The relationship between anxiety and risk taking is moderated by ambiguity by Smith, Andrew R., Ebert, Eva E., Broman-Fulks, Joshua J.

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Caspase‐4 mediates non‐canonical activation of the NLRP3 inflammasome in human myeloid cells by Schmid‐Burgk, Jonathan L., Gaidt, Moritz M., Schmidt, Tobias, Ebert, Thomas S., Bartok, Eva, Hornung, Veit

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Targeting stem cells in myelodysplastic syndromes and acute myeloid leukemia by Woll, Petter S., Yoshizato, Tetsuichi, Hellström‐Lindberg, Eva, Fioretos, Thoas, Ebert, Benjamin L., Jacobsen, Sten Eirik W.

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Genomic profiling for clinical decision making in myeloid neoplasms and acute leukemia by Duncavage, Eric J., Bagg, Adam, Hasserjian, Robert P., DiNardo, Courtney D., Godley, Lucy A., Iacobucci, Ilaria, Jaiswal, Siddhartha, Malcovati, Luca, Vannucchi, Alessandro M., Patel, Keyur P., Arber, Daniel A., Arcila, Maria E., Bejar, Rafael, Berliner, Nancy, Borowitz, Michael J., Branford, Susan, Brown, Anna L., Cargo, Catherine A., Döhner, Hartmut, Falini, Brunangelo, Garcia-Manero, Guillermo, Haferlach, Torsten, Hellström-Lindberg, Eva, Kim, Annette S., Klco, Jeffery M., Komrokji, Rami, Lee-Cheun Loh, Mignon, Loghavi, Sanam, Mullighan, Charles G., Ogawa, Seishi, Orazi, Attilio, Papaemmanuil, Elli, Reiter, Andreas, Ross, David M., Savona, Michael, Shimamura, Akiko, Skoda, Radek C., Solé, Francesc, Stone, Richard M., Tefferi, Ayalew, Walter, Matthew J., Wu, David, Ebert, Benjamin L., Cazzola, Mario

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SF3B1-mutant MDS as a distinct disease subtype: a proposal from the International Working Group for the Prognosis of MDS by Malcovati, Luca, Stevenson, Kristen, Papaemmanuil, Elli, Neuberg, Donna, Bejar, Rafael, Boultwood, Jacqueline, Bowen, David T., Campbell, Peter J., Ebert, Benjamin L., Fenaux, Pierre, Haferlach, Torsten, Heuser, Michael, Jansen, Joop H., Komrokji, Rami S., Maciejewski, Jaroslaw P., Walter, Matthew J., Fontenay, Michaela, Garcia-Manero, Guillermo, Graubert, Timothy A., Karsan, Aly, Meggendorfer, Manja, Pellagatti, Andrea, Sallman, David A., Savona, Michael R., Sekeres, Mikkael A., Steensma, David P., Tauro, Sudhir, Thol, Felicitas, Vyas, Paresh, Van de Loosdrecht, Arjan A., Haase, Detlef, Tüchler, Heinz, Greenberg, Peter L., Ogawa, Seishi, Hellstrom-Lindberg, Eva, Cazzola, Mario

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Cercospora beticola: The intoxicating lifestyle of the leaf spot pathogen of sugar beet by Rangel, Lorena I., Spanner, Rebecca E., Ebert, Malaika K., Pethybridge, Sarah J., Stukenbrock, Eva H., Jonge, Ronnie, Secor, Gary A., Bolton, Melvin D.

