User profiles for Martina Mueller-Nurasyid
Martina Müller-NurasyidUniversitätsmedizin Mainz, Ludwig-Maximilians-Universität München Verified email at uni-mainz.de Cited by 91475 |
Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture
…, WL McArdle, C Medina-Gomez, M Mueller-Nurasyid… - Nature …, 2013 - nature.com
Approaches exploiting trait distribution extremes may be used to identify loci associated
with common traits, but it is unknown whether these loci are generalizable to the broader …
with common traits, but it is unknown whether these loci are generalizable to the broader …
[HTML][HTML] The influence of age and sex on genetic associations with adult body size and shape: a large-scale genome-wide interaction study
…, ME Montasser, G Mueller, M Mueller-Nurasyid… - PLoS …, 2015 - journals.plos.org
Genome-wide association studies (GWAS) have identified more than 100 genetic variants
contributing to BMI, a measure of body size, or waist-to-hip ratio (adjusted for BMI, WHR …
contributing to BMI, a measure of body size, or waist-to-hip ratio (adjusted for BMI, WHR …
Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci
…, G Mirza, TW Muehleisen, M Mueller-Nurasyid… - Nature …, 2015 - nature.com
We performed fine mapping of 39 established type 2 diabetes (T2D) loci in 27,206 cases and
57,574 controls of European ancestry. We identified 49 distinct association signals at these …
57,574 controls of European ancestry. We identified 49 distinct association signals at these …
Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation
…, L Milani, R Mills, N Mononen, M Mueller-Nurasyid… - Nature …, 2015 - nature.com
We carried out a trans-ancestry genome-wide association and replication study of blood
pressure phenotypes among up to 320,251 individuals of East Asian, European and South …
pressure phenotypes among up to 320,251 individuals of East Asian, European and South …
[HTML][HTML] Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits
…, J Marten, RPS Middelberg, M Mueller-Nurasyid… - Nature …, 2017 - nature.com
Few genome-wide association studies (GWAS) account for environmental exposures, like
smoking, potentially impacting the overall trait variance when investigating the genetic …
smoking, potentially impacting the overall trait variance when investigating the genetic …
Incidence of complications related to catheter ablation of atrial fibrillation and atrial flutter: a nationwide in-hospital analysis of administrative data for Germany in 2014
…, MF Sinner, M Lutz, M Mueller-Nurasyid… - European heart …, 2018 - academic.oup.com
Aims Risks of catheter ablation for atrial fibrillation and flutter assessed in retrospective studies,
registries, and controlled trials may underestimate ‘real world’ conditions. Methods and …
registries, and controlled trials may underestimate ‘real world’ conditions. Methods and …
A meta-analysis of 120 246 individuals identifies 18 new loci for fibrinogen concentration
…, S Trompet, M Mueller-Nurasyid… - Human molecular …, 2016 - academic.oup.com
Genome-wide association studies have previously identified 23 genetic loci associated with
circulating fibrinogen concentration. These studies used HapMap imputation and did not …
circulating fibrinogen concentration. These studies used HapMap imputation and did not …
A Low-Frequency Inactivating AKT2 Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk
…, K Strauch, A Peters, M Roden, M Mueller-Nurasyid… - Diabetes, 2017 - Am Diabetes Assoc
To identify novel coding association signals and facilitate characterization of mechanisms
influencing glycemic traits and type 2 diabetes risk, we analyzed 109,215 variants derived …
influencing glycemic traits and type 2 diabetes risk, we analyzed 109,215 variants derived …
[HTML][HTML] Gene-gene interaction analyses for atrial fibrillation
Atrial fibrillation (AF) is a heritable disease that affects more than thirty million individuals
worldwide. Extensive efforts have been devoted to the study of genetic determinants of AF. The …
worldwide. Extensive efforts have been devoted to the study of genetic determinants of AF. The …
Analysis with the exome array identifies multiple new independent variants in lipid loci
…, H Yaghootkar, M Mueller-Nurasyid… - Human molecular …, 2016 - academic.oup.com
It has been hypothesized that low frequency (1–5% minor allele frequency (MAF)) and rare (<1%
MAF) variants with large effect sizes may contribute to the missing heritability in …
MAF) variants with large effect sizes may contribute to the missing heritability in …