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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..

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.

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.

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.

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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.

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..

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.

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.

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.

Radua, Joaquim, Vieta, Eduard, Shinohara, Russell, Kochunov, Peter, Quidé, Yann, Green, Melissa J., Weickert, Cynthia S., Weickert, Thomas, Bruggemann, Jason, Kircher, Tilo, Nenadić, Igor, Cairns, Murray J., Seal, Marc, Schall, Ulrich, Henskens, Frans, Fullerton, Janice M., Mowry, Bryan, Pantelis, Christos, Lenroot, Rhoshel, Cropley, Vanessa, Loughland, Carmel, Scott, Rodney, Wolf, D., Satterthwaite, T. D., Tan, Y., Sim, K., Piras, F., Spalletta, G., Banaj, N., Pomarol-Clotet, E., Gur, R, Solanes, A., Albajes-Eizagirre, A., Canales-Rodríguez, E. J., Sarro, S., Di Giorgio, A., Bertolino, A., Stäblein, M., Oertel, V., Knöchel, C., Borgwardt, S., du Plessis, S., Yun, J-Y., Kwon, J. S., Dannlowski, U., Hahn, T., Grotegerd, D., Alloza, C., Arango, C., Janssen, J., Díaz-Caneja, C., Turner, J, van Erp, T, Glahn, D, Pearlson, G, Hong, E, Krug, A, Carr, V, Tooney, P, Cooper, G, Rasser, P, Michie, P, Catts, S, Gur, R, Yang, F, Jiang, W., Calhoun, V., Ehrlich, S., Yang, K., Cascella, N. G., Takayanagi, Y., Sawa, A., Tomyshev, A., Lebedeva, I., Kaleda, V., Kirschner, M., Hoschl, C., Tomecek, D., Skoch, A., van Amelsvoort, T., Bakker, G., James, A., Preda, A., Weideman, A., Stein, D. J., Howells, F., Uhlmann, A., Temmingh, H., López-Jaramillo, C., Díaz-Zuluaga, A., Fortea, L., Martinez-Heras, E., Solana, E., Llufriu, S., Jahanshad, N., Thompson, P., Turner, Jessica, van Erp, Theo. Elsevier; 2020. Increased power by harmonizing structural MRI site differences with the ComBat batch adjustment method in ENIGMA.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

Scott, Rodney, Lubinski, Jan. Humana Press; 2009. Genetic epidemiology studies in hereditary non-polyposis colorectal cancer.

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.

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.

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.

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.

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.

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.

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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.

