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Author Details

Manal Alaamery
National Centre for Genomic Technologies
2008
36
14
PMIDPaper TitleJournal TitlePublished Year
37998513<i>TGFBR1</i> Variants Can Associate with Non-Syndromic Congenital Heart Disease without Aortopathy.J Cardiovasc Dev Dis2023
34929414Association of KIR gene polymorphisms with COVID-19 disease.Clin Immunol2022
35373199DNA-Mimicking Metal-Organic Frameworks with Accessible Adenine Faces for Complementary Base Pairing.JACS Au2022
36145626Reply to Zandi, M.; Soltani, S. Comment on "Alfassam et al. Development of a Colorimetric Tool for SARS-CoV-2 and Other Respiratory Viruses Detection Using Sialic Acid Fabricated Gold Nanoparticles. <i>Pharmaceutics</i> 2021, <i>13</i>, 502".Pharmaceutics2022
36035137Analysis of chronic kidney disease patients by targeted next-generation sequencing identifies novel variants in kidney-related genes.Front Genet2022
36327219Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative.PLoS Genet2022
34978705Correlation between ABO Blood Group Phenotype and the Risk of COVID-19 Infection and Severity of Disease in a Saudi Arabian Cohort.J Epidemiol Glob Health2022
35214093Fast-Dissolving Nifedipine and Atorvastatin Calcium Electrospun Nanofibers as a Potential Buccal Delivery System.Pharmaceutics2022
35205398Consanguinity and Congenital Heart Disease Susceptibility: Insights into Rare Genetic Variations in Saudi Arabia.Genes (Basel)2022
35205281The Role of the Disrupted Podosome Adaptor Protein (SH3PXD2B) in Frank-Ter Haar Syndrome.Genes (Basel)2022
32402091Role of sphingolipid metabolism in neurodegeneration.J Neurochem2021
33919081Novel Autosomal Recessive Splice-Altering Variant in <i>PRKD1</i> Is Associated with Congenital Heart Disease.Genes (Basel)2021
33918625Development of Epirubicin-Loaded Biocompatible Polymer PLA-PEG-PLA Nanoparticles: Synthesis, Characterization, Stability, and In Vitro Anticancerous Assessment.Polymers (Basel)2021
33917625Development of a Colorimetric Tool for SARS-CoV-2 and Other Respiratory Viruses Detection Using Sialic Acid Fabricated Gold Nanoparticles.Pharmaceutics2021
33838280Interferon-induced transmembrane protein-3 genetic variant rs12252 is associated with COVID-19 mortality.Genomics2021
34043590Rare loss-of-function variants in type I IFN immunity genes are not associated with severe COVID-19.J Clin Invest2021
34145321A homozygous nonsense mutation in DCBLD2 is a candidate cause of developmental delay, dysmorphic features and restrictive cardiomyopathy.Sci Rep2021
34354361Early Prediction of COVID-19 Ventilation Requirement and Mortality from Routinely Collected Baseline Chest Radiographs, Laboratory, and Clinical Data with Machine Learning.J Multidiscip Healthc2021
33398468A cell-based drug delivery platform for treating central nervous system inflammation.J Mol Med (Berl)2021
32286682PDCD6IP, encoding a regulator of the ESCRT complex, is mutated in microcephaly.Clin Genet2020
31998667A Novel Homozygous Nonsense Mutation p.Cys366* in the WNT10B Gene Underlying Split-Hand/Split Foot Malformation in a Consanguineous Pakistani Family.Front Pediatr2020
33398295Failure to replicate the association of rare loss-of-function variants in type I IFN immunity genes with severe COVID-19.medRxiv2020
32679809Optimized Polyethylene Glycolylated Polymer-Lipid Hybrid Nanoparticles as a Potential Breast Cancer Treatment.Pharmaceutics2020
32696233Blood pressure-lowering activity of statins: a systematic literature review and meta-analysis of placebo-randomized controlled trials.Eur J Clin Pharmacol2020
32323311ADAMTS19-associated heart valve defects: Novel genetic variants consolidating a recognizable cardiac phenotype.Clin Genet2020
31068897A Novel Homozygous Non-sense Mutation in the Catalytic Domain of MTHFR Causes Severe 5,10-Methylenetetrahydrofolate Reductase Deficiency.Front Neurol2019
28867658Identification and characterization of a potent and biologically-active PDE4/7 inhibitor via fission yeast-based assays.Cell Signal2017
28143899A missense mutation in the <i>CRBN</i> gene that segregates with intellectual disability and self-mutilating behaviour in a consanguineous Saudi family.J Med Genet2017
29343958Preparation of anastrozole loaded PEG-PLA nanoparticles: evaluation of apoptotic response of breast cancer cell lines.Int J Nanomedicine2017
27302770Anti-inflammatory effects of novel barbituric acid derivatives in T lymphocytes.Int Immunopharmacol2016
25663424Asparagine Synthetase Deficiency: New Inborn Errors of Metabolism.JIMD Rep2015
26102488DNA-Based Nanobiosensors as an Emerging Platform for Detection of Disease.Sensors (Basel)2015
20228279New classes of PDE7 inhibitors identified by a fission yeast-based HTS.J Biomol Screen2010
20474083A novel custom resequencing array for dilated cardiomyopathy.Genet Med2010
19266076Pro-aging effects of glucose signaling through a G protein-coupled glucose receptor in fission yeast.PLoS Genet2009
18430926Schizosaccharomyces pombe Hsp90/Git10 is required for glucose/cAMP signaling.Genetics2008
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Collaborators

National Centre for Genomic Technologies
Co-authored papers 23
King Abdullah International Medical Research Center (KAIMRC)
Co-authored papers 5
Emory School of Medicine
Co-authored papers 5
King Saud bin Abdulaziz Medical City for Science and Technology
Co-authored papers 4
McGill University
Co-authored papers 3
Victor Philip Dahdaleh Institute of Genomic Medicine at McGill University
Co-authored papers 3
5 Prime Sciences Inc.
Co-authored papers 3
Columbia University Irving Medical Center
Co-authored papers 3
Qatar Foundation Research, Qatar Foundation
Co-authored papers 3
King Faisal Specialist Hospital & Research Centre
Co-authored papers 3
McGill University
Co-authored papers 3
Qatar Foundation
Co-authored papers 3
Columbia University
Co-authored papers 3
Victor Philip Dahdaleh Institute of Genomic Medicine at McGill University
Co-authored papers 3
Vrije Universiteit
Co-authored papers 3
Lady Davis Institute for Medical Research, Jewish General Hospital
Co-authored papers 3
Institute for the Advanced Study of Human Biology (ASHBi), Kyoto University
Co-authored papers 3
McGill University
Co-authored papers 3
Institute for Genomic Medicine, Columbia University Irving Medical Center
Co-authored papers 3
Institute for Genomic Medicine, Columbia University Medical Center
Co-authored papers 3
Co-authored papers 2
Dongguk University-Seoul
Co-authored papers 2
School of Pharmacy, University of Southern California
Co-authored papers 2
McGill University
Co-authored papers 2
McGill University
Co-authored papers 2
Vishwakarma University
Co-authored papers 2
The Hospital for Sick Children
Co-authored papers 2
Columbia University College of Physicians and Surgeons
Co-authored papers 2
Qatar Foundation Research, Qatar Foundation
Co-authored papers 2
Co-authored papers 1