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Journal of Neurodevelopmental Disorders
|
April 29, 2023
Rare recurrent copy number variations in metabotropic glutamate receptor interacting genes in children with neurodevelopmental disorders
Joseph T Glessner, Munir E Khan, Xiao Chang, et al.
Nature Communications
|
March 24, 2021
NAC blocks Cystatin C amyloid complex aggregation in a cell system and in skin of HCCAA patients
Michael E March, Alvaro Gutierrez-Uzquiza, Asbjorg Osk Snorradottir, et al.
Brain : a Journal of Neurology
|
May 7, 2026
Targeting glutamatergic pathways: genetic insights into comorbid neurodevelopmental disorders
Joseph T Glessner, Munir E Khan, Xiao Chang, et al.
Peerj
|
August 23, 2017
Genome-wide association study identifies novel type II diabetes risk loci in Jordan subpopulations
Rana Dajani, Jin Li, Zhi Wei, et al.
JAMA Neurology
|
March 31, 2025
N-Acetylcysteine for Hereditary Cystatin C Amyloid Angiopathy: A Nonrandomized Clinical Trial
Asbjorg Osk Snorradottir, Alvaro Gutierrez-Uzquiza, Paloma Bragado, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
August 3, 2024
Secondary ACMG and non-ACMG genetic findings in a multiethnic cohort of 16,713 pediatric participants
Amir Hossein Saeidian, Michael E March, Leila Youssefian, et al.
Annals of the Rheumatic Diseases
|
January 7, 2021
Association of novel rare coding variants with juvenile idiopathic arthritis
Xinyi Meng, Xiaoyuan Hou, Ping Wang, et al.
Medrxiv : the Preprint Server for Health Sciences
|
July 1, 2024
Multi-ancestry Genome-Wide Association Meta-Analysis Identifies Novel Loci in Atopic Dermatitis
Meritxell Oliva, Mrinal K Sarkar, Michael E March, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
July 24, 2024
Novel insights into the phenotypic spectrum and pathogenesis of Hardikar syndrome
Alanna Strong, Michael E March, Christopher J Cardinale, et al.
Genetics in Medicine Open
|
March 5, 2026
Single vs dual genetic disease in children with congenital anomalies and solid tumors
Deborah J Watson, Amir Hossein Saeidian, Xiang Wang, et al.
Page
of 6
Search research articles
Search
Showing results (31-40 of 54) with videos related to
Sort By:
Page
of 6
Journal of Neurodevelopmental Disorders
|
April 29, 2023
Rare recurrent copy number variations in metabotropic glutamate receptor interacting genes in children with neurodevelopmental disorders
Joseph T Glessner, Munir E Khan, Xiao Chang, et al.
Nature Communications
|
March 24, 2021
NAC blocks Cystatin C amyloid complex aggregation in a cell system and in skin of HCCAA patients
Michael E March, Alvaro Gutierrez-Uzquiza, Asbjorg Osk Snorradottir, et al.
Brain : a Journal of Neurology
|
May 7, 2026
Targeting glutamatergic pathways: genetic insights into comorbid neurodevelopmental disorders
Joseph T Glessner, Munir E Khan, Xiao Chang, et al.
Peerj
|
August 23, 2017
Genome-wide association study identifies novel type II diabetes risk loci in Jordan subpopulations
Rana Dajani, Jin Li, Zhi Wei, et al.
JAMA Neurology
|
March 31, 2025
N-Acetylcysteine for Hereditary Cystatin C Amyloid Angiopathy: A Nonrandomized Clinical Trial
Asbjorg Osk Snorradottir, Alvaro Gutierrez-Uzquiza, Paloma Bragado, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
August 3, 2024
Secondary ACMG and non-ACMG genetic findings in a multiethnic cohort of 16,713 pediatric participants
Amir Hossein Saeidian, Michael E March, Leila Youssefian, et al.
Annals of the Rheumatic Diseases
|
January 7, 2021
Association of novel rare coding variants with juvenile idiopathic arthritis
Xinyi Meng, Xiaoyuan Hou, Ping Wang, et al.
Medrxiv : the Preprint Server for Health Sciences
|
July 1, 2024
Multi-ancestry Genome-Wide Association Meta-Analysis Identifies Novel Loci in Atopic Dermatitis
Meritxell Oliva, Mrinal K Sarkar, Michael E March, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
July 24, 2024
Novel insights into the phenotypic spectrum and pathogenesis of Hardikar syndrome
Alanna Strong, Michael E March, Christopher J Cardinale, et al.
Genetics in Medicine Open
|
March 5, 2026
Single vs dual genetic disease in children with congenital anomalies and solid tumors
Deborah J Watson, Amir Hossein Saeidian, Xiang Wang, et al.
Page
of 6