De novo variants in EBF3 are associated with hypotonia, developmental delay, intellectual disability, and autism by Tanaka, Akemi J, Cho, Megan T, Willaert, Rebecca, Retterer, Kyle, Zarate, Yuri A, Bosanko, Katie, Stefans, Vikki, Oishi, Kimihiko, Williamson, Amy, Wilson, Golder N, Basinger, Alice, Barbaro-Dieber, Tina, Ortega, Lucia, Sorrentino, Susanna, Gabriel, Melissa K, Anderson, Ilse J, Sacoto, Maria J Guillen, Schnur, Rhonda E, Chung, Wendy K

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CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language by Snijders Blok, Lot, Rousseau, Justine, Twist, Joanna, Ehresmann, Sophie, Takaku, Motoki, Venselaar, Hanka, Rodan, Lance H, Nowak, Catherine B, Douglas, Jessica, Swoboda, Kathryn J, Steeves, Marcie A, Sahai, Inderneel, Stumpel, Connie T R M, Stegmann, Alexander P A, Wheeler, Patricia, Willing, Marcia, Fiala, Elise, Kochhar, Aaina, Gibson, William T, Cohen, Ana S A, Agbahovbe, Ruky, Innes, A Micheil, Au, P Y Billie, Rankin, Julia, Anderson, Ilse J, Skinner, Steven A, Louie, Raymond J, Warren, Hannah E, Afenjar, Alexandra, Keren, Boris, Nava, Caroline, Buratti, Julien, Isapof, Arnaud, Rodriguez, Diana, Lewandowski, Raymond, Propst, Jennifer, van Essen, Ton, Choi, Murim, Lee, Sangmoon, Chae, Jong H, Price, Susan, Schnur, Rhonda E, Douglas, Ganka, Wentzensen, Ingrid M, Zweier, Christiane, Reis, André, Bialer, Martin G, Moore, Christine, Koopmans, Marije, Brilstra, Eva H, Monroe, Glen R, van Gassen, Koen L I, van Binsbergen, Ellen, Newbury-Ecob, Ruth, Bownass, Lucy, Bader, Ingrid, Mayr, Johannes A, Wortmann, Saskia B, Jakielski, Kathy J, Strand, Edythe A, Kloth, Katja, Bierhals, Tatjana, Roberts, John D, Petrovich, Robert M, Machida, Shinichi, Kurumizaka, Hitoshi, Lelieveld, Stefan, Pfundt, Rolph, Jansen, Sandra, Deriziotis, Pelagia, Faivre, Laurence, Thevenon, Julien, Assoum, Mirna, Shriberg, Lawrence, Kleefstra, Tjitske, Brunner, Han G, Wade, Paul A, Fisher, Simon E, Campeau, Philippe M

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De novo variants in FBXO11 cause a syndromic form of intellectual disability with behavioral problems and dysmorphisms by Jansen, Sandra, van der Werf, Ilse M, Innes, A Micheil, Afenjar, Alexandra, Agrawal, Pankaj B, Anderson, Ilse J, Atwal, Paldeep S, van Binsbergen, Ellen, van den Boogaard, Marie-José, Castiglia, Lucia, Coban-Akdemir, Zeynep H, van Dijck, Anke, Doummar, Diane, van Eerde, Albertien M, van Essen, Anthonie J, van Gassen, Koen L, Guillen Sacoto, Maria J, van Haelst, Mieke M, Iossifov, Ivan, Jackson, Jessica L, Judd, Elizabeth, Kaiwar, Charu, Keren, Boris, Klee, Eric W, Klein Wassink-Ruiter, Jolien S, Meuwissen, Marije E, Monaghan, Kristin G, de Munnik, Sonja A, Nava, Caroline, Ockeloen, Charlotte W, Pettinato, Rosa, Racher, Hilary, Rinne, Tuula, Romano, Corrado, Sanders, Victoria R, Schnur, Rhonda E, Smeets, Eric J, Stegmann, Alexander P A, Stray-Pedersen, Asbjørg, Sweetser, David A, Terhal, Paulien A, Tveten, Kristian, VanNoy, Grace E, de Vries, Petra F, Waxler, Jessica L, Willing, Marcia, Pfundt, Rolph, Veltman, Joris A, Kooy, R Frank, Vissers, Lisenka E L M, de Vries, Bert B A

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New Directions in Cytogenetic and Molecular Testing of the Neonate by Anderson, Ilse J., Matteson, Karla J.

