Trofinetide for the treatment of Rett syndrome: a randomized phase 3 study von Neul, Jeffrey L., Percy, Alan K., Benke, Timothy A., Berry-Kravis, Elizabeth M., Glaze, Daniel G., Marsh, Eric D., Lin, Tim, Stankovic, Serge, Bishop, Kathie M., Youakim, James M.

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Mechanism-Based Treatments in Neurodevelopmental Disorders: Fragile X Syndrome von Berry-Kravis, Elizabeth, MD, PhD

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Effects of mavoglurant on visual attention and pupil reactivity while viewing photographs of faces in Fragile X Syndrome von Hessl, David, Harvey, Danielle, Sansone, Stephanie, Crestodina, Crystal, Chin, Jamie, Joshi, Reshma, Hagerman, Randi J, Berry-Kravis, Elizabeth

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Fragile X Gray Zone Alleles Are Associated With Signs of Parkinsonism and Earlier Death von Hall, Deborah A., Nag, Sukriti, Ouyang, Bichun, Bennett, David A., Liu, Yuanqing, Ali, Aisha, Zhou, Lili, Berry‐Kravis, Elizabeth

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Mild Neurological Signs in FMR1 Premutation Women in an Unselected Community‐Based Cohort von Mailick, Marsha R., Hong, Jinkuk, Movaghar, Arezoo, DaWalt, Leann, Berry‐Kravis, Elizabeth M., Brilliant, Murray H., Boero, Jaime, Todd, Peter K., Hall, Deborah

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The association between mosaicism type and cognitive and behavioral functioning among males with fragile X syndrome von Meng, Lu, Kaufmann, Walter E., Frye, Richard E., Ong, Katherine, Kaminski, Jennifer W., Velinov, Milen, Berry‐Kravis, Elizabeth

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Stress and genetics influence hair cortisol in FMR1 premutation carrier mothers of children with fragile X syndrome von Hong, Jinkuk, Kapoor, Amita, DaWalt, Leann Smith, Maltman, Nell, Kim, Bryan, Berry-Kravis, Elizabeth M., Almeida, David, Coe, Christopher, Mailick, Marsha

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Therapeutic Strategies in Fragile X Syndrome: From Bench to Bedside and Back von Gross, Christina, Hoffmann, Anne, Bassell, Gary J., Berry-Kravis, Elizabeth M.

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Sleep problems in fragile X syndrome: Cross‐sectional analysis of a large clinic‐based cohort von Budimirovic, Dejan B., Protic, Dragana D., Delahunty, Carol M., Andrews, Howard F., Choo, Tse‐Hwei, Xu, Qing, Berry‐Kravis, Elizabeth, Kaufmann, Walter E.

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The comparison of expressed emotion of parents of individuals with fragile X syndrome to other intellectual disabilities von Coleman, Jeanine, Thompson, Talia, Riley, Karen, Allen, Korrie, Michalak, Claire, Shields, Rebecca, Berry‐Kravis, Elizabeth, Hessl, David

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Psychometric Study of the Aberrant Behavior Checklist in Fragile X Syndrome and Implications for Targeted Treatment von Sansone, Stephanie M., Widaman, Keith F., Hall, Scott S., Reiss, Allan L., Lightbody, Amy, Kaufmann, Walter E., Berry-Kravis, Elizabeth, Lachiewicz, Ave, Brown, Elaine C., Hessl, David

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Therapeutic Strategies in Fragile X Syndrome: Dysregulated mGluR Signaling and Beyond von GROSS, Christina, BERRY-KRAVIS, Elizabeth M, BASSELL, Gary J

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Aortic Root Dilation and Genotype Associations in Phelan‐McDermid Syndrome von Gluckman, Jake, Levy, Tess, Friedman, Kate, Garces, Francesca, Filip‐Dhima, Rajna, Quinlan, Aisling, Iannotti, Isabelle, Pekar, Margaret, Hernandez, Alexandra Lopez, Nava, Madison T., Kravets, Elijah, Siegel, Abigail, Bernstein, Jonathan A., Berry‐Kravis, Elizabeth, Powell, Craig M., Soorya, Latha Valluripalli, Thurm, Audrey, Srivastava, Siddharth, Buxbaum, Joseph D., Sahin, Mustafa, Kolevzon, Alexander, Gelb, Bruce D.

