Associated Papers
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
Biosynthesis of Single Thioether c-Type Cytochromes Provides Insight into Mechanisms Intrinsic to Holocytochrome c Synthase (HCCS).
Babbitt SE et al.
Biochemistry, 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
Mutation analysis of WNT10B in obese children, adolescents and adults.
Van Camp JK et al.
Endocrine, 2013
Select a paper to view details