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The Journal of Clinical Psychiatry
|
May 9, 2009
A review of fragile X premutation disorders: expanding the psychiatric perspective
James A Bourgeois, Sarah M Coffey, Susan M Rivera, 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.
Journal of Genetic Counseling
|
May 15, 2007
Recommendations from multi-disciplinary focus groups on cascade testing and genetic counseling for fragile X-associated disorders
Allyn McConkie-Rosell, Liane Abrams, Brenda Finucane, et al.
Journal of Neurodevelopmental Disorders
|
November 19, 2025
Long-term safety and tolerability of transdermal cannabidiol gel in children and adolescents with Fragile X syndrome (ZYN2-CL-017): an interim analysis of an ongoing open-label extension study
Elizabeth Berry-Kravis, Randi Hagerman, Jonathan Cohen, et al.
Journal of Neurodevelopmental Disorders
|
August 12, 2014
AGG interruptions and maternal age affect FMR1 CGG repeat allele stability during transmission
Carolyn M Yrigollen, Loreto Martorell, Blythe Durbin-Johnson, et al.
Journal of Neurodevelopmental Disorders
|
August 7, 2014
Associated features in females with an FMR1 premutation
Anne C Wheeler, Donald B Bailey, Elizabeth Berry-Kravis, et al.
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.
Frontiers in Psychiatry
|
August 23, 2021
The Phenotypic Profile Associated With the <i>FMR1</i> Premutation in Women: An Investigation of Clinical-Behavioral, Social-Cognitive, and Executive Abilities
Nell Maltman, Janna Guilfoyle, Kritika Nayar, 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.
Nature Communications
|
November 12, 2024
A framework for N-of-1 trials of individualized gene-targeted therapies for genetic diseases
Olivia Kim-McManus, Joseph G Gleeson, Laurence Mignon, et al.
Page
of 27
Search research articles
Search
Showing results (191-200 of 265) with videos related to
Sort By:
Page
of 27
The Journal of Clinical Psychiatry
|
May 9, 2009
A review of fragile X premutation disorders: expanding the psychiatric perspective
James A Bourgeois, Sarah M Coffey, Susan M Rivera, 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.
Journal of Genetic Counseling
|
May 15, 2007
Recommendations from multi-disciplinary focus groups on cascade testing and genetic counseling for fragile X-associated disorders
Allyn McConkie-Rosell, Liane Abrams, Brenda Finucane, et al.
Journal of Neurodevelopmental Disorders
|
November 19, 2025
Long-term safety and tolerability of transdermal cannabidiol gel in children and adolescents with Fragile X syndrome (ZYN2-CL-017): an interim analysis of an ongoing open-label extension study
Elizabeth Berry-Kravis, Randi Hagerman, Jonathan Cohen, et al.
Journal of Neurodevelopmental Disorders
|
August 12, 2014
AGG interruptions and maternal age affect FMR1 CGG repeat allele stability during transmission
Carolyn M Yrigollen, Loreto Martorell, Blythe Durbin-Johnson, et al.
Journal of Neurodevelopmental Disorders
|
August 7, 2014
Associated features in females with an FMR1 premutation
Anne C Wheeler, Donald B Bailey, Elizabeth Berry-Kravis, et al.
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.
Frontiers in Psychiatry
|
August 23, 2021
The Phenotypic Profile Associated With the <i>FMR1</i> Premutation in Women: An Investigation of Clinical-Behavioral, Social-Cognitive, and Executive Abilities
Nell Maltman, Janna Guilfoyle, Kritika Nayar, 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.
Nature Communications
|
November 12, 2024
A framework for N-of-1 trials of individualized gene-targeted therapies for genetic diseases
Olivia Kim-McManus, Joseph G Gleeson, Laurence Mignon, et al.
Page
of 27