Associated Papers
Association of folate metabolism-related enzymes (MTHFR, MYD88, and TP53) and their single nucleotide polymorphisms with breast cancer susceptibility in women from Southwest China: a Bayesian network approach.
Li X et al.
Frontiers in Oncology, 2025
The association between methionine synthase reductase c.66A>G variant and the risk of recurrent pregnancy loss: A systematic review and meta-analysis.
Zhou J et al.
Journal of Gynecology Obstetrics and Human Reproduction, 2024
Folate and cobalamin status, indicators, modulators, interactions, and reference ranges from early pregnancy until birth: the Reus-Tarragona birth cohort study.
Santos-Calderón LA et al.
The American Journal of Clinical Nutrition, 2024
Association of c.+677 C>T (rs1801133) and c.+1298 A>C (rs1801131) MTHFR genetic variants with cardiometabolic and disease risk in systemic lupus erythematosus patients: A cross-sectional study.
Pesqueda-Cendejas K et al.
Lupus, 2024
The impact of single nucleotide polymorphisms in MTHFR and MTRR genes on disease activity and the presence of methotrexate treatment side effects in children with juvenile idiopathic arthritis.
Roszkiewicz J et al.
Archives of Medical Science : Ams, 2023
Current perspectives on interethnic variability in multiple myeloma: Single cell technology, population pharmacogenetics and molecular signal transduction.
Gandhi M et al.
Translational Oncology, 2022
Association of homocysteine and polymorphism of methylenetetrahydrofolate reductase with early-onset post stroke depression.
Zhang J et al.
Frontiers in Nutrition, 2022
Association of methionine synthase (rs1805087), methionine synthase reductase (rs1801394), and methylenetetrahydrofolate dehydrogenase 1 (rs2236225) genetic polymorphisms with recurrent implantation failure.
Cho SH et al.
Human Fertility (cambridge, England), 2021
Association of three missense mutations in the homocysteine-related MTHFR and MTRR gene with risk of polycystic ovary syndrome in Southern Chinese women.
Feng W et al.
Reproductive Biology and Endocrinology : Rb&e, 2021
Methionine Synthase Reductase-A66G and -C524T Single Nucleotide Polymorphisms and Prostate Cancer: A Case-Control Trial
Basir A
Asian Pacific Journal of Cancer Prevention : Apjcp, 2019
First report of homocystinuria-megaloblastic anaemia, cobalamin E complementation type, in an Indian child.
Jamwal M et al.
Pathology, 2019
Genetic variation affecting DNA methylation and the human imprinting disorder, Beckwith-Wiedemann syndrome.
Dagar V et al.
Clinical Epigenetics, 2018
Genetic polymorphisms of key enzymes in folate metabolism affect the efficacy of folate therapy in patients with hyperhomocysteinaemia.
Du B et al.
The British Journal of Nutrition, 2018
The role of the folate pathway in pancreatic cancer risk.
Chittiboyina S et al.
Plos One, 2018
Neuro-fuzzy model of homocysteine metabolism.
Naushad SM et al.
Journal of Genetics, 2017
An Inframe Trinucleotide Deletion in MTRR Exon 1 is Associated with the Risk of Spina Bifida.
Zhang J et al.
Neuromolecular Medicine, 2017
Acute lymphoblastic leukemia and genetic variations in BHMT gene: Case-control study and computational characterization.
Bellampalli R et al.
Cancer Biomarkers : Section a of Disease Markers, 2017
[ANALYSIS OF ONE-CARBON METABOLISM GENES AND EPIDERMAL DIFFERENTIATION COMPLEX IN PATIENTS WITH ICHTHYOSIS VULGARIS].
Fedota O et al.
Georgian Medical News, 2017
Comparative analysis of four disease prediction models of Parkinson's disease.
Kumudini N et al.
Molecular and Cellular Biochemistry, 2016
Variants in MTHFR gene and neural tube defects susceptibility in China.
Wang Y et al.
Metabolic Brain Disease, 2015
Methylation diet and methyl group genetics in risk for adenomatous polyp occurrence.
Lucock M et al.
Bba Clinical, 2015
Association of 42 SNPs with genetic risk for cervical cancer: an extensive meta-analysis.
Wang S et al.
Bmc Medical Genetics, 2015
Methionine synthase reductase A66G polymorphism and leukemia risk: evidence from published studies.
Fang DH et al.
Leukemia & Lymphoma, 2014
Association of methionine synthase rs1801394 and methionine synthase reductase rs1805087 polymorphisms with meningioma in adults: A meta-analysis.
Zeng XT et al.
Biomedical Reports, 2014
Betaine-homocysteine methyltransferase 742G>A polymorphism and risk of down syndrome offspring in a Brazilian population.
