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Lista de obras de Thomas Illig

12q14 microdeletion syndrome: A family with short stature and Silver-Russell syndrome (SRS)-like phenotype and review of the literature

artículo científico publicado en 2018

A Low-Frequency Inactivating AKT2 Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk

artículo científico publicado en 2017

A Metabolome-Wide Association Study of Kidney Function and Disease in the General Population ⬇️

artículo científico publicado en 2015

A common FADS2 promoter polymorphism increases promoter activity and facilitates binding of transcription factor ELK1.

artículo científico publicado en 2010

A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization

artículo científico publicado en 2006

A common genetic variant is associated with adult and childhood obesity

artículo científico publicado en 2006

A common variant on chromosome 11q13 is associated with atopic dermatitis.

artículo científico publicado en 2009

A comparison of the accuracy of Illumina HumanHT-12 v3 Expression BeadChip and TaqMan qRT-PCR gene expression results in patient samples from the Tampere Vascular Study.

artículo científico publicado en 2012

A comprehensive analysis of the COL29A1 gene does not support a role in eczema

artículo científico publicado en 2011

A genome-wide association meta-analysis of circulating sex hormone-binding globulin reveals multiple Loci implicated in sex steroid hormone regulation

artículo científico publicado en 2012

A genome-wide association search for type 2 diabetes genes in African Americans

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 three loci associated with mean platelet volume

artículo científico publicado en 2008

A genome-wide association study of atopic dermatitis identifies loci with overlapping effects on asthma and psoriasis

artículo científico publicado en 2013

A genome-wide association study of depressive symptoms

scientific journal article

A genome-wide association study of metabolic traits in human urine

artículo científico publicado en 2011

A genome-wide association study reveals 2 new susceptibility loci for atopic dermatitis.

artículo científico publicado en 2015

A genome-wide association study to identify genetic susceptibility loci that modify ductal and lobular postmenopausal breast cancer risk associated with menopausal hormone therapy use: a two-stage design with replication

scientific article published on 20 February 2013

A genome-wide expression quantitative trait loci analysis of proprotein convertase subtilisin/kexin enzymes identifies a novel regulatory gene variant for FURIN expression and blood pressure

artículo científico publicado en 2015

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

artículo científico publicado en 2009

A genome-wide metabolic QTL analysis in Europeans implicates two loci shaped by recent positive selection

artículo científico publicado en 2011

A genome-wide perspective of genetic variation in human metabolism

artículo científico publicado en 2009

A novel GJA8 mutation causing a recessive triangular cataract.

artículo científico publicado en 2008

A novel polymorphism in the promoter region of ERBB4 is associated with breast and colorectal cancer risk

artículo científico publicado en 2007

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

artículo científico publicado en 2009

A radiation-induced gene expression signature as a tool to predict acute radiotherapy-induced adverse side effects

artículo científico publicado en 2011

A signal transducer and activator of transcription 6 haplotype influences the regulation of serum IgE levels

artículo científico publicado en 2004

A splice site variant in the sodium channel gene SCN1A confers risk of febrile seizures

artículo científico publicado en 2009

A variant in the ABO gene explains the variation in soluble E-selectin levels-results from dense genotyping in two independent populations

artículo científico publicado en 2012

APOA5 variants and metabolic syndrome in Caucasians

artículo científico publicado en 2007

ASXL1 exon 12 mutations are frequent in AML with intermediate risk karyotype and are independently associated with an adverse outcome

artículo científico publicado en 2013

Activated immune-inflammatory pathways are associated with long-standing depressive symptoms: Evidence from gene-set enrichment analyses in the Young Finns Study

artículo científico publicado en 2015

Acute-phase serum amyloid A protein and its implication in the development of type 2 diabetes in the KORA S4/F4 study

artículo científico publicado en 2012

Air Pollution and Inflammatory Response in Myocardial Infarction Survivors: Gene–Environment Interactions in a High-Risk Group

article

Alcohol consumption, alcohol dehydrogenase and risk of coronary heart disease in the MONICA/KORA-Augsburg cohort 1994/1995-2002.

artículo científico publicado en 2007

Alcohol-induced metabolomic differences in humans

artículo científico publicado en 2013

An integrated epigenetic and transcriptomic analysis reveals distinct tissue-specific patterns of DNA methylation associated with atopic dermatitis

artículo científico publicado en 2014

An interferon-induced helicase (IFIH1) gene polymorphism associates with different rates of progression from autoimmunity to type 1 diabetes ⬇️

artículo científico publicado en 2011

Analysis of the high affinity IgE receptor genes reveals epistatic effects of FCER1A variants on eczema risk

artículo científico publicado en 2009

Analysis of the individual and aggregate genetic contributions of previously identified serine peptidase inhibitor Kazal type 5 (SPINK5), kallikrein-related peptidase 7 (KLK7), and filaggrin (FLG) polymorphisms to eczema risk

artículo científico publicado en 2008

Analyzing illumina gene expression microarray data from different tissues: methodological aspects of data analysis in the metaxpress consortium

artículo científico publicado en 2012

Antioxidant defense enzyme genes and asthma susceptibility: gender-specific effects and heterogeneity in gene-gene interactions between pathogenetic variants of the disease

artículo científico publicado en 2014

Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index

artículo científico publicado en 2010

Association analysis between the prostaglandin E synthase 2 R298H polymorphism and body mass index in 8079 participants of the KORA study cohort

artículo científico publicado en 2009

Association analysis of genes involved in cholesterol metabolism located within the linkage region on chromosome 10 and Alzheimer's disease

artículo científico publicado en 2004

Association between DNA Methylation in Whole Blood and Measures of Glucose Metabolism: KORA F4 Study

artículo científico publicado en 2016

Association between functional FABP2 promoter haplotypes and body mass index: analyses of 8072 participants of the KORA cohort study

artículo científico publicado en 2009

Association between variants of PRDM1 and NDP52 and Crohn's disease, based on exome sequencing and functional studies

scientific article published on 25 April 2013

Association between variations in the TLR4 gene and incident type 2 diabetes is modified by the ratio of total cholesterol to HDL-cholesterol

artículos científicos

Association of CARD15 polymorphisms with atopy-related traits in a population-based cohort of Caucasian adults

artículo científico publicado en 2005

Association of NOD1 polymorphisms with atopic eczema and related phenotypes

artículo científico publicado en 2005

Association of a MTNR1B gene variant with fasting glucose and HOMA-B in children and adolescents with high BMI-SDS ⬇️

artículo científico publicado el 8 de noviembre de 2010

Association of a STAT 6 haplotype with elevated serum IgE levels in a population based cohort of white adults

artículo científico publicado en 2004

Association of a variant in the muscarinic acetylcholine receptor 2 gene (CHRM2) with nicotine addiction

artículo científico publicado en 2010

Association of acyl-CoA-binding protein (ACBP) single nucleotide polymorphisms and type 2 diabetes in two German study populations

