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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.
Okbay, Aysu, Beauchamp, Jonathan P., Oskarsson, Sven, , , , , , , , , , , Pickrell, Joseph K., , , , , , , , , , , Thom, Kevin, , , , , , , , , , , Timshel, Pascal, , , , , , , , , , , de Vlaming, Ronald, , , , , , , , , , , Abdellaoui, Abdel, , , , , , , , , , , Ahluwalia, Tarunveer S., , , , , , , , , , , Bacelis, Jonas, , , , , , , , , , , Baumbach, Clemens, , , , , , , , , , , Bjornsdottir, Gyda, , , , , , , , , , , Fontana, Mark Alan, Oldmeadow, Christopher, , , , , , , , , , , Holliday, Elizabeth G., , , , , , , , , , , Scott, Rodney J., , , , , , , , , , , Attia, John R., , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Lee, James J., , , , , , , , , , , Pers, Tune H., , , , , , , , , , , Rietveld, Cornelius A., , , , , , , , , , , Turley, Patrick, , , , , , , , , , , Chen, Guo-Bo, , , , , , , , , , , Emilsson, Valur, , , , , , , , , , , Meddens, S. Fleur W., , , , , , , , , , . Nature Publishing Group; 2016. Genome-wide association study identifies 74 loci associated with educational attainment.
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?.
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.
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.
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.
Stambolian, Dwight, Wojciechowski, Robert, Wong, Tien Y., Simpson, Claire L., Klaver, Caroline C. W., van Duijn, Cornelia M., Verhoeven, Virginie J. M., Baird, Paul N., Vitart, Veronique, Paterson, Andrew D., Mitchell, Paul, Saw, Seang Mei, Oexle, Konrad, Holliday, Elizabeth G., Attia, John, Scott, Rodney J., , , , , , , , Pirastu, Mario, , , , , , , , , , , Li, Xiaohui, , , , , , , , , , , Raffel, Leslie J., , , , , , , , , , , Cotch, Mary Frances, , , Chew, Emily Y., Klein, Barbara, Klein, Ronald. Oxford University Press; 2013. Meta-analysis of genome-wide association studies in five cohorts reveals common variants in RBFOX1, a regulator of tissue-specific splicing, associated with refractive error.
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.
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.
Milne, Elizabeth, Greenop, Kathryn R., Bower, Carol, Miller, Margaret, van Bockxmeer, Frank M., Scott, Rodney J., de Klerk, Nicholas H., Ashton, Lesley J., Gottardo, Nicholas G., Armstrong, Bruce K.. American Association for Cancer Research; 2012. Maternal use of folic acid and other supplements and risk of childhood brain tumors.
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.
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.
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.
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.
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.
Movahedi, Mohammad, Bishop, D. Timothy, Bisgaard, Marie-Luise, Dunlop, Malcolm G., Ho, Judy W. C., Hodgson, Shirley V., Lindblom, Annika, Lubinski, Jan, Morrison, Patrick J., Murday, Victoria, Ramesar, Raj S., Side, Lucy, Macrae, Finlay, Scott, Rodney J., Thomas, Huw J. W., Vasen, Hans F., Burn, John, Mathers, John C., Mecklin, Jukka-Pekka, Moeslein, Gabriela, Olschwang, Sylviane, Eccles, Diana, Evans, D. Gareth, Maher, Eamonn R., Bertario, Lucio. American Society of Clinical Oncology; 2015. Obesity, aspirin, and risk of colorectal cancer in carriers of hereditary colorectal cancer: a prospective investigation in the CAPP2 study.
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.
McCarthy-Jones, Simon, Green, Melissa J., Scott, Rodney J., Tooney, Paul A., Cairns, Murray J., Wu, Jing Qin, Oldmeadow, Christopher, Carr, Vaughn. Pergamon Press; 2014. Preliminary evidence of an interaction between the FOXP2 gene and childhood emotional abuse predicting likelihood of auditory verbal hallucinations in schizophrenia.
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.
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.
Smith, Casey Jo Anne, Bensing, Sophie, Burns, Christine, Robinson, Phillip J., Kasperlik-Zaluska, Anna A., Scott, Rodney J., Kampe, Olle, Crock, Patricia A.. Bioscientifica; 2012. Identification of TPIT and other novel autoantigens in lymphocytic hypophysitis; immunoscreening of a pituitary cDNA library and development of immunoprecipitation assays.
