Author details

Full Name

Jeanette Erdmann

Affiliation

ORCID

Career Start Year

1992

Papers

315

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
36843528	Homozygous frameshift variant in desmoglein 2 geneÂ causes biventricular arrhythmogenic right ventricular cardiomyopathy.		2023
36217027	A novel MAP3K20 mutation causing centronuclear myopathy-6 with fiber-type disproportion in a Pakistani family.	Journal of Human Genetics	2023
35987817	Genetic and modifiable risk factors combine multiplicatively in common disease.	Clin Res Cardiol	2023
35727948	Elucidation of the genetic causes of bicuspid aortic valve disease.	Cardiovasc Res	2023
37675562	ADAMTS-7 Modulates Atherosclerotic Plaque Formation by Degradation of TIMP-1.	Circ Res	2023
37941454	Autoantibodies against the chemokine receptor 3 predict cardiovascular risk.		2023
37596289	The interleukin-11 receptor variant p.W307R results in craniosynostosis in humans.		2023
36884078	The DZHK research platform: maximisation of scientific value by enabling access to health data and biological samples collected in cardiovascular clinical studies.	Clin Res Cardiol	2023
36634218	Genome-wide association studies of cardiovascular disease.		2023
37113769	: Chamber-specific heart phenotype quantification of zebrafish in high-content screens.		2023
35306566	Genetically Determined Reproductive Aging and Coronary Heart Disease: A Bidirectional 2-sample Mendelian Randomization.	J Clin Endocrinol Metab	2022
35381883	Publisher Correction: Transcriptome-wide association study of coronary artery disease identifies novel susceptibility genes.	Basic Res Cardiol	2022
33878186	Cis-epistasis at the LPA locus and risk of cardiovascular diseases.	Cardiovasc Res	2022
34927193	Sex matters? Sex matters!	Cardiovascular Research	2022
35175464	Transcriptome-wide association study of coronary artery disease identifies novel susceptibility genes.	Basic Res Cardiol	2022
34424768	Identification of a Functional <i>PDE5A</i> Variant at the Chromosome 4q27 Coronary Artery Disease Locus in an Extended Myocardial Infarction Family.	Circulation	2021
34070975	Effect of Differences in the Microbiome of <i>Cyp17a1</i>-Deficient Mice on Atherosclerotic Background.	Cells	2021
33633722	Current Developments of Clinical Sequencing and the Clinical Utility of Polygenic Risk Scores in Inflammatory Diseases.	Front Immunol	2021
34011352	Identification of two novel bullous pemphigoid- associated alleles, HLA-DQA105:05 and -DRB107:01, in Germans.	Orphanet J Rare Dis	2021
33478553	What can we learn from common variants associated with unexpected phenotypes in rare genetic diseases?	Orphanet Journal of Rare Diseases	2021
33738695	Induced Pluripotent Stem Cells (iPSCs) in Vascular Research: from Two- to Three-Dimensional Organoids.	Stem Cell Reviews and Reports	2021
33677556	Genome-wide association analysis in dilated cardiomyopathy reveals two new players in systolic heart failure on chromosomes 3p25.1 and 22q11.23.	Eur Heart J	2021
33676559	The CAD risk locus 9p21 increases the risk of vascular calcification in an iPSC-derived VSMC model.	Stem Cell Research and Therapy	2021
34099640	The C5a/C5a receptor 1 axis controls tissue neovascularization through CXCL4 release from platelets.	Nature Communications	2021
33829256	A proteomic atlas of the neointima identifies novel druggable targets for preventive therapy.	Eur Heart J	2021
33561196	Unfolding and disentangling coronary vascular disease through genome-wide association studies.	European Heart Journal	2021
33716783	sGC Activity and Regulation of Blood Flow in a Zebrafish Model System.	Frontiers in Physiology	2021
33822779	Correction: A missense variant in Mitochondrial Amidoxime Reducing Component 1 gene and protection against liver disease.	PLoS Genet	2021
32734504	New technologies for intensive prevention programs after myocardial infarction: rationale and design of the NET-IPP trial.	Clin Res Cardiol	2021
33060817	Identifying multimodal signatures underlying the somatic comorbidity of psychosis: the COMMITMENT roadmap.	Mol Psychiatry	2021
34440456	A Novel Missense Mutation in Causes Recessively Inherited Cardiac Conduction Disease in a Consanguineous Pakistani Family.	Genes	2021
32558485	Genomewide Association Study of Severe Covid-19 with Respiratory Failure.	N Engl J Med	2020
31960029	Genetics of educational attainment and coronary risk in Mendelian randomization studies.	Eur Heart J	2020
31674209	Long-term prevention after myocardial infarction in young patients â¿¤45 years: the Intensive Prevention Program in the Young (IPP-Y) study.	European Journal of Preventive Cardiology	2020
32050579	miR-128a Acts as a Regulator in Cardiac Development by Modulating Differentiation of Cardiac Progenitor Cell Populations.	International Journal of Molecular Sciences	2020
31981480	Sharing lessons learnt across European cardiovascular research consortia.	Drug Discovery Today	2020
31922285	Polygenic risk scores outperform machine learning methods in predicting coronary artery disease status.	Genet Epidemiol	2020
31754706	Osteoclast imbalance in primary familial brain calcification: evidence for its role in brain calcification.	Brain	2020
32472014	CYP17A1 deficient XY mice display susceptibility to atherosclerosis, altered lipidomic profile and atypical sex development.	Scientific Reports	2020
32460060	Retraction notice to "Differentiation of human iPSCs into VSMCs and generation of VSMC-derived calcifying vascular cells" [Stem Cell Res. 31 (2018) 62-70].	Stem Cell Research	2020
32383070	Mendelian randomization analysis does not support causal associations of birth weight with hypertension risk and blood pressure in adulthood.	Eur J Epidemiol	2020
32148083	White Blood Cells and Blood Pressure: A Mendelian Randomization Study.	Circulation	2020
32714944	Dare to Compare. Development of Atherosclerotic Lesions in Human, Mouse, and Zebrafish.	Frontiers in Cardiovascular Medicine	2020
32984406	Studies in Zebrafish Demonstrate That and Are Most Likely the Causal Genes at the Blood Pressure-Associated Locus on Human Chromosome 10q24.32.	Frontiers in Cardiovascular Medicine	2020
32814314	Increased Serum Levels of Asymmetric Dimethylarginine and Symmetric Dimethylarginine and Decreased Levels of Arginine in Sudanese Patients with Essential Hypertension.	Kidney and Blood Pressure Research	2020
32862661	Heterozygous <i>ABCG5</i> Gene Deficiency and Risk of Coronary Artery Disease.	Circ Genom Precis Med	2020
33170024	Population Bias in Polygenic Risk Prediction Models for Coronary Artery Disease.	Circ Genom Precis Med	2020
31152549	CARDIoGRAM celebrates its 10th Anniversary.	European Heart Journal	2019
31824475	Polymorphisms in the Mitochondrial Genome Are Associated With Bullous Pemphigoid in Germans.	Frontiers in Immunology	2019
30218097	Meta-analysis of genome-wide association studies of aggressive and chronic periodontitis identifies two novel risk loci.	Eur J Hum Genet	2019