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Neurogenetics|November 19, 2013
Rare variants in LRRK1 and Parkinson's diseaseEva C Schulte, Daniel C Ellwanger, Sybille Dihanich, et al.
Plos Genetics|September 15, 2017
Correction: Effect of Insulin Resistance on Monounsaturated Fatty Acid Levels: A Multi-cohort Non-targeted Metabolomics and Mendelian Randomization StudyChristoph Nowak, Samira Salihovic, Andrea Ganna, et al.
Plos Genetics|October 22, 2016
Effect of Insulin Resistance on Monounsaturated Fatty Acid Levels: A Multi-cohort Non-targeted Metabolomics and Mendelian Randomization StudyChristoph Nowak, Samira Salihovic, Andrea Ganna, et al.
Aging Cell|July 28, 2012
Human serum metabolic profiles are age dependentZhonghao Yu, Guangju Zhai, Paula Singmann, et al.
Frontiers in Immunology|March 15, 2018
Genome-Wide Association Study on Immunoglobulin G Glycosylation PatternsAnnika Wahl, Erik van den Akker, Lucija Klaric, et al.
BMC Neurology|October 29, 2011
Novel SCARB2 mutation in action myoclonus-renal failure syndrome and evaluation of SCARB2 mutations in isolated AMRF featuresFranziska Hopfner, Barbara Schormair, Franziska Knauf, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|October 2, 2010
Risk gene variants for nicotine dependence in the CHRNA5-CHRNA3-CHRNB4 cluster are associated with cognitive performanceGeorg Winterer, Kirstin Mittelstrass, Ina Giegling, et al.
The Journal of Allergy and Clinical Immunology|August 9, 2015
Atopic dermatitis is associated with an increased risk for rheumatoid arthritis and inflammatory bowel disease, and a decreased risk for type 1 diabetesJochen Schmitt, Kristin Schwarz, Hansjörg Baurecht, et al.
Nature Communications|January 5, 2020
Epigenetics meets proteomics in an epigenome-wide association study with circulating blood plasma protein traitsShaza B Zaghlool, Brigitte Kühnel, Mohamed A Elhadad, et al.
Neurogenetics|March 14, 2012
Replication study of multiple sclerosis (MS) susceptibility alleles and correlation of DNA-variants with disease features in a cohort of Austrian MS patientsMascha C Schmied, Sonja Zehetmayer, Markus Reindl, et al.
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