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One or more keywords matched the following properties of Grundberg, Elin

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keywords Functional genomics
research overview Dr. Elin Grundberg completed her PhD (2006) in Molecular Medicine at Uppsala University, Sweden and following post-doctoral training at the McGill University and Genome Quebec Innovation Centre she joined Wellcome Trust Sanger institute in 2009 to lead the international MuTHER Consortium, which included developing a major resource of detailed genomics and epigenomics data from multiple disease-targeted tissues from twins. In 2012, she was appointed Tenure-Track Assistant Professor at the Department of Human Genetics at McGill University where her group was applying various next-generation sequencing approaches to understand genetic and epigenetic factors underlying complex disease susceptibility. Dr. Grundberg lead two CIHR team grants on this topic including the EpiTriO Consotium with partners in Canada and Europe. She held a Canada Research Chair (tier 2) in Disease Genomics and Epigenomics. In Oct 2017, Dr. Grundberg joined the faculty at Children’s Mercy Kansas City where she holds the Roberta D. Harding & William F. Bradley, Jr. Endowed Chair in Genomic Research. She is building a comprehensive research program leveraging international collaborations (King’s College London, UK; INSERM, France, Helmholtz Zentrum, Germany, McGill, Canada) as well as local collaborators (CM, UMKC, KUMC) for tissue-resources and methodologies essential for contemporary disease genomics and epigenomics. Research areas span genomics medicine applied in pediatric and adult populations including rare diseases, metabolic diseases, social and environmental health and perinatal/maternal health. Dr. Grundberg currently collaborates with a number of large international research consortia and is the author of over 75 scientific papers.

One or more keywords matched the following items that are connected to Grundberg, Elin

Item TypeName
Concept Genomics
Academic Article Systematic assessment of the human osteoblast transcriptome in resting and induced primary cells.
Academic Article Population genomics in a disease targeted primary cell model.
Academic Article Characterization of functional methylomes by next-generation capture sequencing identifies novel disease-associated variants.
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 Functional variation in allelic methylomes underscores a strong genetic contribution and reveals novel epigenetic alterations in the human epigenome.
Academic Article Whole-genome sequence-based analysis of thyroid function.
Academic Article Identification of 153 new loci associated with heel bone mineral density and functional involvement of GPC6 in osteoporosis.
Academic Article Correction to: Functional variation in allelic methylomes underscores a strong genetic contribution and reveals novel epigenetic alterations in the human epigenome.
Award or Honor Receipt Canada Research Chair in Disease Genomics and Epigenomics (Tier 2)
Grant Understanding etiology of metabolic diseases by integrative genomics and epigenomics approaches
Grant Obesity Genes, Energy Regulation in Response to Weight-Loss Diets
Academic Article Capturing functional epigenomes for insight into metabolic diseases.
Grant Understanding Mechanisms Underlying Chronic Stress-Induced Asthma in Children by Population and Single-Cell Epigenomics Approaches

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  • Functional
  • Genomics