Lista de obras -

A Genome-Wide Association Study Suggests Novel Loci Associated with a Schizophrenia-Related Brain-Based Phenotype

artículo científico publicado en 2013

A biomathematical model of immune response and barrier function in mice with pneumococcal lung infection

artículo científico publicado en 2020

A catalog of genetic loci associated with kidney function from analyses of a million individuals

scientific article published on 31 May 2019

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

artículo científico publicado en 2015

Adipocytokines are not associated with gestational diabetes mellitus but with pregnancy status

scientific article published on 10 April 2020

Analysis of a rare functional truncating mutation rs61757459 in vaspin (SERPINA12) on circulating vaspin levels

artículo científico publicado en 2013

Association of Birth Weight With Type 2 Diabetes and Glycemic Traits: A Mendelian Randomization Study

scientific article published on 04 September 2019

Association of Chromosome 9p21 With Subsequent Coronary Heart Disease Events

artículo científico publicado en 2019

Association of Pro12Ala polymorphism in peroxisome proliferator-activated receptor gamma with Pre-diabetic phenotypes: meta-analysis of 57 studies on nondiabetic individuals

artículo científico publicado en 2006

Associations between DNA methylation and schizophrenia-related intermediate phenotypes - a gene set enrichment analysis

artículo científico publicado en 2015

Author Correction: Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function ⬇️

scientific article published on 01 May 2019

Beneficial effects of a 4-week exercise program on plasma concentrations of adhesion molecules

artículo científico publicado en 2007

Catalyzing Transcriptomics Research in Cardiovascular Disease: The CardioRNA COST Action CA17129

scientific article published on 29 March 2019

Cholesterol esterification in plasma as a biomarker for liver function and prediction of mortality

artículo científico publicado en 2017

Circulating Adipokine VASPIN Is Associated with Serum Lipid Profiles in Humans

artículo científico publicado en 2019

Common Genetic Variation Indicates Separate Causes for Periventricular and Deep White Matter Hyperintensities

artículo científico publicado en 2020

Common variants in glyoxalase I do not increase chronic pancreatitis risk

scientific article published on 29 October 2019

DNA methylation patterns reflect individual's lifestyle independent of obesity

artículo científico publicado en 2022

FTO Obesity Risk Variants Are Linked to Adipocyte IRX3 Expression and BMI of Children - Relevance of FTO Variants to Defend Body Weight in Lean Children?

artículo científico publicado en 2016

GWAS and colocalization analyses implicate carotid intima-media thickness and carotid plaque loci in cardiovascular outcomes

artículo científico publicado en 2018

Genetic Architecture of Subcortical Brain Structures in Over 40,000 Individuals Worldwide

scholarly article published 28 August 2017

Genetic Contribution of Variants near SORT1 and APOE on LDL Cholesterol Independent of Obesity in Children

artículo científico publicado en 2015

Genetic Determinants of Cortical Structure (Thickness, Surface Area and Volumes) among Disease Free Adults in the CHARGE Consortium

article published in 2018

Genetic architecture of subcortical brain structures in 38,851 individuals

scientific article published on 21 October 2019

Genetic correlations and genome-wide associations of cortical structure in general population samples of 22,824 adults

scientific article published on 22 September 2020

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

artículo científico publicado en 2010

Genetic variation in the Sorbs of eastern Germany in the context of broader European genetic diversity

artículo científico publicado en 2011

Genetically programmed changes in transcription of the novel progranulin regulator

artículo científico publicado en 2020

Genome wide meta-analysis highlights the role of genetic variation in RARRES2 in the regulation of circulating serum chemerin

artículo científico publicado en 2014

Genome wide meta-analysis identifies novel determinants of circulating serum progranulin

artículo científico publicado en 2017

Genome-wide analysis of carotid plaque burden suggests a role of IL5 in men

artículo científico publicado en 2020

Genome-wide association analysis of pulse wave velocity traits provide new insights into the causal relationship between arterial stiffness and blood pressure

artículo científico publicado en 2020

Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria

artículo científico publicado en 2019

Genome-wide association study identifies inversion in the CTRB1-CTRB2 locus to modify risk for alcoholic and non-alcoholic chronic pancreatitis

artículo científico publicado en 2017

Genome-wide association study of 23,500 individuals identifies 7 loci associated with brain ventricular volume

artículo científico publicado en 2018

HLA Class II Allele Analyses Implicate Common Genetic Components in Type 1 and Non-Insulin-Treated Type 2 Diabetes

scientific article published on 01 March 2020

Harmonization of growth hormone measurements with different immunoassays by data adjustment

artículo científico publicado en 2011

Identification of adipokine clusters related to parameters of fat mass, insulin sensitivity and inflammation

