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Person

Pascal Schlosser

Mathematiker

Name	Pascal Schlosser
Ort	Deutschland
Beruf	Mathematiker (charakteristischer Beruf) Wissenschaftlicher Mitarbeiter
Beziehung	Institut für Medizinische Biometrie und Statistik (Freiburg im Breisgau) (2014-)
Datensatztyp	Person
GND-Nummer	112816373X
Datensatz-ID	112816373X
Beteiligt an alle anzeigen Plasma proteomics of acute tubular injury SLC17A1/3 transporters mediate renal excretion of Lac-Phe in mice and humans Conditional survival to assess prognosis in patients with chronic lymphocytic leukemia 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 Conditional survival to assess prognosis in patients with chronic lymphocytic leukemia Epigenome-wide DNA methylation in unipolar depression - predictive biomarker of antidepressant treatment response? Implication of transcription factor FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT) metaGWASmanager: a toolbox for an automated workflow from phenotypes to meta-analysis in GWAS consortia Plasma proteomics of acute tubular injury SLC17A1/3 transporters mediate renal excretion of Lac-Phe in mice and humans 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 Transcriptome- and proteome-wide association studies nominate determinants of kidney function and damage Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine In vivo kinetics of early, non-random methylome and transcriptome changes induced by DNA-hypomethylating treatment in primary AML blasts In vivo kinetics of early, non-random methylome and transcriptome changes induced by DNA-hypomethylating treatment in primary AML blasts DNA methylation signature of chronic low-grade inflammation and its role in cardio-respiratory diseases Epigenome-wide DNA methylation in obsessive-compulsive disorder Genome-wide studies reveal factors associated with circulating uromodulin and its relations with complex diseases Serum metabolites and kidney outcomes: the atherosclerosis risk in communities study Author Correction: Rare genetic variants affecting urine metabolite levels link population variation to inborn errors of metabolism Discovery and prioritization of variants and genes for kidney function in >1.2 million individuals Epigenome-wide association study of serum urate reveals insights into urate co-regulation and the SLC2A9 locus Meta-analyses identify DNA methylation associated with kidney function and damage Netboost: boosting-supported network analysis improves high-dimensional omics prediction in acute myeloid leukemia and huntington's disease Netboost: boosting-supported network analysis improves high-dimensional Omics prediction in acute myeloid leukemia and Huntington's disease pgainsim: an R-package to assess the mode of inheritance for quantitative trait loci in GWAS Rare genetic variants affecting urine metabolite levels link population variation to inborn errors of metabolism Ttc30a affects tubulin modifications in a model for ciliary chondrodysplasia with polycystic kidney disease Netboost: statistical modeling strategies for high-dimensional data The DNA methylome in panic disorder: a case-control and longitudinal psychotherapy-epigenetic study Combination treatment of acute myeloid leukemia cells with DNMT and HDAC inhibitors: predominant synergistic gene downregulation associated with gene body demethylation Epigenome-wide association studies identify DNA methylation associated with kidney function Epigenome-wide association studies identify DNA methylation associated with kidney function GenToS: use of orthologous gene information to prioritize signals from human GWAS Integrative network-based analysis of magnetic resonance spectroscopy and genome wide expression in glioblastoma multiforme

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Katalog der Deutschen Nationalbibliothek

Pascal Schlosser

Plasma proteomics of acute tubular injury

SLC17A1/3 transporters mediate renal excretion of Lac-Phe in mice and humans

Conditional survival to assess prognosis in patients with chronic lymphocytic leukemia

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

Conditional survival to assess prognosis in patients with chronic lymphocytic leukemia

Epigenome-wide DNA methylation in unipolar depression - predictive biomarker of antidepressant treatment response?

Implication of transcription factor FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT)

metaGWASmanager: a toolbox for an automated workflow from phenotypes to meta-analysis in GWAS consortia

Plasma proteomics of acute tubular injury

SLC17A1/3 transporters mediate renal excretion of Lac-Phe in mice and humans

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

Transcriptome- and proteome-wide association studies nominate determinants of kidney function and damage

Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine

In vivo kinetics of early, non-random methylome and transcriptome changes induced by DNA-hypomethylating treatment in primary AML blasts

In vivo kinetics of early, non-random methylome and transcriptome changes induced by DNA-hypomethylating treatment in primary AML blasts

DNA methylation signature of chronic low-grade inflammation and its role in cardio-respiratory diseases

Epigenome-wide DNA methylation in obsessive-compulsive disorder

Genome-wide studies reveal factors associated with circulating uromodulin and its relations with complex diseases

Serum metabolites and kidney outcomes: the atherosclerosis risk in communities study

Author Correction: Rare genetic variants affecting urine metabolite levels link population variation to inborn errors of metabolism

Discovery and prioritization of variants and genes for kidney function in >1.2 million individuals

Epigenome-wide association study of serum urate reveals insights into urate co-regulation and the SLC2A9 locus

Meta-analyses identify DNA methylation associated with kidney function and damage

Netboost: boosting-supported network analysis improves high-dimensional omics prediction in acute myeloid leukemia and huntington's disease

Netboost: boosting-supported network analysis improves high-dimensional Omics prediction in acute myeloid leukemia and Huntington's disease

pgainsim: an R-package to assess the mode of inheritance for quantitative trait loci in GWAS

Rare genetic variants affecting urine metabolite levels link population variation to inborn errors of metabolism

Ttc30a affects tubulin modifications in a model for ciliary chondrodysplasia with polycystic kidney disease

Netboost: statistical modeling strategies for high-dimensional data

The DNA methylome in panic disorder: a case-control and longitudinal psychotherapy-epigenetic study

Combination treatment of acute myeloid leukemia cells with DNMT and HDAC inhibitors: predominant synergistic gene downregulation associated with gene body demethylation

Epigenome-wide association studies identify DNA methylation associated with kidney function

Epigenome-wide association studies identify DNA methylation associated with kidney function

GenToS: use of orthologous gene information to prioritize signals from human GWAS

Integrative network-based analysis of magnetic resonance spectroscopy and genome wide expression in glioblastoma multiforme