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Bassam R Ali

Showing results (81-90 of 173) with videos related to

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Plos One|January 5, 2012
Identification of new alleles and the determination of alleles and genotypes frequencies at the CYP2D6 gene in EmiratisRula Y Qumsieh, Bassam R Ali, Yousef M Abdulrazzaq, et al.
Omics : a Journal of Integrative Biology|May 10, 2017
Key Pharmacogenomic Considerations for Sickle Cell Disease PatientsAlexandra Kolliopoulou, Apostolos Stratopoulos, Stavroula Siamoglou, et al.
American Journal of Medical Genetics. Part A|July 29, 2018
A recessive truncating variant in thrombospondin-1 domain containing protein 1 gene THSD1 is the underlying cause of nonimmune hydrops fetalis, congenital cardiac defects, and haemangiomas in four patients from a consanguineous familyHanadi A Abdelrahman, Aisha Al-Shamsi, Anne John, et al.
BMC Medical Genetics|February 27, 2010
Molecular and clinical analysis of Ellis-van Creveld syndrome in the United Arab EmiratesBassam R Ali, Nadia A Akawi, Faris Chedid, et al.
Human Genetics|August 1, 2007
Novel Robinow syndrome causing mutations in the proximal region of the frizzled-like domain of ROR2 are retained in the endoplasmic reticulumBassam R Ali, Steve Jeffery, Neha Patel, et al.
Briefings in Bioinformatics|December 27, 2023
A review of genetic variant databases and machine learning tools for predicting the pathogenicity of breast cancerRahaf M Ahmad, Bassam R Ali, Fatma Al-Jasmi, et al.
Human Genomics|October 17, 2021
Development of the pharmacogenomics and genomics literacy framework for pharmacistsAzhar T Rahma, Iffat Elbarazi, Bassam R Ali, et al.
Journal of Personalized Medicine|November 13, 2020
Knowledge, Attitudes, and Perceived Barriers toward Genetic Testing and Pharmacogenomics among Healthcare Workers in the United Arab Emirates: A Cross-Sectional StudyAzhar T Rahma, Mahanna Elsheik, Bassam R Ali, et al.
Journal of Molecular Graphics & Modelling|November 22, 2023
Discovery of pyrimidoindol and benzylpyrrolyl inhibitors targeting SARS-CoV-2 main protease (M<sup>pro</sup>) through pharmacophore modelling, covalent docking, and biological evaluationRadwa E Mahgoub, Feda E Mohamed, Bassam R Ali, et al.
American Journal of Medical Genetics. Part A|March 22, 2017
A novel aberrant splice site mutation in COL27A1 is responsible for Steel syndrome and extension of the phenotype to include hearing lossNesrin Gariballa, Afif Ben-Mahmoud, Makanko Komara, et al.
Pageof 18

Showing results (81-90 of 173) with videos related to

Sort By:
Pageof 18
Plos One|January 5, 2012
Identification of new alleles and the determination of alleles and genotypes frequencies at the CYP2D6 gene in EmiratisRula Y Qumsieh, Bassam R Ali, Yousef M Abdulrazzaq, et al.
Omics : a Journal of Integrative Biology|May 10, 2017
Key Pharmacogenomic Considerations for Sickle Cell Disease PatientsAlexandra Kolliopoulou, Apostolos Stratopoulos, Stavroula Siamoglou, et al.
American Journal of Medical Genetics. Part A|July 29, 2018
A recessive truncating variant in thrombospondin-1 domain containing protein 1 gene THSD1 is the underlying cause of nonimmune hydrops fetalis, congenital cardiac defects, and haemangiomas in four patients from a consanguineous familyHanadi A Abdelrahman, Aisha Al-Shamsi, Anne John, et al.
BMC Medical Genetics|February 27, 2010
Molecular and clinical analysis of Ellis-van Creveld syndrome in the United Arab EmiratesBassam R Ali, Nadia A Akawi, Faris Chedid, et al.
Human Genetics|August 1, 2007
Novel Robinow syndrome causing mutations in the proximal region of the frizzled-like domain of ROR2 are retained in the endoplasmic reticulumBassam R Ali, Steve Jeffery, Neha Patel, et al.
Briefings in Bioinformatics|December 27, 2023
A review of genetic variant databases and machine learning tools for predicting the pathogenicity of breast cancerRahaf M Ahmad, Bassam R Ali, Fatma Al-Jasmi, et al.
Human Genomics|October 17, 2021
Development of the pharmacogenomics and genomics literacy framework for pharmacistsAzhar T Rahma, Iffat Elbarazi, Bassam R Ali, et al.
Journal of Personalized Medicine|November 13, 2020
Knowledge, Attitudes, and Perceived Barriers toward Genetic Testing and Pharmacogenomics among Healthcare Workers in the United Arab Emirates: A Cross-Sectional StudyAzhar T Rahma, Mahanna Elsheik, Bassam R Ali, et al.
Journal of Molecular Graphics & Modelling|November 22, 2023
Discovery of pyrimidoindol and benzylpyrrolyl inhibitors targeting SARS-CoV-2 main protease (M<sup>pro</sup>) through pharmacophore modelling, covalent docking, and biological evaluationRadwa E Mahgoub, Feda E Mohamed, Bassam R Ali, et al.
American Journal of Medical Genetics. Part A|March 22, 2017
A novel aberrant splice site mutation in COL27A1 is responsible for Steel syndrome and extension of the phenotype to include hearing lossNesrin Gariballa, Afif Ben-Mahmoud, Makanko Komara, et al.
Pageof 18