Prognostic markers for colorectal cancer: estimating ploidy and stroma von Danielsen, H.E., Hveem, T.S., Domingo, E., Pradhan, M., Kleppe, A., Syvertsen, R.A., Kostolomov, I., Nesheim, J.A., Askautrud, H.A., Nesbakken, A., Lothe, R.A., Svindland, A., Shepherd, N., Novelli, M., Johnstone, E., Tomlinson, I., Kerr, R., Kerr, D.J.

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Prognostic impact of genomic instability in colorectal cancer von Hveem, T S, Merok, M A, Pretorius, M E, Novelli, M, Bævre, M S, Sjo, O H, Clinch, N, Liestøl, K, Svindland, A, Lothe, R A, Nesbakken, A, Danielsen, H E

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DNA ploidy in curettage specimens identifies high-risk patients and lymph node metastasis in endometrial cancer von Njølstad, T S, Trovik, J, Hveem, T S, Kjæreng, M L, Kildal, W, Pradhan, M, Marcickiewicz, J, Tingulstad, S, Staff, A C, Haugland, H K, Eraker, R, Oddenes, K, Rokne, J A, Tjugum, J, Lode, M S, Amant, F, Werner, H M, Salvesen, H B, Danielsen, H E

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Comparison of nuclear texture analysis and image cytometric DNA analysis for the assessment of dysplasia in Barrett's oesophagus von Dunn, J M, Hveem, T, Pretorius, M, Oukrif, D, Nielsen, B, Albregtsen, F, Lovat, L B, Novelli, M R, Danielsen, H E

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Tumour heterogeneity poses a significant challenge to cancer biomarker research von Cyll, Karolina, Ersvær, Elin, Vlatkovic, Ljiljana, Pradhan, Manohar, Kildal, Wanja, Avranden Kjær, Marte, Kleppe, Andreas, Hveem, Tarjei S, Carlsen, Birgitte, Gill, Silje, Löffeler, Sven, Haug, Erik Skaaheim, Wæhre, Håkon, Sooriakumaran, Prasanna, Danielsen, Håvard E

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Biological and clinical insights from genetics of insomnia symptoms von Lane, Jacqueline M., Jones, Samuel E., Dashti, Hassan S., Wood, Andrew R., Aragam, Krishna G., van Hees, Vincent T., Strand, Linn B., Winsvold, Bendik S., Wang, Heming, Bowden, Jack, Song, Yanwei, Patel, Krunal, Anderson, Simon G., Beaumont, Robin N., Bechtold, David A., Cade, Brian E., Haas, Mary, Kathiresan, Sekar, Little, Max A., Luik, Annemarie I., Loudon, Andrew S., Purcell, Shaun, Richmond, Rebecca C., Scheer, Frank A. J. L., Schormair, Barbara, Tyrrell, Jessica, Winkelman, John W., Winkelmann, Juliane, Hveem, Kristian, Zhao, Chen, Nielsen, Jonas B., Willer, Cristen J., Redline, Susan, Spiegelhalder, Kai, Kyle, Simon D., Ray, David W., Zwart, John-Anker, Brumpton, Ben, Frayling, Timothy M., Lawlor, Deborah A., Rutter, Martin K., Weedon, Michael N., Saxena, Richa

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Avoiding dynastic, assortative mating, and population stratification biases in Mendelian randomization through within-family analyses von Brumpton, Ben, Sanderson, Eleanor, Heilbron, Karl, Hartwig, Fernando Pires, Harrison, Sean, Vie, Gunnhild Åberge, Cho, Yoonsu, Howe, Laura D., Hughes, Amanda, Boomsma, Dorret I., Havdahl, Alexandra, Hopper, John, Neale, Michael, Nivard, Michel G., Pedersen, Nancy L., Reynolds, Chandra A., Tucker-Drob, Elliot M., Grotzinger, Andrew, Howe, Laurence, Morris, Tim, Li, Shuai, Auton, Adam, Windmeijer, Frank, Chen, Wei-Min, Bjørngaard, Johan Håkon, Hveem, Kristian, Willer, Cristen, Evans, David M., Kaprio, Jaakko, Davey Smith, George, Åsvold, Bjørn Olav, Hemani, Gibran, Davies, Neil M.

