Thomas Illig

Thomas Illig's AcademicInfluence.com Rankings

Thomas Illig

Biology

#9736

World Rank

#12977

Historical Rank

Genetics

#999

World Rank

#1097

Historical Rank

Molecular Biology

#1355

World Rank

#1382

Historical Rank

biology Degrees

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Biology

Thomas Illig's Degrees

PhD Genetics Stanford University

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Thomas Illig's Published Works

Number of citations in a given year to any of this author's works

Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author

Published Works

Genetic studies of body mass index yield new insights for obesity biology (2015) (3549)
Discovery and Refinement of Loci Associated with Lipid Levels (2013) (2475)
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk (2010) (2087)
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index (2010) (2011)
Hundreds of variants clustered in genomic loci and biological pathways affect human height (2010) (1961)
Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes (2008) (1882)
Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes (2012) (1839)
Defining the role of common variation in the genomic and biological architecture of adult human height (2014) (1805)
Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis (2010) (1801)
Genome-Wide Association Study reveals genetic risk underlying Parkinson’s disease (2009) (1770)
Large-scale association analysis identifies new risk loci for coronary artery disease (2012) (1507)
Genetic variants regulating ORMDL3 expression contribute to the risk of childhood asthma (2007) (1493)
New genetic loci link adipose and insulin biology to body fat distribution (2014) (1227)
Genome-wide association study identifies eight loci associated with blood pressure (2009) (1225)
Association analyses of 249,796 individuals reveal eighteen new loci associated with body mass index (2010) (1179)
Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility (2014) (933)
Human metabolic individuality in biomedical and pharmaceutical research (2011) (929)
The genetic architecture of type 2 diabetes (2016) (927)
Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution (2010) (897)
Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease (2011) (894)
GWAS of 126,559 Individuals Identifies Genetic Variants Associated with Educational Attainment (2013) (803)
Identification of Serum Metabolites Associated With Risk of Type 2 Diabetes Using a Targeted Metabolomic Approach (2013) (784)
Common variants associated with plasma triglycerides and risk for coronary artery disease (2013) (767)
Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways (2012) (758)
New loci associated with kidney function and chronic kidney disease (2010) (754)
Variants in MTNR1B influence fasting glucose levels (2009) (742)
A Common Genetic Variant Is Associated with Adult and Childhood Obesity (2006) (739)
Genetics Meets Metabolomics: A Genome-Wide Association Study of Metabolite Profiles in Human Serum (2008) (691)
Tobacco Smoking Leads to Extensive Genome-Wide Changes in DNA Methylation (2013) (662)
Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions (2007) (657)
A genome-wide perspective of genetic variation in human metabolism (2010) (639)
Epigenome-wide association study of body mass index, and the adverse outcomes of adiposity (2016) (634)
Identification of ten loci associated with height highlights new biological pathways in human growth (2008) (626)
Meta-Analysis of 28,141 Individuals Identifies Common Variants within Five New Loci That Influence Uric Acid Concentrations (2009) (617)
Loss-of-function variations within the filaggrin gene predispose for atopic dermatitis with allergic sensitizations. (2006) (591)
Novel biomarkers for pre-diabetes identified by metabolomics (2012) (587)
Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture (2013) (568)
Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity (2012) (555)
A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium (2009) (551)
Metabolic Footprint of Diabetes: A Multiplatform Metabolomics Study in an Epidemiological Setting (2010) (544)
Common genetic variants of the FADS1 FADS2 gene cluster and their reconstructed haplotypes are associated with the fatty acid composition in phospholipids. (2006) (544)
A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization (2006) (537)
The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study (2015) (532)
Genome-Wide Association Scan Meta-Analysis Identifies Three Loci Influencing Adiposity and Fat Distribution (2009) (516)
Genome Wide Association (GWA) Study for Early Onset Extreme Obesity Supports the Role of Fat Mass and Obesity Associated Gene (FTO) Variants (2007) (510)
Physical Activity Attenuates the Influence of FTO Variants on Obesity Risk: A Meta-Analysis of 218,166 Adults and 19,268 Children (2011) (508)
KORA-gen--resource for population genetics, controls and a broad spectrum of disease phenotypes. (2005) (506)
Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies (2010) (477)
Mapping the human genetic architecture of COVID-19 (2021) (455)
The transcriptional landscape of age in human peripheral blood (2015) (450)
New gene functions in megakaryopoiesis and platelet formation (2011) (423)
SLC2A9 influences uric acid concentrations with pronounced sex-specific effects (2008) (423)
Metabolite profiling and cardiovascular event risk: a prospective study of 3 population-based cohorts. (2015) (401)
miR-21, miR-210, miR-34a, and miR-146a/b are up-regulated in human atherosclerotic plaques in the Tampere Vascular Study. (2011) (394)
Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function (2016) (388)
Filaggrin mutations, atopic eczema, hay fever, and asthma in children. (2008) (388)
Differences between Human Plasma and Serum Metabolite Profiles (2011) (386)
Sex-stratified Genome-wide Association Studies Including 270,000 Individuals Show Sexual Dimorphism in Genetic Loci for Anthropometric Traits (2013) (365)
Seventy-five genetic loci influencing the human red blood cell (2012) (357)
Genetic fine-mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci (2015) (349)
The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals (2016) (347)
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. (2015) (347)
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 (2010) (337)
Discovery of Sexual Dimorphisms in Metabolic and Genetic Biomarkers (2011) (325)
META-ANALYSIS OF GENOME-WIDE ASSOCIATION STUDIES IDENTIFIES THREE NEW RISK LOCI FOR ATOPIC DERMATITIS (2011) (325)
FADS genotypes and desaturase activity estimated by the ratio of arachidonic acid to linoleic acid are associated with inflammation and coronary artery disease. (2008) (316)
Evidence for a Relationship Between Genetic Variants at the Brain-Derived Neurotrophic Factor (BDNF) Locus and Major Depression (2005) (305)
A common variant on chromosome 11q13 is associated with atopic dermatitis (2009) (302)
Genome-wide association study of intracranial aneurysm identifies three new risk loci (2010) (298)
Gaussian graphical modeling reconstructs pathway reactions from high-throughput metabolomics data (2011) (296)
Genome-Wide Scan on Total Serum IgE Levels Identifies FCER1A as Novel Susceptibility Locus (2008) (289)
Large-scale gene-centric meta-analysis across 39 studies identifies type 2 diabetes loci. (2012) (282)
Impaired glucose tolerance is associated with increased serum concentrations of interleukin 6 and co-regulated acute-phase proteins but not TNF-α or its receptors (2002) (278)
Excessive burden of lysosomal storage disorder gene variants in Parkinson’s disease (2017) (278)
A Two-Stage Meta-Analysis Identifies Several New Loci for Parkinson's Disease (2011) (278)
Loss-of-function mutations in the filaggrin gene and allergic contact sensitization to nickel. (2008) (274)
PTPRD (protein tyrosine phosphatase receptor type delta) is associated with restless legs syndrome (2008) (269)
SNCA variants are associated with increased risk for multiple system atrophy (2009) (263)
Stratifying Type 2 Diabetes Cases by BMI Identifies Genetic Risk Variants in LAMA1 and Enrichment for Risk Variants in Lean Compared to Obese Cases (2012) (263)
SNPs of the FADS Gene Cluster are Associated with Polyunsaturated Fatty Acids in a Cohort of Patients with Cardiovascular Disease (2008) (247)
Human serum metabolic profiles are age dependent (2012) (247)
Filaggrin mutations strongly predispose to early-onset and extrinsic atopic dermatitis. (2007) (242)
A genome-wide association study of metabolic traits in human urine (2011) (241)
Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. (2012) (238)
Large-Scale Gene-Centric Analysis Identifies Novel Variants for Coronary Artery Disease (2011) (228)
Genetic architecture of the APM1 gene and its influence on adiponectin plasma levels and parameters of the metabolic syndrome in 1,727 healthy Caucasians. (2006) (226)
Elevated levels of interleukin-18 predict the development of type 2 diabetes: results from the MONICA/KORA Augsburg Study, 1984-2002. (2005) (224)
Melanocortin-4 receptor gene variant I103 is negatively associated with obesity. (2004) (218)
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 (2008) (216)
A Genome-Wide Association Meta-Analysis of Circulating Sex Hormone–Binding Globulin Reveals Multiple Loci Implicated in Sex Steroid Hormone Regulation (2012) (216)
CUBN is a gene locus for albuminuria. (2011) (214)
Meta-analysis of genome-wide association studies from the CHARGE consortium identifies common variants associated with carotid intima media thickness and plaque (2011) (214)
Toward a major risk factor for atopic eczema: meta-analysis of filaggrin polymorphism data. (2007) (212)
Prevalence, spectrum, and functional characterization of melanocortin-4 receptor gene mutations in a representative population-based sample and obese adults from Germany. (2006) (202)
Genome-wide scan identifies CDH13 as a novel susceptibility locus contributing to blood pressure determination in two European populations (2009) (201)
The Role of Adiposity in Cardiometabolic Traits: A Mendelian Randomization Analysis (2013) (199)
Genetic evidence of assortative mating in humans (2017) (199)
Genetic evidence that raised sex hormone binding globulin (SHBG) levels reduce the risk of type 2 diabetes (2009) (199)
Replication of lung cancer susceptibility loci at chromosomes 15q25, 5p15, and 6p21: a pooled analysis from the International Lung Cancer Consortium. (2010) (198)
