Preparative fractionation of oligoriboguanylates by anion-exchange chromatography on TSK DEAE-5PW von Rockstroh, H., Wangler, W., Ackermann, Th

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A Comparative Calorimetric Study on rRNA Unfolding von Schott, F J, Grubert, M, Wangler, W, Ackermann, T

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A comparative calorimetric study on trna unfolding von Schott, Franz Joachim, Grubert, Michael, Wangler, Wilhelm, Ackermann, Theodor

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A process classification framework for defining and describing Digital Fabrication with Concrete von Buswell, R.A., da Silva, W.R. Leal, Bos, F.P., Schipper, H.R., Lowke, D., Hack, N., Kloft, H., Mechtcherine, V., Wangler, T., Roussel, N.

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Loss-of-Function Variants in MYLK Cause Recessive Megacystis Microcolon Intestinal Hypoperistalsis Syndrome von 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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Lessons learned from additional research analyses of unsolved clinical exome cases von Eldomery, Mohammad K, Coban-Akdemir, Zeynep, Harel, Tamar, Rosenfeld, Jill A, Gambin, Tomasz, Stray-Pedersen, Asbjørg, Küry, Sébastien, Mercier, Sandra, Lessel, Davor, Denecke, Jonas, Wiszniewski, Wojciech, Penney, Samantha, Liu, Pengfei, Bi, Weimin, Lalani, Seema R, Schaaf, Christian P, Wangler, Michael F, Bacino, Carlos A, Lewis, Richard Alan, Potocki, Lorraine, Graham, Brett H, Belmont, John W, Scaglia, Fernando, Orange, Jordan S, Jhangiani, Shalini N, Chiang, Theodore, Doddapaneni, Harsha, Hu, Jianhong, Muzny, Donna M, Xia, Fan, Beaudet, Arthur L, Boerwinkle, Eric, Eng, Christine M, Plon, Sharon E, Sutton, V Reid, Gibbs, Richard A, Posey, Jennifer E, Yang, Yaping, Lupski, James R

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An Integrated Phenotypic and Genotypic Approach Reveals a High‐Risk Subtype Association for EBF3 Missense Variants Affecting the Zinc Finger Domain von Deisseroth, Cole A., Lerma, Vanesa C., Magyar, Christina L., Pfliger, Jessica Mae, Nayak, Aarushi, Bliss, Nathan D., LeMaire, Ashley W., Narayanan, Vinodh, Balak, Christopher, Zanni, Ginevra, Valente, Enza Maria, Bertini, Enrico, Benke, Paul J., Wangler, Michael F., Chao, Hsiao‐Tuan

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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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TNPO2 variants associate with human developmental delays, neurologic deficits, and dysmorphic features and alter TNPO2 activity in Drosophila von Goodman, Lindsey D., Cope, Heidi, Nil, Zelha, Ravenscroft, Thomas A., Charng, Wu-Lin, Lu, Shenzhao, Tien, An-Chi, Pfundt, Rolph, Koolen, David A., Haaxma, Charlotte A., Veenstra-Knol, Hermine E., Wassink-Ruiter, Jolien S. Klein, Wevers, Marijke R., Jones, Melissa, Walsh, Laurence E., Klee, Victoria H., Theunis, Miel, Legius, Eric, Steel, Dora, Barwick, Katy E.S., Kurian, Manju A., Mohammad, Shekeeb S., Dale, Russell C., Terhal, Paulien A., van Binsbergen, Ellen, Kirmse, Brian, Robinette, Bethany, Cogné, Benjamin, Isidor, Bertrand, Grebe, Theresa A., Kulch, Peggy, Hainline, Bryan E., Sapp, Katherine, Morava, Eva, Klee, Eric W., Macke, Erica L., Trapane, Pamela, Spencer, Christopher, Si, Yue, Begtrup, Amber, Moulton, Matthew J., Dutta, Debdeep, Kanca, Oguz, Wangler, Michael F., Yamamoto, Shinya, Bellen, Hugo J., Tan, Queenie K.-G.

