Sifting the wheat from the chaff: prioritizing GWAS results by identifying consistency across analytical methods

- 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.

First recurrent large genomic rearrangement in the BRCA1 gene found in Poland

- Rudnicka, Helena, Masojc, Bartlomiej, van de Wetering, Thierry, Debniak, Tadeusz, Cybulski, Cezary, Gronwald, Jacek, Lubinski, Jan, Gorski, Bohdan, Scott, Rodney

Evidence for genetic overlap between schizophrenia and age at first birth in women.

- 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

Impact of COX-2 rs5275 and rs20417 and GPIIIa rs5918 polymorphisms on 90-day ischemic stroke functional outcome: a novel finding

- Maguire, Jane, Thakkinstian, Ammarin, Levi, Christopher, Lincz, Lisa, Bisset, Linda, Sturm, Jonathan, Scott, Rodney, Whyte, Scott, Attia, John

Genetic determinants of heel bone properties: genome-wide association meta-analysis and replication in the GEFOS/GENOMOS consortium

- 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.

Cohort profile: the Hunter Community Study

- 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

Genetic contribution to all cancers: the first demonstration using the model of breast cancers from Poland stratified by age at diagnosis and tumour pathology

- 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

Submicroscopic duplications of the hydroxysteroid dehydrogenase HSD17B10 and the E3 ubiquitin ligase HUWE1 are associated with mental retardation

- 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

A rare P2X7 variant Arg307Gln with absent pore formation function protects against neuroinflammation in multiple sclerosis

- 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

The CYP27B1 variant associated with an increased risk of autoimmune disease is underexpressed in tolerizing dendritic cells

- 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

Schizophrenia risk from complex variation of complement component 4

- 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

Meta-analysis of genome-wide association studies identifies novel loci that influence cupping and the glaucomatous process

- 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, 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., Christen, William G., Fingert, John, Friedman, David S., Gaasterland, Douglas, Gaasterland, Terry, Gibson, Jane, Hauder, Michael A., Kang, Jae Hee, Kraft, Peter, Lee, Richard K., Lichter, Paul R., Liu, Yutao, 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, Wiggs, Janey L., Janssen, Sarah F., Wollstein, Gadi, Zack, Donald J., Zhang, Kang, Bramon, Elvira, Brown, Matthew A., Casas, Juan P.

Low prevalence of CDKN2A/ARF mutations among early-onset cancers of breast, pancreas and malignant melanoma in Poland

- 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

Australian schizophrenia research bank: a database of comprehensive clinical, endophenotypic and genetic data for aetiological studies of schizophrenia

- 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

Gastrointestinal polyps in McCune Albright syndrome

- Zacharin, Margaret, Bajpai, Anurag, Chow, Chung Wo, Catto-Smith, Anthony, Stratakis, Constantine, Wong, Michelle W., Scott, Rodney

Genome-wide association study identifies FCGR2A as a susceptibility locus for Kawasaki disease

- 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

MLH1 Germline Epimutations as a Factor in Hereditary Nonpolyposis Colorectal Cancer

- 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

Preliminary analysis of potential drug and gene interactions involving tricyclic antidepressant drugs

- Biswas, Mohitosh, Dias, Thilani H., Daneshi, Nilofar, Holliday, Elizabeth, Hancock, Stephen, Attia, John, Scott, Rodney, Newby, David, Kerr, Karen P., Milward, Elizabeth A.

The VEGF_936_C > T 3 ' UTR polymorphism reduces BRCA1-associated breast cancer risk in Polish women

- Jakubowska, Anna, Gronwald, Jacek, Menklszak, Janusz, Gorski, Bohdan, Huzarski, Tomasz, Byrski, Tomasz, Edler, Lutz, Lubinski, Jan, Scott, Rodney, Hamann, Ute

The effect of a muscarinic receptor 1 gene variant on grey matter volume in schizophrenia

- Cropley, Vanessa L., Scarr, Elizabeth, Fornito, Alex, Klauser, Paul, Bousman, Chad A., Scott, Rodney, Cairns, Murray J., Tooney, Paul A., Pantelis, Christos, Dean, Brian