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Current Biology : CB
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January 15, 2019
Male-Specific Conditioned Pain Hypersensitivity in Mice and Humans
Loren J Martin, Erinn L Acland, Chulmin Cho, et al.
HGG Advances
|
October 24, 2022
Large 22q13.3 deletions perturb peripheral transcriptomic and metabolomic profiles in Phelan-McDermid syndrome
Michael S Breen, Xuanjia Fan, Tess Levy, et al.
Journal of the American Academy of Child and Adolescent Psychiatry
|
March 27, 2026
Catatonia in Autism and Neurodevelopmental Disorders: A Scoping Review for Advancing Identification, Practice, and Research
Pilar Trelles, Tess Levy, Sonal Jain, et al.
HGG Advances
|
September 19, 2022
An open-label study evaluating the safety, behavioral, and electrophysiological outcomes of low-dose ketamine in children with ADNP syndrome
Alexander Kolevzon, Tess Levy, Sarah Barkley, et al.
Genes
|
March 6, 2021
Sensory Reactivity Symptoms Are a Core Feature of ADNP Syndrome Irrespective of Autism Diagnosis
Paige M Siper, Christina Layton, Tess Levy, et al.
Journal of Neurodevelopmental Disorders
|
May 10, 2024
Clinical, genetic, and cognitive correlates of seizure occurrences in Phelan-McDermid syndrome
Tess Levy, Jacob Gluckman, Paige M Siper, et al.
American Journal on Intellectual and Developmental Disabilities
|
August 26, 2025
Genetic Subtypes of Phelan-McDermid Syndrome Exhibit Similar Rates of Change Despite Differences in Level of Impairment in Developmental Constructs
Tess Levy, Cristan Farmer, Siddharth Srivastava, et al.
Human Molecular Genetics
|
September 24, 2021
Strong evidence for genotype-phenotype correlations in Phelan-McDermid syndrome: results from the developmental synaptopathies consortium
Tess Levy, Jennifer H Foss-Feig, Catalina Betancur, et al.
Molecular Autism
|
May 17, 2021
Prospective and detailed behavioral phenotyping in DDX3X syndrome
Lara Tang, Tess Levy, Sylvia Guillory, et al.
NPJ Genomic Medicine
|
April 6, 2024
Consensus reporting guidelines to address gaps in descriptions of ultra-rare genetic conditions
Ali AlMail, Ahmed Jamjoom, Amy Pan, et al.
Page
of 4
Search research articles
Search
Showing results (21-30 of 40) with videos related to
Sort By:
Page
of 4
Current Biology : CB
|
January 15, 2019
Male-Specific Conditioned Pain Hypersensitivity in Mice and Humans
Loren J Martin, Erinn L Acland, Chulmin Cho, et al.
HGG Advances
|
October 24, 2022
Large 22q13.3 deletions perturb peripheral transcriptomic and metabolomic profiles in Phelan-McDermid syndrome
Michael S Breen, Xuanjia Fan, Tess Levy, et al.
Journal of the American Academy of Child and Adolescent Psychiatry
|
March 27, 2026
Catatonia in Autism and Neurodevelopmental Disorders: A Scoping Review for Advancing Identification, Practice, and Research
Pilar Trelles, Tess Levy, Sonal Jain, et al.
HGG Advances
|
September 19, 2022
An open-label study evaluating the safety, behavioral, and electrophysiological outcomes of low-dose ketamine in children with ADNP syndrome
Alexander Kolevzon, Tess Levy, Sarah Barkley, et al.
Genes
|
March 6, 2021
Sensory Reactivity Symptoms Are a Core Feature of ADNP Syndrome Irrespective of Autism Diagnosis
Paige M Siper, Christina Layton, Tess Levy, et al.
Journal of Neurodevelopmental Disorders
|
May 10, 2024
Clinical, genetic, and cognitive correlates of seizure occurrences in Phelan-McDermid syndrome
Tess Levy, Jacob Gluckman, Paige M Siper, et al.
American Journal on Intellectual and Developmental Disabilities
|
August 26, 2025
Genetic Subtypes of Phelan-McDermid Syndrome Exhibit Similar Rates of Change Despite Differences in Level of Impairment in Developmental Constructs
Tess Levy, Cristan Farmer, Siddharth Srivastava, et al.
Human Molecular Genetics
|
September 24, 2021
Strong evidence for genotype-phenotype correlations in Phelan-McDermid syndrome: results from the developmental synaptopathies consortium
Tess Levy, Jennifer H Foss-Feig, Catalina Betancur, et al.
Molecular Autism
|
May 17, 2021
Prospective and detailed behavioral phenotyping in DDX3X syndrome
Lara Tang, Tess Levy, Sylvia Guillory, et al.
NPJ Genomic Medicine
|
April 6, 2024
Consensus reporting guidelines to address gaps in descriptions of ultra-rare genetic conditions
Ali AlMail, Ahmed Jamjoom, Amy Pan, et al.
Page
of 4