Rescue of dendritic spine phenotype in Fmr1 KO mice with the mGluR5 antagonist AFQ056/Mavoglurant by Pop, Andreea S., Levenga, Josien, de Esch, Celine E. F., Buijsen, Ronald A. M., Nieuwenhuizen, Ingeborg M., Li, Tracy, Isaacs, Aaron, Gasparini, Fabrizio, Oostra, Ben A., Willemsen, Rob

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Chronic administration of AFQ056/Mavoglurant restores social behaviour in Fmr1 knockout mice by Gantois, Ilse, Pop, Andreea S., de Esch, Celine E.F., Buijsen, Ronald A.M., Pooters, Tine, Gomez-Mancilla, Baltazar, Gasparini, Fabrizio, Oostra, Ben A., D’Hooge, Rudi, Willemsen, Rob

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A novel fragile X syndrome mutation reveals a conserved role for the carboxy‐terminus in FMRP localization and function by Okray, Zeynep, de Esch, Celine EF, Van Esch, Hilde, Devriendt, Koen, Claeys, Annelies, Yan, Jiekun, Verbeeck, Jelle, Froyen, Guy, Willemsen, Rob, de Vrij, Femke MS, Hassan, Bassem A

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Translational endpoints in fragile X syndrome by de Esch, Celine E F, Zeidler, Shimriet, Willemsen, Rob

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Transcriptional consequences of MBD5 disruption in mouse brain and CRISPR-derived neurons by Seabra, Catarina M, Aneichyk, Tatsiana, Erdin, Serkan, Tai, Derek J C, De Esch, Celine E F, Razaz, Parisa, An, Yu, Manavalan, Poornima, Ragavendran, Ashok, Stortchevoi, Alexei, Abad, Clemer, Young, Juan I, Maciel, Patricia, Talkowski, Michael E, Gusella, James F

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Locomotor activity assay in zebrafish larvae: Influence of age, strain and ethanol by de Esch, Celine, van der Linde, Herma, Slieker, Roderick, Willemsen, Rob, Wolterbeek, André, Woutersen, Ruud, De Groot, Didima

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Tissue- and cell-type-specific molecular and functional signatures of 16p11.2 reciprocal genomic disorder across mouse brain and human neuronal models by Tai, Derek J.C., Razaz, Parisa, Erdin, Serkan, Gao, Dadi, Wang, Jennifer, Nuttle, Xander, de Esch, Celine E., Collins, Ryan L., Currall, Benjamin B., O’Keefe, Kathryn, Burt, Nicholas D., Yadav, Rachita, Wang, Lily, Mohajeri, Kiana, Aneichyk, Tatsiana, Ragavendran, Ashok, Stortchevoi, Alexei, Morini, Elisabetta, Ma, Weiyuan, Lucente, Diane, Hastie, Alex, Kelleher, Raymond J., Perlis, Roy H., Talkowski, Michael E., Gusella, James F.

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Epigenetic Characterization of the FMR1 Promoter in Induced Pluripotent Stem Cells from Human Fibroblasts Carrying an Unmethylated Full Mutation by de Esch, Celine E.F., Ghazvini, Mehrnaz, Loos, Friedemann, Schelling-Kazaryan, Nune, Widagdo, W., Munshi, Shashini T., van der Wal, Erik, Douben, Hannie, Gunhanlar, Nilhan, Kushner, Steven A., Pijnappel, W.W.M. Pim, de Vrij, Femke M.S., Geijsen, Niels, Gribnau, Joost, Willemsen, Rob

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Paradoxical effect of baclofen on social behavior in the fragile X syndrome mouse model by Zeidler, Shimriet, Pop, Andreea S., Jaafar, Israa A., Boer, Helen, Buijsen, Ronald A. M., Esch, Celine E. F., Nieuwenhuizen‐Bakker, Ingeborg, Hukema, Renate K., Willemsen, Rob

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Delay and impairment in brain development and function in rat offspring after maternal exposure to methylmercury by Radonjic, Marijana, Cappaert, Natalie L M, de Vries, Erik F J, de Esch, Celine E F, Kuper, Frieke C, van Waarde, Aren, Dierckx, Rudi A J O, Wadman, Wytse J, Wolterbeek, André P M, Stierum, Rob H, de Groot, Didima M G

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Convergent coexpression of autism-associated genes suggests some novel risk genes may not be detectable in large-scale genetic studies by Liao, Calwing, Moyses-Oliveira, Mariana, De Esch, Celine E.F., Bhavsar, Riya, Nuttle, Xander, Li, Aiqun, Yu, Alex, Burt, Nicholas D., Erdin, Serkan, Fu, Jack M., Wang, Minghui, Morley, Theodore, Han, Lide, Dion, Patrick A., Rouleau, Guy A., Zhang, Bin, Brennand, Kristen J., Talkowski, Michael E., Ruderfer, Douglas M.

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Tissue- and cell-type-specific molecular and functional signatures of 16p11.2 reciprocal genomic disorder across mouse brain and human neuronal models by Tai, Derek J.C., Razaz, Parisa, Erdin, Serkan, Gao, Dadi, Wang, Jennifer, Nuttle, Xander, de Esch, Celine E., Collins, Ryan L., Currall, Benjamin B., O’Keefe, Kathryn, Burt, Nicholas D., Yadav, Rachita, Wang, Lily, Mohajeri, Kiana, Aneichyk, Tatsiana, Ragavendran, Ashok, Stortchevoi, Alexei, Morini, Elisabetta, Ma, Weiyuan, Lucente, Diane, Hastie, Alex, Kelleher, Raymond J., Perlis, Roy H., Talkowski, Michael E., Gusella, James F.