Patsopoulos, Nikolaos A., de Bakker, Paul I. W., Kappos, Ludwig, Miller, David, Montalbán, Javier, Polman, Chris H., Freedman, Mark S., Hartung, Hans-Peter, Arnason, Barry G. W., Comi, Giancarlo, Cook, Stuart, Filippi, Massimo, Esposito, Federica, Goodin, Douglas S., Jeffery, Douglas, O'Connor, Paul, Ebers, George C., Langdon, Dawn, Reder, Anthony T., Traboulsee, Anthony, Zipp, Frauke, Schimrigk, Sebastian, Hillert, Jan, Reischl, Joachim, Bahlo, Melanie, Booth, David R., Broadley, Simon, Brown, Matthew A., Browning, Brian L., Browning, Sharon R., Butzkueven, Helmut, Carroll, William M., Chapman, Caron, Foote, Simon J., Lehr, Stephan, Griffiths, Lyn, Kermode, Allan G., Kilpatrick, Trevor J., Lechner-Scott, Jeannette, Marriott, Mark, Mason, Deborah, Moscato, Pablo, Heard, Robert N., Pender, Michael P., Perreau, Victoria M., Bauer, David, Perera, Devindri, Rubio, Justin P., Scott, Rodney J., Slee, Mark, Stankovich, Jim, Stewart, Graeme J., Taylor, Bruce V., Tubridy, Niall, Willoughby, Ernest, Wiley, James, Heubach, Jürgen, Matthews, Paul, Boneschi, Filippo M., Compston, Alastair, Haines, Jonathan, Hauser, Stephen L., McCauley, Jacob, Ivinson, Adrian, Oksenberg, Jorge R., Pericak-Vance, Margaret, Sawcer, Stephen J., Sandbrink, Rupert, De Jager, Philip L., Hafler, David A., Pohl, Christoph, Edan, Gilles. John Wiley & Sons; 2011. Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci.
Kaput, Jim, Cotton, Richard G. H., Bapat, Bharati, Bernstein, Inge T., Bhak, Jong, Bleoo, Stacey L., Blöcker, Helmut, Brenner, Steven E., Burn, John, Bustamante, Mariona, Calzone, Rita, Scott, Rodney J., Hardman, Lauren, Watson, Michael, Aqeel, Aida I. Al, Al-Aama, Jumana Y., Al-Mulla, Fahd, Alonso, Santos, Aretz, Stefan, Auerbach, Arleen D.. John Wiley; 2009. Planning the Human Variome Project: the Spain report.
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.
Lener, Marcin R., Gupta, Satish, Jaworska-Bieniek, Katarzyna, Durda, Katarzyna, Muszyńska, Magdalena, Sukiennicki, Grzegorz, Jakubowska, Anna, Lubiński, Jan, Scott, Rodney J., Tootsi, Martin, Kulp, Maria, Tammesoo, Mari-Liis, Viitak, Anu, Metspalu, Anders, Serrano-Fernandez, Pablo, Kładny, Józef. BioMed Central Ltd; 2013. Can selenium levels act as a marker of colorectal cancer risk?.
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.
Shi, Zumin, Johnstone, Daniel, Lubinski, Jan, Scott, Rodney J., Talseth-Palmer, Bente A., Evans, Tiffany-Jane, Spigelman, Allan D., Groombridge, Claire, Milward, Elizabeth A., Olynyk, John K., Suchy, Janina, Kurzawski, Grzegorz. John Wiley & Sons; 2009. Haemochromatosis HFE gene polymorphisms as potential modifiers of hereditary nonpolyposis colorectal cancer risk and onset age.
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.
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.
Greenop, Kathryn R., Hinwood, Andrea L., Fritschi, Lin, Scott, Rodney J., Attia, John, Ashton, Lesley J., Heath, John A., Armstrong, Bruce K., Milne, Elizabeth. John Wiley & Sons; 2015. Vehicle refuelling, use of domestic wood heaters and the risk of childhood brain tumours: results from an Australian case-control study.