ASXL1 exon 12 mutations are frequent in AML with intermediate risk karyotype and are independently associated with an adverse outcome (2013) (197)
Multiple regions of α‐synuclein are associated with Parkinson's disease (2005) (195)
Association of NOD1 polymorphisms with atopic eczema and related phenotypes. (2005) (191)
Autoantibodies to zinc transporter 8 and SLC30A8 genotype stratify type 1 diabetes risk (2009) (187)
Meta-analysis and a large association study confirm a role for calpain-10 variation in type 2 diabetes susceptibility. (2003) (184)
Genome-Wide Association and Functional Follow-Up Reveals New Loci for Kidney Function (2012) (180)
A genome-wide association study of atopic dermatitis identifies loci with overlapping effects on asthma and psoriasis (2013) (179)
Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels (2015) (179)
Gender-specific pathway differences in the human serum metabolome (2015) (178)
Putative association of a TLR9 promoter polymorphism with atopic eczema (2007) (177)
Epigenetics meets metabolomics: an epigenome-wide association study with blood serum metabolic traits (2013) (177)
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. (2002) (173)
Genome-Wide Association Study Identifies Novel Restless Legs Syndrome Susceptibility Loci on 2p14 and 16q12.1 (2011) (172)
Childhood cancer predisposition syndromes—A concise review and recommendations by the Cancer Predisposition Working Group of the Society for Pediatric Oncology and Hematology (2017) (172)
Genetic variants of the FADS1 FADS2 gene cluster as related to essential fatty acid metabolism (2010) (171)
High-density genotyping study identifies four new susceptibility loci for atopic dermatitis (2013) (170)
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. (2011) (169)
Clear detection of ADIPOQ locus as the major gene for plasma adiponectin: results of genome-wide association analyses including 4659 European individuals. (2010) (168)
Common Variants in Myocardial Ion Channel Genes Modify the QT Interval in the General Population: Results From the KORA Study (2005) (168)
A Genome-Wide Association Study of Depressive Symptoms (2013) (166)
Chemokines as risk factors for type 2 diabetes: results from the MONICA/KORA Augsburg study, 1984–2002 (2006) (160)
Mining the Unknown: A Systems Approach to Metabolite Identification Combining Genetic and Metabolic Information (2012) (156)
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. (2010) (155)
DNA Methylation of Lipid-Related Genes Affects Blood Lipid Levels (2015) (153)
Serum branched-chain amino acid to histidine ratio: a novel metabolomic biomarker of knee osteoarthritis (2010) (152)
Characterization of whole-genome autosomal differences of DNA methylation between men and women (2015) (151)
Genetic Regulation of Serum Phytosterol Levels and Risk of Coronary Artery Disease (2010) (151)
Gene-centric meta-analysis in 87,736 individuals of European ancestry identifies multiple blood-pressure-related loci. (2014) (150)
Association between variants of PRDM1 and NDP52 and Crohn's disease, based on exome sequencing and functional studies. (2013) (149)
G-Protein-coupled receptor polymorphisms are associated with asthma in a large German population. (2005) (148)
Genome-wide meta-analysis uncovers novel loci influencing circulating leptin levels (2016) (147)
Toll-like receptor heterodimer variants protect from childhood asthma. (2008) (146)
Loci influencing blood pressure identified using a cardiovascular gene-centric array. (2013) (145)
Polymorphisms in the angiotensin-converting enzyme gene are associated with unipolar depression, ACE activity and hypercortisolism (2006) (144)
Genome-wide Comparative Analysis of Atopic Dermatitis and Psoriasis Gives Insight into Opposing Genetic Mechanisms (2015) (144)
A Metabolome-Wide Association Study of Kidney Function and Disease in the General Population. (2016) (144)
Identification of FOXP1 Deletions in Three Unrelated Patients with Mental Retardation and Significant Speech and Language Deficits (2010) (143)
Identification of novel immune phenotypes for allergic and nonallergic childhood asthma. (2015) (142)
A Genome-Wide Association Study Identifies LIPA as a Susceptibility Gene for Coronary Artery Disease (2011) (141)
Childhood Obesity Is Associated with Changes in the Serum Metabolite Profile (2012) (140)
Schizophrenia shows a unique metabolomics signature in plasma (2012) (139)
ERCC2 genotypes and a corresponding haplotype are linked with breast cancer risk in a German population. (2004) (138)
Linkage disequilibrium patterns and tagSNP transferability among European populations. (2005) (138)
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. (2005) (137)
SNP-Based Analysis of Genetic Substructure in the German Population (2006) (137)
On the replication of genetic associations: timing can be everything! (2008) (135)
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 (2013) (133)
Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height. (2011) (133)
Dissecting the role of the mitochondrial chaperone mortalin in Parkinson's disease: functional impact of disease-related variants on mitochondrial homeostasis. (2010) (132)
A Genome-Wide Metabolic QTL Analysis in Europeans Implicates Two Loci Shaped by Recent Positive Selection (2011) (129)
Large meta-analysis of genome-wide association studies identifies five loci for lean body mass (2017) (127)
Potential Impact and Study Considerations of Metabolomics in Cardiovascular Health and Disease: A Scientific Statement From the American Heart Association. (2017) (127)
Genome-wide association study identifies a new locus for coronary artery disease on chromosome 10p11.23. (2011) (125)
A novel variant on chromosome 7q22.3 associated with mean platelet volume, counts, and function. (2009) (124)
Multiple Loci Are Associated with White Blood Cell Phenotypes (2011) (123)
A genome-wide association study identifies three loci associated with mean platelet volume. (2009) (123)
Mechanisms of IFN-γ-induced apoptosis of human skin keratinocytes in patients with atopic dermatitis. (2012) (122)
Metabolic Profiling Reveals Distinct Variations Linked to Nicotine Consumption in Humans — First Results from the KORA Study (2008) (122)
Duffy antigen receptor for chemokines (Darc) polymorphism regulates circulating concentrations of monocyte chemoattractant protein-1 and other inflammatory mediators. (2010) (122)
Reliability of Serum Metabolite Concentrations over a 4-Month Period Using a Targeted Metabolomic Approach (2011) (122)
Do FADS genotypes enhance our knowledge about fatty acid related phenotypes? (2010) (121)
Matrix Metalloproteinase 1 (MMP1) Is Associated with Early-Onset Lung Cancer (2008) (121)
Genome-wide Association Studies Identify Genetic Loci Associated With Albuminuria in Diabetes (2015) (121)
Leveraging Cross-Species Transcription Factor Binding Site Patterns: From Diabetes Risk Loci to Disease Mechanisms (2014) (120)
Association of a STAT 6 haplotype with elevated serum IgE levels in a population based cohort of white adults (2004) (118)
STAT6 as an asthma candidate gene: polymorphism-screening, association and haplotype analysis in a Caucasian sib-pair study. (2002) (116)
Common Polymorphisms Influencing Serum Uric Acid Levels Contribute to Susceptibility to Gout, but Not to Coronary Artery Disease (2009) (116)
The transcription factor PITX3 is associated with sporadic Parkinson's disease (2009) (115)
Association of the 103I MC4R allele with decreased body mass in 7937 participants of two population based surveys (2005) (112)
Targeted metabolomics profiles are strongly correlated with nutritional patterns in women (2012) (112)
Genetic Association Study Identifies HSPB7 as a Risk Gene for Idiopathic Dilated Cardiomyopathy (2010) (110)
Significant association of the interleukin-6 gene polymorphisms C-174G and A-598G with type 2 diabetes. (2004) (109)
Variants in the neuronal nitric oxide synthase (nNOS, NOS1) gene are associated with restless legs syndrome (2008) (108)
Metabolites associate with kidney function decline and incident chronic kidney disease in the general population. (2013) (107)
Effects of smoking and smoking cessation on human serum metabolite profile: results from the KORA cohort study (2013) (106)
Mortality Excess in Individuals with Elevated IgA Anti-Transglutaminase Antibodies: The KORA/MONICA Augsburg Cohort Study 1989–1998 (2006) (106)
Targeting 160 Candidate Genes for Blood Pressure Regulation with a Genome-Wide Genotyping Array (2009) (106)
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 (2008) (105)
Serum metabolite concentrations and decreased GFR in the general population. (2012) (104)
Unifying Candidate Gene and GWAS Approaches in Asthma (2010) (104)
Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution (2011) (104)
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). (2008) (104)
Mouse phenotyping. (2011) (103)
Effects of Metformin on Metabolite Profiles and LDL Cholesterol in Patients With Type 2 Diabetes (2015) (103)
Increased efficacy of omalizumab in atopic dermatitis patients with wild‐type filaggrin status and higher serum levels of phosphatidylcholines (2014) (103)
The microRNA-449 family inhibits TGF-β-mediated liver cancer cell migration by targeting SOX4. (2017) (102)
The fragile X tremor ataxia syndrome in the differential diagnosis of multiple system atrophy: data from the EMSA Study Group. (2005) (101)
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. (2012) (99)
Body Fat Free Mass Is Associated with the Serum Metabolite Profile in a Population-Based Study (2012) (98)
An integrated epigenetic and transcriptomic analysis reveals distinct tissue-specific patterns of DNA methylation associated with atopic dermatitis. (2014) (98)
Inflammation and type 2 diabetes: results from KORA Augsburg. (2005) (97)
Sex-Specific Association of the Putative Fructose Transporter SLC2A9 Variants With Uric Acid Levels Is Modified by BMI (2008) (95)
Metabolite Profiling and Cardiovascular Event RiskCLINICAL PERSPECTIVE (2015) (94)
A signal transducer and activator of transcription 6 haplotype influences the regulation of serum IgE levels. (2004) (93)
Association of Novel Genetic Loci With Circulating Fibrinogen Levels: A Genome-Wide Association Study in 6 Population-Based Cohorts (2009) (93)
Breast cancer: a candidate gene approach across the estrogen metabolic pathway (2007) (92)
Large‐scale determination of SNP allele frequencies in DNA pools using MALDI‐TOF mass spectrometry (2002) (89)
