., Biswas, Mohitosh, Daneshi, Nilofar, Holliday, Elizabeth, Hancock, Stephen, Munro, Irene, Kerr, Karen, Attia, John, Scott, Rodney J., Milward, Elizabeth A.. Global Science and Technology Forum (GSTF); 2017. Initial investigations of simple and multifactorial drug-gene interactions related to methotrexate in a community cohort.

Geaghan, Michael P., Atkins, Joshua R., Brichta, Alan M., Tooney, Paul A., Scott, Rodney J., Carr, Vaughan J., Cairns, Murray J.. Elsevier; 2019. Alteration of miRNA-mRNA interactions in lymphocytes of individuals with schizophrenia.

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.

Li, Na, Thompson, Ella R., Gorringe, Kylie L., James, Paul A., Campbell, Ian G., Rowley, Simone M., McInerny, Simone, Devereux, Lisa, Goode, David, LifePool Investigators,, Wong-Brown, Michelle W., Scott, Rodney J., Trainer, Alison H.. Springer; 2016. Reevaluation of RINT1 as a breast cancer predisposition gene.

Talseth-Palmer, Bente A., Scott, Rodney J., Vasen, Hans F. A., Wijnen, Juul T.. Nature Publishing Group; 2012. 8q23.3 and 11q23.1 as modifying loci influencing the risk for CRC in Lynch syndrome.

Talseth-Palmer, Bente A., McPhillips, Mary, Groombridge, Claire, Spigelman, Allan, Scott, Rodney J.. BioMed Central; 2010. MSH6 and PMS2 mutation positive Australian Lynch syndrome families: novel mutations, cancer risk and age of diagnosis of colorectal cancer.

Milne, Elizabeth, Greenop, Kathryn R., Scott, Rodney J., de Klerk, Nicholas H., Bower, Carol, Ashton, Lesley J., Heath, John A., Armstrong, Bruce K.. Springer Netherlands; 2013. Parental alcohol consumption and risk of childhood acute lymphoblastic leukemia and brain tumors.

Avery-Kiejda, Kelly A., Zhang, Xu Dong, Adams, Luke J., Scott, Rodney J., Vojtesek, Borivoj, Lane, David P., Hersey, Peter. American Association for Cancer Research, Inc; 2008. Small molecular weight variants of p53 are expressed in human melanoma cells and are induced by the DNA-damaging agent cisplatin.

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?.

Talseth-Palmer, Bente A., Holliday, Elizabeth G., Evans, Tiffany-Jane, McEvoy, Mark, Attia, John, Grice, Desma M., Masson, Amy L., Meldrum, Cliff, Spigelman, Allan, Scott, Rodney J.. BioMed Central Ltd; 2013. Continuing difficulties in interpreting CNV data: lessons from a genome-wide CNV association study of Australian HNPCC/lynch syndrome patients.

Kim, Kyu-Tae, Mossman, David, Small, Donald, Scott, Rodney J.. Scientific Research Publishing; 2012. Gene expression profiling of human myeloid leukemic MV4-11 cells treated with 5-Aza-2’-deoxycytidine.

Baines, Katherine J., Simpson, Jodie L., Wood, Lisa G., Scott, Rodney J., Gibson, Peter G.. Mosby; 2011. Transcriptional phenotypes of asthma defined by gene expression profiling of induced sputum samples.

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.

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.

Hansen, Maren F., Johansen, Jostein, Sjursen, Wenche, Sylvander, Anna E., Bjørnevoll, Inga, Talseth-Palmer, Bente A., Lavik, Liss A. S., Xavier, Alexandre, Engebretsen, Lars F., Scott, Rodney J., Drabløs, Finn. Wiley-Blackwell; 2017. Use of multigene-panel identifies pathogenic variants in several CRC-predisposing genes in patients previously tested for Lynch Syndrome.

Kennedy, Daniel W., White, Nicole M., Benton, Miles C., Fox, Andrew, Scott, Rodney J., Griffiths, Lyn R., Mengersen, Kerrie, Lea, Rodney A.. Public Library of Science (PLoS); 2018. Critical evaluation of linear regression models for cell-subtype specific methylation signal from mixed blood cell DNA.

Morten, Brianna C., Wong-Brown, Michelle W., Scott, Rodney J., Avery-Kiejda, Kelly A.. Oxford University Press; 2016. The presence of the intron 3 16 bp duplication polymorphism of p53 (rs17878362) in breast cancer is associated with a low ∆40p53:p53 ratio and better outcome.

