Spontaneous usage of different shortcuts based on the commutativity principle von Gaschler, Robert, Vaterrodt, Bianca, Frensch, Peter A, Eichler, Alexandra, Haider, Hilde

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Fostering Formal Commutativity Knowledge with Approximate Arithmetic von Hansen, Sonja Maria, Haider, Hilde, Eichler, Alexandra, Godau, Claudia, Frensch, Peter A, Gaschler, Robert

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The use of recognition information and additional cues in inferences from memory von Bröder, Arndt, Eichler, Alexandra

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An old problem: How can we distinguish between conscious and unconscious knowledge acquired in an implicit learning task? von Haider, Hilde, Eichler, Alexandra, Lange, Thorsten

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How we use what we learn in Math: An integrative account of the development of commutativity von Haider, Hilde, Eichler, Alexandra, Hansen, Sonja, Vaterrodt, Bianca, Gaschler, Robert, Frensch, Peter

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Focus on the human being: Cognitive Ergonomics in intralogistics von Kretschmer, Veronika, Eichler, Alexandra, Rinkenauer, Gerhard, Spee, Detlef

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Schweigen ist Silber, Reden ist Gold? :die Rolle von Sprache als Determinante expliziten Wissens von Eichler, Alexandra

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Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations von O'Roak, Brian J, Deriziotis, Pelagia, Lee, Choli, Vives, Laura, Schwartz, Jerrod J, Girirajan, Santhosh, Karakoc, Emre, MacKenzie, Alexandra P, Ng, Sarah B, Baker, Carl, Rieder, Mark J, Nickerson, Deborah A, Bernier, Raphael, Fisher, Simon E, Shendure, Jay, Eichler, Evan E

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Adaptive archaic introgression of copy number variants and the discovery of previously unknown human genes von Hsieh, PingHsun, Vollger, Mitchell R., Dang, Vy, Porubsky, David, Baker, Carl, Cantsilieris, Stuart, Hoekzema, Kendra, Lewis, Alexandra P., Munson, Katherine M., Sorensen, Melanie, Kronenberg, Zev N., Murali, Shwetha, Nelson, Bradley J., Chiatante, Giorgia, Maggiolini, Flavia Angela Maria, Blanché, Hélène, Underwood, Jason G., Antonacci, Francesca, Deleuze, Jean-François, Eichler, Evan E.

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The structure, function and evolution of a complete human chromosome 8 von Logsdon, Glennis A., Vollger, Mitchell R., Hsieh, PingHsun, Mao, Yafei, Liskovykh, Mikhail A., Koren, Sergey, Nurk, Sergey, Mercuri, Ludovica, Dishuck, Philip C., Rhie, Arang, de Lima, Leonardo G., Dvorkina, Tatiana, Porubsky, David, Harvey, William T., Mikheenko, Alla, Bzikadze, Andrey V., Kremitzki, Milinn, Graves-Lindsay, Tina A., Jain, Chirag, Hoekzema, Kendra, Murali, Shwetha C., Munson, Katherine M., Baker, Carl, Sorensen, Melanie, Lewis, Alexandra M., Surti, Urvashi, Gerton, Jennifer L., Larionov, Vladimir, Ventura, Mario, Miga, Karen H., Phillippy, Adam M., Eichler, Evan E.

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Segmental duplications and their variation in a complete human genome von Vollger, Mitchell R, Guitart, Xavi, Dishuck, Philip C, Mercuri, Ludovica, Harvey, William T, Gershman, Ariel, Diekhans, Mark, Sulovari, Arvis, Munson, Katherine M, Lewis, Alexandra P, Hoekzema, Kendra, Porubsky, David, Li, Ruiyang, Nurk, Sergey, Koren, Sergey, Miga, Karen H, Phillippy, Adam M, Timp, Winston, Ventura, Mario, Eichler, Evan E

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TAD evolutionary and functional characterization reveals diversity in mammalian TAD boundary properties and function von Okhovat, Mariam, VanCampen, Jake, Nevonen, Kimberly A., Harshman, Lana, Li, Weiyu, Layman, Cora E., Ward, Samantha, Herrera, Jarod, Wells, Jackson, Sheng, Rory R., Mao, Yafei, Ndjamen, Blaise, Lima, Ana C., Vigh-Conrad, Katinka A., Stendahl, Alexandra M., Yang, Ran, Fedorov, Lev, Matthews, Ian R., Easow, Sarah A., Chan, Dylan K., Jan, Taha A., Eichler, Evan E., Rugonyi, Sandra, Conrad, Donald F., Ahituv, Nadav, Carbone, Lucia

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Expectations and blind spots for structural variation detection from long-read assemblies and short-read genome sequencing technologies von Zhao, Xuefang, Collins, Ryan L., Lee, Wan-Ping, Weber, Alexandra M., Jun, Yukyung, Zhu, Qihui, Weisburd, Ben, Huang, Yongqing, Audano, Peter A., Wang, Harold, Walker, Mark, Lowther, Chelsea, Fu, Jack, Gerstein, Mark B., Devine, Scott E., Marschall, Tobias, Korbel, Jan O., Eichler, Evan E., Chaisson, Mark J.P., Lee, Charles, Mills, Ryan E., Brand, Harrison, Talkowski, Michael E.

