Associated Papers
Association of cell adhesion molecules levels & single nucleotide polymorphisms with vaso-occlusive crisis in sickle cell disease: A cross sectional study.
Gupta P et al.
The Indian Journal of Medical Research, 2025
The pharmacogenomic landscape in the Chinese: An analytics of pharmacogenetic variants in 206,640 individuals.
Wang LY et al.
Innovation (cambridge (mass.)), 2025
Whole-exome sequencing association study reveals genetic effects on tumor microenvironment components in nasopharyngeal carcinoma.
Zeng Y et al.
The Journal of Clinical Investigation, 2025
ACE Phenotyping in Human Blood and Tissues: Revelation of ACE Outliers and Sex Differences in ACE Sialylation.
Enyedi EE et al.
Biomedicines, 2024
Whole exome sequencing identifies genetic markers of enterovirus susceptibility in East Asians.
Sung CC et al.
Frontiers in Microbiology, 2024
Whole-Exome Sequencing in a Family with an Unexplained Tendency for Venous Thromboembolism: Multicomponent Prediction of Low-Frequency Variant Deleteriousness and of Individual Protein Interaction.
Lunghi B et al.
International Journal of Molecular Sciences, 2023
The Role of Polymorphism in the Endothelial Homeostasis and Vitamin D Metabolism Genes in the Severity of Coronary Artery Disease.
Ponasenko A et al.
Biomedicines, 2023
High Rate of Mutations of Adhesion Molecules and Extracellular Matrix Glycoproteins in Patients with Adult-Onset Focal and Segmental Glomerulosclerosis.
Marcos González S et al.
Biomedicines, 2023
Exomes of Ductal Luminal Breast Cancer Patients from Southwest Colombia: Gene Mutational Profile and Related Expression Alterations.
Cortes-Urrea C et al.
Biomolecules, 2020
Association of E-selectin S128R Polymorphism with Hereditary Breast Carcinoma Susceptibility in Turkish Patients Without BRCA1/2 Germline Mutations.
Yararbas K et al.
Balkan Journal of Medical Genetics : Bjmg, 2018
Investigation of DNA repair-related SNPs underlying susceptibility to papillary thyroid carcinoma reveals MGMT as a novel candidate gene in Belarusian children exposed to radiation.
Lonjou C et al.
Bmc Cancer, 2017
Identification of EGFLAM, SPATC1L and RNASE13 as novel susceptibility loci for aortic aneurysm in Japanese individuals by exome-wide association studies.
Yamada Y et al.
International Journal of Molecular Medicine, 2017
Three-dimensional modelling identifies novel genetic dependencies associated with breast cancer progression in the isogenic MCF10 model.
Maguire SL et al.
The Journal of Pathology, 2016
The E-selectin S149R polymorphisms in breast cancer in a northern Iran population.
Golnarnik G et al.
Cellular and Molecular Biology (noisy-le-grand, France), 2016
The eSNV-detect: a computational system to identify expressed single nucleotide variants from transcriptome sequencing data.
Tang X et al.
Nucleic Acids Research, 2014
Correlations of SELE and SELP genetic polymorphisms with myocardial infarction risk: a meta-analysis and meta-regression.
Zhao YJ et al.
Molecular Biology Reports, 2014
Correlations of SELE genetic polymorphisms with risk of coronary heart disease and myocardial infarction: a meta-analysis.
Dong ZQ et al.
Molecular Biology Reports, 2014
Association of cell adhesion molecule gene polymorphisms with recurrent aphthous stomatitis.
Alkhateeb A et al.
Journal of Oral Pathology & Medicine : Official Publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology, 2013
Effect of the E-selectin gene polymorphism (S149R) on platelet activation and adverse events after coronary artery surgery.
Stępień E et al.
Archives of Medical Research, 2011
Evaluation of variants in the selectin genes in age-related macular degeneration.
Mullins RF et al.
Bmc Medical Genetics, 2011
Single nucleotide polymorphisms in inflammation-related genes are associated with venous thromboembolism.
Beckers MM et al.
European Journal of Internal Medicine, 2010
A CETP polymorphism improves the diagnostic power of clinical examination in patients with cardiovascular disease.
Erzberger P et al.
Swiss Medical Weekly, 2010
Genetic and epidemiological risk factors in the development of bronchopulmonary dysplasia.
Mailaparambil B et al.
Disease Markers, 2010
Identification of novel single nucleotide polymorphisms in inflammatory genes as risk factors associated with trachomatous trichiasis.
Atik B et al.
Plos One, 2008
Common genetic variants in proinflammatory and other immunoregulatory genes and risk for non-Hodgkin lymphoma.
Wang SS et al.
Cancer Research, 2006
Multifactor dimensionality reduction reveals gene-gene interactions associated with multiple sclerosis susceptibility in African Americans.
Brassat D et al.
Genes and Immunity, 2006
Understanding mutations and protein stability through tripeptides.
Anishetty S et al.
Febs Letters, 2006
Genetic inflammatory factors predict restenosis after percutaneous coronary interventions.
Monraats PS et al.
Circulation, 2005
Analysis of Hemicentin-1, hOgg1, and E-selectin single nucleotide polymorphisms in age-related macular degeneration.
Bojanowski CM et al.
Transactions of the American Ophthalmological Society, 2005
Linkage and association with the NOS2A locus on chromosome 17q11 in multiple sclerosis.
Barcellos LF et al.
Annals of Neurology, 2004
Highly multiplexed genotyping of coronary artery disease-associated SNPs using MALDI-TOF mass spectrometry.
Nakai K et al.
Human Mutation, 2002