Debniak, T., Scott, Rodney J., Huzarski, T., Byrski, T., Rozmiarek, A., Debniak, B., Zaluga, E., Maleszka, R., Kladny, J., Gorski, B., Cybulski, C., Gronwald, J., Kurzawski, G., Lubinski, J.. Waverly Press; 2005. CDKN2A common variants and their association with melanoma risk: A population-based study.
Sapkota, Yadav, Low, Siew-Kee, Takahashi, Atsushi, Scott, Rodney J., Kubo, Michiaki, Zondervan, Krina T., Montgomery, Grant W., Nyholt, Dale R., Attia, John, Gordon, Scott D., Henders, Anjali K., Holliday, Elizabeth G., MacGregor, Stuart, Martin, Nicholas G., McEvoy, Mark, Morris, Andrew P.. Oxford University Press; 2015. Association between endometriosis and the interleukin 1A (IL1A) locus.
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.
Bergon, Aurélie, Belzeaux, Raoul, Kelly, Brian, Cairns, Murray J., Kumarasinghe, Nishantha, Schall, Ulrich, Blin, Olivier, Boucraut, José, Tooney, Paul A., Fakra, Eric, Ibrahim, El Chérif, Comte, Magali, Pelletier, Florence, Hervé, Mylène, Gardiner, Erin J., Beveridge, Natalie J., Liu, Bing, Carr, Vaughan, Scott, Rodney J.. Elsevier; 2015. CX3CR1 is dysregulated in blood and brain from schizophrenia patients.
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.
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.
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.
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.
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.
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.
Talseth-Palmer, Bente A., Brenne, Ingvild S., Scott, Rodney J., Ashton, Katie A., Evans, Tiffany-Jane, McPhillips, Mary, Groombridge, Claire, Suchy, Janina, Kurzawski, Grzegorz, Spigelman, Allan, Lubinski, Jan. BMJ Group; 2011. Colorectal cancer susceptibility loci on chromosome 8q23.3 and 11q23.1 as modifiers for disease expression in lynch syndrome.
Hancock, Dana B., Levy, Joshua L., Degenhardt, Louisa, Martin, Nicholas G., Montgomery, Grant W., Attia, John, Holliday, Elizabeth G., McEvoy, Mark, Scott, Rodney J., Bierut, Laura J., Nelson, Elliot C., Kral, Alex H., Gaddis, Nathan C., Johnson, Eric O., Glasheen, Cristie, Saccone, Nancy L., Page, Grier P., Hulse, Gary K., Wildenauer, Dieter, Kelty, Erin A., Schwab, Sibylle G.. Elsevier; 2015. Cis-expression quantitative trait loci mapping reveals replicable associations with heroin addiction in OPRM1.
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.
Finucane, Hilary K., Bulik-Sullivan, Brendan, Ripke, Stephan, Day, Felix R., ReproGen Consortium,, Schizophrenia Working Group of the Psychiatric Genomics Consortium,, The RACI Consortium,, Purcell, Shaun, Stahl, Eli, Lindstrom, Sara, Perry, John R. B., Okada, Yukinori, Gusev, Alexander, Raychaudhuri, Soumya, Daly, Mark J., Patterson, Nick, Neale, Benjamin M., Price, Alkes L., Henskens, Frans A., Loughland, Carmel M., Michie, Patricia T., Schall, Ulrich, Scott, Rodney J., Trynka, Gosia, Tooney, Paul A., Wu, Jing Qin, Reshef, Yakir, Loh, Po-Ru, Anttila, Verneri, Xu, Han, Zang, Chongzhi, Farh, Kyle. Nature Publishing; 2015. Partitioning heritability by functional annotation using genome-wide association summary statistics.
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.