artículo científico publicado en 2014

Indications for potential parent-of-origin effects within the FTO gene

artículo científico publicado en 2015

Integration of Genome-Wide SNP Data and Gene-Expression Profiles Reveals Six Novel Loci and Regulatory Mechanisms for Amino Acids and Acylcarnitines in Whole Blood

artículo científico publicado en 2015

Lineage-Specific Changes in Biomarkers in Great Apes and Humans

artículo científico publicado en 2015

Low sphingosine-1-phosphate plasma levels are predictive for increased mortality in patients with liver cirrhosis

artículo científico publicado en 2017

MB-COMT promoter DNA methylation is associated with working-memory processing in schizophrenia patients and healthy controls

artículo científico publicado en 2014

Markov State Modelling of Disease Courses and Mortality Risks of Patients with Community-Acquired Pneumonia

artículo científico publicado en 2020

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

artículo científico publicado en 2020

Model-based optimization of G-CSF treatment during cytotoxic chemotherapy

artículo científico publicado en 2017

Ninety-nine independent genetic loci influencing general cognitive function include genes associated with brain health and structure (N = 280,360)

Novel loci for childhood body mass index and shared heritability with adult cardiometabolic traits

artículo científico publicado en 2020

On the Parametrization of Epidemiologic Models—Lessons from Modelling COVID-19 Epidemic

artículo científico publicado en 2022

Parameters of pulse wave velocity: determinants and reference values assessed in the population-based study LIFE-Adult

scientific article published on 15 May 2018

Plasma Amino Acid Concentrations Predict Mortality in Patients with End-Stage Liver Disease

artículo científico publicado en 2016

Population-genetic comparison of the Sorbian isolate population in Germany with the German KORA population using genome-wide SNP arrays

artículo científico publicado en 2011

Pro-Neurotensin depends on renal function and is related to all-cause mortality in chronic kidney disease

artículo científico publicado en 2020

Relations between lipoprotein(a) concentrations, LPA genetic variants, and the risk of mortality in patients with established coronary heart disease: a molecular and genetic association study

artículo científico publicado en 2017

Relationship between twelve adipocytokines and distinct components of the metabolic syndrome

artículo científico publicado en 2018

Secretory phospholipase A(2)-IIA and cardiovascular disease: a mendelian randomization study

scientific article published on 31 July 2013

Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function ⬇️

artículo científico publicado en 2018

Subsequent Event Risk in Individuals With Established Coronary Heart Disease

artículo científico publicado en 2019

Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels

artículo científico publicado en 2019

The Effect of FGF21 and Its Genetic Variants on Food and Drug Cravings, Adipokines and Metabolic Traits

artículo científico publicado en 2021

The LIFE-Adult-Study: objectives and design of a population-based cohort study with 10,000 deeply phenotyped adults in Germany

artículo científico publicado en 2015

The Obesity-Susceptibility Gene TMEM18 Promotes Adipogenesis through Activation of PPARG

artículo científico publicado en 2020

The role of rs2237781 within GRM8 in eating behavior

scientific article published on 23 June 2013

Transcriptome Analyses of Adipose Tissue Samples Identify <i>EGFL6</i> as a Candidate Gene Involved in Obesity-Related Adipose Tissue Dysfunction in Children

scientific article published on 14 April 2022

Unraveling the polygenic architecture of complex traits using blood eQTL meta-analysis

scholarly article published 19 October 2018

Lista de obras de

A Genome-Wide Association Study Suggests Novel Loci Associated with a Schizophrenia-Related Brain-Based Phenotype

A biomathematical model of immune response and barrier function in mice with pneumococcal lung infection

A catalog of genetic loci associated with kidney function from analyses of a million individuals

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

Adipocytokines are not associated with gestational diabetes mellitus but with pregnancy status

Analysis of a rare functional truncating mutation rs61757459 in vaspin (SERPINA12) on circulating vaspin levels

Association of Birth Weight With Type 2 Diabetes and Glycemic Traits: A Mendelian Randomization Study

Association of Chromosome 9p21 With Subsequent Coronary Heart Disease Events

Association of Pro12Ala polymorphism in peroxisome proliferator-activated receptor gamma with Pre-diabetic phenotypes: meta-analysis of 57 studies on nondiabetic individuals

Associations between DNA methylation and schizophrenia-related intermediate phenotypes - a gene set enrichment analysis

Author Correction: Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function ⬇️

Beneficial effects of a 4-week exercise program on plasma concentrations of adhesion molecules

Catalyzing Transcriptomics Research in Cardiovascular Disease: The CardioRNA COST Action CA17129

Cholesterol esterification in plasma as a biomarker for liver function and prediction of mortality

Circulating Adipokine VASPIN Is Associated with Serum Lipid Profiles in Humans

Common Genetic Variation Indicates Separate Causes for Periventricular and Deep White Matter Hyperintensities

Common variants in glyoxalase I do not increase chronic pancreatitis risk

DNA methylation patterns reflect individual's lifestyle independent of obesity

FTO Obesity Risk Variants Are Linked to Adipocyte IRX3 Expression and BMI of Children - Relevance of FTO Variants to Defend Body Weight in Lean Children?

