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Lista de obras de Jeanette Erdmann

5-HT2A receptor and bipolar affective disorder: association studies in affected patients

artículo científico publicado en 1997

A common polymorphism in KCNH2 (HERG) hastens cardiac repolarization

artículo científico publicado en 2003

A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease

artículo científico publicado en 2015

A decade of genome-wide association studies for coronary artery disease: The challenges ahead.

artículo científico publicado en 2018

A genome-wide association study for coronary artery disease identifies a novel susceptibility locus in the major histocompatibility complex

artículo científico publicado en 2012

A genome-wide association study identifies LIPA as a susceptibility gene for coronary artery disease

artículo científico publicado en 2011

A genome-wide association study identifies nucleotide variants at SIGLEC5 and DEFA1A3 as risk loci for periodontitis

artículo científico publicado en 2017

A genome-wide association study identifies nucleotide variants at SIGLEC5 and DEFA1A3 as risk loci for periodontitis

artículo científico publicado en 2018

A genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathy

artículo científico publicado en 2011

A genome-wide association study reveals variants in ARL15 that influence adiponectin levels

artículo científico publicado en 2009

A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium

artículo científico publicado en 2009

A genomic approach to therapeutic target validation identifies a glucose-lowering GLP1R variant protective for coronary heart disease

artículo científico publicado en 2016

A genomic exploration identifies mechanisms that may explain adverse cardiovascular effects of COX-2 inhibitors

artículo científico publicado en 2017

A locus on chromosome 10 influences C-reactive protein levels in two independent populations

A missense variant in Mitochondrial Amidoxime Reducing Component 1 gene and protection against liver disease

scientific article published on 13 April 2020

A novel variant on chromosome 7q22.3 associated with mean platelet volume, counts, and function

artículo científico publicado en 2009

A proteomic atlas of the neointima identifies novel druggable targets for preventive therapy

artículo científico publicado en 2021

A trans-acting locus regulates an anti-viral expression network and type 1 diabetes risk

artículo científico publicado en 2010

ADAMTS-7 inhibits re-endothelialization of injured arteries and promotes vascular remodeling through cleavage of thrombospondin-1.

artículo científico publicado en 2015

ANGPTL3 Deficiency and Protection Against Coronary Artery Disease

artículo científico publicado en 2017

APOE alleles are not associated with calcific aortic stenosis

artículo científico publicado en 2006

Additional Candidate Genes for Human Atherosclerotic Disease Identified Through Annotation Based on Chromatin Organization

artículo científico publicado en 2017

Ahnak is critical for cardiac Ca(V)1.2 calcium channel function and its beta-adrenergic regulation

artículo científico publicado en 2005

Aldosterone synthase (CYP11B2) -344 C/T polymorphism is associated with left ventricular structure in human arterial hypertension

artículo científico publicado en 2001

An Alternative Splice Variant inAbcc6, the Gene Causing Dystrophic Calcification, Leads to Protein Deficiency in C3H/He Mice

artículo científico publicado en 2008

Analysis of predicted loss-of-function variants in UK Biobank identifies variants protective for disease.

artículo científico publicado en 2018

Angiotensin II type 2 receptor gene polymorphism and cardiovascular phenotypes: the GLAECO and GLAOLD studies.

artículo científico publicado en 2002

Angiotensin converting enzyme gene polymorphism and myocardial infarction a large association and linkage study

artículo científico publicado en 2003

Arterial calcification in mice after freeze-thaw injury

artículo científico publicado en 2006

Association analyses based on false discovery rate implicate new loci for coronary artery disease ⬇️

artículo científico

Association between PPARalpha gene polymorphisms and myocardial infarction

artículo científico publicado en 2008

Association between arterial pressure and coronary artery calcification

artículo científico publicado en 2007

Association of Genetic Variation at Locus with Vascular Depression

artículo científico publicado en 2018

Association of NOS3 gene polymorphisms with essential hypertension in Sudanese patients: a case control study

artículo científico publicado en 2017

Association of a functional polymorphism in the CYP4A11 gene with systolic blood pressure in survivors of myocardial infarction

article

Association of angiotensin-converting enzyme 2 (ACE2) gene polymorphisms with parameters of left ventricular hypertrophy in men

article

Association of common polymorphisms in GLUT9 gene with gout but not with coronary artery disease in a large case-control study

artículo científico publicado en 2008

Association of low-grade urinary albumin excretion with left ventricular hypertrophy in the general population