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International Consensus Classification of Myeloid Neoplasms and Acute Leukemias: integrating morphologic, clinical, and genomic data by Arber, Daniel A, Orazi, Attilio, Hasserjian, Robert P, Borowitz, Michael J, Calvo, Katherine R, Kvasnicka, Hans-Michael, Wang, Sa A, Bagg, Adam, Barbui, Tiziano, Branford, Susan, Bueso-Ramos, Carlos E, Cortes, Jorge E, Dal Cin, Paola, DiNardo, Courtney D, Dombret, Hervé, Duncavage, Eric J, Ebert, Benjamin L, Estey, Elihu H, Facchetti, Fabio, Foucar, Kathryn, Gangat, Naseema, Gianelli, Umberto, Godley, Lucy A, Gökbuget, Nicola, Gotlib, Jason, Hellström-Lindberg, Eva, Hobbs, Gabriela S, Hoffman, Ronald, Jabbour, Elias J, Kiladjian, Jean-Jacques, Larson, Richard A, Le Beau, Michelle M, Loh, Mignon L-C, Löwenberg, Bob, Macintyre, Elizabeth, Malcovati, Luca, Mullighan, Charles G, Niemeyer, Charlotte, Odenike, Olatoyosi M, Ogawa, Seishi, Orfao, Alberto, Papaemmanuil, Elli, Passamonti, Francesco, Porkka, Kimmo, Pui, Ching-Hon, Radich, Jerald P, Reiter, Andreas, Rozman, Maria, Rudelius, Martina, Savona, Michael R, Schiffer, Charles A, Schmitt-Graeff, Annette, Shimamura, Akiko, Sierra, Jorge, Stock, Wendy A, Stone, Richard M, Tallman, Martin S, Thiele, Jürgen, Tien, Hwei-Fang, Tzankov, Alexandar, Vannucchi, Alessandro M, Vyas, Paresh, Wei, Andrew H, Weinberg, Olga K, Wierzbowska, Agnieszka, Cazzola, Mario, Döhner, Hartmut, Tefferi, Ayalew

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The Gene Ontology resource: enriching a GOld mine by Carbon, Seth, Douglass, Eric, Good, Benjamin M, Unni, Deepak R, Harris, Nomi L, Mungall, Christopher J, Basu, Siddartha, Chisholm, Rex L, Dodson, Robert J, Hartline, Eric, Fey, Petra, Thomas, Paul D, Albou, Laurent-Philippe, Ebert, Dustin, Kesling, Michael J, Mi, Huaiyu, Muruganujan, Anushya, Huang, Xiaosong, Mushayahama, Tremayne, LaBonte, Sandra A, Siegele, Deborah A, Antonazzo, Giulia, Attrill, Helen, Brown, Nick H, Garapati, Phani, Marygold, Steven J, Trovisco, Vitor, dos Santos, Gil, Falls, Kathleen, Tabone, Christopher, Zhou, Pinglei, Goodman, Joshua L, Strelets, Victor B, Thurmond, Jim, Garmiri, Penelope, Ishtiaq, Rizwan, Rodríguez-López, Milagros, Acencio, Marcio L, Kuiper, Martin, Lægreid, Astrid, Logie, Colin, Lovering, Ruth C, Kramarz, Barbara, Saverimuttu, Shirin C C, Pinheiro, Sandra M, Gunn, Heather, Su, Renzhi, Thurlow, Katherine E, Chibucos, Marcus, Giglio, Michelle, Nadendla, Suvarna, Munro, James, Jackson, Rebecca, Duesbury, Margaret J, Del-Toro, Noemi, Meldal, Birgit H M, Paneerselvam, Kalpana, Perfetto, Livia, Porras, Pablo, Orchard, Sandra, Shrivastava, Anjali, Chang, Hsin-Yu, Finn, Robert Daniel, Mitchell, Alexander Lawson, Rawlings, Neil David, Richardson, Lorna, Sangrador-Vegas, Amaia, Blake, Judith A, Christie, Karen R, Dolan, Mary E, Drabkin, Harold J, Hill, David P, Ni, Li, Sitnikov, Dmitry M, Harris, Midori A, Oliver, Stephen G, Rutherford, Kim, Wood, Valerie, Hayles, Jaqueline, Bähler, Jürg, Bolton, Elizabeth R, De Pons, Jeffery L, Dwinell, Melinda R, Hayman, G Thomas, Kaldunski, Mary L, Kwitek, Anne E, Laulederkind, Stanley J F, Plasterer, Cody, Tutaj, Marek A, Vedi, Mahima, Wang, Shur-Jen, D’Eustachio, Peter, Matthews, Lisa, Balhoff, James P, Aleksander, Suzi A, Alexander, Michael J, Cherry, J Michael, Engel, Stacia R, Gondwe, Felix, Karra, Kalpana

