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Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
March 14, 2025
Response to Alkuraya
Hosneara Akter, Nasna Nassir, Mohammed Uddin
Human Genetics
|
November 16, 2022
Overlapping pathogenic de novo CNVs in neurodevelopmental disorders and congenital anomalies impacting constraint genes regulating early development
Seyed Ali Safizadeh Shabestari, Nasna Nassir, Samana Sopariwala, et al.
Neurogenetics
|
March 24, 2022
Detection of copy number variants and genes by chromosomal microarray in an Emirati neurodevelopmental disorders cohort
Nasna Nassir, Isra Sati, Shaiban Al Shaibani, et al.
Genes
|
February 25, 2022
Mutational Landscape of Autism Spectrum Disorder Brain Tissue
Marc Woodbury-Smith, Sylvia Lamoureux, Ghausia Begum, et al.
Translational Psychiatry
|
October 6, 2025
Mapping human brain cell type origin and diseases through single-cell transcriptomics
Anjana Soorajkumar, Bipin Balan, Nasna Nassir, et al.
Nature Medicine
|
March 4, 2025
Advancing clinical genomics with Middle Eastern and South Asian pangenomes
Nasna Nassir, Mohamed A Almarri, Hosneara Akter, et al.
Ebiomedicine
|
May 16, 2019
Antibody-drug conjugate T-DM1 treatment for HER2+ breast cancer induces ROR1 and confers resistance through activation of Hippo transcriptional coactivator YAP1
Syed S Islam, Mohammed Uddin, Abu Shadat M Noman, et al.
Clinical Case Reports
|
August 28, 2018
An <i>ANKRD26</i> nonsense somatic mutation in a female with epidermodysplasia verruciformis (Tree Man Syndrome)
K M Furkan Uddin, Robed Amin, Sabbiha Nadia Majumder, et al.
Human Genetics
|
February 19, 2026
Horizon: CNV interpretation through rapid automated ACMG-aligned pathogenicity analysis
Mariam Eldesouky, Suhana Shiyas, Amirul Islam, et al.
International Journal of Molecular Sciences
|
March 6, 2021
Long-Read Sequencing Improves the Detection of Structural Variations Impacting Complex Non-Coding Elements of the Genome
Ghausia Begum, Ammar Albanna, Asma Bankapur, et al.
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of 3
Search research articles
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Showing results (1-10 of 21) with videos related to
Sort By:
Page
of 3
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
March 14, 2025
Response to Alkuraya
Hosneara Akter, Nasna Nassir, Mohammed Uddin
Human Genetics
|
November 16, 2022
Overlapping pathogenic de novo CNVs in neurodevelopmental disorders and congenital anomalies impacting constraint genes regulating early development
Seyed Ali Safizadeh Shabestari, Nasna Nassir, Samana Sopariwala, et al.
Neurogenetics
|
March 24, 2022
Detection of copy number variants and genes by chromosomal microarray in an Emirati neurodevelopmental disorders cohort
Nasna Nassir, Isra Sati, Shaiban Al Shaibani, et al.
Genes
|
February 25, 2022
Mutational Landscape of Autism Spectrum Disorder Brain Tissue
Marc Woodbury-Smith, Sylvia Lamoureux, Ghausia Begum, et al.
Translational Psychiatry
|
October 6, 2025
Mapping human brain cell type origin and diseases through single-cell transcriptomics
Anjana Soorajkumar, Bipin Balan, Nasna Nassir, et al.
Nature Medicine
|
March 4, 2025
Advancing clinical genomics with Middle Eastern and South Asian pangenomes
Nasna Nassir, Mohamed A Almarri, Hosneara Akter, et al.
Ebiomedicine
|
May 16, 2019
Antibody-drug conjugate T-DM1 treatment for HER2+ breast cancer induces ROR1 and confers resistance through activation of Hippo transcriptional coactivator YAP1
Syed S Islam, Mohammed Uddin, Abu Shadat M Noman, et al.
Clinical Case Reports
|
August 28, 2018
An <i>ANKRD26</i> nonsense somatic mutation in a female with epidermodysplasia verruciformis (Tree Man Syndrome)
K M Furkan Uddin, Robed Amin, Sabbiha Nadia Majumder, et al.
Human Genetics
|
February 19, 2026
Horizon: CNV interpretation through rapid automated ACMG-aligned pathogenicity analysis
Mariam Eldesouky, Suhana Shiyas, Amirul Islam, et al.
International Journal of Molecular Sciences
|
March 6, 2021
Long-Read Sequencing Improves the Detection of Structural Variations Impacting Complex Non-Coding Elements of the Genome
Ghausia Begum, Ammar Albanna, Asma Bankapur, et al.
Page
of 3