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.

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.

Kumarasinghe, Nishantha, Beveridge, Natalie J., Gardiner, Erin, Scott, Rodney J., Yasawardene, Surangi, Perera, Antoinette, Mendis, Jayan, Suriyakumara, Kanishka, Schall, Ulrich, Tooney, Paul A.. Cambridge University Press; 2013. Gene expression profiling in treatment-naive schizophrenia patients identifies abnormalities in biological pathways involving AKT1 that are corrected by antipsychotic medication.

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.

Wong-Brown, Michelle W., Meldrum, Cliff J., Carpenter, Jane E., Clarke, Christine L., Narod, Steven A., Jakubowska, Anna, Rudnicka, Helena, Lubinski, Jan, Scott, Rodney J.. Springer; 2015. Prevalence of BRCA1 and BRCA2 germline mutations in patients with triple-negative breast cancer.

Talseth-Palmer, Bente A., Wijnen, Juul T., Suchy, Janina, Kurzawski, Grzegorz, The Dutch Cancer Genetics Group,, Spigelman, Allan, Møller, Pål, Morreau, Hans M., Van Wezel, Tom, Lubinski, Jan, Vasen, Hans F. A., Scott, Rodney J., Brenne, Ingvild S., Jagmohan-Changur, Shantie, Barker, Daniel, Ashton, Katie A., Tops, Carli M., Evans, Tiffany-Jane, McPhillips, Mary, Groombridge, Claire. John Wiley & Sons; 2013. Combined analysis of three lynch syndrome cohorts confirms the modifying effects of 8q23.3 and 11q23.1 in MLH1 mutation carriers.

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.

Johnstone, Daniel, Graham, Ross M., Trinder, Debbie, Delima, Roheeth D., Riveros, Carlos, Olynyk, John K., Scott, Rodney J., Moscato, Pablo, Milward, Elizabeth. Elsevier; 2012. Brain transcriptome perturbations in the Hfe^-/- mouse model of genetic iron loading.

Ashton, Katie A., Proietto, Anthony, Otton, Geoffrey, Symonds, Ian, Scott, Rodney J.. BioMed Central; 2009. Genetic variants in MUTYH are not associated with endometrial cancer risk.

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

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.

Hnatyszyn, Andrzej, Hryhorowicz, Szymon, Kaczmarek-Rys, Marta, Lis, Emilia, Slomski, Ryszard, Scott, Rodney J., Plawski, Andrzej. BioMed Central; 2019. Colorectal carcinoma in the course of inflammatory bowel diseases.

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.

Picelli, Simone, Lorenzo Bermejo, Justo, Pardini, Barbara, Vodickova, Ludmila, Mueller, Heiko, Talseth-Palmer, Bente A., Stibbard, Geoffrey, Peterlongo, Paolo, Nici, Carmela, Veneroni, Silvia, Li, Li, Casey, Graham, Chang-Claude, Jenny, Tenesa, Albert, Farrington, Susan M., Tomlinson, Ian, Moreno, Victor, van Wezel, Tom, Wijnen, Juul, Dunlop, Malcolm, Radice, Paolo, Scott, Rodney J., Vodicka, Pavel, Hoffmeister, Michael, Ruiz-Ponte, Clara, Brenner, Hermann, Buch, Stephan, Voelzke, Henry, Hampe, Jochen, Schafmayer, Clemens, Lindblom, Annika, Fernandez-Rozadilla, Ceres, Carracedo, Angel, Castells, Antoni, Castellvi-Bel, Sergi, The EPICOLON Consortium, Naccarati, Alessio. Public Library of Science; 2013. Meta-analysis of mismatch repair polymorphisms within the cogent consortium for colorectal cancer susceptibility.

Sjursen, Wenche, McPhillips, Mary, Scott, Rodney J., Talseth-Palmer, Bente A.. John Wiley & Sons; 2016. Lynch syndrome mutation spectrum in New South Wales, Australia, including 55 novel mutations.

Holliday, Elizabeth G., Attia, John, Almazar, Ann E., Saito, Yuri A., Scott, Rodney J., Talley, Nicholas J., Hancock, Stephen, Koloski, Natasha, McEvoy, Mark, Peel, Roseanne, D'Amato, Mauro, Agréus, Lars, Nyhlin, Henry, Andreasson, Anna. Nature Publishing Group; 2014. Genome-wide association study identifies two novel genomic regions in irritable bowel syndrome.

