selected publications
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academic article
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Biological age of the endometrium using DNA methylation.
Reproduction.
155.
2018
Evaluating the Feasibility of DNA Methylation Analyses Using Long-Term Archived Brain Formalin-Fixed Paraffin-Embedded Samples.
Molecular Neurobiology.
55.
2018
Giant jelly eaters on the line: Species distribution and bycatch of three dominant sunfishes in the Southwest Pacific.
Estuarine Coastal and Shelf Science.
207.
2018
Global transcriptional changes in response to cGAMP depend on STING in human THP-1 cells.
Cellular & Molecular Immunology.
15.
2018
Human Calmodulin Mutations.
Frontiers in Molecular Neuroscience.
11.
2018
Interferon priming is essential for human CD34+ cell-derived plasmacytoid dendritic cell maturation and function.
Nature Communications.
9.
2018
Nrf2 negatively regulates STING indicating a link between antiviral sensing and metabolic reprogramming.
Nature Communications.
9.
2018
A 45-SNP genetic risk score is increased in early-onset coronary artery disease but independent of familial disease clustering.
Atherosclerosis.
257.
2017
A GENETIC RISK SCORE PREDICTS CARDIOVASCULAR EVENTS IN PATIENTS WITH STABLE CORONARY ARTERY DISEASE.
Journal of the American College of Cardiology.
69.
2017
A genetic risk score predicts cardiovascular events in patients with stable coronary artery disease.
International Journal of Cardiology.
241.
2017
Analysis of potential protein-modifying variants in 9000 endometriosis patients and 150000 controls of European ancestry.
Scientific Reports.
7.
2017
Blood DNA methylation age is not associated with cognitive functioning in middle-aged monozygotic twins.
Neurobiology of Aging.
50.
2017
Coronary artery disease-associated genetic variants and biomarkers of inflammation.
PLoS ONE.
12.
2017
DNA Methylation Analysis of BRD1 Promoter Regions and the Schizophrenia rs138880 Risk Allele.
PLoS ONE.
12.
2017
Differential DNA methylation at birth associated with mental disorder in individuals with 22q11.2 deletion syndrome.
Translational Psychiatry.
7.
2017
Epigenome-Wide Association Study of Cognitive Functioning in Middle-Aged Monozygotic Twins.
Frontiers in Aging Neuroscience.
9.
2017
IFI16 is required for DNA sensing in human macrophages by promoting production and function of cGAMP.
Nature Communications.
8.
2017
Meta-analysis identifies five novel loci associated with endometriosis highlighting key genes involved in hormone metabolism.
Nature Communications.
8.
2017
Mice heterozygous for an inactivated allele of the schizophrenia associated Brd1 gene display selective cognitive deficits with translational relevance to schizophrenia.
Neurobiology of Learning and Memory.
141.
2017
Molecular classification of tissue from a transformed non-Hogkin’s lymphoma case with unexpected long-time remission.
Experimental Hematology & Oncology.
6.
2017
The Genome-Wide DNA Methylation Profile of Peripheral Blood Is Not Systematically Changed by Short-Time Storage at Room Temperature.
Epigenomes.
1.
2017
The SH2B3 and KCNK5 loci may be implicated in regulation of platelet count, volume, and maturity.
Thrombosis Research.
158.
2017
The Schizophrenia-Associated BRD1 Gene Regulates Behavior, Neurotransmission, and Expression of Schizophrenia Risk Enriched Gene Sets in Mice.
Biological Psychiatry.
82.
2017
Whole-exome sequencing of individuals from an isolated population implicates rare risk variants in bipolar disorder.
Translational Psychiatry.
7.
2017
Abnormal IGF-Binding Protein Profile in the Bone Marrow of Multiple Myeloma Patients.
PLoS ONE.
11.
2016
CACNA1C hypermethylation is associated with bipolar disorder.
Translational Psychiatry.
6.
2016
Characterization of memory B cells from thymus and its impact for DLBCL classification.
Experimental Hematology.
44.
2016
Danish study of Non-Invasive testing in Coronary Artery Disease (Dan-NICAD): study protocol for a randomised controlled trial.
Trials.
17.
2016
Genome-wide DNA methylation profiling with MeDIP-seq using archived dried blood spots.
Clinical Epigenetics.
8.
2016
Hypomethylation of FAM63B in bipolar disorder patients.
Clinical Epigenetics.
8.
2016
Identification of the BRD1 interaction network and its impact on mental disorder risk.
Genome Medicine.
8.
2016
Mannose 6-Phosphate Receptor Is Reduced in -Synuclein Overexpressing Models of Parkinsons Disease.
PLoS ONE.
11.
2016
The insulin-like growth factor system in Multiple Myeloma: diagnostic and therapeutic potential.
Oncotarget.
7.
2016
A Novel Locus Harbouring a Functional CD164 Nonsense Mutation Identified in a Large Danish Family with Nonsyndromic Hearing Impairment.
PLOS Genetics.
11.
2015
A novel single nucleotide splice site mutation in FHL1 confirms an Emery-Dreifuss plus phenotype with pulmonary artery hypoplasia and facial dysmorphology.
European Journal of Medical Genetics.
58.
2015
Calmodulin mutations causing catecholaminergic polymorphic ventricular tachycardia confer opposing functional and biophysical molecular changes.
The FEBS Journal.
282.
2015
Diffuse Large B-Cell Lymphoma Classification System That Associates Normal B-Cell Subset Phenotypes With Prognosis.
Journal of Clinical Oncology.
33.
2015
Experimental validation of methods for differential gene expression analysis and sample pooling in RNA-seq.
BMC Genomics.
16.
