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Search Results to Tomi Pastinen

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One or more keywords matched the following items that are connected to Pastinen, Tomi

Item TypeName
Concept Genetic Predisposition to Disease
Academic Article Immune system genes in multiple sclerosis: genetic association and linkage analyses on TCR beta, IGH, IFN-gamma and IL-1ra/IL-1 beta loci.
Academic Article Contribution of the CCR5 and MBL genes to susceptibility to HIV type 1 infection in the Finnish population.
Academic Article HLA class II associated risk and protection against multiple sclerosis-a Finnish family study.
Academic Article Chromosome 19q13 and multiple sclerosis susceptibility in Finland: a linkage and two-stage association study.
Academic Article Intercellular adhesion molecule-1 K469E polymorphism: study of association with multiple sclerosis.
Academic Article Association study between the CX3CR1 gene and asthma.
Academic Article Genome-wide association study identifies variants at 9p21 and 22q13 associated with development of cutaneous nevi.
Academic Article Population genomics in a disease targeted primary cell model.
Academic Article Allele-specific chromatin remodeling in the ZPBP2/GSDMB/ORMDL3 locus associated with the risk of asthma and autoimmune disease.
Academic Article A cis-acting regulatory variant in the IL2RA locus.
Academic Article A genome-wide association study reveals variants in ARL15 that influence adiponectin levels.
Academic Article An integration of genome-wide association study and gene expression profiling to prioritize the discovery of novel susceptibility Loci for osteoporosis-related traits.
Academic Article Mapping of numerous disease-associated expression polymorphisms in primary peripheral blood CD4+ lymphocytes.
Academic Article Hundreds of variants clustered in genomic loci and biological pathways affect human height.
Academic Article Homozygous BUB1B mutation and susceptibility to gastrointestinal neoplasia.
Academic Article Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture.
Academic Article Promoter polymorphisms in CHI3L1 are associated with asthma.
Academic Article Large-scale association analysis identifies new risk loci for coronary artery disease.
Academic Article Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk.
Academic Article Genome-wide search for exonic variants affecting translational efficiency.
Academic Article Genetic implication of a novel thiamine transporter in human hypertension.
Academic Article Genetic risk factors for decreased bone mineral accretion in children with asthma receiving multiple oral corticosteroid bursts.
Academic Article Whole-genome sequencing identifies EN1 as a determinant of bone density and fracture.
Academic Article Association of breast cancer risk with genetic variants showing differential allelic expression: Identification of a novel breast cancer susceptibility locus at 4q21.
Academic Article Association of breast cancer risk in BRCA1 and BRCA2 mutation carriers with genetic variants showing differential allelic expression: identification of a modifier of breast cancer risk at locus 11q22.3.
Academic Article Genetic Drivers of Epigenetic and Transcriptional Variation in Human Immune Cells.
Academic Article The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
Academic Article Combining omics data to identify genes associated with allergic rhinitis.
Academic Article Genetic Predisposition to Multiple Myeloma at 5q15 Is Mediated by an ELL2 Enhancer Polymorphism.
Academic Article Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes.
Academic Article Genome-wide association study implicates immune dysfunction in the development of Hodgkin lymphoma.
Academic Article Asthma-associated polymorphisms in 17q12-21 locus modulate methylation and gene expression of GSDMA in na?ve CD4+ T cells.
Academic Article Rare variants in KDR, encoding VEGF Receptor 2, are associated with tetralogy of Fallot.

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  • Genetic Predisposition to Disease