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The recurrent de novo c.2011C>T missense variant in MTSS2 causes syndromic intellectual disability von Huang, Yan, Lemire, Gabrielle, Briere, Lauren C., Liu, Fang, Wessels, Marja W., Wang, Xueqi, Osmond, Matthew, Kanca, Oguz, Lu, Shenzhao, High, Frances A., Walker, Melissa A., Rodan, Lance H., Wangler, Michael F., Yamamoto, Shinya, Kernohan, Kristin D., Sweetser, David A., Boycott, Kym M., Bellen, Hugo J.

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A Genocentric Approach to Discovery of Mendelian Disorders von Hansen, Adam W., Murugan, Mullai, Li, He, Khayat, Michael M., Wang, Liwen, Rosenfeld, Jill, Andrews, B. Kim, Jhangiani, Shalini N., Coban Akdemir, Zeynep H., Sedlazeck, Fritz J., Ashley-Koch, Allison E., Liu, Pengfei, Muzny, Donna M., Allori, Alexander, Angrist, Misha, Ashley, Patricia, Bidegain, Margarita, Boyd, Brita, Chambers, Eileen, Cope, Heidi, Cotten, C. Michael, Curington, Theresa, Davis, Erica E., Ellestad, Sarah, Fisher, Kimberley, French, Amanda, Gallentine, William, Goldberg, Ronald, Hill, Kevin, Kansagra, Sujay, Katsanis, Nicholas, Katsanis, Sara, Kurtzberg, Joanne, Marcus, Jeffrey, McDonald, Marie, Mikati, Mohammed, Miller, Stephen, Murtha, Amy, Perilla, Yezmin, Pizoli, Carolyn, Purves, Todd, Ross, Sherry, Sadeghpour, Azita, Smith, Edward, Wiener, John, Davis, Erica E., Katsanis, Nicholas, Sabo, Aniko, Posey, Jennifer E., Yang, Yaping, Wangler, Michael F., Eng, Christine M., Sutton, V. Reid, Lupski, James R., Boerwinkle, Eric, Gibbs, Richard A.

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De novo mutations in MED13, a component of the Mediator complex, are associated with a novel neurodevelopmental disorder von Snijders Blok, Lot, Hiatt, Susan M., Bowling, Kevin M., Prokop, Jeremy W., Engel, Krysta L., Cochran, J. Nicholas, Bebin, E. Martina, Bijlsma, Emilia K., Ruivenkamp, Claudia A. L., Terhal, Paulien, Simon, Marleen E. H., Smith, Rosemarie, Hurst, Jane A., McLaughlin, Heather, Person, Richard, Crunk, Amy, Wangler, Michael F., Streff, Haley, Symonds, Joseph D., Zuberi, Sameer M., Elliott, Katherine S., Sanders, Victoria R., Masunga, Abigail, Hopkin, Robert J., Dubbs, Holly A., Ortiz-Gonzalez, Xilma R., Pfundt, Rolph, Brunner, Han G., Fisher, Simon E., Kleefstra, Tjitske, Cooper, Gregory M.

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The Epilepsy-Linked Lgi1 Protein Assembles into Presynaptic Kv1 Channels and Inhibits Inactivation by Kv beta 1 von Schulte, Uwe, Thumfart, Joerg-Oliver, Kloecker, Nikolaj, Sailer, Claudia A, Bildl, Wolfgang, Biniossek, Martin, Dehn, Doris, Deller, Thomas, Eble, Silke, Abbass, Karen, Wangler, Tanja, Knaus, Hans-Guenther, Fakler, Bernd

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Germline mutation in POLR2A: a heterogeneous, multi-systemic developmental disorder characterized by transcriptional dysregulation von Hansen, Adam W., Arora, Payal, Khayat, Michael M., Smith, Leah J., Lewis, Andrea M., Rossetti, Linda Z., Jayaseelan, Joy, Cristian, Ingrid, Haynes, Devon, DiTroia, Stephanie, Meeks, Naomi, Delgado, Mauricio R., Rosenfeld, Jill A., Pais, Lynn, White, Susan M., Meng, Qingchang, Pehlivan, Davut, Liu, Pengfei, Gingras, Marie-Claude, Wangler, Michael F., Muzny, Donna M., Lupski, James R., Kaplan, Craig D., Gibbs, Richard A.

