Scoliosis in Rett Syndrome: Progression, Comorbidities, and Predictors von Killian, John T., MD, Lane, Jane B., RN, BSN, Lee, Hye-Seung, PhD, Skinner, Steve A., MD, Kaufmann, Walter E., MD, Glaze, Daniel G., MD, Neul, Jeffrey L., MD, PhD, Percy, Alan K., MD

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Intracerebral transplantation of porcine choroid plexus provides structural and functional neuroprotection in a rodent model of stroke von BORLONGAN, Cesar V, SKINNER, Steve J. M, GEANEY, Marilyn, VASCONCELLOS, Alfred V, ELLIOTT, Robert B, EMERICH, Dwaine F

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Characterizing the phenotypic effect of Xq28 duplication size in MECP2 duplication syndrome von Peters, Sarika U., Fu, Cary, Suter, Bernhard, Marsh, Eric, Benke, Timothy A., Skinner, Steve A., Lieberman, David N., Standridge, Shannon, Jones, Mary, Beisang, Arthur, Feyma, Timothy, Heydeman, Peter, Ryther, Robin, Kaufmann, Walter E., Glaze, Daniel G., Neul, Jeffrey L., Percy, Alan K.

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Mental health professionals and telehealth in a rural setting: a cross sectional survey von Nelson, David, Inghels, Maxime, Kenny, Amanda, Skinner, Steve, McCranor, Tracy, Wyatt, Stephen, Phull, Jaspreet, Nanyonjo, Agnes, Yusuff, Ojali, Gussy, Mark

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Discovery and Characterization of a Class of Pyrazole Inhibitors of Bacterial Undecaprenyl Pyrophosphate Synthase von Concha, Nestor, Huang, Jianzhong, Bai, Xiaopeng, Benowitz, Andrew, Brady, Pat, Grady, LaShadric C, Kryn, Luz Helena, Holmes, David, Ingraham, Karen, Jin, Qi, Pothier Kaushansky, Laura, McCloskey, Lynn, Messer, Jeffrey A, O’Keefe, Heather, Patel, Amish, Satz, Alexander L, Sinnamon, Robert H, Schneck, Jessica, Skinner, Steve R, Summerfield, Jennifer, Taylor, Amy, Taylor, J. David, Evindar, Ghotas, Stavenger, Robert A

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Caretaker Quality of Life in Rett Syndrome: Disorder Features and Psychological Predictors von Killian, John T., MA, Lane, Jane B., RN, BSN, Lee, Hye-Seung, PhD, Pelham, James H., BS, Skinner, Steve A., MD, Kaufmann, Walter E., MD, Glaze, Daniel G., MD, Neul, Jeffrey L., MD, PhD, Percy, Alan K., MD

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Development of a small molecule that corrects misfolding and increases secretion of Z α1‐antitrypsin von Lomas, David A, Irving, James A, Arico‐Muendel, Christopher, Belyanskaya, Svetlana, Brewster, Andrew, Brown, Murray, Chung, Chun‐wa, Dave, Hitesh, Denis, Alexis, Dodic, Nerina, Dossang, Anthony, Eddershaw, Peter, Klimaszewska, Diana, Haq, Imran, Holmes, Duncan S, Hutchinson, Jonathan P, Jagger, Alistair M, Jakhria, Toral, Jigorel, Emilie, Liddle, John, Lind, Ken, Marciniak, Stefan J, Messer, Jeff, Neu, Margaret, Olszewski, Allison, Ordonez, Adriana, Ronzoni, Riccardo, Rowedder, James, Rüdiger, Martin, Skinner, Steve, Smith, Kathrine J, Terry, Rebecca, Trottet, Lionel, Uings, Iain, Wilson, Steve, Zhu, Zhengrong, Pearce, Andrew C

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Phenotypic features in MECP2 duplication syndrome: Effects of age von Peters, Sarika U., Fu, Cary, Marsh, Eric D., Benke, Tim A., Suter, Bernard, Skinner, Steve A., Lieberman, David N., Standridge, Shannon, Jones, Mary, Beisang, Arthur, Feyma, Timothy, Heydeman, Peter, Ryther, Robin, Glaze, Daniel G., Percy, Alan K., Neul, Jeffrey L.