GWAS and colocalization analyses implicate carotid intima-media thickness and carotid plaque loci in cardiovascular outcomes

Genetic Architecture of Subcortical Brain Structures in Over 40,000 Individuals Worldwide

Genetic Contribution of Variants near SORT1 and APOE on LDL Cholesterol Independent of Obesity in Children

Genetic Determinants of Cortical Structure (Thickness, Surface Area and Volumes) among Disease Free Adults in the CHARGE Consortium

Genetic architecture of subcortical brain structures in 38,851 individuals

Genetic correlations and genome-wide associations of cortical structure in general population samples of 22,824 adults

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

Genetic variation in the Sorbs of eastern Germany in the context of broader European genetic diversity

Genetically programmed changes in transcription of the novel progranulin regulator

Genome wide meta-analysis highlights the role of genetic variation in RARRES2 in the regulation of circulating serum chemerin

Genome wide meta-analysis identifies novel determinants of circulating serum progranulin

Genome-wide analysis of carotid plaque burden suggests a role of IL5 in men

Genome-wide association analysis of pulse wave velocity traits provide new insights into the causal relationship between arterial stiffness and blood pressure

Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria

Genome-wide association study identifies inversion in the CTRB1-CTRB2 locus to modify risk for alcoholic and non-alcoholic chronic pancreatitis

Genome-wide association study of 23,500 individuals identifies 7 loci associated with brain ventricular volume

HLA Class II Allele Analyses Implicate Common Genetic Components in Type 1 and Non-Insulin-Treated Type 2 Diabetes

Harmonization of growth hormone measurements with different immunoassays by data adjustment

Identification of adipokine clusters related to parameters of fat mass, insulin sensitivity and inflammation

Indications for potential parent-of-origin effects within the FTO gene

Integration of Genome-Wide SNP Data and Gene-Expression Profiles Reveals Six Novel Loci and Regulatory Mechanisms for Amino Acids and Acylcarnitines in Whole Blood

Lineage-Specific Changes in Biomarkers in Great Apes and Humans

Low sphingosine-1-phosphate plasma levels are predictive for increased mortality in patients with liver cirrhosis

MB-COMT promoter DNA methylation is associated with working-memory processing in schizophrenia patients and healthy controls

Markov State Modelling of Disease Courses and Mortality Risks of Patients with Community-Acquired Pneumonia

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

Model-based optimization of G-CSF treatment during cytotoxic chemotherapy

Ninety-nine independent genetic loci influencing general cognitive function include genes associated with brain health and structure (N = 280,360)

Novel loci for childhood body mass index and shared heritability with adult cardiometabolic traits

On the Parametrization of Epidemiologic Models—Lessons from Modelling COVID-19 Epidemic

Parameters of pulse wave velocity: determinants and reference values assessed in the population-based study LIFE-Adult

Plasma Amino Acid Concentrations Predict Mortality in Patients with End-Stage Liver Disease

Population-genetic comparison of the Sorbian isolate population in Germany with the German KORA population using genome-wide SNP arrays

Pro-Neurotensin depends on renal function and is related to all-cause mortality in chronic kidney disease

Relations between lipoprotein(a) concentrations, LPA genetic variants, and the risk of mortality in patients with established coronary heart disease: a molecular and genetic association study

Relationship between twelve adipocytokines and distinct components of the metabolic syndrome

Secretory phospholipase A(2)-IIA and cardiovascular disease: a mendelian randomization study

Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function ⬇️

Subsequent Event Risk in Individuals With Established Coronary Heart Disease

Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels

The Effect of FGF21 and Its Genetic Variants on Food and Drug Cravings, Adipokines and Metabolic Traits

The LIFE-Adult-Study: objectives and design of a population-based cohort study with 10,000 deeply phenotyped adults in Germany

The Obesity-Susceptibility Gene TMEM18 Promotes Adipogenesis through Activation of PPARG

The role of rs2237781 within GRM8 in eating behavior

Transcriptome Analyses of Adipose Tissue Samples Identify <i>EGFL6</i> as a Candidate Gene Involved in Obesity-Related Adipose Tissue Dysfunction in Children

Unraveling the polygenic architecture of complex traits using blood eQTL meta-analysis