Prion protein codon 129 polymorphism and risk of Alzheimer disease (2004) (89)
Association of CARD15 polymorphisms with atopy‐related traits in a population‐based cohort of Caucasian adults (2005) (88)
The ATGL Gene Is Associated With Free Fatty Acids, Triglycerides, and Type 2 Diabetes (2006) (88)
Eight blood pressure loci identified by genome-wide association study of 34,433 people of European ancestry (2009) (88)
Questionnaire-based self-reported nutrition habits associate with serum metabolism as revealed by quantitative targeted metabolomics (2011) (87)
IL6 Gene Promoter Polymorphisms and Type 2 Diabetes (2006) (87)
Analyzing Illumina Gene Expression Microarray Data from Different Tissues: Methodological Aspects of Data Analysis in the MetaXpress Consortium (2012) (86)
Early IFN-α signatures and persistent dysfunction are distinguishing features of NK cells in severe COVID-19 (2021) (86)
Discovery and functional prioritization of Parkinson’s disease candidate genes from large-scale whole exome sequencing (2017) (85)
Meta-Analysis of the INSIG2 Association with Obesity Including 74,345 Individuals: Does Heterogeneity of Estimates Relate to Study Design? (2009) (85)
One-Carbon Metabolism and Breast Cancer Risk: No Association of MTHFR, MTR, and TYMS Polymorphisms in the GENICA Study from Germany (2005) (85)
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) (2010) (83)
Subclinical Inflammation and Diabetic Polyneuropathy (2009) (82)
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. (2008) (82)
The role of polymorphisms in ADAM33, a disintegrin and metalloprotease 33, in childhood asthma and lung function in two German populations (2006) (81)
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 over the duration of lactation. (2011) (80)
Variants of the PPARG, IGF2BP2, CDKAL1, HHEX, and TCF7L2 genes confer risk of type 2 diabetes independently of BMI in the German KORA studies. (2008) (80)
Novel association to the proprotein convertase PCSK7 gene locus revealed by analysing soluble transferrin receptor (sTfR) levels. (2011) (78)
Functional Characterization of Promoter Variants of the Adiponectin Gene Complemented by Epidemiological Data (2008) (78)
APOA5 variants and metabolic syndrome in Caucasianss⃞s⃞ The online version of this article (available at http://www.jlr.org) contains supplementary data in the form of three tables, one figure. Published, JLR Papers in Press, September 3, 2007. (2007) (78)
Causal Effect of Plasminogen Activator Inhibitor Type 1 on Coronary Heart Disease (2017) (78)
Association between DNA Methylation in Whole Blood and Measures of Glucose Metabolism: KORA F4 Study (2016) (78)
Alcohol-induced metabolomic differences in humans (2013) (77)
The adiponectin gene is associated with adiponectin levels but not with characteristics of the insulin resistance syndrome in healthy Caucasians (2006) (77)
A common FADS2 promoter polymorphism increases promoter activity and facilitates binding of transcription factor ELK1 (2010) (76)
The endotoxin receptor TLR4 polymorphism is not associated with diabetes or components of the metabolic syndrome. (2003) (75)
Integrative genetic and metabolite profiling analysis suggests altered phosphatidylcholine metabolism in asthma (2013) (75)
A radiation-induced gene expression signature as a tool to predict acute radiotherapy-induced adverse side effects. (2011) (74)
Genetic variation in the prostate stem cell antigen gene and upper gastrointestinal cancer in white individuals. (2011) (74)
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 (2009) (74)
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. (2007) (73)
Identification of a novel, putative cataract-causing allele in CRYAA (G98R) in an Indian family. (2006) (72)
An Interferon-Induced Helicase (IFIH1) Gene Polymorphism Associates With Different Rates of Progression From Autoimmunity to Type 1 Diabetes (2011) (71)
Congenital cataract and macular hypoplasia in humans associated with a de novo mutation in CRYAA and compound heterozygous mutations in P (2006) (71)
FADS Gene Cluster Polymorphisms: Important Modulators of Fatty Acid Levels and Their Impact on Atopic Diseases (2009) (71)
Changes in the serum metabolite profile in obese children with weight loss (2014) (69)
CYP450 polymorphisms as risk factors for early-onset lung cancer: gender-specific differences. (2009) (69)
Risk gene variants for nicotine dependence in the CHRNA5–CHRNA3–CHRNB4 cluster are associated with cognitive performance (2010) (68)
Integration of genome-wide association studies with biological knowledge identifies six novel genes related to kidney function. (2012) (67)
Long term conservation of human metabolic phenotypes and link to heritability (2014) (65)
Random Survival Forest in practice: a method for modelling complex metabolomics data in time to event analysis. (2016) (65)
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 (2014) (65)
Association of the MC4R V103I Polymorphism With the Metabolic Syndrome: The KORA Study (2008) (64)
Identification of novel Angiogenin (ANG) gene missense variants in German patients with amyotrophic lateral sclerosis (2009) (64)
Genetic Predictors of Fibrin D-Dimer Levels in Healthy Adults (2011) (63)
Preservation of Metabolic Flexibility in Skeletal Muscle by a Combined Use of n-3 PUFA and Rosiglitazone in Dietary Obese Mice (2012) (63)
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 (2006) (62)
Evaluation of Different Biomarkers to Predict Individual Radiosensitivity in an Inter-Laboratory Comparison–Lessons for Future Studies (2012) (62)
International Lung Cancer Consortium: coordinated association study of 10 potential lung cancer susceptibility variants. (2010) (62)
Underlying genetic models of inheritance in established type 2 diabetes associations. (2009) (62)
Association of single nucleotide polymorphisms in the diamine oxidase gene with diamine oxidase serum activities (2011) (62)
Genes and lifestyle factors in obesity: results from 12 462 subjects from MONICA/KORA (2010) (62)
Macrophage migration inhibitory factor (MIF) and risk for coronary heart disease: results from the MONICA/KORA Augsburg case-cohort study, 1984-2002. (2008) (61)
A splice site variant in the sodium channel gene SCN1A confers risk of febrile seizures (2009) (61)
Serum metabolites and risk of myocardial infarction and ischemic stroke: a targeted metabolomic approach in two German prospective cohorts (2017) (61)
Single nucleotide polymorphism screening and association analysis – exclusion of integrin β7 and vitamin D receptor (chromosome 12q) as candidate genes for asthma (2004) (61)
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 (2013) (60)
Do genetic factors protect for early onset lung cancer? A case control study before the age of 50 years (2008) (60)
Association of the interleukin-1 receptor antagonist gene with asthma. (2004) (60)
Association study of mast cell chymase polymorphisms with atopy (2005) (59)
Strong genetic evidence for association of TOR1A/TOR1B with idiopathic dystonia (2006) (59)
Metabolomics approach reveals effects of antihypertensives and lipid-lowering drugs on the human metabolism (2014) (59)
Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability (2020) (58)
Rare exonic deletions of the RBFOX1 gene increase risk of idiopathic generalized epilepsy (2013) (58)
Variation in the human lipidome associated with coffee consumption as revealed by quantitative targeted metabolomics. (2009) (57)
Common variants of LRRK2 are not associated with sporadic Parkinson's disease (2005) (57)
Lack of association between Toll-like receptor 2 and Toll-like receptor 4 polymorphisms and atopic eczema. (2006) (56)
Vaspin (SERPINA12) genotypes and risk of type 2 diabetes: Results from the MONICA/KORA studies. (2008) (56)
Blood hsa-miR-122-5p and hsa-miR-885-5p levels associate with fatty liver and related lipoprotein metabolism—The Young Finns Study (2016) (56)
Impact of common regulatory single-nucleotide variants on gene expression profiles in whole blood (2012) (55)
Lack of support for a genetic association of the XBP1 promoter polymorphism with bipolar disorder in probands of European origin (2004) (55)
Association of nicotinic acetylcholine receptor subunit α4 polymorphisms with nicotine dependence in 5500 Germans (2009) (55)
Genetic polymorphisms of MPO, GSTT1, GSTM1, GSTP1, EPHX1 and NQO1 as risk factors of early‐onset lung cancer (2010) (53)
TBX21 gene variants increase childhood asthma risk in combination with HLX1 variants. (2009) (53)
Exploring beyond clinical routine SARS-CoV-2 serology using MultiCoV-Ab to evaluate endemic coronavirus cross-reactivity (2021) (52)
Associations between BMI and the FTO Gene Are Age Dependent: Results from the GINI and LISA Birth Cohort Studies up to Age 6 Years (2010) (52)
Polymorphisms related to ORMDL3 are associated with asthma susceptibility, alterations in transcriptional regulation of ORMDL3, and changes in TH2 cytokine levels. (2015) (51)
RANTES/CCL5 gene polymorphisms, serum concentrations, and incident type 2 diabetes: results from the MONICA/KORA Augsburg case-cohort study, 1984-2002. (2008) (50)
Multi-omic signature of body weight change: results from a population-based cohort study (2015) (50)
The CYP1B1_1358_GG genotype is associated with estrogen receptor-negative breast cancer (2008) (49)
DNA variants, plasma levels and variability of C-reactive protein in myocardial infarction survivors: results from the AIRGENE study. (2008) (49)
Modification of the Interleukin-6 Response to Air Pollution by Interleukin-6 and Fibrinogen Polymorphisms (2009) (49)
How to analyze many contingency tables simultaneously in genetic association studies (2012) (48)
Genome-Wide Association Study of L-Arginine and Dimethylarginines Reveals Novel Metabolic Pathway for Symmetric Dimethylarginine (2014) (48)
Molecular analysis of cataract families in India: new mutations in the CRYBB2 and GJA3 genes and rare polymorphisms (2010) (48)
Smoking Cessation and Variations in Nicotinic Acetylcholine Receptor Subunits α-5, α-3, and β-4 Genes (2009) (48)
SLC30A8 (ZnT8) Polymorphism is Associated with Young Age at Type 1 Diabetes Onset. (2008) (47)
Meta-analysis of two genome-wide association studies identifies four genetic loci associated with thyroid function. (2012) (46)
Air Pollution and Inflammatory Response in Myocardial Infarction Survivors: Gene–Environment Interactions in a High-Risk Group (2007) (45)
RANTES/CCL5 and Risk for Coronary Events: Results from the MONICA/KORA Augsburg Case-Cohort, Athero-Express and CARDIoGRAM Studies (2011) (45)
