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  • Direct Evidence on the Contribution of a Missense Mutation in GDF9 to Variation in Ovulation Rate of Finnsheep
  • Common Genetic Variation in the Human CTF1 Locus, Encoding Cardiotrophin-1, Determines Insulin Sensitivity
  • Distribution and Medical Impact of Loss-of-Function Variants in the Finnish Founder Population
  • Common Variants in CYP2R1 and GC Genes Predict Vitamin D Concentrations in Healthy Danish Children and Adults
  • Common variants in PERK, JNK, BIP and XBP1 genes are associated with the risk of prediabetes or diabetes-related phenotypes in a Chinese population
  • Common vitamin D pathway gene variants reveal contrasting effects on serum vitamin D levels in African Americans and European Americans
  • CCDC26 Gene Polymorphism and Glioblastoma Risk in the Han Chinese Population
  • CFI-rs7356506 is a genetic protective factor for acute anterior uveitis in Chinese patients
  • Characterisation of Adaptive Genetic Diversity in Environmentally Contrasted Populations of Eucalyptus camaldulensis Dehnh. (River Red Gum)
  • Characterisation of Genetic Variation in ST8SIA2 and Its Interaction Region in NCAM1 in Patients with Bipolar Disorder
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