Association of the Ghrelin Receptor Gene Region With Left Ventricular Hypertrophy in the General Population

article

Association of the T8590C polymorphism of CYP4A11 with hypertension in the MONICA Augsburg echocardiographic substudy

artículo científico publicado en 2005

Associations of autozygosity with a broad range of human phenotypes

scientific article published on 31 October 2019

Bedeutung moderner Genomstudien für das Herzinfarktrisiko

Binding properties of the naturally occurring human 5-HT1A receptor variant with the Ile28Val substitution in the extracellular domain

artículo científico publicado en 1995

Biological, clinical and population relevance of 95 loci for blood lipids

artículo científico publicado en 2010

Bradykinin B2BKR receptor polymorphism and left-ventricular growth response

artículo científico publicado en 2001

CD163+ macrophages promote angiogenesis and vascular permeability accompanied by inflammation in atherosclerosis

artículo científico publicado en 2018

CYP17A1 deficient XY mice display susceptibility to atherosclerosis, altered lipidomic profile and atypical sex development

artículo científico publicado en 2020

Characterization of the GNAQ promoter and association of increased Gq expression with cardiac hypertrophy in humans.

artículo científico publicado en 2008

Cigarette smoking reduces DNA methylation levels at multiple genomic loci but the effect is partially reversible upon cessation

artículo científico publicado en 2014

Circulating brain-derived neurotrophic factor concentrations and the risk of cardiovascular disease in the community

artículo científico publicado en 2015

Classification of ADAMTS binding sites: The first step toward selective ADAMTS7 inhibitors

artículo científico publicado en 2016

Clinical and genetic association of serum paraoxonase and arylesterase activities with cardiovascular risk

artículo científico publicado en 2012

Cloning and characterization of the 5'-flanking region of the human cardiotrophin-1 gene

artículo científico publicado en 1998

Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease

artículo científico publicado en 2016

Common and Rare Genetic Variation in CCR2, CCR5, or CX3CR1 and Risk of Atherosclerotic Coronary Heart Disease and Glucometabolic Traits

scientific article published on 24 March 2016

Common genetic loci influencing plasma homocysteine concentrations and their effect on risk of coronary artery disease

artículo científico publicado en 2013

Common genetic variation in the 3'-BCL11B gene desert is associated with carotid-femoral pulse wave velocity and excess cardiovascular disease risk: the AortaGen Consortium

artículo científico publicado en 2011

Common polymorphisms influencing serum uric acid levels contribute to susceptibility to gout, but not to coronary artery disease

artículo científico publicado en 2009

Common variants at 10 genomic loci influence hemoglobin A₁(C) levels via glycemic and nonglycemic pathways ⬇️

artículo científico publicado en 2010

Comprehensive exploration of the effects of miRNA SNPs on monocyte gene expression

artículo científico publicado en 2012

Coronary Artery Disease-Associated Locus on Chromosome 9p21 and Early Markers of Atherosclerosis

artículo científico publicado en 2008

Coronary Artery Ectasia Are Frequently Observed in Patients With Bicuspid Aortic Valves With and Without Dilatation of the Ascending Aorta

artículo científico publicado en 2016

Coronary artery disease associated gene Phactr1 modulates severity of vascular calcification in vitro

artículo científico publicado en 2017

Coronary heart disease-associated variation in TCF21 disrupts a miR-224 binding site and miRNA-mediated regulation

artículo científico publicado en 2014

Correction: The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study

artículo científico publicado en 2016

DNA Sequence Variation in Encoding the Activin-Receptor Like Kinase 7 Influences Body Fat Distribution and Protects Against Type 2 Diabetes