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Evidence for opposing selective forces operating on human-specific duplicated TCAF genes in Neanderthals and humans von Hsieh, PingHsun, Dang, Vy, Vollger, Mitchell R., Mao, Yafei, Huang, Tzu-Hsueh, Dishuck, Philip C., Baker, Carl, Cantsilieris, Stuart, Lewis, Alexandra P., Munson, Katherine M., Sorensen, Melanie, Welch, AnneMarie E., Underwood, Jason G., Eichler, Evan E.

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Assembly of 43 human Y chromosomes reveals extensive complexity and variation von Hallast, Pille, Ebert, Peter, Loftus, Mark, Yilmaz, Feyza, Audano, Peter A., Logsdon, Glennis A., Bonder, Marc Jan, Zhou, Weichen, Höps, Wolfram, Kim, Kwondo, Li, Chong, Hoyt, Savannah J., Dishuck, Philip C., Porubsky, David, Tsetsos, Fotios, Kwon, Jee Young, Zhu, Qihui, Munson, Katherine M., Hasenfeld, Patrick, Harvey, William T., Lewis, Alexandra P., Kordosky, Jennifer, Hoekzema, Kendra, O’Neill, Rachel J., Korbel, Jan O., Tyler-Smith, Chris, Eichler, Evan E., Shi, Xinghua, Beck, Christine R., Marschall, Tobias, Konkel, Miriam K., Lee, Charles

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Familial long-read sequencing increases yield of de novo mutations von Noyes, Michelle D., Harvey, William T., Porubsky, David, Sulovari, Arvis, Li, Ruiyang, Rose, Nicholas R., Audano, Peter A., Munson, Katherine M., Lewis, Alexandra P., Hoekzema, Kendra, Mantere, Tuomo, Graves-Lindsay, Tina A., Sanders, Ashley D., Goodwin, Sara, Kramer, Melissa, Mokrab, Younes, Zody, Michael C., Hoischen, Alexander, Korbel, Jan O., McCombie, W. Richard, Eichler, Evan E.

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Reconstruction of the human amylase locus reveals ancient duplications seeding modern-day variation von Yilmaz, Feyza, Karageorgiou, Charikleia, Kim, Kwondo, Pajic, Petar, Scheer, Kendra, Beck, Christine R, Torregrossa, Ann-Marie, Lee, Charles, Gokcumen, Omer, Audano, Peter A, Austine-Orimoloye, Olanrewaju, Beck, Christine R, Eichler, Evan E, Hallast, Pille, Harvey, William T, Hastie, Alex R, Hoekzema, Kendra, Hunt, Sarah, Korbel, Jan O, Kordosky, Jennifer, Lee, Charles, Lewis, Alexandra P, Marschall, Tobias, Munson, Katherine M, Pang, Andy, Yilmaz, Feyza

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Structurally divergent and recurrently mutated regions of primate genomes von Mao, Yafei, Harvey, William T., Porubsky, David, Munson, Katherine M., Hoekzema, Kendra, Lewis, Alexandra P., Audano, Peter A., Rozanski, Allison, Yang, Xiangyu, Zhang, Shilong, Yoo, DongAhn, Gordon, David S., Fair, Tyler, Wei, Xiaoxi, Logsdon, Glennis A., Haukness, Marina, Dishuck, Philip C., Jeong, Hyeonsoo, del Rosario, Ricardo, Bauer, Vanessa L., Fattor, Will T., Wilkerson, Gregory K., Mao, Yuxiang, Shi, Yongyong, Sun, Qiang, Lu, Qing, Paten, Benedict, Bakken, Trygve E., Pollen, Alex A., Feng, Guoping, Sawyer, Sara L., Warren, Wesley C., Carbone, Lucia, Eichler, Evan E.

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Profiling variable-number tandem repeat variation across populations using repeat-pangenome graphs von Lu, Tsung-Yu, Chaisson, Mark J. P.

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Haplotype-resolved genome sequencing of a Gujarati Indian individual von Kitzman, Jacob O, Shendure, Jay, MacKenzie, Alexandra P, Adey, Andrew, Hiatt, Joseph B, Patwardhan, Rupali P, Sudmant, Peter H, Ng, Sarah B, Alkan, Can, Qiu, Ruolan, Eichler, Evan E

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