Pentanucleotide repeats at the spinocerebellar ataxia type 31 (SCA31) locus in Caucasians (2011) (45)
No Association Between the Putative Functional ZDHHC8 Single Nucleotide Polymorphism rs175174 and Schizophrenia in Large European Samples (2005) (45)
Whole blood microRNA levels associate with glycemic status and correlate with target mRNAs in pathways important to type 2 diabetes (2019) (45)
Unmasking Differential Effects of Rosiglitazone and Pioglitazone in the Combination Treatment with n-3 Fatty Acids in Mice Fed a High-Fat Diet (2011) (45)
Metabolite profiling reveals new insights into the regulation of serum urate in humans (2013) (44)
MALDI‐TOF MS and TaqMan® assisted SNP genotyping of DNA isolated from formalin‐fixed and paraffin‐embedded tissues (FFPET) (2005) (44)
Metformin Effect on Nontargeted Metabolite Profiles in Patients With Type 2 Diabetes and in Multiple Murine Tissues (2016) (44)
Rationale, design and objectives of ARegPKD, a European ARPKD registry study (2015) (44)
On metabolic reprogramming and tumor biology: A comprehensive survey of metabolism in breast cancer (2016) (44)
Spinocerebellar ataxia type 36 exists in diverse populations and can be caused by a short hexanucleotide GGCCTG repeat expansion (2014) (44)
Elder siblings enhance the effect of filaggrin mutations on childhood eczema: results from the 2 birth cohort studies LISAplus and GINIplus. (2010) (44)
A functional polymorphism within plasminogen activator urokinase (PLAU) is associated with Alzheimer's disease. (2006) (43)
The C718T polymorphism in the 3′-untranslated region of glutathione peroxidase-4 gene is a predictor of cerebral stroke in patients with essential hypertension (2012) (43)
Single nucleotide polymorphisms in Wnt signaling and cell death pathway genes and susceptibility to colorectal cancer. (2010) (43)
A Low-Frequency Inactivating AKT2 Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk (2017) (43)
Mutation analysis of the MCHR1 gene in human obesity. (2005) (42)
IL10 polymorphisms influence neonatal immune responses, atopic dermatitis, and wheeze at age 3 years. (2013) (42)
Acute-Phase Serum Amyloid A Protein and Its Implication in the Development of Type 2 Diabetes in the KORA S4/F4 Study (2013) (42)
IRF-1 gene variations influence IgE regulation and atopy. (2008) (42)
Fibrinogen genes modify the fibrinogen response to ambient particulate matter. (2009) (42)
Stability of targeted metabolite profiles of urine samples under different storage conditions (2016) (42)
Differentially expressed genes and canonical pathway expression in human atherosclerotic plaques – Tampere Vascular Study (2017) (42)
A novel GJA8 mutation causing a recessive triangular cataract (2008) (41)
Possible association between genetic variants at the GRIN1 gene and schizophrenia with lifetime history of depressive symptoms in a German sample (2007) (41)
Mapping the Genetic Architecture of Gene Regulation in Whole Blood (2014) (41)
The identification of pathogenic variants in BRCA1/2 negative, high risk, hereditary breast and/or ovarian cancer patients: High frequency of FANCM pathogenic variants (2019) (40)
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 (2012) (40)
Glucose substitution prolongs maintenance of energy homeostasis and lifespan of telomere dysfunctional mice (2014) (39)
Genetically determined variation in polyunsaturated fatty acid metabolism may result in different dietary requirements. (2008) (39)
A genome-wide association study reveals 2 new susceptibility loci for atopic dermatitis. (2015) (39)
Genetic factors in individual radiation sensitivity. (2014) (39)
Correction: Genome-Wide Association Scan Meta-Analysis Identifies Three Loci Influencing Adiposity and Fat Distribution (2009) (39)
Different FCER1A polymorphisms influence IgE levels in asthmatics and non‐asthmatics (2013) (38)
Original article: Polymorphisms in eosinophil pathway genes, asthma and atopy (2007) (38)
Calpain-10 variants and haplotypes are associated with polycystic ovary syndrome in Caucasians. (2007) (38)
Rare TLR2 mutations reduce TLR2 receptor function and can increase atopy risk (2009) (38)
Correction: The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study (2016) (37)
MMP-9 gene variants increase the risk for non-atopic asthma in children (2010) (37)
Analysis of the high affinity IgE receptor genes reveals epistatic effects of FCER1A variants on eczema risk (2009) (37)
Investigation of the DAOA/G30 locus in panic disorder (2005) (36)
Mutation screen in the GWAS derived obesity gene SH2B1 including functional analyses of detected variants (2012) (36)
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. (2008) (36)
A Variant In the Abo Gene Explains the Variation in Soluble E-Selectin Levels—Results from Dense Genotyping in Two Independent Populations (2012) (36)
Common variants in Mendelian kidney disease genes and their association with renal function. (2013) (35)
Association between variations in the TLR4 gene and incident type 2 diabetes is modified by the ratio of total cholesterol to HDL-cholesterol (2008) (35)
No evidence of association of FLJ10986 and ITPR2 with ALS in a large German cohort (2011) (35)
A Novel Polymorphism in the Promoter Region of ERBB4 Is Associated with Breast and Colorectal Cancer Risk (2007) (35)
Mutation analysis in a German family identified a new cataract-causing allele in the CRYBB2 gene (2007) (35)
Laboratory management of samples in biobanks: European consensus expert group report. (2010) (34)
Childhood asthma is associated with mutations and gene expression differences of ORMDL genes that can interact (2015) (34)
Genetic associations with lipoprotein subfractions provide information on their biological nature. (2012) (34)
Bayesian independent component analysis recovers pathway signatures from blood metabolomics data. (2012) (34)
Association of common variants identified by recent genome-wide association studies with obesity in Chinese children: a case-control study (2016) (33)
Deletion of Late Cornified Envelope 3B and 3C genes is not associated with atopic dermatitis. (2010) (33)
Possible gender-dependent association of vascular endothelial growth factor (VEGF) gene and ALS (2006) (33)
High-resolution SNP scan of chromosome 6p21 in pooled samples from patients with complex diseases. (2003) (33)
Improvement of myocardial infarction risk prediction via inflammation-associated metabolite biomarkers (2017) (33)
Filaggrin loss-of-function mutations and association with allergic diseases. (2008) (33)
Metabolomic profiles in individuals with negative affectivity and social inhibition: A population-based study of Type D personality (2013) (33)
Colorectal cancer and polymorphisms in DNA repair genes WRN, RMI1 and BLM. (2010) (32)
Increased amino acids levels and the risk of developing of hypertriglyceridemia in a 7-year follow-up (2014) (32)
Association of a MTNR1B gene variant with fasting glucose and HOMA-B in children and adolescents with high BMI-SDS. (2011) (32)
Decreased plasma phospholipid concentrations and increased acid sphingomyelinase activity are accurate biomarkers for community-acquired pneumonia (2019) (32)
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). (2006) (32)
MDS1 and EVI1 complex locus (MECOM): a novel candidate gene for hereditary hematological malignancies (2017) (31)
Regulation of TH17 markers early in life through maternal farm exposure. (2014) (31)
Asthma and IL-4 receptor alpha gene variants. (2002) (31)
Common variants in FCER1A influence total serum IgE levels from cord blood up to six years of life (2009) (31)
N-acetyltransferase 2, exposure to aromatic and heterocyclic amines, and receptor-defined breast cancer (2010) (31)
Novel genetic associations with serum level metabolites identified by phenotype set enrichment analyses. (2014) (30)
Lymphotoxin-α and galectin-2 SNPs are not associated with myocardial infarction in two different German populations (2007) (30)
The WST survival assay: an easy and reliable method to screen radiation-sensitive individuals. (2011) (30)
Genetic variation in the vaspin gene affects circulating serum vaspin concentrations (2013) (30)
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. (2007) (29)
Mitochondrial DNA Variants in Obesity (2014) (29)
Disentangling the genetics of lean mass. (2019) (28)
Impaired immune response mediated by prostaglandin E2 promotes severe COVID-19 disease (2021) (28)
Genome-Wide Association Study Identifies Two Novel Regions at 11p15.5-p13 and 1p31 with Major Impact on Acute-Phase Serum Amyloid A (2010) (28)
Fine‐mapping of IgE‐associated loci 1q23, 5q31, and 12q13 using 1000 Genomes Project data (2014) (28)
Strong associations of psoriasis with antigen processing LMP and transport genes TAP differ by gender and phenotype (2007) (28)
Genome-wide and gene-centric analyses of circulating myeloperoxidase levels in the charge and care consortia. (2013) (28)
Low‐risk variants FGFR2, TNRC9 and LSP1 in German familial breast cancer patients (2010) (28)
Identification and MS-assisted interpretation of genetically influenced NMR signals in human plasma (2013) (28)
Common variation in the ADAM8 gene affects serum sADAM8 concentrations and the risk of myocardial infarction in two independent cohorts. (2011) (28)
Metabolomics reveals determinants of weight loss during lifestyle intervention in obese children (2013) (27)
Genetics of type 2 diabetes: impact of interleukin-6 gene variants. (2005) (27)
Genetic variation influencing DNA methylation provides insights into molecular mechanisms regulating genomic function (2022) (27)
CXCR1 and CXCR2 haplotypes synergistically modulate cystic fibrosis lung disease (2011) (27)
Plasma Metabolomics Reveal Alterations of Sphingo- and Glycerophospholipid Levels in Non-Diabetic Carriers of the Transcription Factor 7-Like 2 Polymorphism rs7903146 (2013) (27)
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. (2014) (27)
Genetic variation in CRTh2 influences development of allergic phenotypes (2009) (27)
A unique genetic defect on chromosome 3 is responsible for juvenile obesity in the Berlin Fat Mouse (2010) (26)
Undiagnosed Diabetes Mellitus in Community-Acquired Pneumonia: A Prospective Cohort Study (2017) (26)
IL-6 promoter polymorphisms and quantitative traits related to the metabolic syndrome in KORA S4 (2006) (26)
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 (2015) (26)
HLX1 gene variants influence the development of childhood asthma. (2009) (26)
Predicting sudden cardiac death using common genetic risk variants for coronary artery disease. (2015) (26)
