Ion Channels in Gliomas-From Molecular Basis to Treatment von Elias, Abdallah F, Lin, Bernice C, Piggott, Beverly J

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Experimental analysis of CFRP laminates subjected to compression after impact: The role of impact-induced cracks in failure von Rivallant, Samuel, Bouvet, Christophe, Abi Abdallah, Elias, Broll, Bernhard, Barrau, Jean-Jacques

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Two microcephaly-associated novel missense mutations in CASK specifically disrupt the CASK–neurexin interaction von LaConte, Leslie E. W., Chavan, Vrushali, Elias, Abdallah F., Hudson, Cynthia, Schwanke, Corbin, Styren, Katie, Shoof, Jonathan, Kok, Fernando, Srivastava, Sarika, Mukherjee, Konark

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Pathogenic variants in SQOR encoding sulfide:quinone oxidoreductase are a potentially treatable cause of Leigh disease von Friederich, Marisa W., Elias, Abdallah F., Kuster, Alice, Laugwitz, Lucia, Larson, Austin A., Landry, Aaron P., Ellwood‐Digel, Logan, Mirsky, David M., Dimmock, David, Haven, Jaclyn, Jiang, Hua, MacLean, Kenneth N., Styren, Katie, Schoof, Jonathan, Goujon, Louise, Lefrancois, Thomas, Friederich, Maike, Coughlin, Curtis R., Banerjee, Ruma, Haack, Tobias B., Van Hove, Johan L. K.

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Phenotypic spectrum of GABRA1: From generalized epilepsies to severe epileptic encephalopathies von Johannesen, Katrine, Marini, Carla, Pfeffer, Siona, Møller, Rikke S, Dorn, Thomas, Niturad, Christina, Gardella, Elena, Weber, Yvonne, Søndergård, Marianne, Hjalgrim, Helle, Nikanorova, Mariana, Becker, Felicitas, Larsen, Line H.G, Dahl, Hans A, Maier, Oliver, Mei, Davide, Biskup, Saskia, Klein, Karl M, Reif, Philipp S, Rosenow, Felix, Elias, Abdallah F, Hudson, Cindy, Helbig, Katherine L, Schubert-Bast, Susanne, Scordo, Maria R, Craiu, Dana, Djémié, Tania, Hoffman-Zacharska, Dorota, Caglayan, Hande, Helbig, Ingo, Serratosa, Jose, Striano, Pasquale, De Jonghe, Peter, Weckhuysen, Sarah, Suls, Arvid, Muru, Kai, Talvik, Inga, Talvik, Tiina, Muhle, Hiltrud, Borggraefe, Ingo, Rost, Imma, Guerrini, Renzo, Lerche, Holger, Lemke, Johannes R, Rubboli, Guido, Maljevic, Snezana

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Ensuring equity: Pharmacogenetic implementation in rural and tribal communities von Leitch, Tianna M, Killam, Shayna R, Brown, Karen E, Katseanes, Kirk C, George, Kathleen M, Schwanke, Corbin, Loveland, Joshua, Elias, Abdallah F, Haney, Kerry, Krebsbach, Kate, Muzquiz, LeeAnna I, Trinidad, Susan B, Woodahl, Erica L

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Outer-Surface Protein C of the Lyme Disease Spirochete: A Protein Induced in Ticks for Infection of Mammals von Grimm, Dorothee, Tilly, Kit, Byram, Rebecca, Stewart, Philip E., Krum, Jonathan G., Bueschel, Dawn M., Schwan, Tom G., Policastro, Paul F., Elias, Abdallah F., Rosa, Patricia A., Falkow, Stanley

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Philip D. Pallister of Montana von Opitz, John M., Mullen, Pierce, Elias, Abdallah F.

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Overrepresentation of pregnancies conceived by artificial reproductive technology in prenatally identified fetuses with Beckwith-Wiedemann syndrome von Johnson, John P., Beischel, Linda, Schwanke, Corbin, Styren, Katie, Crunk, Amy, Schoof, Jonathan, Elias, Abdallah F.

