Pouget, Jennie G., Schizophrenia Working Group of the Psychiatric Genomics Consortium,, Martin, Javier, Mayes, Maureen D., Bossini-Castillo, Lara, López-Isac, Elena, Jin, Ying, Santorico, Stephanie A., Spritz, Richard A., Hakonarson, Hakon, Polychronakos, Constantin, Raychaudhuri, Soumya, Han, Buhm, Knight, Jo, Cairns, Murray, Henskens, Frans A., Kelly, Brian J., Loughland, Carrmel M., Michie, Patricia T., Schall, Ulrich A., Scott, Rodney, Tooney, Paul A., Wu, Yang, Mignot, Emmanuel, Ollila, Hanna M., Barker, Jonathan, Spain, Sarah, Dand, Nick, Trembath, Richard. Oxford University Press; 2019. Cross-disorder analysis of schizophrenia and 19 immune-mediated diseases identifies shared genetic risk.

Hess, Jonathan L., Quinn, Thomas P., Kumarasinghe, Nishantha, Ophoff, Roel, Schall, Ulrich, Scott, Rodney, Stamova, Boryana, Tooney, Paul, Kong, Sek Won, Cairns, Murray, Tsuang, Ming T., Faraone, Stephen V., Zhang, Chunling, Glatt, Stephen J., Hearn, Gentry C., Chen, Samuel, Beveridge, Natalie Jane, Carr, Vaughan, de Jong, Simone, Gardiner, Erin, Kelly, Brian. Nature Publishing Group; 2023. BrainGENIE: The Brain Gene Expression and Network Imputation Engine.

Lubiński, Jan, Korzeń, Marcin, Huzarski, Tomasz, Byrski, Tomasz, Gronwald, Jacek, Masojć, Bartłomiej, Lener, Marcin, Szymańska, Anna, Szymańska-Pasternak, Jolanta, Serrano-Fernàndez, Pablo, Piegat, Andrzej, Uciński, Rafał, Górski, Bohdan, Scott, Rodney, Cybulski, Cezary, Dębniak, Tadeusz, Jakubowska, Anna, Jaworska, Katarzyna, Wokołorczyk, Dominika, Mędrek, Krzysztof, Matyjasik, Joanna. Springer; 2009. Genetic contribution to all cancers: the first demonstration using the model of breast cancers from Poland stratified by age at diagnosis and tumour pathology.

Purrington, Kristen S., Slettedahl, Seth, Carpenter, Jane, Ko, Yon-Dschun, Van Deurzen, Carolien H. M., Martens, John W. M., Kriege, Mieke, Figueroa, Jonine D., Chanock, Stephen J., Lissowska, Jolanta, Tomlinson, Ian, Kerin, Michael J., Miller, Nicola, Yannoukakos, Drakoulis, Schneeweiss, Andreas, Tapper, William J., Gerty, Susan M., Durcan, Lorraine, Mclean, Catriona, Milne, Roger L., Baglietto, Laura, dos Santos Silva, Isabel, Fletcher, Olivia, Johnson, Nichola, Haiman, Christopher A., Van'T Veer, Laura J., Cornelissen, Sten, Försti, Ast, Torres, Diana, Rüdiger, Thomas, Rudolph, Anja, Flesch-Janys, Dieter, Nickels, Stefan, Weltens, Caroline, Floris, Giuseppe, Fasching, Peter A., Moisse, Matthieu, Dennis, Joe, Wang, Qin, Dunning, Alison M., Shah, Mitul, Brown, Judith, Simard, Jacques, Anton-Culver, Hoda, Neuhausen, Susan L., Hopper, John L., Mannermaa, Arto, Bogdanova, Natalia, Dörk, Thilo, Zheng, Wei, Radice, Paolo, Jakubowska, Anna, Lubinski, Jan, Devillee, Peter, Brauch, Hiltrud, Hooning, Maartje, García-Closas, Montserrat, Winqvist, Robert, Sawyer, Elinor, Burwinkel, Barbara, Marmee, Frederick, Eccles, Diana M., Giles, Graham G., Peto, Julian, Schmidt, Marjanka, Broeks, Annegien, Hamann, Ute, Chang-Claude, Jenny, Brenner, Hermann, Lambrechts, Diether, Pharoah, Paul D. P., Easton, Douglas, Pankratz, V. Shane, Slager, Susan, Vachon, Celine M., Couch, Fergus J., Lindblom, Annika, Chenevix-Trench, Georgia, Benitez, Javier, Bolla, Manjeet K., Swerdlow, Anthony, Kristensen, Vessela, Guénel, Pascal, Meindl, Alfons, Darabi, Hatef, Eriksson, Michael, Fagerholm, Rainer, Aittomäki, Kristiina, Blomqvist, Carl, Nordestgaard, Børge G., Michailidou, Kyriaki, Nielsen, Sune F., Flyger, Henrik, Wang, Xianshu, Olswold, Curtis, Olson, Janet E., Mulligan, Anna Marie, Knight, Julia A., Tchatchou, Sandrine, Reed, Malcolm W. R., Cross, Simon S., Czene, Kamila, Liu, Jianjun, Li, Jingmei, Humphreys, Keith, Clarke, Christine, Scott, Rodney, ABCTB Investigators, Fostira, Florentia, Fountzilas, George, Konstantopoulou, Irene, Henderson, Brian E., Nevanlinna, Heli, Schumacher, Frederick, Le Marchand, Loic, Ekici, Arif B., Hartmann, Arndt, Beckmann, Matthias W., Hartikainen, Jaana M., Kosma, Veli-Matti, Kataja, Vesa, Jukkola-Vuarinen, Arja, Pylkäs, Katri, Bojesen, Stig E., Kauppila, Saila, Dieffenbach, Aida Karina, Stegmaier, Christa, Arndt, Volker, Margolin, Sara, Australian Ovarian Cancer Study Group, kConFab Investigators, Balleine, Rosemary, Perez, Jose Ignacio Arias, Zamora, M. Pilar, Andrulis, Irene L., Menéndez, Primitiva, Ashworth, Alan, Jones, Michael, Orr, Nick, Arveux, Patrick, Kerbrat, Pierre, Truong, Thérèse, Bugert, Peter, Toland, Amanda E., Ambrosone, Christine B., Cox, Angela, Labrèche, France, Goldberg, Mark S., Dumont, Martine, Ziogas, Argyrios, Lee, Eunjung, Dite, Gillian S., Apicella, Carmel, Southey, Melissa C., Long, Jirong, Shrubsole, Martha, Hall, Per, Deming-Halverson, Sandra, Ficarazzi, Fiolmena, Barile, Monica, Peterlongo, Paolo, Durda, Katarzyna, Jaworska-Bieniek, Katarzyna, Tollenaar, Robert A. E. M., Seynaeve, Caroline, The GENICA Network, Brüning, Thomas. Oxford University Press; 2014. Genetic variation in mitotic regulatory pathway genes is associated with breast tumor grade.

Maguire, Jane, Thakkinstian, Ammarin, Levi, Christopher, Lincz, Lisa, Bisset, Linda, Sturm, Jonathan, Scott, Rodney, Whyte, Scott, Attia, John. W.B. Saunders; 2011. Impact of COX-2 rs5275 and rs20417 and GPIIIa rs5918 polymorphisms on 90-day ischemic stroke functional outcome: a novel finding.

Biswas, Mohitosh, Dias, Thilani H., Daneshi, Nilofar, Holliday, Elizabeth, Hancock, Stephen, Attia, John, Scott, Rodney, Newby, David, Kerr, Karen P., Milward, Elizabeth A.. Global Science and Technology Forum (GSTF); 2017. Preliminary analysis of potential drug and gene interactions involving tricyclic antidepressant drugs.

Ngo, Thi Tuyet Dieu, Lea, Rodney A., Scott, Rodney, Griffiths, Lyn R., Maksemous, Neen, Eccles, David A., Smith, Robert A., Dunn, Paul J., Thao, Van Cao, Ha, Thi Minh Thi, Bùi, Chi Bao, Haupt, Larisa M.. Elsevier; 2021. The MinION as a cost-effective technology for diagnostic screening of the SCN1A gene in epilepsy patients.

Shu, Xiang, Bao, Jiandong, Wu, Lang, Long, Jirong, Shu, Xiao-Ou, Guo, Xingyi, Yang, Yaohua, Michailidou, Kyriaki, Bolla, Manjeet K., Wang, Qin, Dennis, Joe, Andrulis, Irene L., Castelao, Jose E., Dörk, Thilo, Gago-Dominguez, Manuela, García-Closas, Montserrat, Giles, Graham G., Lophatananon, Artitaya, Muir, Kenneth, Olsson, Håkan, Scott, Rodney, , , , , , , , , . John Wiley & Sons; 2020. Evaluation of associations between genetically predicted circulating protein biomarkers and breast cancer risk.

Moayyeri, Alireza, Hsu, Yi-Hsiang, Smith, Albert V., Cooper, Cyrus, Kung, Annie Wai Chee, Lips, Paul, Alen, Markku, Attia, John, Luisa Brandi, Maria, de Groot, Lisette C. P. G. M., Lehtimäeki, Terho, Riancho, José A., Campbell, Harry, Pye, Stephen R., Liu, Yongmei, Harris, Tamara B., Akesson, Kristina, Karlsson, Magnus, Lee, Jong-Young, Wallaschofski, Henri, Duncan, Emma L., O'Neill, Terence W., Gudnason, Vilmundur, Spector, Timothy D., Leo, Paul J., Rousseau, François, Orwoll, Eric, Cummings, Steven R., Wareham, Nick J., Rivadeneira, Fernando, Uitterlinden, Andre G., Prince, Richard L., Kiel, Douglas P., Reeve, Jonathan, Kaptoge, Stephen K., Teumer, Alexander, Hwang, Joo-Yeon, Ohlsson, Claes, McGuigan, Fiona, Minster, Ryan L., Hayward, Caroline, Olmos, José M., Karasik, David, Lyytikäeinen, Leo-Pekka, Lewis, Joshua R., Swart, Karin M. A., Masi, Laura, Oldmeadow, Chris, Holliday, Elizabeth G., Cheng, Sulin, van Schoor, Natasja M., Harvey, Nicholas C., Kruk, Marcin, Estrada, Karol, del Greco M, Fabiola, Igl, Wilmar, Trummer, Olivia, Grigoriou, Efi, Luben, Robert, Liu, Ching-Ti, Zhou, Yanhua, Oei, Ling, Medina-Gomez, Carolina, Zmuda, Joseph, Xiao, Su-Mei, Tranah, Greg, Brown, Suzanne J., Williams, Frances M., Soranzo, Nicole, Jakobsdottir, Jphanna, Siggeirsdottir, Kristin, Holliday, Kate L., Hannemann, Anke, Go, Min Jin, Garcia, Melissa, Nielson, Carrie, Polasek, Ozren, Laaksonen, Marika, Zhu, Kun, Enneman, Anke W., McEvoy, Mark, Peel, Roseanne, Sham, Pak Chung, Jaworski, Maciej, Johansson, Åsa, Hicks, Andrew A., Srikanth, Priya, Pludowski, Pawel, Scott, Rodney, Dhonukshe-Rutten, Rosalie A. M., van der Velde, Nathalie, Käehöenen, Mika, Viikari, Jorma S., Sieväenen, Harri, Raitakari, Olli T., González-Macías, Jesús, Hernández, Jose L., Giroux, Sylvie, Mellströem, Dan, Ljunggren, Östen, Cho, Yoon Shin, Vöelker, Uwe, Nauck, Matthias, Homuth, Georg, Vöelzke, Henry, Haring, Robin, Brown, Matthew A., McCloskey, Eugene, Wilson, Scott G., Nicholson, Geoffrey C., Eastell, Richard, Eisman, John A., Jones, Graeme, Reid, Ian R., Dennison, Elaine M., Wark, John, Boonen, Steven, Vanderschueren, Dirk, Wu, Frederick C. W., Zheng, Hou-Feng, Aspelund, Thor, Richards, J. Brent, Bauer, Doug, Hofman, Albert, Khaw, Kay-Tee, Dedoussis, George, Obermayer-Pietsch, Barbara, Gyllensten, Ulf, Pramstaller, Peter P., Lorenc, Roman S.. Oxford University Press; 2014. Genetic determinants of heel bone properties: genome-wide association meta-analysis and replication in the GEFOS/GENOMOS consortium.

Ahearn, Thomas U., Zhang, Haoyu, Michailidou, Kyriaki, Milne, Roger L., Bolla, Manjeet K., Dennis, Joe, Dunning, Alison M., Lush, Michael, Wang, Qin, Andrulis, Irene L., Anton-Culver, Hoda, Arndt, Volker, Aronson, Kristan J., Auer, Paul L., Augustinsson, Annelie, Baten, Adinda, Becher, Heiko, Behrens, Sabine, Benitez, Javier, Bermisheva, Marina, Michailidou, Kyriaki, Forbes, John, Scott, Rodney. Current Medicine Group; 2022. Common variants in breast cancer risk loci predispose to distinct tumor subtypes.

Iglesias, Adriana I., Mishra, Aniket, Vitart, Veronique, Bykhovskaya, Yelena, Höhn, René, Springelkamp, Henriët, Cuellar-Partida, Gabriel, Gharahkhani, Puya, Bailey, Jessica N. Cooke, Willoughby, Colin E., Li, Xiaohui, Yazar, Seyhan, Nag, Abhishek, Khawaja, Anthony P., Polašek, Ozren, Siscovick, David, Mitchell, Paul, Tham, Yin Chung, Haines, Jonathan L., Kearns, Lisa S., Hayward, Caroline, Shi, Yuan, van Leeuwen, Elisabeth M., Taylor, Kent D., Wang, Jie Jin, Rochtchina, Elena, Attia, John, Scott, Rodney, Holliday, Elizabeth G., Baird, Paul N., Xie, Jing, Inouye, Michael, Viswanathan, Ananth, Sim, Xueling, Bonnemaijer, Pieter, Rotter, Jerome I., Martin, Nicholas G., Zeller, Tanja, Mills, Richard A., Staffieri, Sandra E., Jonas, Jost B., Schmidtmann, Irene, Boutin, Thibaud, Kang, Jae H., Lucas, Sionne E. M., Wong, Tien Yin, Beutel, Manfred E., Wilson, James F., Allingham, R. Rand, Brilliant, Murray H., Budenz, Donald L., Christen, William G., Fingert, John, Friedman, David S., Gaasterland, Douglas, Gaasterland, Terry, Hauser, Michael A., Kraft, Peter, Lee, Richard K., Lichter, Paul R., Liu, Yutao, Loomis, Stephanie J., Moroi, Sayoko E., Pericak-Vance, Margaret A., Realini, Anthony, Richards, Julia E., Schuman, Joel S., Scott, William K., Singh, Kuldev, Sit, Arthur J., Vollrath, Douglas, Weinreb, Robert N., Wollstein, Gadi, Zack, Donald J., Zhang, Kang. Nature Publishing Group; 2018. Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases.

Warren, Helen, Evangelou, Evangelos, Kraja, Aldi T., Drenos, Fotios, Loh, Marie, Verweij, Niek, Marten, Jonathan, Karaman, Ibrahim, Segura Lepe, Marcelo P., O'Reilly, Paul F., Knight, Joanne, Scott, Rodney, Cabrera, Claudia P., Attia, John, Gao, He, Ren, Meixia, Mifsud, Borbala, Ntalla, Ioanna, Surendran, Praveen, Liu, Chunyu, Cook, James P.. Nature Publishing Group; 2017. Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk.

Figlioli, Gisella, Bogliolo, Massimo, Catucci, Irene, Caleca, Laura, Lasheras, Sandra Viz, Pujol, Roser, Kiiski, Johanna I., Muranen, Taru A., Barnes, Daniel R., Dennis, Joe, Michailidou, Kyriaki, Bolla, Manjeet K., Leslie, Goska, Aalfs, Cora M., Adank, Muriel A., Adlard, Julian, Agata, Simona, Cadoo, Karen, Agnarsson, Bjarni A., Ahearn, Thomas, Braye, Stephen, Forbes, John, Scott, Rodney. Nature Publishing Group; 2019. The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer.