Spurdle, Amanda B., Couch, Fergus J., Rhiem, Kerstin, Lissowska, Jolanta, Olson, Janet E., Pankratz, Vernon S., John, Esther M., Whittemore, Alice S., West, Dee W., Hamann, Ute, Torres, Diana, Ulmer, Hans Ulrich, Rüdiger, Thomas, Hahnen, Eric, Devilee, Peter, Tollenaar, Robert AEM, Seynaeve, Caroline, Van Asperen, Christi J, Eccles, Diana M, Tapper, William J, Durcan, Lorraine, Jones, Louise, Peto, Julian, dos-Santos-Silva, Isabel, Engel, Christoph, Fletcher, Olivia, Johnson, Nichola, Dwek, Miriam, Swann, Ruth, Bane, Anita L., Glendon, Gord, Mulligan, Anna M., Giles, Graham G., Milne, Roger L, Baglietto, Laura, Meindl, Alfons, McLean, Catriona, Carpenter, Jane, Clarke, Christine, Scott, Rodney, Brauch, Hiltrud, Brüning, Thomas, Ko, Yon-Dschun, Cox, Angela, Cross, Simon S., Reed, Malcolm W. R., Ditsch, Nina, Lubinski, Jan, Jaworska-Bieniek, Katarzyna, Durda, Katarzyna, Gronwald, Jacek, Dörk, Thilo, Bogdanova, Natalia, Park-Simon, Tjoung-Won, Hillemanns, Peter, Haiman, Christopher A., Henderson, Brian E., Arnold, Norbert, Schumacher, Fredrick, Le Marchand, Loic, Burwinkel, Barbara, Marme, Frederik, Surovy, Harald, Yang, Rongxi, Anton-Culver, Hoda, Ziogas, Argyrios, Hooning, Maartje J., Collée, J. Margriet, Plendl, Hansjoerg, Martens, John W. M., Tilanus-Linthorst, Madeleine M. A., Brenner, Hermann, Dieffenbach, Aida Karina, Arndt, Volke, Stegmaier, Christa, Winqvist, Robert, Pylkäs, Katri, Jukkola-Vuorinen, Arja, Grip, Mervi, Niederacher, Dieter, Lindblom, Annika, Margolin, Sara, Joseph, Vijai, Robson, Mark, Rau-Murthy, Rohini, González-Neira, Anna, Arias, José Ignacio, Zamora, Pilar, Benítez, Javier, Mannermaa, Arto, Sutter, Christian, Kataja, Vesa, Kosma, Veli-Matti, Hartikainen, Jaana M., Peterlongo, Paolo, Zaffaroni, Daniela, Barile, Monica, Capra, Fabio, Radice, Paolo, Teo, Soo H., Easton, Douglas F., Wang-Gohrke, Shan, Antoniou, Antonis C., Chenevix-Trench, Georgia, Goldgar, David E., Parsons, Michael T., Steinemann, Doris, Preisler-Adams, Sabine, Kast, Karin, Varon-Mateeva, Raymonda, Ellis, Steve, Frost, Debra, Platte, Radka, Perkins, Jo, Evans, D. Gareth, Izatt, Louise, McGuffog, Lesley, Eeles, Ros, Adlard, Julian, Davidson, Rosemarie, Cole, Trevor, Scuvera, Giulietta, Manoukian, Siranoush, Bonanni, Bernardo, Mariette, Frederique, Fortuzzi, Stefano, Viel, Alessandra, Barrowdale, Daniel, Pasini, Barbara, Papi, Laura, Varesco, Liliana, Balleine, Rosemary, Nathanson, Katherine L., Domchek, Susan M., Offitt, Kenneth, Jakubowska, Anna, Lindor, Noralane, Thomassen, Mads, Bolla, Manjeet K., Jensen, Uffe Birk, Rantala, Johanna, Borg, Åke, Andrulis, Irene L., Miron, Alexander, Hansen, Thomas V. O., Caldes, Trinidad, Neuhausen, Susan L., Toland, Amanda E., Nevanlinna, Heli, Wang, Qin, Montagna, Marco, Garber, Judy, Godwin, Andrew K., Osorio, Ana, Factor, Rachel E., Terry, Mary B., Rebbeck, Timothy R., Karlan, Beth Y., Southey, Melissa, Rashid, Muhammad Usman, Healey, Sue, Tung, Nadine, Pharoah, Paul D. P., Blows, Fiona M., Dunning, Alison M., Provenzano, Elena, Hall, Per, Czene, Kamila, Schmidt, Marjanka K., Broeks, Annegien, Cornelissen, Sten, Schmutzler, Rita Katharina, Verhoef, Senno, Fasching, Peter A., Beckmann, Matthias W., Ekici, Arif B., Slamon, Dennis J., Bojesen, Stig E., Nordestgaard, Børg G., Nielsen, Sune F., Flyger, Henrik, Chang-Claude, Jenny, Wappenschmidt, Barbara, Flesch-Janys, Dieter, Rudolph, Anja, Seibold, Petra, Aittomäki, Kristiina, Muranen, Taru A., Heikkilä, Päivi, Blomqvist, Carl, Figueroa, Jonine, Chanock, Stephen J., Brinton, Louise. Current Medicine Group; 2014. Refined histopathological predictors of BRCA1 and BRCA2 mutation status: a large-scale analysis of breast cancer characteristics from the BCAC, CIMBA, and ENIGMA consortia.

