Schlosser, Pascal
Pascal Schlosser researcher
VIAF ID: 5886149068374265730000 (Personal)
Permalink: http://viaf.org/viaf/5886149068374265730000
Preferred Forms
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100 0 _ ‡a Pascal Schlosser ‡c researcher
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100 1 _ ‡a Schlosser, Pascal
4xx's: Alternate Name Forms (1)
5xx's: Related Names (1)
Works
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Combination treatment of acute myeloid leukemia cells with DNMT and HDAC inhibitors: predominant synergistic gene downregulation associated with gene body demethylation |
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Conditional survival to assess prognosis in patients with chronic lymphocytic leukemia |
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Discovery and prioritization of variants and genes for kidney function in >1.2 million individuals |
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Discovery of potential serum and urine-based microRNA as minimally-invasive biomarkers for breast and gynecological cancer |
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DNA methylation signature of chronic low-grade inflammation and its role in cardio-respiratory diseases |
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DNA methylome in panic disorder: a case-control and longitudinal psychotherapy-epigenetic study |
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Early diastolic septal movement in patients with myocarditis. |
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Epigenome-wide association studies identify DNA methylation associated with kidney function |
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Epigenome-wide association study of serum urate reveals insights into urate co-regulation and the SLC2A9 locus |
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Epigenome-wide DNA methylation in obsessive-compulsive disorder |
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Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine |
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Genetic studies of urinary metabolites illuminate mechanisms of detoxification and excretion in humans |
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Genome-wide studies reveal factors associated with circulating uromodulin and its relations with complex diseases |
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GenToS: use of orthologous gene information to prioritize signals from human GWAS |
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Implication of transcription factor FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT) |
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In vivo kinetics of early, non-random methylome and transcriptome changes induced by DNA-hypomethylating treatment in primary AML blasts |
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Integration of GWAS Summary Statistics and Gene Expression Reveals Target Cell Types Underlying Kidney Function Traits |
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Integrative network-based analysis of magnetic resonance spectroscopy and genome wide expression in glioblastoma multiforme |
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metaGWASmanager: a toolbox for an automated workflow from phenotypes to meta-analysis in GWAS consortia |
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<i>NAT8</i> Variants, N-Acetylated Amino Acids, and Progression of CKD |
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Netboost: boosting-supported network analysis improves high-dimensional Omics prediction in acute myeloid leukemia and Huntington's disease |
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Netboost: statistical modeling strategies for high-dimensional data |
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pgainsim: an R-package to assess the mode of inheritance for quantitative trait loci in GWAS |
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Rare genetic variants affecting urine metabolite levels link population variation to inborn errors of metabolism |
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Self-Reported Medication Use and Urinary Drug Metabolites in the German Chronic Kidney Disease (GCKD) Study |
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Serum metabolites and kidney outcomes: the atherosclerosis risk in communities study |
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Ttc30a affects tubulin modifications in a model for ciliary chondrodysplasia with polycystic kidney disease |
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X-chromosome and kidney function: evidence from a multi-trait genetic analysis of 908,697 individuals reveals sex-specific and sex-differential findings in genes regulated by androgen response elements |
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