Focal chromosomal copy number aberrations identify CMTM8 and GPR177 as new candidate driver genes in osteosarcoma by Both, Joeri, Krijgsman, Oscar, Bras, Johannes, Schaap, Gerard R, Baas, Frank, Ylstra, Bauke, Hulsebos, Theo J M

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Identification of novel candidate oncogenes in chromosome region 17p11.2-p12 in human osteosarcoma by Both, Joeri, Wu, Thijs, Bras, Johannes, Schaap, Gerard R, Baas, Frank, Hulsebos, Theo J M

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Focal Chromosomal Copy Number Aberrations Identify CMTM8 and GPR177 as New Candidate Driver Genes in Osteosarcoma: e115835 by Both, Joeri, Krijgsman, Oscar, Bras, Johannes, Schaap, Gerard R, Baas, Frank, Ylstra, Bauke, Hulsebos, Theo JM

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Negative selection in humans and fruit flies involves synergistic epistasis by Sohail, Mashaal, Vakhrusheva, Olga A., Sul, Jae Hoon, Pulit, Sara L., Francioli, Laurent C., van den Berg, Leonard H., Veldink, Jan H., de Bakker, Paul I. W., Bazykin, Georgii A., Kondrashov, Alexey S., Sunyaev, Shamil R.

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Solving patients with rare diseases through programmatic reanalysis of genome-phenome data by Matalonga, Leslie, Hernández-Ferrer, Carles, Piscia, Davide, Schüle, Rebecca, Synofzik, Matthis, Töpf, Ana, Vissers, Lisenka E L M, de Voer, Richarda, Tonda, Raul, Laurie, Steven, Fernandez-Callejo, Marcos, Picó, Daniel, Garcia-Linares, Carles, Papakonstantinou, Anastasios, Corvó, Alberto, Joshi, Ricky, Diez, Hector, Gut, Ivo, Hoischen, Alexander, Graessner, Holm, Beltran, Sergi

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iHIVARNA phase IIa, a randomized, placebo-controlled, double-blinded trial to evaluate the safety and immunogenicity of iHIVARNA-01 in chronically HIV-infected patients under stabl... by de Jong, Wesley, Aerts, Joeri, Allard, Sabine, Brander, Christian, Buyze, Jozefien, Florence, Eric, van Gorp, Eric, Vanham, Guido, Leal, Lorna, Mothe, Beatriz, Thielemans, Kris, Plana, Montse, Garcia, Félipe, Gruters, Rob

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European Cardiomyopathy Pilot Registry: EURObservational Research Programme of the European Society of Cardiology by Elliott, Perry, Charron, Philippe, Blanes, Juan Ramon Gimeno, Tavazzi, Luigi, Tendera, Michal, Konté, Marème, Laroche, Cécile, Maggioni, Aldo P

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Exome reanalysis and proteomic profiling identified TRIP4 as a novel cause of cerebellar hypoplasia and spinal muscular atrophy (PCH1) by Töpf, Ana, Pyle, Angela, Griffin, Helen, Matalonga, Leslie, Schon, Katherine, Sickmann, Albert, Schara-Schmidt, Ulrike, Hentschel, Andreas, Chinnery, Patrick F, Kölbel, Heike, Roos, Andreas, Horvath, Rita

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Improved imputation quality of low-frequency and rare variants in European samples using the 'Genome of The Netherlands' by Deelen, Patrick, Menelaou, Androniki, van Leeuwen, Elisabeth M, Kanterakis, Alexandros, van Dijk, Freerk, Medina-Gomez, Carolina, Francioli, Laurent C, Hottenga, Jouke Jan, Karssen, Lennart C, Estrada, Karol, Kreiner-Møller, Eskil, Rivadeneira, Fernando, van Setten, Jessica, Gutierrez-Achury, Javier, Westra, Harm-Jan, Franke, Lude, van Enckevort, David, Dijkstra, Martijn, Byelas, Heorhiy, van Duijn, Cornelia M, de Bakker, Paul I W, Wijmenga, Cisca, Swertz, Morris A

