A C–H Functionalization Protocol for the Direct Synthesis of Benzobisthiazole Derivatives by Bon, Jennifer L, Feng, Daijun, Marder, Seth R, Blakey, Simon B

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Environmental Sensitivity of Ru(II) Complexes: The Role of the Accessory Ligands by Dixon, Eileen N, Snow, Michael Z, Bon, Jennifer L, Whitehurst, Alison M, DeGraff, Benjamin A, Trindle, Carl, Demas, James N

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Human-to-monkey transfer learning identifies the frontal white matter as a key determinant for predicting monkey brain age by He, Sheng, Guan, Yi, Cheng, Chia Hsin, Moore, Tara L, Luebke, Jennifer I, Killiany, Ronald J, Rosene, Douglas L, Koo, Bang-Bon, Ou, Yangming

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YY1 Haploinsufficiency Causes an Intellectual Disability Syndrome Featuring Transcriptional and Chromatin Dysfunction by 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, Patrier, Sophie, Lynch, Sally A., Kjaergaard, Susanne, Tørring, Pernille M., Brasch-Andersen, Charlotte, Ronan, Anne, van Haeringen, Arie, Anderson, Peter J., Powis, Zöe, Brunner, Han G., Pfundt, Rolph, Schuurs-Hoeijmakers, Janneke H.M., van Bon, Bregje W.M., Lelieveld, Stefan, Gilissen, Christian, Nillesen, Willy M., Vissers, Lisenka E.L.M., Gecz, Jozef, Koolen, David A., Testa, Giuseppe, de Vries, Bert B.A.

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Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt Signaling by Snijders Blok, Lot, Madsen, Erik, Juusola, Jane, Gilissen, Christian, Baralle, Diana, Reijnders, Margot R.F., Venselaar, Hanka, Helsmoortel, Céline, Cho, Megan T., Hoischen, Alexander, Vissers, Lisenka E.L.M., Koemans, Tom S., Wissink-Lindhout, Willemijn, Eichler, Evan E., Romano, Corrado, Van Esch, Hilde, Stumpel, Connie, Vreeburg, Maaike, Smeets, Eric, Oberndorff, Karin, van Bon, Bregje W.M., Shaw, Marie, Gecz, Jozef, Haan, Eric, Bienek, Melanie, Jensen, Corinna, Loeys, Bart L., Van Dijck, Anke, Innes, A. Micheil, Racher, Hilary, Vermeer, Sascha, Di Donato, Nataliya, Rump, Andreas, Tatton-Brown, Katrina, Parker, Michael J., Henderson, Alex, Lynch, Sally A., Fryer, Alan, Ross, Alison, Vasudevan, Pradeep, Kini, Usha, Newbury-Ecob, Ruth, Chandler, Kate, Male, Alison, Dijkstra, Sybe, Schieving, Jolanda, Giltay, Jacques, van Gassen, Koen L.I., Schuurs-Hoeijmakers, Janneke, Tan, Perciliz L., Pediaditakis, Igor, Haas, Stefan A., Retterer, Kyle, Reed, Patrick, Monaghan, Kristin G., Haverfield, Eden, Natowicz, Marvin, Myers, Angela, Kruer, Michael C., Stein, Quinn, Strauss, Kevin A., Brigatti, Karlla W., Keating, Katherine, Burton, Barbara K., Kim, Katherine H., Charrow, Joel, Norman, Jennifer, Foster-Barber, Audrey, Kline, Antonie D., Kimball, Amy, Zackai, Elaine, Harr, Margaret, Fox, Joyce, McLaughlin, Julie, Lindstrom, Kristin, Haude, Katrina M., van Roozendaal, Kees, Brunner, Han, Chung, Wendy K., Kooy, R. Frank, Pfundt, Rolph, Kalscheuer, Vera, Mehta, Sarju G., Katsanis, Nicholas, Kleefstra, Tjitske

