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Search Results to Tomi Pastinen

This is a "connection" page, showing the details of why an item matched the keywords from your search.

                     
                     

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

Item TypeName
Concept Chromosome Aberrations
Concept Chromosome Mapping
Concept Chromosomes, Human, Pair 11
Concept Chromosomes, Human, Pair 14
Concept Chromosomes, Human, Pair 17
Concept Chromosomes, Human, Pair 19
Concept Chromosomes, Human, Pair 22
Concept Chromosomes, Human, Pair 3
Concept Chromosomes, Human, Pair 4
Concept Chromosomes, Human, Pair 5
Concept Chromosomes, Human, Pair 8
Concept Chromosomes, Human, Pair 9
Concept Y Chromosome
Concept Physical Chromosome Mapping
Concept Chromosome Disorders
Concept X Chromosome Inactivation
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 Y-chromosomal SNPs in Finno-Ugric-speaking populations analyzed by minisequencing on microarrays.
Academic Article Chromosome 19q13 and multiple sclerosis susceptibility in Finland: a linkage and two-stage association study.
Academic Article Cis-acting regulatory variation in the human genome.
Academic Article Mapping common regulatory variants to human haplotypes.
Academic Article A low-cost open-source SNP genotyping platform for association mapping applications.
Academic Article Mapping cis-acting regulatory variation in recombinant congenic strains.
Academic Article Influence of human genome polymorphism on gene expression.
Academic Article Bone mineral density, osteoporosis, and osteoporotic fractures: a genome-wide association study.
Academic Article Targeted screening of cis-regulatory variation in human haplotypes.
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 Cell culture-induced aberrant methylation of the imprinted IG DMR in human lymphoblastoid cell lines.
Academic Article Fine mapping of the insulin-induced gene 2 identifies a variant associated with LDL cholesterol and total apolipoprotein B levels.
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 Identification, replication, and fine-mapping of Loci associated with adult height in individuals of african ancestry.
Academic Article Interaction between genetic and epigenetic variation defines gene expression patterns at the asthma-associated locus 17q12-q21 in lymphoblastoid cell lines.
Academic Article Powerful identification of cis-regulatory SNPs in human primary monocytes using allele-specific gene expression.
Academic Article Genome-wide signatures of differential DNA methylation in pediatric acute lymphoblastic leukemia.
Academic Article Analysis of expressed SNPs identifies variable extents of expression from the human inactive X chromosome.
Academic Article Fusion of TTYH1 with the C19MC microRNA cluster drives expression of a brain-specific DNMT3B isoform in the embryonal brain tumor ETMR.
Academic Article Allelic expression mapping across cellular lineages to establish impact of non-coding SNPs.
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 Predisposition to Multiple Myeloma at 5q15 Is Mediated by an ELL2 Enhancer Polymorphism.
Academic Article Asthma-associated polymorphisms in 17q12-21 locus modulate methylation and gene expression of GSDMA in naïve CD4+ T cells.

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  • Chromosomes Human Pair 6