Bowden, Nikola A., Weidenhofer, Judith C., Scott, Rodney, Schall, Ulrich A., Todd, Juanita, Michie, Patricia T., Tooney, Paul A.. Human Genetics Society of Australasia; 2005. Classification of schizophrenia using differential gene expression in peripheral blood lymphocytes.

Froyen, Guy, Corbett, Mark, Chelly, Jamel, Sanlaville, Damien, van Bokhoven, Hans, Ropers, Hans-Hilger, Laumonnier, Frederic, Ranieri, Enzo, Schwartz, Charles E., Abidi, Fatima, Tarpey, Patrick S., Futreal, P. Andrew, Vandewalle, Joke, Whibley, Annabel, Raymond, F. Lucy, Stratton, Michael R., Fryns, Jean-Pierre, Scott, Rodney, Peippo, Maarit, Sipponen, Marjatta, Partington, Michael, Mowat, David, Field, Michael, Jarvela, Irma, Hackett, Anna, Marynen, Peter, Turner, Gillian, Gécz, Jozef, Lawrence, Owen, Meldrum, Cliff, Bauters, Marijke, Govaerts, Karen, Vandeleur, Lucianne, Van Esch, Hilde. Elsevier; 2008. Submicroscopic duplications of the hydroxysteroid dehydrogenase HSD17B10 and the E3 ubiquitin ligase HUWE1 are associated with mental retardation.

Gould, Tiffany, Jamaluddin, Muhammad Fairuz B., Petit, Joel, King, Simon J., Nixon, Brett, Scott, Rodney, Pockney, Peter, Dun, Matthew D.. IntechOpen; 2019. Finding needles in haystacks: the use of quantitative proteomics for the early detection of colorectal cancer.

Oldmeadow, Christopher, Holliday, Elizabeth G., McEvoy, Mark, Scott, Rodney, Kwok, John B. J., Mather, Karen, Sachdev, Perminder, Schofield, Peter, Attia, John. IOS Press; 2014. Concordance between direct and imputed APOE genotypes using 1000 genomes data.

Hauberg, Mads Engel, Roussos, Panos, Schall, Ulli, Scott, Rodney, Tooney, Paul, Wu, Jing Qin, Grove, Jakob, Børglum, Anders Dupont, Mattheisen, Manual, Cairns, Murray, Henskens, Frans, Kelly, Brian, Loughland, Carmel, Michie, Patricia. American Medical Association; 2016. Analyzing the role of microRNAs in schizophrenia in the context of common genetic risk variants.

Cropley, Vanessa L., Scarr, Elizabeth, Fornito, Alex, Klauser, Paul, Bousman, Chad A., Scott, Rodney, Cairns, Murray J., Tooney, Paul A., Pantelis, Christos, Dean, Brian. Elsevier; 2015. The effect of a muscarinic receptor 1 gene variant on grey matter volume in schizophrenia.

Jakubowska, Anna, Gronwald, Jacek, Menklszak, Janusz, Gorski, Bohdan, Huzarski, Tomasz, Byrski, Tomasz, Edler, Lutz, Lubinski, Jan, Scott, Rodney, Hamann, Ute. Elsevier; 2008. The VEGF_936_C > T 3 ' UTR polymorphism reduces BRCA1-associated breast cancer risk in Polish women.

Rudnicka, Helena, Masojc, Bartlomiej, van de Wetering, Thierry, Debniak, Tadeusz, Cybulski, Cezary, Gronwald, Jacek, Lubinski, Jan, Gorski, Bohdan, Scott, Rodney. Elsevier; 2014. First recurrent large genomic rearrangement in the BRCA1 gene found in Poland.

Loughland, Carmel, Draganic, Daren, Mowry, Bryan, Pantelis, Christos, Schall, Ulrich, Scott, Rodney, Tooney, Paul, Carr, Vaughan, McCabe, Kathryn, Richards, Jacqueline, Nasir, Aslam, Allen, Joanne, Catts, Stanley, Jablensky, Assen, Henskens, Frans, Michie, Patricia. The Royal Australian and New Zealand College of Psychiatrists; 2010. Australian schizophrenia research bank: a database of comprehensive clinical, endophenotypic and genetic data for aetiological studies of schizophrenia.

Yari, Hamed, Jin, Lei, Teng, Liu, Wang, Yufang, Wu, Yongyan, Liu, Guang Zhi, Gao, Wei, Liang, Jin, Xi, Yanfeng, Feng, Yu Chen, Zhang, Chunming, Zhang, Yuan Yuan, Tabatabaee, Hessam, La, Ting, Yang, Rui Hong, Wang, Fu Hua, Yan, Xu Guang, Farrelly, Margaret, Scott, Rodney, Liu, Tao, Thorne, Rick F., Guo, Su Tang, Zhang, Xu Dong. Nature Publishing Group; 2019. LncRNA REG1CP promotes tumorigenesis through an enhancer complex to recruit FANCJ helicase for REG3A transcription.

Lee, Phil H., Anttila, Verneri, Wang, Meg M.-J., Cairns, Murray, Henskens, Frans A., Kelly, Brian J., Loughland, Carmel M., Schall, Ulrich A., Scott, Rodney, Tooney, Paul A., Yu, Dongmei, Stahl, Eli A., Walters, Raymond K., Anney, Richard J. L., Duncan, Laramie E., Ge, Tian, Adolfsson, Rolf, Banaschewski, Tobias, Belangero, Sintia, Won, Hyejung, Cook, Edwin H., Coppola, G, Derks, EM, Hoekstra, PJ, Kaprio, J, Keski-Rahkonen, A, Kirov, G, Kranzler, HR, Luykx, JJ, Rohde, LA, Feng, Yen-Chen A., Zai, CC, Agerbo, E, Arranz, MJ, Asherson, P, Bækvad-Hansen, M, Baldursson, G, Bellgrove, M, Belliveau, RA, Buitelaar, J, Burton, CL, Rosenthal, Jacob, Bybjerg-Grauholm, J, Casas, M, Cerrato, F, Chambert, K, Churchhouse, C, Cormand, B, Crosbie, J, Dalsgaard, S, Demontis, D, Doyle, AE, Zhu, Zhaozhong, Dumont, A, Elia, J, Grove, J, Gudmundsson, OO, Haavik, J, Hakonarson, H, Hansen, CS, Hartman, CA, Hawi, Z, Hervás, A, Tucker-Drob, Elliot M., Hougaard, DM, Howrigan, DP, Huang, H, Kuntsi, J, Langley, K, Lesch, KP, Leung, PWL, Loo, SK, Martin, J, Martin, AR, Nivard, Michel G., McGough, JJ, Medland, SE, Moran, JL, Mors, O, Mortensen, PB, Oades, RD, Palmer, DS, Pedersen, CB, Pedersen, MG, Peters, T, Grotzinger, Andrew D., Poterba, T, Poulsen, JB, Ramos-Quiroga, JA, Reif, A, Ribasés, M, Rothenberger, A, Rovira, P, Sánchez-Mora, C, Satterstrom, FK, Schachar, R, Posthuma, Danielle, Artigas, MS, Steinberg, S, Stefansson, H, Turley, P, Walters, GB, Werge, T, Zayats, T, Arking, DE, Bettella, F, Buxbaum, JD. Cell Press; 2019. Genomic relationships, novel loci, and pleiotropic mechanisms across eight psychiatric disorders.

Johnson, Natalie A., Kypri, Kypros, Latter, Joanna, Attia, John, McEvoy, Mark, Dunlop, Adrian, Scott, Rodney. Sax Institute; 2016. Genetic feedback to reduce alcohol consumption in hospital outpatients with risky drinking: feasibility and acceptability.