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SPEN haploinsufficiency causes a neurodevelopmental disorder overlapping proximal 1p36 deletion syndrome with an episignature of X chromosomes in females by Radio, Francesca Clementina, Ciolfi, Andrea, Levy, Michael A., Hernández-García, Andrés, Pedace, Lucia, Pantaleoni, Francesca, Liu, Zhandong, de Boer, Elke, Jackson, Adam, Bruselles, Alessandro, McConkey, Haley, Stellacci, Emilia, Lo Cicero, Stefania, Motta, Marialetizia, Carrozzo, Rosalba, McWalter, Kirsty, Desai, Megha, Monaghan, Kristin G., Telegrafi, Aida, Philippe, Christophe, Vitobello, Antonio, Au, Margaret, Grand, Katheryn, Baez, Joanne, Lindstrom, Kristin, Kulch, Peggy, Sebastian, Jessica, Madan-Khetarpal, Suneeta, Roadhouse, Chelsea, MacKenzie, Jennifer J., Monteleone, Berrin, Saunders, Carol J., Jean Cuevas, July K., Zhou, Dihong, Sawyer, Sarah L., Monteiro, Fabíola Paoli, Secches, Tania Vertemati, Kok, Fernando, Schultz-Rogers, Laura E., Morava, Eva, Klee, Eric W., Kemppainen, Jennifer, Iascone, Maria, Selicorni, Angelo, Tenconi, Romano, Pais, Lynn, Gallacher, Lyndon, Turnpenny, Peter D., Stals, Karen, Ellard, Sian, Cabet, Sara, Lesca, Gaetan, Pascal, Joset, Steindl, Katharina, Weiss, Karin, Carter, Melissa T., Kalsner, Louisa, de Vries, Bert B.A., van Bon, Bregje W., Wevers, Marijke R., Pfundt, Rolph, Stegmann, Alexander P.A., Kerr, Bronwyn, Chandler, Kate E., Sheehan, Willow, Elias, Abdallah F., Shinde, Deepali N., Towne, Meghan C., Robin, Nathaniel H., Goodloe, Dana, Vanderver, Adeline, Sherbini, Omar, Bluske, Krista, Faletra, Flavio, Musante, Luciana, Kurtz-Nelson, Evangeline C., Earl, Rachel K., Anderlid, Britt-Marie, Morin, Gilles, van Slegtenhorst, Marjon, Diderich, Karin E.M., Brooks, Alice S., Gribnau, Joost, Boers, Ruben G., Finestra, Teresa Robert, Carter, Lauren B., Rauch, Anita, Gasparini, Paolo, Boycott, Kym M., Barakat, Tahsin Stefan, Graham, John M., Faivre, Laurence, Banka, Siddharth, Wang, Tianyun, Eichler, Evan E., Dallapiccola, Bruno, Vissers, Lisenka E.L.M., Sadikovic, Bekim, Holder, Jimmy Lloyd, Tartaglia, Marco

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Single-cell RNA sequencing of neurofibromas reveals a tumor microenvironment favorable for neural regeneration and immune suppression in a neurofibromatosis type 1 porcine model by McLean, Dalton T, Meudt, Jennifer J, Lopez Rivera, Loren D, Schomberg, Dominic T, Pavelec, Derek M, Duellman, Tyler T, Buehler, Darya G, Schwartz, Patrick B, Graham, Melissa, Lee, Laura M, Graff, Keri D, Reichert, Jamie L, Bon-Durant, Sandra S, Konsitzke, Charles M, Ronnekleiv-Kelly, Sean M, Shanmuganayagam, Dhanansayan, Rubinstein, C Dustin