De Vivo, Immaculata, Prescott, Jennifer, Cook, Linda S., Crous-Bou, Marta, Doherty, Jennifer, Dunning, Alison M., Easton, Douglas F., Friedenreich, Christine M., Garcia-Closas, Montserrat, Gaudet, Mia M., Haiman, Christopher, Hankinson, Susan E., Setiawan, Veronica Wendy, Hartge, Patricia, Henderson, Brian E., Holliday, Elizabeth, Horn-Ross, Pamela L., Hunter, David J., Le Marchand, Loic, Liang, Xiaolin, Lissowska, Jolanta, Long, Jirong, Lu, Lingeng, Olson, Sara H., Magliocco, Anthony M., McEvoy, Mark, O'Mara, Tracy A., Orlow, Irene, Painter, Jodie N., Pooler, Loreall, Rastogi, Radhai, Rebbeck, Timothy R., Risch, Harvey, Sacerdote, Carlotta, Wentzensen, Nicolas, Schumacher, Frederick, Scott, Rodney J., Sheng, Xin, Shu, Xiao-ou, Spurdle, Amanda B., Thompson, Deborah, VanDen Berg, David, Weiss, Noel S., Xia, Lucy, Xiang, Yong-Bing, Attia, John, Yang, Hannah P., Yu, Herbert, Zheng, Wei, Chanock, Stephen, Kraft, Peter, Black, Amanda, Brinton, Louise, Chen, Chu, Chen, Constance. Springer; 2014. Genome-wide association study of endometrial cancer in E2C2.

Spurdle, Amanda B., Thompson, Deborah J., Fahey, Paul, Montgomery, Grant W., Webb, Penelope M., Fasching, Peter A., Beckmann, Matthias W., Ekici, Arif B., Hein, Alexander, Lambrechts, Diether, Coenegrachts, Lieve, Vergote, Ignace, Ahmed, Shahana, Amant, Frederic, Salvesen, Helga B., Trovik, Jone, Njolstad, Tormund S., Helland, Harald, Scott, Rodney J., Ashton, Katie, Proietto, Tony, Otton, Geoffrey, National Study of Endometrial Cancer Genetics Group,, Ferguson, Kaltin, Tomlinson, Ian, Gorman, Maggie, Howarth, Kimberley, Hodgson, Shirley, Garcia-Closas, Montserrat, Wentzensen, Nicolas, Yang, Hannah, Chanock, Stephen, Hall, Per, Czene, Kamila, Healey, Catherine S., Liu, Jianjun, Li, Jingmei, Shu, Xiao-Ou, Zheng, Wei, Long, Jirong, Xiang, Yong-Bing, Shah, Mitul, Morrison, Jonathan, Michailidou, Kyriaki, Pharoah, Paul D., O'Mara, Tracy, Dunning, Alison M., Easton, Douglas F., Walker, Logan C,, Montgomery, Stephen B., Dermitzakis, Emmanouil T., Australian National Endometrial Cancer Study Group,. Nature Publishing Group; 2011. Genome-wide association study identifies a common variant associated with risk of endometrial cancer.

Lubiński, Jan, Sijmons, Rolf H., Scott, Rodney J.. BioMed Central; 2009. Hereditary cancer in clinical practice transfers to BioMed Central (editorial).

Johnstone, Daniel M., Graham, Ross M., Trinder, Debbie, Riveros, Carlos, Olynyk, John K., Scott, Rodney J., Moscato, Pablo, Milward, Elizabeth A.. IOS Press; 2012. Changes in brain transcripts related to Alzheimer's disease in a model of HFE hemochromatosis are not consistent with increased Alzheimer's disease risk.

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.

Dun, Matthew D., Chalkley, Robert J., Hondermarck, Hubert, Faulkner, Sam, Keene, Sheridan, Avery-Kiejda, Kelly A., Scott, Rodney J., Falkenby, Lasse G., Cairns, Murray J., Larsen, Martin R., Bradshaw, Ralph A.. American Society for Biochemistry and Molecular Biology; 2015. Proteotranscriptomic profiling of 231-BR breast cancer cells: identification of potential biomarkers and therapeutic targets for brain metastasis.

