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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.
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.
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..
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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