The "unnatural" history of colorectal cancer in Lynch syndrome: lessons from colonoscopy surveillance

- 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.

Common variants in breast cancer risk loci predispose to distinct tumor subtypes

- 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, Forbes, John, Scott, Rodney

Analysis of shared heritability in common disorders of the brain

- 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

Common and low frequency variants in MERTK are independently associated with multiple sclerosis susceptibility with discordant association dependent upon HLA-DRB1*15:01 status

- 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.

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.

Potential simple and multifactorial drug-gene interactions of tricyclic antidepressants in older Australians

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

Classification of schizophrenia using differential gene expression in peripheral blood lymphocytes

- Bowden, Nikola A., Weidenhofer, Judith C., Scott, Rodney, Schall, Ulrich A., Todd, Juanita, Michie, Patricia T., Tooney, Paul A.

Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer

- 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

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

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

Rare germline copy number variants (CNVs) and breast cancer risk

- 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

Two truncating variants in FANCC and breast cancer risk

- 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

The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer

- 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

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

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,

Paracingulate sulcus morphology is associated with hallucinations in the human brain

- 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

Genetically determined risk of depression and functional outcome after Ischemic Stroke: mendelian randomization study

- 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.

Finding needles in haystacks: the use of quantitative proteomics for the early detection of colorectal cancer

- Gould, Tiffany, Jamaluddin, Muhammad Fairuz B., Petit, Joel, King, Simon J., Nixon, Brett, Scott, Rodney, Pockney, Peter, Dun, Matthew D.

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

Analyzing the role of microRNAs in schizophrenia in the context of common genetic risk variants

- 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