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Journal of Neurodevelopmental Disorders
|
April 30, 2025
Protein-truncating variants and deletions of SHANK2 are associated with autism spectrum disorder and other neurodevelopmental concerns
Hailey Silver, Rori Greenberg, Paige M Siper, et al.
American Journal on Intellectual and Developmental Disabilities
|
August 26, 2025
Longitudinal Trajectory of Adaptive Skills in Phelan-McDermid Syndrome
Siddharth Srivastava, Kristina Johnson, Cristan Farmer, et al.
Human Mutation
|
June 28, 2013
The Sac1 domain of SYNJ1 identified mutated in a family with early-onset progressive Parkinsonism with generalized seizures
Catharine E Krebs, Siamak Karkheiran, James C Powell, et al.
Pediatric Neurology
|
November 7, 2018
Volumetric Analysis of the Basal Ganglia and Cerebellar Structures in Patients with Phelan-McDermid Syndrome
Siddharth Srivastava, Benoit Scherrer, Anna K Prohl, et al.
Molecular Autism
|
May 3, 2018
Delineation of the genetic and clinical spectrum of Phelan-McDermid syndrome caused by <i>SHANK3</i> point mutations
Silvia De Rubeis, Paige M Siper, Allison Durkin, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
June 29, 2005
Altered ultrasonic vocalization in mice with a disruption in the Foxp2 gene
Weiguo Shu, Julie Y Cho, Yuhui Jiang, et al.
Plos Genetics
|
August 23, 2013
Integrated model of de novo and inherited genetic variants yields greater power to identify risk genes
Xin He, Stephan J Sanders, Li Liu, et al.
European Child & Adolescent Psychiatry
|
May 7, 2014
The increasing prevalence of reported diagnoses of childhood psychiatric disorders: a descriptive multinational comparison
Hjördis O Atladottir, David Gyllenberg, Amanda Langridge, et al.
Medrxiv : the Preprint Server for Health Sciences
|
May 18, 2026
Modeling rare coding variation on chromosome X provides insight into the genetics and differential sex prevalence of autism spectrum disorder
F Kyle Satterstrom, Kiana Jodeiry, Behrang Mahjani, et al.
Autism : the International Journal of Research and Practice
|
May 10, 2021
Reduced engagement of visual attention in children with autism spectrum disorder
Christopher S McLaughlin, Hannah E Grosman, Sylvia B Guillory, et al.
Page
of 37
Search research articles
Search
Showing results (201-210 of 361) with videos related to
Sort By:
Page
of 37
Journal of Neurodevelopmental Disorders
|
April 30, 2025
Protein-truncating variants and deletions of SHANK2 are associated with autism spectrum disorder and other neurodevelopmental concerns
Hailey Silver, Rori Greenberg, Paige M Siper, et al.
American Journal on Intellectual and Developmental Disabilities
|
August 26, 2025
Longitudinal Trajectory of Adaptive Skills in Phelan-McDermid Syndrome
Siddharth Srivastava, Kristina Johnson, Cristan Farmer, et al.
Human Mutation
|
June 28, 2013
The Sac1 domain of SYNJ1 identified mutated in a family with early-onset progressive Parkinsonism with generalized seizures
Catharine E Krebs, Siamak Karkheiran, James C Powell, et al.
Pediatric Neurology
|
November 7, 2018
Volumetric Analysis of the Basal Ganglia and Cerebellar Structures in Patients with Phelan-McDermid Syndrome
Siddharth Srivastava, Benoit Scherrer, Anna K Prohl, et al.
Molecular Autism
|
May 3, 2018
Delineation of the genetic and clinical spectrum of Phelan-McDermid syndrome caused by <i>SHANK3</i> point mutations
Silvia De Rubeis, Paige M Siper, Allison Durkin, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
June 29, 2005
Altered ultrasonic vocalization in mice with a disruption in the Foxp2 gene
Weiguo Shu, Julie Y Cho, Yuhui Jiang, et al.
Plos Genetics
|
August 23, 2013
Integrated model of de novo and inherited genetic variants yields greater power to identify risk genes
Xin He, Stephan J Sanders, Li Liu, et al.
European Child & Adolescent Psychiatry
|
May 7, 2014
The increasing prevalence of reported diagnoses of childhood psychiatric disorders: a descriptive multinational comparison
Hjördis O Atladottir, David Gyllenberg, Amanda Langridge, et al.
Medrxiv : the Preprint Server for Health Sciences
|
May 18, 2026
Modeling rare coding variation on chromosome X provides insight into the genetics and differential sex prevalence of autism spectrum disorder
F Kyle Satterstrom, Kiana Jodeiry, Behrang Mahjani, et al.
Autism : the International Journal of Research and Practice
|
May 10, 2021
Reduced engagement of visual attention in children with autism spectrum disorder
Christopher S McLaughlin, Hannah E Grosman, Sylvia B Guillory, et al.
Page
of 37