2015
Investigating interactions between early life stress and two single nucleotide polymorphisms in HSD11B2 on the risk of schizophrenia.
Psychoneuroendocrinology.
60.
2015
Paternal Hemizygosity in 11p15 in Mole-like Conceptuses.
Medicine.
94.
2015
Predicting response to multidrug regimens in cancer patients using cell line experiments and regularised regression models.
BMC Cancer.
15.
2015
The importance of distinguishing between the odds ratio and the incidence rate ratio in GWAS.
BMC Medical Genetics.
16.
2015
Triploidy—Observations in 154 Diandric Cases.
PLoS ONE.
10.
2015
A Diffuse Large B-Cell Lymphoma Classification System That Associates Normal B-Cell Subset Phenotypes with Prognosis.
Blood.
124.
2014
Exposure time independent summary statistics for assessment of drug dependent cell line growth inhibition.
BMC Bioinformatics.
15.
2014
Genome-wide study of association and interaction with maternal cytomegalovirus infection suggests new schizophrenia loci.
Molecular Psychiatry.
19.
2014
The Hypercholesterolemia-Risk Gene SORT1 Facilitates PCSK9 Secretion.
Cell Metabolism.
19.
2014
The IGF-1 receptor inhibitor picropodophyllin potentiates the anti-myeloma activity of a BH3-mimetic.
Oncotarget.
5.
2014
Validation and implementation of a method for microarray gene expression profiling of minor B-cell subpopulations in man.
BMC Immunology.
15.
2014
World Endometriosis Research Foundation Endometriosis Phenome and Biobanking Harmonisation Project: I. Surgical phenotype data collection in endometriosis research.
Fertility and Sterility.
102.
2014
World Endometriosis Research Foundation Endometriosis Phenome and Biobanking Harmonisation Project: IV. Tissue collection, processing, and storage in endometriosis research.
Fertility and Sterility.
102.
2014
World Endometriosis Research Foundation Endometriosis Phenome and Biobanking Harmonization Project: III. Fluid biospecimen collection, processing, and storage in endometriosis research.
Fertility and Sterility.
102.
2014
World Endometriosis Research Foundation Endometriosis Phenome and biobanking harmonization project: II. Clinical and covariate phenotype data collection in endometriosis research.
Fertility and Sterility.
102.
2014
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dataset
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Associations between presumed inflammation-related SNPs and inflammatory proteins..
public-library-of-science.
2017
Associations between remaining CAD-related SNPs and inflammatory proteins..
public-library-of-science.
2017
Coronary artery disease-associated genetic variants and biomarkers of inflammation.
public-library-of-science.
2017
DNA Methylation Analysis of BRD1 Promoter Regions and the Schizophrenia rs138880 Risk Allele.
public-library-of-science.
2017
Patient characteristics..
public-library-of-science.
2017
Additional file 12: of Identification of the BRD1 interaction network and its impact on mental disorder risk.
springer-nature.
2016
Additional file 14: of Identification of the BRD1 interaction network and its impact on mental disorder risk.
springer-nature.
2016
Additional file 16: of Identification of the BRD1 interaction network and its impact on mental disorder risk.
springer-nature.
2016
Additional file 9: of Identification of the BRD1 interaction network and its impact on mental disorder risk.
springer-nature.
2016
Patient characteristics..
public-library-of-science.
2016
qPCR on mRNA from ASOtg/tg and wildtype mice brain tissues..
public-library-of-science.
2016
A Novel Locus Harbouring a Functional CD164 Nonsense Mutation Identified in a Large Danish Family with Nonsyndromic Hearing Impairment.
public-library-of-science.
2015
Additional file 1: of The importance of distinguishing between the odds ratio and the incidence rate ratio in GWAS.
springer-nature.
2015
Number of fully informative loci in 152 (near) triploid cases with vesicular chorionic villi, analyzed along with a maternal sample..
public-library-of-science.
2015
Parental types in triploid conceptuses with molar phenotype..
public-library-of-science.
2015
Triploidy—Observations in 154 Diandric Cases.
public-library-of-science.
2015
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hide from search
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Performance Comparison of Affymetrix SNP6.0 and Cytogenetic 2.7M Whole-Genome Microarrays in Complex Cancer Samples.
Cytogenetic and Genome Research.
2013
Polymorphisms of Muscle Genes Are Associated with Bone Mass and Incident Osteoporotic Fractures in Caucasians.
Calcified Tissue International.
2013
The human oviduct transcriptome reveals an anti-inflammatory, anti-angiogenic, secretory and matrix-stable environment during embryo transit.
Reproductive BioMedicine Online.
2013
Supplementary Material for: Performance Comparison of Affymetrix SNP6.0 and Cytogenetic 2.7M Whole-Genome Microarrays in Complex Cancer Samples.
karger-publishers.
2012
Association of multiple sclerosis with rs391745 located near HERV-Fc1..
public-library-of-science.
2011
Association of multiple sclerosis with the polymorphism rs3802981 located in the first intron of TRIM5..
public-library-of-science.
2011
Comparison of clinical and morphometric findings in Seckel (SCKL2) and Jawad patients..
public-library-of-science.
2011
CtIP Mutations Cause Seckel and Jawad Syndromes.
public-library-of-science.
2011
Generation of a Predictive Melphalan Resistance Index by Drug Screen
of B-Cell Cancer Cell Lines.
public-library-of-science.
2011
The Etiology of Multiple Sclerosis: Genetic Evidence for the Involvement of the Human Endogenous Retrovirus HERV-Fc1.
public-library-of-science.
2011
The generated probesets predicting melphalan resistance..
public-library-of-science.
2011
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patent
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preprint