Associated Papers
Role of the mitochondrial regulatory factor CHCHD2 in neurodegenerative diseases.
Guo X et al.
Frontiers in Neuroscience, 2025
SERPINE1 and MTHFR genetic variants in patients with embolic stroke of undetermined source: links with fibrin clot properties.
Klajmon A et al.
Neurologia I Neurochirurgia Polska, 2024
Genomic and phenotypic insights from an atlas of genetic effects on DNA methylation.
Min JL et al.
Nature Genetics, 2021
34493871 (PubMed )
Supplement: EMS131971-supplement-Supplementary_Note.pdf
Blood triglyceride levels are associated with DNA methylation at the serine metabolism gene PHGDH.
Truong V et al.
Scientific Reports, 2017
Single nucleotide polymorphisms in an intergenic chromosome 2q region associated with tissue factor pathway inhibitor plasma levels and venous thromboembolism.
Dennis J et al.
Journal of Thrombosis and Haemostasis : Jth, 2016
Familial thrombotic risk based on the genetic background of Protein C Deficiency in a Portuguese Study.
Fidalgo T et al.
European Journal of Haematology, 2015
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