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 (2007) (25)
Sequence data and association statistics from 12,940 type 2 diabetes cases and controls (2017) (25)
Associations between thyroid hormones and serum metabolite profiles in an euthyroid population (2013) (25)
SDCCAG8 Obesity Alleles and Reduced Weight Loss After a Lifestyle Intervention in Overweight Children and Adolescents (2012) (25)
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 (2015) (25)
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. (2013) (25)
N-acetyltransferase 2 Phenotype, Occupation, and Bladder Cancer Risk: Results from the EPIC Cohort (2013) (25)
Evidence for a Pathogenic Role of Different Mutations at Codon 188 of PRNP (2008) (25)
Talin and vinculin are downregulated in atherosclerotic plaque; Tampere Vascular Study. (2016) (25)
Polymorphic loci of E2F2, CCND1 and CCND3 are associated with HER2 status of breast tumors (2009) (24)
Comparison of metabolic profiles of acutely ill and short-term weight recovered patients with anorexia nervosa reveals alterations of 33 out of 163 metabolites. (2012) (24)
Non-replication of an association of CTNNBL1 polymorphisms and obesity in a population of Central European ancestry (2009) (23)
Association of variants in gastric inhibitory polypeptide receptor gene with impaired glucose homeostasis in obese children and adolescents from Berlin. (2010) (23)
Association of a variant in the muscarinic acetylcholine receptor 2 gene (CHRM2) with nicotine addiction (2010) (23)
Changes in metabolite profiles caused by genetically determined obesity in mice (2013) (23)
Replication study of multiple sclerosis (MS) susceptibility alleles and correlation of DNA-variants with disease features in a cohort of Austrian MS patients (2012) (23)
Genetic variants of the FADS gene cluster are associated with erythrocyte membrane LC PUFA levels in patients with mild cognitive impairment (2016) (23)
High-throughput DNA methylation analysis in anorexia nervosa confirms TNXB hypermethylation (2018) (23)
Alcohol consumption, alcohol dehydrogenase and risk of coronary heart disease in the MONICA/KORA-Augsburg cohort 1994/1995-2002 (2007) (23)
Multicentric investigation of ionising radiation-induced cell death as a predictive parameter of individual radiosensitivity (2009) (23)
The KORA Eye Study: a population-based study on eye diseases in Southern Germany (KORA F4). (2011) (23)
Weak independent association signals between IDE polymorphisms, Alzheimer's disease and cognitive measures (2007) (23)
Wnt status-dependent oncogenic role of BCL9 and BCL9L in hepatocellular carcinoma (2019) (23)
Association of prostaglandin E synthase 2 (PTGES2) Arg298His polymorphism with type 2 diabetes in two German study populations. (2007) (22)
Further support for the association of CCR5 allelic variants with asthma susceptibility. (2002) (22)
Upstream Transcription Factor 1 (USF1) allelic variants regulate lipoprotein metabolism in women and USF1 expression in atherosclerotic plaque (2014) (22)
STAT1 gene variations, IgE regulation and atopy (2007) (22)
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. (2015) (22)
Early onset lung cancer, cigarette smoking and the SNP309 of the murine double minute-2 (MDM2) gene (2008) (22)
Gastric inhibitory polypeptide receptor: association analyses for obesity of several polymorphisms in large study groups (2009) (22)
The effect of BDNF gene variants on asthma in German children (2009) (21)
Monocyte‐derived dendritic cells from highly atopic individuals are not impaired in their pro‐inflammatory response to toll‐like receptor ligands (2006) (21)
Genetics of asthma and related phenotypes. (2002) (21)
Serum metabolomic profiling highlights pathways associated with liver fat content in a general population sample (2017) (21)
Mutation screen and association studies for the fatty acid amide hydrolase (FAAH) gene and early onset and adult obesity (2010) (21)
Erratum: New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk (Nature Genetics (2010) 42 (105-116)) (2010) (20)
Diagnosis of monogenic liver diseases in childhood by next‐generation sequencing (2018) (20)
Comparative analysis of plasma metabolomics response to metabolic challenge tests in healthy subjects and influence of the FTO obesity risk allele (2014) (20)
Genetic variation in TLR pathway and the risk of pulmonary tuberculosis in a Moldavian population. (2019) (20)
Genome-Wide Association Study Pinpoints a New Functional Apolipoprotein B Variant Influencing Oxidized Low-Density Lipoprotein Levels But Not Cardiovascular Events: AtheroRemo Consortium (2013) (19)
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 (2013) (18)
Genetic variation in Fcγ receptor IIa and risk of coronary heart disease: negative results from two large independent populations (2009) (18)
Detection of ATM gene mutations in young lung cancer patients: a population-based control study. (2008) (18)
Association analysis of genes involved in cholesterol metabolism located within the linkage region on chromosome 10 and Alzheimer’s disease (2004) (18)
Estimating the single nucleotide polymorphism genotype misclassification from routine double measurements in a large epidemiologic sample. (2008) (18)
Interrogating causal pathways linking genetic variants, small molecule metabolites, and circulating lipids (2014) (18)
Differentially expressed genes and canonical pathways in the ascending thoracic aortic aneurysm – The Tampere Vascular Study (2017) (18)
Gene-Gene Interaction between APOA5 and USF1: Two Candidate Genes for the Metabolic Syndrome (2009) (18)
Activated immune-inflammatory pathways are associated with long-standing depressive symptoms: Evidence from gene-set enrichment analyses in the Young Finns Study. (2015) (18)
Genetic Variation in Glutathione S-Transferase Genes and Risk of Nonfatal Cerebral Stroke in Patients Suffering from Essential Hypertension (2012) (17)
Polymorphisms in inflammatory pathway genes and their association with colorectal cancer risk (2010) (17)
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. (2016) (17)
Motivations for (non)participation in population-based health studies among the elderly – comparison of participants and nonparticipants of a prospective study on influenza vaccination (2017) (17)
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. (2011) (17)
Variants in COMT and spontaneous smoking cessation: retrospective cohort analysis of 925 cessation events. (2009) (17)
No association of two functional polymorphisms in human ALOX15 with myocardial infarction. (2009) (17)
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. (2013) (17)
Association study between variants in the fibrinogen gene cluster, fibrinogen levels and hypertension: Results from the MONICA/ KORA study (2009) (16)
The ATGL gene is associated with free fatty acids, triglycerides and type 2 diabetes (2006) (16)
Expression and regulation of interferon-related development regulator-1 in cystic fibrosis neutrophils. (2013) (16)
Synergistic Expression of Histone Deacetylase 9 and Matrix Metalloproteinase 12 in M4 Macrophages in Advanced Carotid Plaques. (2017) (16)
Variation of the N-Acetyltransferase 2 Gene in a Romanian and a Kyrgyz Population (2006) (16)
How to link call rate and p‐values for Hardy–Weinberg equilibrium as measures of genome‐wide SNP data quality (2010) (16)
Antioxidant Defense Enzyme Genes and Asthma Susceptibility: Gender-Specific Effects and Heterogeneity in Gene-Gene Interactions between Pathogenetic Variants of the Disease (2014) (16)
Current practices for access, compensation, and prioritization in biobanks. Results from an interview study (2018) (15)
Genetic variants in Protocadherin‐1, bronchial hyper‐responsiveness, and asthma subphenotypes in German children (2012) (15)
Corrigendum: Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis (2011) (15)
A comprehensive analysis of the COL29A1 gene does not support a role in eczema. (2011) (15)
Further Genetic Heterogeneity for Autosomal Dominant Human Sutural Cataracts (2003) (15)
First investigation of two obesity-related loci (TMEM18, FTO) concerning their association with educational level as well as income: the MONICA/KORA study (2010) (15)
Evidence for the Thr79Met polymorphism of the ileal fatty acid binding protein (FABP6) to be associated with type 2 diabetes in obese individuals. (2009) (14)
Night Shift Work Affects Urine Metabolite Profiles of Nurses with Early Chronotype (2018) (14)
Association of acyl-CoA-binding protein (ACBP) single nucleotide polymorphisms and type 2 diabetes in two German study populations. (2007) (14)
Association study between genetic variants at the PIP5K2A gene locus and schizophrenia and bipolar affective disorder (2006) (14)
Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention (2022) (14)
Association of humoral immunity to human Hsp60 with the IL-6 gene polymorphism C-174G in patients with type 2 diabetes and controls. (2005) (14)
No impact of obesity susceptibility loci on weight regain after a lifestyle intervention in overweight children (2013) (14)
HHEX-IDE polymorphism is associated with low birth weight in offspring with a family history of type 1 diabetes. (2009) (14)
Rare compound heterozygous variants in PNKP identified by whole exome sequencing in a German patient with ataxia‐oculomotor apraxia 4 and pilocytic astrocytoma (2018) (14)
A common atopy‐associated variant in the Th2 cytokine locus control region impacts transcriptional regulation and alters SMAD3 and SP1 binding (2014) (13)
Long-term health sequelae and quality of life at least 6 months after infection with SARS-CoV-2: design and rationale of the COVIDOM-study as part of the NAPKON population-based cohort platform (POP) (2021) (13)
No association between the serine racemase gene (SRR) and schizophrenia in a German case-control sample. (2007) (13)
The GJA8 allele encoding CX50I247M is a rare polymorphism, not a cataract-causing mutation (2009) (13)
New susceptibility loci for severe COVID-19 by detailed GWAS analysis in European populations (2021) (13)
Genome-wide association study identifies novel restless legs syndrome susceptibility loci on 2 p 14 and 16 q 12 . 1 (2017) (13)
Detailed stratified GWAS analysis for severe COVID-19 in four European populations (2022) (13)
BMI at Age 8 Years Is Influenced by the Type 2 Diabetes Susceptibility Genes HHEX-IDE and CDKAL1 (2010) (13)
Genetic variants harbored in the forkhead box protein 3 locus increase hay fever risk. (2010) (13)
