Associated Papers
The pharmacogenomic landscape in the Chinese: An analytics of pharmacogenetic variants in 206,640 individuals.
Wang LY et al.
Innovation (cambridge (mass.)), 2025
39991480 (PubMed )
Supplement: mmc5.xlsx › Sheet1
Molecular characterization of sub-frontal recurrent medulloblastomas reveals potential clinical relevance.
Chen Z et al.
Frontiers in Neurology, 2023
37181548 (PubMed )
Supplement: Data_Sheet_2.xlsx › Germline_mutation-case_2
Association of single nucleotide polymorphisms in CXCR1, CXCR2 and CXCL5 with Behçet disease: a study in the Denizli province of Turkey.
Arıkan S et al.
Clinical and Experimental Dermatology, 2021
Comprehensive pharmacogenetic profiling of the epidermal growth factor receptor pathway for biomarkers of response to, and toxicity from, cetuximab.
Madi A et al.
Journal of Medical Genetics, 2017
Innate immunity and genetic determinants of urinary tract infection susceptibility.
Godaly G et al.
Current Opinion in Infectious Diseases, 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
25671699 (PubMed )
Supplement: pgen.1004955.s006.xlsx › SNVs
Next generation exome sequencing of paediatric inflammatory bowel disease patients identifies rare and novel variants in candidate genes.
Christodoulou K et al.
Gut, 2013
[M31R and R335C polymorphic variants of the IL8RA gene in Russian and Buryat patients with atopic bronchial asthma].
Voron'ko OE et al.
Genetika, 2011
Genetic risk for recurrent urinary tract infections in humans: a systematic review.
Zaffanello M et al.
Journal of Biomedicine & Biotechnology, 2010
Genetic variation of the human urinary tract innate immune response and asymptomatic bacteriuria in women.
Hawn TR et al.
Plos One, 2009
Genetic determinants of HIV-1 infection and progression to AIDS: susceptibility to HIV infection.
Kaur G et al.
Tissue Antigens, 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
19139070 (PubMed )
Supplement: gkn1008_nar-01723-s-2008-File006.xls › TypeII-
Impact of IL8 and IL8-receptor alpha polymorphisms on the genetics of bronchial asthma and severe RSV infections.
Puthothu B et al.
Clinical and Molecular Allergy : Cma, 2006
Polymorphisms in interleukin 8 and its receptors (IL8, IL8RA and IL8RB) and association of common IL8 receptor variants with peripheral blood eosinophil counts.
Cheong HS et al.
Journal of Human Genetics, 2006
Association of interleukin-8 receptor alpha polymorphisms with chronic obstructive pulmonary disease and asthma.
Stemmler S et al.
Genes and Immunity, 2005
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