Associated Papers
Genetic Variants in Cytokines IL-10 and IL-17A Are Associated with the Risk and Severity of Sporadic Parkinson's Disease in Mexican Patients.
Monroy-Jaramillo N et al.
Life (basel, Switzerland), 2025
Molecular Determinants of the Human Retinal Pigment Epithelium Cell Fate and Potential Pharmacogenomic Targets for Precision Medicine.
Zibetti C
International Journal of Molecular Sciences, 2025
GWAS meta-analysis of psoriasis identifies new susceptibility alleles impacting disease mechanisms and therapeutic targets.
Dand N et al.
Nature Communications, 2025
IL13 gene polymorphisms among Sudanese patients with bronchial asthma: a case-control study.
Abdalla MA et al.
Molecular Biology Research Communications, 2025
Multiple sclerosis susceptibility may be associated with the coding rs20541 (R130Q) IL-13 gene polymorphism in the Polish population.
Grunwald C et al.
Scientific Reports, 2023
Targeting the non-coding genome and temozolomide signature enables CRISPR-mediated glioma oncolysis.
Tan IL et al.
Cell Reports, 2023
GWAS meta-analysis of psoriasis identifies new susceptibility alleles impacting disease mechanisms and therapeutic targets.
Dand N et al.
Medrxiv : the Preprint Server for Health Sciences, 2023
Relevance of Coding Variation in FLG And DOCK8 in Finnish Pediatric Patients with Early-Onset Moderate-To-Severe Atopic Dermatitis.
Perälä M et al.
Jid Innovations : Skin Science From Molecules to Population Health, 2023
Network expansion of genetic associations defines a pleiotropy map of human cell biology.
Barrio-Hernandez I et al.
Nature Genetics, 2023
Biochemical Characteristics of iPSC-Derived Dopaminergic Neurons from N370S GBA Variant Carriers with and without Parkinson's Disease.
Grigor'eva EV et al.
International Journal of Molecular Sciences, 2023
FinnGen provides genetic insights from a well-phenotyped isolated population.
Kurki MI et al.
Nature, 2023
Exome variants associated with asthma and allergy.
Wjst M
Scientific Reports, 2022
Genetic susceptibility of bladder cancer in the Lebanese population.
Kourie HR et al.
Bmc Medical Genomics, 2022
A novel missense variant in CEACAM16 gene causes autosomal dominant nonsyndromic hearing loss.
Zhang D et al.
Annals of Human Genetics, 2022
Multidisciplinary In-Depth Investigation in a Young Athlete Suffering from Syncope Caused by Myocardial Bridge.
Brancaccio M et al.
Diagnostics (basel, Switzerland), 2021
Pathogenic nsSNPs that increase the risks of cancers among the Orang Asli and Malays.
Khoruddin NA et al.
Scientific Reports, 2021
Familial Temperature-Sensitive Auditory Neuropathy: Distinctive Clinical Courses Caused by Variants of the OTOF Gene.
Zhu YM et al.
Frontiers in Cell and Developmental Biology, 2021
Association of IL13 genetic polymorphisms with atopic dermatitis: Fine mapping and haplotype analysis.
Lee E et al.
Annals of Allergy, Asthma & Immunology : Official Publication of the American College of Allergy, Asthma, & Immunology, 2020
A deep analysis using panel-based next-generation sequencing in an Ecuadorian pediatric patient with anaplastic astrocytoma: a case report.
García-Cárdenas JM et al.
Journal of Medical Case Reports, 2020
Introducing the first whole genomes of nationals from the United Arab Emirates.
AlSafar HS et al.
Scientific Reports, 2019
Whole-Exome Sequencing Characterized the Landscape of Somatic Mutations and Pathways in Colorectal Cancer Liver Metastasis.
Feng L et al.
Journal of Oncology, 2019
Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biology.
Ferreira MA et al.
Nature Genetics, 2017
Exome-wide association study reveals novel psoriasis susceptibility locus at TNFSF15 and rare protective alleles in genes contributing to type I IFN signalling.
Dand N et al.
Human Molecular Genetics, 2017
Genetic variation at the Th2 immune gene IL13 is associated with IgE-mediated paediatric food allergy.
Ashley SE et al.
Clinical and Experimental Allergy : Journal of the British Society for Allergy and Clinical Immunology, 2017
A rare coding allele in IFIH1 is protective for psoriatic arthritis.
Budu-Aggrey A et al.
Annals of the Rheumatic Diseases, 2017
Mutational profiling in the peripheral blood leukocytes of patients with systemic mast cell activation syndrome using next-generation sequencing.
Altmüller J et al.
Immunogenetics, 2017
Detection and interpretation of shared genetic influences on 42 human traits.
Pickrell JK et al.
Nature Genetics, 2016
Pooled Resequencing of 122 Ulcerative Colitis Genes in a Large Dutch Cohort Suggests Population-Specific Associations of Rare Variants in MUC2.
Visschedijk MC et al.
Plos One, 2016
The immunogenetics of Psoriasis: A comprehensive review.
Harden JL et al.
Journal of Autoimmunity, 2015
Clinical associations of host genetic variations in the genes of cytokines in critically ill patients.
Belopolskaya OB et al.
Clinical and Experimental Immunology, 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
Whole-exome sequencing in patients with ichthyosis reveals modifiers associated with increased IgE levels and allergic sensitizations.
Kiritsi D et al.
The Journal of Allergy and Clinical Immunology, 2015
A meta-analysis of Hodgkin lymphoma reveals 19p13.3 TCF3 as a novel susceptibility locus.
Cozen W et al.
Nature Communications, 2014
Genome-wide pathway analysis of a genome-wide association study on psoriasis and Behcet's disease.
Lee YH et al.
Molecular Biology Reports, 2012
IL13 gene polymorphism is a marker for psoriatic arthritis among psoriasis patients.
Eder L et al.
Annals of the Rheumatic Diseases, 2011
Disparity of innate immunity-related gene effects on asthma and allergy on Karelia.
Zhang G et al.
Pediatric Allergy and Immunology : Official Publication of the European Society of Pediatric Allergy and Immunology, 2011
Evidence to support IL-13 as a risk locus for psoriatic arthritis but not psoriasis vulgaris.
Bowes J et al.
Annals of the Rheumatic Diseases, 2011
Genetic and epidemiological risk factors in the development of bronchopulmonary dysplasia.
Mailaparambil B et al.
Disease Markers, 2010
Association between IL13 polymorphisms and psoriatic arthritis is modified by smoking.
Duffin KC et al.
The Journal of Investigative Dermatology, 2009
Single nucleotide polymorphisms in inflammation-related genes and mortality in a community-based cohort in Washington County, Maryland.
Gallicchio L et al.
American Journal of Epidemiology, 2008
Variants in the 5q31 cytokine gene cluster are associated with psoriasis.
Chang M et al.
Genes and Immunity, 2008
Genotype frequency and F ST analysis of polymorphisms in immunoregulatory genes in Chinese and Caucasian populations.
Lan Q et al.
Immunogenetics, 2007
Association of IL4R gene polymorphisms with asthma in Chinese populations.
Zhang H et al.
Human Mutation, 2007
Common genetic variants in proinflammatory and other immunoregulatory genes and risk for non-Hodgkin lymphoma.
Wang SS et al.
Cancer Research, 2006