Strumidło, Agnieszka, Skiba, Sylwia, Scott, Rodney J., Lubiński, Jan. BioMed Central; 2017. The potential role of miRNAs in therapy of breast and ovarian cancers associated with BRCA1 mutation.

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.

Thompson, Ella R., Gorringe, Kylie L., Lupat, Richard, Delatycki, Martin B., LifePool Investigators,, Mitchell , Gillian, James , Paul A., Scott, Rodney J., Campbell, Ian G., Rowley, Simone M., Wong-Brown, Michelle W., McInerny, Simone, Li, Na, Trainer, Alison H., Devereux, Lisa, Doyle, Maria A., Li, Jason. BioMed Central; 2015. Prevalence of PALB2 mutations in Australian familial breast cancer cases and controls.

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.

Li, Na, Zethoven, Magnus, Nguyen-Dumont, Tu, Southey, Melissa C., Hopper, John L., Simard, Jacques, Dumont, Martine, Soucy, Penny, Meindl, Alfons, Schmutzler, Rita, Schmidt, Marjanka K., Adank, Muriel A., McInerny, Simone, Andrulis, Irene L., Hahnen, E, Engel, C, Lesueur, F, Girard, E, Neuhausen, SL, Ziv, E, Allen, J, Easton, DF, Scott, Rodney J., Devereux, Lisa, Gorringe, KL, James, PA, Campbell, IG, Huang, Yu-Kuan, Thio, Niko, Cheasley, Dane, Gutiérrez-Enríquez, Sara, Moles-Fernández, Alejandro, Diez, Orland. Nature Publishing Group; 2021. Evaluation of the association of heterozygous germline variants in NTHL1 with breast cancer predisposition: an international multi-center study of 47,180 subjects.

Nead, Kevin T., Sharp, Stephen J., Easton, Douglas F., Holliday, Elizabeth, Lotta, Luca A., O'Mara, Tracy, McEvoy, Mark, Pharoah, Paul D. P., Scott, Rodney J., Spurdle, Amanda B., Langenberg, Claudia, Wareham, Nicholas J., Thompson, Deborah J., Scott, Robert A., , Painter, Jodie N., Savage, David B., Semple, Robert K., Barker, Adam, Perry, John R. B., Attia, John, Dunning, Alison M.. Oxford University Press; 2015. Evidence of a causal association between insulinemia and endometrial cancer: a Mendelian randomization analysis.

Delforce, Sarah J., Lumbers, Eugenie R., Corbisier de Meaultsart, Celine, Wang, Yu, Proietto, Anthony, Otton, Geoffrey, Scurry, Jim, Verrills, Nicole M., Scott, Rodney J., Pringle, Kirsty G.. Bioscientifica; 2017. Expression of renin–angiotensin system (RAS) components in endometrial cancer.

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.

Riveros, Carlos, Vimieiro, Renato, Holliday, Elizabeth G., Oldmeadow, Christopher, Wang, Jie Jin, Mitchell, Paul, Attia, John, Scott, Rodney J., Moscato, Pablo A.. Springer; 2015. Identification of genome-wide SNP-SNP and SNP-clinical Boolean interactions in age-related macular degeneration.

Jensen, Cathy J., Stankovich, Jim, Field, Judith, Danoy, Patrick, Brown, Matthew A., The Australian and New Zealand Multiple Sclerosis Genetics Consortium (ANZgene), Lechner-Scott, Jeanette, Moscato, Pablo, Scott, Rodney J., Rubio, Justin P,, Butzkueven, Helmut, Van der Walt, Anneke, Bahlo, Melanie, Taylor, Bruce V,, van der Mei, Ingrid A. F., Foote, Simon J., Kilpatrick, Trevor J,, Johnson, Laura J., Wilkins, Ella. Public Library of Science; 2010. Multiple sclerosis susceptibility-associated SNPs do not influence disease severity measures in a cohort of Australian MS patients.

Masson, Amy L., Talseth-Palmer, Bente A., Evans, Tiffany-Jane, Grice, Desma M., Hannan, Garry N., Scott, Rodney J.. BioMed Central; 2014. Expanding the genetic basis of copy number variation in familial breast cancer.

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.

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.

Moscovis, Sophia M., Cox, Amanda, Hall, Sharron T., Burns, Christine J., Scott, Rodney J., Blackwell, C. Caroline. Sage; 2015. Effects of gender, cytokine gene polymorphisms and environmental factors on inflammatory responses.

