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Bassam R Ali

Showing results (91-100 of 173) with videos related to

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Pediatric Neurology|June 19, 2014
Clinical and molecular analysis of a novel COLQ missense mutation causing congenital myasthenic syndrome in a Syrian familyHussein N Matlik, Reham M Milhem, Imad Y Saadeldin, et al.
Human Genomics|December 30, 2025
Strategic insights into pharmacogenomics coverage: a theory-informed SWOT analysis of UAE insurance stakeholders' perspectivesMaram O Abbas, Azhar T Rahma, Iffat Elbarazi, et al.
Frontiers in Cell and Developmental Biology|December 29, 2023
Extracellular molecular signals shaping dendrite architecture during brain developmentMohammad I K Hamad, Bright Starling Emerald, Kukkala K Kumar, et al.
Omics : a Journal of Integrative Biology|April 27, 2021
Mapping the Educational Environment of Genomics and Pharmacogenomics in the United Arab Emirates: A Mixed-Methods Triangulated DesignAzhar T Rahma, Luai A Ahmed, Mahanna Elsheik, et al.
Metabolic Brain Disease|September 18, 2014
Asparagine synthetase deficiency detected by whole exome sequencing causes congenital microcephaly, epileptic encephalopathy and psychomotor delaySalma Ben-Salem, Joseph G Gleeson, Aisha M Al-Shamsi, et al.
Scientific Reports|December 5, 2020
Variation in 100 relevant pharmacogenes among emiratis with insights from understudied populationsZeina N Al-Mahayri, George P Patrinos, Sukanya Wattanapokayakit, et al.
Orphanet Journal of Rare Diseases|October 23, 2016
A homozygous splicing mutation in ELAC2 suggests phenotypic variability including intellectual disability with minimal cardiac involvementNadia A Akawi, Salma Ben-Salem, Jozef Hertecant, et al.
Human Molecular Genetics|March 13, 2010
Trafficking defects and loss of ligand binding are the underlying causes of all reported DDR2 missense mutations found in SMED-SL patientsBassam R Ali, Huifang Xu, Nadia A Akawi, et al.
Human Genomics|September 10, 2024
AI-derived comparative assessment of the performance of pathogenicity prediction tools on missense variants of breast cancer genesRahaf M Ahmad, Bassam R Ali, Fatma Al-Jasmi, et al.
Molecular Biology Reports|November 7, 2013
Analysis of two Arab families reveals additional support for a DFNB2 nonsyndromic phenotype of MYO7ASalma Ben-Salem, Heidi L Rehm, Patrick J Willems, et al.
Pageof 18

Showing results (91-100 of 173) with videos related to

Sort By:
Pageof 18
Pediatric Neurology|June 19, 2014
Clinical and molecular analysis of a novel COLQ missense mutation causing congenital myasthenic syndrome in a Syrian familyHussein N Matlik, Reham M Milhem, Imad Y Saadeldin, et al.
Human Genomics|December 30, 2025
Strategic insights into pharmacogenomics coverage: a theory-informed SWOT analysis of UAE insurance stakeholders' perspectivesMaram O Abbas, Azhar T Rahma, Iffat Elbarazi, et al.
Frontiers in Cell and Developmental Biology|December 29, 2023
Extracellular molecular signals shaping dendrite architecture during brain developmentMohammad I K Hamad, Bright Starling Emerald, Kukkala K Kumar, et al.
Omics : a Journal of Integrative Biology|April 27, 2021
Mapping the Educational Environment of Genomics and Pharmacogenomics in the United Arab Emirates: A Mixed-Methods Triangulated DesignAzhar T Rahma, Luai A Ahmed, Mahanna Elsheik, et al.
Metabolic Brain Disease|September 18, 2014
Asparagine synthetase deficiency detected by whole exome sequencing causes congenital microcephaly, epileptic encephalopathy and psychomotor delaySalma Ben-Salem, Joseph G Gleeson, Aisha M Al-Shamsi, et al.
Scientific Reports|December 5, 2020
Variation in 100 relevant pharmacogenes among emiratis with insights from understudied populationsZeina N Al-Mahayri, George P Patrinos, Sukanya Wattanapokayakit, et al.
Orphanet Journal of Rare Diseases|October 23, 2016
A homozygous splicing mutation in ELAC2 suggests phenotypic variability including intellectual disability with minimal cardiac involvementNadia A Akawi, Salma Ben-Salem, Jozef Hertecant, et al.
Human Molecular Genetics|March 13, 2010
Trafficking defects and loss of ligand binding are the underlying causes of all reported DDR2 missense mutations found in SMED-SL patientsBassam R Ali, Huifang Xu, Nadia A Akawi, et al.
Human Genomics|September 10, 2024
AI-derived comparative assessment of the performance of pathogenicity prediction tools on missense variants of breast cancer genesRahaf M Ahmad, Bassam R Ali, Fatma Al-Jasmi, et al.
Molecular Biology Reports|November 7, 2013
Analysis of two Arab families reveals additional support for a DFNB2 nonsyndromic phenotype of MYO7ASalma Ben-Salem, Heidi L Rehm, Patrick J Willems, et al.
Pageof 18