Publikationer i DiVA – Claes Wadelius
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Organ-specific metabolic pathways distinguish prediabetes, type 2 diabetes, and normal tissues
Ingår i Cell Reports Medicine, 2022.
DOI för Organ-specific metabolic pathways distinguish prediabetes, type 2 diabetes, and normal tissues Ladda ner fulltext (pdf) av Organ-specific metabolic pathways distinguish prediabetes, type 2 diabetes, and normal tissues
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scSPLAT, a scalable plate-based protocol for single cell WGBS library preparation
Ingår i Scientific Reports, 2022.
DOI för scSPLAT, a scalable plate-based protocol for single cell WGBS library preparation Ladda ner fulltext (pdf) av scSPLAT, a scalable plate-based protocol for single cell WGBS library preparation
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Genome-wide association study of liver enzyme elevation in rheumatoid arthritis patients starting methotrexate
Ingår i Pharmacogenomics (London), s. 973-982, 2021.
DOI för Genome-wide association study of liver enzyme elevation in rheumatoid arthritis patients starting methotrexate Ladda ner fulltext (pdf) av Genome-wide association study of liver enzyme elevation in rheumatoid arthritis patients starting methotrexate
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Polymorphisms rs55710213 and rs56334587 regulate SCD1 expression by modulating HNF4A binding
Ingår i Biochimica et Biophysica Acta. Gene Regulatory Mechanisms, 2021.
DOI för Polymorphisms rs55710213 and rs56334587 regulate SCD1 expression by modulating HNF4A binding Ladda ner fulltext (pdf) av Polymorphisms rs55710213 and rs56334587 regulate SCD1 expression by modulating HNF4A binding
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Single nucleus transcriptomics data integration recapitulates the major cell types in human liver
Ingår i Hepatology Research, s. 233-238, 2021.
DOI för Single nucleus transcriptomics data integration recapitulates the major cell types in human liver Ladda ner fulltext (pdf) av Single nucleus transcriptomics data integration recapitulates the major cell types in human liver
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The Thioesterase ACOT1 as a Regulator of Lipid Metabolism in Type 2 Diabetes Detected in a Multi-Omics Study of Human Liver
Ingår i Omics, s. 652-659, 2021.
DOI för The Thioesterase ACOT1 as a Regulator of Lipid Metabolism in Type 2 Diabetes Detected in a Multi-Omics Study of Human Liver Ladda ner fulltext (pdf) av The Thioesterase ACOT1 as a Regulator of Lipid Metabolism in Type 2 Diabetes Detected in a Multi-Omics Study of Human Liver
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A Multi-Omics Approach to Liver Diseases: Integration of Single Nuclei Transcriptomics with Proteomics and HiCap Bulk Data in Human Liver
Ingår i Omics, s. 180-194, 2020.
DOI för A Multi-Omics Approach to Liver Diseases: Integration of Single Nuclei Transcriptomics with Proteomics and HiCap Bulk Data in Human Liver Ladda ner fulltext (pdf) av A Multi-Omics Approach to Liver Diseases: Integration of Single Nuclei Transcriptomics with Proteomics and HiCap Bulk Data in Human Liver
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Cancer LncRNA Census reveals evidence for deep functional conservation of long noncoding RNAs in tumorigenesis
Ingår i Communications Biology, 2020.
DOI för Cancer LncRNA Census reveals evidence for deep functional conservation of long noncoding RNAs in tumorigenesis Ladda ner fulltext (pdf) av Cancer LncRNA Census reveals evidence for deep functional conservation of long noncoding RNAs in tumorigenesis
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Combined burden and functional impact tests for cancer driver discovery using DriverPower
Ingår i Nature Communications, 2020.
DOI för Combined burden and functional impact tests for cancer driver discovery using DriverPower Ladda ner fulltext (pdf) av Combined burden and functional impact tests for cancer driver discovery using DriverPower
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Genome-wide association study of angioedema induced by angiotensin-converting enzyme inhibitor and angiotensin receptor blocker treatment.
Ingår i The Pharmacogenomics Journal, s. 770-783, 2020.
DOI för Genome-wide association study of angioedema induced by angiotensin-converting enzyme inhibitor and angiotensin receptor blocker treatment. Ladda ner fulltext (pdf) av Genome-wide association study of angioedema induced by angiotensin-converting enzyme inhibitor and angiotensin receptor blocker treatment.
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Integration of whole-body [18F]FDG PET/MRI with non-targeted metabolomics can provide new insights on tissue-specific insulin resistance in type 2 diabetes
Ingår i Scientific Reports, 2020.