O'Mara, Tracy A., Glubb, Dylan M., Ashton, Katie, Proietto, Tony, Otton, Geoffrey, Shah, Mitul, Ahmed, Shahana, Healey, Catherine S., Gorman, Maggie, Martin, Lynn, National Study of Endometrial Cancer Genetics Group (NSECG),, Hodgson, Shirley, Painter, Jodie N., Fasching, Peter A., Hein, Alexander, Beckmann, Matthias W., Ekici, Arif B., Hall, Per, Czene, Kamila, Darabi, Hatef, Li, Jingmei, Dürst, Matthias, Runnebaum, Ingo, Cheng, Timothy, Hillemanns, Peter, Dörk, Thilo, Lambrechts, Diether, Depreeuw, Jeroen, Annibali, Daniela, Amant, Frederic, Zhao, Hui, Goode, Ellen L., Dowdy, Sean C., Fridley, Brooke L., Dennis, Joe, Winham, Stacey J., Salvesen, Helga B., Njølstad, Tormund S., Trovik, Jone, Werner, Henrica M. J., Tham, Emma, Liu, Tao, Mints, Miriam, RENDOCAS,, Bolla, Manjeet K., Australian National Endometrial Cancer Study Group (ANECS),, Michailidou, Kyriaki, Tyrer, Jonathan P., Wang, Qin, Hopper, John L., AOCS Group,, Peto, Julian, Swerdlow, Anthony J., Burwinkel, Barbara, Brenner, Hermann, Meindl, Alfons, Attia, John, Brauch, Hiltrud, Lindblom, Annika, Chang-Claude, Jenny, Couch, Fergus J., Giles, Graham G., Kristensen, Vessela N., Cox, Angela, Pharoah, Paul D. P., Dunning, Alison M., Tomlinson, Ian, Holliday, Elizabeth G., Easton, Douglas F., Thompson, Deborah J., Spurdle, Amanda B., McEvoy, Mark, Scott, Rodney J.. BioScientifica; 2015. Comprehensive genetic assessment of the ESR1 locus identifies a risk region for endometrial 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.
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.
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.
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.
Williams, Frances M. K., Carter, Angela M., Sudlow, Cathie, Farrall, Martin, Silander, Kaisa, Kaunisto, Mari, Wagner, Peter, Saarela, Olli, Kuulasmaa, Kari, Virtamo, Jarmo, Salomaa, Veikko, Amouyel, Philippe, Hysi, Pirro G., Bis, Joshua C., Levi, Christopher, Attia, John, Holliday, Elizabeth G., Scott, Rodney J., , , , , , Surdulescu, Gabriela, , , , , , , , , , , Hodgkiss, Dylan, , , , , , , , , , , Soranzo, Nicole, , , , , , , , , , , Traylor, Matthew, , Bevan, Steve, Dichgans, Martin, Rothwell, Peter M. W.. John Wiley & Sons; 2013. Ischemic stroke is associated with the ABO locus: the EuroCLOT Study.
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.
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.
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.
Cotton, Richard G. H., Al Aqeel , Aida I., Patrinos, George P., Qi, Ming, Ramesar, Rajkumar S., Scott, Rodney J., Sijmons, Rolf H., Sobrido, Maria-Jesus, Vihinen, Mauno, Al-Mulla, Fahd, Carrera, Paola, Claustres, Mireille, Ekong, Rosemary, Hyland, Valentine J., Macrae, Finlay A., Marafie, Makia J., Paalman, Mark H.. Lippincott Williams & Wilkins; 2009. Capturing all disease-causing mutations for clinical and research use: toward an effortless system for the Human Variome Project.
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.
Burn, John, Gerdes, Anne-Marie, Bisgaard, Marie Louise, Dunlop, Malcolm G., Ho, Judy W. C., Hodgson, Shirley V., Lindblom, Annika, Lubinski, Jan, Morrison, Patrick J., Murday, Victoria, Ramesar, Raj, Side, Lucy, Macrae, Finlay, Scott, Rodney J., Thomas, Huw J. W., Vasen, Hans F., Barker, Gail, Crawford, Gillian, Elliott, Faye, Movahedi, Mohammad, Pylvanainen, Kirsi, Wijnen, Juul T., Fodde, Riccardo, Mecklin, Jukka-Pekka, Lynch, Henry T., Mathers, John C., Bishop, D. Timothy, Moeslein, Gabriela, Olschwang, Sylviane, Eccles, Diane, Evans, D. Gareth, Maher, Eamonn R., Bertario, Lucio. Lancet Publishing Group; 2011. Long-term effect of aspirin on cancer risk in carriers of hereditary colorectal cancer: an analysis from the CAPP2 randomised controlled trial.
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.
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.
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.