The effects of social comparison and depressive mood on adolescent social decision-making von Hu, Yixin, Zhou, Mengmeng, Shao, Yunru, Wei, Jing, Li, Zhenying, Xu, Shike, Maguire, Phil, Wang, Dawei

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De Novo Truncating Variants in SON Cause Intellectual Disability, Congenital Malformations, and Failure to Thrive von Tokita, Mari J., Braxton, Alicia A., Shao, Yunru, Lewis, Andrea M., Vincent, Marie, Küry, Sébastien, Besnard, Thomas, Isidor, Bertrand, Latypova, Xénia, Bézieau, Stéphane, Liu, Pengfei, Motter, Connie S., Melver, Catherine Ward, Robin, Nathaniel H., Infante, Elena M., McGuire, Marianne, El-Gharbawy, Areeg, Littlejohn, Rebecca O., McLean, Scott D., Bi, Weimin, Bacino, Carlos A., Lalani, Seema R., Scott, Daryl A., Eng, Christine M., Yang, Yaping, Schaaf, Christian P., Walkiewicz, Magdalena A.

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Phenotypic expansion in DDX3X – a common cause of intellectual disability in females von Wang, Xia, Posey, Jennifer E., Rosenfeld, Jill A., Bacino, Carlos A., Scaglia, Fernando, Immken, LaDonna, Harris, Jill M., Hickey, Scott E., Mosher, Theresa M., Slavotinek, Anne, Zhang, Jing, Beuten, Joke, Leduc, Magalie S., He, Weimin, Vetrini, Francesco, Walkiewicz, Magdalena A., Bi, Weimin, Xiao, Rui, Liu, Pengfei, Shao, Yunru, Gezdirici, Alper, Gulec, Elif Y., Jiang, Yunyun, Darilek, Sandra A., Hansen, Adam W., Khayat, Michael M., Pehlivan, Davut, Piard, Juliette, Muzny, Donna M., Hanchard, Neil, Belmont, John W., Van Maldergem, Lionel, Gibbs, Richard A., Eldomery, Mohammad K., Akdemir, Zeynep C., Adesina, Adekunle M., Chen, Shan, Lee, Yi‐Chien, Lee, Brendan, Lupski, James R., Eng, Christine M., Xia, Fan, Yang, Yaping, Graham, Brett H., Moretti, Paolo

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Recurrent De Novo and Biallelic Variation of ATAD3A, Encoding a Mitochondrial Membrane Protein, Results in Distinct Neurological Syndromes von Harel, Tamar, Yoon, Wan Hee, Garone, Caterina, Gu, Shen, Coban-Akdemir, Zeynep, Eldomery, Mohammad K., Posey, Jennifer E., Jhangiani, Shalini N., Rosenfeld, Jill A., Cho, Megan T., Fox, Stephanie, Withers, Marjorie, Brooks, Stephanie M., Chiang, Theodore, Duraine, Lita, Erdin, Serkan, Yuan, Bo, Shao, Yunru, Moussallem, Elie, Lamperti, Costanza, Donati, Maria A., Smith, Joshua D., McLaughlin, Heather M., Eng, Christine M., Walkiewicz, Magdalena, Xia, Fan, Pippucci, Tommaso, Magini, Pamela, Seri, Marco, Zeviani, Massimo, Hirano, Michio, Hunter, Jill V., Srour, Myriam, Zanigni, Stefano, Lewis, Richard Alan, Muzny, Donna M., Lotze, Timothy E., Boerwinkle, Eric, Gibbs, Richard A., Hickey, Scott E., Graham, Brett H., Yang, Yaping, Buhas, Daniela, Martin, Donna M., Potocki, Lorraine, Graziano, Claudio, Bellen, Hugo J., Lupski, James R.

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Research and Evaluation of a Cyberchondria Severity Scale in a Chinese Context von Wang, Dawei, Sun, Lingchao, Shao, Yunru, Zhang, Xiaoyan, Maguire, Phil, Hu, Yixin

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MED27 Variants Cause Developmental Delay, Dystonia, and Cerebellar Hypoplasia von Meng, Linyan, Isohanni, Pirjo, Shao, Yunru, Graham, Brett H., Hickey, Scott E., Brooks, Stephanie, Suomalainen, Anu, Joset, Pascal, Steindl, Katharina, Rauch, Anita, Hackenberg, Annette, High, Frances A., Armstrong‐Javors, Amy, Mencacci, Niccolò E., Gonzàlez‐Latapi, Paulina, Kamel, Walaa A., Al‐Hashel, Jasem Y., Bustos, Bernabé I., Hernandez, Alejandro V., Krainc, Dimitri, Lubbe, Steven J., Van Esch, Hilde, De Luca, Chiara, Ballon, Katleen, Ravelli, Claudia, Burglen, Lydie, Qebibo, Leila, Calame, Daniel G., Mitani, Tadahiro, Marafi, Dana, Pehlivan, Davut, Saadi, Nebal W., Sahin, Yavuz, Maroofian, Reza, Efthymiou, Stephanie, Houlden, Henry, Maqbool, Shazia, Rahman, Fatima, Gu, Shen, Posey, Jennifer E., Lupski, James R., Hunter, Jill V., Wangler, Michael F., Carroll, Christopher J., Yang, Yaping