MTTP variants and body mass index, waist circumference and serum cholesterol level: Association analyses in 7582 participants of the KORA study cohort. (2008) (12)
Genome-wide association study identifies a new locus for coronary artery disease on chromosome 10 p 11 . 23 (2010) (12)
Genetic Variation in the Epidermal Transglutaminase Genes Is Not Associated with Atopic Dermatitis (2012) (12)
Genetic variation in TH17 pathway genes, childhood asthma, and total serum IgE levels. (2014) (12)
Association of genetic variation in KCNQ1 with type 2 diabetes in the KORA surveys. (2010) (12)
SARS-CoV-2 seroprevalence in Germany - a population based sequential study in five regions (2021) (12)
No association between genetic variants at the ASCT1 gene and schizophrenia or bipolar disorder in a German sample. (2006) (12)
Gene variants of monocyte chemoattractant protein 1 and components of metabolic syndrome in KORA S4, Augsburg. (2007) (12)
A tandem duplication of BRCA1 exons 1–19 through DHX8 exon 2 in four families with hereditary breast and ovarian cancer syndrome (2018) (12)
Look beyond one's own nose: combination of information from publicly available sources reveals an association of GATA4 polymorphisms with plasma triglycerides. (2011) (11)
Genetic predisposition to an adverse lipid profile limits the improvement in total cholesterol in response to weight loss (2013) (11)
CX3CR1 Polymorphisms Are Associated with Atopy but Not Asthma in German Children (2007) (11)
Genetic association between obstructive bronchitis and enzymes of oxidative stress. (2012) (11)
Determination of nasal and oropharyngeal microbiomes in a multicenter population-based study – findings from Pretest 1 of the German National Cohort (2017) (11)
Gene Set of Nuclear-Encoded Mitochondrial Regulators Is Enriched for Common Inherited Variation in Obesity (2013) (11)
Discrimination of SARS-CoV-2 Infections From Other Viral Respiratory Infections by Scent Detection Dogs (2021) (11)
Fatty liver is associated with blood pathways of inflammatory response, immune system activation and prothrombotic state in Young Finns Study (2018) (10)
NCAM2 deletion in a boy with macrocephaly and autism: Cause, association or predisposition? (2016) (10)
Polymorphisms in MUC1, MUC2, MUC5B and MUC6 genes are not associated with the risk of chronic atrophic gastritis. (2012) (9)
A common FADS 2 promoter polymorphism increases promoter activity and facilitates binding of transcription factor ELK 1 (2009) (9)
Dopamine-related genes and spontaneous smoking cessation in ever-heavy smokers. (2011) (9)
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 (2014) (9)
The Pharmacogenetic Footprint of ACE Inhibition: A Population-Based Metabolomics Study (2016) (9)
Optical genome mapping identifies rare structural variations as predisposition factors associated with severe COVID-19 (2022) (9)
No association between genetic variants at the GRIN1 gene and bipolar disorder in a German sample. (2006) (9)
Sex Dependency of Human Metabolic Profiles Revisited (2012) (9)
Fine Mapping of a GWAS-Derived Obesity Candidate Region on Chromosome 16p11.2 (2015) (9)
Diagnosing Fatty Liver Disease: A Comparative Evaluation of Metabolic Markers, Phenotypes, Genotypes and Established Biomarkers (2013) (9)
Genetic variation in the Toll-like receptor signaling pathway is associated with childhood asthma. (2013) (9)
Breast cancer patients suggestive of Li-Fraumeni syndrome: mutational spectrum, candidate genes, and unexplained heredity (2018) (9)
Correction: Genome-Wide Association Study Identifies Novel Restless Legs Syndrome Susceptibility Loci on 2p14 and 16q12.1 (2011) (9)
Going beyond clinical routine in SARS-CoV-2 antibody testing - A multiplex corona virus antibody test for the evaluation of cross-reactivity to endemic coronavirus antigens (2020) (8)
Feasibility and quality development of biomaterials in the pretest studies of the German National Cohort (2014) (8)
Using genome-Wwide complex trait analysis to quantify 'missing heritability' in Parkinson's disease (2012) (8)
Children and Adolescents’ Behavioral Patterns in Response to Escalating COVID-19 Restriction Reveal Sex and Age Differences (2021) (8)
PLA1A2 platelet polymorphism predicts mortality in prediabetic subjects of the population based KORA S4-Cohort (2014) (8)
Association between Single Nucleotide Polymorphisms and Weight Reduction in Behavioural Interventions—A Pooled Analysis (2021) (8)
GT198 (PSMC3IP) germline variants in early-onset breast cancer patients from hereditary breast and ovarian cancer families (2017) (8)
[Centralized biobanks: a basis for medical research]. (2016) (8)
The fatal trajectory of pulmonary COVID-19 is driven by lobular ischemia and fibrotic remodelling (2022) (8)
Erratum: Large meta-analysis of genome-wide association studies identifies five loci for lean body mass (2017) (8)
No association between genetic variants at the GLYT2 gene and bipolar affective disorder and schizophrenia. (2006) (7)
Response to Comment on Xu et al. Effects of Metformin on Metabolite Profiles and LDL Cholesterol in Patients With Type 2 Diabetes. Diabetes Care 2015;38:1858–1867 (2015) (7)
Polymorphisms in the IRF‐4 gene, asthma and recurrent bronchitis in children (2013) (7)
Association analysis between the prostaglandin E synthase 2 R298H polymorphism and body mass index in 8079 participants of the KORA study cohort. (2009) (7)
Response to Comments on "A Common Genetic Variant Is Associated with Adult and Childhood Obesity" (2007) (7)
MTF1 binds to metal‐responsive element e within the ATP7B promoter and is a strong candidate in regulating the ATP7B expression (2020) (7)
Functional classification of RUNX1 variants in familial platelet disorder with associated myeloid malignancies (2021) (7)
Quality Assessment of the Preanalytical Workflow in Liquid Biobanking: Taurine as a Serum-Specific Quality Indicator for Preanalytical Process Variations. (2019) (7)
No evidence for an association between variants at the ??-amino-n-butyric acid type A receptor ??2 locus and schizophrenia (2007) (7)
Self-reported diabetes and herpes zoster are associated with a weak humoral response to the seasonal influenza A H1N1 vaccine antigen among the elderly (2019) (6)
The German National Pandemic Cohort Network (NAPKON): rationale, study design and baseline characteristics (2022) (6)
Lack of association between neuropeptide S receptor 1 gene (NPSR1) and eczema in five European populations. (2008) (6)
Erratum: Large-scale gene-centric meta-analysis across 39 studies identifies type 2 diabetes loci (American Journal of Human Genetics (2012) 90 (410-425)) (2012) (6)
Polymorphisms in the receptor for GDNF (RET) are not associated with Parkinson's disease in Southern Germany (2010) (6)
Lack of Association of Delta-Aminolevulinate Dehydratase Polymorphisms with Blood Lead Levels and Hemoglobin in Romanian Women from a Lead-Contaminated Region (2008) (6)
Haplotype Misclassification Resulting from Statistical Reconstruction and Genotype Error, and Its Impact on Association Estimates (2010) (6)
12q14 microdeletion syndrome: A family with short stature and Silver-Russell syndrome (SRS)-like phenotype and review of the literature. (2018) (6)
Observational study on variability between biobanks in the estimation of DNA concentration (2009) (6)
Genetic variants in the Upstream Stimulatory Factor 1 (USF1) gene are associated with LDL cholesterol levels and incident T2DM in women: Results from the MONICA/KORA Augsburg case-cohort study, 1984-2002 (2008) (5)
Transcriptional and Mutational Profiling of B-Other Acute Lymphoblastic Leukemia for Improved Diagnostics (2021) (5)
The gender-specific association of the putative fructose transporter SLC2A9 variants with uric acid levels is modified by BMI (2008) (5)
Comparative Magnitude and Persistence of Humoral SARS-CoV-2 Vaccination Responses in the Adult Population in Germany (2022) (5)
Homozygous frame shift variant in ATP7B exon 1 leads to bypass of nonsense-mediated mRNA decay and to a protein capable of copper export (2019) (5)
PedCAPNETZ – prospective observational study on community acquired pneumonia in children and adolescents (2019) (5)
Establishment of a cohort for deep phenotyping of the immune response to influenza vaccination among elderly individuals recruited from the general population (2017) (5)
No SARS-CoV-2 detection in the German CAPNETZ cohort of community acquired pneumonia before COVID-19 peak in March 2020 (2020) (5)
Genetic Variation in CRTh2 Influences Development of Allergy (2008) (4)
Genetic variants in the GATA3 gene are not associated with asthma and atopic diseases in German children. (2009) (4)
Canine real-time detection of SARS-CoV-2 infections in the context of a mass screening event (2022) (4)
Metabolomic Signature of Coronary Artery Disease in Type 2 Diabetes Mellitus (2017) (4)
IL15 gene variants are not associated with asthma and atopy (2009) (4)
Smokers with COPD Show a Shift in Energy and Nitrogen Metabolism at Rest and During Exercise (2020) (4)
Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls (2018) (4)
Blood cis-eQTL Analysis Fails to Identify Novel Association Signals among Sub-Threshold Candidates from Genome-Wide Association Studies in Restless Legs Syndrome (2014) (4)
[The BSD Health Study: a pilot study to examine the comparability of Bavarian blood donors with the Bavarian general population by a comparison with KORA S4]. (2009) (4)
[How about the uncertainty in the haplotypes in the population-based KORA studies?]. (2005) (4)
Rational therapy with vigabatrin and a ketogenic diet in a patient with GAD1 deficiency. (2020) (4)
Validation and clinical application of transactivation assays for RUNX1 variant classification (2022) (3)
Association between functional FABP2 promoter haplotypes and body mass index: analyses of 8072 participants of the KORA cohort study. (2009) (3)
MicroRNA‐192‐5p inhibits migration of triple negative breast cancer cells and directly regulates Rho GTPase activating protein 19 (2021) (3)
Supplementary Material 3 (2015) (3)
Synergistic effect of genetic polymorphisms in TLR6 and TLR10 genes on the risk of pulmonary tuberculosis in a Moldavian population (2020) (3)
The European Nutrigenomics Organisation (2009) (3)
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). (2007) (3)
A comparison of curated gene sets versus transcriptomics-derived gene signatures for detecting pathway activation in immune cells (2020) (3)
Discovery of mitochondrial DNA variants associated with genome-wide blood cell gene expression: a population-based mtDNA sequencing study. (2019) (3)