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TP53 mutation status divides myelodysplastic syndromes with complex karyotypes into distinct prognostic subgroups by Haase, Detlef, Stevenson, Kristen E., Neuberg, Donna, Maciejewski, Jaroslaw P., Nazha, Aziz, Sekeres, Mikkael A., Ebert, Benjamin L., Garcia-Manero, Guillermo, Haferlach, Claudia, Haferlach, Torsten, Kern, Wolfgang, Ogawa, Seishi, Nagata, Yasunobu, Yoshida, Kenichi, Graubert, Timothy A., Walter, Matthew J., List, Alan F., Komrokji, Rami S., Padron, Eric, Sallman, David, Papaemmanuil, Elli, Campbell, Peter J., Savona, Michael R., Seegmiller, Adam, Adès, Lionel, Fenaux, Pierre, Shih, Lee-Yung, Bowen, David, Groves, Michael J., Tauro, Sudhir, Fontenay, Michaela, Kosmider, Olivier, Bar-Natan, Michal, Steensma, David, Stone, Richard, Heuser, Michael, Thol, Felicitas, Cazzola, Mario, Malcovati, Luca, Karsan, Aly, Ganster, Christina, Hellström-Lindberg, Eva, Boultwood, Jacqueline, Pellagatti, Andrea, Santini, Valeria, Quek, Lynn, Vyas, Paresh, Tüchler, Heinz, Greenberg, Peter L., Bejar, Rafael

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Molecular and clinical presentation of UBA1-mutated myelodysplastic syndromes by Sirenko, Maria, Bernard, Elsa, Creignou, Maria, Domenico, Dylan, Farina, Andrea, Arango Ossa, Juan E., Kosmider, Olivier, Hasserjian, Robert, Jädersten, Martin, Germing, Ulrich, Sanz, Guillermo, van de Loosdrecht, Arjan A., Gurnari, Carmelo, Follo, Matilde Yung, Thol, Felicitas, Zamora, Lurdes, Pinheiro, Ronald Feitosa, Pellagatti, Andrea, Elias, Harold K., Haase, Detlef, Sander, Birgitta, Orna, Elisa, Zoldan, Katharina, Eder, Lea Naomi, Sperr, Wolfgang R., Thalhammer, Renate, Ganster, Christina, Adès, Lionel, Tobiasson, Magnus, Palomo, Laura, Della Porta, Matteo Giovanni, Huberman, Kety, Fenaux, Pierre, Belickova, Monika, Savona, Michael R., Klimek, Virginia M., Santos, Fabio P. S., Boultwood, Jacqueline, Kotsianidis, Ioannis, Santini, Valeria, Solé, Francesc, Platzbecker, Uwe, Heuser, Michael, Valent, Peter, Finelli, Carlo, Voso, Maria Teresa, Shih, Lee-Yung, Ogawa, Seishi, Fontenay, Michaela, Jansen, Joop H., Cervera, Jose, Ebert, Benjamin L., Bejar, Rafael, Greenberg, Peter L., Gattermann, Norbert, Malcovati, Luca, Cazzola, Mario, Beck, David B., Hellström-Lindberg, Eva, Papaemmanuil, Elli

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Recurrent inversion polymorphisms in humans associate with genetic instability and genomic disorders by Porubsky, David, Höps, Wolfram, Ashraf, Hufsah, Hsieh, PingHsun, Rodriguez-Martin, Bernardo, Yilmaz, Feyza, Ebler, Jana, Hallast, Pille, Maria Maggiolini, Flavia Angela, Harvey, William T., Henning, Barbara, Audano, Peter A., Gordon, David S., Ebert, Peter, Hasenfeld, Patrick, Benito, Eva, Zhu, Qihui, Lee, Charles, Antonacci, Francesca, Steinrücken, Matthias, Beck, Christine R., Sanders, Ashley D., Marschall, Tobias, Eichler, Evan E., Korbel, Jan O.