DNA methylation and body-mass index: a genome-wide analysis

artículo científico publicado en 2014

Defining the role of common variation in the genomic and biological architecture of adult human height

artículo científico publicado en 2014

Design of the Coronary ARtery DIsease Genome-Wide Replication And Meta-Analysis (CARDIoGRAM) Study: A Genome-wide association meta-analysis involving more than 22 000 cases and 60 000 controls

artículo científico publicado en 2010

Detection of four polymorphic sites in the human dopamine D1 receptor gene (DRD1)

article

Die Herzinsuffizienz als komplexe genetische Erkrankung

Differentiation of human iPSCs into VSMCs and generation of VSMC-derived calcifying vascular cells

retracted paper

Dinucleotide repeat polymorphism at the D18S365 locus

artículo científico publicado en 1993

Dinucleotide repeat polymorphism at the D18S99 locus

scientific article published on 01 January 1993

Discovery and Fine-Mapping of Glycaemic and Obesity-Related Trait Loci Using High-Density Imputation

artículo científico publicado en 2015

Dissecting the roles of microRNAs in coronary heart disease via integrative genomic analyses

artículo científico publicado en 2015

Distinct Heritable Patterns of Angiographic Coronary Artery Disease in Families With Myocardial Infarction

Druggability of Coronary Artery Disease Risk Loci

scientific article published on 01 August 2018

Dysfunctional nitric oxide signalling increases risk of myocardial infarction

artículo científico publicado en 2013

Effect of the angiotensin II type 2-receptor gene (+1675 G/A) on left ventricular structure in humans

artículo científico publicado en 2001

Epistatic interaction between haplotypes of the ghrelin ligand and receptor genes influence susceptibility to myocardial infarction and coronary artery disease

article

Etidronate prevents dystrophic cardiac calcification by inhibiting macrophage aggregation.

artículo científico publicado en 2018

Exome sequencing and directed clinical phenotyping diagnose cholesterol ester storage disease presenting as autosomal recessive hypercholesterolemia

artículo científico publicado en 2013

Expression quantitative trait Loci acting across multiple tissues are enriched in inherited risk for coronary artery disease

artículo científico publicado en 2015

FTO genotype is associated with phenotypic variability of body mass index

artículo científico publicado en 2012

Familial aggregation of left main coronary artery disease and future risk of coronary events in asymptomatic siblings of affected patients

artículo científico publicado en 2007

Fifteen new risk loci for coronary artery disease highlight arterial-wall-specific mechanisms

artículo científico publicado en 2017

Forty-five years to diagnosis

artículo científico

Functional Characterization of the GUCY1A3 Coronary Artery Disease Risk Locus

artículo científico publicado en 2017

Functional evaluation of GUCY1A3 mutations associated with myocardial infarction risk.

artículo científico publicado en 2015

Functional interaction of osteogenic transcription factors Runx2 and Vdr in transcriptional regulation of Opn during soft tissue calcification

artículo científico publicado en 2013

Gendered innovation in cardiovascular science: implementation of sex and gender into clinical and biomedical research

artículo científico publicado en 2013

Genetic Loci associated with C-reactive protein levels and risk of coronary heart disease

artículo científico publicado en 2009

Genetic Susceptibility Loci for Cardiovascular Disease and Their Impact on Atherosclerotic Plaques

Genetic analysis for a shared biological basis between migraine and coronary artery disease

artículo científico publicado en 2015

Genetic association study identifies HSPB7 as a risk gene for idiopathic dilated cardiomyopathy

artículo científico publicado en 2010

Genetic basis of myocardial infarction: Novel insights from genome-wide association studies

Genetic causes of myocardial infarction: new insights from genome-wide association studies

artículo científico publicado en 2010

Genetic determinants of circulating sphingolipid concentrations in European populations

scientific article published on 02 October 2009

Genetic evidence for PLASMINOGEN as a shared genetic risk factor of coronary artery disease and periodontitis

artículo científico publicado en 2014

Genetic evidence of assortative mating in humans

article

Genetic factors for overweight and CAD.

