Behavioural phenotype of SYNGAP1‐related intellectual disability von Kranak, M. P., Rooker, G., Smith‐Hicks, C.

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Resolution of severe neurobehavioral difficulties in an individual with Primrose syndrome with sertraline von Moon, Young Min, Park, Sa Eun, Smith‐Hicks, Constance, Hauptman, Aaron

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An exploratory study of sleep quality and quantity in children with causal variants in SYNGAP1, an autism risk gene von Paasch, Valerie, Doucoure, Aida, Bifano, Morgan, Smith-Hicks, Constance L

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Caregivers' perception of and experience with variants of uncertain significance from whole exome sequencing for children with undiagnosed conditions von Li, Xin, Nusbaum, Rachel, Smith‐Hicks, Constance, Jamal, Leila, Dixon, Shannan, Mahida, Sonal

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A PIGH mutation leading to GPI deficiency is associated with developmental delay and autism von Nguyen, Thi Tuyet Mai, Mahida, Sonal, Smith‐Hicks, Constance, Campeau, Philippe M.

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Factors Associated with Listing Decisions under the U.S. Endangered Species Act von Smith-Hicks, Kathryn N., Morrison, Michael L.

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GABAergic dysfunction in pediatric neuro-developmental disorders von Smith-Hicks, Constance L

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De Novo HECW2 Mutation Associated With Epilepsy, Developmental Decline, and Intellectual Disability: Case Report and Review of Literature von Ullman, Natalie L., Smith-Hicks, Constance L., Desai, Sonal, Stafstrom, Carl E.

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The Impact of X-Chromosome Inactivation on Phenotypic Expression of X-Linked Neurodevelopmental Disorders von Brand, Boudewien A, Blesson, Alyssa E, Smith-Hicks, Constance L.

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Neuroimaging abnormalities in a child with infantile spasms on high dose vigabatrin von Sun, Lisa R., MD, Bosemani, Thangamadhan, MD, Smith-Hicks, Constance L., MD PhD

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Elongation Factor 2 and Fragile X Mental Retardation Protein Control the Dynamic Translation of Arc/Arg3.1 Essential for mGluR-LTD von Park, Sungjin, Park, Joo Min, Kim, Sangmok, Kim, Jin-Ah, Shepherd, Jason D., Smith-Hicks, Constance L., Chowdhury, Shoaib, Kaufmann, Walter, Kuhl, Dietmar, Ryazanov, Alexey G., Huganir, Richard L., Linden, David J., Worley, Paul F.

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Increased Sparsity of Hippocampal CA1 Neuronal Ensembles in a Mouse Model of Down Syndrome Assayed by Arc Expression von Smith-Hicks, Constance L, Cai, Peiling, Savonenko, Alena V, Reeves, Roger H, Worley, Paul F

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Activity-Induced Notch Signaling in Neurons Requires Arc/Arg3.1 and Is Essential for Synaptic Plasticity in Hippocampal Networks von Alberi, Lavinia, Liu, Shuxi, Wang, Yue, Badie, Ramy, Smith-Hicks, Constance, Wu, Jing, Pierfelice, Tarran J., Abazyan, Bagrat, Mattson, Mark P., Kuhl, Dietmar, Pletnikov, Mikhail, Worley, Paul F., Gaiano, Nicholas

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POLR3B is associated with a developmental and epileptic encephalopathy with myoclonic‐atonic seizures and ataxia von Symonds, Joseph D., Park, Kristen L., Mignot, Cyril, Macleod, Stewart, Armstrong, Martin, Ashrafian, Houman, Bernard, Geneviève, Brown, Kathleen, Brunklaus, Andreas, Callaghan, Mary, Classen, Georg, Cohen, Julie S., Cutcutache, Ioana, Sainte Agathe, Jean‐Madeleine, Dyment, David, Elliot, Katherine S., Isapof, Arnaud, Joss, Shelagh, Keren, Boris, Marble, Michael, McTague, Amy, Osmond, Matthew, Page, Matthew, Planes, Marc, Platzer, Konrad, Redon, Sylvia, Reese, James, Saenz, Margarita, Smith‐Hicks, Constance, Stobo, Daniel, Stockhaus, Christian, Vuillaume, Marie‐Laure, Wolf, Nicole I., Wakeling, Emma L., Yoon, Grace, Knight, Julian C., Zuberi, Sameer M.