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Application of non-HDL cholesterol for population-based cardiovascular risk stratification: results from the Multinational Cardiovascular Risk Consortium von Brunner, Fabian J, Waldeyer, Christoph, Ojeda, Francisco, Salomaa, Veikko, Kee, Frank, Sans, Susana, Thorand, Barbara, Giampaoli, Simona, Brambilla, Paolo, Tunstall-Pedoe, Hugh, Moitry, Marie, Iacoviello, Licia, Veronesi, Giovanni, Grassi, Guido, Mathiesen, Ellisiv B, Söderberg, Stefan, Linneberg, Allan, Brenner, Hermann, Amouyel, Philippe, Ferrières, Jean, Tamosiunas, Abdonas, Nikitin, Yuriy P, Drygas, Wojciech, Melander, Olle, Jöckel, Karl-Heinz, Leistner, David M, Shaw, Jonathan E, Panagiotakos, Demosthenes B, Simons, Leon A, Kavousi, Maryam, Vasan, Ramachandran S, Dullaart, Robin P F, Wannamethee, S Goya, Risérus, Ulf, Shea, Steven, de Lemos, James A, Omland, Torbjørn, Kuulasmaa, Kari, Landmesser, Ulf, Blankenberg, Stefan, Zeller, Tanja, Kontto, Jukka, Männistö, Satu, Metspalu, Andres, Lackner, Karl, Wild, Philipp, Peters, Annette, Meisinger, Christa, Donfrancesco, Chiara, Signorini, Stefano G., Alver, Maris, Woodward, Mark, Gianfagna, Francesco, Costanzo, Simona, Wilsgaard, Tom, Eliasson, Mats, Jørgensen, Torben, Völzke, Henry, Dörr, Marcus, Nauck, Matthias, Schöttker, Ben, Lorenz, Thiess, Makarova, Nataliya, Twerenbold, Raphael, Dallongeville, Jean, Dobson, Annette, Malyutina, Sofia, Pajak, Andrzej, Engström, Gunnar, Bobak, Martin, Schmidt, Börge, Jääskeläinen, Tuija, Niiranen, Teemu, Jousilahti, Pekka, Giles, Graham, Hodge, Allison, Klotsche, Jens, Magliano, Dianna J., Lyngbakken, Magnus N., Hveem, Kristian, Pitsavos, Christos, Benjamin, Emelia J., Bakker, Stephan J.L., Whincup, Peter, Ikram, M. Kamran, Ingelsson, Martin, Koenig, Wolfgang

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O-016A prognostic marker for colorectal cancer: combining analyses of ploidy and stroma von Fotheringham, S, Danielsen, H, Hveem, T, Domingo, E, Pradhan, M, Syvertsen, R, Kostolomov, I, Nesheim, J, Johnstone, E, Novelli, M, Tomlinson, I, Kerr, R, Kerr, D

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O-016 A prognostic marker for colorectal cancer: combining analyses of ploidy and stroma von Fotheringham, S., Danielsen, H., Hveem, T., Domingo, E., Pradhan, M., Syvertsen, R., Kostolomov, I., Nesheim, J., Johnstone, E., Novelli, M., Tomlinson, I., Kerr, R., Kerr, D.