artículo científico publicado en 2006

Genetic linkage and association of the growth hormone secretagogue receptor (ghrelin receptor) gene in human obesity

artículo científico publicado en 2005

Genetic markers enhance coronary risk prediction in men: the MORGAM prospective cohorts

artículo científico publicado en 2012

Genetic predisposition to higher blood pressure increases coronary artery disease risk

artículo científico publicado en 2013

Genetic regulation of serum phytosterol levels and risk of coronary artery disease

artículo científico publicado en 2010

Genetic studies of body mass index yield new insights for obesity biology

artículo científico publicado en 2015

Genetic variants associated with cardiac structure and function: a meta-analysis and replication of genome-wide association data

artículo científico publicado en 2009

Genetic variants associated with celiac disease and the risk for coronary artery disease

artículo científico publicado en 2015

Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk

artículo científico publicado en 2011

Genetic variants primarily associated with type 2 diabetes are related to coronary artery disease risk

artículo científico publicado en 2015

Genetic variation at chromosome 1p13.3 affects sortilin mRNA expression, cellular LDL-uptake and serum LDL levels which translates to the risk of coronary artery disease

artículo científico publicado en 2009

Genetic variation in the arachidonate 5-lipoxygenase-activating protein (ALOX5AP) is associated with myocardial infarction in the German population

artículo científico publicado en 2008

Genetic variation of the 5-HT2A receptor and response to clozapine

artículo científico publicado en 1995

Genetically determined height and coronary artery disease

artículo científico publicado en 2015

Genetics and heritability of coronary artery disease and myocardial infarction

artículo científico publicado en 2006

Genetics of (Premature) Coronary Artery Disease

article

Genetics of coronary artery disease and myocardial infarction--2013.

artículo científico publicado en 2013

Genetics of coronary artery disease: Short people at risk?

article

Genetics of educational attainment and coronary risk in Mendelian randomization studies

scientific article published on 01 February 2020

Genetics of myocardial infarction: a progress report

artículo científico publicado en 2010

Genetik der koronaren Herzkrankheit und des Herzinfarkts

Genetik des Herzinfarktes. Der lange Weg von der positiven Familienanamnese zum Gen

Genetische Analysen als Basis einer individualisierten Medizin bei koronarer Herzkrankheit

Genetische Einflüsse beim Herzinfarkt

Genome-Wide Association and Functional Studies Identify SCML4 and THSD7A as Novel Susceptibility Genes for Coronary Artery Disease.

artículo científico publicado en 2018

Genome-wide and gene-centric analyses of circulating myeloperoxidase levels in the charge and care consortia

artículo científico publicado en 2013

Genome-wide association analysis in dilated cardiomyopathy reveals two new players in systolic heart failure on chromosomes 3p25.1 and 22q11.23

artículo científico publicado en 2021

Genome-wide association meta-analysis of coronary artery disease and periodontitis reveals a novel shared risk locus

scientific article published in Scientific Reports

Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants

artículo científico publicado en 2009

Genome-wide association study and targeted metabolomics identifies sex-specific association of CPS1 with coronary artery disease

artículo científico publicado en 2016

Genome-wide association study identifies a new locus for coronary artery disease on chromosome 10p11.23

scholarly article by Jeanette Erdmann et al published 18 November 2010 in European Heart Journal

Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure

artículo científico publicado en 2011

Genome-wide association study in Han Chinese identifies four new susceptibility loci for coronary artery disease

artículo científico publicado en 2012

Genome-wide association study in takotsubo syndrome - Preliminary results and future directions

artículo científico publicado en 2017

Genome-wide association study of L-arginine and dimethylarginines reveals novel metabolic pathway for symmetric dimethylarginine

artículo científico publicado en 2014

Genome-wide haplotype association study identifies the SLC22A3-LPAL2-LPA gene cluster as a risk locus for coronary artery disease

artículo científico publicado en 2009

Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture

scientific journal article

Genome-wide meta-analysis of common variant differences between men and women

artículo científico publicado en 2012

Genomewide association analysis of coronary artery disease

artículo científico publicado en 2007

Genomic correlates of glatiramer acetate adverse cardiovascular effects lead to a novel locus mediating coronary risk

artículo científico publicado en 2017

How to include chromosome X in your genome-wide association study

artículo científico publicado en 2014

Human 5-HT5AReceptor Gene: Systematic Screening for DNA Sequence Variation and Linkage Mapping on Chromosome 7q34–q36 Using a Polymorphism in the 5′ Untranslated Region

article

Human metabolic individuality in biomedical and pharmaceutical research

artículo científico publicado en 2011

Hundreds of variants clustered in genomic loci and biological pathways affect human height

artículo científico publicado en 2010

Hypertrophe Kardiomyopathie

Identification of ADAMTS7 as a novel locus for coronary atherosclerosis and association of ABO with myocardial infarction in the presence of coronary atherosclerosis: two genome-wide association studies

artículo científico publicado en 2011

Identification of a novel ovine LH-beta promoter region, which dramatically enhances its promoter activity

artículo científico publicado en 2015

Identification of a single SNP that affects the promoter activity in the Moroccan prolific D'man breed

artículo científico publicado en 2015

Identification of genetic variation in the human serotonin 1D beta receptor gene.

