Flexible and Insoluble Artificial Synapses Based on Chemical Cross‐Linked Wool Keratin von Shi, Chenyang, Lan, Jinling, Wang, Jingjuan, Zhang, Shuai, Lin, Youhui, Zhu, Shuihong, Stegmann, Amy E., Yu, Rui, Yan, Xiaobing, Liu, Xiang Yang

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Phase Control of Nanocrystalline Inclusions in Bioprecipitated Titania with a Panel of Mutant Silica-Binding Proteins von Hellner, Brittney, Stegmann, Amy E, Pushpavanam, Karthik, Bailey, Matthew J, Baneyx, François

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De novo variants in FRYL are associated with developmental delay, intellectual disability, and dysmorphic features von Pan, Xueyang, Tao, Alice M., Lu, Shenzhao, Ma, Mengqi, Hannan, Shabab B., Slaugh, Rachel, Drewes Williams, Sarah, O'Grady, Lauren, Kanca, Oguz, Person, Richard, Carter, Melissa T., Platzer, Konrad, Schnabel, Franziska, Abou Jamra, Rami, Roberts, Amy E., Newburger, Jane W., Revah-Politi, Anya, Granadillo, Jorge L., Stegmann, Alexander P.A., Sinnema, Margje, Accogli, Andrea, Salpietro, Vincenzo, Capra, Valeria, Ghaloul-Gonzalez, Lina, Brueckner, Martina, Simon, Marleen E.H., Sweetser, David A., Glinton, Kevin E., Kirk, Susan E., Burrage, Lindsay C., Heaney, Jason D., Kim, Seon-Young, Lanza, Denise G., Liu, Zhandong, Mao, Dongxue, Milosavljevic, Aleksander, Nagamani, Sandesh C.S., Posey, Jennifer E., Ramamurthy, Uma, Ramanathan, Vivek, Rogers, Jeffrey, Rosenfeld, Jill A., Roth, Matthew, Zahedi Darshoori, Ramin, Wangler, Michael F., Yamamoto, Shinya, Chung, Wendy K., Bellen, Hugo J.

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Five-years of a mandatory single-embryo transfer (mSET) policy dramatically reduces twinning rate without lowering pregnancy rates von Kresowik, Jessica D., M.D, Stegmann, Barbara J., M.D., M.P.H, Sparks, Amy E., Ph.D, Ryan, Ginny L., M.D., M.A, van Voorhis, Bradley J., M.D

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PSMD11 loss-of-function variants correlate with a neurobehavioral phenotype, obesity, and increased interferon response von Deb, Wallid, Rosenfelt, Cory, Vignard, Virginie, Papendorf, Jonas Johannes, Möller, Sophie, Wendlandt, Martin, Studencka-Turski, Maja, Cogné, Benjamin, Besnard, Thomas, Ruffier, Léa, Toutain, Bérénice, Poirier, Léa, Cuinat, Silvestre, Kritzer, Amy, Crunk, Amy, diMonda, Janette, Vengoechea, Jaime, Mercier, Sandra, Kleinendorst, Lotte, van Haelst, Mieke M., Zuurbier, Linda, Sulem, Telma, Katrínardóttir, Hildigunnur, Friðriksdóttir, Rún, Sulem, Patrick, Stefansson, Kari, Jonsdottir, Berglind, Zeidler, Shimriet, Sinnema, Margje, Stegmann, Alexander P.A., Naveh, Natali, Skraban, Cara M., Gray, Christopher, Murrell, Jill R., Isikay, Sedat, Pehlivan, Davut, Calame, Daniel G., Posey, Jennifer E., Nizon, Mathilde, McWalter, Kirsty, Lupski, James R., Isidor, Bertrand, Bolduc, François V., Bézieau, Stéphane, Krüger, Elke, Küry, Sébastien, Ebstein, Frédéric

