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Parkinsonism & Related Disorders|August 2, 2016
Systematic TOR1A non-c.907_909delGAG variant analysis in isolated dystonia and controlsMichael Zech, Angela Jochim, Sylvia Boesch, et al.
Nature Communications|February 25, 2021
Revealing the role of the human blood plasma proteome in obesity using genetic driversShaza B Zaghlool, Sapna Sharma, Megan Molnar, et al.
Human Molecular Genetics|September 28, 2022
Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populationsGaurav Thareja, Aziz Belkadi, Matthias Arnold, et al.
Clinical Epigenetics|March 23, 2021
Epigenome-wide association study of whole blood gene expression in Framingham Heart Study participants provides molecular insight into the potential role of CHRNA5 in cigarette smoking-related lung diseasesChen Yao, Roby Joehanes, Rory Wilson, et al.
European Journal of Human Genetics : EJHG|June 14, 2012
Impact of common regulatory single-nucleotide variants on gene expression profiles in whole bloodDivya Mehta, Katharina Heim, Christian Herder, et al.
American Journal of Human Genetics|February 7, 2008
On the use of general control samples for genome-wide association studies: genetic matching highlights causal variantsDiana Luca, Steven Ringquist, Lambertus Klei, et al.
Obesity (Silver Spring, Md.)|August 1, 2017
Metabolomic Profiling of Long-Term Weight Change: Role of Oxidative Stress and Urate Levels in Weight GainCristina Menni, Marie Migaud, Gabi Kastenmüller, et al.
Scientific Reports|April 5, 2017
Genome-wide association analysis for chronic venous disease identifies EFEMP1 and KCNH8 as susceptibility lociEva Ellinghaus, David Ellinghaus, Petra Krusche, et al.
Annals of Neurology|December 11, 2012
Genetic variants in the immunoglobulin heavy chain locus are associated with the IgG index in multiple sclerosisDorothea Buck, Eva Albrecht, Muhammad Aslam, et al.
Liver International : Official Journal of the International Association for the Study of the Liver|January 24, 2024
Penetrance, cancer incidence and survival in HFE haemochromatosis-A population-based cohort studyBenedikt Schaefer, Lorenz M Pammer, Bernhard Pfeifer, et al.
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