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.

Morten, Brianna C., Chiu, Simon, Oldmeadow, Christopher, Lubinski, Jan, Scott, Rodney J., Avery-Kiejda, Kelly A.. Springer; 2019. The intron 3 16 bp duplication polymorphism of p53 (rs17878362) is not associated with increased risk of developing triple-negative breast cancer.

Jaworowska, Ewa, Serrano-Fernandez, Pablo, Lubinski, Jan, Tarnowska, Czeslawa, Lubinski, Jakub, Brzosko, Marek, Flicinski, Jacek, Masojc, Bartolomej, Matyjasik, Joanna, Scott, Rodney J., Narod, Steven A.. Springer; 2008. Familial association of laryngeal, lung, stomach and early-onset breast cancer.

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.

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.

Greenop, Kathryn R., Peters, Susan, Milne, Elizabeth, Bailey, Helen D., Fritschi, Lin, Attia, John, Scott, Rodney J., Glass, Deborah C., de Klerk, Nicholas H., Alvaro, Frank, Armstrong, Bruce K.. Springer Netherlands; 2013. Exposure to pesticides and the risk of childhood brain tumors.

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.

Wan, Charles, Latter, Joanna L., Amirshahi, Ashkan, Symonds, Ian, Finnie, Jane, Bowden, Nikola, Scott, Rodney J., Cunningham, Kelly A., Timms, Peter, Beagley, Kenneth W.. Wiley-Blackwell; 2014. Progesterone activates multiple innate immune pathways in <i>Chlamydia trachomatis</i>-infected endocervical cells.

Jaworska-Bieniek, Katarzyna, Lener, Marcin, Grodzki, Tomasz, Jaworowska, Ewa, Lubiński, Jakub, Górecka-Szyld, Barbara, Wilk, Grażyna, Huzarski, Tomasz, Byrski, Tomasz, Cybulski, Cezary, Gronwald, Jacek, Dębniak, Tadeusz, Muszyńska, Magdalena, Scott, Rodney J., Serrano-Fernández, Pablo, Sukiennicki, Grzegorz, Durda, Katarzyna, Gromowski, Tomasz, Gupta, Satish, Kladny, Józef, Wiechowska-Kozłowska, Anna. Royal Society of Chemistry; 2015. Selenium and cancer.

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.

Smith, Casey Jo Anne, Bensing, Sophie, Maltby, Vicki E., Zhang, Mingdong, Scott, Rodney J., Smith, Roger, Kämpe, Olle, Hökfelt, Tomas, Crock, Patricia A.. Springer; 2014. Intermediate lobe immunoreactivity in a patient with suspected lymphocytic hypophysis.

Ashton, Katie A., Proietto, Anthony, Otton, Geoffrey, Symonds, Ian, McEvoy, Mark, Attia, John, Gilbert, Michael, Hamann, Ute, Scott, Rodney J.. Elsevier; 2009. Polymorphisms in TP53 and MDM2 combined are associated with high grade endometrial cancer.

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.

Bowden, Nikola A., Weidenhofer, Judith, Scott, Rodney J., Schall, Ulrich, Todd, Juanita, Michie, Patricia T., Tooney, Paul A.. Elsevier; 2006. Preliminary investigation of gene expression profiles in peripheral blood lymphocytes in schizophrenia.

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.

Ni, Guiyan, Moser, Gerhard, Ripke, Stephan, Neale, Benjamin M., Corvin, Aiden, Walters, James T. R., Farh, Kai-How, Holmans, Peter A., Lee, Phil, Bulik-Sullivan, Brendan, Collier, David A., Huang, Hailiang, Pers, Tune H., Agartz, Ingrid, Agerbo, Esben, Albus, Margot, Alexander, Madeline, Amin, Farooq, Bacanu, Silviu A., Henskens, Frans A., Loughland, Carmel A., Michie, Patricia T., Schall, Ulrich, Scott, Rodney J., Wray, Naomi R., Lee, S. Hong. Cell Press; 2018. Estimation of Genetic Correlation via Linkage Disequilibrium Score Regression and Genomic Restricted Maximum Likelihood.