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SCORE2 risk prediction algorithms: new models to estimate 10-year risk of cardiovascular disease in Europe von Hageman, Steven, Pennells, Lisa, Ojeda, Francisco, Kaptoge, Stephen, Kuulasmaa, Kari, de Vries, Tamar, Xu, Zhe, Kee, Frank, Chung, Ryan, Wood, Angela, McEvoy, John William, Veronesi, Giovanni, Bolton, Thomas, Achenbach, Stephan, Aleksandrova, Krasimira, Amiano, Pilar, Sebastian, Donostia-San, Amouyel, Philippe, Andersson, Jonas, Bakker, Stephan J L, Da Providencia Costa, Rui Bebiano, Beulens, Joline W J, Blaha, Michael, Bobak, Martin, Boer, Jolanda M A, Bonet, Catalina, Bonnet, Fabrice, Boutron-Ruault, Marie-Christine, Braaten, Tonje, Brenner, Hermann, Brunner, Fabian, Brunner, Eric J, Brunström, Mattias, Buring, Julie, Butterworth, Adam S, Capkova, Nadezda, Cesana, Giancarlo, Chrysohoou, Christina, Colorado-Yohar, Sandra, Cook, Nancy R, Cooper, Cyrus, Dahm, Christina C, Davidson, Karina, Dennison, Elaine, Di Castelnuovo, Augusto, Donfrancesco, Chiara, Dörr, Marcus, Doryńska, Agnieszka, Eliasson, Mats, Engström, Gunnar, Ferrari, Pietro, Ferrario, Marco, Ford, Ian, Fu, Michael, Gansevoort, Ron T, Giampaoli, Simona, Gillum, Richard F, Gómez de la Cámara, Agustin, Grassi, Guido, Hansson, Per-Olof, Huculeci, Radu, Hveem, Kristian, Iacoviello, Licia, Ikram, M Kamran, Jørgensen, Torben, Joseph, Bijoy, Jousilahti, Pekka, Wouter Jukema, J, Kaaks, Rudolf, Katzke, Verena, Kavousi, Maryam, Kiechl, Stefan, Klotsche, Jens, König, Wolfgang, Kronmal, Richard A, Kubinova, Ruzena, Kucharska-Newton, Anna, Läll, Kristi, Lehmann, Nils, Leistner, David, Linneberg, Allan, Pablos, David Lora, Lorenz, Thiess, Lu, Wentian, Luksiene, Dalia, Lyngbakken, Magnus, Magnussen, Christina, Malyutina, Sofia, Ibañez, Alejandro Marín, Masala, Giovanna, Mathiesen, Ellisiv B, Matsushita, Kuni, Meade, Tom W, Melander, Olle, Meyer, Haakon E, Moons, Karel G M, Moreno-Iribas, Conchi, Muller, David, Münzel, Thomas, Nikitin, Yury

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Changes in Chromatin Structure in Curettage Specimens Identifies High-Risk Patients in Endometrial Cancer von Hveem, Tarjei S, Njølstad, Tormund S, Nielsen, Birgitte, Syvertsen, Rolf Anders, Nesheim, John Arne, Kjæreng, Marna L, Kildal, Wanja, Pradhan, Manohar, Marcickiewicz, Janusz, Tingulstad, Solveig, Staff, Anne C, Haugland, Hans K, Eraker, Runar, Oddenes, Klaus, Rokne, Jan A, Tjugum, Jostein, Lode, Margaret S, Amant, Frederic, Werner, Henrica M J, Bjørge, Line, Albregtsen, Fritz, Liestøl, Knut, Salvesen, Helga B, Trovik, Jone, Danielsen, Håvard E

