Autism genetics: opportunities and challenges for clinical translation von Vorstman, Jacob A. S., Parr, Jeremy R., Moreno-De-Luca, Daniel, Anney, Richard J. L., Nurnberger Jr, John I., Hallmayer, Joachim F.

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Vitrimeric Silicone Elastomers Enabled by Dynamic Meldrum’s Acid-Derived Cross-Links von Ishibashi, Jacob S. A, Kalow, Julia A

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The Least Stable Isomer of BN Naphthalene: Toward Predictive Trends for the Optoelectronic Properties of BN Acenes von Liu, Zhiqiang, Ishibashi, Jacob S. A, Darrigan, Clovis, Dargelos, Alain, Chrostowska, Anna, Li, Bo, Vasiliu, Monica, Dixon, David A, Liu, Shih-Yuan

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Cross-linker control of vitrimer flow von El-Zaatari, Bassil M, Ishibashi, Jacob S. A, Kalow, Julia A

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A genetics-first approach to understanding autism and schizophrenia spectrum disorders: the 22q11.2 deletion syndrome von Fiksinski, Ania M., Hoftman, Gil D., Vorstman, Jacob A. S., Bearden, Carrie E.

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Defining the Macromolecules of Tomorrow through Synergistic Sustainable Polymer Research von Haque, Farihah M, Ishibashi, Jacob S. A, Lidston, Claire A. L, Shao, Huiling, Bates, Frank S, Chang, Alice B, Coates, Geoffrey W, Cramer, Christopher J, Dauenhauer, Paul J, Dichtel, William R, Ellison, Christopher J, Gormong, Ethan A, Hamachi, Leslie S, Hoye, Thomas R, Jin, Mengyuan, Kalow, Julia A, Kim, Hee Joong, Kumar, Gaurav, LaSalle, Christopher J, Liffland, Stephanie, Lipinski, Bryce M, Pang, Yutong, Parveen, Riffat, Peng, Xiayu, Popowski, Yanay, Prebihalo, Emily A, Reddi, Yernaidu, Reineke, Theresa M, Sheppard, Daylan T, Swartz, Jeremy L, Tolman, William B, Vlaisavljevich, Bess, Wissinger, Jane, Xu, Shu, Hillmyer, Marc A

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Microfluidics-free single-cell genomics with templated emulsification von Clark, Iain C., Fontanez, Kristina M., Meltzer, Robert H., Xue, Yi, Hayford, Corey, May-Zhang, Aaron, D’Amato, Chris, Osman, Ahmad, Zhang, Jesse Q., Hettige, Pabodha, Ishibashi, Jacob S. A., Delley, Cyrille L., Weisgerber, Daniel W., Replogle, Joseph M., Jost, Marco, Phong, Kiet T., Kennedy, Vanessa E., Peretz, Cheryl A. C., Kim, Esther A., Song, Siyou, Karlon, William, Weissman, Jonathan S., Smith, Catherine C., Gartner, Zev J., Abate, Adam R.

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Two BN Isosteres of Anthracene: Synthesis and Characterization von Ishibashi, Jacob S. A, Marshall, Jonathan L, Mazière, Audrey, Lovinger, Gabriel J, Li, Bo, Zakharov, Lev N, Dargelos, Alain, Graciaa, Alain, Chrostowska, Anna, Liu, Shih-Yuan

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A framework for an evidence-based gene list relevant to autism spectrum disorder von Schaaf, Christian P., Betancur, Catalina, Yuen, Ryan K. C., Parr, Jeremy R., Skuse, David H., Gallagher, Louise, Bernier, Raphael A., Buchanan, Janet A., Buxbaum, Joseph D., Chen, Chun-An, Dies, Kira A., Elsabbagh, Mayada, Firth, Helen V., Frazier, Thomas, Hoang, Ny, Howe, Jennifer, Marshall, Christian R., Michaud, Jacques L., Rennie, Olivia, Szatmari, Peter, Chung, Wendy K., Bolton, Patrick F., Cook, Edwin H., Scherer, Stephen W., Vorstman, Jacob A. S.

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BN Tetracene: Extending the Reach of BN/CC Isosterism in Acenes von Ishibashi, Jacob S. A, Dargelos, Alain, Darrigan, Clovis, Chrostowska, Anna, Liu, Shih-Yuan

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Neurodevelopmental Trajectories and Psychiatric Morbidity: Lessons Learned From the 22q11.2 Deletion Syndrome von Fiksinski, Ania M., Schneider, Maude, Zinkstok, Janneke, Baribeau, Danielle, Chawner, Samuel J. R. A., Vorstman, Jacob A. S.

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The aromatic Claisen rearrangement of a 1,2-azaborine von Robichaud, Hannah M, Ishibashi, Jacob S. A, Ozaki, Tomoya, Lamine, Walid, Miqueu, Karinne, Liu, Shih-Yuan

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The Dewar Isomer of 1,2‐Dihydro‐1,2‐azaborinines: Isolation, Fragmentation, and Energy Storage von Edel, Klara, Yang, Xinyu, Ishibashi, Jacob S. A., Lamm, Ashley N., Maichle‐Mössmer, Cäcilia, Giustra, Zachary X., Liu, Shih‐Yuan, Bettinger, Holger F.

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Superelectrophilicity of 1,2‐Azaborine: Formation of Xenon and Carbon Monoxide Adducts von Edel, Klara, Ishibashi, Jacob S. A., Liu, Shih‐Yuan, Bettinger, Holger F.

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Executive functioning in preschoolers with 22q11.2 deletion syndrome and the impact of congenital heart defects von Everaert, Emma, Vorstman, Jacob A S, Selten, Iris S, Slieker, Martijn G, Wijnen, Frank, Boerma, Tessel D, Houben, Michiel L

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Understanding the pediatric psychiatric phenotype of 22q11.2 deletion syndrome von Fiksinski, Ania M., Schneider, Maude, Murphy, Clodagh M., Armando, Marco, Vicari, Stefano, Canyelles, Jaume M., Gothelf, Doron, Eliez, Stephan, Breetvelt, Elemi J., Arango, Celso, Vorstman, Jacob A. S.

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Rare coding variants as risk modifiers of the 22q11.2 deletion implicate postnatal cortical development in syndromic schizophrenia von Lin, Jhih-Rong, Zhao, Yingjie, Jabalameli, M. Reza, Nguyen, Nha, Mitra, Joydeep, Swillen, Ann, Vorstman, Jacob A. S., Chow, Eva W. C., van den Bree, Marianne, Emanuel, Beverly S., Vermeesch, Joris R., Owen, Michael J., Williams, Nigel M., Bassett, Anne S., McDonald-McGinn, Donna M., Gur, Raquel E., Bearden, Carrie E., Morrow, Bernice E., Lachman, Herbert M., Zhang, Zhengdong D.

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Within-family influences on dimensional neurobehavioral traits in a high-risk genetic model von Fiksinski, Ania M., Heung, Tracy, Corral, Maria, Breetvelt, Elemi J., Costain, Gregory, Marshall, Christian R., Kahn, Rene S., Vorstman, Jacob A.S., Bassett, Anne S.

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From Genes to Therapy in Autism Spectrum Disorder von Vorstman, Jacob A. S, Freitag, Christine M, Persico, Antonio M

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Bone morphogenetic proteins: Signaling periodontal bone regeneration and repair von Anusuya, G, Kandasamy, M, Jacob Raja, S, Sabarinathan, S, Ravishankar, P, Kandhasamy, Balu

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