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De Novo Mutations in Protein Kinase Genes CAMK2A and CAMK2B Cause Intellectual Disability by Küry, Sébastien, van Woerden, Geeske M., Besnard, Thomas, Proietti Onori, Martina, Latypova, Xénia, Towne, Meghan C., Cho, Megan T., Ploeg, Melissa A., Sanders, Stephan, Stessman, Holly A.F., Pujol, Aurora, Distel, Ben, Robak, Laurie A., Bernstein, Jonathan A., Denommé-Pichon, Anne-Sophie, Lesca, Gaëtan, Sellars, Elizabeth A., Berg, Jonathan, Carré, Wilfrid, Busk, Øyvind Løvold, van Bon, Bregje W.M., Waugh, Jeff L., Deardorff, Matthew, Hoganson, George E., Bosanko, Katherine B., Johnson, Diana S., Dabir, Tabib, Holla, Øystein Lunde, Sarkar, Ajoy, Tveten, Kristian, de Bellescize, Julitta, Braathen, Geir J., Terhal, Paulien A., Grange, Dorothy K., van Haeringen, Arie, Lam, Christina, Mirzaa, Ghayda, Burton, Jennifer, Bhoj, Elizabeth J., Douglas, Jessica, Santani, Avni B., Nesbitt, Addie I., Helbig, Katherine L., Andrews, Marisa V., Begtrup, Amber, Tang, Sha, van Gassen, Koen L.I., Juusola, Jane, Foss, Kimberly, Enns, Gregory M., Moog, Ute, Hinderhofer, Katrin, Paramasivam, Nagarajan, Lincoln, Sharyn, Kusako, Brandon H., Lindenbaum, Pierre, Charpentier, Eric, Nowak, Catherine B., Cherot, Elouan, Simonet, Thomas, Ruivenkamp, Claudia A.L., Hahn, Sihoun, Brownstein, Catherine A., Xia, Fan, Schmitt, Sébastien, Deb, Wallid, Bonneau, Dominique, Nizon, Mathilde, Chelly, Jamel, Rudolf, Gabrielle, Sanlaville, Damien, Parent, Philippe, Gilbert-Dussardier, Brigitte, Toutain, Annick, Sutton, Vernon R., Thies, Jenny, Peart-Vissers, Lisenka E.L.M., Boisseau, Pierre, Vincent, Marie, Grabrucker, Andreas M., Dubourg, Christèle, Tan, Wen-Hann, Verbeek, Nienke E., Granzow, Martin, Santen, Gijs W.E., Shendure, Jay, Pasquier, Laurent, Redon, Richard, Yang, Yaping, State, Matthew W., Kleefstra, Tjitske, Cogné, Benjamin, Petrovski, Slavé, Retterer, Kyle, Eichler, Evan E., Rosenfeld, Jill A., Agrawal, Pankaj B., Bézieau, Stéphane, Odent, Sylvie, Mercier, Sandra

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Behavior Profiles at 2 Years for Children Born Extremely Preterm with Bronchopulmonary Dysplasia by Bell, Edward F., Grey, Scott F., Vohr, Betty R., Harmon, Heidi M., Logan, J. Wells, Colaizy, Tarah T., Peralta-Carcelen, Myriam A., McGowan, Elisabeth C., Stoll, Barbara J., Caplan, Michael S., Keszler, Martin, Hensman, Angelita M., Vieira, Elisa, Newman, Nancy S., Siner, Bonnie S., Pallotto, Eugenia K., Gauldin, Cheri, Holmes, Anne, Johnson, Kathy, Knutson, Allison, Schibler, Kurt, Gratton, Teresa L., Wuertz, Sandra, Adams-Chapman, Ira, Hale, Ellen C., Bottcher, Diane I., Goldberg, Ronald N., Goldstein, Ricki F., Malcolm, William F., Ashley, Patricia L., Finkle, Joanne, Bernhardt, Janice, Wilson Archer, Stephanie, Papile, Lu Ann, Hines, Abbey C., Gunn, Susan, Smiley, Lucy, Wright, Sharon L., Nelin, Leif D., Luzader, Patricia, Parikh, Nehal A., Newman, Jamie E., Leblond, David, Adams, Marian M., Huffman, Lynne C., Palmquist, Andrew W., Sankar, Meera N., Frantz, Ivan D., Fiascone, John M., Nylen, Ellen, Brussa, Ana K., Whitley, Sally, Garg, Meena, Vaucher, Yvonne E., Demetrio, Clarence, Rich, Wade, Hogden, Laurie A., Broadbent, Megan, Schmelzel, Mendi L., Walker, Jacky R., Watterberg, Kristi L., Ohls, Robin K., Backstrom Lacy, Conra, Fuller, Janell, Hanson, Mary Ruffner, Kuan, Elizabeth, Mancini, Toni, Bernbaum, Judy C., D'Angio, Carl T., Guillet, Ronnie, Lakshminrusimha, Satyan, Sacilowski, Michael G., Hunn, Julianne, Fallone, Cait, Vasil, Diana M., Chen, Lijun, De Leon, Maria M., Madden, Linda A., Sepulveda, Pollieanna, Faix, Roger G., Yoder, Bradley A., Baserga, Mariana, Bird, Karie, Burnett, Jill, Davis, Brandy, Elmont, Jennifer O., Jensen, Jennifer J., Loertscher, Manndi C., Maxson, Earl, Rau, Carrie A., Chawla, Sanjay, Bajaj, Monika, Johnson, Mary E., Wiggins, Stephanie A., Christensen, Mary K., Carlson, Martha, White, Diane F., Jacobs, Harris, Cervone, Patricia, Greisman, Sheila