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AHDC1 missense mutations in Xia-Gibbs syndrome von Khayat, Michael M., Hu, Jianhong, Jiang, Yunyun, Li, He, Chander, Varuna, Dawood, Moez, Hansen, Adam W., Li, Shoudong, Friedman, Jennifer, Cross, Laura, Bijlsma, Emilia K., Ruivenkamp, Claudia A.L., Sansbury, Francis H., Innis, Jeffrey W., Omark O’Shea, Jessica, Meng, Qingchang, Rosenfeld, Jill A., McWalter, Kirsty, Wangler, Michael F., Lupski, James R., Posey, Jennifer E., Murdock, David, Gibbs, Richard A.

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Visual Prediction of Bounce Trajectories von Paulun, Vivian C., Schmidt, Filipp, Bayer, Florian S., Wangler, Julia, Tenenbaum, Joshua B., Fleming, Roland W.

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Fibrochondrogenesis Results from Mutations in the COL11A1 Type XI Collagen Gene von Tompson, Stuart W., Bacino, Carlos A., Safina, Nicole P., Bober, Michael B., Proud, Virginia K., Funari, Tara, Wangler, Michael F., Nevarez, Lisette, Ala-Kokko, Leena, Wilcox, William R., Eyre, David R., Krakow, Deborah, Cohn, Daniel H.

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Conservation planning for pollinators in the U.S. Great Plains: considerations of context, treatments, and scale von Niemuth, Neal D., Wangler, Brian, LeBrun, Jaymi J., Dewald, David, Larson, Scott, Schwagler, Todd, Bradbury, Curtis W., Pritchert, Ronald D., Iovanna, Rich

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The recurrent de novo c.2011C>T missense variant in MTSS2 causes syndromic intellectual disability von Huang, Yan, Lemire, Gabrielle, Briere, Lauren C., Liu, Fang, Wessels, Marja W., Wang, Xueqi, Osmond, Matthew, Kanca, Oguz, Lu, Shenzhao, High, Frances A., Walker, Melissa A., Rodan, Lance H., Wangler, Michael F., Yamamoto, Shinya, Kernohan, Kristin D., Sweetser, David A., Boycott, Kym M., Bellen, Hugo J.

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Expanding the clinical phenotype of individuals with a 3-bp in-frame deletion of the NF1 gene (c.2970_2972del): an update of genotype–phenotype correlation von Koczkowska, Magdalena, Callens, Tom, Gomes, Alicia, Sharp, Angela, Chen, Yunjia, Hicks, Alesha D., Aylsworth, Arthur S., Azizi, Amedeo A., Basel, Donald G., Bellus, Gary, Bird, Lynne M., Blazo, Maria A., Burke, Leah W., Cannon, Ashley, Collins, Felicity, DeFilippo, Colette, Denayer, Ellen, Digilio, Maria C., Dills, Shelley K., Dosa, Laura, Greenwood, Robert S., Griffis, Cristin, Gupta, Punita, Hachen, Rachel K., Hernández-Chico, Concepción, Janssens, Sandra, Jones, Kristi J., Jordan, Justin T., Kannu, Peter, Korf, Bruce R., Lewis, Andrea M., Listernick, Robert H., Lonardo, Fortunato, Mahoney, Maurice J., Ojeda, Mayra Martinez, McDonald, Marie T., McDougall, Carey, Mendelsohn, Nancy, Miller, David T., Mori, Mari, Oostenbrink, Rianne, Perreault, Sebastién, Pierpont, Mary Ella, Piscopo, Carmelo, Pond, Dinel A., Randolph, Linda M., Rauen, Katherine A., Rednam, Surya, Rutledge, S. Lane, Saletti, Veronica, Schaefer, G. Bradley, Schorry, Elizabeth K., Scott, Daryl A., Shugar, Andrea, Siqveland, Elizabeth, Starr, Lois J., Syed, Ashraf, Trapane, Pamela L., Ullrich, Nicole J., Wakefield, Emily G., Walsh, Laurence E., Wangler, Michael F., Zackai, Elaine, Claes, Kathleen B. M., Wimmer, Katharina, van Minkelen, Rick, De Luca, Alessandro, Martin, Yolanda, Legius, Eric, Messiaen, Ludwine M.

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