Köttgen, Anna 1974-
Anna Köttgen researcher
VIAF ID: 45210332 (Personal)
Permalink: http://viaf.org/viaf/45210332
Preferred Forms
- 100 0 _ ‡a Anna Köttgen ‡c researcher
- 100 1 _ ‡a Köttgen, Anna ‡d 1974-
- 100 1 _ ‡a Köttgen, Anna ‡d 1974-
4xx's: Alternate Name Forms (3)
5xx's: Related Names (1)
- 500 1 _ ‡a Hopf, Anna ‡d 1974-
Works
Title | Sources |
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Association of eGFR-related loci identified by GWAS with incident CKD and ESRD | |
Association of omega 3 polyunsaturated fatty acids with incident chronic kidney disease: pooled analysis of 19 cohorts | |
Associations between known genetic risk variants and CKD stage and etiology in the GCKD study | |
Associations of baseline and longitudinal serum uromodulin with kidney failure and mortality: results from the African American Study of Kidney Disease and Hypertension (AASK) trial | |
Blood pressure control in chronic kidney disease: A cross-sectional analysis from the German Chronic Kidney Disease (GCKD) study | |
Bucket fuser: statistical signal extraction for 1D 1H NMR metabolomic data | |
Cardiovascular disease protein biomarkers are associated with kidney function: The Framingham Heart Study | |
Clock genes rescue nphp mutations in zebrafish | |
Clonal hematopoiesis of indeterminate potential is associated with acute kidney injury | |
A common pathomechanism in GMAP-210– and LBR-related diseases | |
Control procedures and estimators of the false discovery rate and their application in low-dimensional settings: an empirical investigation | |
Corrigendum: 1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function | |
Differential prognostic utility of adiposity measures in chronic kidney disease | |
Discovery and prioritization of variants and genes for kidney function in >1.2 million individuals | |
DNA methylation signature of chronic low-grade inflammation and its role in cardio-respiratory diseases | |
DNA methylome in panic disorder: a case-control and longitudinal psychotherapy-epigenetic study | |
effect of LPA Thr3888Pro on lipoprotein(a) and coronary artery disease is modified by the LPA KIV-2 variant 4925G>A | |
Epigenome-wide association study of serum urate reveals insights into urate co-regulation and the SLC2A9 locus | |
Epigenome-wide DNA methylation in obsessive-compulsive disorder | |
Framework and baseline examination of the German National Cohort (NAKO) | |
From discovery to translation: characterization of the novel kidney function markers C-mannosyltryptophan and pseudouridine | |
genetic architecture of membranous nephropathy and its potential to improve non-invasive diagnosis | |
Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function | |
Genetic drivers of heterogeneity in type 2 diabetes pathophysiology | |
Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine | |
Genetics in chronic kidney disease: conclusions from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference | |
Genetics of serum urate concentrations and gout in a high-risk population, patients with chronic kidney disease | |
Genome-wide analyses identify a role for SLC17A4 and AADAT in thyroid hormone regulation | |
Genome-wide association and functional follow-up reveals new Loci for kidney function | |
Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria | |
Genome-wide association study of 1,5-anhydroglucitol identifies novel genetic loci linked to glucose metabolism | |
Genome-wide studies reveal factors associated with circulating uromodulin and its relations with complex diseases | |
GenToS: use of orthologous gene information to prioritize signals from human GWAS | |
High detection rate for disease-causing variants in a cohort of 30 Iranian pediatric steroid resistant nephrotic syndrome cases | |
Identification of a sudden cardiac death susceptibility locus at 2q24.2 through genome-wide association in european ancestry individuals | |
Implication of transcription factor FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT) | |
An intermediate-effect size variant in UMOD confers risk for chronic kidney disease | |
Investigation of a nonsense mutation located in the complex KIV-2 copy number variation region of apolipoprotein(a) in 10,910 individuals | |
KLKB1 and CLSTN2 are associated with HDL-mediated cholesterol efflux capacity in a genome-wide association study | |
Large-scale whole-exome sequencing association studies identify rare functional variants influencing serum urate levels | |
Mapping eGFR loci to the renal transcriptome and phenome in the VA Million Veteran Program | |
Mapping of the gene network that regulates glycan clock of ageing | |
Mechanismen der CFTR-vermittelten Hemmung des epithelialen Na+-Kanals | |
Meta-analyses identify DNA methylation associated with kidney function and damage | |
Meta-Analysis of genome-wide association studies identifies six new loci for serum calcium concentrations | |
Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline | |
Meta-GWAS on PCSK9 concentrations reveals associations of novel loci outside the PCSK9 locus in White populations | |
Mild-to-moderate kidney dysfunction and cardiovascular disease: observational and mendelian randomization analyses | |
Mitochondrial DNA copy number is associated with mortality and infections in a large cohort of patients with chronic kidney disease | |
Modulation of genetic associations with serum urate levels by body-mass-index in humans | |
Multi-trait analysis characterizes the genetics of thyroid function and identifies causal associations with clinical implications | |
De novo mutations across 1,465 diverse genomes reveal mutational insights and reductions in the Amish founder population | |
Patterns of medication use and the burden of polypharmacy in patients with chronic kidney disease: the German Chronic Kidney Disease study | |
A polygenic score for reduced kidney function and adverse outcomes in a cohort with chronic kidney disease | |
Posttranslationale Integration kleiner Membranproteine in Escherichia Coli : eine neue Funktion des Signal Recognition Particle | |
Prevalence and risk factors of thyroid dysfunction in older adults in the community | |
Prospective cohort study of soluble urokinase plasminogen activation receptor and cardiovascular events in patients with CKD | |
Rare genetic variants affecting urine metabolite levels link population variation to inborn errors of metabolism | |
Rare variants in SLC5A10 are associated with serum 1,5-anhydroglucitol (1,5-AG) in the Atherosclerosis Risk in Communities (ARIC) Study | |
Refining risk factors via metabolomics - a general methodology and its application | |
Regional variation in hemoglobin distribution among individuals with CKD: the ISN international network of CKD cohorts | |
relationship between blood metabolites of the tryptophan pathway and kidney function: a bidirectional Mendelian randomization analysis | |
A saturated map of common genetic variants associated with human height | |
Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program | |
SLC26A1 is a major determinant of sulfate homeostasis in humans | |
A slit-diaphragm-associated protein network for dynamic control of renal filtration | |
Stratifying type 2 diabetes cases by BMI identifies genetic risk variants in LAMA1 and enrichment for risk variants in lean compared to obese cases | |
Therapeutic effects of inhibition of sphingosine-1-phosphate signaling in HIF-2[alpha] inhibitor-resistant clear cell renal cell carcinoma | |
Trans-ethnic Mendelian-randomization study reveals causal relationships between cardiometabolic factors and chronic kidney disease | |
Ttc30a affects tubulin modifications in a model for ciliary chondrodysplasia with polycystic kidney disease | |
Urine 6-bromotryptophan: associations with genetic variants and incident end-stage kidney disease | |
Whole genome sequence analyses of eGFR in 23,732 people representing multiple ancestries in the NHLBI trans-omics for precision medicine (TOPMed) consortium | |
Wildtype heterogeneity contributes to clonal variability in genome edited cells | |
X-chromosome and kidney function: evidence from a multi-trait genetic analysis of 908,697 individuals reveals sex-specific and sex-differential findings in genes regulated by androgen response elements | |
Zirkulierende Angiopoietin-2- und Tie-2-Konzentrationen in Assoziation zur Nierenfunktion in einer populationsbasierten Studie |