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Variants in TCF20 in neurodevelopmental disability: description of 27 new patients and review of literature by Torti, Erin, Keren, Boris, Palmer, Elizabeth E., Zhu, Zehua, Afenjar, Alexandra, Anderson, Ilse. J., Andrews, Marisa V., Atkinson, Celia, Au, Margaret, Berry, Susan A., Bowling, Kevin M., Boyle, Jackie, Buratti, Julien, Cathey, Sara S., Charles, Perrine, Cogne, Benjamin, Courtin, Thomas, Escobar, Luis F., Finley, Sabra Ledare, Graham, John M., Grange, Dorothy K., Heron, Delphine, Hewson, Stacy, Hiatt, Susan M., Hibbs, Kathleen A., Jayakar, Parul, Kalsner, Louisa, Larcher, Lise, Lesca, Gaetan, Mark, Paul R., Miller, Kathryn, Nava, Caroline, Nizon, Mathilde, Pai, G. Shashidhar, Pappas, John, Parsons, Gretchen, Payne, Katelyn, Putoux, Audrey, Rabin, Rachel, Sabatier, Isabelle, Shinawi, Marwan, Shur, Natasha, Skinner, Steven A., Valence, Stephanie, Warren, Hannah, Whalen, Sandra, Crunk, Amy, Douglas, Ganka, Monaghan, Kristin G., Person, Richard E., Willaert, Rebecca, Solomon, Benjamin D., Juusola, Jane

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Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language by Snijders Blok, Lot, Rousseau, Justine, Twist, Joanna, Ehresmann, Sophie, Takaku, Motoki, Venselaar, Hanka, Rodan, Lance H, Nowak, Catherine B, Douglas, Jessica, Swoboda, Kathryn J, Steeves, Marcie A, Sahai, Inderneel, Stumpel, Connie T R M, Stegmann, Alexander P A, Wheeler, Patricia, Willing, Marcia, Fiala, Elise, Kochhar, Aaina, Gibson, William T, Cohen, Ana S A, Agbahovbe, Ruky, Innes, A Micheil, Au, P Y Billie, Rankin, Julia, Anderson, Ilse J, Skinner, Steven A, Louie, Raymond J, Warren, Hannah E, Afenjar, Alexandra, Keren, Boris, Nava, Caroline, Buratti, Julien, Isapof, Arnaud, Rodriguez, Diana, Lewandowski, Raymond, Propst, Jennifer, van Essen, Ton, Choi, Murim, Lee, Sangmoon, Chae, Jong H, Price, Susan, Schnur, Rhonda E, Douglas, Ganka, Wentzensen, Ingrid M, Zweier, Christiane, Reis, André, Bialer, Martin G, Moore, Christine, Koopmans, Marije, Brilstra, Eva H, Monroe, Glen R, van Gassen, Koen L I, van Binsbergen, Ellen, Newbury-Ecob, Ruth, Bownass, Lucy, Bader, Ingrid, Mayr, Johannes A, Wortmann, Saskia B, Jakielski, Kathy J, Strand, Edythe A, Kloth, Katja, Bierhals, Tatjana, Roberts, John D, Petrovich, Robert M, Machida, Shinichi, Kurumizaka, Hitoshi, Lelieveld, Stefan, Pfundt, Rolph, Jansen, Sandra, Deriziotis, Pelagia, Faivre, Laurence, Thevenon, Julien, Assoum, Mirna, Shriberg, Lawrence, Kleefstra, Tjitske, Brunner, Han G, Wade, Paul A, Fisher, Simon E, Campeau, Philippe M

