Clinical, genetic and imaging findings identify new causes for corpus callosum development syndromes by EDWARDS, Timothy J, SHERR, Elliott H, BARKOVICH, A. James, RICHARDS, Linda J

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Dual-Mode Modulation of Smad Signaling by Smad-Interacting Protein Sip1 Is Required for Myelination in the Central Nervous System by Weng, Qinjie, Chen, Ying, Wang, Haibo, Xu, Xiaomei, Yang, Bo, He, Qiaojun, Shou, Weinian, Chen, Yan, Higashi, Yujiro, van den Berghe, Veronique, Seuntjens, Eve, Kernie, Steven G., Bukshpun, Polina, Sherr, Elliott H., Huylebroeck, Danny, Lu, Q. Richard

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White Matter Changes of Neurite Density and Fiber Orientation Dispersion during Human Brain Maturation by Chang, Yi Shin, Owen, Julia P, Pojman, Nicholas J, Thieu, Tony, Bukshpun, Polina, Wakahiro, Mari L J, Berman, Jeffrey I, Roberts, Timothy P L, Nagarajan, Srikantan S, Sherr, Elliott H, Mukherjee, Pratik

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Pathogenic DDX3X Mutations Impair RNA Metabolism and Neurogenesis during Fetal Cortical Development by Lennox, Ashley L., Hoye, Mariah L., Jiang, Ruiji, Johnson-Kerner, Bethany L., Suit, Lindsey A., Venkataramanan, Srivats, Sheehan, Charles J., Alsina, Fernando C., Fregeau, Brieana, Aldinger, Kimberly A., Moey, Ching, Lobach, Iryna, Afenjar, Alexandra, Babovic-Vuksanovic, Dusica, Bézieau, Stéphane, Blackburn, Patrick R., Bunt, Jens, Burglen, Lydie, Campeau, Philippe M., Charles, Perrine, Chung, Brian H.Y., Cogné, Benjamin, Curry, Cynthia, D’Agostino, Maria Daniela, Di Donato, Nataliya, Faivre, Laurence, Héron, Delphine, Innes, A. Micheil, Isidor, Bertrand, Keren, Boris, Kimball, Amy, Klee, Eric W., Kuentz, Paul, Küry, Sébastien, Martin-Coignard, Dominique, Mirzaa, Ghayda, Mignot, Cyril, Miyake, Noriko, Matsumoto, Naomichi, Fujita, Atsushi, Nava, Caroline, Nizon, Mathilde, Rodriguez, Diana, Blok, Lot Snijders, Thauvin-Robinet, Christel, Thevenon, Julien, Vincent, Marie, Ziegler, Alban, Dobyns, William, Richards, Linda J., Barkovich, A. James, Floor, Stephen N., Silver, Debra L., Sherr, Elliott H.

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The variant landscape and function of DDX3X in cancer and neurodevelopmental disorders by Gadek, Margaret, Sherr, Elliott H., Floor, Stephen N.

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The role of corpus callosum development in functional connectivity and cognitive processing by Hinkley, Leighton B N, Marco, Elysa J, Findlay, Anne M, Honma, Susanne, Jeremy, Rita J, Strominger, Zoe, Bukshpun, Polina, Wakahiro, Mari, Brown, Warren S, Paul, Lynn K, Barkovich, A James, Mukherjee, Pratik, Nagarajan, Srikantan S, Sherr, Elliott H

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Ultra-rare genetic variation in common epilepsies: a case-control sequencing study by Allen, Andrew S, Bellows, Susannah T, Berkovic, Samuel F, Bridgers, Joshua, Burgess, Rosemary, Cavalleri, Gianpiero, Chung, Seo-Kyung, Cossette, Patrick, Delanty, Norman, Dlugos, Dennis, Epstein, Michael P, Freyer, Catharine, Goldstein, David B, Heinzen, Erin L, Hildebrand, Michael S, Johnson, Michael R, Kuzniecky, Ruben, Lowenstein, Daniel H, Marson, Anthony G, Mayeux, Richard, Mebane, Caroline, Mefford, Heather C, O'Brien, Terence J, Ottman, Ruth, Petrou, Steven, Petrovski, Slavgé, Pickrell, William O, Poduri, Annapurna, Radtke, Rodney A, Rees, Mark I, Regan, Brigid M, Ren, Zhong, Scheffer, Ingrid E, Sills, Graeme J, Thomas, Rhys H, Wang, Quanli, Abou-Khalil, Bassel, Alldredge, Brian K, Amrom, Dina, Andermann, Eva, Andermann, Frederick, Bautista, Jocelyn F., Bluvstein, Judith, Boro, Alex, Cascino, Gregory D, Consalvo, Damian, Crumrine, Patricia, Devinsky, Orrin, Fiol, Miguel, Fountain, Nathan B, French, Jacqueline, Friedman, Daniel, Geller, Eric B, Glauser, Tracy, Glynn, Simon, Haas, Kevin, Haut, Sheryl R, Hayward, Jean, Helmers, Sandra L, Joshi, Sucheta, Kanner, Andres, Kirsch, Heidi E, Knowlton, Robert C, Kossoff, Eric H, Kuperman, Rachel, Motika, Paul V, Novotny, Edward J, Paolicchi, Juliann M, Parent, Jack M, Park, Kristen, Sadleir, Lynette G, Shellhaas, Renée A., Sherr, Elliott H, Shih, Jerry J., Shinnar, Shlomo, Singh, Rani K, Sirven, Joseph, Smith, Michael C, Sullivan, Joseph, Thio, Liu Lin, Venkat, Anu, Vining, Eileen P.G, Von Allmen, Gretchen K, Weisenberg, Judith L, Widdess-Walsh, Peter, Winawer, Melodie R

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Early Predictors of Impaired Social Functioning in Male Rhesus Macaques (Macaca mulatta) by Sclafani, Valentina, Del Rosso, Laura A, Seil, Shannon K, Calonder, Laura A, Madrid, Jesus E, Bone, Kyle J, Sherr, Elliott H, Garner, Joseph P, Capitanio, John P, Parker, Karen J

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16p11.2 deletion syndrome by Chung, Wendy K, Roberts, Timothy PL, Sherr, Elliott H, Snyder, LeeAnne Green, Spiro, John E

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Epileptic Encephalopathies: New Genes and New Pathways by Esmaeeli Nieh, Sahar, Sherr, Elliott H.