artículo científico publicado en 2007

Association of common variants identified by recent genome-wide association studies with obesity in Chinese children: a case-control study

artículo científico publicado en 2016

Association of genetic variation in KCNQ1 with type 2 diabetes in the KORA surveys

artículo científico publicado en 2009

Association of humoral immunity to human Hsp60 with the IL-6 gene polymorphism C-174G in patients with type 2 diabetes and controls

artículo científico publicado en 2005

Association of nicotinic acetylcholine receptor subunit alpha 4 polymorphisms with nicotine dependence in 5500 Germans

artículo científico publicado en 2009

Association of novel genetic Loci with circulating fibrinogen levels: a genome-wide association study in 6 population-based cohorts

scientific article published on April 2009

Association of prostaglandin E synthase 2 (PTGES2) Arg298His polymorphism with type 2 diabetes in two German study populations

artículo científico publicado en 2007

Association of the 103I MC4R allele with decreased body mass in 7937 participants of two population based surveys

artículo científico publicado en 2005

Association of the MC4R V103I polymorphism with the metabolic syndrome: the KORA Study

artículo científico publicado en 2008

Association of the interleukin-1 receptor antagonist gene with asthma

artículo científico publicado en 2004

Association of variants in gastric inhibitory polypeptide receptor gene with impaired glucose homeostasis in obese children and adolescents from Berlin

artículo científico publicado en 2010

Association study between genetic variants at the PIP5K2A gene locus and schizophrenia and bipolar affective disorder

article

Association study between the D10S1423 microsatellite marker and Alzheimer's disease.

artículo científico publicado en 2005

Association study between variants in the fibrinogen gene cluster, fibrinogen levels and hypertension: results from the MONICA/KORA study.

artículo científico publicado en 2009

Association study of mast cell chymase polymorphisms with atopy

artículo científico publicado en 2005

Associations between thyroid hormones and serum metabolite profiles in an euthyroid population

artículo científico publicado en 2013

Associations of IGF-1 gene variants and milk protein intake with IGF-I concentrations in infants at age 6 months - results from a randomized clinical trial

artículo científico publicado en 2013

BMI at age 8 years is influenced by the type 2 diabetes susceptibility genes HHEX-IDE and CDKAL1

artículo científico publicado en 2010

Bayesian independent component analysis recovers pathway signatures from blood metabolomics data

artículo científico publicado en 2012

Blood cis-eQTL analysis fails to identify novel association signals among sub-threshold candidates from genome-wide association studies in restless legs syndrome

artículo científico publicado en 2014

Blood hsa-miR-122-5p and hsa-miR-885-5p levels associate with fatty liver and related lipoprotein metabolism-The Young Finns Study

artículo científico publicado en 2016

Blood microRNA profile associates with the levels of serum lipids and metabolites associated with glucose metabolism and insulin resistance and pinpoints pathways underlying metabolic syndrome: the cardiovascular risk in Young Finns Study.

artículo científico publicado en 2014

Blood pathway analyses reveal differences between prediabetic subjects with or without dyslipidaemia. The Cardiovascular Risk in Young Finns Study

artículo científico publicado en 2017

Body fat free mass is associated with the serum metabolite profile in a population-based study

artículo científico publicado en 2012

Breast cancer: a candidate gene approach across the estrogen metabolic pathway

artículo científico publicado en 2007

CX3CR1 polymorphisms are associated with atopy but not asthma in German children

artículo científico publicado en 2007

CXCR1andCXCR2haplotypes synergistically modulate cystic fibrosis lung disease

scientific article published on 16 November 2011

CYP450 polymorphisms as risk factors for early-onset lung cancer: gender-specific differences

artículo científico publicado en 2009

Calpain-10 variants and haplotypes are associated with polycystic ovary syndrome in Caucasians

Changes in metabolite profiles caused by genetically determined obesity in mice

artículo científico publicado en 2013

Changes in the serum metabolite profile in obese children with weight loss

artículo científico publicado en 2014

Characterization of whole-genome autosomal differences of DNA methylation between men and women

artículo científico publicado en 2015

Chemokines as risk factors for type 2 diabetes: results from the MONICA/KORA Augsburg study, 1984-2002.

artículo científico publicado en 2006

Childhood cancer predisposition syndromes-A concise review and recommendations by the Cancer Predisposition Working Group of the Society for Pediatric Oncology and Hematology.

artículo científico publicado en 2017

Childhood obesity is associated with changes in the serum metabolite profile

artículo científico publicado en 2012

Clear detection of ADIPOQ locus as the major gene for plasma adiponectin: results of genome-wide association analyses including 4659 European individuals

artículo científico publicado en 2009

Colorectal cancer and polymorphisms in DNA repair genes WRN , RMI1 and BLM

article

Common Variants in Myocardial Ion Channel Genes Modify the QT Interval in the General Population

article

Common genetic variants of the FADS1 FADS2 gene cluster and their reconstructed haplotypes are associated with the fatty acid composition in phospholipids

artículo científico publicado en 2006

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 associated with plasma triglycerides and risk for coronary artery disease

artículo científico publicado en 2013

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

artículo científico publicado en 2010

Common variants in FCER1A influence total serum IgE levels from cord blood up to six years of life

artículo científico publicado en 2009

Common variants in Mendelian kidney disease genes and their association with renal function

artículo científico publicado en 2013

Common variants near MC4R are associated with fat mass, weight and risk of obesity

artículo científico publicado en 2008

Common variants of LRRK2 are not associated with sporadic Parkinson's disease

scholarly article by Saskia Biskup et al published December 2005 in Annals of Neurology

Common variation in the ADAM8 gene affects serum sADAM8 concentrations and the risk of myocardial infarction in two independent cohorts

artículo científico publicado en 2011

Comparative analysis of plasma metabolomics response to metabolic challenge tests in healthy subjects and influence of the FTO obesity risk allele

article

Comparison of metabolic profiles of acutely ill and short-term weight recovered patients with anorexia nervosa reveals alterations of 33 out of 163 metabolites

artículo científico publicado en 2012

Congenital cataract and macular hypoplasia in humans associated with a de novo mutation in CRYAA and compound heterozygous mutations in P.

artículo científico publicado en 2006

Correction: Evidence for a Pathogenic Role of Different Mutations at Codon 188 of PRNP.

artículo científico publicado en 2008

Correction: Genome-Wide Association Study Identifies Novel Restless Legs Syndrome Susceptibility Loci on 2p14 and 16q12.1

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

Corrigendum: Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis

scholarly article published in Nature Genetics

DNA methylation of lipid-related genes affects blood lipid levels

scientific article published on 12 January 2015

DNA repair gene polymorphisms and risk of chronic atrophic gastritis: a case-control study

artículo científico publicado en 2011

DNA variants, plasma levels and variability of C-reactive protein in myocardial infarction survivors: results from the AIRGENE study

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

artículo científico publicado en 2014

Detection of ATM gene mutations in young lung cancer patients: a population-based control study.