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.

Seppala, Toni T., Ahadova, Aysel, Bernstein, Inge, Holinski-Feder, Elke, Pylvanainen, Kirsi, Renkonen-Sinisalo, Laura, Lepisto, Anna, Lautrup, Charlotte Kvist, Lindblom, Annika, Plazzer, John-Paul, Winship, Ingrid, Tjandra, Douglas, Dominguez-Valentin, Mev, Katz, Lior H., Aretz, S, Hueneburg, R, Holzapfel, S, Heinimann, K, Della Valle, A, Neffa, F, Gluck, N, Cappel, WHDVTN, Vasen, H, Macrae, Finlay, Morak, M, Steinke-Lange, V, Engel, C, Rahner, N, Schmiegel, W, Vangala, D, Thomas, H, Green, K, Lalloo, F, Crosbie, EJ, Evans, D. Gareth, Hill, J, Capella, G, Pineda, M, Navarro, M, Blanco, I, ten Broeke, S, Nielsen, M, Ljungmann, K, Nakken, S, Lindor, N, Therkildsen, Christina, Frayling, I, Hovig, E, Sunde, L, Kloor, M, Mecklin, J-P, Kalager, M, Moller, P, Sampson, Julian, Scott, Rodney, Burn, John, Moeslein, Gabriela. BioMed Central; 2019. Lack of association between screening interval and cancer stage in Lynch syndrome may be accounted for by over-diagnosis; a prospective Lynch syndrome database report.

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.

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.

Hitchins, Megan, Williams, Rachel, Cheong, Kayfong, Halani, Nimita, Lin, Vita A.P., Packham, Deborah, Ku, Sue, Buckle, Andrew, Hawkins, Nicholas, Burn, John, Steven Gallinger, Jack Goldblattshort, Judy Kirk, Ian Tomlinson, Scott, Rodney, Spigelman, Allan, Catherine Suter, David Martin, Graeme Suthers, Robyn Ward. W.B. Saunders; 2005. MLH1 Germline Epimutations as a Factor in Hereditary Nonpolyposis Colorectal Cancer.

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

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.

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.

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.

Mavaddat, Nasim, Pharoah, Paul D. P., Michailidou, Kyriaki, Tyrer, Jonathan, Brook, Mark N., Bolla, Manjeet K., Wang, Qin, Dennis, Joe, Dunning, Alison M., Shah, Mitul, Luben, Robert, Brown, Judith, Bojesen, Stig E., Nordestgaard, Børge G., Nielsen, Sune F., Flyger, Henrik, Czene, Kamila, Darabi, Hatef, Eriksson, Mikael, Peto, Julian, Dos-Santos-Silva, Isabel, Dudbridge, Frank, Scott, Rodney, Yang, Rui. Oxford University Press; 2015. Prediction of breast cancer risk based on profiling with common genetic variants.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

Wang, Yunpeng, Thompson, Wesley K., Devor, Anna, Bipolar Disorder and Schizophrenia Working Group of the Psychiatric Genomics Consortium,, Enhancing Neuro Imaging Genetics through Meta Analysis Consortium,, Cairns, Murray J., Henskens, Fran A., Kelly, Brian J., Loughland, Carmel M., Michie, Patricia T., Schall, Ulrich A., Scott, Rodney, Schork, Andrew J., Tooney, Paul A., Wu, Jing Qin, Holland, Dominic, Chen, Chi-Hua, Bettella, Francesco, Desikan, Rahul S., Li, Wen, Witoelar, Aree, Zuber, Verena. Public Library of Science (PLoS); 2016. Leveraging genomic annotations and pleiotropic enrichment for improved replication rates in schizophrenia GWAS.

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.

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.

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.

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.

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.