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A Case Series of Familial ARID1B Variants Illustrating Variable Expression and Suggestions to Update the ACMG Criteria by van der Sluijs, Pleuntje J, Alders, Mariëlle, Dingemans, Alexander J M, Parbhoo, Kareesma, van Bon, Bregje W, Dempsey, Jennifer C, Doherty, Dan, den Dunnen, Johan T, Gerkes, Erica H, Milller, Ilana M, Moortgat, Stephanie, Regier, Debra S, Ruivenkamp, Claudia A L, Schmalz, Betsy, Smol, Thomas, Stuurman, Kyra E, Vincent-Delorme, Catherine, de Vries, Bert B A, Sadikovic, Bekim, Hickey, Scott E, Rosenfeld, Jill A, Maystadt, Isabelle, Santen, Gijs W E

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A novel hTERT promoter–driven E1A therapeutic for ovarian cancer by Xie, Xiaoming, Hsu, Jennifer L, Choi, Min-Gew, Xia, Weiya, Yamaguchi, Hirohito, Chen, Chun-Te, Trinh, Bon Q, Lu, Zhen, Ueno, Naoto T, Wolf, Judith K, Bast, Jr, Robert C, Hung, Mien-Chie

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Socioeconomic disparities in changes to preterm birth and stillbirth rates during the first year of the COVID-19 pandemic: a study of 21 European countries by Zeitlin, Jennifer, Philibert, Marianne, Barros, Henrique, Broeders, Lisa, Cap, Jan, Draušnik, Željka, Engjom, Hilde, Farr, Alex, Fresson, Jeanne, Gatt, Miriam, Gissler, Mika, Heller, Günther, Isakova, Jelena, Källén, Karin, Kyprianou, Theopisti, Loghi, Marzia, Monteath, Kirsten, Mortensen, Laust, Rihs, Tonia, Sakkeus, Luule, Sikora, Izabela, Szamotulska, Katarzyna, Velebil, Petr, Verdenik, Ivan, Weber, Guy, Zile, Irisa, Zurriaga, Oscar, Smith, Lucy

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First Reported Case of a Brodie Abscess in the Hand: A Rare Complication of a “Fight Bite” Injury by Lam, Bon, Stone, Jill P., Matthews, Jennifer L. K.

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First Reported Case of a Brodie Abscess in the Hand by Lam, Bon, Stone, Jill P, Matthews Jennifer L K

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An annotated cDNA library of juvenile Euprymna scolopes with and without colonization by the symbiont Vibrio fischeri by Chun, Carlene K, Scheetz, Todd E, Bonaldo, Maria de Fatima, Brown, Bartley, Clemens, Anik, Crookes-Goodson, Wendy J, Crouch, Keith, DeMartini, Tad, Eyestone, Mari, Goodson, Michael S, Janssens, Bernadette, Kimbell, Jennifer L, Koropatnick, Tanya A, Kucaba, Tamara, Smith, Christina, Stewart, Jennifer J, Tong, Deyan, Troll, Joshua V, Webster, Sarahrose, Winhall-Rice, Jane, Yap, Cory, Casavant, Thomas L, McFall-Ngai, Margaret J, Soares, M Bento

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