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Annals of Saudi Medicine|March 22, 2016
Investigation of KIF6 Trp719Arg gene polymorphism in a case-control study of coronary artery disease and non-fatal myocardial infarction in the Eastern Province of Saudi ArabiaChittibabu Vatte, Cyril Cyrus, Abdullah Mohammed Al Shehri, et al.
Human Genomics|March 4, 2016
The impact of common polymorphisms in CETP and ABCA1 genes with the risk of coronary artery disease in Saudi ArabiansCyril Cyrus, Chittibabu Vatte, Awatif Al-Nafie, et al.
Lipids in Health and Disease|February 21, 2022
Insulin resistance induced by de novo pathway-generated C16-ceramide is associated with type 2 diabetes in an obese populationShahanas Chathoth, Mona H Ismail, Hanan M Alghamdi, et al.
The EMBO Journal|November 2, 2014
IκΒα inhibits apoptosis at the outer mitochondrial membrane independently of NF-κB retentionEvangelos Pazarentzos, Anne-Laure Mahul-Mellier, Christoph Datler, et al.
Genome Medicine|September 1, 2023
Interplay of Mendelian and polygenic risk factors in Arab breast cancer patientsMohammed Al-Jumaan, Hoyin Chu, Abdullah Alsulaiman, et al.
BMC Nephrology|April 19, 2018
Assessing known chronic kidney disease associated genetic variants in Saudi Arabian populationsCyril Cyrus, Samir Al-Mueilo, Chittibabu Vatte, et al.
Genetics and Molecular Biology|September 2, 2017
Type 2 diabetes associated variants of KCNQ1 strongly confer the risk of cardiovascular disease among the Saudi Arabian populationMaha S Al-Shammari, Rhaya Al-Ali, Nader Al-Balawi, et al.
Plos One|February 6, 2016
Exome-Wide Association Analysis of Coronary Artery Disease in the Kingdom of Saudi Arabia PopulationCarolien G de Kovel, Flip Mulder, Jessica van Setten, et al.
Stem Cell Reports|January 24, 2017
A Comprehensive, Ethnically Diverse Library of Sickle Cell Disease-Specific Induced Pluripotent Stem CellsSeonmi Park, Andreia Gianotti-Sommer, Francisco Javier Molina-Estevez, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 9, 2016
Genetic, immunological, and clinical features of patients with bacterial and fungal infections due to inherited IL-17RA deficiencyRomain Lévy, Satoshi Okada, Vivien Béziat, et al.
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