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Hosneara Akter

Showing results (1-10 of 21) with videos related to

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Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 14, 2025
Response to AlkurayaHosneara 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 developmentSeyed 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 cohortNasna Nassir, Isra Sati, Shaiban Al Shaibani, et al.
Genes|February 25, 2022
Mutational Landscape of Autism Spectrum Disorder Brain TissueMarc Woodbury-Smith, Sylvia Lamoureux, Ghausia Begum, et al.
Translational Psychiatry|October 6, 2025
Mapping human brain cell type origin and diseases through single-cell transcriptomicsAnjana Soorajkumar, Bipin Balan, Nasna Nassir, et al.
Nature Medicine|March 4, 2025
Advancing clinical genomics with Middle Eastern and South Asian pangenomesNasna 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 YAP1Syed 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 analysisMariam 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 GenomeGhausia Begum, Ammar Albanna, Asma Bankapur, et al.
Pageof 3

Showing results (1-10 of 21) with videos related to

Sort By:
Pageof 3
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 14, 2025
Response to AlkurayaHosneara 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 developmentSeyed 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 cohortNasna Nassir, Isra Sati, Shaiban Al Shaibani, et al.
Genes|February 25, 2022
Mutational Landscape of Autism Spectrum Disorder Brain TissueMarc Woodbury-Smith, Sylvia Lamoureux, Ghausia Begum, et al.
Translational Psychiatry|October 6, 2025
Mapping human brain cell type origin and diseases through single-cell transcriptomicsAnjana Soorajkumar, Bipin Balan, Nasna Nassir, et al.
Nature Medicine|March 4, 2025
Advancing clinical genomics with Middle Eastern and South Asian pangenomesNasna 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 YAP1Syed 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 analysisMariam 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 GenomeGhausia Begum, Ammar Albanna, Asma Bankapur, et al.
Pageof 3