Gene profiling in the amygdala in schizophrenia

- Weidenhofer, J., Bowden, N. A., Scott, R. J., Tooney, P. A.

Association of forced vital capacity with the developmental gene NCOR2

- 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.

The discovery of novel biomarkers improves breast cancer intrinsic subtype prediction and reconciles the labels in the METABRIC data set

- Milioli, Heloisa Helena, Vimieiro, Renato, Riveros, Carlos, Tishchenko, Inna, Berretta, Regina, Moscato, Pablo

Comparing genotyping algorithms for Illumina's Infinium whole-genome SNP BeadChips

- Ritchie, Matthew E., Ruijie, Liu, Kilpatrick, Trevor J., Lechner-Scott, Jeannette, Moscato, Pablo, Perreau, Victoria M., Rubio, Justin P., Scott, Rodney J., Stankovich, Jim, Stewart, Graeme J., Taylor, Bruce V., Wiley, James, Carvalho, Benilton S., Booth, David R., Clarke, Glynnis, Cox, Mathew B., Csurhes, Peter A., Danoy, Patrick, Dickinson, Joanne L., Drysdale, Karen, Field, Judith, Greer, Judith M., Griffiths, Lyn R., Irizarry, Rafael A., Guru, Preethi, Hadler, Johanna, Hoban, Ella, McMorran, Brendan J., Jensen, Cathy J., Johnson, Laura J., McCallum, Ruth, Merriman, Marilyn, Merriman, Tony, Polanowski, Andrea, Bahlo, Melanie, Pryce, Karena, Tajouri, Lotfi, Whittock, Lucy, Wilkins, Ella J., Browning, Brian L., Browning, Sharon R., Perera, Devindri, Butzkueven, Helmut, Carroll, William M., Chapman, Caron, Kermode, Allan G., Marriott, Mark, Mason, Deborah, Heard, Robert N., Pender, Michael P., Slee, Mark, Tubridy, Niall, Willoughby, Ernest, Broadley, Simon A., Brown, Matthew A., Foote, Simon J.

Genes related with Alzheimer's disease: a comparison of evolutionary search, statistical and integer programming approaches

- Moscato, Pablo Alberto, Berretta, Regina Esther, Hourani, Mou'ath, Mendes, Alexandre, Cotta, Carlos

RNA modulators of complex phenotypes in mammalian cells

- Lai, Angela, Cairns, Murray J., Tran, Nham, Zhang, Hong-Ping, Cullen, Lara, Arndt, Greg M.

A coagulopathic dilemma: snakes or genes

- Chiew, Angela L., Isbister, Geoffrey K.

Microwaves for chromogenic in situ hybridization

- Leong, Anthony S. -Y., Haffajee, Zenobia

Pyrimidine-based inhibitors of dynamin I GTPase activity: competitive inhibition at the pleckstrin homology domain

- Odell, Luke R., Abdel-Hamid, Mohammed K., McCluskey, Adam, Hill, Timothy A., Chau, Ngoc, Young, Kelly A., Deane, Fiona M., Sakoff, Jennette A., Andersson, Sofia, Daniel, James A., Robinson, Phillip J.

Meta-analysis of genome-wide association studies identifies common susceptibility polymorphisms for colorectal and endometrial cancer near SH2B3 and TSHZ1

- Cheng, Timothy H. T., Thompson, Deborah, Hopper, John, Tomlinson, Ian, Jenkins, Mark, Lindor, Noralane M., Newcomb, Polly A., Gallinger, Steve, Conti, David, Schumacher, Fred, Casey, Graham, Giles, Graham G., Pharoah, Paul, Painter, Jodie, Peto, Julian, Cox, Angela, Swerdlow, Anthony, Couch, Fergus, Cunningham, Julie M., Goode, Ellen L., Winham, Stacey J., Lambrechts, Diether, Fasching, Peter, Burwinkel, Barbara, O'Mara, Tracy, Brenner, Hermann, Brauch, Hiltrud, Chang-Claude, Jenny, Salvesen, Helga B., Kristensen, Vessela, Darabi, Hatef, Li, Jingmei, Liu, Tao, Lindblom, Annika, Hall, Per, Gorman, Maggie, de Polanco, Magdalena Echeverry, Sans, Monica, Carracedo, Angel, Castellvi-Bel, Sergi, Rojas-Martinez, Augusto, Aguiar Jnr, Samuel, Teixeira, Manuel R., Dunning, Alison M., Dennis, Joe, Otton, Geoffrey, Martin, Lynn, Proietto, Tony, Holliday, Elizabeth, Attia, John, Ashton, Katie, Scott, Rodney J., McEvoy, Mark, Dowdy, Sean C., Fridley, Brooke L., Werner, Henrica M. J., Trovik, Jone, Palles, Claire, Njolstad, Tormund S., Tham, Emma, Mints, Miriam, Runnebaum, Ingo, Hillemanns, Peter, Dörk, Thilo, Amant, Frederic, Schrauwen, Stefanie, Hein, Alexander, Beckmann, Matthias W., Jones, Angela, Ekici, Arif, Czene, Kamila, Meindl, Alfons, Bolla, Manjeet K., Michailidou, Kyriaki, Tyrer, Jonathan P., Wang, Qin, Ahmed, Shahana, Healey, Catherine S., Shah, Mitul, Buchanan, Daniel D., Annibali, Daniela, Depreeuw, Jeroen, Al-Tassan, Nada A., Harris, Rebecca, Meyer, Brian F., Whiffin, Nicola, Hosking, Fay J., Kinnersley, Ben, Farrington, Susan M., Timofeeva, Maria, Ko Win, Aung, Tenesa, Albert, Campbell, Harry, Haile, Robert W., Hodgson, Shirley, Carvajal-Carmona, Luis, Cheadle, Jeremy P., Easton, Douglas, Dunlop, Malcolm, Houlston, Richard, Spurdle, Amanda

