Tess Levy (T Levy)

Publication Activity (10 Years)

Years Active: 2021-2023
Publications (10 Years): 6

Top Topics

Autism Spectrum Disorder

Intellectual Disability

Top Venues

Human molecular genetics

Molecular autism

This page only lists publications with an associated author ORCID identifier.

Publications

Tess Levy, Thariana Pichardo, Hailey Silver, Bonnie Lerman, Jessica Zweifach, Danielle Halpern, Paige M Siper, Alexander Kolevzon, Joseph D Buxbaum
Prospective phenotyping of CHAMP1 disorder indicates that coding mutations may not act through haploinsufficiency. Human genetics (2023)
Swathi Sethuram, Tess Levy, Jennifer H Foss-Feig, Danielle Halpern, Sven Sandin, Paige M Siper, H Walker, Joseph D Buxbaum, Robert Rapaport, Alexander Kolevzon
A proof-of-concept study of growth hormone in children with Phelan-McDermid syndrome. Molecular autism 13 (1) (2022)
Tess Levy, Bonnie Lerman, Danielle Halpern, Yitzchak Frank, Christina Layton, Jessica Zweifach, Paige M Siper, Joseph D Buxbaum, Alexander Kolevzon
CHAMP1 disorder is associated with a complex neurobehavioral phenotype including autism, ADHD, repetitive behaviors and sensory symptoms. Human molecular genetics 31 (15) (2022)
Lara Tang, Tess Levy, Sylvia B Guillory, Danielle Halpern, Jessica Zweifach, Ivy Giserman-Kiss, Jennifer H Foss-Feig, Yitzchak Frank, Reymundo Lozano, Puneet B Belani, Christina Layton, Bonnie Lerman, Emanuel Frowner, Michael S Breen, Silvia De Rubeis, Ana Kostic, Alexander Kolevzon, Joseph D Buxbaum, Paige M Siper, Dorothy E Grice
Prospective and detailed behavioral phenotyping in DDX3X syndrome. Molecular autism 12 (1) (2021)
Tess Levy, Jennifer H Foss-Feig, Catalina Betancur, Paige M Siper, Maria Pilar Trelles-Thorne, Danielle Halpern, Yitzchak Frank, Reymundo Lozano, Christina Layton, Bari Britvan, Jonathan A Bernstein, Joseph D Buxbaum, Elizabeth Berry-Kravis, Craig M Powell, Siddharth Srivastava, Mustafa Sahin, Latha Soorya, Audrey Thurm, Alexander Kolevzon, null null
Strong evidence for genotype-phenotype correlations in Phelan-McDermid syndrome: Results from the developmental Synaptopathies consortium. Human molecular genetics (2021)
Teresa Tavassoli, Christina Layton, Tess Levy, Mikaela Rowe, Julia George-Jones, Jessica Zweifach, Stacey Lurie, Joseph D Buxbaum, Alexander Kolevzon, Paige M Siper
Sensory Reactivity Phenotype in Phelan-McDermid Syndrome Is Distinct from Idiopathic ASD. Genes 12 (7) (2021)