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Stroke genetics informs drug discovery and risk prediction across ancestries von Jürgenson, Tuuli, Namba, Shinichi, Posner, Daniel C., Kamanu, Frederick K., Koido, Masaru, He, Yunye, Caro, Ilana, Krebs, Kristi, Liaw, Yi-Ching, Parodi, Livia, Bae, Hee-Joon, Chong, Michael R., Tomppo, Liisa, Akinyemi, Rufus, Roshchupkin, Gennady V., Habib, Naomi, Jee, Yon Ho, Thomassen, Jesper Qvist, Abedi, Vida, Cárcel-Márquez, Jara, Nygaard, Marianne, Yonova-Doing, Ekaterina, Knol, Maria J., Lewis, Adam J., Judy, Renae L., Amouyel, Philippe, Bakker, Mark K., Bennett, David A., Bis, Joshua C., Bordes, Constance, Børte, Sigrid, Cain, Anael, Ridker, Paul M., Cho, Kelly, Chen, Zhengming, Cruchaga, Carlos, Cole, John W., de Cid, Rafael, Ferreira, Leslie E., He, Jing, Jeon, Christina E., Jern, Christina, Kamouchi, Masahiro, Keene, Keith L., Konuma, Takahiro, Kumar, Amit, Launer, Lenore J., Lee, Keon-Joo, Li, Jiang, Li, Liming, Manichaikul, Ani, Markus, Hugh S., Meitinger, Thomas, Mitchell, Braxton D., Morisaki, Takayuki, O’Donnell, Martin J., Onland-Moret, N. Charlotte, Ovbiagele, Bruce, Peters, Annette, Rosand, Jonathan, Sabatine, Marc S., Sacco, Ralph L., Saleheen, Danish, Schmidt, Carsten O., Smith, Nicholas L., Sloane, Kelly L., Sutoh, Yoichi, Tiwari, Hemant K., Wennberg, Patrik, Wilson, Peter W. F., Yang, Qiong, Yoon, Kyungheon, Gieger, Christian, Ninomiya, Toshiharu, Grabe, Hans J., Jukema, J. Wouter, Kim, Young Jin, Chen, Pei-Hsin, Mayerhofer, Ernst, Ikram, Mohammad A., Worrall, Bradford B., Lathrop, G. Mark, Riaz, Moeen, Simonsick, Eleanor M., Kõrv, Janika, Zand, Ramin, Prasad, Kameshwar, Frikke-Schmidt, Ruth, Liman, Thomas, Ruigrok, Ynte M., Bastarache, Lisa, Damrauer, Scott M., Rotter, Jerome I., Niiranen, Teemu J., Walters, Robin G., Owolabi, Mayowa O., Huffman, Jennifer E., Kamatani, Yoichiro, Dichgans, Martin, Debette, Stephanie

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Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects von Howe, Laurence J., Nivard, Michel G., Morris, Tim T., Hansen, Ailin F., Rasheed, Humaira, Cho, Yoonsu, Chittoor, Geetha, Ahlskog, Rafael, Lind, Penelope A., Palviainen, Teemu, van der Zee, Matthijs D., Cheesman, Rosa, Mangino, Massimo, Wang, Yunzhang, Li, Shuai, Klaric, Lucija, Ratliff, Scott M., Bielak, Lawrence F., Nygaard, Marianne, Giannelis, Alexandros, Willoughby, Emily A., Reynolds, Chandra A., Balbona, Jared V., Andreassen, Ole A., Ask, Helga, Baras, Aris, Bauer, Christopher R., Boomsma, Dorret I., Campbell, Archie, Campbell, Harry, Chen, Zhengming, Christofidou, Paraskevi, Corfield, Elizabeth, Dahm, Christina C., Dokuru, Deepika R., Evans, Luke M., de Geus, Eco J. C., Giddaluru, Sudheer, Gordon, Scott D., Harden, K. Paige, Hill, W. David, Hughes, Amanda, Kerr, Shona M., Kim, Yongkang, Kweon, Hyeokmoon, Latvala, Antti, Lawlor, Deborah A., Li, Liming, Lin, Kuang, Magnus, Per, Magnusson, Patrik K. E., Mallard, Travis T., Martikainen, Pekka, Mills, Melinda C., Njølstad, Pål Rasmus, Overton, John D., Pedersen, Nancy L., Porteous, David J., Reid, Jeffrey, Silventoinen, Karri, Southey, Melissa C., Stoltenberg, Camilla, Tucker-Drob, Elliot M., Wright, Margaret J., Hewitt, John K., Keller, Matthew C., Stallings, Michael C., Lee, James J., Christensen, Kaare, Kardia, Sharon L. R., Peyser, Patricia A., Smith, Jennifer A., Wilson, James F., Hopper, John L., Hägg, Sara, Spector, Tim D., Pingault, Jean-Baptiste, Plomin, Robert, Havdahl, Alexandra, Bartels, Meike, Martin, Nicholas G., Oskarsson, Sven, Justice, Anne E., Millwood, Iona Y., Hveem, Kristian, Naess, Øyvind, Willer, Cristen J., Åsvold, Bjørn Olav, Koellinger, Philipp D., Kaprio, Jaakko, Medland, Sarah E., Walters, Robin G., Benjamin, Daniel J., Turley, Patrick, Evans, David M., Davey Smith, George, Hayward, Caroline, Brumpton, Ben, Hemani, Gibran, Davies, Neil M.