Phenotypic expansion and further characterisation of the 17q21.31 microdeletion syndrome

- Tan, T. Y., Aftimos, S., Slavotinek, A., Hogue, J., Moeschler, J. B., Ozmore, J., Widmer, R., Savarirayan, R., Peters, G., Worgan, L., Susman, R., Wilson, M., Ghedia, S., Kirk, E. P., Love, D., Ronan, A., Darmanian, A.

Differential effect of disease-associated ST8SIA2 haplotype on cerebral white matter diffusion properties in schizophrenia and healthy controls

- 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,

Characterisation of the legume SERK-NIK gene superfamily including splice variants: implications for development and defence

- Nolan, Kim E., Kurdyukov, Sergey, Rose, Ray J.

The role of 5-HTT LPR and GNβ3 825C>T polymorphisms and gene–environment interactions in Irritable Bowel Syndrome (IBS)

- Saito, Yuri A., Larson, Joseph J., Atkinson, Elizabeth J., Ryu, Euijung, Almazar, Ann E., Peterson, Gloria M., Talley, Nicholas J.

Common variation in COL4A1/COL4A2 is associated with sporadic cerebral small vessel disease

- Rannikmäe, Kristiina, Davies, Gail, Deka, Ranjan, Woo, Jessica G., Martin, Lisa J., Jimenez-Conde, Jordi, Selim, Magdy, Brown, Devin L., Silliman, Scott L., Kidwell, Chelsea S., Montaner, Joan, Langefeld, Carl D., Thomson, Pippa A., Holliday, Elizabeth G., Levi, Christopher R., Attia, John, Rothwell, Peter M., Poole, Deborah L., Bevan, Steve, Devan, William J., Falcone, Guido J., Traylor, Matthew, Anderson, Christopher D., Battey, Thomas W. K., Radmanesh, Farid

Electrochemical detection of short DNA sequences related to the Escherichia coli pathogen using a zirconia-modified screen-printed DNA biosensor

- Zuo, Shao-Hua, Zhang, Ling-Fan, Zhao, Yan-Hui, Yuan, Hui-Hui, Lan, Min-Bo, Lawrance, Geoffrey A., Wei, Gang

Genome-wide association and functional follow-up reveals new loci for kidney function