Amorim MR et al.
Molecular Biology Reports, 2013
Haplotype analysis of the folate-related genes MTHFR, MTRR, and MTR and migraine with aura.
Roecklein KA et al.
Cephalalgia : an International Journal of Headache, 2013
Role of NOS3 DNA variants in externalizing behavioral problems observed in childhood leukemia survivors.
Marcoux S et al.
Journal of Pediatric Hematology/oncology, 2013
Complex interaction between serum folate levels and genetic polymorphisms in folate pathway genes: biomarkers of prostate cancer aggressiveness.
Jackson MD et al.
Genes & Nutrition, 2013
Functional variant in methionine synthase reductase decreases the risk of Down syndrome in China.
Wang SS et al.
The Journal of Obstetrics and Gynaecology Research, 2013
[Clinical and genetic characteristics of long-livers in Moscow region].
Artem'eva OV et al.
Advances in Gerontology = Uspekhi Gerontologii, 2013
Solar cycle predicts folate-sensitive neonatal genotypes at discrete phases of the first trimester of pregnancy: a novel folate-related human embryo loss hypothesis.
Lucock M et al.
Medical Hypotheses, 2012
Folate gene polymorphisms MTR A2756G, MTRR A66G, and BHMT G742A and risk for coronary artery disease: a meta-analysis.
Singh PR et al.
Genetic Testing and Molecular Biomarkers, 2012
Importance of gene variants and co-factors of folate metabolic pathway in the etiology of idiopathic intellectual disability.
Dutta S et al.
Nutritional Neuroscience, 2011
Genes and abdominal aortic aneurysm.
Hinterseher I et al.
Annals of Vascular Surgery, 2011
MTHFR and MTRR genotype and haplotype analysis and colorectal cancer susceptibility in a case-control study from the Czech Republic.
Pardini B et al.
Mutation Research, 2011
Update on the role of genetics in the onset of age-related macular degeneration.
Francis PJ et al.
Clinical Ophthalmology (auckland, N.z.), 2011
Impact of coagulation-balance gene predictors on efficacy of photodynamic therapy for choroidal neovascularization in pathologic myopia.
Parmeggiani F et al.
Ophthalmology, 2010
Methionine synthase reductase (MTRR) A66G polymorphism is not related to plasma homocysteine concentration and the risk for vascular disease.
Scazzone C et al.
Experimental and Molecular Pathology, 2009
Methylenetetrahydrofolate reductase and methionine synthase reductase gene polymorphisms and protection from microvascular complications in adolescents with type 1 diabetes.
Wiltshire EJ et al.
Pediatric Diabetes, 2008
Coagulation gene predictors of photodynamic therapy for occult choroidal neovascularization in age-related macular degeneration.
Parmeggiani F et al.
Investigative Ophthalmology & Visual Science, 2008
Prevalence and effects of gene-gene and gene-nutrient interactions on serum folate and serum total homocysteine concentrations in the United States: findings from the third National Health and Nutrition Examination Survey DNA Bank.
Yang QH et al.
The American Journal of Clinical Nutrition, 2008
First trimester diagnosis of iniencephaly associated with fetal malformations and trisomy 18: report of a new case and gene analysis on folate metabolism in parents.
Tonni G et al.
Congenital Anomalies, 2007
Polymorphisms in genes MTHFR, MTR and MTRR are not risk factors for cleft lip/palate in South Brazil.
Brandalize AP et al.
Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologica, 2007
Folate metabolic gene polymorphisms and childhood acute lymphoblastic leukemia: a case-control study.
Gast A et al.
Leukemia, 2007
Defects in homocysteine metabolism: diversity among hyperhomocyst(e)inemias.
Matthews RG et al.
Clinical Chemistry and Laboratory Medicine, 2007
Methionine synthase reductase polymorphisms are associated with serum osteocalcin levels in postmenopausal women.
Kim DJ et al.
Experimental & Molecular Medicine, 2006
Effects of single-nucleotide polymorphisms in MTHFR and MTRR on mortality and allograft loss in kidney transplant recipients.
Winkelmayer WC et al.
Kidney International, 2005
Genetic polymorphisms predisposing to hyperhomocysteinemia in cardiac transplant patients.
Miriuka SG et al.
Transplant International : Official Journal of the European Society for Organ Transplantation, 2005
Congenital heart defects and abnormal maternal biomarkers of methionine and homocysteine metabolism.
Hobbs CA et al.
The American Journal of Clinical Nutrition, 2005
Genetic polymorphisms in folate and homocysteine metabolism as risk factors for DNA damage.
Botto N et al.
European Journal of Human Genetics : Ejhg, 2003