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16p11.2 deletion and duplication: Characterizing neurologic phenotypes in a large clinically ascertained cohort by Steinman, Kyle J., Spence, Sarah J., Ramocki, Melissa B., Proud, Monica B., Kessler, Sudha K., Marco, Elysa J., Green Snyder, LeeAnne, D'Angelo, Debra, Chen, Qixuan, Chung, Wendy K., Sherr, Elliott H.

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Opposing brain differences in 16p11.2 deletion and duplication carriers by Qureshi, Abid Y, Mueller, Sophia, Snyder, Abraham Z, Mukherjee, Pratik, Berman, Jeffrey I, Roberts, Timothy P L, Nagarajan, Srikantan S, Spiro, John E, Chung, Wendy K, Sherr, Elliott H, Buckner, Randy L

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Vasopressin deficiency: a hypothesized driver of both social impairment and fluid imbalance in autism spectrum disorder by Clarke, Lauren, Gesundheit, Neil, Sherr, Elliott H., Hardan, Antonio Y., Parker, Karen J.

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Astroglial-Mediated Remodeling of the Interhemispheric Midline Is Required for the Formation of the Corpus Callosum by Gobius, Ilan, Morcom, Laura, Suárez, Rodrigo, Bunt, Jens, Bukshpun, Polina, Reardon, William, Dobyns, William B., Rubenstein, John L.R., Barkovich, A. James, Sherr, Elliott H., Richards, Linda J.

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Deletion of Tmtc4 activates the unfolded protein response and causes postnatal hearing loss by Li, Jiang, Akil, Omar, Rouse, Stephanie L, McLaughlin, Conor W, Matthews, Ian R, Lustig, Lawrence R, Chan, Dylan K, Sherr, Elliott H

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Modulating the unfolded protein response with ISRIB mitigates cisplatin ototoxicity by Li, Jiang, Rouse, Stephanie L., Matthews, Ian R., Park, Yesai, Eltawil, Yasmin, Sherr, Elliott H., Chan, Dylan K.

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De novo CLCN3 variants affecting Gly327 cause severe neurodevelopmental syndrome with brain structural abnormalities by Nakashima, Mitsuko, Argilli, Emanuela, Nakano, Sayaka, Sherr, Elliott H, Kato, Mitsuhiro, Saitsu, Hirotomo

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De novo mutations in epileptic encephalopathies by Allen, Andrew S, Berkovic, Samuel F, Cossette, Patrick, Delanty, Norman, Dlugos, Dennis, Eichler, Evan E, Epstein, Michael P, Glauser, Tracy, Goldstein, David B, Han, Yujun, Heinzen, Erin L, Hitomi, Yuki, Howell, Katherine B, Johnson, Michael R, Kuzniecky, Ruben, Lowenstein, Daniel H, Lu, Yi-Fan, Madou, Maura R Z, Marson, Anthony G, Mefford, Heather C, Esmaeeli Nieh, Sahar, O'Brien, Terence J, Ottman, Ruth, Petrovski, Slavé, Poduri, Annapurna, Ruzzo, Elizabeth K, Scheffer, Ingrid E, Sherr, Elliott H, Yuskaitis, Christopher J, Abou-Khalil, Bassel, Alldredge, Brian K, Bautista, Jocelyn F, Boro, Alex, Cascino, Gregory D, Consalvo, Damian, Crumrine, Patricia, Devinsky, Orrin, Fiol, Miguel, Fountain, Nathan B, French, Jacqueline, Friedman, Daniel, Geller, Eric B, Glynn, Simon, Haut, Sheryl R, Hayward, Jean, Helmers, Sandra L, Joshi, Sucheta, Kanner, Andres, Kirsch, Heidi E, Knowlton, Robert C, Kossoff, Eric H, Kuperman, Rachel, McGuire, Shannon M, Motika, Paul V, Novotny, Edward J, Paolicchi, Juliann M, Parent, Jack M, Park, Kristen, Shellhaas, Renée A, Shih, Jerry J, Singh, Rani, Sirven, Joseph, Smith, Michael C, Sullivan, Joseph, Lin Thio, Liu, Venkat, Anu, Vining, Eileen P G, Von Allmen, Gretchen K, Weisenberg, Judith L, Widdess-Walsh, Peter, Winawer, Melodie R

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De Novo GLI3 Pathogenic Variants May Cause Hypotonia and a Range of Brain Malformations Without Skeletal Abnormalities by Siafa, Lyna, Argilli, Emanuela, Sherr, Elliott H., Myers, Kenneth A.

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Altered structural connectivity networks in a mouse model of complete and partial dysgenesis of the corpus callosum by Edwards, Timothy J., Fenlon, Laura R., Dean, Ryan J., Bunt, Jens, Sherr, Elliott H., Richards, Linda J.

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