Integration Analysis of Three Omics Data Using Penalized Regression Methods: An Application to Bladder Cancer by Pineda, Silvia, Real, Francisco X, Kogevinas, Manolis, Carrato, Alfredo, Chanock, Stephen J, Malats, Núria, Van Steen, Kristel

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Genetic variation in the TP53 pathway and bladder cancer risk. a comprehensive analysis by Pineda, Silvia, Milne, Roger L, Calle, M Luz, Rothman, Nathaniel, López de Maturana, Evangelina, Herranz, Jesús, Kogevinas, Manolis, Chanock, Stephen J, Tardón, Adonina, Márquez, Mirari, Guey, Lin T, García-Closas, Montserrat, Lloreta, Josep, Baum, Erin, González-Neira, Anna, Carrato, Alfredo, Navarro, Arcadi, Silverman, Debra T, Real, Francisco X, Malats, Núria

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FGF receptor genes and breast cancer susceptibility: results from the Breast Cancer Association Consortium by Agarwal, D, Herranz, J, Pita, G, Moreno, L T, Alonso, M R, Bolla, M K, Hardisson, D, González-Neira, A, Lindblom, A, Swerdlow, A, Matsuo, K, Ito, H, Iwata, H, Hartman, M, Iau, P T -C, Sawyer, E, Kerin, M, Miller, N, Yip, C H, Sivanandan, K, Tay, W -T, Brüning, T, Hamann, U, Shah, M, Andrulis, I L, Tchatchou, S, Schmidt, M K, Broeks, A, Rosenberg, E H, Fasching, P A, Blot, W, Cai, Q, Wu, A H, Cox, A, Muir, K, Lophatananon, A, Deming-Halverson, S, Long, J, Shu, X -O, Lu, W, Peterlongo, P, Manoukian, S, Mariette, F, Sangrajrang, S, McKay, J, Couch, F J, Yannoukakos, D, Johnson, N, dos Santos Silva, I, Marme, F, Truong, T, Sanchez, M, Mulot, C, Flyer, H, Dieffenbach, A K, Stegmaier, C, Mannermaa, A, Kosma, V -M, Hartikainen, J M, Lambrechts, D, Yesilyurt, B T, Floris, G, Chang-Claude, J, Seibold, P, Flesch-Janys, D, Vachon, C, Schumacher, F, Marchand, L Le, Simard, J, Goldberg, M S, Labréche, F, Winqvist, R, Jukkola-Vuorinen, A, Grip, M, Devilee, P, Tollenaar, R A E M, Seynaeve, C, Chanock, S J, Figueroa, J D, Czene, K, Eriksson, M, Humphreys, K, Darabi, H, Hooning, M J, Collée, J M, Tilanus-Linthorst, M, Li, J, Jakubowska, A, Jaworska-Bieniek, K, Durda, K, Muranen, T A, Aittomäki, K, Blomqvist, C, Bogdanova, N, Chenevix-Trench, G, Easton, D F, Pharroah, P D P, Zamora, P, Benítez, J, Milne, R L

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Framework for the integration of genomics, epigenomics, and transcriptomics in complex diseases by Pineda San Juan, Silvia, Gómez-Rubio, Paulina, Antoni, Picornell, Bessonov, Kyrylo, Márquez, Mirari, Kogevinas, Manolis, Real, FX, Van Steen, Kristel, Malats, Nuria

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Author Correction: Common variants in Alzheimer's disease and risk stratification by polygenic risk scores by Tesi, Niccolo, Jansen, Iris E, Stringa, Najada, Montrreal, Laura, Antonell, Anna, Franco-Macías, Emilio, Menéndez-González, Manuel, Royo, Jose Luís, Lage, Carmen, Naj, Adam C, Lemstra, Afina W, Benaque, Alba, Benussi, Alberto, Rábano, Alberto, de Mendonça, Alexandre, Arias Pastor, Alfonso, Kok, Almar A L, Espinosa, Ana, Corma-Gómez, Anaïs, Sanabria, Ángela, Haapasalo, Annakaisa, Kinhult Ståhlbom, Anne, Hartmann, Annette M, Spottke, Annika, Borroni, Barbara, Arosio, Beatrice, Nacmias, Benedetta, Nordestgaard, Børge G, Martínez Rodríguez, Carmen, Dufouil, Carole, Holmes, Clive, Aarsland, Dag, Rujescu, Dan, Alcolea, Daniel, Grünblatt, Edna, Dardiotis, Efthimios, Scarpini, Elio, Conti, Elisa, Gelpi, Ellen, Boerwinkle, Eric, Sanchez-Garcia, Florentino, Chêne, Geneviève, Rossi, Giacomina, Spalletta, Gianfranco, Binetti, Giuliano, Bailly, Henri, Zetterberg, Henrik, Appollonio, Ildebrando, Giegling, Ina, Rosas Allende, Irene, Van Dongen, Jasper, Vidal, Jean-Sebastien, Thomassen, Jesper Qvist, Fortea, Juan, Morgan, Kevin, Weinhold, Leonie, Farrer, Lindsay A, Wang, Li-San, Parnetti, Lucilla, Ikram, M Arfan, Tsolaki, Magda, Hulsman, Marc, Pericak-Vance, Margaret A, Esiri, Margaret, Dalmasso, Maria Carolina, Arcaro, Marina, Dichgans, Martin, Ingelsson, Martin, Scherer, Martin, Vyhnalek, Martin, Ewers, Michael, Wagner, Michael, Hiltunen, Mikko, Fornage, Myriam, Seidu, Nazib M, Scarmeas, Nikolaos, Skrobot, Olivia Anna, Lerch, Ondrej, Dionigi Rossi, Paolo, Yang, Qiong, Mayeux, Richard, Vandenberghe, Rik, Kern, Silke, Fostinelli, Silvia, Grimmer, Timo, Jian, Xueqiu, Sánchez-Juan, Pascual, Pastor, Pau, Pérez-Tur, Jordi, Piñol-Ripoll, Gerard, García-Alberca, Jose María, Álvarez, Victoria, Medina, Miguel, Schellenberg, Gerard D, Mather, Karen A, Serrano-Ríos, Manuel, Huisman, Martijn, Clarimón, Jordi, Boada, Mercè, Ramirez, Alfredo

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The utility of Next Generation Sequencing for molecular diagnostics in Rett syndrome by Vidal, Silvia, Brandi, Núria, Pacheco, Paola, Gerotina, Edgar, Blasco, Laura, Trotta, Jean-Rémi, Derdak, Sophia, Del Mar O'Callaghan, Maria, Garcia-Cazorla, Àngels, Pineda, Mercè, Armstrong, Judith

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