Michailidou, Kyriaki, Lindström, Sara, Bolla, Manjeet K., , , , , , , , , , , Wang, Qin, , , , , , , , , , , Tyrer, Jonathan, , , , , , , , , , , Dicks, Ed, , , , , , , , , , , Lee, Andrew, , , , , , , , , , , Wang, Zhaoming, , , , , , , , , , , Allen, Jamie, , , , , , , , , , , Keeman, Renske, , , , , , , , , , , Eilber, Ursula, , , , , , , , , , , French, Juliet D., , , , , , , , , , , Dennis, Joe, Scott, Rodney J., , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Beesley, Jonathan, , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Hui, Shirley, , , , , , , , , , , Kar, Siddhartha, , , , , , , , , , , Lemaçon, Audrey, , , , , , , , , , , Soucy, Penny, , , , , , , , , , , Glubb, Dylan, , , , , , , , , , , Rostamianfar, Asha, , , , , , , , , , . Nature Publishing Group; 2017. Association analysis identifies 65 new breast cancer risk loci.

Cheng, Yu-Ching, Anderson, Christopher D., Barlera, Simona, Biffi, Alessandro, Bookman, Ebony, Brott, Thomas G., Brown, Robert D., Chen, Fang, Chen, Wei-Min, Ciusani, Emilio, Cole, John W., Cortellini, Lynelle, Bione, Silvia, Danesh, John, Doheny, Kimberley, Ferrucci, Luigi, Franzosi, Maria Grazia, Frossard, Philippe, Furie, Karen L., Golledge, Jonathan, Hankey, Graeme J., Hernandez, Dena, Holliday, Elizabeth G., Keene, Keith, Hsu, Fang-Chi, Jannes, Jim, Kamal, Ayeesha, Khan, Muhammad Saleem, Kittner, Steven J., Koblar, Simon A., Lewis, Martin, Lincz, Lisa, Lisa, Antonella, Matarin, Mar, Maguire, Jane M., Moscato, Pablo, Mychaleckyj, Josyf C., Parati, Eugenio A., Parolo, Silvia, Pugh, Elizabeth, Rost, Natalia S., Schallert, Michael, Schmidt, Helena, Scott, Rodney J., Sturm, Jonathan W., Nalls, Michael, Yadav, Sunaina, Zaidi, Moazzam, Boncoraglio, Giorgio B., Levi, Christopher Royce, Meschia, James F., Rosand, Jonathan, Sale, Michele, Saleheen, Danish, Schmidt, Reinhold, Sharma, Pankaj, Rasheed, Asif, Worrall, Bradford, Mitchell, Branxton D., Zeginigg, Marion, Attia, John, Baker, Ross. Lippincott Williams & Wilkins; 2012. Are myocardial infarction-associated single-nucleotide polymorphisms associated with ischemic stroke?.

Revelas, Mary, Thalamuthu, Anbupalam, Attia, John R., Sachdev, Perminder S., Mather, Karen A., Oldmeadow, Christopher, Evans, Tiffany-Jane, Armstrong, Nicola J., Riveros, Carlos, Kwok, John B., Schofield, Peter R., Brodaty, Henry, Scott, Rodney J.. MDPI AG; 2019. Exceptional longevity and polygenic risk for cardiovascular health.

Ashton, Katie A., Proietto, Anthony, Otton, Geoffrey, Symonds, Ian, McEvoy, Mark, Attia, John, Scott, Rodney J.. BioMed Central; 2010. Toll-like receptor (TLR) and nucleosome-binding oligomerization domain (NOD) gene polymorphisms and endometrial cancer risk.

O'Brien, Aidan R., Saunders, Neil F. W., Guo, Yi, Buske, Fabian A., Scott, Rodney J., Bauer, Denis C.. BioMed Central; 2015. VariantSpark: population scale clustering of genotype information.

Avery-Kiejda, Kelly A., Morten, Brianna, Wong-Brown, Michelle W., Mathe, Andrea, Scott, Rodney J.. Oxford University Press; 2014. The relative mRNA expression of p53 isoforms in breast cancer is associated with clinical features and outcome..

Young, Kathleen M. N., Scurry, James, Jaaback, Kenneth, Bowden, Nikola A., Scott, Rodney J.. Lippincott Williams & Wilkins; 2012. Bilateral dysgerminoma associated with gonadoblastoma and sex-cord stromal tumour with annular tubules in a 28-year-old fertile woman with normal karyotype.

