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

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.

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.

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

Pan, Xin, Bowman, Maria, Scott, Rodney J., Fitter, John, Smith, Roger, Zakar, Tamas. Public Library of Science (PLoS); 2017. Promoter methylation pattern controls corticotropin releasing hormone gene activity in human trophoblasts.

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.

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.

Painter, Jodie N., Kaufmann, Susanne, Hoivik, Erling A., Goode, Ellen L., Scott, Rodney J., Tomlinson, Ian, Dunning, Alison M., Easton, Douglas F., French, Juliet D., Salvesen, Helga B., Pollock, Pamela M., Thompson, Deborah J., O'Mara, Tracy A., Spurdle, Amanda B., Edwards, Stacey L., Hillman, Kristine M., Sivakumaran, Haran, Darabi, Hatef, Cheng, Timothy H.T., Pearson, John, Kazakoff, Stephen, Waddell, Nicola. Cell Press; 2016. A common variant at the 14q32 endometrial cancer risk locus activates AKT1 through YY1 binding.

McLaughlin, Russell L., Schijven, Dick, Schall, Ulrich, Scott, Rodney J., , , , , , , , , van Rheenen, Wouter, , , , , , , , , , , van Eijk, Kristel R., , , , , , , , , , , O'Brien, Margaret, , , , , , , , , , , Project MinE GWAS Consortium,, , , , , , , , , , , Schizophrenia Working Group of the Psychiatric Genomics Consortium,, , , , , , , , , , , Henskens, Frans A., , , , , , , , , , , Loughland, Carmel M., , Michie, Patricia T., Khan, René S., Ophoff, Roel A., Goris, An, Bradley, Daniel G., Al-Chalabi, Ammar, van den Berg, Leonard H., Luykx, Jurjen J.. Nature Publishing Group; 2017. Genetic correlation between amyotrophic lateral sclerosis and schizophrenia.

Berry, Nadine K., Scott, Rodney J., Rowlings, Philip, Enjeti, Anoop K.. Elsevier; 2019. Clinical use of SNP-microarrays for the detection of genome-wide changes in haematological malignancies.

Wiik, Mariann Unhjem, Evans, Tiffany-Jane, Belhadj, Sami, Bolton, Katherine A., Dymerska, Dagmara, Jagmohan-Changur, Shantie, Capellá, Gabriel, Kurzawski, Grzegorz, Wijnen, Juul T., Valle, Laura, Vasen, Hans F. A., Lubinski, Jan, Scott, Rodney J., Talseth-Palmer, Bente A.. Nature Publishing Group; 2021. A genetic variant in telomerase reverse transcriptase (TERT) modifies cancer risk in Lynch syndrome patients harbouring pathogenic MSH2 variants.

Gromowski, Tomasz, Gapska, Paulina, Kaczmarek, Katarzyna, Jaworska-Bieniek, Katarzyna, Paszkowska-Szczur, Katarzyna, Waloszczyk, Piotr, Lubinski, Jan, Debniak, Tadeusz, Scott, Rodney J., Kaklewski, Krzysztof, Marciniak, Wojciech, Durda, Katarzyna, Lener, Marcin, Górski, Bohdan, Cybulski, Cezary, Sukiennicki, Grzegorz. John Wiley; 2017. Serum 25(OH)D concentration, common variants of the VDR gene and lung cancer occurrence.

Cox, Mathew B., Bowden, Nikola A., Scott, Rodney J., Lechner-Scott, Jeannette. Sage; 2014. Common genetic variants in the plasminogen activation pathway are not associated with multiple sclerosis.

Cox, Amanda J., Gleeson, Maree, Pyne, David B., Callister, Robin, Fricker, Peter A., Scott, Rodney J.. Verein zur Foerderung der Sportmedizin; 2010. Cytokine gene polymorphisms and risk for upper respiratory symptoms in highly-trained athletes.

Kurzawski, Grzegorz, Suchy, Janina, Domagala, Wenancjusz, Scott, Rodney J., Lubinski, Jan, Kladny, Jozef, Grabowska, Ewa, Mierzejewski, Marek, Jakubowska, Anna, Debniak, Tadeusz, Cybulski, Cezary, Kowalska, Elsbieta, Szych, Zbigniew. American Association Cancer Research; 2004. The NOD2 3020insC mutation and the risk of colorectal cancer.