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Disruptive mutations in TANC2 define a neurodevelopmental syndrome associated with psychiatric disorders von Guo, Hui, Bettella, Elisa, Marcogliese, Paul C., Zhao, Rongjuan, Andrews, Jonathan C., Nowakowski, Tomasz J., Gillentine, Madelyn A., Hoekzema, Kendra, Wang, Tianyun, Wu, Huidan, Jangam, Sharayu, Liu, Cenying, Ni, Hailun, Willemsen, Marjolein H., van Bon, Bregje W., Rinne, Tuula, Stevens, Servi J. C., Kleefstra, Tjitske, Brunner, Han G., Yntema, Helger G., Long, Min, Zhao, Wenjing, Hu, Zhengmao, Colson, Cindy, Richard, Nicolas, Schwartz, Charles E., Romano, Corrado, Castiglia, Lucia, Bottitta, Maria, Dhar, Shweta U., Erwin, Deanna J., Emrick, Lisa, Keren, Boris, Afenjar, Alexandra, Zhu, Baosheng, Bai, Bing, Stankiewicz, Pawel, Herman, Kristin, Mercimek-Andrews, Saadet, Juusola, Jane, Wilfert, Amy B., Abou Jamra, Rami, Büttner, Benjamin, Mefford, Heather C., Muir, Alison M., Scheffer, Ingrid E., Regan, Brigid M., Malone, Stephen, Gecz, Jozef, Cobben, Jan, Weiss, Marjan M., Waisfisz, Quinten, Bijlsma, Emilia K., Hoffer, Mariëtte J. V., Ruivenkamp, Claudia A. L., Sartori, Stefano, Xia, Fan, Rosenfeld, Jill A., Bernier, Raphael A., Wangler, Michael F., Yamamoto, Shinya, Xia, Kun, Stegmann, Alexander P. A., Bellen, Hugo J., Murgia, Alessandra, Eichler, Evan E.

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In vitro fertilization patients support a single blastocyst transfer policy von Martini, Sarina, B.A, Van Voorhis, Bradley J., M.D, Stegmann, Barbara J., M.D., M.P.H, Sparks, Amy E.T., Ph.D, Shochet, Tara, Ph.D, Zimmerman, Miriam B., Ph.D, Ryan, Ginny L., M.D., M.A. (Bioethics)

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One hundred years of EEG for brain and behaviour research von Mushtaq, Faisal, Welke, Dominik, Gallagher, Anne, Pavlov, Yuri G., Kouara, Layla, Bosch-Bayard, Jorge, van den Bosch, Jasper J. F., Arvaneh, Mahnaz, Bland, Amy R., Chaumon, Maximilien, Borck, Cornelius, He, Xun, Luck, Steven J., Machizawa, Maro G., Pernet, Cyril, Puce, Aina, Segalowitz, Sidney J., Rogers, Christine, Awais, Muhammad, Babiloni, Claudio, Bailey, Neil W., Baillet, Sylvain, Bendall, Robert C. A., Brady, Daniel, Bringas-Vega, Maria L., Busch, Niko A., Calzada-Reyes, Ana, Chatard, Armand, Clayson, Peter E., Cohen, Michael X., Cole, Jonathan, Constant, Martin, Corneyllie, Alexandra, Coyle, Damien, Cruse, Damian, Delis, Ioannis, Delorme, Arnaud, Fair, Damien, Falk, Tiago H., Gamer, Matthias, Ganis, Giorgio, Gloy, Kilian, Gregory, Samantha, Hassall, Cameron D., Hiley, Katherine E., Ivry, Richard B., Jerbi, Karim, Jenkins, Michael, Kaiser, Jakob, Keil, Andreas, Knight, Robert T., Kochen, Silvia, Kotchoubey, Boris, Krigolson, Olave E., Langer, Nicolas, Liesefeld, Heinrich R., Lippé, Sarah, London, Raquel E., MacNamara, Annmarie, Makeig, Scott, Marinovic, Welber, Martínez-Montes, Eduardo, Marzuki, Aleya A., Mathew, Ryan K., Michel, Christoph, Millán, José d. R., Mon-Williams, Mark, Morales-Chacón, Lilia, Naar, Richard, Nilsonne, Gustav, Niso, Guiomar, Nyhus, Erika, Oostenveld, Robert, Paul, Katharina, Paulus, Walter, Pfabigan, Daniela M., Pourtois, Gilles, Rampp, Stefan, Rausch, Manuel, Robbins, Kay, Rossini, Paolo M., Ruzzoli, Manuela, Schmidt, Barbara, Senderecka, Magdalena, Srinivasan, Narayanan, Stegmann, Yannik, Thompson, Paul M., Valdes-Sosa, Mitchell, van der Molen, Melle J. W., Veniero, Domenica, Verona, Edelyn, Voytek, Bradley, Yao, Dezhong, Evans, Alan C., Valdes-Sosa, Pedro