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Genome-wide variant calling in reanalysis of exome sequencing data uncovered a pathogenic TUBB3 variant by de Boer, Elke, Yaldiz, Burcu, Denommé-Pichon, Anne-Sophie, Matalonga, Leslie, Laurie, Steve, Steyaert, Wouter, de Reuver, Rick, Gilissen, Christian, Kwint, Michael, Pfundt, Rolph, Verloes, Alain, Willemsen, Michèl A.A.P., Vries, Bert B.A. de, Vitobello, A., Kleefstra, Tjitske, Vissers, Lisenka E.L.M., Boer, Elke de, Cohen, Enzo, Cuesta, Isabel, Danis, Daniel, Denommé-Pichon, Anne-Sophie, Gao, Fei, Gilissen, Christian, Horvath, Rita, Johari, Mridul, Johanson, Lennart, Li, Shuang, Matalonga, Leslie, Morsy, Heba, Nelson, Isabelle, Paramonov, Ida, Paske, Iris B.A.W. te, Robinson, Peter, Savarese, Marco, Steyaert, Wouter, Töpf, Ana, Trimouille, Aurélien, van der Velde, Joeri K., Vandrovcova, Jana, Vitobello, Antonio, Zurek, Birte, Abbot, Kristin M., Banka, Siddharth, Benetti, Elisa, de Boer, Elke, Casari, Giorgio, Ciolfi, Andrea, Clayton-Smith, Jill, Dallapiccola, Bruno, Ellwanger, Kornelia, Faivre, Laurence, Graessner, Holm, Haack, Tobias B., Hammarsjö, Anna, Havlovicova, Marketa, Hoischen, Alexander, Hugon, Anne, Jackson, Adam, Kerstjens, Mieke, Kleefstra, Tjitske, Lindstrand, Anna, Martín, Estrella López, Macek, Milan, Maystadt, Isabelle, Morleo, Manuela, Nigro, Vicenzo, Nordgren, Ann, Pettersson, Maria, Pinelli, Michele, Pizzi, Simone, Posada, Manuel, Radio, Francesca C., Renieri, Alessandra, Rooryck, Caroline, Ryba, Lukas, Santen, Gijs W.E., Schwarz, Martin, Tartaglia, Marco, Thauvin, Christel, Torella, Annalaura, Verloes, Alain, Vissers, Lisenka, Votypka, Pavel, Vyshka, Klea, Zguro, Kristina

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A MT-TL1 variant identified by whole exome sequencing in an individual with intellectual disability, epilepsy, and spastic tetraparesis by de Boer, Elke, Ockeloen, Charlotte W, Matalonga, Leslie, Horvath, Rita, Rodenburg, Richard J, Coenen, Marieke J H, Janssen, Mirian, Henssen, Dylan, Gilissen, Christian, Steyaert, Wouter, Paramonov, Ida, Trimouille, Aurélien, Kleefstra, Tjitske, Verloes, Alain, Vissers, Lisenka E L M

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Analysis of exonic deletions in a large population study provides novel insights into NRXN1 pathology by Montalbano, Simone, Krebs, Morten Dybdahl, Rosengren, Anders, Vaez, Morteza, Hellberg, Kajsa-Lotta Georgii, Mortensen, Preben B., Børglum, Anders D., Geschwind, Daniel H., Raznahan, Armin, Thompson, Wesley K., Helenius, Dorte, Werge, Thomas, Ingason, Andrés

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Correction: A MT-TL1 variant identified by whole exome sequencing in an individual with intellectual disability, epilepsy, and spastic tetraparesis by de Boer, Elke, Ockeloen, Charlotte W, Matalonga, Leslie, Horvath, Rita, Rodenburg, Richard J, Coenen, Marieke J H, Janssen, Mirian, Henssen, Dylan, Gilissen, Christian, Steyaert, Wouter, Paramonov, Ida, Trimouille, Aurélien, Kleefstra, Tjitske, Verloes, Alain, Vissers, Lisenka E L M