Baines, Katherine J., Simpson, Jodie L., Scott, Rodney J., Gibson, Peter G.. Informa Healthcare; 2009. Immune responses of airway neutrophils are impaired in asthma.

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

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.

Sanders, Katherine A., Benton, Miles C., Lea, Rod A., Maltby, Vicki E., Agland, Susan, Griffin, Nathan, Scott, Rodney J., Tajouri, Lotto, Lechner-Scott, Jeannette. BioMed Central; 2016. Next-generation sequencing reveals broad down-regulation of microRNAs in secondary progressive multiple sclerosis CD4+T cells.

Le Hellard, Stephanie, Wang, Yunpeng, Schork, Andrew J., Thompson, Wesley K., Dale, Anders M., Djurovic, Srdjan, Andreassen, Ole A., Cairns, Murray J., Henskens, Frans, Kelly, Brian J., Loughland, Carmel, Michie, Patricia T., Witoelar, Aree, Schall, Ulrich, Scott, Rodney J., Tooney, Paul A., Wu, Jing Qin, Zuber, Verena, Bettella, Francesco, Hugdahl, Kenneth, Espeseth, Thomas, Steen, Vidar M., Melle, Ingrid, Desikan, Rahul. Oxford University Press; 2017. Identification of gene loci that overlap between schizophrenia and educational attainment.

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.

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.

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

Talseth-Palmer, Bente A., Wijnen, Juul T., Grice, Desma M., Scott, Rodney J.. Springer Netherlands; 2013. Genetic modifiers of cancer risk in Lynch syndrome: a review.

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.

Abdullah, Noraidatulakma, Attia, John, Oldmeadow, Christopher, Scott, Rodney J., Holliday, Elizabeth G.. Hindawi Publishing Corporation; 2014. The architecture of risk for type 2 diabetes: understanding Asia in the context of global findings.

Bialkowska, Katarzyna, Marciniak, Wojciech, Cybulski, Cezary, Huzarski, Tomasz, Gronwald, Jacek, Debniak, Tadeusz, Scott, Rodney J., Lubinski, Jan, Jakubowska, Anna, Muszynska, Magdalena, Baszuk, Piotr, Gupta, Satish, Jaworska-Bieniek, Katarzyna, Sukiennicki, Grzegorz, Durda, Katarzyna, Gromowski, Tomasz, Prajzendanc, Karolina. Public Library of Science; 2018. Association of zinc level and polymorphism in MMP-7 gene with prostate cancer in Polish population.

Talseth-Palmer, Bente A., Bowden, Nikola A., Hill, Alyssa, Meldrum, Cliff, Scott, Rodney J.. Biomed Central; 2008. Whole genome amplification and its impact on CGH array profiles.

Masson, Amy L., Talseth-Palmer, Bente A., Evans, Tiffany-Jane, Grice, Desma M., Duesing, Konsta, Hannan, Garry N., Scott, Rodney J.. MDPI; 2013. Copy number variation in hereditary non-polyposis colorectal cancer.

Scott, Rodney J., Reeves, Stuart, Talseth-Palmer, Bente. InTech; 2012. The role of modifier genes in Lynch Syndrome.

Yadav, Sunaina, Cotlarciuc, Ioana, Holliday, Elizabeth G., Speed, Douglas, Hasan, Nazeeha, Pucek, Mateusz, Rinne, Paul E., Sever, Peter, Stanton, Alice, Shields, Denis C., Maguire, Jane M., McEvoy, Mark, Munroe, Patricia B., Scott, Rodney J., Ferrucci, Luigi, Macleod, Mary J., Attia, John, Markus, Hugh S., Sale, Michele M., Worrall, Bradford B., Mitchell, Braxton D., Dichgans, Martin, Sudlow, Cathy, Khan, Muhammad S., Meschia, James F., Rothwell, Peter M., Caulfield, Mark, Sharma, Pankaj, International Stroke Genetics Consortium,, Nalls, Michael A., Bevan, Steve, Cheng, Yu-Ching, Chen, Wei-Min, Malik, Rainer, McCarthy, Nina S.. Lippincott Williams & Wilkins; 2013. Genome-wide analysis of blood pressure variability and ischemic stroke.

Groen, Kira, Maltby, Vicki E., Scott, Rodney J., Tajouri, Lotti, Lechner-Scott, Jeannette. Elsevier; 2020. Concentrations of plasma-borne extracellular particles differ between multiple sclerosis disease courses and compared to healthy controls.