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Histone H3.3 beyond cancer : Germline mutations in Histone 3 Family 3A and 3B cause a previously unidentified neurodegenerative disorder in 46 patients von Bryant, Laura, Li, Dong, Marchione, Dylan, Joiner, Evan F, Wilson, Khadija, Lee, Pearl, March, Michael E, Nair, Divya, Sherr, Elliott, Fregeau, Brieana, Wadley, Alexandrea, Mancini, Grazia M. S, Powell-Hamilton, Nina, van de Kamp, Jiddeke, Dean, John, Ross, Alison, Crawford, Heather P, Powis, Zoe, Cho, Megan T, Willing, Marcia C, Manwaring, Linda, Schot, Rachel, Nava, Caroline, Lessel, Davor, Wagner, Matias, Winkelmann, Juliane, Schuette, Jane L, Innis, Jeffrey W, Pizzino, Amy, Lüttgen, Sabine, Strom, Tim M, Monaghan, Kristin G, Dubbs, Holly, Bend, Renee, Lee, Jennifer A, Lyons, Michael J, Hoefele, Julia, Reutter, Heiko, Radtke, Kelly, Sherbini, Omar, Mrokse, Cameron, Helbig, Katherine L, Odent, Sylvie, Cogne, Benjamin, Mercier, Sandra, Besnard, Thomas, Kury, Sebastien, Redon, Richard, Reinson, Karit, Wojcik, Monica H, Õunap, Katrin, Ilves, Pilvi, Innes, A. Micheil, Kernohan, Kristin D, Meyn, M. Stephen, Lehman, Anna, Kitson, Hilary, Martin, Martin G, Martinez-Agosto, Julian A, Palmer, Christina G. S, Papp, Jeanette C, Parker, Neil H, Vilain, Eric, Wan, Jijun, Yoon, Amanda J, Ferrero, Giovanni Battista, Radio, Francesca Clementina, Carli, Diana, Barresi, Sabina, Brusco, Alfredo, Stuurman, K. E, Thompson, Michelle L, McWalter, Kirsty, Stegmann, Alexander P. A, Tveten, Kristian, Vøllo, Arve, Prescott, Trine, Fagerberg, Christina, Laulund, Lone Walentin, Larsen, Martin J, Byler, Melissa, Lebel, Robert Roger, Dean, Joy, Schrier Vergano, Samantha A, Norman, Jennifer, Mercimek-Andrews, Saadet, Neira, Juanita, Longo, Nicola, Sellars, Elizabeth, Louie, Raymond J, Cathey, Sara S, Heron, Delphine, Vanderver, Adeline, Simon, Celeste, Padilla Sirera, Natàlia, Chung, Wendy, Garcia, Benjamin, Hakonarson, Hakon, Bhoj, Elizabeth J, Universitat Autònoma de Barcelona

