The Collaborative Literacy Coaching Framework for Transformation: Humanizing Prerequisites for Reflective Practitioners von Caylor, Emily C.

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Enhanced thermoelectric performance in PbTe-based superlattice structures from reduction of lattice thermal conductivity von Caylor, J. C., Coonley, K., Stuart, J., Colpitts, T., Venkatasubramanian, R.

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Nonrandom X Chromosome Inactivation Detection von Caylor, Raymond C.

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The Caenorhabditis elegans voltage-gated calcium channel subunits UNC-2 and UNC-36 and the calcium-dependent kinase UNC-43/CaMKII regulate neuromuscular junction morphology von Caylor, Raymond C, Jin, Yishi, Ackley, Brian D

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Analysis of X‐inactivation status in a Rett syndrome natural history study cohort von Fang, Xiaolan, Butler, Kameryn M., Abidi, Fatima, Gass, Jennifer, Beisang, Arthur, Feyma, Timothy, Ryther, Robin C., Standridge, Shannon, Heydemann, Peter, Jones, Mary, Haas, Richard, Lieberman, David N, Marsh, Eric D., Benke, Tim A., Skinner, Steve, Neul, Jeffrey L., Percy, Alan K., Friez, Michael J., Caylor, Raymond C.

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HSD10 disease in a female: A case report and review of literature von Upadia, Jariya, Walano, Nicolette, Noh, Grace S., Liu, Jiao, Li, Yuwen, Deputy, Stephen, Elliott, Lindsay T., Wong, Joaquin, Lee, Jennifer A., Caylor, Raymond C., Andersson, Hans C.

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Sound Velocity and Elasticity of Tetragonal Lysozyme Crystals by Brillouin Spectroscopy von Speziale, S., Jiang, F., Caylor, C.L., Kriminski, S., Zha, C.-S., Thorne, R.E., Duffy, T.S.

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Flash-cooling and annealing of protein crystals von Kriminski, S., Caylor, C. L., Nonato, M. C., Finkelstein, K. D., Thorne, R. E.

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Identification of a DNA methylation signature for Renpenning syndrome (RENS1), a spliceopathy von Haghshenas, Sadegheh, Foroutan, Aidin, Bhai, Pratibha, Levy, Michael A, Relator, Raissa, Kerkhof, Jennifer, McConkey, Haley, Skinner, Cindy D, Caylor, Raymond C, Tedder, Matthew L, Stevenson, Roger E, Sadikovic, Bekim, Schwartz, Charles E

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Round-robin measurements of two candidate materials for a Seebeck coefficient Standard Reference Material von Lowhorn, N. D., Wong-Ng, W., Zhang, W., Lu, Z. Q., Otani, M., Thomas, E., Green, M., Tran, T. N., Dilley, N., Ghamaty, S., Elsner, N., Hogan, T., Downey, A. D., Jie, Q., Li, Q., Obara, H., Sharp, J., Caylor, C., Venkatasubramanian, R., Willigan, R., Yang, J., Martin, J., Nolas, G., Edwards, B., Tritt, T.

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Clinical case report: mosaic ANK3 pathogenic variant in a patient with autism spectrum disorder and neurodevelopmental delay von Fang, Xiaolan, Fee, Timothy, Davis, Jessica, Stolerman, Elliot S, Caylor, Raymond C

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Delineation of a KDM2B-related neurodevelopmental disorder and its associated DNA methylation signature von van Jaarsveld, Richard H., Reilly, Jack, Cornips, Marie-Claire, Hadders, Michael A., Agolini, Emanuele, Ahimaz, Priyanka, Anyane-Yeboa, Kwame, Bellanger, Severine Audebert, van Binsbergen, Ellen, van den Boogaard, Marie-Jose, Brischoux-Boucher, Elise, Caylor, Raymond C., Ciolfi, Andrea, van Essen, Ton A.J., Fontana, Paolo, Hopman, Saskia, Iascone, Maria, Javier, Margaret M., Kamsteeg, Erik-Jan, Kerkhof, Jennifer, Kido, Jun, Kim, Hyung-Goo, Kleefstra, Tjitske, Lonardo, Fortunato, Lai, Abbe, Lev, Dorit, Levy, Michael A., Lewis, M.E. Suzanne, Lichty, Angie, Mannens, Marcel M.A.M., Matsumoto, Naomichi, Maya, Idit, McConkey, Haley, Megarbane, Andre, Michaud, Vincent, Miele, Evelina, Niceta, Marcello, Novelli, Antonio, Onesimo, Roberta, Pfundt, Rolph, Popp, Bernt, Prijoles, Eloise, Relator, Raissa, Redon, Sylvia, Rots, Dmitrijs, Rouault, Karen, Saida, Ken, Schieving, Jolanda, Tartaglia, Marco, Tenconi, Romano, Uguen, Kevin, Verbeek, Nienke, Walsh, Christopher A., Yosovich, Keren, Yuskaitis, Christopher J., Zampino, Giuseppe, Sadikovic, Bekim, Alders, Mariëlle, Oegema, Renske

