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Bassam R Ali

Showing results (161-170 of 173) with videos related to

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Frontiers in Pharmacology|September 15, 2025
A multi-centre observational cohort study on pharmacogenomic predictors of rosuvastatin discontinuation in a multiethnic populationMais N Alqasrawi, Zeina N Al-Mahayri, Lubna Q Khasawneh, et al.
Frontiers in Molecular Biosciences|October 16, 2024
Profiling genetic variants in cardiovascular disease genes among a Heterogeneous cohort of Mendelian conditions patients and electronic health recordsNadia Akawi, Ghadeera Al Mansoori, Anwar Al Zaabi, et al.
American Journal of Human Genetics|July 19, 2011
Faulty initiation of proteoglycan synthesis causes cardiac and joint defectsSevjidmaa Baasanjav, Lihadh Al-Gazali, Taishi Hashiguchi, et al.
Human Genomics|November 13, 2016
Novel genetic risk variants for pediatric celiac diseaseAngeliki Balasopoulou, Biljana Stanković, Angeliki Panagiotara, et al.
Cell|July 20, 2010
SRD5A3 is required for converting polyprenol to dolichol and is mutated in a congenital glycosylation disorderVincent Cantagrel, Dirk J Lefeber, Bobby G Ng, et al.
Human Molecular Genetics|February 7, 2014
METTL23, a transcriptional partner of GABPA, is essential for human cognitionRachel E Reiff, Bassam R Ali, Byron Baron, et al.
American Journal of Human Genetics|August 5, 2008
Mutations in the cilia gene ARL13B lead to the classical form of Joubert syndromeVincent Cantagrel, Jennifer L Silhavy, Stephanie L Bielas, et al.
Human Genomics|December 9, 2017
Genomic variants in the FTO gene are associated with sporadic amyotrophic lateral sclerosis in Greek patientsKonstantinos Mitropoulos, Eleni Merkouri Papadima, Georgia Xiromerisiou, et al.
Human Genome Variation|February 5, 2021
Prevalence of pharmacogenomic variants in 100 pharmacogenes among Southeast Asian populations under the collaboration of the Southeast Asian Pharmacogenomics Research Network (SEAPharm)Chakkaphan Runcharoen, Koya Fukunaga, Insee Sensorn, et al.
Human Genetics|March 3, 2017
Haploinsufficiency of the E3 ubiquitin-protein ligase gene TRIP12 causes intellectual disability with or without autism spectrum disorders, speech delay, and dysmorphic featuresJing Zhang, Tomasz Gambin, Bo Yuan, et al.
Pageof 18

Showing results (161-170 of 173) with videos related to

Sort By:
Pageof 18
Frontiers in Pharmacology|September 15, 2025
A multi-centre observational cohort study on pharmacogenomic predictors of rosuvastatin discontinuation in a multiethnic populationMais N Alqasrawi, Zeina N Al-Mahayri, Lubna Q Khasawneh, et al.
Frontiers in Molecular Biosciences|October 16, 2024
Profiling genetic variants in cardiovascular disease genes among a Heterogeneous cohort of Mendelian conditions patients and electronic health recordsNadia Akawi, Ghadeera Al Mansoori, Anwar Al Zaabi, et al.
American Journal of Human Genetics|July 19, 2011
Faulty initiation of proteoglycan synthesis causes cardiac and joint defectsSevjidmaa Baasanjav, Lihadh Al-Gazali, Taishi Hashiguchi, et al.
Human Genomics|November 13, 2016
Novel genetic risk variants for pediatric celiac diseaseAngeliki Balasopoulou, Biljana Stanković, Angeliki Panagiotara, et al.
Cell|July 20, 2010
SRD5A3 is required for converting polyprenol to dolichol and is mutated in a congenital glycosylation disorderVincent Cantagrel, Dirk J Lefeber, Bobby G Ng, et al.
Human Molecular Genetics|February 7, 2014
METTL23, a transcriptional partner of GABPA, is essential for human cognitionRachel E Reiff, Bassam R Ali, Byron Baron, et al.
American Journal of Human Genetics|August 5, 2008
Mutations in the cilia gene ARL13B lead to the classical form of Joubert syndromeVincent Cantagrel, Jennifer L Silhavy, Stephanie L Bielas, et al.
Human Genomics|December 9, 2017
Genomic variants in the FTO gene are associated with sporadic amyotrophic lateral sclerosis in Greek patientsKonstantinos Mitropoulos, Eleni Merkouri Papadima, Georgia Xiromerisiou, et al.
Human Genome Variation|February 5, 2021
Prevalence of pharmacogenomic variants in 100 pharmacogenes among Southeast Asian populations under the collaboration of the Southeast Asian Pharmacogenomics Research Network (SEAPharm)Chakkaphan Runcharoen, Koya Fukunaga, Insee Sensorn, et al.
Human Genetics|March 3, 2017
Haploinsufficiency of the E3 ubiquitin-protein ligase gene TRIP12 causes intellectual disability with or without autism spectrum disorders, speech delay, and dysmorphic featuresJing Zhang, Tomasz Gambin, Bo Yuan, et al.
Pageof 18