artículo científico publicado en 2007

Determination of nasal and oropharyngeal microbiomes in a multicenter population-based study - findings from Pretest 1 of the German National Cohort

artículo científico publicado en 2017

Diagnosing fatty liver disease: a comparative evaluation of metabolic markers, phenotypes, genotypes and established biomarkers

artículo científico publicado en 2013

Die BSD Gesundheitsstudie: eine Pilotstudie zur Untersuchung der Vergleichbarkeit bayerischer Blutspender mit der Allgemein-bevölkerung Bayerns durch einen Vergleich mit KORA S4

Differences between human plasma and serum metabolite profiles

artículo científico publicado en 2011

Different FCER1A polymorphisms influence IgE levels in asthmatics and non-asthmatics

artículo científico publicado en 2013

Differentially expressed genes and canonical pathway expression in human atherosclerotic plaques - Tampere Vascular Study

artículo científico publicado en 2017

Differentially expressed genes and canonical pathways in the ascending thoracic aortic aneurysm - The Tampere Vascular Study

artículo científico publicado en 2017

Discovery and refinement of loci associated with lipid levels

artículo científico publicado en 2013

Discovery of sexual dimorphisms in metabolic and genetic biomarkers

artículo científico publicado en 2011

Dissecting the role of the mitochondrial chaperone mortalin in Parkinson's disease: functional impact of disease-related variants on mitochondrial homeostasis

artículo científico publicado en 2010

Do FADS genotypes enhance our knowledge about fatty acid related phenotypes?

artículo científico publicado en 2009

Do common variants separate between obese melanocortin-4 receptor gene mutation carriers and non-carriers? The impact of cryptic relatedness.

artículo científico publicado en 2012

Do genetic factors protect for early onset lung cancer? A case control study before the age of 50 years

artículos científicos

Dopamine-related genes and spontaneous smoking cessation in ever-heavy smokers

article

Doublesex and mab-3 related transcription factor 1 (DMRT1) is a sex-specific genetic determinant of childhood-onset asthma and is expressed in testis and macrophages

artículo científico publicado en 2016

ERCC2 genotypes and a corresponding haplotype are linked with breast cancer risk in a German population.

artículo científico publicado en 2004

ERRATUM: Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height

article by Matthew B. Lanktree et al published June 2012 in American Journal of Human Genetics

Early onset lung cancer, cigarette smoking and the SNP309 of the murine double minute-2 (MDM2) gene

artículo científico publicado en 2008

Effect of macrophage migration inhibitory factor (MIF) gene variants and MIF serum concentrations on the risk of type 2 diabetes: results from the MONICA/KORA Augsburg Case–Cohort Study, 1984–2002

article

Effects of metformin on metabolite profiles and LDL cholesterol in patients with type 2 diabetes

artículo científico publicado en 2015

Effects of smoking and smoking cessation on human serum metabolite profile: results from the KORA cohort study

artículo científico publicado en 2013

Eight genetic loci associated with variation in lipoprotein-associated phospholipase A2 mass and activity and coronary heart disease: meta-analysis of genome-wide association studies from five community-based studies

artículo científico publicado en 2011

Elder siblings enhance the effect of filaggrin mutations on childhood eczema: results from the 2 birth cohort studies LISAplus and GINIplus

artículo científico publicado en 2010

Elevated levels of interleukin-18 predict the development of type 2 diabetes: results from the MONICA/KORA Augsburg Study, 1984-2002.

artículo científico publicado en 2005

Epigenetics meets metabolomics: an epigenome-wide association study with blood serum metabolic traits

artículo científico publicado en 2013

Epigenome-wide association of DNA methylation markers in peripheral blood from Indian Asians and Europeans with incident type 2 diabetes: a nested case-control study

artículo científico publicado en 2015

Epigenome-wide association study of body mass index, and the adverse outcomes of adiposity

artículo científico publicado en 2016

Erratum: Large meta-analysis of genome-wide association studies identifies five loci for lean body mass

artículo científico publicado en 2017

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

Erratum: New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk

artículo científico publicado en 2010

Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls

artículo científico publicado en 2018

Estimating the single nucleotide polymorphism genotype misclassification from routine double measurements in a large epidemiologic sample

artículo científico publicado en 2008

Ethics Reporting in Biospecimen and Genetic Research: Current Practice and Suggestions for Changes

artículo científico publicado en 2016

Evaluation of different biomarkers to predict individual radiosensitivity in an inter-laboratory comparison--lessons for future studies

artículo científico publicado en 2012

Evidence for a pathogenic role of different mutations at codon 188 of PRNP

artículo científico publicado en 2008

Evidence for a relationship between genetic variants at the brain-derived neurotrophic factor (BDNF) locus and major depression

artículo científico publicado en 2005

Evidence for an association between genetic variants of the fatty acid desaturase 1 fatty acid desaturase 2 ( FADS1 FADS2) gene cluster and the fatty acid composition of erythrocyte membranes.

artículo científico publicado en 2008

Evidence for the Thr79Met polymorphism of the ileal fatty acid binding protein (FABP6) to be associated with type 2 diabetes in obese individuals

artículo científico publicado en 2009

Extensive alterations of the whole-blood transcriptome are associated with body mass index: results of an mRNA profiling study involving two large population-based cohorts

artículo científico publicado en 2015

FADS gene cluster polymorphisms: important modulators of fatty acid levels and their impact on atopic diseases

artículo científico publicado en 2009

FADS genotypes and desaturase activity estimated by the ratio of arachidonic acid to linoleic acid are associated with inflammation and coronary artery disease

artículo científico publicado en 2008

Fat mass and obesity-associated gene (FTO) in eating disorders: evidence for association of the rs9939609 obesity risk allele with bulimia nervosa and anorexia nervosa

artículo científico publicado en 2012

Fatty liver is associated with blood pathways of inflammatory response, immune system activation and prothrombotic state in Young Finns Study.

artículo científico publicado en 2018

Feasibility and quality development of biomaterials in the pretest studies of the German National Cohort

artículo científico publicado en 2014

Fibrinogen genes modify the fibrinogen response to ambient particulate matter

artículo científico publicado en 2009

Filaggrin loss-of-function mutations and association with allergic diseases

artículo científico publicado en 2008

Filaggrin mutations, atopic eczema, hay fever, and asthma in children

artículo científico publicado en 2008

Fine Mapping of a GWAS-Derived Obesity Candidate Region on Chromosome 16p11.2.

artículo científico publicado en 2015

First investigation of two obesity-related loci (TMEM18, FTO) concerning their association with educational level as well as income: the MONICA/KORA study

artículo científico publicado en 2010

Functional characterization of promoter variants of the adiponectin gene complemented by epidemiological data

artículo científico publicado en 2008

Further genetic heterogeneity for autosomal dominant human sutural cataracts.