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Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function von Pattaro, Cristian, Teumer, Alexander, Tin, Adrienne, Sorice, Rossella, Foster, Meredith, Johnson, Andrew D., Nalls, Michael, Dehghan, Abbas, Dieffenbach, Aida Karina, Nolte, Ilja M., van der Most, Peter J., Shuldiner, Alan R., Morrison, Alanna C., Hofman, Albert, Lupo, Antonio, Robino, Antonietta, Johansson, Åsa, Freedman, Barry I., Mitchell, Braxton D., Hayward, Caroline, Shaffer, Christian M., Toniolo, Daniela, Lu, Yingchang, Siscovick, David S., Ruderfer, Douglas, Atkinson, Elizabeth J., Boerwinkle, Eric, Rivadeneira, Fernando, Hu, Frank B., Navis, Gerjan J., Curhan, Gary C., Ehret, George B., Coassin, Stefan, Thun, Gian-Andri, Eiriksdottir, Gudny, Wichmann, H-Erich, Brenner, Hermann, Ford, Ian, Guessous, Idris, Rudan, Igor, Heid, Iris M., Kolcic, Ivana, Persico, Ivana, Jukema, J. Wouter, Wilson, James F., Divers, Jasmin, Stafford, Jeanette M., Smith, Jennifer A., Wang, Jie Jin, Viikari, Jorma, Coresh, Josef, Butterbach, Katja, Lohman, Kurt, Portas, Laura, Lyytikäinen, Leo-Pekka, Yengo, Loic, Ferrucci, Luigi, Cavalieri, Margherita, Haun, Margot, Pirastu, Mario, McEvoy, Mark A., Woodward, Mark, Adam, Martin, Nauck, Matthias, Stumvoll, Michael, Sale, Michele M., Boban, Mladen, Bochud, Murielle, Verweij, Niek, Probst-Hensch, Nicole, Soranzo, Nicole, Gottesman, Omri, Polasek, Ozren, Ridker, Paul M., Mitchell, Paul, Muntner, Paul, Meisinger, Christa, Smit, Johannes H., Wild, Philipp S., Biffar, Reiner, Carroll, Robert J., Penninx, Brenda W., Scott, Rodney J., Katz, Ronit, Hwang, Shih-Jen, Kloiber, Stefan, Rosas, Sylvia E., Harris, Tamara B., Aspelund, Thor, Nikopensius, Tiit, Chen, Wei-Min, Igl, Wilmar, Lieb, Wolfgang, Loos, Ruth J. F., Liu, Yongmei, Parsa, Afshin, Hamet, Pavel, Tremblay, Johanne, Goessling, Wolfram, Fox, Caroline S.