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Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language by Blok, Lot Snijders, Rousseau, Justine, Twist, Joanna, Ehresmann, Sophie, Takaku, Motoki, Venselaar, Hanka, Rodan, Lance H, Nowak, Catherine B, Douglas, Jessica, Swoboda, Kathryn J, Steeves, Marcie A, Sahai, Inderneel, Stumpel, Connie T R M, Stegmann, Alexander P A, Wheeler, Patricia, Willing, Marcia, Fiala, Elise, Kochhar, Aaina, Gibson, William T, Cohen, Ana S A, Agbahovbe, Ruky, Innes, A Micheil, Au, P Y Billie, Rankin, Julia, Anderson, Ilse J, Skinner, Steven A, Louie, Raymond J, Warren, Hannah E, Afenjar, Alexandra, Keren, Boris, Nava, Caroline, Buratti, Julien, Isapof, Arnaud, Rodriguez, Diana, Lewandowski, Raymond, Propst, Jennifer, van Essen, Ton, Choi, Murim, Lee, Sangmoon, Chae, Jong H, Price, Susan, Schnur, Rhonda E, Douglas, Ganka, Wentzensen, Ingrid M, Zweier, Christiane, Reis, André, Bialer, Martin G, Moore, Christine, Koopmans, Marije, Brilstra, Eva H, Monroe, Glen R, van Gassen, Koen L I, van Binsbergen, Ellen, Newbury-Ecob, Ruth, Bownass, Lucy, Bader, Ingrid, Mayr, Johannes A, Wortmann, Saskia B, Jakielski, Kathy J, Strand, Edythe A, Kloth, Katja, Bierhals, Tatjana, Roberts, John D, Petrovich, Robert M, Machida, Shinichi, Kurumizaka, Hitoshi, Lelieveld, Stefan, Pfundt, Rolph, Jansen, Sandra, Deriziotis, Pelagia, Faivre, Laurence, Thevenon, Julien, Assoum, Mirna, Shriberg, Lawrence, Kleefstra, Tjitske, Brunner, Han G, Wade, Paul A, Fisher, Simon E, Campeau, Philippe M

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Mutation detection in an equivocal case of Friedreich’s ataxia by Potter, Nicholas T, Miller, Christopher A, Anderson, Ilse J

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Spondyloepiphyseal dysplasia congenita : genetic linkage to type II collagen (COL2AI) by ANDERSON, I. J, GOLDBERG, R. B, MARION, R. W, UPHOLT, W. B, TSIPOURAS, P

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Predicting beef tenderness using color and multispectral image texture features by Sun, X., Chen, K.J., Maddock-Carlin, K.R., Anderson, V.L., Lepper, A.N., Schwartz, C.A., Keller, W.L., Ilse, B.R., Magolski, J.D., Berg, E.P.

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The high optical brightness of the BlueWalker 3 satellite by Nandakumar, Sangeetha, Eggl, Siegfried, Tregloan-Reed, Jeremy, Adam, Christian, Anderson-Baldwin, Jasmine, Bannister, Michele T., Battle, Adam, Benkhaldoun, Zouhair, Campbell, Tanner, Colque, J. P., Damke, Guillermo, Plauchu Frayn, Ilse, Ghachoui, Mourad, Guillen, Pedro F., Kaeouach, Aziz Ettahar, Krantz, Harrison R., Langbroek, Marco, Rattenbury, Nicholas, Reddy, Vishnu, Ridden-Harper, Ryan, Young, Brad, Unda-Sanzana, Eduardo, Watson, Alan M., Walker, Constance E., Barentine, John C., Benvenuti, Piero, Di Vruno, Federico, Peel, Mike W., Rawls, Meredith L., Bassa, Cees, Flores-Quintana, Catalina, García, Pablo, Kim, Sam, Longa-Peña, Penélope, Ortiz, Edgar, Otarola, Ángel, Romero-Colmenares, María, Sanhueza, Pedro, Siringo, Giorgio, Soto, Mario

