Author details

Full Name

Monika Stoll

Affiliation

ORCID

Career Start Year

1968

Papers

185

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
35348614	A genome-wide association study in autoimmune neurological syndromes with anti-GAD65 autoantibodies.	Brain	2023
36970523	Evidence of polygenic regulation of the physiological presence of neurofilament light chain in human serum.	Front Neurol	2023
36715011	Studies in Zebrafish and Rat Models Support Dual Blockade of EP2 and EP4 (Prostaglandin E Receptors Type 2 and 4) for Renoprotection in Glomerular Hyperfiltration and Albuminuria.		2023
36574650	Enhanced pathogenicity of Th17 cells due to natalizumab treatment: Implications for MS disease rebound.		2023
37073128	MicroRNA-216a is essential for cardiac angiogenesis.		2023
36756698	DNA repair in cardiomyocytes is critical for maintaining cardiac function in mice.	Aging Cell	2023
37191590	Cell-intrinsic genomic reassortment of pandemic H1N1 2009 and Eurasian avian-like swine influenza viruses results in potentially zoonotic variants.		2023
36526599	Blood Milieu in Acute Myocardial Infarction Reprograms Human Macrophages for Trauma Repair.		2023
35012583	Polymorphisms in the mTOR-PI3K-Akt pathway, energy balance-related exposures and colorectal cancer risk in the Netherlands Cohort Study.	BioData Mining	2022
35379829	Monocyte subpopulation profiling indicates CDK6-derived cell differentiation and identifies subpopulation-specific miRNA expression sets in acute and stable coronary artery disease.	Scientific Reports	2022
35625889	Low Density Lipoprotein Exposure of Plasmacytoid Dendritic Cells Blunts Toll-like Receptor 7/9 Signaling via NUR77.	Biomedicines	2022
35359237	Assessment of angiogenesis-related parameters in juvenile idiopathic arthritis-associated uveitis.	Molecular Biology Reports	2022
35859757	The Impact of Varying Food Availability on Gene Expression in the Liver: Testing the Match-Mismatch Hypothesis.	Frontiers in Nutrition	2022
36533130	Transcriptional profiles in the mouse amygdala after a cognitive judgment bias test largely depend on the genotype.		2022
34916661	Cpxm2 as a novel candidate for cardiac hypertrophy and failure in hypertension.	Hypertension Research	2022
34729582	Empirical Investigation of Genomic Clusters Associated With Height and the Risk of Postmenopausal Breast and Colorectal Cancer in the Netherlands Cohort Study.	American Journal of Epidemiology	2022
35218871	Cardiac chamber-specific genetic alterations suggest candidate genes and pathways implicating the left ventricle in the pathogenesis of atrial fibrillation.	Genomics	2022
34506887	Evolutionarily conserved transcriptional landscape of the heart defining the chamber specific physiology.	Genomics	2021
34128785	Insights into evolution and coexistence of the colibactin- and yersiniabactin secondary metabolite determinants in enterobacterial populations.	Microbial genomics	2021
33592630	Single- and Multimarker Genome-Wide Scans Evidence Novel Genetic Risk Modifiers for Venous Thromboembolism.	Thromb Haemost	2021
33506376	Reappraisal of Atrial fibrillation: interaction between hyperCoagulability, Electrical remodelling and Vascular destabilisation in the progression of AF (RACEÂ V) Tissue Bank Project: study design.	Netherlands Heart Journal	2021
33713866	Leukocyte gene expression in post-thrombotic syndrome.	Thrombosis Research	2021
33555020	Dynamic risk assessment to improve quality of care in patients with atrial fibrillation: the 7th AFNET/EHRA Consensus Conference.	Europace	2021
34313541	A genetic variant alters the secondary structure of the lncRNA H19 and is associated with dilated cardiomyopathy.	RNA Biol	2021
32594420	Role of prothrombin 19911 A>G polymorphism, blood group and male gender in patients with venous thromboembolism: Results of a German cohort study.	J Thromb Thrombolysis	2021
33067869	Climate change facilitates a parasite's host exploitation via temperature-mediated immunometabolic processes.	Glob Chang Biol	2021
34465617	Genomic instability in the naturally and prematurely aged myocardium.	Proceedings of the National Academy of Sciences of the United States of America	2021
32602979	Induction of ICER is superseded by smICER, challenging the impact of ICER under chronic beta-adrenergic stimulation.	FASEB Journal	2020
32199911	CD163 expression defines specific, IRF8-dependent, immune-modulatory macrophages in the bone marrow.	J Allergy Clin Immunol	2020
32424227	Dichotomy between the transcriptomic landscape of naturally versus accelerated aged murine hearts.	Scientific Reports	2020
32443579	A Year in the Life of the EU-CardioRNA COST Action: CA17129 Catalysing Transcriptomics Research in Cardiovascular Disease.	Non-coding RNA	2020
33208780	JavaCyte, a novel open-source tool for automated quantification of key hallmarks of cardiac structural remodeling.	Scientific Reports	2020
32887511	Non-Coding RNA Databases in Cardiovascular Research.	Non-coding RNA	2020
32817637	ADAMTS12, a new candidate gene for pediatric stroke.	PLoS ONE	2020
32814717	Reduced left atrial cardiomyocyte PITX2 and elevated circulating BMP10 predict atrial fibrillation after ablation.	JCI insight	2020
30709035	Evolutionary Patterns of Non-Coding RNA in Cardiovascular Biology.	Non-coding RNA	2019
31575673	Recurrent stroke: the role of thrombophilia in a large international pediatric stroke population.	Haematologica	2019
30192927	Complement 5a Receptor Polymorphisms Are Associated With Panton-Valentine Leukocidin-positive Staphylococcus aureus Colonization in African Pygmies.	Clinical Infectious Diseases	2019
30816678	Suppressor of Cytokine Signaling 1 is Involved in Gene Regulation Which Controls the Survival of Ly6C Monocytes in Mice.	Cellular Physiology and Biochemistry	2019
30737279	A novel isoform of myosin 18A (Myo18AÎ³) is an essential sarcomeric protein in mouse heart.	J Biol Chem	2019
30679327	Recurrent stroke: the role of thrombophilia in a large international pediatric stroke population.	Haematologica	2019
30900988	Analysis of the genomic architecture of a complex trait locus in hypertensive rat models links to kidney damage.	eLife	2019
30934986	Catalyzing Transcriptomics Research in Cardiovascular Disease: The CardioRNA COST Action CA17129.	Noncoding RNA	2019
30885419	Transcriptomic and proteomic analysis of iris tissue and aqueous humor in juvenile idiopathic arthritis-associated uveitis.	J Autoimmun	2019
31043571	Teriflunomide treatment for multiple sclerosis modulates T cell mitochondrial respiration with affinity-dependent effects.	Science Translational Medicine	2019
29540468	Genetic Reduction in Left Ventricular Protein Kinase C-Î± and Adverse Ventricular Remodeling in Human Subjects.	Circ Genom Precis Med	2018
29934777	Targeted resequencing of a locus for heparin-induced thrombocytopenia on chromosome 5 identified in a genome-wide association study.	Journal of Molecular Medicine	2018
30072431	Nur77 serves as a molecular brake of the metabolic switch during T cell activation to restrict autoimmunity.	Proceedings of the National Academy of Sciences of the United States of America	2018
29265336	Advances in predicting venous thromboembolism risk in children.	British Journal of Haematology	2018
29611822	Autoinhibitory regulation of S100A8/S100A9 alarmin activity locally restricts sterile inflammation.	Journal of Clinical Investigation	2018