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Identification and characterization of Cercospora beticola necrosis‐inducing effector CbNip1 by Ebert, Malaika K., Rangel, Lorena I., Spanner, Rebecca E., Taliadoros, Demetris, Wang, Xiaoyun, Friesen, Timothy L., Jonge, Ronnie, Neubauer, Jonathan D., Secor, Gary A., Thomma, Bart P. H. J., Stukenbrock, Eva H., Bolton, Melvin D.

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Dairying, diseases and the evolution of lactase persistence in Europe by Evershed, Richard P., Davey Smith, George, Roffet-Salque, Mélanie, Timpson, Adrian, Diekmann, Yoan, Lyon, Matthew S., Cramp, Lucy J. E., Casanova, Emmanuelle, Smyth, Jessica, Whelton, Helen L., Dunne, Julie, Brychova, Veronika, Šoberl, Lucija, Gerbault, Pascale, Gillis, Rosalind E., Heyd, Volker, Johnson, Emily, Manning, Katie, Marciniak, Arkadiusz, Outram, Alan K., Vigne, Jean-Denis, Shennan, Stephen, Bevan, Andrew, Colledge, Sue, Allason-Jones, Lyndsay, Amkreutz, Luc, Arbogast, Rose-Marie, Bălăşescu, Adrian, Bánffy, Eszter, Barclay, Alistair, Behrens, Anja, Bogucki, Peter, Carrancho Alonso, Ángel, Carretero, José Miguel, Cavanagh, Nigel, Claßen, Erich, Conrad, Matthias, Csengeri, Piroska, Czerniak, Lech, Dębiec, Maciej, Denaire, Anthony, Domboróczki, László, Donald, Christina, Ebert, Julia, Evans, Christopher, Francés-Negro, Marta, Gronenborn, Detlef, Haack, Fabian, Halle, Matthias, Hülshoff, Roman, Ilett, Michael, Iriarte, Eneko, Jakucs, János, Jeunesse, Christian, Johnson, Melanie, Jones, Andy M., Karul, Necmi, Kiosak, Dmytro, Kotova, Nadezhda, Krause, Rüdiger, Kretschmer, Saskia, Krüger, Marta, Lefranc, Philippe, Lelong, Olivia, Lenneis, Eva, Logvin, Andrey, Lüth, Friedrich, Marton, Tibor, Marley, Jane, Mortimer, Richard, Oosterbeek, Luiz, Oross, Krisztián, Pavúk, Juraj, Pechtl, Joachim, Pétrequin, Pierre, Pollard, Joshua, Pollard, Richard, Powlesland, Dominic, Pyzel, Joanna, Richardson, Andrew, Rowe, Peter, Rowland, Stephen, Sebők, Katalin, Schier, Wolfram, Schmalfuß, Germo, Sharapova, Svetlana, Sharp, Helen, Sheridan, Alison, Shevnina, Irina, Sobkowiak-Tabaka, Iwona, Stadler, Peter, Stäuble, Harald, Stobbe, Astrid, Stojanovski, Darko, Tasić, Nenad, van Wijk, Ivo, Vostrovská, Ivana, Wolfram, Sabine, Zeeb-Lanz, Andrea, Thomas, Mark G.

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External Validation of a Predictive Model of Urethral Strictures for Prostate Patients Treated With HDR Brachytherapy Boost by Panettieri, Vanessa, Rancati, Tiziana, Onjukka, Eva, Ebert, Martin A., Joseph, David J., Denham, James W., Steigler, Allison, Millar, Jeremy L.

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Large eQTL meta-analysis reveals differing patterns between cerebral cortical and cerebellar brain regions by Sieberts, Solveig K., Perumal, Thanneer M., Carrasquillo, Minerva M., Allen, Mariet, Reddy, Joseph S., Hoffman, Gabriel E., Dang, Kristen K., Calley, John, Ebert, Philip J., Eddy, James, Wang, Xue, Greenwood, Anna K., Mostafavi, Sara, Omberg, Larsson, Peters, Mette A., Logsdon, Benjamin A., De Jager, Philip L., Ertekin-Taner, Nilüfer, Mangravite, Lara M.