artículo científico publicado en 1994

Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders

artículo científico publicado en 2013

Identification of risk genes for myocardial infarction by genome wide association studies

artículo científico publicado en 2010

Identification of seven loci affecting mean telomere length and their association with disease

artículo científico publicado en 2013

Identification of the BCAR1-CFDP1-TMEM170A locus as a determinant of carotid intima-media thickness and coronary artery disease risk

artículo científico publicado en 2012

Identifying multimodal signatures underlying the somatic comorbidity of psychosis: the COMMITMENT roadmap

artículo científico publicado en 2020

Impact of Diabetes on QT Dynamicity in Patients With and Without Myocardial Infarction: The KORA Family Heart Study

Inactivating mutations in NPC1L1 and protection from coronary heart disease

artículo científico publicado en 2014

Inheritance of coronary artery disease in men: an analysis of the role of the Y chromosome

artículo científico publicado en 2012

Integrating genome-wide genetic variations and monocyte expression data reveals trans-regulated gene modules in humans

artículo científico publicado en 2011

Integrative genomics reveals novel molecular pathways and gene networks for coronary artery disease.

artículo científico publicado en 2014

Interleukin-6 receptor pathways in coronary heart disease: a collaborative meta-analysis of 82 studies

artículo científico publicado en 2012

Introduction

Intronic ANG II type 2 receptor gene polymorphism 1675 G/A modulates receptor protein expression but not mRNA splicing.

artículo científico publicado en 2005

Investigation of the human serotonin 6 (5HT6) receptor gene in bipolar affective disorder and schizophrenia

article

KCNJ11 polymorphisms and sudden cardiac death in patients with acute myocardial infarction

artículo científico publicado en 2004

Knock-out of nexilin in mice leads to dilated cardiomyopathy and endomyocardial fibroelastosis

LDL triglycerides, hepatic lipase activity, and coronary artery disease: An epidemiologic and Mendelian randomization study

scholarly article by Günther Silbernagel et al published March 2019 in Atherosclerosis

Lack of Association Between the MEF2A Gene and Myocardial Infarction

article

Lack of association between a common polymorphism near the INSIG2 gene and BMI, myocardial infarction, and cardiovascular risk factors.

artículo científico publicado en 2009

Lack of association of a 9 bp insertion/deletion polymorphism within the bradykinin 2 receptor gene with myocardial infarction

article

Lack of association of genetic variants in the LRP8 gene with familial and sporadic myocardial infarction

article

Lack of genetically determined structural variants of the human serotonin-1E (5-HT1E) receptor protein points to its evolutionary conservation

artículo científico publicado en 1995

Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease

artículo científico publicado en 2011

Large-scale association analysis identifies new risk loci for coronary artery disease

artículo científico publicado en 2012

Lifelong reduction of LDL-cholesterol related to a common variant in the LDL-receptor gene decreases the risk of coronary artery disease--a Mendelian Randomisation study

artículo científico publicado en 2008

Long-range DNA looping and gene expression analyses identify DEXI as an autoimmune disease candidate gene

artículo científico publicado en 2011

Loss-of-function mutations in APOC3, triglycerides, and coronary disease

artículo científico publicado en 2014

Lp-PLA2, scavenger receptor class B type I gene (SCARB1) rs10846744 variant, and cardiovascular disease

artículo científico publicado en 2018

Lymphotoxin-α and galectin-2 SNPs are not associated with myocardial infarction in two different German populations

article

Macrophage cholesterol efflux correlates with lipoprotein subclass distribution and risk of obstructive coronary artery disease in patients undergoing coronary angiography

