Towards a therapy for Angelman syndrome by targeting a long non-coding RNA by Meng, Linyan, Ward, Amanda J, Chun, Seung, Bennett, C Frank, Beaudet, Arthur L, Rigo, Frank

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Using fetal cells for prenatal diagnosis: History and recent progress by Beaudet, Arthur L.

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Truncation of Ube3a-ATS unsilences paternal Ube3a and ameliorates behavioral defects in the Angelman syndrome mouse model by Meng, Linyan, Person, Richard Erwin, Huang, Wei, Zhu, Ping Jun, Costa-Mattioli, Mauro, Beaudet, Arthur L

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Molecular Findings Among Patients Referred for Clinical Whole-Exome Sequencing by Yang, Yaping, Muzny, Donna M, Xia, Fan, Niu, Zhiyv, Person, Richard, Ding, Yan, Ward, Patricia, Braxton, Alicia, Wang, Min, Buhay, Christian, Veeraraghavan, Narayanan, Hawes, Alicia, Chiang, Theodore, Leduc, Magalie, Beuten, Joke, Zhang, Jing, He, Weimin, Scull, Jennifer, Willis, Alecia, Landsverk, Megan, Craigen, William J, Bekheirnia, Mir Reza, Stray-Pedersen, Asbjorg, Liu, Pengfei, Wen, Shu, Alcaraz, Wendy, Cui, Hong, Walkiewicz, Magdalena, Reid, Jeffrey, Bainbridge, Matthew, Patel, Ankita, Boerwinkle, Eric, Beaudet, Arthur L, Lupski, James R, Plon, Sharon E, Gibbs, Richard A, Eng, Christine M

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Use of array CGH in the evaluation of dysmorphology, malformations, developmental delay, and idiopathic mental retardation by Stankiewicz, Pawel, Beaudet, Arthur L

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The Angelman syndrome ubiquitin ligase localizes to the synapse and nucleus, and maternal deficiency results in abnormal dendritic spine morphology by Dindot, Scott V., Antalffy, Barbara A., Bhattacharjee, Meenakshi B., Beaudet, Arthur L.

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Synaptic dysfunction and abnormal behaviors in mice lacking major isoforms of Shank3 by Wang, Xiaoming, McCoy, Portia A., Rodriguiz, Ramona M., Pan, Yanzhen, Je, H. Shawn, Roberts, Adam C., Kim, Caroline J., Berrios, Janet, Colvin, Jennifer S., Bousquet-Moore, Danielle, Lorenzo, Isabel, Wu, Gangyi, Weinberg, Richard J., Ehlers, Michael D., Philpot, Benjamin D., Beaudet, Arthur L., Wetsel, William C., Jiang, Yong-hui

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Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism by Sanders, Stephan J., Ercan-Sencicek, A. Gulhan, Hus, Vanessa, Luo, Rui, Murtha, Michael T., Moreno-De-Luca, Daniel, Chu, Su H., Moreau, Michael P., Gupta, Abha R., Thomson, Susanne A., Mason, Christopher E., Bilguvar, Kaya, Celestino-Soper, Patricia B.S., Choi, Murim, Crawford, Emily L., Davis, Lea, Davis Wright, Nicole R., Dhodapkar, Rahul M., DiCola, Michael, DiLullo, Nicholas M., Fernandez, Thomas V., Fielding-Singh, Vikram, Fishman, Daniel O., Frahm, Stephanie, Garagaloyan, Rouben, Goh, Gerald S., Kammela, Sindhuja, Klei, Lambertus, Lowe, Jennifer K., Lund, Sabata C., McGrew, Anna D., Meyer, Kyle A., Moffat, William J., Murdoch, John D., O'Roak, Brian J., Ober, Gordon T., Pottenger, Rebecca S., Raubeson, Melanie J., Song, Youeun, Wang, Qi, Yaspan, Brian L., Yu, Timothy W., Yurkiewicz, Ilana R., Beaudet, Arthur L., Cantor, Rita M., Curland, Martin, Grice, Dorothy E., Günel, Murat, Lifton, Richard P., Mane, Shrikant M., Martin, Donna M., Shaw, Chad A., Sheldon, Michael, Tischfield, Jay A., Walsh, Christopher A., Morrow, Eric M., Ledbetter, David H., Fombonne, Eric, Lord, Catherine, Martin, Christa Lese, Brooks, Andrew I., Sutcliffe, James S., Cook, Edwin H., Geschwind, Daniel, Roeder, Kathryn, Devlin, Bernie, State, Matthew W.

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Prediction of long‐term sustainability of constructed urban soil: impact of high amounts of organic matter on soil physical properties and water transfer by Cannavo, P, Vidal‐Beaudet, L, Grosbellet, C

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Altered ultrasonic vocalization and impaired learning and memory in Angelman syndrome mouse model with a large maternal deletion from Ube3a to Gabrb3 by Jiang, Yong-Hui, Pan, Yanzhen, Zhu, Li, Landa, Luis, Yoo, Jong, Spencer, Corinne, Lorenzo, Isabel, Brilliant, Murray, Noebels, Jeffrey, Beaudet, Arthur L