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Genome of the Netherlands population-specific imputations identify an ABCA6 variant associated with cholesterol levels by van Leeuwen, Elisabeth M., Karssen, Lennart C., Deelen, Joris, Isaacs, Aaron, Medina-Gomez, Carolina, Mbarek, Hamdi, Kanterakis, Alexandros, Trompet, Stella, Postmus, Iris, Verweij, Niek, van Enckevort, David J., Huffman, Jennifer E., White, Charles C., Feitosa, Mary F., Bartz, Traci M., Manichaikul, Ani, Joshi, Peter K., Peloso, Gina M., Deelen, Patrick, van Dijk, Freerk, Willemsen, Gonneke, de Geus, Eco J., Milaneschi, Yuri, Penninx, Brenda W.J.H., Francioli, Laurent C., Menelaou, Androniki, Pulit, Sara L., Rivadeneira, Fernando, Hofman, Albert, Oostra, Ben A., Franco, Oscar H., Leach, Irene Mateo, Beekman, Marian, de Craen, Anton J.M., Uh, Hae-Won, Trochet, Holly, Hocking, Lynne J., Porteous, David J., Sattar, Naveed, Packard, Chris J., Buckley, Brendan M., Brody, Jennifer A., Bis, Joshua C., Rotter, Jerome I., Mychaleckyj, Josyf C., Campbell, Harry, Duan, Qing, Lange, Leslie A., Wilson, James F., Hayward, Caroline, Polasek, Ozren, Vitart, Veronique, Rudan, Igor, Wright, Alan F., Rich, Stephen S., Psaty, Bruce M., Borecki, Ingrid B., Kearney, Patricia M., Stott, David J., Adrienne Cupples, L., Jukema, J. Wouter, van der Harst, Pim, Sijbrands, Eric J., Hottenga, Jouke-Jan, Uitterlinden, Andre G., Swertz, Morris A., van Ommen, Gert-Jan B., de Bakker, Paul I.W., Eline Slagboom, P., Boomsma, Dorret I., Wijmenga, Cisca, van Duijn, Cornelia M.

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A framework for the detection of de novo mutations in family-based sequencing data by Francioli, Laurent C, Cretu-Stancu, Mircea, Garimella, Kiran V, Fromer, Menachem, Kloosterman, Wigard P, Samocha, Kaitlin E, Neale, Benjamin M, Daly, Mark J, Banks, Eric, DePristo, Mark A, de Bakker, Paul Iw

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Dynamic Metabolic Flux Analysis Demonstrated on Cultures Where the Limiting Substrate Is Changed from Carbon to Nitrogen and Vice Versa by Beauprez, Joeri, Lequeux, Gaspard, Maertens, Jo, Van Horen, Ellen, Soetaert, Wim, Vandamme, Erick, Vanrolleghem, Peter A.

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Consensus guidance for banking and supply of human embryonic stem cell lines for research purposes by Andrews, PW, Auerbach, J, Alvarez, M, Ahrlund-Richter, L, Baker, D, Benvenisty, N, Ben-Josef, D, Blin, G, Borghese, L, Borstlap, J, Bruce, K, Brustle, O, Buckle, R, Camby, C, Choo, A, Chen, W, Collins, D, Colman, A, Crombie, C, Crook, J, Cypess, R, De Sousa, P, Dhawan, J, Douay, L, Dvorak, P, Dyke, T, Eriksson, L, Firpo, M, Fitzgerald, C, Glover, C, Greene, M, Ha, HY, Hampl, A, Healy, L, Hei, D, Holm, F, Hovatta, O, Hunt, C, Hwang, SM, Inamdar, M, Isasi, R, Itskovitz-Eldor, J, Jessie, N, Kim, DW, Kirzner, R, Kiatpongsan, S, Knowles, B, Kuo, HC, Laughlin, M, Lavon, N, Ludwig, T, Lakov, M, Macauley, J, Mckay, R, Menasche, P, Menendez, P, Mileikovskaia, M, Minger, S, Mishra, G, Moody, J, Montgomery, K, Morris, C, Mummery, C, Nagy, A, Nakamura, Y, Nakatsuji, N, Nishikawa, SI, Oh, S, Oh, SK, Olson, P, Otonkoski, T, Patole, M, Park, HS, Pei, XT, Pera, M, Puceat, M, Reubinoff, B, Robins, A, Rooke, H, Rumayor, V, Scotman, H, Sherlock, J, Simon, C, Sipp, D, Skinner, R, Smith, D, Stacey, G, Stefanovic, S, Strehl, R, Takahashi, T, Talib, S, Terstegge, S, Turner, R, Tuuri, T, Yu, J, Zandstra, P, Zapata, A, Zeng, FY, Zhou, Q, Tannenbaum, S

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Marion, Jean-Luc

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Street Trends - How Today's Alternative Youth Cultures are Creating Tomorrow's Mainstream Markets

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Net zero targets in science and policy by Rogelj, Joeri

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