- Pattaro, Cristian, Kottgen, Anna, Li, Man, Uitterlinden, Andre G., Rivadeneira, Fernando, Aulchenko, Yurii S., Polasek, Ozren, Hastie, Nick, Vitart, Veronique, Helmer, Catherine, Wang, Jie Jin, Ruggiero, Daniela, Bergmann, Sven, Gao, Xiaoyi, Kahonen, Mika, Viikari, Jorma, Nikopensius, Tiit, Province, Michael, Ketkar, Shamika, Colhoun, Helen, Doney, Alex, Robino, Antonietta, Giulianini, Franco, Kramer, Bernhard K., Gorski, Mathias, Portas, Laura, Ford, Ian, Buckley, Brendan M., Adam, Martin, Thun, Gian-Andri, Paulweber, Bernhard, Haun, Margot, Sala, Cinzia, Metzger, Marie, Mitchell, Paul, Yang, Qiong, Ciullo, Marina, King, Stuart K., Vollenweider, Peter, Raitakari, Olli, Metspalu, Andres, Palmer, Colin, Gasparini, Paolo, Pirastu, Mario, Jukema, J. Wouter, Probst-Hensch, Nicole M., Hundertmark, Claudia, Kronenberg, Florian, Toniolo, Daniela, Gudnason, Vilmundur, Shuldiner, Alan R., Coresh, Josef, Schmidt, Reinhold, Ferrucci, Luigi, Siscovick, David S., van Duijn, Cornelia M., Borecki, Ingrid, Foster, Meredith C., Kardia, Sharon L. R., Liu, Yongmei, Curhan, Gary C., Rudan, Igor, Gyllensten, Ulf, Wilson, James F., Franke, Andre, Pramstaller, Peter P., Retting, Rainer, Prokopenko, Inga, O'Seaghdha, Conall M., Witteman, Jacqueline C. M., Hayward, Caroline, Ridker, Paul, Parsa, Afshin, Bochud, Murielle, Heid, Iris M., Goessling, Wolfram, Chasman, Daniel I., Kao, W. H. Linda, Fox, Caroline S., Glazer, Nicole, Isaacs, Aaron, Liu, Ching-Ti, Teumer, Alexander, Smith, Albert V., O'Connell, Jeffrey R., Struchalin, Maksim, Tanaka, Toshiko, Li, Guo, Johnson, Andrew D., Gierman, Hinco J., Feitosa, Mary, Hwang, Shih-Jen, Atkinson, Elizabeth J., Garnaas, Maija, Lohman, Kurt, Cornelis, Marilyn C., Johansson, Asa, Tonjes, Anke, Dehghan, Abbas, Chouraki, Vincent, Holliday, Elizabeth G., Sorice, Rossella, Kutalik, Zoltan, Lehtimaki, Terho, Boger, Carsten A., Esko, Tonu, Deshmukh, Harshal, Ulivi, Sheila, Chu, Audrey Y., Murgia, Federico, Trompet, Stella, Imboden, Medea, Kollerits, Barbara, Pistis, Giorgio, CARDIoGRAM Consortium, Fuchsberger, Christian, ICBP Consortium, CARe Consortium, Wellcome Trust Case Control Consortium 2 (WTCCC2), Harris, Tamara B., Launer, Lenore J., Aspelund, Thor, Eiriksdottir, Gudny, Mitchell, Braxton D., Boerwinkle, Eric, Schmidt, Helena, Olden, Matthias, Cavalieri, Margherita, Rao, Madhumathi, Hu, Frank B., Demirkan, Ayse, Oostra, Ben A., de Andrade, Mariza, Turner, Stephen T., Ding, Jingzhong, Andrews, Jeanette S., Freedma, Barry I., Chen, Ming-Huei, Koenig, Wolfgang, Illig, Thomas, Doring, Angela, Wichmann, H.-Erich, Kolcic, Ivana, Zemunik, Tatijana, Boban, Mladen, Minelli, Cosetta, Wheeler, Heather E., Igl, Wilmar, Tin, Adrienne, Zaboli, Ghazal, Wild, Sarah H., Wright, Alan F., Campbell, Harry, Ellinghaus, David, Nothlings, Ute, Jacobs, Gunnar, Biffar, Reiner, Endlich, Karlhans, Ernst, Florian, Taliun, Daniel, Homuth, Georg, Kroemer, Heyo K., Nauck, Matthias, Stracke, Sylvia, Volker, Uwe, Volzke, Henry, Kovacs, Peter, Stumvoll, Michael, Magi, Reedik, Hofman, Albert

Smchd1 is a maternal effect gene required for genomic imprinting

- Wanigasuriya, Iromi, Gouil, Quentin, Keniry, Andrew, Ritchie, Matthew E., Blewitt, Marnie E., Kinkel, Sarah A., del Fierro, Andres Tapia, Beck, Tamara, Roper, Ellise A., Breslin, Kelsey, Stringer, Jessica, Hutt, Karla, Lee, Heather J.

A "candidate-interactome" aggregate analysis of genome-wide association data in multiple sclerosis

- Mechelli, Rosella, Umeton, Renato, Wellcome Trust Case Control Consortium 2,, Romano, Silvia, Salvetti, Marco, Ristori, Giovanni, Cox, Mathew B., Lechner-Scott, Jeannette S., Scott, Rodney J., Policano, Claudia, Annibali, Viviana, Coarelli, Giulia, Ricigliano, Vito A. G., Vittori, Danila, Fornasiero, Arianna, Buscarinu, Maria Chiara, International Multiple Sclerosis Genetics Consortium,

Regulation of expression of key genes in uterine myocytes

- Ilicic, Marina