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Loss of MAGEL2 in Prader-Willi syndrome leads to decreased secretory granule and neuropeptide production by Chen, Helen, Victor, A Kaitlyn, Klein, Jonathon, Tacer, Klementina Fon, Tai, Derek Jc, de Esch, Celine, Nuttle, Alexander, Temirov, Jamshid, Burnett, Lisa C, Rosenbaum, Michael, Zhang, Yiying, Ding, Li, Moresco, James J, Diedrich, Jolene K, Yates, 3rd, John R, Tillman, Heather S, Leibel, Rudolph L, Talkowski, Michael E, Billadeau, Daniel D, Reiter, Lawrence T, Potts, Patrick Ryan

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P159: Variants in cohesin release factors WAPL, PDS5A, and PDS5B define a new class of cohesinopathies by Boone, Philip, Faour, Kamli, Mohajeri, Kiana, Lemanski, John, Jana, Bimal, Fu, Jack, Kerkhof, Jennifer, McConkey, Haley, Collins, Ryan, Lucente, Diane, de Esch, Celine, Moysés-Oliveira, Mariana, Nuttle, Alexander, Domingo, Aloysius, Erdin, Serkan, Hanley, Maris, Watt, Amy, Surette, Eric, Lima, Gloria, Smith, Laura, Salani, Monica, Yadav, Rachita, Harripaul, Ricardo, O’Keefe, Kathryn, Burt, Nicholas, Larson, Matthew, Bhavsar, Riya, Currall, Benjamin, Sell, Susan, Ladda, Roger, Immken, LaDonna, Buchanan, Catherine, Yuan, Bo, Lynch, Sally, Gilissen, Christian, Pfundt, Rolph, Ockeloen, Charlotte, Kleefstra, Tjitske, Vanhoutte, Els, Sinnema, Margje, Stegmann, Sander, Stevens, Servi, Iascone, Maria, Maitz, Silvia, Cogne, Benjamin, Le Caignec, Cedric, Vincent, Marie, Nizon, Mathilde, Male, Alison, Agrawal, Pankaj, Thompson, Michelle, Torring, Pernille, Brasch-Andersen, Charlotte, Faivre, Laurence, Bruel, Ange-Line, Isidor, Bertrand, Philippe, Christophe, Morleo, Manuela, Wojcik, Monica, Genetti, Casie, Srivastava, Siddharth, Ballal, Sonia, Schließke, Sophia, Jamra, Rami Abou, Delahaye, Andree, von Wintzingerode, Lydia, Bothe, Viktoria, Houlier, Marine, Stout, Timothy, Bergant, Gaber, Peterlin, Borut, Moldovan, Oana, Martínez-Gil, Núria, Argilli, Emanuela, Sherr, Elliott, Harel, Tamar, Rosenberg-Fogler, Hallel, Rosenfeld, Jill, Wentzensen, Ingrid, Westphal, Dominik, Riedhammer, Korbinian, Orec, Laura, Gusella, James, Sadikovic, Bekim, Tai, Derek, Talkowski, Michael

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Zebrafish as potential model for developmental neurotoxicity testing: A mini review by DE ESCH, Celine, SLIEKER, Roderick, WOLTERBEEK, Andre, WOUTERSEN, Ruud, DE GROOT, Didima

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Beyond the exome: What’s next in diagnostic testing for Mendelian conditions by Wojcik, Monica H., Reuter, Chloe M., Marwaha, Shruti, Mahmoud, Medhat, Duyzend, Michael H., Barseghyan, Hayk, Yuan, Bo, Boone, Philip M., Groopman, Emily E., Délot, Emmanuèle C., Jain, Deepti, Sanchis-Juan, Alba, Starita, Lea M., Talkowski, Michael, Montgomery, Stephen B., Bamshad, Michael J., Chong, Jessica X., Wheeler, Matthew T., Berger, Seth I., O'Donnell-Luria, Anne, Sedlazeck, Fritz J., Miller, Danny E.

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Positioning of leukocyte subsets in the portal and lobular compartments of hepatitis C virus-infected liver correlates with local chemokine expression by Nguyen, Nam, de Esch, Celine, Cameron, Barbara, Kumar, Rakesh K, Zekry, Amany, Lloyd, Andrew R

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Perinatal exposure to the immune-suppressant di-n-octyltin dichloride affects brain development in rats by de Groot, Didima M G, Linders, Louisa, Kayser, Reinier, Nederlof, Rianne, de Esch, Celine, Slieker, Roderick C, Kuper, C Frieke, Wolterbeek, Andre, de Groot, V Jeroen, Veltien, Andor, Heerschap, Arend, van Waarde, Aren, Dierckx, Rudi A J O, de Vries, Erik F J

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CXorf56, a dendritic neuronal protein, identified as a new candidate gene for X-linked intellectual disability by Verkerk, Annemieke J M H, Zeidler, Shimriet, Breedveld, Guido, Overbeek, Lydia, Huigh, Daphne, Koster, Linda, van der Linde, Herma, de Esch, Celine, Severijnen, Lies-Anne, de Vries, Bert B A, Swagemakers, Sigrid M A, Willemsen, Rob, Hoogeboom, A Jeannette M, van der Spek, Peter J, Oostra, Ben A

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Zebrafish as potential model for developmental neurotoxicity testing by de Esch, Celine, Slieker, Roderick, Wolterbeek, André, Woutersen, Ruud, de Groot, Didima

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