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Fragile X-associated tremor/ataxia syndrome: Clinical features, genetics, and testing guidelines von Berry-Kravis, Elizabeth, Abrams, Liane, Coffey, Sarah M., Hall, Deborah A., Greco, Claudia, Gane, Louise W., Grigsby, Jim, Bourgeois, James A., Finucane, Brenda, Jacquemont, Sebastien, Brunberg, James A., Zhang, Lin, Lin, Janet, Tassone, Flora, Hagerman, Paul J., Hagerman, Randi J., Leehey, Maureen A.

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Anesthetic management of pediatric patients with Niemann‐Pick disease type C for intrathecal 2‐hydroxypropyl‐β‐cyclodextrin injection von Ulloa, Morgan L., Froyshteter, Alexander B., Kret, Lauren N., Chang, Denise P., Sarah, Gabriel E., McCarthy, Robert J., Barnes, Steve D., Berry‐Kravis, Elizabeth M., Veyckemans, Francis

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Mutation update for the SATB2 gene von Zarate, Yuri A., Bosanko, Katherine A., Caffrey, Aisling R., Bernstein, Jonathan A., Martin, Donna M., Williams, Marc S., Berry‐Kravis, Elizabeth M., Mark, Paul R., Manning, Melanie A., Bhambhani, Vikas, Vargas, Marcelo, Seeley, Andrea H., Estrada‐Veras, Juvianee I., Dooren, Marieke F., Schwab, Maria, Vanderver, Adeline, Melis, Daniela, Alsadah, Adnan, Sadler, Laurie, Esch, Hilde, Callewaert, Bert, Oostra, Ann, Maclean, Jane, Dentici, Maria Lisa, Orlando, Valeria, Lipson, Mark, Sparagana, Steven P., Maarup, Timothy J., Alsters, Suzanne IM, Brautbar, Ariel, Kovitch, Eliana, Naidu, Sakkubai, Lees, Melissa, Smith, Douglas M., Turner, Lesley, Raggio, Víctor, Spangenberg, Lucía, Garcia‐Miñaúr, Sixto, Roeder, Elizabeth R., Littlejohn, Rebecca O., Grange, Dorothy, Pfotenhauer, Jean, Jones, Marilyn C., Balasubramanian, Meena, Martinez‐Monseny, Antonio, Blok, Lot Snijders, Gavrilova, Ralitza, Fish, Jennifer L.

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Cholesterol levels in Fragile X syndrome von Berry-Kravis, Elizabeth, Levin, Rebecca, Shah, Haroon, Mathur, Shaguna, Darnell, Jennifer C., Ouyang, Bichun

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Congenital central hypoventilation syndrome: Severe disease caused by co‐occurrence of two PHOX2B variants inherited separately from asymptomatic family members von Sivan, Yakov, Zhou, Amy, Jennings, Lawrence J., Berry‐Kravis, Elizabeth M., Yu, Min, Zhou, Lili, Rand, Casey M., Weese‐Mayer, Debra E.

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Fragile X AGG analysis provides new risk predictions for 45-69 repeat alleles von Nolin, Sarah L., Sah, Sachin, Glicksman, Anne, Sherman, Stephanie L., Allen, Emily, Berry-Kravis, Elizabeth, Tassone, Flora, Yrigollen, Carolyn, Cronister, Amy, Jodah, Marcia, Ersalesi, Nicole, Dobkin, Carl, Brown, W. Ted, Shroff, Raghav, Latham, Gary J., Hadd, Andrew G.

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Idiopathic congenital central hypoventilation syndrome: Analysis of genes pertinent to early autonomic nervous system embryologic development and identification of mutations in PHO... von Weese-Mayer, Debra E., Berry-Kravis, Elizabeth M., Zhou, Lili, Maher, Brion S., Silvestri, Jean M., Curran, Mark E., Marazita, Mary L.

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