Ripke, Stephan, Neale, Benjamin M., Pers, Tune H., Julià, Antonio, Kahn, René S., Kalaydjieva, Luba, Karachanak-Yankova, Sena, Karjalainen, Juha, Kavanagh, David, Keller, Matthew C., Kennedy, James L., Khrunin, Audrey, Kim, Yunjung, Agartz, Iingrid, Klovins, Janis, Knowles, James A., Konte, Bettina, Kucinskas, Vaidutis, Ausrele Kucinskiene, Zita, Kuzelova-Ptackova, Hana, Kähler, Anna K., Laurent, Claudine, Lee Chee Keong, Jimmy, Hong Lee, S., Agerbo, Esben, Legge, Sophie E., Lerer, Bernard, Li, Miaoxin, Li, Tao, Liang, Kung-Yee, Lieberman, Jeffrey, Limborska, Svetlana, Loughland, Carmel M., Lubinski, Jan, Lönnqvist, Jouko, Albus, Margot, Macek Jr, Milan, Magnusson, Patrik K. E., Maher, Brion S., Maier, Wolfgang, Mallet, Jacques, Marsal, Sara, Mattheisen, Manuel, Mattingsdal, Morten, McCarley, Robert W., McDonald, Colm, Alexander, Madeline, McIntosh, Andrew M., Meier, Sandra, Meijer, Carin J., Melegh, Bela, Melle, Iingrid, Mesholam-Gately, Raquelle I., Metspalu, Andres, Michie, Patricia T., Milani, Lili, Milanova, Virha, Amin, Farooq, Mokrab, Younes, Morris, Derek W., Mors, Ole, Murphy, Kieran C., Murray, Robin M., Myin-Germeys, Inez, Müller-Myhsok, Bertram, Nelis, Mari, Nenadic, Igor, Nertney, Deborah A., Bacanu, Silviu A., Nestadt, Gerald, Nicodemus, Kristin K., Nikitina-Zake, Liene, Nisenbaum, Laura, Nordin, Annelie, O'Callaghan, Eadbhard, O'Dushlaine, Colm, O'Neill, F. Anthony, Oh, Sang-Yun, Olincy, Ann, Begemann, Martin, Olsen, Line, Van Os, Jim, Psychosis Endophenotypes International Consortium, Pantelis, Christos, Papadimitriou, George N., Papiol, Sergi, Parkhomenko, Elena, Pato, Michele T., Paunio, Tiina, Pejovic-Milovancevic, Milica, Belliveau Jr, Richard A., Perkins, Diana O., Pietiläinen, Olli, Pimm, Jonathan, Pocklington, Andrew J., Powell, John, Price, Alkes, Pulver, Ann E., Purcell, Shaun M., Quested, Digby, Rasmussen, Henrik B., Bene, Judit, Reichenberg, Abraham, Reimers, Mark A., Richards, Alexander L., Roffman, Joshua L., Roussos, Panos, Ruderfer, Douglas M., Salomaa, Veikko, Sanders, Alan R., Schall, Ulrich, Schubert, Christian R., Corvin, Aiden, Bergen, Sarah E., Schulze, Thomas G., Schwab, Sibylle G., Scolnick, Edward M., Scott, Rodney J., Seidman, Larry J., Shi, Jianxin, Sigurdsson, Engilbert, Silagadze, Teimuraz, Silverman, Jeremy M., Sim, Kang, Bevilacqua, Elizabeth, Slominsky, Petr, Smoller, Jordan W., So, Hon-Cheong, Spencer, Chris C. A., Stahl, Eli A., Stefansson, Hreinn, Steinberg, Stacy, Stogmann, Elisabeth, Straub, Richard E., Strengman, Eric, Bigdeli, Tim B., Strohmaier, Jana, Scott Stroup, T., Subramaniam, Mythily, Suvisaari, Jaana, Svrakic, Dragan M., Szatkiewicz, Jin P., Söderman, Erik, Thirumalai, Srinivas, Toncheva, Draga, Tosato, Sarah, Black, Donald W., Veijola, Juha, Waddington, John, Walsh, Dermot, Wang, Dai, Wang, Qiang, Webb, Bradley