DOI för Integration of whole-body [18F]FDG PET/MRI with non-targeted metabolomics can provide new insights on tissue-specific insulin resistance in type 2 diabetes Ladda ner fulltext (pdf) av Integration of whole-body [18F]FDG PET/MRI with non-targeted metabolomics can provide new insights on tissue-specific insulin resistance in type 2 diabetes
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Integrative pathway enrichment analysis of multivariate omics data.
Ingår i Nature Communications, 2020.
DOI för Integrative pathway enrichment analysis of multivariate omics data.
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Retrospective evaluation of whole exome and genome mutation calls in 746 cancer samples.
Ingår i Nature Communications, 2020.
DOI för Retrospective evaluation of whole exome and genome mutation calls in 746 cancer samples. Ladda ner fulltext (pdf) av Retrospective evaluation of whole exome and genome mutation calls in 746 cancer samples.
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rs953413 Regulates Polyunsaturated Fatty Acid Metabolism by Modulating ELOVL2 Expression
Ingår i iScience, 2020.
DOI för rs953413 Regulates Polyunsaturated Fatty Acid Metabolism by Modulating ELOVL2 Expression Ladda ner fulltext (pdf) av rs953413 Regulates Polyunsaturated Fatty Acid Metabolism by Modulating ELOVL2 Expression
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Sex differences in oncogenic mutational processes.
Ingår i Nature Communications, 2020.
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Allele specific chromatin signals, 3D interactions, and motif predictions for immune and B cell related diseases
Ingår i Scientific Reports, 2019.
DOI för Allele specific chromatin signals, 3D interactions, and motif predictions for immune and B cell related diseases Ladda ner fulltext (pdf) av Allele specific chromatin signals, 3D interactions, and motif predictions for immune and B cell related diseases
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Detailed Functional Characterization of a Waist-Hip Ratio Locus in 7p15.2 Defines an Enhancer Controlling Adipocyte Differentiation
Ingår i iScience, s. 42-59, 2019.
DOI för Detailed Functional Characterization of a Waist-Hip Ratio Locus in 7p15.2 Defines an Enhancer Controlling Adipocyte Differentiation Ladda ner fulltext (pdf) av Detailed Functional Characterization of a Waist-Hip Ratio Locus in 7p15.2 Defines an Enhancer Controlling Adipocyte Differentiation
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Intra- and inter-individual metabolic profiling highlights carnitine and lysophosphatidylcholine pathways as key molecular defects in type 2 diabetes
Ingår i Scientific Reports, 2019.
DOI för Intra- and inter-individual metabolic profiling highlights carnitine and lysophosphatidylcholine pathways as key molecular defects in type 2 diabetes Ladda ner fulltext (pdf) av Intra- and inter-individual metabolic profiling highlights carnitine and lysophosphatidylcholine pathways as key molecular defects in type 2 diabetes
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Pandemrix-induced narcolepsy is associated with genes related to immunity and neuronal survival
Ingår i EBioMedicine, s. 595-604, 2019.
DOI för Pandemrix-induced narcolepsy is associated with genes related to immunity and neuronal survival Ladda ner fulltext (pdf) av Pandemrix-induced narcolepsy is associated with genes related to immunity and neuronal survival
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Studies of liver tissue identify functional gene regulatory elements associated to gene expression, type 2 diabetes, and other metabolic diseases
Ingår i Human Genomics, 2019.
DOI för Studies of liver tissue identify functional gene regulatory elements associated to gene expression, type 2 diabetes, and other metabolic diseases Ladda ner fulltext (pdf) av Studies of liver tissue identify functional gene regulatory elements associated to gene expression, type 2 diabetes, and other metabolic diseases
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Genetic variants associated with angiotensin-converting enzyme inhibitor-induced cough: a genome-wide association study in a Swedish population
Ingår i Pharmacogenomics (London), s. 201-213, 2017.
DOI för Genetic variants associated with angiotensin-converting enzyme inhibitor-induced cough: a genome-wide association study in a Swedish population Ladda ner fulltext (pdf) av Genetic variants associated with angiotensin-converting enzyme inhibitor-induced cough: a genome-wide association study in a Swedish population
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PATZ1 down-regulates FADS1 by binding to rs174557 and is opposed by SP1/SREBP1c
Ingår i Nucleic Acids Research, s. 2408-2422, 2017.
DOI för PATZ1 down-regulates FADS1 by binding to rs174557 and is opposed by SP1/SREBP1c
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Allele-specific transcription factor binding in liver and cervix cells unveils many likely drivers of GWAS signals
Ingår i Genomics, s. 248-254, 2016.
DOI för Allele-specific transcription factor binding in liver and cervix cells unveils many likely drivers of GWAS signals Ladda ner fulltext (pdf) av Allele-specific transcription factor binding in liver and cervix cells unveils many likely drivers of GWAS signals
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Allele-specific transcription factor binding to common and rare variants associated with disease and gene expression
Ingår i Human Genetics, s. 485-497, 2016.
