Loading...
Keywords
Last Name
Institution
Back to Search Results

Connection

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 properties of Pastinen, Tomi

PropertyValue
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 Child
Concept Child Abuse
Concept Child, Preschool
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 Allele-specific chromatin remodeling in the ZPBP2/GSDMB/ORMDL3 locus associated with the risk of asthma and autoimmune disease.
Academic Article Phosphodiesterase type 4D gene polymorphism: association with the response to short-acting bronchodilators in paediatric asthma patients.
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 Fusion of TTYH1 with the C19MC microRNA cluster drives expression of a brain-specific DNMT3B isoform in the embryonal brain tumor ETMR.
Academic Article An epigenome-wide association study of total serum immunoglobulin E concentration.
Academic Article Genetic risk factors for decreased bone mineral accretion in children with asthma receiving multiple oral corticosteroid bursts.
Academic Article Demonstration of Autosomal Monoallelic Expression in Thyroid Tissue Assessed by Whole-Exome and Bulk RNA Sequencing.
Academic Article DNA methylome analysis of acute lymphoblastic leukemia cells reveals stochastic de novo DNA methylation in CpG islands.
Academic Article Combining omics data to identify genes associated with allergic rhinitis.
Academic Article Mutations in THAP11 cause an inborn error of cobalamin metabolism and developmental abnormalities.
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 High-resolution analyses of human sperm dynamic methylome reveal thousands of novel age-related epigenetic alterations.
Academic Article Non-CG methylation and multiple histone profiles associate child abuse with immune and small GTPase dysregulation.
Academic Article High-resolution epigenome analysis in nasal samples derived from children with respiratory viral infections reveals striking changes upon SARS-CoV-2 infection.
Academic Article Immune cell residency in the nasal mucosa may partially explain respiratory disease severity across the age range.
Academic Article HLA-B*07:02 and HLA-C*07:02 are associated with trimethoprim-sulfamethoxazole respiratory failure.
Academic Article Genomic answers for children: Dynamic analyses of >1000 pediatric rare disease genomes.
Academic Article Differentially methylated CpGs in response to growth hormone administration in children with idiopathic short stature.
Academic Article The post-diagnostics world: charting a path for pediatric genomic medicine in the twenty-first century.
Academic Article The Role of Dynamic DNA Methylation in Liver Transplant Rejection in Children.
Academic Article Insurance denials and diagnostic rates in a pediatric genomic research cohort.
Academic Article Solving inherited white matter disorder etiologies in the neurology clinic: Challenges and lessons learned using next-generation sequencing.
Academic Article Committing to genomic answers for all kids: Evaluating inequity in genomic research enrollment.
Academic Article The cellular and immunological dynamics of early and transitional human milk.
Academic Article A Recurrent De Novo Variant in EIF2AK2 Causes a Hypomyelinating Leukodystrophy.
Academic Article Comparing Attitudes About Genomic Privacy and Data Sharing in Adolescents and Parents of Children Enrolled in a Genomic Research Repository.

Search Criteria
  • Child
  • Neurology