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ROCK signaling promotes collagen remodeling to facilitate invasive pancreatic ductal adenocarcinoma tumor cell growth by Rath, Nicola, Morton, Jennifer P, Julian, Linda, Helbig, Lena, Kadir, Shereen, McGhee, Ewan J, Anderson, Kurt I, Kalna, Gabriela, Mullin, Margaret, Pinho, Andreia V, Rooman, Ilse, Samuel, Michael S, Olson, Michael F

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Dementia Prevention Research Clinic: a longitudinal study investigating factors influencing the development of Alzheimer's disease in Aotearoa, New Zealand by Tippett, Lynette J., Cawston, Erin E., Morgan, Catherine A., Melzer, Tracy R., Brickell, Kiri L., Ilse, Christina, Cheung, Gary, Kirk, Ian J., Roberts, Reece P., Govender, Jane, Griner, Leon, Le Heron, Campbell, Buchanan, Sarah, Port, Waiora, Dudley, Makarena, Anderson, Tim J., Williams, Joanna M., Cutfield, Nicholas J., Dalrymple-Alford, John C., Wood, Phil

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Effects of increasing field pea (Pisum sativum) level in high-concentrate diets on growth performance and carcass traits in finishing steers and heifers by Lardy, G.P, Loken, B.A, Anderson, V.L, Larson, D.M, Maddock-Carlin, K.R, Ilse, B.R, Maddock, R, Leupp, J.L, Clark, R, Paterson, J.A, Bauer, M.L

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Understanding the long‐term risks of neutering dogs

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The congenital great toe malformation of fibrodysplasia ossificans progressiva? - A close call by Towler, O. Will, Shore, Eileen M, Xu, Meiqi, Bamford, Abbey, Anderson, Ilse, Pignolo, Robert J, Kaplan, Frederick S

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Automated image analysis of cytokinesis-blocked micronuclei: an adapted protocol and a validated scoring procedure for biomonitoring by Decordier, Ilse, Papine, Alexander, Plas, Gina, Roesems, Sam, Vande Loock, Kim, Moreno-Palomo, Jennifer, Cemeli, Eduardo, Anderson, Diana, Fucic, Aleksandra, Marcos, Ricardo, Soussaline, Françoise, Kirsch-Volders, Micheline

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Proximal microdeletions and microduplications of 1q21.1 contribute to variable abnormal phenotypes by Rosenfeld, Jill A, Traylor, Ryan N, Schaefer, G Bradley, McPherson, Elizabeth W, Ballif, Blake C, Klopocki, Eva, Mundlos, Stefan, Shaffer, Lisa G, Aylsworth, Arthur S

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Abstract C22: ROCK kinases drive invasive pancreatic tumor growth by Rath, Nicola, Kadir, Shereen, Morton, Jennifer P., Pinho, Andreia V., Helbig, Lena, Julian, Linda, McGhee, Ewan J., Kalna, Gabriela, Vazquez, Alexei, Anderson, Kurt I., Rooman, Ilse, Samuel, Michael S., Olson, Michael F.

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LOFAR: Recent Imaging Results and Future Prospects by Heald, George, Bell, Michael R., Horneffer, Andreas, Offringa, André R., Pizzo, Roberto, van der Tol, Sebastiaan, van Weeren, Reinout J., van Zwieten, Joris E., Anderson, James M., Beck, Rainer, van Bemmel, Ilse, Bîrzan, Laura, Bonafede, Annalisa, Conway, John, Ferrari, Chiara, De Gasperin, Francesco, Haverkorn, Marijke, Jackson, Neal, Macario, Giulia, McKean, John, Miraghaei, Halime, Orrù, Emanuela, Rafferty, David, Röttgering, Huub, Scaife, Anna, Shulevski, Aleksandar, Sotomayor, Carlos, Tasse, Cyril, Trasatti, Monica, Wucknitz, Olaf

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