T., Weiser, Mark, Wildenauer, Dieter B., Williams, Nigel M., Williams, Stephanie, Bruggeman, Richard, Witt, Stephanie H., Wolen, Aaron R., Wong, Emily H. M., Wormley, Brandon K., Simon Xi, Hualin, Zai, Clement C., Zheng, Xuebin, Zimprich, Fritz, Wray, Naomi R., Stefansson, Kari, Buccola, Nancy G., Visscher, Peter M., Welcome Trust Case-Control Consortium,, Adolfsson, Rolf, Andreassen, Ole A., Blackwood, Douglas H. R., Bramon, Elvira, Buxbaum, Joseph D., Børglum, Anders D., Cichon, Sven, Darvasi, Ariel, Buckner, Randy L., Domenici, Enrico, Ehrenreich, Hannelore, Esko, Tõnu, Gejman, Pablo V., Gill, Michael, Gurling, Hugh, Hultman, Christina M., Iwata, Nakao, Jablensky, Assen V., Jönsson, Erik G., Byerley, William, Kendler, Kenneth S., Kirov, George, Knight, Jo, Lencz, Todd, Levinson, Douglas F., Li, Qingqin S., Liu, Jianjun, Malhotra, Anil K., McCarroll, Steven A., McQuillin, Andrew, Cahn, Wiepke, Moran, Jennifer L., Mortensen, Preben B., Mowry, Bryan J., Nöthen, Markus M., Ophoff, Roel A., Owen, Michael J., Palotie, Aarno, Pato, Carlos N., Petryshen, Tracey L., Posthuma, Danielle, Cai, Guiqing, Rietschel, Marcella, Riley, Brien P., Rujescu, Dan, Sham, Pak C., Sklar, Pamela, St Clair, David, Weinberger, David R., Wendland, Jens R., Werge, Thomas, Daly, Mark J., Walters, James T. R., Campion, Dominique, Sullivan, Patrick F., O'Donovan, Michael C., Cantor, Rita M., Carr, Vaughan J., Carrera, Noa, Catts, Stanley V., Chambert, Kimberly D., Chan, Raymond C. K., Chen, Ronald Y. L., Chen, Eric Y. H., Cheng, Wei, Farh, Kai-How, Cheung, Eric F. C., Ann Chong, Siow, Robert Cloninger, C., Cohen, David, Cohen, Nadine, Cormican, Paul, Craddock, Nick, Crowley, James J., Curtis, David, Davidson, Michael, Holmans, Peter A., Davis, Kenneth L., Degenhardt, Franziska, Del Favero, Jurgen, Demontis, Ditte, Dikeos, Dimitris, Dinan, Timothy, Djurovic, Srdjan, Donohoe, Gary, Drapeau, Elodie, Duan, Jubao, Lee, Phil, Dudbridge, Frank, Durmishi, Naser, Eichhammer, Peter, Eriksson, Johan, Escott-Price, Valentina, Essioux, Laurent, Fanous, Ayman H., Farrell, Martilias S., Frank, Josef, Franke, Lude, Bulik-Sullivan, Brendan, Freedman, Robert, Freimer, Nelson B., Friedl, Marion, Friedman, Joseph I., Fromer, Menachem, Genovese, Giulio, Georgieva, Lyudmila, Giegling, Ina, Giusti-Rodríguez, Paola, Godard, Stephanie, Collier, David A., Goldstein, Jacqueline I., Golimbet, Vera, Gopal, Srihari, Gratten, Jacob, de Haan, Lieuwe, Hammer, Christian, Hamshere, Marian L., Hansen, Mark, Hansen, Thomas, Haroutunian, Vahram, Huang, Hailiang, Hartmann, Annette M., Henskens, Frans A., Herms, Stefan, Hirschhorn, Joel N., Hoffmann, Per, Hofman, Andrea, Hollegaard, Mads V., Hougaard, David M., Ikeda, Masashi, Joa, Inge. Nature Publishing Group; 2014. Biological insights from 108 schizophrenia-associated genetic loci.

