Ulrika Liljedahl
Head of unit at Department of Medical Sciences; SNP&SEQ Technology Platform
- Mobile phone:
- +46 70 167 94 59
- E-mail:
- Ulrika.Liljedahl@medsci.uu.se
- Visiting address:
- BMC, Husargatan 3
752 37 Uppsala - Postal address:
- Molekylär Medicin, Box 1432, BMC
751 44 Uppsala
Publications
Recent publications
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A human pan-disease blood atlas of the circulating proteome
Part of Science, 2025
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Genomic, transcriptomic and epigenomic sequencing data of the B-cell leukemia cell line REH
Part of BMC Research Notes, 2023
- DOI for Genomic, transcriptomic and epigenomic sequencing data of the B-cell leukemia cell line REH
- Download full text (pdf) of Genomic, transcriptomic and epigenomic sequencing data of the B-cell leukemia cell line REH
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Next Generation Plasma Proteomics Identifies High-Precision Biomarker Candidates for Ovarian Cancer.
Part of Cancers, 2022
- DOI for Next Generation Plasma Proteomics Identifies High-Precision Biomarker Candidates for Ovarian Cancer.
- Download full text (pdf) of Next Generation Plasma Proteomics Identifies High-Precision Biomarker Candidates for Ovarian Cancer.
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Part of Scientific Data, 2021
- DOI for Whole genome and exome sequencing reference datasets from a multi-center and cross-platform benchmark study
- Download full text (pdf) of Whole genome and exome sequencing reference datasets from a multi-center and cross-platform benchmark study
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The SEQC2 epigenomics quality control (EpiQC) study
Part of Genome Biology, 2021
- DOI for The SEQC2 epigenomics quality control (EpiQC) study
- Download full text (pdf) of The SEQC2 epigenomics quality control (EpiQC) study
All publications
Articles in journal
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A human pan-disease blood atlas of the circulating proteome
Part of Science, 2025
-
Genomic, transcriptomic and epigenomic sequencing data of the B-cell leukemia cell line REH
Part of BMC Research Notes, 2023
- DOI for Genomic, transcriptomic and epigenomic sequencing data of the B-cell leukemia cell line REH
- Download full text (pdf) of Genomic, transcriptomic and epigenomic sequencing data of the B-cell leukemia cell line REH
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Next Generation Plasma Proteomics Identifies High-Precision Biomarker Candidates for Ovarian Cancer.
Part of Cancers, 2022
- DOI for Next Generation Plasma Proteomics Identifies High-Precision Biomarker Candidates for Ovarian Cancer.
- Download full text (pdf) of Next Generation Plasma Proteomics Identifies High-Precision Biomarker Candidates for Ovarian Cancer.
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Part of Scientific Data, 2021
- DOI for Whole genome and exome sequencing reference datasets from a multi-center and cross-platform benchmark study
- Download full text (pdf) of Whole genome and exome sequencing reference datasets from a multi-center and cross-platform benchmark study
-
The SEQC2 epigenomics quality control (EpiQC) study
Part of Genome Biology, 2021
- DOI for The SEQC2 epigenomics quality control (EpiQC) study
- Download full text (pdf) of The SEQC2 epigenomics quality control (EpiQC) study
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Part of Nature Biotechnology, p. 1151-1160, 2021
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De novo mutations implicate novel genes in systemic lupus erythematosus
Part of Human Molecular Genetics, p. 421-429, 2018
- DOI for De novo mutations implicate novel genes in systemic lupus erythematosus
- Download full text (pdf) of De novo mutations implicate novel genes in systemic lupus erythematosus
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Data quality of whole genome bisulfite sequencing on Illumina platforms
Part of PLOS ONE, 2018
- DOI for Data quality of whole genome bisulfite sequencing on Illumina platforms
- Download full text (pdf) of Data quality of whole genome bisulfite sequencing on Illumina platforms
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Part of European Journal of Human Genetics, p. 1253-1260, 2017
- DOI for SweGen: a whole-genome data resource of genetic variability in a cross-section of the Swedish population
- Download full text (pdf) of SweGen: a whole-genome data resource of genetic variability in a cross-section of the Swedish population
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Part of PLOS ONE, 2013
- DOI for Adaptive Mutations and Replacements of Virulence Traits in the Escherichia coli O104:H4 Outbreak Population
- Download full text (pdf) of Adaptive Mutations and Replacements of Virulence Traits in the Escherichia coli O104:H4 Outbreak Population
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Part of PLOS ONE, 2012
- DOI for Powerful Identification of Cis-regulatory SNPs in Human Primary Monocytes Using Allele-Specific Gene Expression
- Download full text (pdf) of Powerful Identification of Cis-regulatory SNPs in Human Primary Monocytes Using Allele-Specific Gene Expression
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Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis
Part of Nature, p. 214-219, 2011
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SUMOylation mediates the nuclear translocation and signaling of the IGF-1 receptor
Part of Science Signaling, 2010
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Geographical structure and differential natural selection among North European populations
Part of Genome Research, p. 804-814, 2009
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Part of American Journal of Hypertension, p. 836-839, 2008
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Evaluation of HapMap data in six populations of European descent
Part of European Journal of Human Genetics, p. 1142-1150, 2008
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Part of Genes, Chromosomes and Cancer, p. 697-711, 2008
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Part of Arthritis and Rheumatism, p. 2202-2210, 2007
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Hypertension and SNP genotyping in antihypertensive treatment.
Part of Cardiovasc Toxicol, p. 133-42, 2005
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Detecting imbalanced expression of SNP alleles by minisequencing on microarrays
Part of BMC Biotechnology, p. 1-10, 2004
- DOI for Detecting imbalanced expression of SNP alleles by minisequencing on microarrays
- Download full text (pdf) of Detecting imbalanced expression of SNP alleles by minisequencing on microarrays
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Part of Clinical Cardiology, p. 169-73, 2004
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Part of BMC Cardiovascular Disorders, p. 16, 2004
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Part of American Journal of Hypertension, p. 8-13, 2004
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Part of Journal of Hypertension, p. 2321-8, 2004
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Adipocyte-derived leucine aminopeptidase genotype and response to antihypertensive therapy
Part of BMC Cardiovascular Disorders, p. 11, 2003
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A microarray minisequencing system for pharmacogenetic profiling of antihypertensive drug response
Part of Pharmacogenetics, p. 7-17, 2003