Discovery and functional prioritization of Parkinson’s disease candidate genes from large-scale whole exome sequencing (2017) (3)
Do Common Variants Separate between Obese Melanocortin-4 Receptor Gene Mutation Carriers and Non-Carriers? The Impact of Cryptic Relatedness (2012) (3)
DNA repair gene polymorphisms and risk of chronic atrophic gastritis: a case-control study (2011) (3)
Supplementary Material 5 (2014) (3)
Supplementary Material 6 (2014) (3)
Copy Number Analysis in a Large Cohort Suggestive of Inborn Errors of Immunity Indicates a Wide Spectrum of Relevant Chromosomal Losses and Gains (2022) (3)
The transplant cohort of the German center for infection research (DZIF Tx-Cohort): study design and baseline characteristics (2021) (3)
Large meta-analysis of genome-wide association studies identifies five loci for lean body mass (2017) (3)
Supplementary Material 7 (2014) (3)
Blood pathway analyses reveal differences between prediabetic subjects with or without dyslipidaemia. The Cardiovascular Risk in Young Finns Study (2017) (3)
Supportive evidence for a relationship between genetic variants at the brain-derived neurotrophic factor (BDNF) locus and depressive symptoms in affective disorder and schizophrenia (2004) (3)
Further delineation of the association signal on chromosome 5 from the first whole genome association study in Parkinson's disease (2009) (2)
No evidence for an association between variants at the gamma-amino-n-butyric acid type A receptor beta2 locus and schizophrenia. (2007) (2)
Positional cloning of susceptibility genes for atopic dermatitis in the epidermal differentiation complex (2007) (2)
Sample selection algorithm to improve quality of genotyping from plasma‐derived DNA: to separate the wheat from the chaff (2007) (2)
University of Groningen Physical Activity Attenuates the Influence of FTO Variants on Obesity Risk (2011) (2)
Analysis of the individual and aggregate genetic contributions of previously identified SPINK 5 , KLK 7 and FLG polymorphisms to eczema risk (2015) (2)
22nd European Congress on Obesity (ECO2015), Prague, Czech Republic, May 6-9, 2015: Abstracts (2015) (2)
Characterization of whole-genome autosomal differences of DNA methylation between men and women (2015) (2)
SARS-CoV-2-induced impaired immune response by Prostaglandin E2 is accelerated by age, male sex and air pollution (2020) (2)
Ethics Reporting in Biospecimen and Genetic Research: Current Practice and Suggestions for Changes (2016) (2)
Gene-Gene Interaction between textitAPOA5 and textitUSF1: Two Candidate Genes for the Metabolic Syndrome (2009) (2)
An association between a variation in the PSCA gene and upper gastrointestinal cancer in Caucasians (2011) (2)
Abstract 1879: 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 (2009) (2)
Plasma markers of COVID-19 severity: a pilot study (2022) (2)
Somatic Mutations and Inborn Variants in Exon 12 of ASXL1 in Different Myeloid Neoplasms (2011) (2)
Unbalanced translocation der(5;17) resulting in a TP53 loss as recurrent aberration in myelodysplastic syndrome and acute myeloid leukemia with complex karyotype (2021) (2)
Network-based SNP meta-analysis identifies joint and disjoint genetic features across common human diseases (2012) (2)
Correction: Evidence for a Pathogenic Role of Different Mutations at Codon 188 of PRNP (2008) (2)
Ago-RIP Sequencing Identifies New MicroRNA-449a-5p Target Genes Increasing Sorafenib Efficacy in Hepatocellular Carcinoma (2022) (2)
MiR-129-5p exerts Wnt signaling-dependent tumor-suppressive functions in hepatocellular carcinoma by directly targeting hepatoma-derived growth factor HDGF (2022) (2)
Are further genetic factors associated with the risk of developing variant Creutzfeldt–Jakob disease? (2009) (2)
Consumption of Green Vegetables, GSTM1 Genotype and the Association of Air Pollution with Inflammatory Responses (2009) (1)
Reprogramming of Amino Acid Metabolism Differs between Community-Acquired Pneumonia and Infection-Associated Exacerbation of Chronic Obstructive Pulmonary Disease (2022) (1)
Stability of targeted metabolite profiles of urine samples under different storage conditions (2016) (1)
Polymorphisms in extracellular signal-regulated kinase family influence genetic susceptibility to asthma. (2013) (1)
Are metabolomic markers associated with spirometric lung function indices? Results of the KORAF4 Study (2013) (1)
Abstract 1808: Duffy Antigen Receptor for Chemokines (Darc) Polymorphism Regulates Circulating Concentrations of Monocyte Chemoattractant Protein-1 and Other Circulating Inflammatory Mediators (2009) (1)
Distinct immunological and molecular signatures underpinning influenza vaccine responsiveness in the elderly (2022) (1)
Interrogating causal pathways linking genetic variants, small molecule metabolites, and circulating lipids (2014) (1)
The Hannover Unified Biobank (HUB) – Centralized Standardised Biobanking at Hannover Medical School (2021) (1)
No association between the serine racemase gene (SRR) and bipolar disorder in a German case-control sample. (2007) (1)
A Common Single Nucleotide Polymorphism in the Chromosome 7q22.3 Region, Which Is Frequently Deleted in Myeloid Malignancies, Is Associated with Mean Platelet Volume and Platelet Function in Healthy Individuals (2008) (1)
Supplementary Material 4 (2015) (1)
Supplementary Material 15 (2013) (1)
ORMDL3 haplotype is associated with asthma in an italian familial collection (2009) (1)
The SLC30A8 gene polymorphism R325W can stratify type 1 diabetes risk among ZnT8 autoantibody positive children (2009) (1)
Discovery and Refinement Supplementary (2015) (1)
Polymorphisms in the proteasomal subunit alpha4 are not associated with Parkinson's disease (2008) (1)
Pathogen spectra in hospitalised and nonhospitalised children with community-acquired pneumonia (2022) (1)
Clinical studies in CKD (2012) (1)
AREGPKD - A European ARPKD Registry Study (2015) (1)
Supplementary Material 9 (2013) (1)
Breast cancer risk is linked with ERCC2 genotypes and a corresponding haplotype in a German population (2005) (1)
Case-control study of genetic susceptibility in early onset lung cancer: Investigation of Matrix Metalloproteinase-1 (MMP1) (2008) (1)
Glutathione-S-transferase T1, M1 and P1 polymorphisms as risk factors for early onset lung cancer (2008) (1)
Abstract 2923: Association Mapping Of QT-interval In a 500k Genome-wide Scan: Confirmation Of NOS1AP And Identification Of A Spectrum Of Additional QTLs (2007) (1)
Human serum metabolic profiles are age dependent: Metabolic profiles associated with age (2012) (1)
Air Pollution and Inflammation: Gene-Environment Interactions in Myocardial Infarction Survivors (2009) (1)
Association between the vascular endothelial growth factor (VEGF) gene and amyotrophic lateral sclerosis (ALS): possible gender-dependent effect (2006) (1)
Genetic variation influencing DNA methylation provides insights into molecular mechanisms regulating genomic function (2022) (1)
Publisher Correction: Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability (2021) (1)
osteoarthritis ratio : a novel metabolomic biomarker of knee Serum branched-chain amino acid to histidine (2010) (1)
Loci influencing blood pressure identified using a cardiovascular gene-centric array (Correction to Ganesh et al. 22 (8): 1663) (2013) (1)
The role of adiposity in cardiometabolic traits (2013) (1)
Erratum: Meta-analysis of dense genecentric association studies reveals common and uncommon variants associated with height ((The American Journal of Human Genetics (2010) 88 (6-18)) (2012) (1)
IT-Systems for Biobanking - A brief Overview (2014) (1)
Altered and allele-specific open chromatin landscape reveals epigenetic and genetic regulators of innate immunity in COVID-19 (2022) (1)
Identification and MS-assisted interpretation of genetically influenced NMR signals in human plasma (2013) (1)
Network-based SNP meta-analysis identifies joint and disjoint genetic features across common human diseases (2012) (0)
P192 SERUM URIC ACID, BUT NOT RS7442295 POLYMORPHISM OF SCL2A9 GENE, PREDICTS TOTAL AND CARDIOVASCULAR MORTALITY IN SEVERE CORONARY ARTERY DISEASE (2010) (0)
MiR-129-5p exerts Wnt signaling-dependent tumor-suppressive functions in hepatocellular carcinoma by directly targeting hepatoma-derived growth factor HDGF (2022) (0)
ANovel Polymorphism in the Promoter Region of ERBB4 Is Associated with Breast and Colorectal Cancer Risk (2007) (0)
Associations between thyroid hormones and serum metabolite profiles in an euthyroid population (2013) (0)
Distinct profiles and kinetics of soluble inflammatory markers in patients with acute and chronic HCV-infections and SARS-CoV-2-infections: Implications for the long-term consequences of viral infections? (2023) (0)
Comparative analysis of plasma metabolomics response to metabolic challenge tests in healthy subjects and influence of the FTO obesity risk allele (2013) (0)
Contents Vol. 77, 2012 (2012) (0)
O3-02-02 The chromosome 10 locus and AD: recent progress of the German national genome network initiative (2004) (0)
University of Groningen Gene-centric meta-analysis in 87,736 individuals of European ancestry identifies multiple blood-pressure-related loci Tragante, (2014) (0)
Plasma Metabolome Signature Indicative of BRCA1 Germline Status Independent of Cancer Incidence (2021) (0)
Replication study of multiple sclerosis (MS) susceptibility alleles and correlation of DNA-variants with disease features in a cohort of Austrian MS patients (2012) (0)
Supplementary Table S16 (2012) (0)
Supplemental Human Genetics Point of View. (2019) (0)
Distribution of characteristics of the study population (n = 3,000) by PTSD status. (2013) (0)
Explorer Novel association to the proprotein convertase PCSK 7 gene locus revealed by analysing soluble transferrin receptor ( sTfR ) levels (2018) (0)
Fatty liver is associated with blood pathways of inflammatory response, immune system activation and prothrombotic state in Young Finns Study (2018) (0)
' s response to reviews Title : Multi-omic signature of body weight change : results from a population-based cohort study (2014) (0)
A comparison of curated gene sets versus transcriptomics-derived gene signatures for detecting pathway activation in immune cells (2020) (0)
Identification of treatment predictive markers for breast cancer patients with chemotherapy (2005) (0)
Biobanking, Ethics, and Relevant Legal Issues (2018) (0)
ASSOCIATION OF GENE TRL2 POLYMORPHISM WITH PULMONARY TUBERCULOSIS IN THE POPULATION OF MOLDOVA (2018) (0)