Patel, Yash, Shin, Jean, Auzias, Guilllaume, Lebedeva, I, Luna, B, Lundervold, AJ, MacMaster, FP, Maglanoc, LA, Mathalon, DH, McDonald, C, McIntosh, A, Meinert, S, Michie, Patricia T., Ayesa-Arriola, Rosa, Mitchell, P, Moreno-Alcazar, A, Mowry, B, Muratori, F, Nabulsi, L, Nenadic, I, Tuura, RO, Oosterlaan, J, Overs, B, Pantelis, C, Banaj, Nerisa, Parellada, M, Pariente, JC, Pauli, P, Pergola, G, Piarulli, FM, Picon, F, Piras, F, Pomarol-Clotet, E, Pretus, C, Quide, Y, Banaschewski, Tobias, Radua, J, Ramos-Quiroga, JA, Rasser, Paul E., Reif, A, Retico, A, Roberts, G, Rossell, S, Rovaris, DL, Rubia, K, Sacchet, M, Bandeira, Cibele, Salavert, J, Salvador, R, Sarro, S, Sawa, A, Schall, Ulrich, Scott, Rodney, Selvaggi, P, Silk, T, Sim, K, Skoch, A, Basgoze, Zeynep, Spalletta, G, Spaniel, F, Stein, DJ, Steinstrater, O, Stolicyn, A, Takayanagi, Y, Tamm, L, Tavares, M, Teumer, A, Thiel, K, Cupertino, Renata Basso, Thomopoulos, SI, Tomecek, D, Tomyshev, AS, Tordesillas-Gutierrez, D, Tosetti, M, Uhlmann, A, Van Rheenen, T, Vazquez-Bourgon, J, Vernooij, MW, Vieta, E, Bau, Claiton H. D., Vilarroya, O, Weickert, C, Weickert, T, Westlye, LT, Whalley, H, Willinger, D, Winter, A, Wittfeld, K, Yang, TT, Yoncheva, Y, Bauer, Jochen, Zijlmans, JL, Hoogman, M, Franke, B, van Rooij, D, Buitelaar, J, Ching, CRK, Andreassen, OA, Pozzi, E, Veltman, D, Schmaal, L, Baumeister, Sarah, van Erp, TGM, Turner, J, Castellanos, FX, Pausova, Z, Thompson, P, Paus, T, Abé, Christoph, Bernardoni, Fabio, Bertolino, A, del Mar Bonnin, C, Brandeis, D, Brem, S, Bruggemann, J, Bulow, R, Bustillo, JR, Calderoni, S, Calvo, R, Agartz, Ingrid, Canales-Rodriguez, EJ, Cannon, DM, Carmona, S, Carr, VJ, Catts, SV, Chenji, S, Chew, QH, Coghill, D, Connolly, CG, Conzelmann, A, Alloza, Clara, Craven, AR, Crespo-Facorro, B, Cullen, K, Dahl, A, Dannlowski, U, Davey, CG, Deruelle, C, Diaz-Caneja, CM, Dohm, K, Ehrlich, S, Alnaes, Dag, Epstein, J, Erwin-Grabner, T, Eyler, LT, Fedor, J, Fitzgerald, J, Foran, W, Ford, JM, Fortea, L, Fuentes-Claramonte, P, Fullerton, J, Ambrogi, Sonia, Furlong, L, Gallagher, L, Gao, B, Gao, S, Goikolea, JM, Gotlib, I, Goya-Maldonado, R, Grabe, HJ, Green, M, Grevet, EH, Antonucci, Linda A., Groenewold, NA, Grotegerd, D, Gruber, O, Haavik, J, Hahn, T, Harrison, BJ, Heindel, W, Henskens, Frans, Heslenfeld, DJ, Hilland, E, Arango, Celso, Hoekstra, PJ, Hohmann, S, Holz, N, Howells, FM, Ipser, JC, Jahanshad, N, Jakobi, B, Jansen, A, Janssen, J, Jonassen, R, Arolt, Volker, Kaiser, A, Kaleda, V, Karantonis, J, King, JA, Kircher, T, Kochunov, P, Koopowitz, S-M, Landen, M, Landro, NI, Lawrie, S. Elsevier; 2022. Virtual Ontogeny of Cortical Growth Preceding Mental Illness.

Lin, Rui, Charlesworth, Jac, Stankovich, Jim, Perreau, Victoria M., Brown, Matthew A., ANZgene Consortium,, Scott, Rodney, Taylor, Bruce V.. Public Library of Science (PLoS); 2013. Identity-by-descent mapping to detect rare variants conferring susceptibility to multiple sclerosis.

Ahadova, Aysel, Seppälä, Toni T., Laghi, Luigi, Dominguez-Valentin, Mev, Capella, Gabriel, Macrae, Finlay, Scott, Rodney, Hüneburg, Robert, Nattermann, Jacob, Hoffmeister, Michael, Brenner, Hermann, Bläker, Hendrik, Engel, Christoph, von Knebel Doeberitz, Magnus, Sampson, Julien R., Vasen, Hans, Mecklin, Jukka-Pekka, Møller, Pal, Kloor, Matthias, Gallon, Richard, Burn, John, Holinski-Feder, Elke, Steinke-Lange, Verena, Möslein, Gabriela, Nielsen, Maartje, ten Broeke, Sanne W.. John Wiley & Sons; 2021. The "unnatural" history of colorectal cancer in Lynch syndrome: lessons from colonoscopy surveillance.

Anttila, Verneri, Bulik-Sullivan, Brendan, Patsopoulos, Nikolaos A., Ripke, Stephan, Wei, Zhi, Yu, Dongmei, Lee, Phil H., Turley, Patrick, Grenier-Boley, Benjamin, Chouraki, Vincent, Kamatani, Yoichiro, Berr, Claudine, Finucane, Hilary K., Holliday, Elizabeth, Attia, John, Cairns, Murray, Loughland, Carmel, Schall, Ulrich, Henskens, Frans, Scott, Rodney, Reitz, C, Goate, AM, Huentelman, MJ, Walters, Raymond K., Ilyas Kamboh, M, Larson, EB, Rogaeva, E, George-Hyslop, PS, Hakonarson, H, Kukull, WA, Farrer, LA, Barnes, LL, Beach, TG, Yesim Demirci, F, Bras, Jose, Head, E, Hulette, CM, Jicha, GA, Kauwe, JSK, Kaye, JA, Leverenz, JB, Levey, AI, Lieberman, AP, Pankratz, VS, Poon, WW, Duncan, Laramie, Quinn, JF, Saykin, AJ, Schneider, LS, Smith, AG, Escott-Price, Valentina, Falcone, Guido J., Gormley, Padhraig, Malik, Rainer. American Association for the Advancement of Science; 2018. Analysis of shared heritability in common disorders of the brain.

Ten Broeke, Sanne W., van der Klift, Heleen M., Gallinger, Steven, Gomez Garcia, Encarna, Figueiredo, Jane C., Haile, Robert, Hampel, Heather L., Hopper, John L., Hoogerbrugge, Nicoline, von Knebel Doeberitz, Magnus, Le Marchand, Loic, Letteboer, Tom G. W., Tops, Carli M. J., Jenkins, MA, Lindblom, A, Lindor, NM, Mensenkamp, AR, Møller, P, Newcomb, PA, van Os, TAM, Pearlman, R, Pineda, M, Rahner, N, Aretz, Stefan, Redeker, EJW, Olderode-Berends, MJW, Rosty, C, Schackert, HK, Scott, Rodney, Senter, L, Spruijt, L, Steinke-Lange, V, Suerink, M, Thibodeau, S, Bernstein, Inge, Vos, YJ, Wagner, A, Winship, I, Hes, FJ, Vasen, HFA, Wijnen, JT, Nielsen, M, Win, AK, Buchanan, Daniel D., de la Chapelle, Albert, Capella, Gabriel, Clendenning, Mark, Engel, Christoph. American Society of Clinical Oncology; 2018. Cancer Risks for PMS2-Associated Lynch Syndrome..

Sekar, Aswin, Bialas, Allison R., Genovese, Giulio, Rose, Samuel A., Handsaker, Robert E., Schizophrenia Working Group of the Psychiatric Genomics Consortium,, Daly, Mark J., Carroll, Michael C., Stevens, Beth, McCarroll, Steven A., Tooney, Paul A., Henskens, Frans A., de Rivera, Heather, Michie, Patricia, Schall, Ulrich, Loughland, Carmel, Cairns, Murray J., Kelly, Brian J., Scott, Rodney, Davis, Avery, Hammond, Timothy R., Kamitaki, Nolan, Tooley, Katherine, Presumey, Jessy, Baum, Matthew, Van Doren, Vanessa. Nature Publishing Group; 2016. Schizophrenia risk from complex variation of complement component 4.