artículo científico publicado en 2003

G-Protein-coupled receptor polymorphisms are associated with asthma in a large German population

artículo científico publicado en 2005

GT198 (PSMC3IP) germline variants in early-onset breast cancer patients from hereditary breast and ovarian cancer families

artículo científico publicado en 2017

GWAS of 126,559 individuals identifies genetic variants associated with educational attainment

artículo científico publicado en 2013

Gender-specific pathway differences in the human serum metabolome

artículo científico publicado en 2015

Gene set of nuclear-encoded mitochondrial regulators is enriched for common inherited variation in obesity

artículo científico publicado en 2013

Gene variants of monocyte chemoattractant protein 1 and components of metabolic syndrome in KORA S4, Augsburg

artículo científico publicado en 2007

Gene-centric meta-analyses for central adiposity traits in up to 57 412 individuals of European descent confirm known loci and reveal several novel associations

artículo científico publicado en 2013

Gene-centric meta-analysis in 87,736 individuals of European ancestry identifies multiple blood-pressure-related loci

artículo científico publicado en 2014

Gene-gene interaction between APOA5 and USF1: two candidate genes for the metabolic syndrome

artículo científico publicado en 2009

Genes and lifestyle factors in obesity: results from 12,462 subjects from MONICA/KORA.

artículo científico publicado en 2010

Genetic architecture of the APM1 gene and its influence on adiponectin plasma levels and parameters of the metabolic syndrome in 1,727 healthy Caucasians

artículo científico publicado en 2006

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

artículo científico publicado en 2010

Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function

artículo científico publicado en 2016

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 evidence that raised sex hormone binding globulin (SHBG) levels reduce the risk of type 2 diabetes

artículo científico publicado en 2009

Genetic factors in individual radiation sensitivity

artículo científico publicado en 2014

Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci

artículo científico publicado en 2015

Genetic polymorphisms of MPO, GSTT1, GSTM1, GSTP1, EPHX1 and NQO1 as risk factors of early-onset lung cancer

artículo científico publicado en 2010

Genetic predictors of fibrin D-dimer levels in healthy adults

artículo científico publicado en 2011

Genetic predisposition to an adverse lipid profile limits the improvement in total cholesterol in response to weight loss

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 harbored in the forkhead box protein 3 locus increase hay fever risk.

artículo científico publicado en 2010

Genetic variants in Protocadherin-1, bronchial hyper-responsiveness, and asthma subphenotypes in German children.

artículo científico publicado en 2012

Genetic variants in the FADS gene cluster are associated with arachidonic acid concentrations of human breast milk at 1.5 and 6 mo postpartum and influence the course of milk dodecanoic, tetracosenoic, and trans-9-octadecenoic acid concentrations ov

artículo científico publicado en 2010

Genetic variants in the GATA3 gene are not associated with asthma and atopic diseases in German children.

artículo científico publicado en 2009

Genetic variants in the USF1 gene are associated with low-density lipoprotein cholesterol levels and incident type 2 diabetes mellitus in women: results from the MONICA/KORA Augsburg case-cohort study, 1984-2002.

artículo científico publicado en 2008

Genetic variants in the leukemia-associated Rho guanine nucleotide exchange factor (ARHGEF12) gene are not associated with T2DM and related parameters in Caucasians (KORA study).

artículo científico publicado en 2007

Genetic variants of the FADS1 FADS2 gene cluster as related to essential fatty acid metabolism

artículo científico publicado en 2010

Genetic variants of the fatty acid desaturase gene cluster predict amounts of red blood cell docosahexaenoic and other polyunsaturated fatty acids in pregnant women: findings from the Avon Longitudinal Study of Parents and Children ⬇️

artículo científico publicado el 24 de noviembre de 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

Genetic variation in CRTh2 influences development of allergic phenotypes

artículo científico publicado en 2009

Genetic variation in Fc gamma receptor IIa and risk of coronary heart disease: negative results from two large independent populations

artículo científico publicado en 2009

Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge

scientific journal article

Genetic variation in the epidermal transglutaminase genes is not associated with atopic dermatitis

artículo científico publicado en 2012

Genetic variation in the prostate stem cell antigen gene and upper gastrointestinal cancer in white individuals

artículo científico publicado en 2010

Genetic variation in the vaspin gene affects circulating serum vaspin concentrations

artículo científico publicado en 2012

Genetically determined variation in polyunsaturated fatty acid metabolism may result in different dietary requirements

artículo científico publicado en 2008

Genetics meets metabolomics: a genome-wide association study of metabolite profiles in human serum

artículo científico publicado en 2008

Genetics of asthma and related phenotypes

artículo científico publicado en 2002

Genetics of type 2 diabetes: impact of interleukin-6 gene variants

artículo científico publicado en 2005

Genome wide association (GWA) study for early onset extreme obesity supports the role of fat mass and obesity associated gene (FTO) variants

artículo científico publicado en 2007

Genome-Wide Association Study Pinpoints a New Functional Apolipoprotein B Variant Influencing Oxidized Low-Density Lipoprotein Levels But Not Cardiovascular Events

scholarly article by Kari-Matti Mäkelä et al published February 2013 in Circulation: Cardiovascular Genetics

Genome-wide Association Studies Identify Genetic Loci Associated With Albuminuria in Diabetes.

artículo científico publicado en 2015

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

artículo científico publicado en 2013

Genome-wide association and functional follow-up reveals new loci for kidney function

artículo científico publicado en 2012

Genome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distribution

artículo científico publicado en 2009

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 eight loci associated with blood pressure

artículo científico publicado en 2009

Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels

artículo científico publicado en 2015

Genome-wide association study identifies novel restless legs syndrome susceptibility loci on 2p14 and 16q12.1

scientific journal article

Genome-wide association study identifies two novel regions at 11p15.5-p13 and 1p31 with major impact on acute-phase serum amyloid A.

artículo científico publicado en 2010

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

artículo científico publicado en 2014

Genome-wide association study of intracranial aneurysm identifies three new risk loci

artículo científico publicado en 2010

Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions

artículo científico publicado en 2007

Genome-wide association study reveals genetic risk underlying Parkinson's disease

artículo científico publicado en 2009

Genome-wide comparative analysis of atopic dermatitis and psoriasis gives insight into opposing genetic mechanisms

artículo científico publicado en 2015

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

scientific journal article

Genome-wide meta-analysis uncovers novel loci influencing circulating leptin levels

artículo científico publicado en 2016

Genome-wide scan identifies CDH13 as a novel susceptibility locus contributing to blood pressure determination in two European populations

artículo científico publicado en 2009

Genome-wide scan on total serum IgE levels identifies FCER1A as novel susceptibility locus

artículo científico publicado en 2008

Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility

artículo científico publicado en 2014

Genotype-phenotype studies in bipolar disorder showing association between the DAOA/G30 locus and persecutory delusions: a first step toward a molecular genetic classification of psychiatric phenotypes.

