Lista de obras -

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 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

Association of early repolarization pattern on ECG with risk of cardiac and all-cause mortality: a population-based prospective cohort study (MONICA/KORA).

artículo científico publicado en 2010

Chances and challenges of machine learning-based disease classification in genetic association studies illustrated on age-related macular degeneration

artículo científico publicado en 2020

Erratum: Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution

artículo científico publicado en 2011

Exome-wide association study reveals novel susceptibility genes to sporadic dilated cardiomyopathy

artículo científico publicado en 2017

FGF21 signalling pathway and metabolic traits - genetic association analysis

artículo científico publicado en 2010

FTO genotype is associated with phenotypic variability of body mass index

artículo científico publicado en 2012

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

artículo científico publicado en 2010

Genetic associations with lipoprotein subfractions provide information on their biological nature

artículo científico publicado en 2011

Genetic evidence of assortative mating in humans

article

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

artículo científico publicado en 2010

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

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 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

IDGenerator: unique identifier generator for epidemiologic or clinical studies

artículo científico publicado en 2016

Identification and MS-assisted interpretation of genetically influenced NMR signals in human plasma

artículo científico publicado en 2013

Investigating the modulation of genetic effects on late AMD by age and sex: Lessons learned and two additional loci.

artículo científico publicado en 2018

Lack of association between the Trp719Arg polymorphism in kinesin-like protein-6 and coronary artery disease in 19 case-control studies

artículo científico publicado en 2010

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

Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution

artículo científico publicado en 2010

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

artículo científico publicado en 2009

On the impact of different approaches to classify age-related macular degeneration: Results from the German AugUR study.

artículo científico publicado en 2018

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

Lista de obras de

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

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

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

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

Association of early repolarization pattern on ECG with risk of cardiac and all-cause mortality: a population-based prospective cohort study (MONICA/KORA).

Chances and challenges of machine learning-based disease classification in genetic association studies illustrated on age-related macular degeneration

Erratum: Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution

Exome-wide association study reveals novel susceptibility genes to sporadic dilated cardiomyopathy

FGF21 signalling pathway and metabolic traits - genetic association analysis

FTO genotype is associated with phenotypic variability of body mass index

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

Genetic associations with lipoprotein subfractions provide information on their biological nature

Genetic evidence of assortative mating in humans

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

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

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

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

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

IDGenerator: unique identifier generator for epidemiologic or clinical studies

Identification and MS-assisted interpretation of genetically influenced NMR signals in human plasma

Investigating the modulation of genetic effects on late AMD by age and sex: Lessons learned and two additional loci.

Lack of association between the Trp719Arg polymorphism in kinesin-like protein-6 and coronary artery disease in 19 case-control studies

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

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

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

Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution

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

On the impact of different approaches to classify age-related macular degeneration: Results from the German AugUR study.

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