Shahijanian, Fernando, Parnell, Grant P., Baxter, Alan, Kermode, Allan, Carroll, William, Butzkueven, Helmut, Booth, David, Stewart, Graeme, Vucic, Steve, Wiley, James, Field, Judith, Tajouri, Lotti, McKay, Fiona C., Griffiths, Lyn, Barnett, Michael, Scott, Rodney, Lechner-Scott, Jeannette, Moscato, Pablo, Broadley, Simon, Slee, Mark, Kilpatrick, Trevor, Taylor, Bruce, Charlesworth, Jac, Gatt, Prudence N., Brown, Matt, Mason, Deborah, Stewart, Graeme J., Booth, David R., Shojoei, Maryam, O'Connor, Kate S., Schibeci, Stephen D., Brilot, Fabienne, Liddle, Christopher, Batten, Marcel. Oxford University Press; 2014. The CYP27B1 variant associated with an increased risk of autoimmune disease is underexpressed in tolerizing dendritic cells.

Gill, Dipender, James, Nicole E., Monori, Grace, Lorentzen, Erik, Fernandez-Cadenas, Israel, Lemmens, Robin, Thijs, Vincent, Rost, Natalia S., Scott, Rodney, Hankey, Graeme J., Lindgren, Arne, Jern, Christina, Maguire, Jane M.. Lippincott Williams & Wilkins; 2019. Genetically determined risk of depression and functional outcome after Ischemic Stroke: mendelian randomization study.

Minelli, Cosetta, Dean, Charlotte H., Bossé, Yohan, Postma, Dirkje S., Sin, Don, Thompson, John, Attia, John, Gu, Xin, Holiday, Liz, Oldmeadow, Christopher, Scott, Rodney, Wang, Cindy, Hind, Matthew, , , , , , , , , , , Alves, Alexessander Couto, , , , , , , , , , , Amaral, André F. S, , , , , , , , , , , Siroux, Valerie, , , , , , , Huikari, Ville, Soler Artigas, María, Evans, David M., Loth, Daan W.. Public Library of Science; 2016. Association of forced vital capacity with the developmental gene NCOR2.

Khor, Chiea Chuen, Davila, Sonia, Wong, Tien Yin, Pang, Junxiong, Mitchell, Paul, Cimaz, Rolando, Dahdah, Nagib, Cheung, Yiu-Fai, Huang, Guo-Ying, Yang, Wanling, Park, In-Sook, Lee, Jong-Keuk, Breunis, Willemijn B., Wu, Jer-Yuarn, Levin, Michael, Burns, Jane C., Burgner, David, Kuijpers, Taco W., Hibberd, Martin L., Attia, John, Scott, Rodney, Holliday, Elizabeth, Lee, Yi-Ching, Shimizu, Chisato, Wright, Victoria J., Yeung, Rae S. M, Tan, Dennis E. K., Sim, Kar Seng, Wang, Jie Jin. Nature Publishing Group; 2011. Genome-wide association study identifies FCGR2A as a susceptibility locus for Kawasaki disease.

Wain, Louise V., Vaez, Ahmad, Verwoert, Germaine C., , , , , , , , , , , Hottenga, Jouke-Jan, , , , , , , , , , , Strawbridge, Rona J., , , , , , , , , , , Esko, Tonu, , , , , , , , , , , Arking, Dan E., , , , , , , , , , , Hwang, Shih-Jen, , , , , , , , , , , Guo, Xiuqing, , , , , , , , , , , Kutalik, Zoltan, , , , , , , , , , , Trompet, Stella, , , , , , , , , , , Shrine, Nick, , , , , , , , , , , Jansen, Rick, Oldmeadow, Christopher, , , , , , , , , , , Scott, Rodney, , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Joehanes, Roby, , , , , , , , , , , van Der Most, Peter J., , , , , , , , , , , Erzurumluoglu, A. Mesut, , , , , , , , , , , O'Reilly, Paul F., , , , , , , , , , , Cabrera, Claudia P., , , , , , , , , , , Warren, Helen R., , , , , , , , , , , Rose, Lynda M., , , , , , , , , , . Lippincott Williams & Wilkins; 2017. Novel blood pressure locus and gene discovery using genome-wide association study and expression data sets from blood and the kidney.

Simpson, Jodie L., Scott, Rodney, Boyle, Michael J., Gibson, Peter G.. American Lung Association; 2005. Differential proteolytic enzyme activity in eosinophilic and neutrophilic asthma.

Schmidt, Amand F., Holmes, Michael V., Preiss, David, Swerdlow, Daniel I., Denaxas, Spiros, Fatemifar, Ghazaleh, Faraway, Rupert, Finan, Chris, Valentine, Dennis, Fairhurst-Hunter, Zammy, Hartwig, Fernando Pires, Horta, Bernardo Lessa, Hypponen, Elina, Power, Christine, Moldovan, Max, van Iperen, Erik, Hovingh, Kees, Demuth, Ilja, Norman, Kristina, Steinhagen-Thiessen, Elisabeth, Hancock, Stephen, Attia, John, Holliday, Elizabeth, Scott, Rodney, Teumer, A, Baumeister, S, Doerr, M, Lerch, MM, Voelker, U, Voelzke, H, Ward, J, Pell, JP, Meade, T, Christophersen, IE, Maitland-van der Zee, AH, Baranova, EV, Young, R, Ford, I, Campbell, A, Padmanabhan, S, Bots, ML, Grobbee, DE, Froguel, P, Thuillier, D, Roussel, R, Bonnefond, A, Cariou, B, Smart, M, Bao, Y, Kumari, M, Mahajan, A, Hopewell, JC, Seshadri, S, Dale, C, Costa, RPE, Ridker, PM, Chasman, DI, Reiner, AP, Ritchie, MD, Lange, LA, Cornish, AJ, Dobbins, SE, Hemminki, K, Kinnersley, B, Sanson, M, Labreche, K, Simon, M, Bondy, M, Law, P, Speedy, H, Allan, J, Li, N, Went, M, Weinhold, N, Morgan, G, Sonneveld, P, Nilsson, B, Goldschmidt, H, Sud, A, Engert, A, Hansson, M, Hemingway, H, Asselbergs, FW, Patel, RS, Keating, BJ, Sattar, N, Houlston, R, Casas, JP, Hingorani, AD, Demuth, Juri, Bertram, L, Lill, CM, Coassin, S, Willeit, J, Kiechl, S, Willeit, K, Mason, D, Wright, J, Morris, R, Wanamethee, G, Whincup, P, Ben-Shlomo, Y, McLachlan, S, Price, JF, Kivimaki, M, Welch, C, Sanchez-Galvez, A, Marques-Vidal, P, Nicolaides, A, Panayiotou, AG, Onland-Moret, NC, van der Schouw, YT, Matullo, G, Fiorito, G, Guarrera, S, Sacerdote, C, Wareham, NJ, Langenberg, C, Scott, RA, Luan, J, Bobak, M, Malyutina, S, Pajak, A, Kubinova, R, Tamosiunas, A, Pikhart, H, Grarup, N, Pedersen, O, Hansen, T, Linneberg, A, Jess, T, Cooper, J, Humphries, SE, Brilliant, M, Kitchner, T, Hakonarson, H, Carrell, DS, McCarty, CA, Lester, KH, Larson, EB, Crosslin, DR, de Andrade, M, Roden, DM, Denny, JC, Carty, C, Schofield, P, O'Donnell, M, Yusuf, S, Chong, M, Pare, G, van der Harst, P, Said, MA, Eppinga, RN, Verweij, N, Snieder, H, Christen, T, Mook-Kanamori, DO, Gustafsson, S, Lind, L, Ingelsson, E, Pazoki, R, Franco, O, Hofman, A, Uitterlinden, A, Dehghan, A. BioMed Central Ltd; 2019. Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in PCSK9.

Moscovis, Sophia, Hall, Sharron, Burns, Christine, Scott, Rodney, Blackwell, Caroline. Sage; 2013. Development of an experimental model for assessing the effects of cigarette smoke and virus infections on inflammatory responses to bacterial antigens.

