Rare variants in MTHFR predispose to occurrence and recurrence of pulmonary embolism

Association between congenital thrombophilia and outcomes in pulmonary embolism patients

(2020) Tian-Yu Lian et al.   Blood Advances

Factor V Leiden paradox in a middle-aged Swedish population: A prospective study

(2018) Bengt Zöller et al.   VASCULAR MEDICINE

Surgical Management of Acute and Chronic Pulmonary Embolism

(2018) Barbara L. LeVarge et al.   CLINICS IN CHEST MEDICINE

Germline BMP9 mutation causes idiopathic pulmonary arterial hypertension

(2018) Xiao-Jian Wang et al.   EUROPEAN RESPIRATORY JOURNAL

Insights into Severe 5,10-Methylenetetrahydrofolate Reductase Deficiency: Molecular Genetic and Enzymatic Characterization of 76 Patients

(2015) Patricie Burda et al.   HUMAN MUTATION

The role of inherited thrombophilia in patients with isolated pulmonary embolism: A systematic review and a meta-analysis of the literature

(2014) Fulvio Pomero et al.   THROMBOSIS RESEARCH

Association of the C677T Polymorphism in the MTHFR Gene with Hemorrhagic Stroke: A Meta-Analysis

(2013) Shan Kang et al.   Genetic Testing and Molecular Biomarkers

Association of MTHFR 677T variant allele with risk of intracerebral haemorrhage: A meta-analysis

(2012) Shan Gao et al.   JOURNAL OF THE NEUROLOGICAL SCIENCES

Prospective study of homocysteine and MTHFR 677TT genotype and risk for venous thrombosis in a general population – results from the HUNT 2 study

(2008) Inger Anne Næss et al.   BRITISH JOURNAL OF HAEMATOLOGY

The prevalence of folate-remedial MTHFR enzyme variants in humans

(2008) N. J. Marini et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA