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Search Results to Tomi Pastinen

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One or more keywords matched the following properties of Pastinen, Tomi

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research overview Dr. Pastinen has been the Director of the Center for Pediatric Genomic Medicine (CPGM) since 2017. Dr. Pastinen joined Children's Mercy from McGill University. He held the Canada Research Chair from 2007 to 2017 and has a significant track record of academic achievement. He has authored over 120 peer-reviewed publications, including papers in top-tier journals Cell and Nature Genetics. Prior to joining Children’s Mercy, he led the epigenome mapping center at McGill as part of the International Human Epigenome Consortium, which provides maps of genome function to the global research community. Dr. Pastinen is leading Genomic Answers for Kids, a foundational initiative for future genomic research at Children’s Mercy that aims to learn from 30,000 children with genetic conditions.

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

Item TypeName
Concept Adolescent
Concept Family Health
Concept Multigene Family
Concept Genetics, Medical
Concept Parents
Concept Precancerous Conditions
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 Association study between the CX3CR1 gene and asthma.
Academic Article A risk haplotype of STAT4 for systemic lupus erythematosus is over-expressed, correlates with anti-dsDNA and shows additive effects with two risk alleles of IRF5.
Academic Article Genome-wide association study identifies variants at 9p21 and 22q13 associated with development of cutaneous nevi.
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 Human genetics in full resolution.
Academic Article Genome-wide association study of age at menarche in African-American women.
Academic Article Integration of high-resolution methylome and transcriptome analyses to dissect epigenomic changes in childhood acute lymphoblastic leukemia.
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 Reply to Rational drug repositioning by medical genetics.
Academic Article An epigenome-wide association study of total serum immunoglobulin E concentration.
Academic Article Demonstration of Autosomal Monoallelic Expression in Thyroid Tissue Assessed by Whole-Exome and Bulk RNA Sequencing.
Academic Article Combining omics data to identify genes associated with allergic rhinitis.
Academic Article APRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patients.
Academic Article Genomic prediction of relapse in recipients of allogeneic haematopoietic stem cell transplantation.
Academic Article Exploring rare and low-frequency variants in the Saguenay-Lac-Saint-Jean population identified genes associated with asthma and allergy traits.
Academic Article Very long intergenic non-coding RNA transcripts and expression profiles are associated to specific childhood acute lymphoblastic leukemia subtypes.
Academic Article H3K27M induces defective chromatin spread of PRC2-mediated repressive H3K27me2/me3 and is essential for glioma tumorigenesis.
Academic Article Eosinophil microRNAs Play a Regulatory Role in Allergic Diseases Included in the Atopic March.
Academic Article Immune cell residency in the nasal mucosa may partially explain respiratory disease severity across the age range.
Academic Article Comparing Attitudes About Genomic Privacy and Data Sharing in Adolescents and Parents of Children Enrolled in a Genomic Research Repository.
Academic Article Heterozygous loss-of-function variants in DOCK4 cause neurodevelopmental delay and microcephaly.
Academic Article Independent expansion, selection and hypervariability of the TBC1D3 gene family in humans.
Academic Article Refining the phenotype of SINO syndrome: A comprehensive cohort report of 14 novel cases.
Academic Article Independent expansion, selection, and hypervariability of the TBC1D3 gene family in humans.
Academic Article Genomic insights into pediatric intestinal inflammatory and eosinophilic disorders using single-cell RNA-sequencing.
Academic Article Structural variation, selection, and diversification of the NPIP gene family from the human pangenome.

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