Malińska, Karolina, Deptula, Jakub, Cybulski, Cezary, Kram, Andrzej, Boer, Magdalena, Kiedrowicz, Magdalena, Lubiński, Jan, Dębniak, Tadeusz, Rogoża-Janiszewska, Emilia, Górski, Bohdan, Scott, Rodney, Rudnicka, Helena, Kashyap, Aniruddh, Domagala, Pawel, Hybiak, Jolanta, Masojć, Bartlomiej. Lippincott Williams & Wilkins; 2020. Constitutional variants in POT1, TERF2IP, and ACDgenes in patients with melanoma in the Polish population.

Zacharin, Margaret, Bajpai, Anurag, Chow, Chung Wo, Catto-Smith, Anthony, Stratakis, Constantine, Wong, Michelle W., Scott, Rodney. BMJ Group; 2011. Gastrointestinal polyps in McCune Albright syndrome.

Wong, Stephen Q., Scott, Rodney, Fox, Stephen B.. Future Medicine; 2016. KRAS mutation testing in colorectal cancer: the model for molecular pathology testing in the future.

Dörk, Thilo, Peterlongo, Paolo, Aronson, Kristan J., Menon, U, Milne, RL, Taib, NAM, Muir, K, Mulligan, AM, Neuhausen, SL, Nevanlinna, H, Neven, P, Newman, WG, Offit, K, Augustinsson, Annelie, Olopade, O, Olshan, AF, Olson, JE, Olsson, H, Park, SK, Park-Simon, T-W, Peto, J, Plaseska-Karanfilska, D, Pohl-Rescigno, E, Presneau, N, Freeman, Laura E. Beane, Rack, B, Radice, P, Rashid, MU, Rennert, G, Rennert, HS, Romero, A, Ruebner, M, Saloustros, E, Schmidt, MK, Schmutzler, RK, Beckmann, Matthias W., Schneider, MO, Schoemaker, MJ, Scott, C, Shen, C-Y, Shu, X-O, Simard, J, Slager, S, Smichkoska, S, Southey, MC, Spinelli, JJ, Beeghly-Fadiel, Alicia, Stone, J, Surowy, H, Swerdlow, AJ, Tamimi, RM, Tapper, WJ, Teo, SH, Terry, MB, Toland, AE, Tollenaar, RAEM, Torres, D, Behrens, Sabine, Torres-Mejia, G, Troester, MA, Truong, T, Tsugane, S, Untch, M, Vachon, CM, van den Ouweland, AMW, van Veen, EM, Vijai, J, Wendt, C, Bermisheva, Marina, Wolk, A, Yu, J-C, Zheng, W, Ziogas, A, Ziv, E, Dunning, AM, Pharoah, PDP, Schindler, D, Devilee, P, Easton, DF, Blomqvist, Carl, Balleine, R, Baxter, R, Braye, S, Carpenter, J, Dahlstrom, J, Forbes, John, Lee, CS, Marsh, D, Morey, A, Pathmanathan, N, Bogdanova, Natalia V., Scott, Rodney, Simpson, P, Spigelman, A, Wilcken, N, Yip, D, Zeps, N, Borresen-Dale, A-L, Alnaes, GIG, Sahlberg, KK, Ottestad, L, Bojesen, Stig E., Karesen, R, Schlichting, E, Holmen, MM, Sauer, T, Haakensen, V, Engebraten, O, Naume, B, Fossa, A, Kiserud, CE, Reinertsen, K, Mannermaa, Arto, Brauch, H, Helland, A, Riis, M, Geisler, J, Brenner, H, Burwinkel, B, Canzian, F, Chan, TL, Chang-Claude, J, Chanock, SJ, Choi, J-Y, Christiansen, H, Clarke, CL, Bolla, Manjeet K., Couch, FJ, Czene, K, Daly, MB, dos-Santos-Silva, I, Dwek, M, Eccles, DM, Ekici, AB, Eriksson, M, Evans, DG, Fasching, PA, Wang, Qin, Figueroa, J, Flyger, H, Fritschisl, L, Gabrielson, M, Gago-Dominguez, M, Gao, C, Gapstur, SM, Garcia-Closas, M, Garcia-Saenz, JA, Gaudet, MM, Dennis, Joe, Giles, GG, Goldberg, MS, Goldgar, DE, Guenel, P, Haeberle, L, Haiman, CA, Hakansson, N, Hall, P, Hamann, U, Hartman, M, Ahearn, Thomas, Hauke, J, Hein, A, Hillemanns, P, Hogervorst, FBL, Hooning, MJ, Hopper, JL, Howell, T, Huo, D, Ito, H, Iwasaki, M, Andrulis, Irene L., Jakubowska, A, Janni, W, John, EM, Jung, A, Kaaks, R, Kang, D, Kapoor, PM, Khusnutdinova, E, Kim, S-W, Kitahara, CM, Anton-Culver, Hoda, Koutros, S, Kraft, P, Kristensen, VN, Kwon, A, Lambrechts, D, Le Marchand, L, Li, J, Lindstrom, S, Linet, M, Lo, W-Y, Arndt, Volker, Long, J, Lophatananon, A, Lubinski, J, Manoochehri, M, Manoukian, S, Margolin, S, Martinez, E, Matsuo, K, Mavroudis, D, Meindl, A. Nature Publishing Group; 2019. Two truncating variants in FANCC and breast cancer risk.

Fullerton, Janice M., Klauser, Paul, Schofield, Peter R., Weikert, Cyndi Shannon, Pantelis, Christos, Fornito, Alex, Whitford, Thomas J., Weickert, Thomas W., Zalesky, Andrew, Lenroot, Rhosel K., Shaw, Alex D., Overs, Bronwyn, Heath, Anna, Cairns, Murray J., Atkins, Joshua, Scott, Rodney, Australian Schizophrenia Research Bank,. Nature Publishing Group; 2018. Differential effect of disease-associated ST8SIA2 haplotype on cerebral white matter diffusion properties in schizophrenia and healthy controls.

Oldmeadow, Christopher, Riveros, Carlos, Klein, Ronald, Attia, John, Holliday, Elizabeth G., Scott, Rodney, Moscato, Pablo, Wang, Jie Jin, Mitchell, Paul, Buitendijk, Gabrielle H. S., Vingerling, Johannes R., Klaver, Caroline C. W.. John Wiley & Sons; 2011. Sifting the wheat from the chaff: prioritizing GWAS results by identifying consistency across analytical methods.

Mehta, Divya, Tropf, Felix C., Metspalu, Andres, Snieder, Harold, Mowry, Bryan J., , , , , , , , Gratten, Jacob, , , , , Cairns, Murray, , , , , , Bakshi, Andrew, , , , , , , , , , Henskens, Frans, Zhu, Zhihong, , , , , , Loughland, Carmel, , , , , Bacanu, Silviu-Alin, , , , Michie, Patricia, , , , , , , Hemani, Gibran, , , Schall, Ulli, Scott, Rodney, , , Tooney, Paul, , , , Magnusson, Patrik K. E., , , Barban, Nicola, Esko, Tõnu. American Medical Association; 2016. Evidence for genetic overlap between schizophrenia and age at first birth in women..

Biswas, Mohitosh, Dias, Thilani H., Daneshi, Nilofar, Holliday, Elizabeth, Hancock, Stephen, Attia, John, Scott, Rodney, Newby, David, Kerr, Karen P., Milward, Elizabeth A.. Global Science and Technology Forum; 2017. Potential simple and multifactorial drug-gene interactions of tricyclic antidepressants in older Australians.

Sukiennicki, Grzegorz Mariusz, Marciniak, Wojciech, Gromowski, Tomasz, Prajzendanc, Karolina, Lukomska, Alicja, Waloszczyk, Piotr, Wojcik, Janusz Zenon, Scott, Rodney, Lubinski, Jan, Jakubowska, Anna, Muszynska, Magdalena, Baszuk, Piotr, Gupta, Satish, Bialkowska, Katarzyna, Jaworska-Bieniek, Katarzyna, Durda, Katarzyna, Lener, Marcin, Pietrzak, Sandra. Public Library of Science (PLoS); 2019. Iron levels, genes involved in iron metabolism and antioxidative processes and lung cancer incidence.

