Objects
Temprano-Sagrera, Gerard, Sitlani, Colleen M., Dehghan, Abbas, Heath, Adam S., Reiner, Alex P., Johnson, Andrew, Richmond, Anne, Peters, Annette, van Hylckama Vlieg, Astrid, McKnight, Barbara, Psaty, Bruce M., Hayward, Caroline, Bone, William P., Holliday, Elizabeth G., Attia, John, Levi, Christopher R., Chasman, D, Strachan, DP, Tregouet, DA, Mook-Kanamori, D, Gill, D, Thibord, F, Asselbergs, FW, Martin-Bornez, Miguel, Leebeek, FWG, Rosendaal, FR, Davies, G, Homuth, G, Temprano, G, Campbell, H, Taylor, HA, Bressler, J, Huffman, JE, Rotter, JI, Voight, Benjamin F., Yao, J, Wilson, JF, Bis, JC, Hahn, JM, Desch, KC, Wiggins, KL, Raffield, LM, Bielak, LF, Yanek, LR, Kleber, ME, Morrison, Alanna C., Sabater-Lleal, M, Mueller, M, Kavousi, M, Mangino, M, Liu, M, Brown, MR, Conomos, MP, Jhun, MA, Chen, MH, de Maat, MPM, Damrauer, Scott M., Pankratz, N, Peyser, PA, Elliot, P, Wei, P, Wild, PS, Morange, PE, van der Harst, P, Yang, Q, Le, NQ, Marioni, R, de Vries, Paul S., Li, R, Damrauer, SM, Cox, SR, Trompet, S, Felix, SB, Völker, U, Tang, W, Koenig, W, Jukema, JW, Guo, X, Smith, Nicholas L., Lindstrom, S, Wang, L, Smith, EN, Gordon, W, van Hylckama Vlieg, A, de Andrade, M, Brody, JA, Pattee, JW, Haessler, J, Brumpton, BM, Sabater-Lleal, Maria, Chasman, DI, Suchon, P, Chen, MH, Turman, C, Germain, M, Wiggins, KL, MacDonald, J, Braekkan, SK, Armasu, SM. Wiley-Blackwell; 2022. Multi-phenotype analyses of hemostatic traits with cardiovascular events reveal novel genetic associations.
Ballinger, Mandy L., Pattnaik, Swetansu, van der Graaf, Winette T. A., Fennelly, V, Wicht, A, Zielony, B, Galligan, E, Glavich, G, Stoeckert, J, Williams, L, Djandjgava, L, Buettner, I, Osinki, C, Puri, Ajay, Stephens, S, Rogasik, M, Bouclier, L, Girodet, M, Charreton, A, Fayet, Y, Crasto, S, Sandupatla, B, Yoon, Y, Je, N, Duffaud, Florence, Thompson, L, Fowler, T, Johnson, B, Petrikova, G, Hambridge, T, Hutchins, A, Bottero, D, Scanlon, D, Stokes-Denson, J, Génin, E, Le Cesne, Axel, Campion, D, Dartigues, J-F, Deleuze, J-F, Lambert, J-C, Redon, R, Ludwig, T, Grenier-Boley, B, Letort, S, Lindenbaum, P, Meyer, V, Seddon, Beatrice, Quenez, O, Dina, C, Bellenguez, C, Le Clézio, CC, Giemza, J, Chatel, S, Férec, C, Le Marec, H, Letenneur, L, Nicolas, G, Chandrasekar, Coonoor, Rouault, K, Schiffman, Joshua D., Brohl, Andrew S., James, Paul A., Kurtz, Jean-Emmanuel, Mundra, Piyushkumar A., Penel, Nicolas, Myklebost, Ola, Meza-Zepeda, LA, Pickett, H, Kansara, M, Waddell, N, Kondrashova, O, Pearson, JV, Barbour, AP, Li, S, Zaheed, Milita, Nguyen, TL, Fatkin, D, Graham, RM, Giannoulatou, E, Green, MJ, Kaplan, W, Ravishankar, S, Copty, J, Powell, JE, Cuppen, E, Rath, Emma, van Eijk, K, Veldink, J, Ahn, J-H, Kim, JE, Randall, RL, Tucker, K, Judson, I, Sarin, R, Ludwig, T, Genin, E, Priestley, Peter, Deleuze, J-F, French Exome Project Consortium,, Haber, M, Marshall, G, Cairns, Murray J., Blay, J-Y, International Sarcoma Kindred Study,, Thomas, DM, Tattersall, M, Neuhaus, S, Baber, Jonathan, Lewis, C, Tucker, K, Carey-Smith, R, Wood, D, Porceddu, S, Dickinson, I, Thorne, H, James, P, Ray-Coquard, I, Blay, J-Y, Ray-Coquard, Isabelle, Cassier, P, Le Cesne, A, Duffaud, F, Penel, N, Isambert, N, Kurtz, J-E, Puri, A, Sarin, R, Ahn, J-H, Kim, JE, Isambert, Nicholas, Ward, I, Judson, I, van der Graaf, W, Seddon, B, Chandrasekar, C, Rickar, R, Hennig, I, Schiffman, J, Randall, RL, Silvestri, A, Causeret, Sylvain, Zaratzian, A, Tayao, M, Walwyn, K, Niedermayr, E, Mang, D, Clark, R, Thorpe, T, MacDonald, J, Riddell, K, Mar, J. American Association for the Advancement of Science (AAAS); 2023. Heritable defects in telomere and mitotic function selectively predispose to sarcomas.