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Evaluation of two-year Jewish genetic disease screening program in Atlanta: insight into community genetic screening approaches von Shao, Yunru, Liu, Shuling, Grinzaid, Karen

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MED27 variansts cause Developmental Delay, Dystonia, and Cerebellar Hypoplasia von Meng, Linyan, Isohanni, Pirjo, Shao, Yunru, Graham, Brett H, Hickey, Scott E, Brooks, Stephanie, Suomalainen, Anu, Joset, Pascal, Steindl, Katharina, Rauch, Anita, Hackenberg, Annette, High, Frances A, Armstrong-Javors, Amy, Mencacci, Niccolò E, Gonzàlez-Latapi, Paulina, Kamel, Walaa A, Al-Hashel, Jasem Y, Bustos, Bernabé I, Hernandez, Alejandro V, Krainc, Dimitri, Lubbe, Steven J, Van Esch, Hilde, De Luca, Chiara, Ballon, Katleen, Ravelli, Claudia, Burglen, Lydie, Qebibo, Leila, Calame, Daniel G, Mitani, Tadahiro, Marafi, Dana

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MED27 Variants Cause Developmental Delay, Dystonia, and Cerebellar Hypoplasia von Meng, Linyan, Isohanni, Pirjo, Shao, Yunru, Graham, Brett H, Hickey, Scott E, Brooks, Stephanie, Suomalainen, Anu, Joset, Pascal, Steindl, Katharina, Rauch, Anita, Hackenberg, Annette, High, Frances A, Armstrong-Javors, Amy, Mencacci, Niccolo E, Gonzalez-Latapi, Paulina, Kamel, Walaa A, Al-Hashel, Jasem Y, Bustos, Bernabe, Hernandez, Alejandro, Krainc, Dimitri, Lubbe, Steven J, Van Esch, Hilde, De Luca, Chiara, Ballon, Katleen, Ravelli, Claudia, Burglen, Lydie, Qebibo, Leila, Calame, Daniel G, Mitani, Tadahiro, Marafi, Dana, Pehlivan, Davut, Saadi, Nebal W, Sahin, Yavuz, Maroofian, Reza, Efthymiou, Stephanie, Houlden, Henry, Maqbool, Shazia, Rahman, Fatima, Gu, Shen, Posey, Jennifer E, Lupski, James R, Hunter, Jill, Wangler, Michael F, Carroll, Christopher J, Yang, Yaping

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De novo missense variants in PPP1CB are associated with intellectual disability and congenital heart disease von Ma, Lijiang, Bayram, Yavuz, McLaughlin, Heather M., Cho, Megan T., Krokosky, Alyson, Turner, Clesson E., Lindstrom, Kristin, Bupp, Caleb P., Mayberry, Katey, Mu, Weiyi, Bodurtha, Joann, Weinstein, Veronique, Zadeh, Neda, Alcaraz, Wendy, Powis, Zöe, Shao, Yunru, Scott, Daryl A., Lewis, Andrea M., White, Janson J., Jhangiani, Shalani N., Gulec, Elif Yilmaz, Lalani, Seema R., Lupski, James R., Retterer, Kyle, Schnur, Rhonda E., Wentzensen, Ingrid M., Bale, Sherri, Chung, Wendy K.

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YY1 Haploinsufficiency Causes an Intellectual Disability Syndrome Featuring Transcriptional and Chromatin Dysfunction von Gabriele, Michele, Vulto-van Silfhout, Anneke T, Germain, Pierre-Luc, Vitriolo, Alessandro, Kumar, Raman, Douglas, Evelyn, Haan, Eric, Kosaki, Kenjiro, Takenouchi, Toshiki, Rauch, Anita, Steindl, Katharina, Frengen, Eirik, Misceo, Doriana, Pedurupillay, Christeen Ramane J, Stromme, Petter, Rosenfeld, Jill A, Shao, Yunru, Craigen, William J, Schaaf, Christian P, Rodriguez-Buritica, David, Farach, Laura, Friedman, Jennifer, Thulin, Perla, McLean, Scott D, Nugent, Kimberly M, Morton, Jenny, Nicholl, Jillian, Andrieux, Joris, Stray-Pedersen, Asbjørg, Chambon, Pascal