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.

Okbay, Aysu, Wu, Yeda, Jiang, Yunxuan, Hicks, Barry, Tian, Chao, Hinds, David A., Ahlskog, Rafael, Magnusson, Patrik K. E., Oskarsson, Sven, Hayward, Caroline, Campbell, Archie, Porteous, David J., Wang, Nancy, Holliday, Elizabeth J., Scott, Rodney J., Attia, John R., Oldmeadow, Christopher, Auton, A, Bell, RK, Bryc, K, Elson, SL, Fontanillas, P, Furlotte, NA, Jayashankar, Hariharan, Hinds, DA, Huber, KE, Kleinman, A, Litterman, NK, McCreight, JC, McIntyre, MH, Mountain, JL, Northover, CAM, Pitts, SJ, Sathirapongsasuti, JF, Bennett, Michael, Sazonova, OV, Shelton, JF, Shringarpure, S, Tung, JY, Vacic, V, Wilson, CH, Fontana, MA, Pers, TH, Rietveld, CA, Chen, GB, Nehzati, Seyed Moeen, Emilsson, V, Meddens, SFW, Pickrell, JK, Thom, K, Timshel, P, de Vlaming, R, Abdellaoui, A, Ahluwalia, TS, Bacelis, J, Baumbach, C, Sidorenko, Julia, Bjornsdottir, G, Brandsma, JH, Concas, MP, Derringer, J, Galesloot, TE, Girotto, G, Gupta, R, Hall, LM, Harris, SE, Hofer, E, Kweon, Hyeokmoon, Horikoshi, M, Huffman, JE, Kaasik, K, Kalafati, IP, Karlsson, R, Lahti, J, van der Lee, SJ, de Leeuw, C, Lind, PA, Lindgren, KO, Goldman, Grant, Liu, T, Mangino, M, Marten, J, Mihailov, E, Miller, MB, van der Most, PJ, Oldmeadow, C, Payton, A, Pervjakova, N, Peyrot, WJ, Gjorgjieva, Tamara, Qian, Y, Raitakari, O, Rueedi, R, Salvi, E, Schmidt, B, Schraut, KE, Shi, J, Smith, AV, Poot, RA, Pourcain, BS. Nature Publishing Group; 2022. Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals.

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.

Tan, Ava Grace, Kifley, Annette, Klein, Barbara E. K., Cheng, Ching-Yu, Iyengar, Sudha K., Wang, Jie Jin, Mitchell, Paul, Rochtchina, Elena, Flood, Victoria M., Cumming, Robert G., Jun, Gyungah, Holliday, Elizabeth G., Scott, Rodney J., Teo, Yik Ying. American Medical Association; 2016. Associations between methylenetetrahydrofolate reductase polymorphisms, serum homocysteine levels, and incident cortical cataract.

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.

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.

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.

Bahlo, Melanie, Booth, David R., Rubio, Justin P., Scott, Rodney J., Stankovich, Jim, Stewart, Graeme J., Taylor, Bruce V., Wiley, James, Clarke, Glynnis, Cox, Mathew B., Csurhes, Peter A., Danoy, Patrick, Broadley, Simon A., Brown, Matthew A., Foote, Simon J., Griffiths, Lyn R., Kilpatrick, Trevor J., Lechner-Scott, Jeannette, Moscato, Pablo, Perreau, Victoria M.. Nature Publishing Group; 2009. Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20.

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.

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.

Simpson, Jodie L., Baines, Katherine J., Boyle, Michael J., Scott, Rodney J., Gibson, Peter G.. Informa Healthcare; 2009. Oncostatin M (OSM) is increased in asthma with incompletely reversible airflow obstruction.

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. B: are the results of the study valid?.

White, Cassandra, Scott, Rodney J., Paul, Christine, Ziolkowski, Andrew, Mossman, David, Ackland, Stephen. Dove Medical Press; 2021. Ethnic Diversity of DPD Activity and the DPYD Gene: Review of the Literature.

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?.

Bowden, Nikola A., Ashton, Katie A., Scott, Rodney J., Vilain, Ricardo E., Avery-Kiejda, Kelly A., Davey, Ryan J., Murray, Heather C., Budden, Timothy, Braye, Stephen G., Zhang, Xu Dong, Hersey, Peter. Public Library of Science; 2013. Regulators of global genome repair do not respond to DNA damaging therapy but correlate with survival in melanoma.

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.