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Normalized Clinical Severity Scores Reveal a Correlation between X Chromosome Inactivation and Disease Severity in Rett Syndrome von Merritt, Jonathan K, Fang, Xiaolan, Caylor, Raymond C, Skinner, Steven A, Friez, Michael J, Percy, Alan K, Neul, Jeffrey L

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Parental age effects and Rett syndrome von Fang, Xiaolan, Baggett, Lauren M., Caylor, Raymond C., Percy, Alan K., Neul, Jeffrey L., Lane, Jane B., Glaze, Daniel G., Benke, Tim A., Marsh, Eric D., Motil, Kathleen J., Barrish, Judy O., Annese, Fran E., Skinner, Steven A.

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Expansion and mechanistic insights into de novo DEAF1 variants in DEAF1-associated neurodevelopmental disorders von McGee, Stacey R, Rajamanickam, Shivakumar, Adhikari, Sandeep, Falayi, Oluwatosin C, Wilson, Theresa A, Shayota, Brian J, Cooley Coleman, Jessica A, Skinner, Cindy, Caylor, Raymond C, Stevenson, Roger E, Quaio, Caio Robledo D' Angioli Costa, Wilke, Berenice Cunha, Bain, Jennifer M, Anyane-Yeboa, Kwame, Brown, Kaitlyn, Greally, John M, Bijlsma, Emilia K, Ruivenkamp, Claudia A L, Politi, Keren, Arbogast, Lydia A, Collard, Michael W, Huggenvik, Jodi I, Elsea, Sarah H, Jensik, Philip J

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De novo missense variants in the E3 ubiquitin ligase adaptor KLHL20 cause a developmental disorder with intellectual disability, epilepsy, and autism spectrum disorder von Sleyp, Yoeri, Valenzuela, Irene, Accogli, Andrea, Ballon, Katleen, Ben-Zeev, Bruria, Berkovic, Samuel F., Broly, Martin, Callaerts, Patrick, Caylor, Raymond C., Charles, Perrine, Chatron, Nicolas, Cohen, Lior, Coppola, Antonietta, Cordeiro, Dawn, Cuccurullo, Claudia, Cuscó, Ivon, Janette diMonda, Duran-Romaña, Ramon, Ekhilevitch, Nina, Fernández-Alvarez, Paula, Gordon, Christopher T., Isidor, Bertrand, Keren, Boris, Lesca, Gaetan, Maljaars, Jarymke, Mercimek-Andrews, Saadet, Morrow, Michelle M., Muir, Alison M., Rousseau, Frederic, Salpietro, Vincenzo, Scheffer, Ingrid E., Schnur, Rhonda E., Schymkowitz, Joost, Souche, Erika, Steyaert, Jean, Stolerman, Elliot S., Vengoechea, Jaime, Ville, Dorothée, Washington, Camerun, Weiss, Karin, Zaid, Rinat, Sadleir, Lynette G., Mefford, Heather C., Peeters, Hilde

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High-performance flat-panel solar thermoelectric generators with high thermal concentration von Kraemer, Daniel, Poudel, Bed, Feng, Hsien-Ping, Caylor, J. Christopher, Yu, Bo, Yan, Xiao, Ma, Yi, Wang, Xiaowei, Wang, Dezhi, Muto, Andrew, McEnaney, Kenneth, Chiesa, Matteo, Ren, Zhifeng, Chen, Gang

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Dynamic response of tetragonal lysozyme crystals to changes in relative humidity: implications for post-growth crystal treatments von Dobrianov, I., Kriminski, S., Caylor, C. L., Lemay, S. G., Kimmer, C., Kisselev, A., Finkelstein, K. D., Thorne, R. E.

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Incidental diagnosis of tuberous sclerosis complex by exome sequencing in three families with subclinical findings von Caylor, R. C., Grote, L., Thiffault, I., Farrow, E. G., Willig, L., Soden, S., Amudhavalli, S. M., Nopper, A. J., Horii, K. A., Fleming, E., Jenkins, J., Welsh, H., Ilyas, M., Engleman, K., Abdelmoity, A., Saunders, C. J.

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Macromolecular impurities and disorder in protein crystals von Caylor, C.L., Dobrianov, I., Lemay, S.G., Kimmer, C., Kriminski, S., Finkelstein, K.D., Zipfel, W., Webb, W.W., Thomas, B.R., Chernov, A.A., Thorne, R.E.

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