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Journal of Sleep Research|July 12, 2017
Sleep disturbance by pramipexole is modified by Meis1 in miceAaro V Salminen, Barbara Schormair, Cornelia Flachskamm, et al.
Circulation. Genomic and Precision Medicine|November 10, 2020
Population Bias in Polygenic Risk Prediction Models for Coronary Artery DiseaseDamian Gola, Jeanette Erdmann, Kristi Läll, et al.
Human Genetics|October 21, 2019
A different view on fine-scale population structure in Western African populationsKridsadakorn Chaichoompu, Fentaw Abegaz, Bruno Cavadas, et al.
Arthritis Research & Therapy|May 15, 2004
Association of a specific haplotype across the genes MMP1 and MMP3 with radiographic joint destruction in rheumatoid arthritisSylvia Dörr, Nadine Lechtenböhmer, Rolf Rau, et al.
Psychiatric Genetics|March 15, 2011
Evidence for associations between MDGA2 polymorphisms and harm avoidance: replication and extension of a genome-wide association findingAngela Heck, Hildegard Pfister, Darina Czamara, et al.
European Neuropsychopharmacology : the Journal of the European College of Neuropsychopharmacology|September 18, 2009
HTR2A gene variation is involved in antidepressant treatment responseSusanne Lucae, Marcus Ising, Sonja Horstmann, et al.
Plos One|September 11, 2020
Investigation of gene-gene interactions in cardiac traits and serum fatty acid levels in the LURIC Health StudyJiayan Zhou, Kristin Passero, Nicole E Palmiero, et al.
Stroke|March 8, 2008
Genetic variation in soluble epoxide hydrolase (EPHX2) is associated with an increased risk of ischemic stroke in white EuropeansAndreas Gschwendtner, Stephan Ripke, Tobias Freilinger, et al.
Neuroscience Letters|April 22, 2005
Mutations in the pantothenate kinase gene PANK2 are not associated with Parkinson diseaseThomas Klopstock, Matthias Elstner, Christoph B Lücking, et al.
Inflammatory Bowel Diseases|November 25, 2005
Association of polymorphisms in the interleukin-18 gene in patients with Crohn's disease depending on the CARD15/NOD2 genotypeJürgen Glas, Helga-Paula Török, Laurian Tonenchi, et al.
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