Painter, Jodie N., O'Mara, Tracy A., Henders, Anjali K., Attia, John, McEvoy, Mark, Holliday, Elizabeth G., Scott, Rodney J., Webb, Penelope M., Fasching, Peter A., Beckmann, Matthias W., Ekici, Arif B., Hein, Alexander, Morris, Andrew P., Rübner, Matthias, Hall, P, Czene, K, Dörk, T, Dürst, M, Hillemanns, P, Runnebaum, I, Lambrechts, D, Amant, F, Annibali, D, Cheng, Timothy H. T., Depreeuw, J, Vanderstichele, A, Goode, EL, Cunningham, JM, Dowdy, SC, Winham, SJ, Trovik, J, Hoivik, E, Werner, HMJ, Krakstad, C, Gorman, Maggie, Ashton, Katie, Otton, Geoffrey, Proietto, Tony, Tham, E, Mints, M, Ahmed, S, Healey, CS, Shah, M, Pharoah, PDP, Dunning, AM, Martin, Lynn, Dennis, J, Bolla, MK, Michailidou, K, Wang, Q, Tyrer, JP, Hopper, JL, Peto, J, Swerdlow, AJ, Burwinkel, B, Brenner, H, Hodson, Shirley, Meindl, A, Brauch, H, Lindblom, A, Chang-Claude, J, Couch, FJ, Giles, GG, Kristensen, VN, Cox, A, Zondervan, KT, Nyholt, DR, Jones, Angela, Macgregor, S, Montgomery, GW, Martin, Nnicholas G., Gordon, Scott. John Wiley & Sons; 2018. Genetic overlap between endometriosis and endometrial cancer: Evidence from cross-disease genetic correlation and GWAS meta-analyses.

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.

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.

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.

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.

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?.

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.

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.

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.

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.

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.

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.

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

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.

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.

Southey, Melissa C., Goldgar, David E., Heikkinen, Tuomas, Nevanlinna, Heli, Hopper, John L., Dörk, Thilo, Claes, Kathleen B. M., Reis-Filho, Jorge, Teo, Zhi Ling, Radice, Paolo, Catucci, Irene, Peterlongo, Paolo, Winqvist, Robert, Tsimiklis, Helen, Odefrey, Fabrice A., Dowty, JG, Schmidt, MK, Broeks, A, Hogervorst, FB, Verhoef, S, Carpenter, J, Clarke, C, Scott, Rodney J., Pylkäs, Katri, Fasching, PA, Haeberle, L, Ekici, AB, Beckmann, MW, Peto, J, dos-Santos-Silva, I, Fletcher, O, Johnson, N, Bolla, MK, Sawyer, EJ, Couch, Fergus, Tomlinson, I, Kerin, MJ, Miller, N, Marme, F, Burwinkel, B, Yang, R, Guénel, P, Truong, T, Menegaux, F, Sanchez, M, Tischkowitz, Marc, Bojesen, S, Nielsen, SF, Flyger, H, Benitez, J, Zamora, MP, Perez, JIA, Menéndez, P, Anton-Culver, H, Neuhausen, S, Ziogas, A, Foulkes, William D., Clarke, CA, Brenner, H, Arndt, V, Stegmaier, C, Brauch, H, Brüning, T, Ko, YD, Muranen, TA, Aittomäki, K, Blomqvist, C, Dennis, Joe, Bogdanova, NV, Antonenkova, NN, Lindblom, A, Margolin, S, Mannermaa, A, Kataja, V, Kosma, VM, Hartikainen, JM, Spurdle, AB, Michailidou, Kyriaki, van Rensburg, Elizabeth J.. BMJ Group; 2016. PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS.

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.

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.

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

Smith-Anttila, Casey J. A., Bensing, Sophie, Fransson, Anette, Nordmark, Gunnel, Rönnblom, Lars, Meloni, Antonella, Scott, Rodney J., Hökfelt, Tomas, Crock, Patricia A., Kämpe, Olle, Alimohammadi, Mohammad, Dalin, Frida, Oscarson, Mikael, Zhang, Ming-Dong, Perheentupa, Jaakko, Husebye, Eystein S., Gustafsson, Jan, Björklund, Peyman. Taylor & Francis; 2017. Identification of endothelin-converting enzyme-2 as an autoantigen in autoimmune polyendocrine syndrome type 1.

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.

Greenop, Kathryn R., Scott, Rodney J., Ashton, Lesley J., Armstrong, Bruce K., Milne, Elizabeth, Attia, John, Bower, Carol, de Klerk, Nicholas H., Norris, Murray D., Haber, Michelle, Jamieson, Sarra E., van Bockxmeer, Frank M., Gottardo, Nicholas G.. American Association for Cancer Research; 2015. Folate pathway gene polymorphisms and risk of childhood brain tumors: results from an Australian case-control study.