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Mutations in PURA Cause Profound Neonatal Hypotonia, Seizures, and Encephalopathy in 5q31.3 Microdeletion Syndrome by Lalani, Seema R., Zhang, Jing, Schaaf, Christian P., Brown, Chester W., Magoulas, Pilar, Tsai, Anne Chun-Hui, El-Gharbawy, Areeg, Wierenga, Klaas J., Bartholomew, Dennis, Fong, Chin-To, Barbaro-Dieber, Tina, Kukolich, Mary K., Burrage, Lindsay C., Austin, Elise, Keller, Kory, Pastore, Matthew, Fernandez, Fabio, Lotze, Timothy, Wilfong, Angus, Purcarin, Gabriela, Zhu, Wenmiao, Craigen, William J., McGuire, Marianne, Jain, Mahim, Cooney, Erin, Azamian, Mahshid, Bainbridge, Matthew N., Muzny, Donna M., Boerwinkle, Eric, Person, Richard E., Niu, Zhiyv, Eng, Christine M., Lupski, James R., Gibbs, Richard A., Beaudet, Arthur L., Yang, Yaping, Wang, Meng C., Xia, Fan

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The Cognitive and Behavioral Phenotypes of Individuals with CHRNA7 Duplications by Gillentine, M. A., Berry, L. N., Goin-Kochel, R. P., Ali, M. A., Ge, J., Guffey, D., Rosenfeld, J. A., Hannig, V., Bader, P., Proud, M., Shinawi, M., Graham, B. H., Lin, A., Lalani, S. R., Reynolds, J., Chen, M., Grebe, T., Minard, C. G., Stankiewicz, P., Beaudet, A. L., Schaaf, C. P.

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Large-Eddy Simulation of wind turbines wakes including geometrical effects by Benard, P., Viré, A., Moureau, V., Lartigue, G., Beaudet, L., Deglaire, P., Bricteux, L.

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Comparative analysis of single-stranded DNA donors to generate conditional null mouse alleles by Lanza, Denise G, Gaspero, Angelina, Lorenzo, Isabel, Liao, Lan, Zheng, Ping, Wang, Ying, Deng, Yu, Cheng, Chonghui, Zhang, Chuansheng, Seavitt, John R, DeMayo, Francesco J, Xu, Jianming, Dickinson, Mary E, Beaudet, Arthur L, Heaney, Jason D

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Loss-of-Function Variants in MYLK Cause Recessive Megacystis Microcolon Intestinal Hypoperistalsis Syndrome by Halim, Danny, Brosens, Erwin, Muller, Françoise, Wangler, Michael F., Beaudet, Arthur L., Lupski, James R., Akdemir, Zeynep H. Coban, Doukas, Michael, Stoop, Hans J., de Graaf, Bianca M., Brouwer, Rutger W.W., van Ijcken, Wilfred F.J., Oury, Jean-François, Rosenblatt, Jonathan, Burns, Alan J., Tibboel, Dick, Hofstra, Robert M.W., Alves, Maria M.

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A Genome-wide Association Study of Autism Using the Simons Simplex Collection: Does Reducing Phenotypic Heterogeneity in Autism Increase Genetic Homogeneity? by Chaste, Pauline, Klei, Lambertus, Sanders, Stephan J, Hus, Vanessa, Murtha, Michael T, Lowe, Jennifer K, Willsey, A. Jeremy, Moreno-De-Luca, Daniel, Yu, Timothy W, Fombonne, Eric, Geschwind, Daniel, Grice, Dorothy E, Ledbetter, David H, Mane, Shrikant M, Martin, Donna M, Morrow, Eric M, Walsh, Christopher A, Sutcliffe, James S, Lese Martin, Christa, Beaudet, Arthur L, Lord, Catherine, State, Matthew W, Cook, Edwin H, Devlin, Bernie

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The next generation of population-based spinal muscular atrophy carrier screening: comprehensive pan-ethnic SMN1 copy-number and sequence variant analysis by massively parallel seq... by Feng, Yanming, Ge, Xiaoyan, Meng, Linyan, Scull, Jennifer, Li, Jianli, Tian, Xia, Zhang, Tao, Jin, Weihong, Cheng, Hanyin, Wang, Xia, Tokita, Mari, Liu, Pengfei, Mei, Hui, Wang, Yue, Li, Fangyuan, Schmitt, Eric S, Zhang, Wei V, Muzny, Donna, Wen, Shu, Chen, Zhao, Yang, Yaping, Beaudet, Arthur L, Liu, Xiaoming, Eng, Christine M, Xia, Fan, Wong, Lee-Jun, Zhang, Jinglan

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Three-dimensional microCT imaging of mouse development from early post-implantation to early postnatal stages by Hsu, Chih-Wei, Wong, Leeyean, Rasmussen, Tara L., Kalaga, Sowmya, McElwee, Melissa L., Keith, Lance C., Bohat, Ritu, Seavitt, John R., Beaudet, Arthur L., Dickinson, Mary E.

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Evidence for feasibility of fetal trophoblastic cell-based noninvasive prenatal testing by Breman, Amy M., Chow, Jennifer C., U'Ren, Lance, Normand, Elizabeth A., Qdaisat, Sadeem, Zhao, Li, Henke, David M., Chen, Rui, Shaw, Chad A., Jackson, Laird, Yang, Yaping, Vossaert, Liesbeth, Needham, Rachel H. V., Chang, Elizabeth J., Campton, Daniel, Werbin, Jeffrey L., Seubert, Ron C., Van den Veyver, Ignatia B., Stilwell, Jackie L., Kaldjian, Eric P., Beaudet, Arthur L.

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Epigenetics and human disease by Jiang, Yong-Hui, Bressler, Jan, Beaudet, Arthur L

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