artículo científico publicado en 2009

Making Genomes Visible

Mendelian randomization analysis does not support causal associations of birth weight with hypertension risk and blood pressure in adulthood

artículo científico publicado en 2020

Mental Health and Psychosocial Functioning Over the Lifespan of German Patients Undergoing Cardiac Catheterization for Coronary Artery Disease

article

Meta-analysis of genome-wide association studies of aggressive and chronic periodontitis identifies two novel risk loci

artículo científico publicado en 2018

MicroRNAs and regulation of cardiometabolic phenotypes: novel insights into the complexity of genome-wide association studies loci

scientific article published on 01 September 2019

Molecular signatures of cardiovascular disease risk: potential for test development and clinical application

artículo científico publicado en 2008

Molecular variants of soluble guanylyl cyclase affecting cardiovascular risk

artículo científico publicado en 2015

Multiethnic meta-analysis of genome-wide association studies in >100 000 subjects identifies 23 fibrinogen-associated Loci but no strong evidence of a causal association between circulating fibrinogen and cardiovascular disease

artículo científico publicado en 2013

Mutation in the beta amyloid precursor protein gene and schizophrenia.

artículo científico publicado en 1993

Mutation spectrum in a large cohort of unrelated consecutive patients with hypertrophic cardiomyopathy

artículo científico publicado en 2003

Myeloid CD34+CD13+ precursor cells transdifferentiate into chondrocyte-like cells in atherosclerotic intimal calcification

artículo científico publicado en 2010

Network analysis of coronary artery disease risk genes elucidates disease mechanisms and druggable targets

artículo científico publicado en 2018

New gene functions in megakaryopoiesis and platelet formation

artículo científico publicado en 2011

New insights into the genetics of X-linked dystonia-parkinsonism (XDP, DYT3).

artículo científico publicado en 2015

New susceptibility locus for coronary artery disease on chromosome 3q22.3.

artículo científico publicado en 2009

Nexilin mutations destabilize cardiac Z-disks and lead to dilated cardiomyopathy

artículo científico publicado en 2009

No Association of Coronary Artery Disease with X-Chromosomal Variants in Comprehensive International Meta-Analysis ⬇️

scientific article published on 12 October 2016

No association of interleukin-6 gene polymorphism (-174 G/C) with myocardial infarction or traditional cardiovascular risk factors

artículo científico publicado en 2004

No association of theCYP3A5*1allele with blood pressure and left ventricular mass and geometry: the KORA/MONICA Augsburg echocardiographic substudy

Novel correlations between the genotype and the phenotype of hypertrophic and dilated cardiomyopathy: results from the German Competence Network Heart Failure

artículo científico publicado en 2011

Novel genetic approach to investigate the role of plasma secretory phospholipase A2 (sPLA2)-V isoenzyme in coronary heart disease: modified Mendelian randomization analysis using PLA2G5 expression levels

artículo científico publicado en 2014

Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals

artículo científico publicado en 2012

Novel missense mutations (p.T596M and p.P1797H) in NOTCH1 in patients with bicuspid aortic valve

scientific article published in 2006

Novel mutations in sarcomeric protein genes in dilated cardiomyopathy.

artículo científico publicado en 2002

Outcome of clinical versus genetic family screening in hypertrophic cardiomyopathy with focus on cardiac beta-myosin gene mutations Prediction of clinical status—is molecular genetics a new tool for the management of hypertrophic cardiomyopathy in

article

Peroxisome proliferator--activated receptor alpha gene regulates left ventricular growth in response to exercise and hypertension

artículo científico publicado en 2002

Phenotypic Consequences of a Genetic Predisposition to Enhanced Nitric Oxide Signaling

artículo científico publicado en 2017

Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study

artículo científico publicado en 2012

Polymorphisms in the promoter region of the dimethylarginine dimethylaminohydrolase 2 gene are associated with prevalence of hypertension

artículo científico publicado en 2009

Powerful identification of cis-regulatory SNPs in human primary monocytes using allele-specific gene expression

artículo científico publicado en 2012

Prediction of Causal Candidate Genes in Coronary Artery Disease Loci

artículo científico publicado en 2015

Proatherosclerotic Effect of the α1-Subunit of Soluble Guanylyl Cyclase by Promoting Smooth Muscle Phenotypic Switching

artículo científico publicado en 2016

Psoriasis and cardiometabolic traits: modest association but distinct genetic architectures

artículo científico publicado en 2015

Pyrophosphate Supplementation Prevents Chronic and Acute Calcification in ABCC6-Deficient Mice

artículo científico publicado en 2017

Quantitative analysis of cardiomyocyte dynamics with optical coherence phase microscopy