artículo científico publicado en 2005

HHEX-IDE polymorphism is associated with low birth weight in offspring with a family history of type 1 diabetes

artículo científico publicado en 2009

HLX1 gene variants influence the development of childhood asthma

artículo científico publicado en 2008

Haplotype misclassification resulting from statistical reconstruction and genotype error, and its impact on association estimates

artículo científico publicado en 2010

High-density genotyping study identifies four new susceptibility loci for atopic dermatitis

scientific article published on 02 June 2013

High-resolution SNP scan of chromosome 6p21 in pooled samples from patients with complex diseases

artículo científico publicado en 2003

How about the uncertainty in the haplotypes in the population-based KORA studies?

artículo científico publicado en 2005

How to link call rate and p-values for Hardy-Weinberg equilibrium as measures of genome-wide SNP data quality

artículo científico publicado en 2010

Human metabolic individuality in biomedical and pharmaceutical research

artículo científico publicado en 2011

Human serum metabolic profiles are age dependent

artículo científico publicado en 2012

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

artículo científico publicado en 2010

IL-6 promoter polymorphisms and quantitative traits related to the metabolic syndrome in KORA S4.

artículo científico publicado en 2006

IL10 polymorphisms influence neonatal immune responses, atopic dermatitis, and wheeze at age 3 years

article

IL15 gene variants are not associated with asthma and atopy

artículo científico publicado en 2008

IL6 gene promoter polymorphisms and type 2 diabetes: joint analysis of individual participants' data from 21 studies

artículo científico publicado en 2006

IRF-1Gene Variations Influence IgE Regulation and Atopy

article

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

artículo científico publicado en 2013

Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits

artículo científico publicado en 2010

Identification of novel Angiogenin (ANG) gene missense variants in German patients with amyotrophic lateral sclerosis

artículo científico publicado en 2009

Identification of novel immune phenotypes for allergic and nonallergic childhood asthma

artículo científico publicado en 2014

Identification of serum metabolites associated with risk of type 2 diabetes using a targeted metabolomic approach

artículo científico publicado en 2012

Identification of ten loci associated with height highlights new biological pathways in human growth

artículo científico publicado en 2008

Impact of common regulatory single-nucleotide variants on gene expression profiles in whole blood

artículo científico publicado en 2012

Impaired glucose tolerance is associated with increased serum concentrations of interleukin 6 and co-regulated acute-phase proteins but not TNF-alpha or its receptors

artículo científico publicado en 2002

Improvement of myocardial infarction risk prediction via inflammation-associated metabolite biomarkers

artículo científico publicado en 2017

Increased amino acids levels and the risk of developing of hypertriglyceridemia in a 7-year follow-up

artículo científico publicado en 2014

Increased efficacy of omalizumab in atopic dermatitis patients with wild-type filaggrin status and higher serum levels of phosphatidylcholines

artículo científico publicado en 2013

Inflammation and type 2 diabetes: results from KORA Augsburg

artículo científico publicado en 2005

Integration of genome-wide association studies with biological knowledge identifies six novel genes related to kidney function

artículo científico publicado en 2012

Integrative genetic and metabolite profiling analysis suggests altered phosphatidylcholine metabolism in asthma

artículo científico publicado en 2013

International Lung Cancer Consortium: coordinated association study of 10 potential lung cancer susceptibility variants

artículo científico publicado en 2010

Interrogating causal pathways linking genetic variants, small molecule metabolites, and circulating lipids

artículo científico publicado en 2014

Investigation of the DAOA/G30 locus in panic disorder.

artículo científico publicado en 2005

Joint analysis of individual participants' data from 17 studies on the association of the IL6 variant -174G>C with circulating glucose levels, interleukin-6 levels, and body mass index

artículo científico publicado en 2009

KORA-gen--resource for population genetics, controls and a broad spectrum of disease phenotypes

artículo científico publicado en 2005

Kindlin 3 (FERMT3) is associated with unstable atherosclerotic plaques, anti-inflammatory type II macrophages and upregulation of beta-2 integrins in all major arterial beds

artículo científico publicado en 2015

Laboratory management of samples in biobanks: European consensus expert group report

artículo científico publicado en 2010

Lack of association between neuropeptide S receptor 1 gene (NPSR1) and eczema in five European populations.

artículo científico publicado en 2009

Lack of association of delta-aminolevulinate dehydratase polymorphisms with blood lead levels and hemoglobin in Romanian women from a lead-contaminated region

artículo científico publicado en 2008

Lack of support for a genetic association of the XBP1 promoter polymorphism with bipolar disorder in probands of European origin

artículo científico publicado en 2004

Large effects on body mass index and insulin resistance of fat mass and obesity associated gene (FTO) variants in patients with polycystic ovary syndrome (PCOS).

artículo científico publicado en 2010

Large meta-analysis of genome-wide association studies identifies five loci for lean body mass

artículo científico publicado en 2017

Large-Scale Gene-Centric Meta-Analysis across 39 Studies Identifies Type 2 Diabetes Loci.

artículo científico publicado en 2012

Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways

artículo científico publicado en 2012

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

Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes

artículo científico publicado en 2012

Large-scale determination of SNP allele frequencies in DNA pools using MALDI-TOF mass spectrometry

artículo científico publicado en 2002

Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci

artículo científico publicado en 2012

Large-scale gene-centric meta-analysis across 39 studies identifies type 2 diabetes loci

artículo científico publicado en 2012

Leveraging cross-species transcription factor binding site patterns: from diabetes risk loci to disease mechanisms

artículo científico publicado en 2014

Linkage disequilibrium patterns and tagSNP transferability among European populations

artículo científico publicado en 2005

Loci influencing blood pressure identified using a cardiovascular gene-centric array

artículo científico publicado en 2013

Loci influencing blood pressure identified using a cardiovascular gene-centric array.

artículo científico publicado en 2013

Long term conservation of human metabolic phenotypes and link to heritability

artículo científico publicado en 2014

Look beyond one's own nose: combination of information from publicly available sources reveals an association of GATA4 polymorphisms with plasma triglycerides

artículo científico publicado en 2011

Loss-of-function mutations in the filaggrin gene and allergic contact sensitization to nickel

artículo científico publicado en 2007

Low-risk variants FGFR2, TNRC9 and LSP1 in German familial breast cancer patients

artículo científico publicado en 2010

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

article

MALDI-TOF MS and TaqMan assisted SNP genotyping of DNA isolated from formalin-fixed and paraffin-embedded tissues (FFPET).

artículo científico publicado en 2005

MMP-9 gene variants increase the risk for non-atopic asthma in children

artículo científico publicado en 2010

MTTP variants and body mass index, waist circumference and serum cholesterol level: Association analyses in 7582 participants of the KORA study cohort

artículo científico publicado en 2008

Macrophage migration inhibitory factor (MIF) and risk for coronary heart disease: Results from the MONICA/KORA Augsburg case-cohort study, 1984–2002