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Anxiety-like behavior and anxiolytic treatment in the Rett syndrome natural history study von Buchanan, Caroline B, Stallworth, Jennifer L, Joy, Aubin E, Dixon, Rebekah E, Scott, Alexandra E, Beisang, Arthur A, Benke, Timothy A, Glaze, Daniel G, Haas, Richard H, Heydemann, Peter T, Jones, Mary D, Lane, Jane B, Lieberman, David N, Marsh, Eric D, Neul, Jeffrey L, Peters, Sarika U, Ryther, Robin C, Skinner, Steve A, Standridge, Shannon M, Kaufmann, Walter E, Percy, Alan K

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Longevity in Rett Syndrome: Analysis of the North American Database von Kirby, Russell S., PhD, Lane, Jane B., BSN, Childers, Jerry, Skinner, Steve A., MD, Annese, Fran, LMSW, Barrish, Judy O., BSN, Glaze, Daniel G., MD, MacLeod, Patrick, MD, Percy, Alan K., MD

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Assessment of Caregiver Inventory for Rett Syndrome von Lane, Jane B., Salter, Amber R., Jones, Nancy E., Cutter, Gary, Horrigan, Joseph, Skinner, Steve A., Kaufmann, Walter E., Glaze, Daniel G., Neul, Jeffrey L., Percy, Alan K.

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Neuroprotection by encapsulated choroid plexus in a rodent model of Huntingtonʼs disease von Borlongan, Cesario V, Skinner, Steve J. M, Geaney, Marilyn, Vasconcellos, Alfred V, Elliott, Robert B, Emerich, Dwaine F

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Functional analysis of a novel mutation in the TIMM8A gene that causes deafness‐dystonia‐optic neuronopathy syndrome von Neighbors, Addison, Moss, Tonya, Holloway, Lynda, Yu, Seok‐Ho, Annese, Fran, Skinner, Steve, Saneto, Russell, Steet, Richard

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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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Rett syndrome: Revised diagnostic criteria and nomenclature von Jeffrey L. Neul, Kaufmann, Walter E., Glaze, Daniel G., Christodoulou, John, Clarke, Angus J., Bahi-Buisson, Nadia, Leonard, Helen, Bailey, Mark E. S., Schanen, N. Carolyn, Zappella, Michele, Renieri, Alessandra, Huppke, Peter, Percy, Alan K.

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Double-blind, randomized, placebo-controlled study of trofinetide in pediatric Rett syndrome von Glaze, Daniel G, Neul, Jeffrey L, Kaufmann, Walter E, Berry-Kravis, Elizabeth, Condon, Sean, Stoms, George, Oosterholt, Sean, Della Pasqua, Oscar, Glass, Larry, Jones, Nancy E, Percy, Alan K

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Importance of genetic testing in global health during the evaluation of familial microcephaly von Molinero, Isaac, Broman‐Fulks, Jordan, Lyons, Michael J., Matheus, Maria Gisele, Chaubey, Alka, DuPont, Barbara R., Friez, Michael J., Skinner, Steve A., Holden, Kenton R.

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Mucolipidosis Type IV: A Subtle Pediatric Neurodegenerative Disorder von Geer, Joseph S., MD, Skinner, Steve A., MD, Goldin, Ehud, PhD, Holden, Kenton R., MD

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The XMM-Newton extended survey of the Taurus molecular cloud (XEST) von Güdel, M., Briggs, K. R., Arzner, K., Audard, M., Bouvier, J., Feigelson, E. D., Franciosini, E., Glauser, A., Grosso, N., Micela, G., Monin, J.-L., Montmerle, T., Padgett, D. L., Palla, F., Pillitteri, I., Rebull, L., Scelsi, L., Silva, B., Skinner, S. L., Stelzer, B., Telleschi, A.

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Exome sequencing of 457 autism families recruited online provides evidence for autism risk genes von Feliciano, Pamela, Zhou, Xueya, Astrovskaya, Irina, Turner, Tychele N., Wang, Tianyun, Brueggeman, Leo, Barnard, Rebecca, Hsieh, Alexander, Snyder, LeeAnne Green, Muzny, Donna M., Sabo, Aniko, Gibbs, Richard A., Eichler, Evan E., O’Roak, Brian J., Michaelson, Jacob J., Volfovsky, Natalia, Shen, Yufeng, Chung, Wendy K.

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