RANTES/CCL5 and risk for coronary events: results from the MONICA/KORA Augsburg case-cohort, Athero-Express and CARDIoGRAM studies

artículo científico publicado en 2011

Rare variant in scavenger receptor BI raises HDL cholesterol and increases risk of coronary heart disease

scientific journal article

Relation of the G Protein β 3 -Subunit Polymorphism With Left Ventricle Structure and Function

artículo científico publicado en 2002

Repeated replication and a prospective meta-analysis of the association between chromosome 9p21.3 and coronary artery disease

scientific article published on 24 March 2008

Retrospective study of the parental origin of the extra chromosome in trisomy 18 (Edwards syndrome)

artículo científico publicado en 1993

Rheumatoid Arthritis and Coronary Artery Disease: Genetic Analyses Do Not Support a Causal Relation

artículo científico publicado en 2016

Robust association of the APOE ?4 allele with premature myocardial infarction especially in patients without hypercholesterolaemia: the Aachen study

Role of sGC-dependent NO signalling and myocardial infarction risk

artículo científico publicado en 2015

Runs of Homozygosity: Association with Coronary Artery Disease and Gene Expression in Monocytes and Macrophages

artículo científico publicado en 2015

SNPboost: Interaction Analysis and Risk Prediction on GWA Data

SNPtoGO: characterizing SNPs by enriched GO terms

artículo científico publicado en 2007

SPG7 variant escapes phosphorylation-regulated processing by AFG3L2, elevates mitochondrial ROS, and is associated with multiple clinical phenotypes

artículo científico publicado en 2014

Sequenzen und Menschen : Zur Transparenz genetischer Information

article by Malte Dreyer et. al. published in Merkur (2014), issue 778, pp. 260-266.

Serum microRNA-1233 is a specific biomarker for diagnosing acute pulmonary embolism

artículo científico publicado en 2016

Sex in basic research: concepts in the cardiovascular field

artículo científico publicado en 2017

Sex-stratified genome-wide association studies including 270,000 individuals show sexual dimorphism in genetic loci for anthropometric traits

artículo científico publicado en 2013

Shared genetic aetiology of coronary artery disease and atherosclerotic stroke - 2015.

artículo científico publicado en 2015

Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants

artículo científico publicado en 2014

Spectrum of clinical phenotypes and gene variants in cardiac myosin-binding protein C mutation carriers with hypertrophic cardiomyopathy.

artículo científico publicado en 2001

Stimulators of the soluble guanylyl cyclase: promising functional insights from rare coding atherosclerosis-related GUCY1A3 variants

artículo científico publicado en 2016

Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease ⬇️

artículo científico publicado en 2017

Systematic analysis of variants related to familial hypercholesterolemia in families with premature myocardial infarction

artículo científico publicado en 2015

Systematic screening for mutations in the human serotonin 1F receptor gene in patients with bipolar affective disorder and schizophrenia

article

Systematic screening for mutations in the promoter and the coding region of the 5-HT1A gene

article

The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study

artículo científico publicado en 2015

The assertion that a G21V mutation in AGTR2 causes mental retardation is not supported by other studies.

artículo científico publicado en 2004

The common Y402H variant in complement factor H gene is not associated with susceptibility to myocardial infarction and its related risk factors

article

The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals

artículo científico publicado en 2016

The impact of low-frequency and rare variants on lipid levels

artículo científico publicado en 2015

The impact of newly identified loci on coronary heart disease, stroke and total mortality in the MORGAM prospective cohorts

artículo científico publicado en 2009

The metabochip, a custom genotyping array for genetic studies of metabolic, cardiovascular, and anthropometric traits

artículo científico publicado en 2012

The novel genetic variant predisposing to coronary artery disease in the region of the PSRC1 and CELSR2 genes on chromosome 1 associates with serum cholesterol

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