Mapping the genetic architecture of gene regulation in whole blood

artículo científico publicado en 2014

Matrix metalloproteinase 1 (MMP1) is associated with early-onset lung cancer

artículo científico publicado en 2008

Mechanisms of IFN-γ-induced apoptosis of human skin keratinocytes in patients with atopic dermatitis

artículo científico publicado en 2012

Melanocortin-4 receptor gene variant I103 is negatively associated with obesity

artículo científico publicado en 2004

Meta-analysis and a large association study confirm a role for calpain-10 variation in type 2 diabetes susceptibility

artículo científico publicado en 2003

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

Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations

artículo científico publicado en 2009

Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height

artículo científico publicado en 2010

Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes

artículo científico publicado en 2008

Meta-analysis of genome-wide association studies from the CHARGE consortium identifies common variants associated with carotid intima media thickness and plaque

artículo científico publicado en 2011

Meta-analysis of genome-wide association studies identifies three new risk loci for atopic dermatitis

artículo científico publicado en 2012

Meta-analysis of the INSIG2 association with obesity including 74,345 individuals: does heterogeneity of estimates relate to study design?

artículo científico publicado en 2009

Meta-analysis of two genome-wide association studies identifies four genetic loci associated with thyroid function

artículo científico publicado en 2012

Metabolic footprint of diabetes: a multiplatform metabolomics study in an epidemiological setting

artículo científico publicado en 2010

Metabolic profiling reveals distinct variations linked to nicotine consumption in humans--first results from the KORA study

artículo científico publicado en 2008

Metabolite profiling and cardiovascular event risk: a prospective study of 3 population-based cohorts

artículo científico publicado en 2015

Metabolite profiling reveals new insights into the regulation of serum urate in humans

artículo científico publicado en 2013

Metabolites associate with kidney function decline and incident chronic kidney disease in the general population

artículo científico publicado en 2013

Metabolomic Signature of Coronary Artery Disease in Type 2 Diabetes Mellitus

artículo científico publicado en 2017

Metabolomic profiles in individuals with negative affectivity and social inhibition: a population-based study of Type D personality

artículo científico publicado en 2012

Metabolomics approach reveals effects of antihypertensives and lipid-lowering drugs on the human metabolism

artículo científico publicado en 2014

Metabolomics reveals determinants of weight loss during lifestyle intervention in obese children

Metformin Effect on Nontargeted Metabolite Profiles in Patients With Type 2 Diabetes and in Multiple Murine Tissues

artículo científico publicado en 2016

Mining the unknown: a systems approach to metabolite identification combining genetic and metabolic information

artículo científico publicado en 2012

Mitochondrial DNA variants in obesity

artículo científico publicado en 2014

Modification of the interleukin-6 response to air pollution by interleukin-6 and fibrinogen polymorphisms

artículo científico publicado en 2009

Molecular analysis of cataract families in India: new mutations in the CRYBB2 and GJA3 genes and rare polymorphisms ⬇️

artículo científico publicado el 10 de septiembre de 2010

Mortality excess in individuals with elevated IgA anti-transglutaminase antibodies: the KORA/MONICA Augsburg cohort study 1989-1998.

artículo científico publicado en 2006

Mouse phenotyping

artículo científico publicado en 2010

Multi-omic signature of body weight change: results from a population-based cohort study

artículo científico publicado en 2015

Multicentric investigation of ionising radiation-induced cell death as a predictive parameter of individual radiosensitivity

artículo científico publicado en 2009

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

Multiple loci are associated with white blood cell phenotypes

artículo científico publicado en 2011

Multiple regions of alpha-synuclein are associated with Parkinson's disease

artículo científico publicado en 2005

Mutation analysis in a German family identified a new cataract-causing allele in the CRYBB2 gene.

scientific article published on 19 June 2007

Mutation analysis of the MCHR1 gene in human obesity

artículo científico publicado en 2005

Mutation screen and association studies for the fatty acid amide hydrolase (FAAH) gene and early onset and adult obesity

artículo científico publicado en 2010

Mutation screen in the GWAS derived obesity gene SH2B1 including functional analyses of detected variants

artículo científico publicado en 2012

N-acetyltransferase 2 phenotype, occupation, and bladder cancer risk: results from the EPIC cohort

artículo científico

N-acetyltransferase 2, exposure to aromatic and heterocyclic amines, and receptor-defined breast cancer

artículo científico publicado en 2010

NCAM2 deletion in a boy with macrocephaly and autism: Cause, association or predisposition?

artículo científico publicado en 2016

Network-based SNP meta-analysis identifies joint and disjoint genetic features across common human diseases

artículo científico publicado en 2012

New gene functions in megakaryopoiesis and platelet formation

artículo científico publicado en 2011

New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk

artículo científico publicado en 2010

New genetic loci link adipose and insulin biology to body fat distribution

artículo científico publicado en 2015

New loci associated with kidney function and chronic kidney disease

artículo científico publicado en 2010

Night Shift Work Affects Urine Metabolite Profiles of Nurses with Early Chronotype

scholarly article by Markus Rotter published in August 2018

No association between genetic variants at the ASCT1 gene and schizophrenia or bipolar disorder in a German sample

article

No association between genetic variants at the GLYT2 gene and bipolar affective disorder and schizophrenia

artículo científico publicado en 2006

No association between genetic variants at the GRIN1 gene and bipolar disorder in a German sample.

artículo científico publicado en 2006

No association between the putative functional ZDHHC8 single nucleotide polymorphism rs175174 and schizophrenia in large European samples

artículo científico publicado en 2005

No association between the serine racemase gene (SRR) and bipolar disorder in a German case-control sample

artículo científico publicado en 2007

No association between the serine racemase gene (SRR) and schizophrenia in a German case-control sample.

artículo científico publicado en 2007

No association of two functional polymorphisms in human ALOX15 with myocardial infarction

artículo científico publicado en 2008

No evidence for an association between variants at the gamma-amino-n-butyric acid type A receptor beta2 locus and schizophrenia

artículo científico publicado en 2007

No evidence for genome-wide interactions on plasma fibrinogen by smoking, alcohol consumption and body mass index: results from meta-analyses of 80,607 subjects

artículo científico publicado en 2014

No evidence of association of FLJ10986 and ITPR2 with ALS in a large German cohort

artículo científico publicado en 2009

No impact of obesity susceptibility loci on weight regain after a lifestyle intervention in overweight children

artículo científico publicado en 2013

Non-replication of an association of CTNNBL1 polymorphisms and obesity in a population of Central European ancestry

artículo científico publicado en 2009

Novel association to the proprotein convertase PCSK7 gene locus revealed by analysing soluble transferrin receptor (sTfR) levels

artículo científico publicado en 2010

Novel associations for coronary artery disease derived from genome wide association studies are not associated with increased carotid intima-media thickness, suggesting they do not act via early atherosclerosis or vessel remodeling

artículo científico publicado en 2011

Novel biomarkers for pre-diabetes identified by metabolomics

artículo científico publicado en 2012

Novel genetic associations with serum level metabolites identified by phenotype set enrichment analyses