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Molecular taxonomy of myelodysplastic syndromes and its clinical implications by Bernard, Elsa, Hasserjian, Robert P., Greenberg, Peter L., Arango Ossa, Juan E., Creignou, Maria, Tuechler, Heinz, Gutierrez-Abril, Jesus, Domenico, Dylan, Medina-Martinez, Juan S., Levine, Max, Liosis, Konstantinos, Farnoud, Noushin, Sirenko, Maria, Jädersten, Martin, Germing, Ulrich, Sanz, Guillermo, van de Loosdrecht, Arjan A., Nannya, Yasuhito, Kosmider, Olivier, Follo, Matilde Y., Thol, Felicitas, Zamora, Lurdes, Pinheiro, Ronald F., Pellagatti, Andrea, Elias, Harold K., Haase, Detlef, Ganster, Christina, Ades, Lionel, Tobiasson, Magnus, Palomo, Laura, Della Porta, Matteo Giovanni, Fenaux, Pierre, Belickova, Monika, Savona, Michael R., Klimek, Virginia M., Santos, Fabio P. S., Boultwood, Jacqueline, Kotsianidis, Ioannis, Santini, Valeria, Solé, Francesc, Platzbecker, Uwe, Heuser, Michael, Valent, Peter, Finelli, Carlo, Voso, Maria Teresa, Shih, Lee-Yung, Fontenay, Michaela, Jansen, Joop H., Cervera, José, Gattermann, Norbert, Ebert, Benjamin L., Bejar, Rafael, Malcovati, Luca, Ogawa, Seishi, Cazzola, Mario, Hellström-Lindberg, Eva, Papaemmanuil, Elli

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Incidence, Clinical Associations, and Co-Mutation Patterns of UBA1 Mutations in MDS by Sirenko, Maria, Bernard, Elsa, Beck, David B., Creignou, Maria, Domenico, Dylan, Farina, Andrea, Arango, Juan E, Kosmider, Olivier, Hasserjian, Robert P., Jadersten, Martin, Germing, Ulrich, Sanz, Guillermo, van de Loosdrecht, Arjan A., Follo, Matilde Y, Thol, Felicitas R., Zamora, Lurdes, Pinheiro, Ronald Feitosa, Pellagatti, Andrea, Elias, Harold K., Haase, Detlef, Ganster, Christina, Ades, Lionel, Tobiasson, Magnus, Palomo, Laura, Della Porta, Matteo G., Huberman, Kety, Fenaux, Pierre, Belickova, Monika, Savona, Michael R., Klimek, Virginia M., Santos, Fabio Pires de Souza, Boultwood, Jacqueline, Kotsianidis, Ioannis, Santini, Valeria, Solé, Francesc, Platzbecker, Uwe, Heuser, Michael, Valent, Peter, Finelli, Carlo, Voso, Maria Teresa, Shih, Lee-Yung, Ogawa, Seishi, Fontenay, Michaela, Jansen, Joop H., Cervera, Jose, Ebert, Benjamin L., Bejar, Rafael, Greenberg, Peter L, Gattermann, Norbert, Malcovati, Luca, Cazzola, Mario, Hellström-Lindberg, Eva, Papaemmanuil, Elli

