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

Identity-by-descent mapping to detect rare variants conferring susceptibility to multiple sclerosis

- Lin, Rui, Charlesworth, Jac, Stankovich, Jim, Perreau, Victoria M., Brown, Matthew A., ANZgene Consortium,, Scott, Rodney, Taylor, Bruce V.

Genomic relationships, novel loci, and pleiotropic mechanisms across eight psychiatric disorders

- 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

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.

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

Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in PCSK9

- 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

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

Concordance between direct and imputed APOE genotypes using 1000 genomes data

- Oldmeadow, Christopher, Holliday, Elizabeth G., McEvoy, Mark, Scott, Rodney, Kwok, John B. J., Mather, Karen, Sachdev, Perminder, Schofield, Peter, Attia, John

Refined histopathological predictors of BRCA1 and BRCA2 mutation status: a large-scale analysis of breast cancer characteristics from the BCAC, CIMBA, and ENIGMA consortia

- 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

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.

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

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.

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

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

- 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

Gastrointestinal polyps in McCune Albright syndrome

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

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

Genome-wide association meta-analysis of functional outcome after ischemic stroke

- Söderholm, Martin, Pedersen, Annie, Jood, Katarina, Lee, Jin-Moo, Lemmens, Robin, Levi, Christopher, Mitchell, Braxton D., Norrving, Bo, Rannikmäe, Kristiina, Rost, Natalia S., Rosand, Jonathan, Rothwell, Peter M., Lorentzen, Erik, Scott, Rodney, Strbian, Daniel, Sturm, Jonathan W., Sudlow, Cathie, Traylor, Matthew, Thijs, Vincent, Tatlisumak, Turgut, Woo, Daniel, Worrall, Bradford B., Maguire, Jane M., Stanne, Tara M., Lindgren, Arne, Jern, Christina, Bevan, Steve, Olsson, Maja, Cole, John W., Fernandez-Cadenas, Israel, Hankey, Graeme J., Jimenez-Conde, Jordi

A polygenic resilience score moderates the genetic risk for schizophrenia

- Hess, Jonathan L., Tylee, Daniel S., Mattheisen, Manuel, Schizophrenia Working Group of the Psychiatric Genomics Consortium, Lundbeck Foundation Initiative for Integrative Psychiatric Research (iPSYCH), Børglum, Anders D., Als, Thomas D., Grove, Jakob, Werge, Thomas, Mortensen, Preben Bo, Mors, Ole, Nordentoft, Merete, Hougaard, David M., Byberg-Grauholm, Jonas, Bækvad-Hansen, Maree, Greenwood, Tiffany A., Tsuang, Ming T., Curtis, David, Steinberg, Stacy, Sigurdsson, Engilbert, Stefánsson, Hreinn, Stefánsson, Kári, Edenberg, Howard J., Holmans, Peter, Faraone, Stephen V., Glatt, Steven J., Cairns, Murray J., Carr, Vaughan J., Henskens, Frans A., Kelly, Brian J., Loughland, Carmel M., Michie, Patricia T., Schall, Ulrich A,, Scott, Rodney, Tooney, Paul

KRAS mutation testing in colorectal cancer: the model for molecular pathology testing in the future

- Wong, Stephen Q., Scott, Rodney, Fox, Stephen B.

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