Kairupan, Carla F., Meldrum, Cliff J., Williams, Rachel, Scott, Rodney J., Crooks, Renee, Milward, Elizabeth A., Spigelman, Allan D., Burgess, Bronwyn, Groombridge, Claire, Kirk, Judy, Tucker, Kathy, Ward, Robyn. Wiley-Liss, Inc.; 2005. Mutation analysis of the MYH gene in an Australian series of colorectal polyposis patients with or without germline APC mutations.

Sapkota, Yadav, Attia, John, Scott, Rodney J., Zondervan, Krina T., Montgomery, Grant W., Nyholt, Dale R., Gordon, Scott D., Henders, Anjali K., Holliday, Elizabeth G., Rahmioglu, Nilufer, MacGregor, Stuart, Martin, Nicholas G., McEvoy, Mark, Morris, Andrew P.. Oxford University Press; 2015. Genetic burden associated with varying degrees of disease severity in endometriosis.

Li, Wen, Fan, Chun Chieh, Mäki-Marttunen, Tuomo, Thompson, Wesley K., Schork, Andrew J., Bettella, Francesco, Ripke, Stephan, Neal, Benjamin M., Corvin, Aiden, Walters, James T. R., Farh, Kai-How, Holmans, Peter A., Lee, Phil, Bulik-Sullivan, Brendan, Collier, David A., Huang, Hailiang, Cairns, Murray J., Henskens, Frans A., Kelly, Brian J., Michie, Patricia T., Schall, Ulrich, Scott, Rodney J., Tooney, Paul A., Wu, Jing Qin, Djurovic, Srdjan, Dale, Andrew M., Andreassen, Ole A., Wang, Yunpeng. Wiley; 2018. A molecule-based genetic association approach implicates a range of voltage-gated calcium channels associated with schizophrenia.

Suchy, Janina, Kłujszo-Grabowska, Ewa, Kładny, Józef, Cybulski, Cezary, Wokołorczyk, Dominika, Szymańska-Pasternak, Jolanta, Kurzawski, Grzegorz, Scott, Rodney J., Lubiński, Jan. BioMed Central; 2008. Inflammatory response gene polymorphisms and their relationship with colorectal cancer risk.

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.

Scott, Rodney J.. Nature Publishing Group; 2008. Variable phenotypic expression in HNPCC and the search for modifier genes.

Nyholt, Dale R., Low, Siew-Kee, Attia, John, Holliday, Elizabeth G., McEvoy, Mark, Scott, Rodney J., Kennedy, Stephen H., Treloar, Susan A., Missmer, Stacey A., Adachi, Sosuke, Tanaka, Knichi, Nakamura, Yusuke, Anderson, Carl A., Zondervan, Krina T., Zembutsu, Hitoshi, Montgomery, Grant W., Painter Jodie N., Yun-Chul, Uno, Satoko, Morris, Andrew P., MacGregor, Stuart, Gordon, Scott D., Henders, Anjali K., Martin, Nicholas G.. Nature Publishing Group; 2012. Genome-wide association meta-analysis identifies new endometriosis risk loci.

Titmarsh, Callum J., Moscovis, Sophia M., Hall, Sharron, Tzanakaki, Georgina, Kesanopoulos, Konstantinos, Xirogianni, Athanasia, Scott, Rodney J., Blackwell, C. Caroline. Society for General Microbiology; 2013. Comparison of cytokine gene polymorphisms among Greek patients with invasive meningococcal disease or viral meningitis.

Field, Judith, Shahijanian, Fernando, Butzkueven, Helmut, Booth, David, Baxter, Alan, Kermode, Allan G., Taylor, Bruce, Booth, David R., Mason, Deborah, Stewart, Graeme J., Butzkueven, Helmut, Charlesworth, Jac, Schibeci, Stephen, Wiley, James, Lechner-Scott, Jeannette, Field, Judith, Tajouri, Lotti, Griffiths, Lyn, Slee, Mark, Brown, Matthew A., Moscato, Pablo, Scott, Rodney J., Broadley, Simon, Johnson, Laura, Vucic, Steve, Kilpatrick, Trevor, Carroll, William M., Gresle, Melissa, Laverick, Louise, Parnell, Grant, Stewart, Graeme, McKay, Fiona, Kilpatrick, Trevor. Public Library of Science (PLOS); 2015. The MS risk allele of CD40 is associated with reduced cell-membrane bound expression in antigen presenting cells: implications for gene function.

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.