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Experimental analysis of damage creation and permanent indentation on highly oriented plates von Abdallah, Elias Abi, Bouvet, Christophe, Rivallant, Samuel, Broll, Bernhard, Barrau, Jean-Jacques

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N‐glycome analysis detects dysglycosylation missed by conventional methods in SLC39A8 deficiency von Park, Julien H., Mealer, Robert G., Elias, Abdallah F., Hoffmann, Susanne, Grüneberg, Marianne, Biskup, Saskia, Fobker, Manfred, Haven, Jaclyn, Mangels, Ute, Reunert, Janine, Rust, Stephan, Schoof, Jonathan, Schwanke, Corbin, Smoller, Jordan W., Cummings, Richard D., Marquardt, Thorsten

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O25: Strategies for equitable genetic care in underserved regions von Elias, Abdallah, Schwanke, Corbin, Sheehan, Willow, Stypka, Laura, Trout, Maija, VanPaepeghem, Brenna

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P800: Non-mosaic trisomy 9: Prenatal and fetal autopsy findings with further delineation of the clinical phenotype von Elias, Abdallah, Gordon, Michael, Holbrook, Bradley, Maher, Olivia, Poorvu, Tabitha, Schwalbe, Tammy, Trout, Maija, Wojcik, Monica, Zearfoss, Amy

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Clonal Polymorphism of Borrelia burgdorferi Strain B31 MI: Implications for Mutagenesis in an Infectious Strain Background von ELIAS, Abdallah F, STEWART, Philip E, ROSA, Patricia, GRIMM, Dorothee, CAIMANO, Melissa J, EGGERS, Christian H, TILLY, Kit, BONO, James L, AKINS, Darrin R, RADOLF, Justin D, SCHWAN, Tom G

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Second Pallister-Opitz Genetics Symposium, Helena, Montana, July 2015 von Elias, Abdallah F., Opitz, John M.

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P775: Maternally inherited 11p15 duplication involving only part of the ICR1 H19/IGF2 domain: Unraveling mild Russell-Silver syndrome phenotype von Thomas-Wilson, Amanda, Harkavy, Nina, Schwanke, Corbin, Schoof, Jonathan, Srinivasa, Sowmya Thirumalai, Guha, Saurav, Rehman, Atteeq, Okur, Volkan, Giordano, Jessica, Elias, Abdallah, Wapner, Ronald, Jobanputra, Vaidehi

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A Quality Improvement Collaborative to Improve Pediatric Primary Care Genetic Services von Rinke, Michael L, Driscoll, Amy, Mikat-Stevens, Natalie, Healy, Jill, Colantuoni, Elizabeth, Elias, Abdallah F, Pletcher, Beth A, Gubernick, Ruth S, Larson, Ingrid, Chung, Wendy K, Tarini, Beth A

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Confirmation of 6q21-6q22.1 deletion in Acro-cardio-facial syndrome and further delineation of this contiguous gene deletion syndrome von Hudson, Cindy, Schwanke, Corbin, Johnson, John P., Elias, Abdallah F., Phillips, Sandy, Schwalbe, Tammy, Tunby, Mary, Xu, Dongbin

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Profiling of Temperature-Induced Changes in Borrelia burgdorferi Gene Expression by Using Whole Genome Arrays von OJAIMI, Caroline, BROOKS, Chad, CAIMANO, Melissa, SKARE, Jon, SWINGLE, Kristen, AKINS, Darrin, SCHWARTZ, Ira, CASJENS, Sherwood, ROSA, Patricia, ELIAS, Abdallah, BARBOUR, Alan, JASINSKAS, Algis, BENACH, Jorge, KATONA, Laura, RADOLF, Justin

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Experimental Assessment of the Roles of Linear Plasmids lp25 and lp28-1 of Borrelia burgdorferi throughout the Infectious Cycle von GRIMM, Dorothee, EGGERS, Christian H, CAIMANO, Melissa J, TILLY, Kit, STEWART, Philip E, ELIAS, Abdallah F, RADOLF, Justin D, ROSA, Patricia A

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