Johnson, Nichola, Maguire, Sarah, Dennis, Joe, Ahearn, Thomas U., Andrulis, Irene L., Anton-Culver, Hoda, Antonenkova, Natalia N., Arndt, Volker, Aronson, Kristan J., Augustinsson, Annelie, Baynes, Caroline, Freeman, Laura E. Beane, Morra, Anna, Beckmann, MW, Benitez, J, Bermisheva, M, Blomqvist, C, Boeckx, B, Bogdanova, NV, Bojesen, SE, Brauch, H, Brenner, H, Burwinkel, B, Kapoor, Pooja Middha, Campa, D, Canzian, F, Castelao, JE, Chanock, SJ, Chenevix-Trench, G, Clarke, CL, Børresen-Dale, AL, Alnæs, GIG, Sahlberg, KK, Ottestad, L, Tomczyk, Katarzyna, Kåresen, R, Schlichting, E, Holmen, MM, Sauer, T, Haakensen, V, Engebråten, O, Naume, B, Fosså, A, Kiserud, CE, Reinertsen, KV, Jones, Michael E., Helland, Å, Riis, M, Geisler, J, Conroy, DM, Couch, FJ, Cox, A, Cross, SS, Czene, K, Dörk, T, Eliassen, AH, Schoemaker, Minouk J., Engel, C, Evans, DG, Fasching, PA, Figueroa, J, Floris, G, Flyger, H, Gago-Dominguez, M, Gapstur, SM, García-Closas, M, Gaudet, MM, Gilham, Clare, Giles, GG, Goldberg, MS, González-Neira, A, Bowtell, DDL, deFazio, A, Webb, PM, Guénel, P, Hahnen, E, Haiman, CA, Håkansson, N, Bolla, Manjeet K., Hall, P, Hamann, U, Harrington, PA, Hart, SN, Hooning, MJ, Hopper, JL, Howell, A, Hunter, DJ, Clarke, C, Marsh, D, Wang, Qin, Scott, Rodney, Baxter, R, Yip, D, Carpenter, J, Davis, A, Pathmanathan, N, Simpson, P, Graham, D, Sachchithananthan, M, Amor, D. Nature Publishing Group; 2021. CYP3A7*1C allele: linking premenopausal oestrone and progesterone levels with risk of hormone receptor-positive breast cancers.

Binder, Michele D., Fox, Andrew D., Laverick, Louise, Foo, Grace, Fabis-Pedrini, Marzena J., Spelman, Timothy, Jordan, Margaret A., Baxter, Alan G., Foote, Simon, , , , Merlo, Daniel, , , , , , , , , , Lechner-Scott, Jeannette, Johnson, Laura J., , , , , , Moscato, Pablo, Scott, Rodney, , , , Giuffrida, Sarah E., , Calvert, Rainer, Akkermann, Rainer, Ma, Gerry Z. M., Perera, Ashwyn A., Gresle, Melissa M.. Public Library of Science (PLoS); 2016. Common and low frequency variants in MERTK are independently associated with multiple sclerosis susceptibility with discordant association dependent upon HLA-DRB1*15:01 status.

Gu, Ben J., Field, Judith, Butzkueven, Helmut, Gresle, Melissa, Laws, Simon M., Petrou, Steven, Hoffjan, Sabine, Akkad, Denis A., Graham, Colin A., Hawkins, Stanley, Glaser, Anna, Bedri, Sahl Khalid, Dutertre, Sébastien, Hillert, Jan, Matute, Carlos, Antiguedad, Alfredo, Wiley, James S., Ou, Amber, Kilpatrick, Trevor J., Lechner-Scott, Jeannette, Scott, Rodney, Lea, Rodney, Taylor, Bruce V., Stankovich, Jim. Oxford University Press; 2015. A rare P2X7 variant Arg307Gln with absent pore formation function protects against neuroinflammation in multiple sclerosis.

Purrington, Kristen S., Visscher, Daniel W., Kotoula, Vassiliki, Fountzilas, George, Kabisch, Maria, Rüdiger, Thomas, Heikkilä, Päivi, Blomqvist, Carl, Cross, Simon S., Southey, Melissa C., Olson, Janet E., Gilbert, Judy, Wang, Chen, Scott, Rodney, Yannoukakos, Drakoulis, Hamann, Ute, Nevanlinna, Heli, Cox, Angela, Giles, Graham G., Eckel-Passow, Jeanette E., Lakis, Sotiris. Springer; 2016. Genes associated with histopathologic features of triple negative breast tumors predict molecular subtypes.

McEvoy, Mark, Smith, Wayne, Hancock, Stephen, Smith, Derek, Attia, John, D'Este, Catherine, Duke, Janine, Peel, Roseanne, Schofield, Peter, Scott, Rodney, Byles, Julie, Henry, David, Ewald, Ben. Oxford University Press; 2010. Cohort profile: the Hunter Community Study.

Hess, Jonathan L., Tylee, Daniel S., Mattheisen, Manuel, Schizophrenia Working Group of the Psychiatric Genomics Consortium, Lundbeck Foundation Initiative for Integrative Psychiatric Research (iPSYCH), Børglum, Anders D., Als, Thomas D., Grove, Jakob, Werge, Thomas, Mortensen, Preben Bo, Mors, Ole, Nordentoft, Merete, Hougaard, David M., Byberg-Grauholm, Jonas, Bækvad-Hansen, Maree, Greenwood, Tiffany A., Tsuang, Ming T., Curtis, David, Steinberg, Stacy, Sigurdsson, Engilbert, Stefánsson, Hreinn, Stefánsson, Kári, Edenberg, Howard J., Holmans, Peter, Faraone, Stephen V., Glatt, Steven J., Cairns, Murray J., Carr, Vaughan J., Henskens, Frans A., Kelly, Brian J., Loughland, Carmel M., Michie, Patricia T., Schall, Ulrich A,, Scott, Rodney, Tooney, Paul. Nature Publishing; 2021. A polygenic resilience score moderates the genetic risk for schizophrenia.

Springelkamp, Henriët, Höhn, René, Luo, Xiaoyan, Deloukas, Panos, Duncanson, Audrey, Jankowski, Janusz, Markus, Hugh S., Mathew, Christopher G., Palmer, Colin N. A., Plomin, Robert, Rautanen, Anna, Sawcer, Stephen J., Trembath, Richard C., Ramdas, Wishal D., Viswanathan, Ananth C., Wood, Nicholas W., Spencer, Chris C. A., Band, Gavin, Bellenguez, Céline, Freeman, Colin, Hellenthal, Garrett, Giannoulatou, Eleni, Pirinen, Matti, Pearson, Richard, Vithana, Eranga, Strange, Amy, Su, Zhan, Vukcevic, Damjan, Donnelly, Peter, Langford, Cordelia, Hunt, Sarah E., Edkins, Sarah, Gwilliam, Rhian, Blackburn, Hannah, Bumpstead, Suzannah J., Nongpiur, Monisha E., Droniv, Serge, Gillman, Matthew, Gray, Emma, Hammond, Naomi, Jayakumar, Alagurevathi, McCann, Owen T., Liddle, Jennifer, Potter, Simon C., Ravindrarajah, Alagurevathi, Rocketts, Michelle, Montgomery, Grant W., Waller, Matthew, Weston, Paul, Widaa, Sara, Whittaker, Pamela, Barroso, Ines, Deloukas, Panos, Mathew, Christopher G., Blackwell, Jenefer M., Brown , Matthew A., Corvin, Aiden, Xu, Liang, Spencer , Chris C. A., Spector, Timothy D., Mirshahi, Alireza, Saw, Seang-Mei, Vingerling, Johannes R., Teo, Yik-Ying, Haines, Jonathan L., Wolfs, Roger C. W., Lemij, Hans G., Tai, E-Shyong, Mountain, Jenny E., Jansonius, Nomdo M., Jonas, Jost B., Hammond, CJ, Gharahkhani, Puya, Lu, Yi, Amin, Najaf, Mishra, Aniket, Karssen, Lennart C., Sim, Kar-seng, van Leeuwen, Elisabeth M., Iglesias, Adriana I., Verhoeven, Virginie J. M., Hauser, Michael A., Loon, Seng-Chee, Despriet, Dominiek D. G., Nag, Abhishek, Venturini, Cristina, Hysi, Pirro G., Sanfilippo, Paul G., Schillert, Arne, Kang, Jae H., Landers, John, Jonasson, Fridbert, Cree, Angela J., van Koolwijk, Leonieke M. E., Rivadeneira, Fernando, Souzeau, Emmanuelle, Jonsson, Vesteinn, Khor, Chiea-Cheun, Menon, Geeta, Mitchell, Paul, Wang, Jie Jin, Rochtchina, Elena, Attia, John, Scott, Rodney, Holliday, Elizabeth G., Wong, Tien-Yin, Baird, Paul N., Xie, Jing, Loomis, Stephanie J., Inouye, Michael, Viswanathan, Ananth, Sim, Xueling, Weinreb, Robert N., de Jong, Paulus T. V. M., Oostra, Ben A., Uitterlinden, André G., Hofman, Albert, Ennis, Sarah, Thorsteinsdottir, Unnu, Bailey, Jessica N. Cooke, Burdon, Kathryn, Allingham, R. Band, Brilliant, Murray H., Budenz, Donald L., Bailey, Jessica N. Cooke, Christen, William G., Fingert, John, Friedman, David S., Gaasterland, Douglas, Gaasterland, Terry, Gibson, Jane, Haines, Jonathan L., Hauder, Michael A., Kang, Jae Hee, Kraft, Peter, Lee, Richard K., Lichter, Paul R., Liu, Yutao, Loomis, Stephanie J., Moroi, Sayoko E., Pasquale, Louis R., Thorleifsson, Gudmar, Pericak-Vance, Margaret A., Realini, Anthony, Richards, Julia E., Schuman, Joel S., Scott, William K., Singh, Kuldev, Sit, Arthur J., Vollrath, Douglas, Weinreb, Robert N., Wiggs, Janey L., Janssen, Sarah F., Wollstein, Gadi, Zack, Donald J., Zhang, Kang, Donnelly, Peter, Barroso, Ines, Blackwell, Jenefer M., Bramon, Elvira, Brown, Matthew A., Casas, Juan P., Corvin, Aiden. Nature Publishing Group; 2014. Meta-analysis of genome-wide association studies identifies novel loci that influence cupping and the glaucomatous process.