DOI för Allele-specific transcription factor binding to common and rare variants associated with disease and gene expression Ladda ner fulltext (pdf) av Allele-specific transcription factor binding to common and rare variants associated with disease and gene expression
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Genetic determinants of warfarin maintenance dose and time in therapeutic treatment range: a RE-LY genomics substudy
Ingår i Pharmacogenomics (London), s. 1425-1439, 2016.
DOI för Genetic determinants of warfarin maintenance dose and time in therapeutic treatment range: a RE-LY genomics substudy Ladda ner fulltext (pdf) av Genetic determinants of warfarin maintenance dose and time in therapeutic treatment range: a RE-LY genomics substudy
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Looking beyond GWAS: allele-specific transcription factor binding drives the association of GALNT2 to HDL-C plasma levels
Ingår i Lipids in Health and Disease, 2016.
DOI för Looking beyond GWAS: allele-specific transcription factor binding drives the association of GALNT2 to HDL-C plasma levels Ladda ner fulltext (pdf) av Looking beyond GWAS: allele-specific transcription factor binding drives the association of GALNT2 to HDL-C plasma levels
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Maps of context-dependent putative regulatory regions and genomic signal interactions
Ingår i Nucleic Acids Research, s. 9110-9120, 2016.
DOI för Maps of context-dependent putative regulatory regions and genomic signal interactions Ladda ner fulltext (pdf) av Maps of context-dependent putative regulatory regions and genomic signal interactions
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Novel regulatory variant detected on the VKORC1 haplotype that is associated with warfarin dose
Ingår i Pharmacogenomics (London), s. 1305-1314, 2016.
DOI för Novel regulatory variant detected on the VKORC1 haplotype that is associated with warfarin dose Ladda ner fulltext (pdf) av Novel regulatory variant detected on the VKORC1 haplotype that is associated with warfarin dose
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Different distribution of histone modifications in genes with unidirectional and bidirectional transcription and a role of CTCF and cohesin in directing transcription
Ingår i BMC Genomics, 2015.
DOI för Different distribution of histone modifications in genes with unidirectional and bidirectional transcription and a role of CTCF and cohesin in directing transcription Ladda ner fulltext (pdf) av Different distribution of histone modifications in genes with unidirectional and bidirectional transcription and a role of CTCF and cohesin in directing transcription
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Best vitelliform macular dystrophy in a Swedish family: genetic analysis and a seven-year follow-up of photodynamic treatment of a young boy with choroidal neovascularization
Ingår i Acta Ophthalmologica, s. 238-242, 2014.
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Integration of genome-wide of Stat3 binding and epigenetic modification mapping with transcriptome reveals novel Stat3 target genes in glioma cells
Ingår i Biochimica et Biophysica Acta, s. 1341-1350, 2014.
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Nucleosome regulatory dynamics in response to TGF beta
Ingår i Nucleic Acids Research, s. 6921-6934, 2014.
DOI för Nucleosome regulatory dynamics in response to TGF beta
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Nucleosome regulatory dynamics in response to TGF-beta treatment in HepG2 cells
Ingår i Nucleic Acids Research, s. 6921-6934, 2014.
DOI för Nucleosome regulatory dynamics in response to TGF-beta treatment in HepG2 cells
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ChIP-seq in steatohepatitis and normal liver tissue identifies candidate disease mechanisms related to progression to cancer
Ingår i BMC Medical Genomics, s. 50-, 2013.
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A strand specific high resolution normalization method for chip-sequencing data employing multiple experimental control measurements
Ingår i Algorithms for Molecular Biology, s. 2-, 2012.
DOI för A strand specific high resolution normalization method for chip-sequencing data employing multiple experimental control measurements Ladda ner fulltext (pdf) av A strand specific high resolution normalization method for chip-sequencing data employing multiple experimental control measurements
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Cancer associated epigenetic transitions identified by genome-wide histone methylation binding profiles in human colorectal cancer samples and paired normal mucosa
Ingår i BMC Cancer, s. 450-, 2011.
DOI för Cancer associated epigenetic transitions identified by genome-wide histone methylation binding profiles in human colorectal cancer samples and paired normal mucosa Ladda ner fulltext (pdf) av Cancer associated epigenetic transitions identified by genome-wide histone methylation binding profiles in human colorectal cancer samples and paired normal mucosa
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Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma
Ingår i Nature Genetics, s. 906-909, 2010.
DOI för Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma
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Integrative epigenomic and genomic analysis of malignant pheochromocytoma.
Ingår i Experimental and Molecular Medicine, s. 484-502, 2010.
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Integrative epigenomic and genomic analysis of malignant pheochromocytoma
Ingår i Experimental and Molecular Medicine, s. 484-502, 2010.