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

Observational study on variability between biobanks in the estimation of DNA concentration

artículo científico publicado en 2009

On metabolic reprogramming and tumor biology: A comprehensive survey of metabolism in breast cancer

artículo científico publicado en 2016

On the replication of genetic associations: timing can be everything!

artículo científico publicado en 2008

One-carbon metabolism and breast cancer risk: no association of MTHFR, MTR, and TYMS polymorphisms in the GENICA study from Germany

artículo científico publicado en 2005

PLA1A2 platelet polymorphism predicts mortality in prediabetic subjects of the population based KORA S4-Cohort

artículo científico publicado en 2014

PTPRD (protein tyrosine phosphatase receptor type delta) is associated with restless legs syndrome

artículo científico publicado en 2008

Pentanucleotide repeats at the spinocerebellar ataxia type 31 (SCA31) locus in Caucasians

artículo científico publicado en 2011

Physical activity attenuates the influence of FTO variants on obesity risk: a meta-analysis of 218,166 adults and 19,268 children

artículo científico publicado en 2011

Plasma metabolomics reveal alterations of sphingo- and glycerophospholipid levels in non-diabetic carriers of the transcription factor 7-like 2 polymorphism rs7903146

artículo científico publicado en 2013

Polymorphic loci of E2F2, CCND1 and CCND3 are associated with HER2 status of breast tumors

artículo científico publicado en 2009

Polymorphism of the DNA repair enzyme XRCC1 is associated with treatment prediction in anthracycline and cyclophosphamide/methotrexate/5-fluorouracil-based chemotherapy of patients with primary invasive breast cancer

artículo científico publicado en 2007

Polymorphisms in MUC1, MUC2, MUC5B and MUC6 genes are not associated with the risk of chronic atrophic gastritis

article

Polymorphisms in eosinophil pathway genes, asthma and atopy

artículo científico publicado en 2007

Polymorphisms in extracellular signal-regulated kinase family influence genetic susceptibility to asthma

artículo científico publicado en 2013

Polymorphisms in inflammatory pathway genes and their association with colorectal cancer risk

artículo científico publicado en 2010

Polymorphisms in the angiotensin-converting enzyme gene are associated with unipolar depression, ACE activity and hypercortisolism

artículo científico publicado en 2006

Polymorphisms in the proteasomal subunit alpha4 are not associated with Parkinson's disease

artículo científico publicado en 2008

Polymorphisms in the receptor for GDNF (RET) are not associated with Parkinson's disease in Southern Germany

artículo científico publicado en 2008

Possible association between genetic variants at the GRIN1 gene and schizophrenia with lifetime history of depressive symptoms in a German sample.

artículo científico publicado en 2007

Possible gender-dependent association of vascular endothelial growth factor (VEGF) gene and ALS.

artículo científico publicado en 2006

Posttraumatic stress disorder and not depression is associated with shorter leukocyte telomere length: findings from 3,000 participants in the population-based KORA F4 study

artículo científico publicado en 2013

Potential Impact and Study Considerations of Metabolomics in Cardiovascular Health and Disease: A Scientific Statement From the American Heart Association

artículo científico publicado en 2017

Predicting sudden cardiac death using common genetic risk variants for coronary artery disease

artículo científico publicado en 2015

Preservation of metabolic flexibility in skeletal muscle by a combined use of n-3 PUFA and rosiglitazone in dietary obese mice

artículo científico publicado en 2012

Prevalence, spectrum, and functional characterization of melanocortin-4 receptor gene mutations in a representative population-based sample and obese adults from Germany

artículo científico publicado en 2006

Prion protein codon 129 polymorphism and risk of Alzheimer disease.

artículo científico publicado en 2004

Questionnaire-based self-reported nutrition habits associate with serum metabolism as revealed by quantitative targeted metabolomics

artículo científico publicado en 2010

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

RANTES/CCL5 gene polymorphisms, serum concentrations, and incident type 2 diabetes: results from the MONICA/KORA Augsburg case–cohort study, 1984–2002

article

Random Survival Forest in practice: a method for modelling complex metabolomics data in time to event analysis

artículo científico publicado en 2016

Rare TLR2 mutations reduce TLR2 receptor function and can increase atopy risk

artículo científico publicado en 2009

Rare exonic deletions of the RBFOX1 gene increase risk of idiopathic generalized epilepsy

artículo científico publicado en 2013

Rationale, design and objectives of ARegPKD, a European ARPKD registry study

artículo científico publicado en 2015

Regulation of TH17 markers early in life through maternal farm exposure

artículo científico publicado en 2013

Reliability of serum metabolite concentrations over a 4-month period using a targeted metabolomic approach ⬇️

artículo científico publicado en 2011

Replication of lung cancer susceptibility loci at chromosomes 15q25, 5p15, and 6p21: a pooled analysis from the International Lung Cancer Consortium

artículo científico publicado en 2010

Replication study of multiple sclerosis (MS) susceptibility alleles and correlation of DNA-variants with disease features in a cohort of Austrian MS patients

Risk gene variants for nicotine dependence in the CHRNA5-CHRNA3-CHRNB4 cluster are associated with cognitive performance

artículo científico publicado en 2010

SDCCAG8 obesity alleles and reduced weight loss after a lifestyle intervention in overweight children and adolescents

artículo científico publicado en 2011

SLC2A9 influences uric acid concentrations with pronounced sex-specific effects

artículo científico publicado en 2008

SLC30A8 (ZnT8) Polymorphism is Associated with Young Age at Type 1 Diabetes Onset

artículo científico publicado en 2008

SNCA variants are associated with increased risk for multiple system atrophy

artículo científico publicado en 2009

SNP-based analysis of genetic substructure in the German population.

artículo científico publicado en 2006

SNPs of the FADS gene cluster are associated with polyunsaturated fatty acids in a cohort of patients with cardiovascular disease

artículo científico publicado en 2008

STAT1 gene variations, IgE regulation and atopy

artículo científico publicado en 2007

STAT6 as an asthma candidate gene: polymorphism-screening, association and haplotype analysis in a Caucasian sib-pair study.