Couch, Fergus J., Kuchenbaecker, Karoline B., Aittomäki, Kristiina, Ambrosone, Christine, Andrulis, Irene L., Anton-Culver, Hoda, Arndt, Volker, Arun, Banu K., Arver, Brita, Barile, Monica, Barkardottir, Rosa B., Barrowdale, Daniel, Michailidou, Kyriaki, Scott, Rodney, Mendoza-Fandino, Gustavo A., Nord, Siljie, Lilyquist, Janna, Olswold, Curtis, Hallberg, Emily, Agata, Simona, Ahsan, Habibul. Nature Publishing Group; 2016. Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer.

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Debniak, Tadeusz, van de Wetering, Thierry, Byrski, Tomasz, Nej-Wolosiak, Katarzyna, Kladny, Jozef, Maleszka, Romuald, Lubinski, Jan, Scott, Rodney, Nagay, Leszek, Cybulski, Cezary, Gorski, Bohdan, Jakubowska, Annaa, Gronwald, Jacek, Masojc, Bartlomiej, Huzarski, Tomasz. Wolters Kluwer Health; 2008. Low prevalence of CDKN2A/ARF mutations among early-onset cancers of breast, pancreas and malignant melanoma in Poland.

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Dennis, Joe, Tyrer, Jonathan P., Antonenkova, Natalia N., Arndt, Volker, Aronson, Kristan J., Freeman, Laura E. Beane, Beckmann, Matthias W., Behrens, Sabine, Benitez, Javier, Bermisheva, Marina, Bogdanova, Natalia V., Bojesen, Stig E., Walker, Logan C., Brenner, Hermann, Scott, Rodney, .,, .,, .,, .,, .,, .,, .,, .,, Michailidou, Kyriaki, .,, .,, .,, .,, .,, .,, .,, .,, .,, .,, Dorling, Leila, .,, .,, .,, .,, .,, .,, .,, .,, .,, .,, Bolla, Manjeet K., .,, .,, .,, .,, .,, .,, .,, .,, .,, .,, Wang, Qin, .,, .,, .,, .,, .,, .,, .,, .,, ..,, .,, Ahearn, Thomas U., .,, .,, .,, .,, .,, .,, .,, .,, .,, .,, Andrulis, Irene L., .,, .,, .,, .,, .,, .,, .,, .,, .,, .,, Anton-Culver, Hoda, .,, .,, .,, .,, .,, .,, .,, .,, .,. Nature Publishing Group; 2022. Rare germline copy number variants (CNVs) and breast cancer risk.

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Møller, Pal, Seppälä, Toni T., Kohut, Kelly E., Ryan, Neil, Bauerfeind, Peter, Thomas, Laura E., Evans, D. Gareth, Aretz, Stefan, Sijmons, Rolf H., Half, Elizabeth, Heinimann, Karl, Horisberger, Karoline, Ahadova, Aysel, Monahan, Kevin, .,, .,, .,, .,, .,, .,, .,, .,, .,, Crosbie, Emma J., .,, .,, .,, .,, .,, .,, .,, .,, .,, .,, Holinski-Feder, Elke, .,, .,, .,, .,, .,, .,, .,, .,, .,, .,, Scott, Rodney, Haupt, Saskia, Möslein, Gabriela, Winship, Ingrid, Bajwa-ten Broeke, Sanne W.. BioMed Central; 2023. Dominantly inherited micro-satellite instable cancer - the four Lynch syndromes - an EHTG, PLSD position statement..

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Garrison, Jane R., Fernyhough, Charles, Catts, Stanley, Henskens, Frans, Pantelis, Christos, Loughland, Carmel, Simons, Jon S., McCarthy-Jones, Simon, Haggard, Mark, Carr, Vaughan, Schall, Ulrich, Scott, Rodney, Jablensky, Assen, Mowry, Bryan, Michie, Patricia. Nature Publishing Group; 2015. Paracingulate sulcus morphology is associated with hallucinations in the human brain.

Jensen, Richard A., Sim, Xueling, Launer, Lenore J., Smith, Albert Vernon, Boerwinkle, Eric, Cheung, Ning, Hewitt, Alex W., Liew, Gerald, Mitchell, Paul, Wang, Jie Jin, Attia, John, Scott, Rodney, Li, Xiaohui, Glazer, Nicole L., Lumley, Thomas, McKnight, Barbara, Psaty, Bruce M., Taylor, Kent, Hofman, Albert, de Jong, Paulus T. V. M., Rivadeneira, Fernando, Uitterlinden, Andre G., Tay, Wan-Ting, Cotch, Mary Frances, Teo, Yik Ying, Seielstad, Mark, Liu, Jianjun, Cheng, Ching-Yu, Saw, Seang-Mei, Aung, Tin, Ganesh, Santhi K., O'Donnell, Christopher J., Nalls, Mike A., Wiggins, Kerri L., Ikram, M. Kamran, Kuo, Jane Z., The Blue Mountains Eye Study GWAS Team, CKDGen Consortium, Klein, Cornelia M., van Duijn, Cornelia M., Gudnason, Vilmundur, Klein, Ronald, Siscovick, David S., Rotter, Jerome I., Tai, E. Shong, Holliday, Elizabeth G., Vingerling, Johannes, Wong, Tien Y., Eiriksdottir, Gudny, Harris, Tamara B., Jonasson, Fridbert, Klein, Barbara E. K.. Public Library of Science; 2013. Genome-wide association study of retinopathy in individuals without diabetes.

Paul, Christine L., Verrills, Nicole M., Ackland, Stephen, Scott, Rodney, Goode, Susan, Thomas, Ann, Lukeman, Sarah, Nielsen, Sarah, Weidenhofer, Judith, Lynam, James, Fradgley, Elizabeth A., Martin, Jarad, Greer, Peter, Smith, Stephen, Griffin, Cassandra, Avery-Kiejda, Kelly A., Zdenkowski, Nick, Searles, Andrew, Ramanathan, Shanthi. BioMed Central Ltd; 2024. The impact of a regionally based translational cancer research collaborative in Australia using the FAIT methodology.

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Smith, Wayne, Attia, John, D'Este, Catherine, McEvoy, Mark, Peel, Roseanne, Scott, Rodney, Schofield, Peter. Health and ageing data from the Hunter Community Study, NSW, Australia. 2011.

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