Bolton, Katherine A., Avery-Kiejda, Kelly A., Holliday, Elizabeth G., Attia, John, Bowden, Nikola A., Scott, Rodney J.. BioScientifica; 2016. A polymorphic repeat in the IGF1 promoter influences the risk of endometrial cancer.

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

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.

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?.

Karlsson Linnér, Richard, Kalnapenkis, A, Kasela, S, Kettunen, J, Kim, Y, Kirsten, H, Kovacs, P, Krohn, K, Kronberg-Guzman, J, Kukushkina, V, Kutalik, Z, Lee, B, Lehtimäki, T, Loeffler, M, Marigorta, UM, Metspalu, A, Milani, L, Montgomery, GW, Müller-Nurasyid, M, Nauck, M, Penninx, B, Perola, M, Biroli, Poetro, Nivard, Michel G., Okbay, Aysu, Rietveld, Cornelius A., Timshel, Pascal N., Trzaskowski, Maciej, de Vlaming, Ronald, Zünd, Christian L., Bao, Yanchun, Buzdugan, Laura, Caplin, Ann H., Kong, Edward, Chen, Chia-Yen, Eibich, P, Fontanillas, P, Gonzalez, JR, Joshi, PK, Karhunen, V, Kleinman, A, Levin, RZ, Lill, CM, Meddens, GA, Meddens, S. Fleur W., Muntané, G, Sanchez-Roige, S, Rooij, FJV, Taskesen, E, Wu, Y, Zhang, F, Agee, M, Alipanahi, B, Bell, RK, Bryc, K, Wedow, Robbee, Elson, SL, Furlotte, NA, Huber, KE, Litterman, NK, McCreight, JC, McIntyre, MH, Mountain, JL, Northover, CAM, Pitts, SJ, Sathirapongsasuti, JF, Fontana, Mark Alan, Sazonova, OV, Shelton, JF, Shringarpure, S, Tian, C, Tung, JY, Vacic, V, Wilson, CH, Agbessi, M, Ahsan, H, Alves, I, Lebreton, Maël, Andiappan, A, Awadalla, P, Battle, A, Beutner, F, Jan Bonder, M, Boomsma, DI, Christiansen, M, Claringbould, A, Deelen, P, Esko, T, Tino, Stephen P., Favé, MJ, Franke, L, Frayling, T, Gharib, SA, Gibson, G, Oldmeadow, Christopher, Holliday, Elizabeth G., Scott, Rodney J., Attia, John R., Abdellaoui, Abdel, Hammerschlag, Anke R.. Nature Publishing Group; 2019. Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences.

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.

Pundavela, Jay, Roselli, Severine, Hondermarck, Hubert, Faulkner, Sam, Attia, John, Scott, Rodney J., Thorne, Rick F., Forbes, John F., Bradshaw, Ralph A., Walker, Marjorie M., Jobling, Phillip. John Wiley & Sons; 2015. Nerve fibers infiltrate the tumor microenvironment and are associated with nerve growth factor production and lymph node invasion in breast cancer.

Yotova, Vania, Lefebvre, Jean-Francois, Avogbe, Patrice Hodonou, Chabi, Nicodeme, Dicko, Mamoudou Hama, Kou' Santa Amouzou , Emile Sabiba, Sanni, Ambaliou, Roberts-Thomson, June, Boettcher, Barry, Scott, Rodney J., Labuda, Damian, Moreau, Claudia, Gbeha, Elias, Hovhannesyan, Kristine, Bourgeois, Stephane, Bédarida, Sandra, Azevedo, Luisa, Amorim, Antonio, Sarkisian, Tamara. Oxford University Press; 2011. An X-linked haplotype of Neandertal origin is present among all non-African populations.

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.

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.

