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Search Results to Tomi Pastinen

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Pastinen, Tomi

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

Item Type	Name
Concept	Autoimmune Diseases
Concept	Bone Diseases, Developmental
Concept	Cardiovascular Diseases
Concept	Charcot-Marie-Tooth Disease
Concept	Coronary Artery Disease
Concept	Coronary Disease
Concept	Disease
Concept	Disease Models, Animal
Concept	Disease Susceptibility
Concept	Graft vs Host Disease
Concept	Hodgkin Disease
Concept	Immune System Diseases
Concept	Metabolic Diseases
Concept	Rheumatic Diseases
Concept	Disease Progression
Concept	Disease-Free Survival
Concept	Platelet Glycoprotein GPIIb-IIIa Complex
Concept	Genetic Predisposition to Disease
Concept	Genetic Diseases, Inborn
Concept	Rare Diseases
Concept	Polycomb Repressive Complex 2
Concept	Non-alcoholic Fatty Liver 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	Golli-MBP gene in multiple sclerosis susceptibility.
Academic Article	Contribution of the CCR5 and MBL genes to susceptibility to HIV type 1 infection in the Finnish population.
Academic Article	Array-based multiplex analysis of candidate genes reveals two independent and additive genetic risk factors for myocardial infarction in the Finnish population.
Academic Article	Dissecting a population genome for targeted screening of disease mutations.
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	The effect of polymorphisms in the enhancer of split gene complex on bristle number variation in a large wild-caught cohort of Drosophila melanogaster.
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	Genome-wide allele-specific analysis: insights into regulatory variation.
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	Human genetics in full resolution.
Academic Article	Use of genome-wide association studies for drug repositioning.
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	Genome-wide signatures of differential DNA methylation in pediatric acute lymphoblastic leukemia.
Academic Article	Genetic implication of a novel thiamine transporter in human hypertension.
Academic Article	Interrogation of allelic chromatin states in human cells by high-density ChIP-genotyping.
Academic Article	Long-range epigenetic regulation is conferred by genetic variation located at thousands of independent loci.
Academic Article	Characterization of functional methylomes by next-generation capture sequencing identifies novel disease-associated variants.
Academic Article	Genetic risk factors for decreased bone mineral accretion in children with asthma receiving multiple oral corticosteroid bursts.
Academic Article	Erratum: Characterization of functional methylomes by next-generation capture sequencing identifies novel disease-associated variants.
Academic Article	Whole-genome sequencing identifies EN1 as a determinant of bone density and fracture.
Academic Article	funtooNorm: an R package for normalization of DNA methylation data when there are multiple cell or tissue types.
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	Novel insights into systemic autoimmune rheumatic diseases using shared molecular signatures and an integrative analysis.
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	Hidden genomic MHC disparity between HLA-matched sibling pairs in hematopoietic stem cell transplantation.
Academic Article	Genomic prediction of relapse in recipients of allogeneic haematopoietic stem cell transplantation.
Academic Article	Genome-wide association study implicates immune dysfunction in the development of Hodgkin lymphoma.
Academic Article	Dissecting features of epigenetic variants underlying cardiometabolic risk using full-resolution epigenome profiling in regulatory elements.
Academic Article	H3K27M induces defective chromatin spread of PRC2-mediated repressive H3K27me2/me3 and is essential for glioma tumorigenesis.
Academic Article	Integrative analysis of vascular endothelial cell genomic features identifies AIDA as a coronary artery disease candidate gene.
Academic Article	Computational Analysis of HLA-presentation of Non-synonymous Recipient Mismatches Indicates Effect on the Risk of Chronic Graft-vs.-Host Disease After Allogeneic HSCT.
Academic Article	Introducing the Endotype Concept to Address the Challenge of Disease Heterogeneity in Type 1 Diabetes.
Academic Article	Single-cell analysis of human adipose tissue identifies depot and disease specific cell types.
Academic Article	Asthma-associated polymorphisms in 17q12-21 locus modulate methylation and gene expression of GSDMA in na?ve CD4+ T cells.
Academic Article	Eosinophil microRNAs Play a Regulatory Role in Allergic Diseases Included in the Atopic March.
Academic Article	Genetic perturbation of PU.1 binding and chromatin looping at neutrophil enhancers associates with autoimmune disease.
Academic Article	Rare variants in KDR, encoding VEGF Receptor 2, are associated with tetralogy of Fallot.
Academic Article	Immune cell residency in the nasal mucosa may partially explain respiratory disease severity across the age range.
Academic Article	Genetic associations at regulatory phenotypes improve fine-mapping of causal variants for 12 immune-mediated diseases.
Academic Article	Genomic answers for children: Dynamic analyses of >1000 pediatric rare disease genomes.
Academic Article	Massively parallel identification of functionally consequential noncoding genetic variants in undiagnosed rare disease patients.
Academic Article	Direct haplotype-resolved 5-base HiFi sequencing for genome-wide profiling of hypermethylation outliers in a rare disease cohort.
Academic Article	Adverse Maternal Environments Perturb Hepatic DNA Methylome and Transcriptome Prior to the Adult-Onset Non-Alcoholic Fatty Liver Disease in Mouse Offspring.
Academic Article	Monoallelic variation in DHX9, the gene encoding the DExH-box helicase DHX9, underlies neurodevelopment disorders and Charcot-Marie-Tooth disease.
Academic Article	Pangenome graphs improve the analysis of structural variants in rare genetic diseases.
Academic Article	Complex trait associations in rare diseases and impacts on Mendelian variant interpretation.

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