Associated Papers
Prediction of the most deleterious non-synonymous SNPs in the human IL1B gene: evidence from bioinformatics analyses.
Abuzaid O et al.
Bmc Genomic Data, 2024
ACE Phenotyping in Human Blood and Tissues: Revelation of ACE Outliers and Sex Differences in ACE Sialylation.
Enyedi EE et al.
Biomedicines, 2024
Association of genetic variation in COL11A1 with adolescent idiopathic scoliosis.
Yu H et al.
Elife, 2024
Association of genetic variation in COL11A1 with adolescent idiopathic scoliosis.
Yu H et al.
Biorxiv : the Preprint Server for Biology, 2023
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
Association of Single Nucleotide Polymorphisms of Cytokine Genes with Depression, Schizophrenia and Bipolar Disorder.
Mikhalitskaya EV et al.
Genes, 2023
Genetic variants of TLR4, including the novel variant, rs5030719, and related genes are associated with susceptibility to clinical malaria in African children.
Ariff A et al.
Malaria Journal, 2023
Bi-allelic mutation in SEC16B alters collagen trafficking and increases ER stress.
El-Gazzar A et al.
Embo Molecular Medicine, 2023
Genetic variants determine intrafamilial variability of SARS-CoV-2 clinical outcomes in 19 Italian families.
Azzarà A et al.
Plos One, 2022
Impact of rare and common genetic variation in the interleukin-1 pathway on human cytokine responses.
van Deuren RC et al.
Genome Medicine, 2021
Role of the Host Genetic Susceptibility to 2009 Pandemic Influenza A H1N1.
Pérez-Rubio G et al.
Viruses, 2021
NGS study of glucocorticoid response genes in inflammatory bowel disease patients.
Skrzypczak-Zielinska M et al.
Archives of Medical Science : Ams, 2021
Prioritization of candidate genes for a South African family with Parkinson's disease using in-silico tools.
Sebate B et al.
Plos One, 2021
Mannose-binding lectin 2 gene polymorphisms and their association with tuberculosis in a Chinese population.
Zhang JX et al.
Infectious Diseases of Poverty, 2020
Interleukin 1 alpha (IL1A) polymorphisms and risk of endometriosis in Iranian population: a case-control study.
Badie A et al.
Gynecological Endocrinology : the Official Journal of the International Society of Gynecological Endocrinology, 2020
Host Single Nucleotide Polymorphisms Modulating Influenza A Virus Disease in Humans.
Nogales A et al.
Pathogens (basel, Switzerland), 2019
Plasticity of Drug-Naïve and Vemurafenib- or Trametinib-Resistant Melanoma Cells in Execution of Differentiation/Pigmentation Program.
Czyz M et al.
Journal of Oncology, 2019
Host genetic polymorphisms and serological response against malaria in a selected population in Sri Lanka.
Dewasurendra RL et al.
Malaria Journal, 2018
Inflammatory Gene Polymorphisms in Lung Cancer Susceptibility.
Eaton KD et al.
Journal of Thoracic Oncology : Official Publication of the International Association for the Study of Lung Cancer, 2018
Meta-analyses of IL1A polymorphisms and the risk of several autoimmune diseases published in databases.
Su H et al.
Plos One, 2018
Evaluating the Causal Link Between Malaria Infection and Endemic Burkitt Lymphoma in Northern Uganda: A Mendelian Randomization Study.
Legason ID et al.
Ebiomedicine, 2017
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
Polymorphisms in host immune response associated genes and risk of nasopharyngeal carcinoma development in Portugal.
Sousa H et al.
Immunobiology, 2016
Interleukin polymorphisms associated with overall survival, disease-free survival, and recurrence in non-small cell lung cancer patients.
Woods NT et al.
Molecular Carcinogenesis, 2015
Pooled sequencing of 531 genes in inflammatory bowel disease identifies an associated rare variant in BTNL2 and implicates other immune related genes.
Prescott NJ et al.
Plos Genetics, 2015
Polymorphisms in cytokine genes IL6, TNF, IL10, IL17A and IFNG influence susceptibility to complicated skin and skin structure infections.
Stappers MH et al.
European Journal of Clinical Microbiology & Infectious Diseases : Official Publication of the European Society of Clinical Microbiology, 2014
Interleukin-1β genotype and circulating levels in cancer patients: metastatic status and pain perception.
Oliveira A et al.
Clinical Biochemistry, 2014
Genetic variations in IL1A and IL1RN are associated with the risk of preeclampsia in Chinese Han population.
Li J et al.
Scientific Reports, 2014
Risk of ovarian cancer and the NF-κB pathway: genetic association with IL1A and TNFSF10.
Charbonneau B et al.
Cancer Research, 2014
Integrated mRNA and microRNA transcriptome sequencing characterizes sequence variants and mRNA-microRNA regulatory network in nasopharyngeal carcinoma model systems.
Szeto CY et al.
Febs Open Bio, 2014
Symptom clusters of pain, depressed mood, and fatigue in lung cancer: assessing the role of cytokine genes.
Reyes-Gibby CC et al.
Supportive Care in Cancer : Official Journal of the Multinational Association of Supportive Care in Cancer, 2013
Genetic variants in IL1A and IL1B contribute to the susceptibility to 2009 pandemic H1N1 influenza A virus.
Liu Y et al.
Bmc Immunology, 2013
A nonsynonymous variant of IL1A is associated with endometriosis in Japanese population.
Hata Y et al.
Journal of Human Genetics, 2013
Substitution at IL1RN and deletion at SLC4A11 segregating with phenotype in familial keratoconus.
Nowak DM et al.
Investigative Ophthalmology & Visual Science, 2013
Ovarian cancer risk associated with inherited inflammation-related variants.
White KL et al.
Cancer Research, 2012
Host immune gene polymorphisms were associated with the prognosis of non-small-cell lung cancer in Chinese.
Dai J et al.
International Journal of Cancer, 2012
Genetic variants associated with breast-cancer risk: comprehensive research synopsis, meta-analysis, and epidemiological evidence.
Zhang B et al.
The Lancet. Oncology, 2011
Coding single-nucleotide polymorphisms of interleukin-1 gene cluster are not associated with Kawasaki disease in the Korean population.
Kim SK et al.
Pediatric Cardiology, 2011
The dopamine β-hydroxylase -1021C/T polymorphism is associated with the risk of Alzheimer's disease in the Epistasis Project.
Combarros O et al.
Bmc Medical Genetics, 2010
Genetic variants in inflammation-related genes are associated with radiation-induced toxicity following treatment for non-small cell lung cancer.
Hildebrandt MA et al.
Plos One, 2010
Role of inflammation gene polymorphisms on pain severity in lung cancer patients.
Reyes-Gibby CC et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology, 2009
Cytokine and cytokine receptor single-nucleotide polymorphisms predict risk for non-small cell lung cancer among women.
Van Dyke AL et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology, 2009
Cytokine SNPs: Comparison of allele frequencies by race and implications for future studies.
Van Dyke AL et al.
Cytokine, 2009
Genome-wide analysis to predict protein sequence variations that change phosphorylation sites or their corresponding kinases.
Ryu GM et al.
Nucleic Acids Research, 2009