Constantinides, Constantinos, Han, Laura K. M., Bustillo, Juan, Bykhovski, Oleg, Calhoun, Vince, Carr, Vaughan, Catts, Stanley, Chung, Young-Chul, Crespo-Facorro, Benedicto, Díaz-Caneja, Covadonga M., Donohoe, Gary, Plessis, Stefan Du, Alloza, Clara, Edmond, Jesse, Ehrlich, Stefan, Emsley, R, Eyler, LT, Fuentes-Claramonte, P, Georgiadis, F, Green, M, Guerrero-Pedraza, A, Ha, M, Hahn, T, Antonucci, Linda Antonella, Henskens, Frans A., Holleran, L, Homan, S, Homan, P, Jahanshad, N, Janssen, J, Ji, E, Kaiser, S, Kaleda, V, Kim, M, Arango, Celso, Kim, W-S, Kirschner, M, Kochunov, P, Kwak, YB, Kwon, JS, Lebedeva, I, Liu, J, Mitchie, Patricia, Michielse, S, Mothersill, D, Ayesa-Arriola, Rosa, Mowry, B, de la Foz, VO-G, Pantelis, C, Pergola, G, Piras, F, Pomarol-Clotet, E, Preda, A, Quidé, Y, Rasser, Paul E., Rootes-Murdy, K, Banaj, Nerisa, Salvador, R, Sangiuliano, M, Sarró, S, Schall, Ulrich, Schmidt, A, Scott, Rodney J., Selvaggi, P, Sim, K, Skoch, A, Spalletta, G, Bertolino, Alessandro, Spaniel, F, Thomopoulos, SI, Tomecek, D, Tomyshev, AS, Tordesillas-Gutiérrez, D, van Amelsvoort, T, Vázquez-Bourgon, J, Vecchio, D, Voineskos, A, Weickert, CS, Borgwardt, Stefan, Weickert, T, Thompson, PM, Schmaal, L, van Erp, TGM, Turner, J, Cole, JH, ENIGMA Schizophrenia Consortium,, Du Plessis, S, Bin Kwak, Y, Dima, D, Bruggemann, Jason, Walton, E. Nature Publishing Group; 2023. Brain ageing in schizophrenia: evidence from 26 international cohorts via the ENIGMA Schizophrenia consortium.

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.

Simpson, Jodie L., Powell, Heather, Boyle, Michael J., Scott, Rodney J., Gibson, Peter G.. American Thoracic Society; 2008. Clarithromycin targets neutrophilic airway inflammation in refractory asthma.

Ikram, M. Kamran, Xueling, Sim, Jensen, Richard A., Cotch, Mary Frances, Hewitt, Alex W., Attia, John, Holliday, Elizabeth G., Scott, Rodney J., Ikram, M. Arfan, Wang, Jie Jin, Klein, Ronald, Klein, Barbara E. K., Breteler, Monique M. B.. Public Library of Science; 2010. Four novel loci (19q13, 6q24, 12q24, and 5q14) influence the microcirculation in vivo.

Xavier, Miguel J., Mitchell, Lisa A., McEwan, Kristen E., Scott, Rodney J., Aitken, R. John. Society for Reproduction and Fertility; 2018. Genomic integrity in the male germ line: evidence in support of the disposable soma hypothesis.

Fazekas-Lavu, Monika, Parker, Andrew, Spigelman, Allan D., Scott, Rodney J., Epstein, Richard J., Jensen, Michael, Samaras, Katherine. Dove Medical Press; 2017. Thyroid cancer in a patient with Lynch syndrome - case report and literature review.

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.

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.

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.

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.

Greenop, Kathryn R., de Klerk, Nicholas H., Bower, Carol, Milne, Elizabeth, Miller, Margaret, Scott, Rodney J., Attia, John, Ashton, Lesley J., Dalla-Pozza, Luciano, Armstrong, Bruce K.. Routledge; 2014. Maternal dietary intake of folate and vitamins B6 and B12 during pregnancy and risk of childhood brain tumors.

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.

Beveridge, Natalie J., Tooney, Paul A., Carroll, Adam P., Gardiner, Erin, Bowden, Nikola A., Scott, Rodney J., Tran, Nham, Dedova, Irina, Cairns, Murray J.. Oxford University Press; 2008. Dysregulation of miRNA 181b in the temporal cortex in schizophrenia.

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.

The International Multiple Sclerosis Genetics Consortium, The Wellcome Trust Case Control Consortium 2, Cox, Mathew B., Lechner-Scott, Jeannette S., Scott, Rodney J.. Nature Publishing Group; 2011. Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.

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.

Ashton, Katie A., Proietto, Anthony, Otton, Geoffrey, Symonds, Ian, McEvoy, Mark, Attia, John, Gilbert, Michael, Hamann, Ute, Scott, Rodney J.. BioMed Central; 2008. The influence of the Cyclin D1 870 G>A polymorphism as an endometrial cancer risk factor.

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.