DOI för Integrative epigenomic and genomic analysis of malignant pheochromocytoma
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Differential binding and co-binding pattern of FOXA1 and FOXA3 and their relation to H3K4me3 in HepG2 cells revealed by ChIP-seq
Ingår i Genome Biology, s. R129-, 2009.
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Histone H3 lysine 27 trimethylation in adult differentiated colon associated to cancer DNA hypermethylation
Ingår i Epigenetics, s. 107-113, 2009.
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Identification of candidate regulatory SNPs by combination of transcription-factor-binding site prediction, SNP genotyping and haploChIP
Ingår i Nucleic Acids Research, s. e85-, 2009.
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Integrating genome and epigenome in human disease
Ingår i Epigenomics, s. 343-368, 2009.
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Nucleosomes are well positioned in exons and carry characteristic histone modifications
Ingår i Genome Research, s. 1732-1741, 2009.
DOI för Nucleosomes are well positioned in exons and carry characteristic histone modifications
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Two polypyrimidine tracts in the nitric oxide synthase 2 gene: similar regulatory sequences with different properties.
Ingår i Molecular Biology Reports, s. 2021-2030, 2009.
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Influence of adenosine triphosphate and ABCB1 (MDR1) genotype on the P-glycoprotein-dependent transfer of saquinavir in the dually perfused human placenta
Ingår i Human and Experimental Toxicology, s. 65-71, 2008.
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Monte Carlo feature selection for supervised classification
Ingår i Bioinformatics, s. 110-117, 2008.
DOI för Monte Carlo feature selection for supervised classification
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ORegAnno: an open-access community-driven resource for regulatory annotation
Ingår i Nucleic Acids Research, s. D107-D113, 2008.
DOI för ORegAnno: an open-access community-driven resource for regulatory annotation
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Whole-genome maps of USF1 and USF2 binding and histone H3 acetylation reveal new aspects of promoter structure and candidate genes for common human disorders
Ingår i Genome Research, s. 380-392, 2008.
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Association of warfarin dose with genes involved in its action and metabolism
Ingår i Human Genetics, s. 23-34, 2007.
DOI för Association of warfarin dose with genes involved in its action and metabolism
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Butyrate mediates decrease of histone acetylation centered on transcription start sites and down-regulation of associated genes
Ingår i Genome Research, s. 708-719, 2007.
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Enhanced accumulation of A2E in individuals homozygous or heterozygous for mutations in BEST1 (VMD2)
Ingår i Experimental Eye Research, s. 34-43, 2007.
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In vitro analysis of DNA-protein interactions by proximity ligation
Ingår i Proceedings of the National Academy of Sciences of the United States of America, s. 3067-3072, 2007.
DOI för In vitro analysis of DNA-protein interactions by proximity ligation
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Placental transfer of quetiapine in relation to P-glycoprotein activity
Ingår i Journal of Psychopharmacology, s. 751-756, 2007.
DOI för Placental transfer of quetiapine in relation to P-glycoprotein activity
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Expression of bestrophin-1, the product of the VMD2 gene, modulates voltage-dependent Ca2+ channels in retinal pigment epithelial cells
Ingår i The FASEB Journal, s. 178-80, 2006.
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Binding sites for metabolic disease related transcription factors inferred at base pair resolution by chromatin immunoprecipitation and genomic microarrays
Ingår i Human Molecular Genetics, s. 3435-3447, 2005.
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Common VKORC1 and GGCX polymorphisms associated with warfarin dose
Ingår i The Pharmacogenomics Journal, s. 262-70, 2005.
DOI för Common VKORC1 and GGCX polymorphisms associated with warfarin dose
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Functional role of P-glycoprotein in the human blood-placental barrier
Ingår i Clinical Pharmacology and Therapeutics, s. 123-31, 2005.
DOI för Functional role of P-glycoprotein in the human blood-placental barrier
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Warfarin sensitivity related to CYP2C9, CYP3A5, ABCB1 (MDR1) and other factors
Ingår i The Pharmacogenomics Journal, s. 40-8, 2004.
DOI för Warfarin sensitivity related to CYP2C9, CYP3A5, ABCB1 (MDR1) and other factors
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Polymorphisms in NAT2, CYP2D6, CYP2C19 and GSTP1 and their association with prostate cancer
Ingår i Pharmacogenetics, s. 333-40, 1999.
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Prostate cancer associated with CYP17 genotype
Ingår i Pharmacogenetics, s. 635-9, 1999.
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Lamotrigine and toxic epidermal necrolysis
Ingår i The Lancet, s. 1041-, 1996.
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Molecular analysis of chromosome 21 in a patient with a phenotype of down syndrome and apparently normal karyotype
Ingår i American Journal of Medical Genetics. Part A, s. 566-572, 1996.