artículo científico publicado en 2002

Sample selection algorithm to improve quality of genotyping from plasma-derived DNA: to separate the wheat from the chaff

artículo científico publicado en 2007

Schizophrenia shows a unique metabolomics signature in plasma

artículo científico publicado en 2012

Sequence data and association statistics from 12,940 type 2 diabetes cases and controls

artículo científico publicado en 2017

Serum branched-chain amino acid to histidine ratio: a novel metabolomic biomarker of knee osteoarthritis

artículo científico publicado en 2010

Serum metabolite concentrations and decreased GFR in the general population

artículo científico publicado en 2012

Serum metabolites and risk of myocardial infarction and ischemic stroke: a targeted metabolomic approach in two German prospective cohorts

artículo científico publicado en 2017

Serum metabolomic profiling highlights pathways associated with liver fat content in a general population sample

artículo científico publicado en 2017

Seventy-five genetic loci influencing the human red blood cell

artículo científico publicado en 2012

Sex-specific association of the putative fructose transporter SLC2A9 variants with uric acid levels is modified by BMI

artículo científico publicado en 2008

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

artículo científico publicado en 2013

Significant association of a M129V independent polymorphism in the 5' UTR of the PRNP gene with sporadic Creutzfeldt-Jakob disease in a large German case-control study

artículo científico publicado en 2006

Significant association of the interleukin-6 gene polymorphisms C-174G and A-598G with type 2 diabetes

artículo científico publicado en 2004

Single nucleotide polymorphisms in Wnt signaling and cell death pathway genes and susceptibility to colorectal cancer

article

Smoking cessation and variations in nicotinic acetylcholine receptor subunits alpha-5, alpha-3, and beta-4 genes

artículo científico publicado en 2008

Spinocerebellar ataxia type 36 exists in diverse populations and can be caused by a short hexanucleotide GGCCTG repeat expansion

artículo científico publicado en 2014

Stability of targeted metabolite profiles of urine samples under different storage conditions

artículo científico publicado en 2016

Stratifying type 2 diabetes cases by BMI identifies genetic risk variants in LAMA1 and enrichment for risk variants in lean compared to obese cases

artículo científico publicado en 2012

Strong genetic evidence for association of TOR1A/TOR1B with idiopathic dystonia

artículo científico publicado en 2006

Subclinical inflammation and diabetic polyneuropathy: MONICA/KORA Survey F3 (Augsburg, Germany)

artículo científico publicado en 2009

Supplemental Human Genetics Point of View.

artículo científico publicado en 2019

Systemic monocyte chemoattractant protein-1 concentrations are independent of type 2 diabetes or parameters of obesity: results from the Cooperative Health Research in the Region of Augsburg Survey S4 (KORA S4).

artículo científico publicado en 2006

TBX21 gene variants increase childhood asthma risk in combination with HLX1 variants

artículo científico publicado en 2009

Talin and vinculin are downregulated in atherosclerotic plaque; Tampere Vascular Study

artículo científico publicado en 2016

Targeted metabolomics profiles are strongly correlated with nutritional patterns in women

artículo científico publicado en 2012

Targeting 160 candidate genes for blood pressure regulation with a genome-wide genotyping array

artículo científico publicado en 2009

The ATGL gene is associated with free fatty acids, triglycerides, and type 2 diabetes

artículo científico publicado en 2006

The C718T polymorphism in the 3'-untranslated region of glutathione peroxidase-4 gene is a predictor of cerebral stroke in patients with essential hypertension

artículo científico publicado en 2011

The CYP1B1_1358_GG genotype is associated with estrogen receptor-negative breast cancer

artículo científico publicado en 2007

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 KORA Eye Study: a population-based study on eye diseases in Southern Germany (KORA F4).

artículo científico publicado en 2011

The Pharmacogenetic Footprint of ACE Inhibition: A Population-Based Metabolomics Study

artículo científico publicado en 2016

The WST survival assay: an easy and reliable method to screen radiation-sensitive individuals

artículo científico publicado en 2010

The common non-synonymous variant G38S of the KCNE1-(minK)-gene is not associated to QT interval in Central European Caucasians: results from the KORA study

article

The effect of BDNF gene variants on asthma in German children

artículo científico publicado en 2009

The fragile X tremor ataxia syndrome in the differential diagnosis of multiple system atrophy: data from the EMSA Study Group

artículo científico publicado en 2005

The genetic architecture of type 2 diabetes

artículo científico publicado en 2016

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

artículo científico publicado en 2016

The microRNA-449 family inhibits TGF-β-mediated liver cancer cell migration by targeting SOX4.

artículo científico publicado en 2017

The non-synonymous coding IKr-channel variant KCNH2-K897T is associated with atrial fibrillation: results from a systematic candidate gene-based analysis of KCNH2 (HERG)

article

The role of adiposity in cardiometabolic traits: a Mendelian randomization analysis

artículo científico publicado en 2013

The role of polymorphisms in ADAM33, a disintegrin and metalloprotease 33, in childhood asthma and lung function in two German populations

artículo científico publicado en 2006

The transcription factor PITX3 is associated with sporadic Parkinson's disease

artículo científico publicado en 2009

The transcriptional landscape of age in human peripheral blood

artículo científico publicado en 2015

Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies

artículo científico publicado en 2010

Tobacco smoking leads to extensive genome-wide changes in DNA methylation

artículo científico publicado en 2013

Toll-like receptor heterodimer variants protect from childhood asthma

artículo científico publicado en 2008

Toward a major risk factor for atopic eczema: meta-analysis of filaggrin polymorphism data

artículo científico publicado en 2007

Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis

artículo científico publicado en 2010

Two new Loci for body-weight regulation identified in a joint analysis of genome-wide association studies for early-onset extreme obesity in French and german study groups

scientific journal article

Underlying genetic models of inheritance in established type 2 diabetes associations

artículo científico publicado en 2009

Unifying candidate gene and GWAS Approaches in Asthma

artículo científico publicado en 2010

Unmasking differential effects of rosiglitazone and pioglitazone in the combination treatment with n-3 fatty acids in mice fed a high-fat diet

artículo científico publicado en 2011

Upstream Transcription Factor 1 (USF1) allelic variants regulate lipoprotein metabolism in women and USF1 expression in atherosclerotic plaque

artículo científico publicado en 2014

Variants in COMT and spontaneous smoking cessation: retrospective cohort analysis of 925 cessation events.

artículo científico publicado en 2009

Variants in MTNR1B influence fasting glucose levels

artículo científico publicado en 2008

Variants in the neuronal nitric oxide synthase (nNOS, NOS1) gene are associated with restless legs syndrome

artículo científico publicado en 2008

Variants of the PPARG, IGF2BP2, CDKAL1, HHEX, and TCF7L2 genes confer risk of type 2 diabetes independently of BMI in the German KORA studies

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Variants of the transcription factor 7-like 2 gene (TCF7L2) are strongly associated with type 2 diabetes but not with the metabolic syndrome in the MONICA/KORA surveys

artículo científico publicado en 2007

Variation in the human lipidome associated with coffee consumption as revealed by quantitative targeted metabolomics

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Variation of the N-acetyltransferase 2 gene in a Romanian and a Kyrgyz population

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Vaspin (SERPINA12) genotypes and risk of type 2 diabetes: Results from the MONICA/KORA studies

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Weak independent association signals between IDE polymorphisms, Alzheimer's disease and cognitive measures.

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[Centralized biobanks: a basis for medical research].

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miR-21, miR-210, miR-34a, and miR-146a/b are up-regulated in human atherosclerotic plaques in the Tampere Vascular Study

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40 EASD Annual Meeting of the European Association for the Study of Diabetes : Munich, Germany, 5-9 September 2004 ⬇️

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