Search Results - Tess Levy

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  1. 1

    P672: The evolving genetic landscape of Phelan-McDermid syndrome and implications for diagnostics by Mary Hames, Alexander Kolevzon, Elizabeth Berry-Kravis, Larry Glass, Nancy Jones, Brian Eisinger, Liza Squires, Tess Levy

    Published in Genetics in Medicine Open (2025-01-01)
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  2. 2

    Adolescents and adults with FOXP1 syndrome show high rates of anxiety and externalizing behaviors but not psychiatric decompensation or skill loss by Tess Levy, Tess Levy, Hailey Silver, Hailey Silver, Renee Soufer, Renee Soufer, Audrey Rouhandeh, Audrey Rouhandeh, Audrey Rouhandeh, Alexander Kolevzon, Alexander Kolevzon, Alexander Kolevzon, Alexander Kolevzon, Joseph D. Buxbaum, Joseph D. Buxbaum, Joseph D. Buxbaum, Joseph D. Buxbaum, Joseph D. Buxbaum, Joseph D. Buxbaum, Paige M. Siper, Paige M. Siper, Paige M. Siper

    Published in Frontiers in Psychiatry (2025-02-01)
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  3. 3

    Individuals with FOXP1 syndrome present with a complex neurobehavioral profile with high rates of ADHD, anxiety, repetitive behaviors, and sensory symptoms by M. Pilar Trelles, Tess Levy, Bonnie Lerman, Paige Siper, Reymundo Lozano, Danielle Halpern, Hannah Walker, Jessica Zweifach, Yitzchak Frank, Jennifer Foss-Feig, Alexander Kolevzon, Joseph Buxbaum

    Published in Molecular Autism (2021-09-01)
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  4. 4

    Transient peripheral blood transcriptomic response to ketamine treatment in children with ADNP syndrome by Ariela S. Buxbaum Grice, Laura Sloofman, Tess Levy, Hannah Walker, Gauri Ganesh, Miguel Rodriguez de los Santos, Pardis Amini, Joseph D. Buxbaum, Alexander Kolevzon, Ana Kostic, Michael S. Breen

    Published in Translational Psychiatry (2024-07-01)
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  5. 5

    An open-label study evaluating the safety and efficacy of AMO-01 for the treatment of seizures in Phelan-McDermid syndrome by Tess Levy, J. Lloyd Holder, Jr., Joseph P. Horrigan, Michael F. Snape, Alison McMorn, Christina Layton, Hailey Silver, Kate Friedman, Hannah Grosman, Slayton Underwood, Danielle Halpern, Jessica Zweifach, Paige M. Siper, Alexander Kolevzon

    Published in HGG Advances (2025-04-01)
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  6. 6

    Protein-truncating variants and deletions of SHANK2 are associated with autism spectrum disorder and other neurodevelopmental concerns by Hailey Silver, Rori Greenberg, Paige M. Siper, Jessica Zweifach, Renee Soufer, Mustafa Sahin, Elizabeth Berry-Kravis, Latha Valluripalli Soorya, Audrey Thurm, Jonathan A. Bernstein, Alexander Kolevzon, Dorothy E. Grice, Joseph D. Buxbaum, Tess Levy

    Published in Journal of Neurodevelopmental Disorders (2025-04-01)
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  7. 7

    Clinical, genetic, and cognitive correlates of seizure occurrences in Phelan-McDermid syndrome by Tess Levy, Jacob Gluckman, Paige M. Siper, Danielle Halpern, Jessica Zweifach, Rajna Filip-Dhima, J. Lloyd Holder, M. Pilar Trelles, Kristina Johnson, Jonathan A. Bernstein, Elizabeth Berry-Kravis, Craig M. Powell, Latha Valluripalli Soorya, Audrey Thurm, Joseph D. Buxbaum, Mustafa Sahin, Alexander Kolevzon, Siddharth Srivastava, on behalf of the Developmental Synaptopathies Consortium

    Published in Journal of Neurodevelopmental Disorders (2024-05-01)
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  8. 8

    P249: Gaps in the phenotype descriptions of ultra-rare genetic conditions: Review and multi-center consensus reporting guidelines by Ali AlMail, Ahmed Jamjoom, Amy Pan, Anna Feng, Vann Chau, Alissa D'Gama, Katherine Howell, Nicole Si Yan Liang, Amy McTague, Annapurna Poduri, Kimberly Wiltrout, Anne Bassett, John Christodoulou, Lucie Dupuis, Peter Gill, Tess Levy, Paige Siper, Zornitza Stark, Jacob Vorstman, Catherine Diskin, Natalie Jewitt, Danielle Baribeau, Gregory Costain

    Published in Genetics in Medicine Open (2024-01-01)
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  9. 9

    P205: Investigating sex differences in the behavioral phenotypes of Phelan-McDermid syndrome, tuberous sclerosis complex, and PTEN hamartoma tumor syndrome by Kate Friedman, Tess Levy, Paige Siper, Martina Bebin, Elizabeth Berry-Kravis, Jonathan Bernstein, Robyn Busch, Patricia Klaas, Kristn Currans, Amanda Gulsrud, Ellen Hanson, Antonio Hardan, Darcy Krueger, Julian Martinez-Agosto, Hope Northrup, Sarah O'Kelley, Deborah Pearson, Jennifer Phillips, Brenda Porter, Rajsekar Rajaraman, Mustafa Sahin, Joseph Buxbaum, Latha Valluripalli Soorya, Audrey Thurm, Alexander Kolevzon

    Published in Genetics in Medicine Open (2025-01-01)
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  10. 10

    Consensus reporting guidelines to address gaps in descriptions of ultra-rare genetic conditions by Ali AlMail, Ahmed Jamjoom, Amy Pan, Min Yi Feng, Vann Chau, Alissa M. D’Gama, Katherine Howell, Nicole S. Y. Liang, Amy McTague, Annapurna Poduri, Kimberly Wiltrout, IPCHiP Executive Committee, Anne S. Bassett, John Christodoulou, Lucie Dupuis, Peter Gill, Tess Levy, Paige Siper, Zornitza Stark, Jacob A. S. Vorstman, Catherine Diskin, Natalie Jewitt, Danielle Baribeau, Gregory Costain

    Published in npj Genomic Medicine (2024-04-01)
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