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Histone H3.3 beyond cancer : Germline mutations in Histone 3 Family 3A and 3B cause a previously unidentified neurodegenerative disorder in 46 patients von Bryant, Laura, Li, Dong, Marchione, Dylan, Joiner, Evan F, Wilson, Khadija, Lee, Pearl, March, Michael E, Nair, Divya, Sherr, Elliott, Fregeau, Brieana, Wadley, Alexandrea, Mancini, Grazia M. S, Powell-Hamilton, Nina, van de Kamp, Jiddeke, Dean, John, Ross, Alison, Crawford, Heather P, Powis, Zoe, Cho, Megan T, Willing, Marcia C, Manwaring, Linda, Schot, Rachel, Nava, Caroline, Lessel, Davor, Wagner, Matias, Winkelmann, Juliane, Schuette, Jane L, Innis, Jeffrey W, Pizzino, Amy, Lüttgen, Sabine, Strom, Tim M, Monaghan, Kristin G, Dubbs, Holly, Bend, Renee, Lee, Jennifer A, Lyons, Michael J, Hoefele, Julia, Reutter, Heiko, Radtke, Kelly, Sherbini, Omar, Mrokse, Cameron, Helbig, Katherine L, Odent, Sylvie, Cogne, Benjamin, Mercier, Sandra, Besnard, Thomas, Kury, Sebastien, Redon, Richard, Reinson, Karit, Wojcik, Monica H, Õunap, Katrin, Ilves, Pilvi, Innes, A. Micheil, Kernohan, Kristin D, Meyn, M. Stephen, Lehman, Anna, Kitson, Hilary, Martin, Martin G, Martinez-Agosto, Julian A, Palmer, Christina G. S, Papp, Jeanette C, Parker, Neil H, Vilain, Eric, Wan, Jijun, Yoon, Amanda J, Ferrero, Giovanni Battista, Radio, Francesca Clementina, Carli, Diana, Barresi, Sabina, Brusco, Alfredo, Stuurman, K. E, Thompson, Michelle L, McWalter, Kirsty, Stegmann, Alexander P. A, Tveten, Kristian, Vøllo, Arve, Prescott, Trine, Fagerberg, Christina, Laulund, Lone Walentin, Larsen, Martin J, Byler, Melissa, Lebel, Robert Roger, Dean, Joy, Schrier Vergano, Samantha A, Norman, Jennifer, Mercimek-Andrews, Saadet, Neira, Juanita, Longo, Nicola, Sellars, Elizabeth, Louie, Raymond J, Cathey, Sara S, Heron, Delphine, Vanderver, Adeline, Simon, Celeste, Padilla Sirera, Natàlia, Chung, Wendy, Garcia, Benjamin, Hakonarson, Hakon, Bhoj, Elizabeth J, Universitat Autònoma de Barcelona

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Histone H3.3 beyond cancer: Germline mutations in Histone 3 Family 3A and 3B cause a previously unidentified neurodegenerative disorder in 46 patients von Bryant, Laura, Li, Dong, Marchione, Dylan, Joiner, Evan F, Wilson, Khadija, Lee, Pearl, March, Michael E, Nair, Divya, Sherr, Elliott, Fregeau, Brieana, Wadley, Alexandrea, Mancini, Grazia M. S, Powell-Hamilton, Nina, Kamp, Jiddeke van de, Dean, John, Ross, Alison, Crawford, Heather P, Powis, Zoe, Cho, Megan T, Willing, Marcia C, Manwaring, Linda, Schot, Rachel, Nava, Caroline, Lessel, Davor, Wagner, Matias, Winkelmann, Juliane, Schuette, Jane L, Innis, Jeffrey W, Pizzino, Amy, Luttgen, Sabine, Strom, Tim M, Monaghan, Kristin G, Dubbs, Holly, Bend, Renee, Lee, Jennifer A, Lyons, Michael J, Hoefele, Julia, Reutter, Heiko, Radtke, Kelly, Sherbini, Omar, Mrokse, Cameron, Helbig, Katherine L, Odent, Sylvie, Cogne, Benjamin, Mercier, Sandra, Besnard, Thomas, Kury, Sebastien, Redon, Richard, Reinson, Karit, Wojcik, Monica H, Ilves, Pilvi, Innes, A. Micheil, Kernohan, Kristin D, Meyn, M. Stephen, Lehman, Anna, Kitson, Hilary, Martin, Martin G, Martinez-Agosto, Julian A, Palmer, Christina G. S, Papp, Jeanette C, Parker, Neil H, Vilain, Eric, Wan, Jijun, Yoon, Amanda J, Ferrero, Giovanni Battista, Radio, Francesca Clementina, Carli, Diana, Barresi, Sabina, Brusco, Alfredo, Thomas, Jennifer Muncy, Stuurman, K. E, Thompson, Michelle L, McWalter, Kirsty, Stegmann, Alexander P. A, Tveten, Kristian, Vollo, Arve, Prescott, Trine, Fagerberg, Christina, Laulund, Lone Walentin, Larsen, Martin J, Byler, Melissa, Lebel, Robert Roger, Dean, Joy, Vergano, Samantha A. Schrier, Norman, Jennifer, Mercimek-Andrews, Saadet, Neira, Juanita, Allen, Margot van, Longo, Nicola, Sellars, Elizabeth, Louie, Raymond J, Cathey, Sara S, Heron, Delphine, Vanderver, Adeline, Simon, Celeste, Padilla, Natalia, Chung, Wendy, Garcia, Benjamin, Hakonarson, Hakon H, Bhoj, Elizabeth J

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