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De Novo Missense Variants in PPP1CB Are Associated with Intellectual Disabilities and Congenital Heart Disease von Ma, Lijiang, Bayram, Yavuz, McLaughlin, Heather M, Cho, Megan T, Krokosky, Alyson, Turner, Clesson E, Lindstrom, Kristin, Bupp, Caleb, Mayberry, Katey, Mu, Weiyi, Bodurtha, Joann, Weinstein, Veronique, Zadeh, Neda, Alcaraz, Wendy, Powis, Zöe, Shao, Yunru, Scott, Daryl A, Lewis, Andrea M, White, Janson J, Jhangiani, Shalani N, Gulec, Elif Yilmaz, Lalani, Seema R, Lupski, James R, Retterer, Kyle, Schnur, Rhonda E, Wentzensen, Ingrid, Bale, Sherri, Chung, Wendy K

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De Novo Missense Variants in TRAF7 Cause Developmental Delay, Congenital Anomalies, and Dysmorphic Features von Tokita, Mari J., Chen, Chun-An, Chitayat, David, Macnamara, Ellen, Rosenfeld, Jill A., Hanchard, Neil, Lewis, Andrea M., Brown, Chester W., Marom, Ronit, Shao, Yunru, Novacic, Danica, Wolfe, Lynne, Wahl, Colleen, Tifft, Cynthia J., Toro, Camilo, Bernstein, Jonathan A., Hale, Caitlin L., Silver, Julia, Hudgins, Louanne, Ananth, Amitha, Hanson-Kahn, Andrea, Shuster, Shirley, Magoulas, Pilar L., Patel, Vipulkumar N., Zhu, Wenmiao, Chen, Stella M., Jiang, Yanjun, Liu, Pengfei, Eng, Christine M., Batkovskyte, Dominyka, di Ronza, Alberto, Sardiello, Marco, Lee, Brendan H., Schaaf, Christian P., Yang, Yaping, Wang, Xia

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Phenotypic expansion in DDX 3X – a common cause of intellectual disability in females von Wang, Xia, Posey, Jennifer E., Rosenfeld, Jill A., Bacino, Carlos A., Scaglia, Fernando, Immken, LaDonna, Harris, Jill M., Hickey, Scott E., Mosher, Theresa M., Slavotinek, Anne, Zhang, Jing, Beuten, Joke, Leduc, Magalie S., He, Weimin, Vetrini, Francesco, Walkiewicz, Magdalena A., Bi, Weimin, Xiao, Rui, Liu, Pengfei, Shao, Yunru, Gezdirici, Alper, Gulec, Elif Y., Jiang, Yunyun, Darilek, Sandra A., Hansen, Adam W., Khayat, Michael M., Pehlivan, Davut, Piard, Juliette, Muzny, Donna M., Hanchard, Neil, Belmont, John W., Van Maldergem, Lionel, Gibbs, Richard A., Eldomery, Mohammad K., Akdemir, Zeynep C., Adesina, Adekunle M., Chen, Shan, Lee, Yi‐Chien, Lee, Brendan, Lupski, James R., Eng, Christine M., Xia, Fan, Yang, Yaping, Graham, Brett H., Moretti, Paolo

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Microfluidic 3D Printing Responsive Scaffolds with Biomimetic Enrichment Channels for Bone Regeneration von Wang, Xiaocheng, Yu, Yunru, Yang, Chaoyu, Shao, Changmin, Shi, Keqing, Shang, Luoran, Ye, Fangfu, Zhao, Yuanjin

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Porous scaffolds from droplet microfluidics for prevention of intrauterine adhesion von Cai, Yunlang, Wu, Fangyuan, Yu, Yunru, Liu, Yuxiao, Shao, Changmin, Gu, Hongcheng, Li, Minli, Zhao, Yuanjin

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Bioinspired Helical Micromotors as Dynamic Cell Microcarriers von Yu, Yunru, Guo, Jiahui, Wang, Yuetong, Shao, Changmin, Wang, Yu, Zhao, Yuanjin

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Organ-on-a-chip for dynamic tumor drug resistance investigation von Shao, Changmin, Yu, Yunru, Lei, Xin, Cao, Jie, Zhao, Yuanjin, Ye, Fangfu

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Polyurethane‐polypyrrole hybrid structural color films for dual‐signal mechanics sensing von Shao, Changmin, Yu, Yunru, Fan, Qihui, Wang, Xiaochen, Ye, Fangfu

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Microfluidic 3D Printing Responsive Scaffolds with Biomimetic Enrichment Channels for Bone Regeneration von Wang, Xiaocheng, Yu, Yunru, Yang, Chaoyu, Shao, Changmin, Shi, Keqing, Shang, Luoran, Ye, Fangfu, Zhao, Yuanjin

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