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ZBTB33 is mutated in clonal hematopoiesis and myelodysplastic syndromes and impacts RNA splicing by Beauchamp, Ellen M, Leventhal, Matthew, Bernard, Elsa, Hoppe, Emma R, Todisco, Gabriele, Creignou, Maria, Gallì, Anna, Castellano, Cecilia A, McConkey, Marie, Tarun, Akansha, Wong, Waihay, Schenone, Monica, Stanclift, Caroline, Tanenbaum, Benjamin, Malolepsza, Edyta, Nilsson, Björn, Bick, Alexander G, Weinstock, Joshua S, Miller, Mendy, Niroula, Abhishek, Dunford, Andrew, Taylor-Weiner, Amaro, Wood, Timothy, Barbera, Alex, Anand, Shankara, Psaty, Bruce M, Desai, Pinkal, Cho, Michael H, Johnson, Andrew D, Loos, Ruth, MacArthur, Daniel G, Lek, Monkol, Neuberg, Donna S, Lage, Kasper, Carr, Steven A, Hellstrom-Lindberg, Eva, Malcovati, Luca, Papaemmanuil, Elli, Stewart, Chip, Getz, Gad, Bradley, Robert K, Jaiswal, Siddhartha, Ebert, Benjamin L

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Author Correction: Dairying, diseases and the evolution of lactase persistence in Europe by Evershed, Richard P., Davey Smith, George, Roffet-Salque, Mélanie, Timpson, Adrian, Diekmann, Yoan, Lyon, Matthew S., Cramp, Lucy J. E., Casanova, Emmanuelle, Smyth, Jessica, Whelton, Helen L., Dunne, Julie, Brychova, Veronika, Šoberl, Lucija, Gerbault, Pascale, Gillis, Rosalind E., Heyd, Volker, Johnson, Emily, Manning, Katie, Marciniak, Arkadiusz, Outram, Alan K., Vigne, Jean-Denis, Shennan, Stephen, Bevan, Andrew, Colledge, Sue, Allason-Jones, Lyndsay, Amkreutz, Luc, Arbogast, Rose-Marie, Bălăşescu, Adrian, Bánffy, Eszter, Barclay, Alistair, Behrens, Anja, Bogucki, Peter, Carrancho Alonso, Ángel, Carretero, José Miguel, Cavanagh, Nigel, Claßen, Erich, Conrad, Matthias, Csengeri, Piroska, Czerniak, Lech, Dębiec, Maciej, Denaire, Anthony, Domboróczki, László, Donald, Christina, Ebert, Julia, Evans, Christopher, Francés-Negro, Marta, Gronenborn, Detlef, Haack, Fabian, Halle, Matthias, Hülshoff, Roman, Ilett, Michael, Iriarte, Eneko, Jakucs, János, Jeunesse, Christian, Johnson, Melanie, Jones, Andy M., Karul, Necmi, Kiosak, Dmytro, Kotova, Nadezhda, Krause, Rüdiger, Kretschmer, Saskia, Krüger, Marta, Lefranc, Philippe, Lelong, Olivia, Lenneis, Eva, Logvin, Andrey, Lüth, Friedrich, Marton, Tibor, Marley, Jane, Mortimer, Richard, Oosterbeek, Luiz, Oross, Krisztián, Pavúk, Juraj, Pechtl, Joachim, Pétrequin, Pierre, Pollard, Joshua, Pollard, Richard, Powlesland, Dominic, Pyzel, Joanna, Richardson, Andrew, Rowe, Peter, Rowland, Stephen, Sebők, Katalin, Schier, Wolfram, Schmalfuß, Germo, Sharapova, Svetlana, Sharp, Helen, Sheridan, Alison, Shevnina, Irina, Sobkowiak-Tabaka, Iwona, Stadler, Peter, Stäuble, Harald, Stobbe, Astrid, Stojanovski, Darko, Tasić, Nenad, van Wijk, Ivo, Vostrovská, Ivana, Wolfram, Sabine, Zeeb-Lanz, Andrea, Thomas, Mark G.

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Diminutive somatic deletions in the 5q region lead to a phenotype atypical of classical 5q− syndrome by Vlachos, Adrianna, Farrar, Jason E., Atsidaftos, Eva, Muir, Ellen, Narla, Anupama, Markello, Thomas C., Singh, Sharon A., Landowski, Michael, Gazda, Hanna T., Blanc, Lionel, Liu, Johnson M., Ellis, Steven R., Arceci, Robert J., Ebert, Benjamin L., Bodine, David M., Lipton, Jeffrey M.

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