Author details

Full Name

Ulrika Liljedahl

Affiliation

ORCID

Career Start Year

2001

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37817248	Genomic, transcriptomic and epigenomic sequencing data of the B-cell leukemia cell line REH.	BMC Res Notes	2023
35406529	Next Generation Plasma Proteomics Identifies High-Precision Biomarker Candidates for Ovarian Cancer.	Cancers (Basel)	2022
34872606	The SEQC2 epigenomics quality control (EpiQC) study.	Genome Biol	2021
34504347	Establishing community reference samples, data and call sets for benchmarking cancer mutation detection using whole-genome sequencing.	Nat Biotechnol	2021
34504346	Toward best practice in cancer mutation detection with whole-genome and whole-exome sequencing.	Nat Biotechnol	2021
34949218	Author Correction: The SEQC2 epigenomics quality control (EpiQC) study.	Genome Biol	2021
29177435	De novo mutations implicate novel genes in systemic lupus erythematosus.	Hum Mol Genet	2018
29668744	Data quality of whole genome bisulfite sequencing on Illumina platforms.	PLoS One	2018
28832569	SweGen: a whole-genome data resource of genetic variability in a cross-section of the Swedish population.	Eur J Hum Genet	2017
23675451	Adaptive mutations and replacements of virulence traits in the Escherichia coli O104:H4 outbreak population.	PLoS ONE	2013
23031429	A genome-wide association study of monozygotic twin-pairs suggests a locus related to variability of serum high-density lipoprotein cholesterol.	Twin Res Hum Genet	2012
23300628	Powerful identification of cis-regulatory SNPs in human primary monocytes using allele-specific gene expression.	PLoS One	2012
21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Nature	2011
20145208	SUMOylation mediates the nuclear translocation and signaling of the IGF-1 receptor.	Science Signaling	2010
19265028	Geographical structure and differential natural selection among North European populations.	Genome Res	2009
18398430	Evaluation of HapMap data in six populations of European descent.	Eur J Hum Genet	2008
18464745	The relationship between the plasma concentration of irbesartan and the antihypertensive response is disclosed by an angiotensin II type 1 receptor polymorphism: results from the Swedish Irbesartan Left Ventricular Hypertrophy Investigation vs. Atenolol (SILVHIA) Trial.	Am J Hypertens	2008
18484635	Screening for copy-number alterations and loss of heterozygosity in chronic lymphocytic leukemia--a comparative study of four differently designed, high resolution microarray platforms.	Genes Chromosomes and Cancer	2008
17599733	Association of a haplotype in the promoter region of the interferon regulatory factor 5 gene with rheumatoid arthritis.		2007
16786507	A quality assessment survey of SNP genotyping laboratories.	Hum Mutat	2006
16311014	Tag/anti-tag liquid-phase primer extension array: a flexible and versatile genotyping platform.	Genomics	2006
16046789	Hypertension and SNP genotyping in antihypertensive treatment.	Cardiovasc Toxicol	2005
15049387	Transforming growth factor beta1 genotype and change in left ventricular mass during antihypertensive treatment--results from the Swedish Irbesartan Left Ventricular Hypertrophy Investigation versus Atenolol (SILVHIA).	Clin Cardiol	2004
15614026	Single nucleotide polymorphisms predict the change in left ventricular mass in response to antihypertensive treatment.	J Hypertens	2004
15453913	Single nucleotide polymorphisms in the apolipoprotein B and low density lipoprotein receptor genes affect response to antihypertensive treatment.	BMC Cardiovasc Disord	2004
15500681	Detecting imbalanced expression of SNP alleles by minisequencing on microarrays.	BMC Biotechnology	2004
15188945	Gender-specific association between preproendothelin-1 genotype and reduction of systolic blood pressure during antihypertensive treatment--results from the Swedish Irbesartan Left Ventricular Hypertrophy Investigation versus Atenolol (SILVHIA).	Clin Cardiol	2004
14671647	Assessing hematopoietic chimerism after allogeneic stem cell transplantation by multiplexed SNP genotyping using microarrays and quantitative analysis of SNP alleles.	Leukemia	2004
14700505	Angiotensinogen gene polymorphisms: relationship to blood pressure response to antihypertensive treatment. Results from the Swedish Irbesartan Left Ventricular Hypertrophy Investigation vs Atenolol (SILVHIA) trial.	Am J Hypertens	2004
14576329	Quantitative evaluation by minisequencing and microarrays reveals accurate multiplexed SNP genotyping of whole genome amplified DNA.	Nucleic Acids Research	2003
12491909	Quantitative analysis of SNPs in pooled DNA samples by solid-phase minisequencing.	Methods in Molecular Biology	2003
12491908	Genotyping SNPs by minisequencing primer extension using oligonucleotide microarrays.	Methods in Molecular Biology	2003
13678427	Adipocyte-derived leucine aminopeptidase genotype and response to antihypertensive therapy.	BMC Cardiovasc Disord	2003
12544508	A microarray minisequencing system for pharmacogenetic profiling of antihypertensive drug response.	Pharmacogenetics	2003
11433045	Minisequencing on oligonucleotide microarrays: comparison of immobilisation chemistries.	Nucleic Acids Research	2001