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Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci von Reschen, Michael E, Mahajan, Anubha, William Rayner, N, Scott, Laura J, Yengo, Loic, Wahl, Simone, Kestler, Hans, Chheda, Himanshu, Eisele, Lewin, Steinthorsdottir, Valgerdur, Chen, Han, Fuchsberger, Christian, Kwan, Phoenix, Thomsen, Soren K, Rundle, Jana K, van de Bunt, Martijn, Voight, Benjamin F, Abecasis, Gonçalo R, Baldassarre, Damiano, Carey, Jason, Chines, Peter S, Crenshaw, Andrew T, Edkins, Sarah, Eury, Elodie, Fontanillas, Pierre, Franks, Paul W, Gertow, Karl, Groves, Christopher J, Hassinen, Maija, Herder, Christian, Hreidarsson, Astradur B, Jackson, Anne U, Jonsson, Anna, Jørgensen, Marit E, Jørgensen, Torben, Kao, Wen-Hong L, Kerrison, Nicola D, Kinnunen, Leena, Kravic, Jasmina, Langford, Cordelia, Lichtner, Peter, Lindholm, Eero, Lobbens, Stéphane, Luan, Jian'an, Meyer, Julia, Mihailov, Evelin, Mühleisen, Thomas W, Navarro, Carmen, Oskolkov, Nikolay N, Pechlivanis, Sonali, Platou, Carl G P, Rybin, Denis, van der Schouw, Yvonne T, Sennblad, Bengt, Steinbach, Gerald, Storm, Petter, Sun, Qi, Thorand, Barbara, Tikkanen, Emmi, Trakalo, Joseph, Tremoli, Elena, Wood, Andrew R, Zeggini, Eleftheria, Birney, Ewan, Pasquali, Lorenzo, Pankow, James S, van Duijn, Cornelia, Sijbrands, Eric, Hu, Frank B, Thorsteinsdottir, Unnur, Stefansson, Kari, Lakka, Timo A, Rauramaa, Rainer, Stumvoll, Michael, Korpi-Hyövälti, Eeva, Kuusisto, Johanna, Metspalu, Andres, Jöcke, Karl-Heinz, Moebus, Susanne, Bergman, Richard N, Collins, Francis S, Mohlke, Karen L, Koistinen, Heikki, Tuomilehto, Jaakko, Deloukas, Panagiotis, Donnelly, Peter J, Frayling, Timothy M, Sladek, Rob, Froguel, Philippe, Hansen, Torben, Kathiresan, Sekar, Barroso, Inês, Langenberg, Claudia, Wareham, Nicholas J, O'Callaghan, Christopher A, Gloyn, Anna L, Altshuler, David, Boehnke, Michael, Teslovich, Tanya M, Morris, Andrew P

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Dissecting the shared genetic basis of migraine and mental disorders using novel statistical tools von Bahrami, Shahram, Hindley, Guy, Winsvold, Bendik Slagsvold, O'Connell, Kevin S, Frei, Oleksandr, Shadrin, Alexey, Cheng, Weiqiu, Bettella, Francesco, Rødevand, Linn, Odegaard, Ketil J, Fan, Chun C, Pirinen, Matti J, Hautakangas, Heidi M, Dale, Anders M, Djurovic, Srdjan, Smeland, Olav B, Andreassen, Ole A

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Genome-wide analysis identifies impaired axonogenesis in chronic overlapping pain conditions von Khoury, Samar, Parisien, Marc, Thompson, Scott J, Vachon-Presseau, Etienne, Roy, Mathieu, Martinsen, Amy E, Winsvold, Bendik S, Mundal, Ingunn P, Zwart, John-Anker, Kania, Artur, Mogil, Jeffrey S, Diatchenko, Luda

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The blood proteome of imminent lung cancer diagnosis von Albanes, Demetrius, Alcala, Karine, Alcala, Nicolas, Amos, Christopher I., Arslan, Alan A., Bassett, Julie K., Brennan, Paul, Cai, Qiuyin, Chen, Chu, Feng, Xiaoshuang, Freedman, Neal D., Guida, Florence, Hung, Rayjean J., Hveem, Kristian, Johansson, Mikael, Johansson, Mattias, Koh, Woon-Puay, Langhammer, Arnulf, Milne, Roger L., Muller, David, Onwuka, Justina, Sørgjerd, Elin Pettersen, Robbins, Hilary A., Sesso, Howard D., Severi, Gianluca, Shu, Xiao-Ou, Sieri, Sabina, Smith-Byrne, Karl, Stevens, Victoria, Tinker, Lesley, Tjønneland, Anne, Visvanathan, Kala, Wang, Ying, Wang, Renwei, Weinstein, Stephanie, Yuan, Jian-Min, Zahed, Hana, Zhang, Xuehong, Zheng, Wei

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Using multivariable Mendelian randomization to estimate the causal effect of bone mineral density on osteoarthritis risk, independently of body mass index von Hartley, April, Sanderson, Eleanor, Granell, Raquel, Paternoster, Lavinia, Zheng, Jie, Smith, George Davey, Southam, Lorraine, Hatzikotoulas, Konstantinos, Boer, Cindy G, van Meurs, Joyce, Zeggini, Eleftheria, Gregson, Celia L, Tobias, Jon H

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