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Neurologic phenotypes associated with COL4A1/2 mutations: Expanding the spectrum of disease von Zagaglia, Sara, Selch, Christina, Nisevic, Jelena Radic, Mei, Davide, Michalak, Zuzanna, Hernandez-Hernandez, Laura, Krithika, S, Vezyroglou, Katharina, Varadkar, Sophia M, Pepler, Alexander, Biskup, Saskia, Leão, Miguel, Gärtner, Jutta, Merkenschlager, Andreas, Jaksch, Michaela, Møller, Rikke S, Gardella, Elena, Kristiansen, Britta Schlott, Hansen, Lars Kjærsgaard, Vari, Maria Stella, Helbig, Katherine L, Desai, Sonal, Smith-Hicks, Constance L, Hino-Fukuyo, Naomi, Talvik, Tiina, Laugesaar, Rael, Ilves, Pilvi, Õunap, Katrin, Körber, Ingrid, Hartlieb, Till, Kudernatsch, Manfred, Winkler, Peter, Schimmel, Mareike, Hasse, Anette, Knuf, Markus, Heinemeyer, Jan, Makowski, Christine, Ghedia, Sondhya, Subramanian, Gopinath M, Striano, Pasquale, Thomas, Rhys H, Micallef, Caroline, Thom, Maria, Werring, David J, Kluger, Gerhard Josef, Cross, J Helen, Guerrini, Renzo, Balestrini, Simona, Sisodiya, Sanjay M

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Quantifying neurobehavioral profiles across neurodevelopmental genetic syndromes and idiopathic neurodevelopmental disorders von Frazier, Thomas W, Busch, Robyn M, Klaas, Patricia, Lachlan, Katherine, Loth, Eva, Smith-Hicks, Constance, Sahin, Mustafa, Hardan, Antonio Y, Uljarevic, Mirko

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Functional integration of new neurons into hippocampal networks and poststroke comorbidities following neonatal stroke in mice von Kadam, S.D, Smith-Hicks, C.L, Smith, D.R, Worley, P.F, Comi, A.M

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Development of informant‐report neurobehavioral survey scales for PTEN hamartoma tumor syndrome and related neurodevelopmental genetic syndromes von Frazier, Thomas W., Busch, Robyn M., Klaas, Patricia, Lachlan, Katherine, Jeste, Shafali, Kolevzon, Alexander, Loth, Eva, Harris, Jacqueline, Speer, Leslie, Pepper, Tom, Anthony, Kristin, Graglia, J. Michael, Delagrammatikas, Christal, Bedrosian‐Sermone, Sandra, Beekhuyzen, Jenine, Smith‐Hicks, Constance, Sahin, Mustafa, Eng, Charis, Hardan, Antonia Y., Uljarević, Mirko

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Heterozygous NOTCH1 Variants Cause CNS Immune Activation and Microangiopathy von Helman, Guy, Zarekiani, Parand, Tromp, Samantha A.M., Andrews, Ashley, Botto, Lorenzo D., Bonkowsky, Joshua L., Chassevent, Anna, Giorgio, Elisa, Pippucci, Tommaso, Wei, Shen, Smith‐Hicks, Constance, Vaula, Giovanna, Willemsen, Michèl A.A.P, Schimmel, Mareike, Vollert, Kurt, Shimizu, Fumitaka, Kanda, Takashi, Lynch, Matthew, Roscioli, Tony, Taft, Ryan J., Simons, Cas, Bugiani, Marianna, Kuijpers, Taco W., Knaap, Marjo S.

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Natural history and genotype‐phenotype correlations in 72 individuals with SATB2‐associated syndrome von Zarate, Yuri A., Smith‐Hicks, Constance L., Greene, Carol, Abbott, Mary‐Alice, Siu, Victoria M., Calhoun, Amy R. U. L., Pandya, Arti, Li, Chumei, Sellars, Elizabeth A., Kaylor, Julie, Bosanko, Katherine, Kalsner, Louisa, Basinger, Alice, Slavotinek, Anne M., Perry, Hazel, Saenz, Margarita, Szybowska, Marta, Wilson, Louise C., Kumar, Ajith, Brain, Caroline, Balasubramanian, Meena, Dubbs, Holly, Ortiz‐Gonzalez, Xilma R., Zackai, Elaine, Stein, Quinn, Powell, Cynthia M., Schrier Vergano, Samantha, Britt, Allison, Sun, Angela, Smith, Wendy, Bebin, E. Martina, Picker, Jonathan, Kirby, Amelia, Pinz, Hailey, Bombei, Hannah, Mahida, Sonal, Cohen, Julie S., Fatemi, Ali, Vernon, Hilary J., McClellan, Rebecca, Fleming, Leah R., Knyszek, Brittney, Steinraths, Michelle, Velasco Gonzalez, Cruz, Beck, Anita E., Golden‐Grant, Katie L., Egense, Alena, Parikh, Aditi, Raimondi, Chantalle, Angle, Brad, Allen, William, Schott, Suzanna, Algrabli, Adi, Robin, Nathaniel H., Ray, Joseph W., Everman, David B., Gambello, Michael J., Chung, Wendy K.

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