Genetic variations in the TLR signaling pathway are associated with childhood asthma (2012) (0)
Mutation screen in the GWAS derived obesity gene SH2B1including functional analyses of detected variants (2012) (0)
The role of MEIS1, BTBD9 and MAP2K5/LBXCOR1 in uraemic RLS – a case-control study in patients with end stage renal disease on maintenance hemodialysis (2008) (0)
Characterisation of Gene Variations in the Transcription Factors T-bet and HLX1 and their Functional Role in the Development of Asthma (2008) (0)
Serum uric acid, but not rs7442295 polymorphism of SCL2A9 gene, predicts total and cardiovascular mortality in severe coronary artery disease. (2011) (0)
Errata (2011) (0)
Advanced biobanking and good management (2013) (0)
Metabolomics and Molecular Imaging in the Post-genomic Era (2017) (0)
Current practices for access, compensation, and prioritization in biobanks. Results from an interview study (2018) (0)
Differentially expressed genes and canonical pathways in the ascending thoracic aortic aneurysm – The Tampere Vascular Study (2017) (0)
Mendelian Randomization Studies of the Role of Biomarkers in Type 2 Diabetes (2009) (0)
Genetic polymorphisms of myeloperoxidase (MPO), epoxide hydrolase 1 (EPHX1) and NAD(P)H dehydrogenase 1 (NQO1) as risk factors of early onset lung caner (2008) (0)
002 IDENTIFICATION OF A NOVEL HTRA1-SUSCEPTIBLE CLEAVAGE SITE IN HUMAN AGGRECAN: EVIDENCE FOR THE INVOLVEMENT OF HTRA1 IN AGGRECAN PROTEOLYSIS IN VIVO (2009) (0)
GBA/GBN-position on the feedback of incidental findings in biobank-based research: consensus-based workflow for hospital-based biobanks. (2023) (0)
Characterization of potential risk markers of the renal ARPKD Phenotype (2017) (0)
Changes in metabolite profiles caused by genetically determined obesity in mice (2013) (0)
COPD_A_217474 1..13 (2020) (0)
Metabolomics reveals determinants of weight loss during lifestyle intervention in obese children (2013) (0)
PS1326 IMPLEMENTATION OF FUNCTIONAL ASSAYS TO CHARACTERIZE AND DETERMINE THE CLINICAL IMPACT OF RUNX1 VARIANTS OF UNCERTAIN SIGNIFICANCE IN SPORADIC DISEASES AS WELL AS IN THE CONTEXT OF FPDMM (2019) (0)
Genetic Variation in Glutathione S-Transferase Genes and Risk of Nonfatal Cerebral Stroke in Patients Suffering from Essential Hypertension (2012) (0)
DZL-Platform Biobanking (2014) (0)
Two Gja8 Mutations: An Insertion Causing a Recessive Triangular Cataract, and a Rare Polymorphism (2008) (0)
Decreased plasma phospholipid concentrations and increased acid sphingomyelinase activity are accurate biomarkers for community-acquired pneumonia (2019) (0)
001 NOVEL BIOMARKERS OF KNEE OSTEOARTHRITIS IDENTIFIED USING METABOLIC PROFILING (2009) (0)
AIRGENE - AIR POLLUTION AND INFLAMMATORY RESPONSE IN MYOCARDIAL INFARCTION SURVIVORS: GENE-ENVIRONMENT INTERACTION IN A HIGH RISK GROUP (2005) (0)
Genome-wide association and functional follow-up reveals new loci for kidney function | NOVA. The University of Newcastle's Digital Repository (2012) (0)
Determination of nasal and oropharyngeal microbiomes in a multicenter population-based study – findings from Pretest 1 of the German National Cohort (2017) (0)
Edinburgh Research Explorer Large meta-analysis of genome-wide association studies identifies five loci for lean body mass (2018) (0)
Genetic Predisposition to Neurological Complications in Patients with COVID-19 (2023) (0)
Running title: Pfeiffer et al.; genome-wide DNA methylation and blood lipid levels (2015) (0)
Genome-wide association study reveals new risk variants for atopic dermatitis on chromosome 11 and in the epidermal differentiation complex (EDC) on chromosome 1q21 (2009) (0)
Melanocortin-4-receptor gene variants: hotspot or identical by descent? (2009) (0)
Abstract 17304: Dense Genotyping of Candidate Gene Loci Identifies Variants Associated with Soluble E-Selectin Levels (2011) (0)
Breast cancer patients suggestive of Li-Fraumeni syndrome: mutational spectrum, candidate genes, and unexplained heredity (2018) (0)
Functional characterization of a JAG1 5'UTR variant in a patient with clinically observed Alagille syndrome (2022) (0)
Association study between the D10S1423 microsatellite marker and Alzheimer's disease (2006) (0)
Association of FcER1A and RAD50 polymorphisms with serum IgE levels, asthma and rhinitis (2009) (0)
Whole blood microRNA levels associate with glycemic status and correlate with target mRNAs in pathways important to type 2 diabetes (2019) (0)
Review Process File (2012) (0)
Polymorphisms in all three ORMDL genes are associated with asthma and their mRNA expression is increased in asthmatics (2014) (0)
P305: COMPREHENSIVE TRANSCRIPTIONAL AND CYTOGENETIC PROFILING IMPROVES CLASSIFICATION AND DETECTION OF RISK-STRATIFYING MARKERS IN THE B-OTHER PEDIATRIC ACUTE LYMPHOBLASTIC LEUKEMIA (2022) (0)
Homozygous frame shift variant in ATP7B exon 1 leads to bypass of nonsense-mediated mRNA decay and to a protein capable of copper export (2019) (0)
Method and apparatus for optimizing cross machining operations (2007) (0)
Association study on three single nucleotide polymorphisms upstream and in the GIPR in obese and lean children from Berlin (2008) (0)
IgE levels in asthmatics and non-asthmatics are affected by different SNPs in FCER1A (2012) (0)
Targeted metabolomics profiles are strongly correlated with nutritional patterns in women (2012) (0)
Claussnitzer et al manuscript coauthor review-Cell (2014) (0)
A pilot study on DNA methylation and RNA expression in diverse tissues reveals epigenetic changes in atopic dermatitis. (2014) (0)
PrP type 1 from a sporadic CJD case (2011) (0)
Long term conservation of human metabolic phenotypes and link to heritability (2014) (0)
Correction to: Functional classification of RUNX1 variants in familial platelet disorder with associated myeloid malignancies (2022) (0)
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 (2015) (0)
Genome-wide DNA methylation analysis reveals several loci important for blood lipid levels (2015) (0)
Erratum: Large meta-analysis of genome-wide association studies identifies five loci for lean body mass (2017) (0)
Asthma and the genes : from GWAS to next generation transcriptome analyses 1862 Meta-analysis of genome-wide association studies of single nucleotide polymorphisms in selected genes of the WNT signaling pathway (2012) (0)
A polymorphism in DMRT1 is associated with asthma in boys only and affects promoter activity by allele-specific transcription factor binding (2012) (0)
Polymorphisms in inflammatory pathway genes and their associations with colorectal cancer risk (2010) (0)
Analysis of the IDH1G105 (SNPrs11554137) Polymorphism in 961 AML Patients and in a Large Cohort of 475 Healthy Controls (2011) (0)
Age-related cataracts in a German population-based study (KORA S4) (2007) (0)
other inflammatory mediators circulating concentrations of monocyte chemoattractant protein-1 and Duffy antigen receptor for chemokines (Darc) polymorphism regulates (2014) (0)
Single nucleotide polymorphisms in Wnt signaling and apoptotic pathway genes and susceptibility to colorectal cancer (2010) (0)
Effect of genome-wide simultaneous hypotheses tests on the discovery rate. (2011) (0)
Wednesday, 29 August 2012 (2012) (0)
Gender-specific pathway differences in the human serum metabolome (2015) (0)
No association between seven single nucleotide polymorphisms in the human gene encoding Calpain-10 and endstage renal disease because of diabetic nephropathy in type 2 diabetic patients in a German case-control study (2002) (0)
Effects of Repeated Freeze and Thaw Cycles on the Genome-Wide DNA Methylation Profile of Isolated Genomic DNA. (2023) (0)
Statistical Applications in Genetics and Molecular Biology (2012) (0)
Effect Modification of Interleukin-6 Response to Ambient Carbon Monoxide Levels by Fibrinogen and Interleukin-6 Polymorphisms (2008) (0)
A polymorphism of the DNA repair enzyme XRCC1 is associated with treatment prediction in anthracycline and CMF-based chemotherapy of patients with primary invasive breast cancer (2006) (0)
Author and Subject Index (2009) (0)
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 (2015) (0)
Long-term human spaceflight and inflammaging: Does it promote aging? (2023) (0)
Formyl peptide receptors 1-3 and annexin 1 in atherosclerotic plaques —tampere vascular study (2018) (0)
Genetic epidemiology in age-related cataract research (2008) (0)
Epigenome-wide association reveals extensive perturbations in DNA methylation associated with adiposity and its adverse metabolic consequences. Authors (2015) (0)
Increase arachidonic/linoleic acid ratio and a polygenic model of desaturases polymorphism are associated with increase risk of coronary artery disease (2007) (0)
Associations between variations in the TLR4 gene and incident coronary heart disease (CHD) in middle-aged men and women: Results from the MONICA/KORA Augsburg case-cohort study, 1984–2002 (2010) (0)
Subject Index Vol. 77, 2012 (2012) (0)
CAPON is a Novel QT-Interval Modifier Gene with Gender Dependent Effect Identified through Genomewide Association Analysis in Individuals from the General Population1 (2007) (0)
Myocardial ion channel IKr-alpha-Subunit genes KCNH2 and KCNE2: Haplotype structure and modulation of the QTc interval (2003) (0)
Functional characterization of RUNX1 variants in the context of FPDMM (2019) (0)
Functional Polymorphisms in the IRF1 Gene May Influence IgE Regulation and Atopy (2008) (0)
MicroRNA-449a Inhibits Triple Negative Breast Cancer by Disturbing DNA Repair and Chromatid Separation (2022) (0)
Candidate genes and sequence variants for susceptibility to mycobacterial infection identified by whole-exome sequencing (2022) (0)
Pre-conditions for High Quality Biobanking in Large Human Epidemiological Cohorts for Metabolomics and Other – Omics Studies (2012) (0)
' s response to reviews Title : Do genetic factors protected for early onset lung cancer ?-A case-control study before the age of 50 years (2007) (0)
Issue Information (2019) (0)
Serum uric acid, but not rs7442295 polymorphism of SCL2A9 gene, predicts total and cardiovascular mortality in advanced coronary artery disease. (2010) (0)
Metabolite profiling reveals new insights into the regulation of serum urate in humans (2013) (0)

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Thomas Illig is affiliated with the following schools:

Boston University
University of Bristol
Ludwig Maximilian University of Munich
University of Verona
Hannover Medical School
Technical University of Munich

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