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Plos Genetics|December 19, 2014
Genome wide meta-analysis highlights the role of genetic variation in RARRES2 in the regulation of circulating serum chemerinAnke Tönjes, Markus Scholz, Jana Breitfeld, et al.
Plos One|July 27, 2011
The use of genome-wide eQTL associations in lymphoblastoid cell lines to identify novel genetic pathways involved in complex traitsJosine L Min, Jennifer M Taylor, J Brent Richards, et al.
Addiction Biology|December 3, 2019
Alcohol consumption is associated with widespread changes in blood DNA methylation: Analysis of cross-sectional and longitudinal dataPierre-Antoine Dugué, Rory Wilson, Benjamin Lehne, et al.
American Journal of Respiratory and Critical Care Medicine|July 28, 2012
A novel sarcoidosis risk locus for Europeans on chromosome 11q13.1Annegret Fischer, Benjamin Schmid, David Ellinghaus, et al.
Genome Medicine|April 1, 2014
Interrogating causal pathways linking genetic variants, small molecule metabolites, and circulating lipidsSo-Youn Shin, Ann-Kristin Petersen, Simone Wahl, et al.
Oncotarget|December 13, 2017
Bayesian and frequentist analysis of an Austrian genome-wide association study of colorectal cancer and advanced adenomasPhilipp Hofer, Michael Hagmann, Stefanie Brezina, et al.
Clinical Epigenetics|April 29, 2025
Regulation of nc886 (vtRNA2-1) RNAs is associated with cardiometabolic risk factors and diseasesSonja Rajić, Thomas Delerue, Justiina Ronkainen, et al.
Diabetes|September 12, 2023
A Fecal Metabolite Signature of Impaired Fasting Glucose: Results From Two Independent Population-Based CohortsAna Nogal, Francesca Tettamanzi, Qiuling Dong, et al.
Pancreatology : Official Journal of the International Association of Pancreatology (IAP) ... [Et Al.]|March 25, 2022
Colocalization analysis of pancreas eQTLs with risk loci from alcoholic and novel non-alcoholic chronic pancreatitis GWAS suggests potential disease causing mechanismsAndreas W Schmidt, Andreas Kühnapfel, Holger Kirsten, et al.
Nature Communications|May 24, 2017
Pseudoexfoliation syndrome-associated genetic variants affect transcription factor binding and alternative splicing of LOXL1Francesca Pasutto, Matthias Zenkel, Ursula Hoja, et al.
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