Detail page

Knowledge Web

Person

Jan Haas

Biologe

Name	Jan Haas
Place	Heidelberg (Geburtsort) Deutschland
Gender	männlich
Academic degree	Dr. rer. nat.
Profession	Biologe (characteristic profession)
Further information	Diss. Naturwiss.-Mathematische Gesamtfakultät der Ruprecht-Karls-Universität Heidelberg; Mitarbeiter, Analysezentrum III, Innere Medizin III, Medizinische Klinik, Universitätsklinikum Heidelberg
Record type	Person
GND-Identifier	1030297231
Record ID	1030297231
Involved in show all Improving sudden cardiac death risk stratification in hypertrophic cardiomyopathy using established clinical variables and genetic information Genotype complements the phenotype: identification of the pathogenicity of an LMNA splice variant by nanopore long-read sequencing in a large DCM family Identification of SCN5a p.C335R variant in a large family with dilated cardiomyopathy and conduction disease Novel Nongenetic Murine Model of Hyperglycemia and Hyperlipidemia-Associated Aggravated Atherosclerosis NIMA-related kinase 9 regulates the phosphorylation of the essential myosin light chain in the heart Reduction of A-to-I RNA editing in the failing human heart regulates formation of circular RNAs Doxorubicin induces cardiotoxicity in a pluripotent stem cell model of aggressive B cell lymphoma cancer patients Controlling my genome with my smartphone: first clinical experiences of the PROMISE system Multi-omics assessment of dilated cardiomyopathy using non-negative matrix factorization Controlling my genome with my smartphone: first clinical experiences of the PROMISE system Energy Metabolites as Biomarkers in Ischemic and Dilated Cardiomyopathy Marathon-Induced Cardiac Strain as Model for the Evaluation of Diagnostic microRNAs for Acute Myocardial Infarction Epigenetic Regulation of Alternative mRNA Splicing in Dilated Cardiomyopathy Clinical and genetic insights into non-compaction: a meta-analysis and systematic review on 7598 individuals Genomic structural variations lead to dysregulation of important coding and non‐coding RNA species in dilated cardiomyopathy Genomic structural variations lead to dysregulation of important coding and non-coding RNA species in dilated cardiomyopathy Clinical outcomes associated with sarcomere mutations in hypertrophic cardiomyopathy: a meta-analysis on 7675 individuals The cardiac microenvironment uses non‐canonical WNT signaling to activate monocytes after myocardial infarction Genotype-phenotype associations in dilated cardiomyopathy: meta-analysis on more than 8000 individuals Deep characterization of blood cell miRNomes by NGS Next-generation sequencing identifies altered whole blood microRNAs in neuromyelitis optica spectrum disorder which may permit discrimination from multiple sclerosis Systematic permutation testing in GWAS pathway analyses: identification of genetic networks in dilated cardiomyopathy and ulcerative colitis miFRame: analysis and visualization of miRNA sequencing data in neurological disorders Systematic permutation testing in GWAS pathway analyses: identification of genetic networks in dilated cardiomyopathy and ulcerative colitis A blood based 12-miRNA signature of Alzheimer disease patients Alterations in cardiac DNA methylation in human dilated cardiomyopathy A blood based 12-miRNA signature of Alzheimer disease patients miRTrail - a comprehensive webserver for analyzing gene and miRNA patterns to enhance the understanding of regulatory mechanisms in diseases Etablierung der nächsten Generation molekularer Diagnostik von Kardiomyopathien

Please note

The beta version does not yet contain all functions and information of the DNB portal catalogue. If you are missing information or want to order a medium, please visit the page in the DNB portal catalogue via the following link:

Katalog der Deutschen Nationalbibliothek

Jan Haas

Improving sudden cardiac death risk stratification in hypertrophic cardiomyopathy using established clinical variables and genetic information

Genotype complements the phenotype: identification of the pathogenicity of an LMNA splice variant by nanopore long-read sequencing in a large DCM family

Identification of SCN5a p.C335R variant in a large family with dilated cardiomyopathy and conduction disease

Novel Nongenetic Murine Model of Hyperglycemia and Hyperlipidemia-Associated Aggravated Atherosclerosis

NIMA-related kinase 9 regulates the phosphorylation of the essential myosin light chain in the heart

Reduction of A-to-I RNA editing in the failing human heart regulates formation of circular RNAs

Doxorubicin induces cardiotoxicity in a pluripotent stem cell model of aggressive B cell lymphoma cancer patients

Controlling my genome with my smartphone: first clinical experiences of the PROMISE system

Multi-omics assessment of dilated cardiomyopathy using non-negative matrix factorization

Controlling my genome with my smartphone: first clinical experiences of the PROMISE system

Energy Metabolites as Biomarkers in Ischemic and Dilated Cardiomyopathy

Marathon-Induced Cardiac Strain as Model for the Evaluation of Diagnostic microRNAs for Acute Myocardial Infarction

Epigenetic Regulation of Alternative mRNA Splicing in Dilated Cardiomyopathy

Clinical and genetic insights into non-compaction: a meta-analysis and systematic review on 7598 individuals

Genomic structural variations lead to dysregulation of important coding and non‐coding RNA species in dilated cardiomyopathy

Genomic structural variations lead to dysregulation of important coding and non-coding RNA species in dilated cardiomyopathy

Clinical outcomes associated with sarcomere mutations in hypertrophic cardiomyopathy: a meta-analysis on 7675 individuals

The cardiac microenvironment uses non‐canonical WNT signaling to activate monocytes after myocardial infarction

Genotype-phenotype associations in dilated cardiomyopathy: meta-analysis on more than 8000 individuals

Deep characterization of blood cell miRNomes by NGS

Next-generation sequencing identifies altered whole blood microRNAs in neuromyelitis optica spectrum disorder which may permit discrimination from multiple sclerosis

Systematic permutation testing in GWAS pathway analyses: identification of genetic networks in dilated cardiomyopathy and ulcerative colitis

miFRame: analysis and visualization of miRNA sequencing data in neurological disorders

Systematic permutation testing in GWAS pathway analyses: identification of genetic networks in dilated cardiomyopathy and ulcerative colitis

A blood based 12-miRNA signature of Alzheimer disease patients

Alterations in cardiac DNA methylation in human dilated cardiomyopathy

A blood based 12-miRNA signature of Alzheimer disease patients

miRTrail - a comprehensive webserver for analyzing gene and miRNA patterns to enhance the understanding of regulatory mechanisms in diseases

Etablierung der nächsten Generation molekularer Diagnostik von Kardiomyopathien