Associated Papers
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
[Assessment of the role of nutritional and genetic determinants in the formation of the risk of diseases associated with folate cycle disorders in the population of the Omsk region].
Vilms EA et al.
Voprosy Pitaniia, 2023
Genetic Polymorphisms of GGH and ABCC2 Are Associated with Methotrexate Intolerance in Patients with Rheumatoid Arthritis.
Escudero-Contreras A et al.
Journal of Clinical Medicine, 2021
The Roles of Reduced Folate Carrier-1 (RFC1) A80G (rs1051266) Polymorphism in Congenital Heart Disease: A Meta-Analysis.
Yi K et al.
Medical Science Monitor : International Medical Journal of Experimental and Clinical Research, 2021
Paternal genetic variants and risk of obstructive heart defects: A parent-of-origin approach.
Patel J et al.
Plos Genetics, 2021
Methylenetetrahydrofolate reductase C677T (Ala>Val, rs1801133 C>T) polymorphism decreases the susceptibility of hepatocellular carcinoma: a meta-analysis involving 12,628 subjects.
Zhang S et al.
Bioscience Reports, 2020
Effect of genetic polymorphisms involved in folate metabolism on the concentration of serum folate and plasma total homocysteine (p-tHcy) in healthy subjects after short-term folic acid supplementation: a randomized, double blind, crossover study.
Cabo R et al.
Genes & Nutrition, 2015
Pharmacogenetic considerations for acute lymphoblastic leukemia therapies.
Dulucq S et al.
Expert Opinion on Drug Metabolism & Toxicology, 2014
Polymorphisms in genes RFC-1/CBS as maternal risk factors for Down syndrome in China.
Wang SS et al.
Archives of Gynecology and Obstetrics, 2013
Reduced folate carrier A80G polymorphism and susceptibility to neural tube defects: a meta-analysis.
Wang HG et al.
Gene, 2012
Association of reduced folate carrier gene polymorphism and maternal folic acid use with neural tube defects.
Pei L et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics, 2009
Folate-related gene polymorphisms as risk factors for cleft lip and cleft palate.
Mills JL et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology, 2008
Genetic variation of infant reduced folate carrier (A80G) and risk of orofacial defects and congenital heart defects in China.
Pei L et al.
Annals of Epidemiology, 2006
Interactions among polymorphisms in folate-metabolizing genes and serum total homocysteine concentrations in a healthy elderly population.
Devlin AM et al.
The American Journal of Clinical Nutrition, 2006
[Epidemiological study on reduced folate carrier gene(RFC1 A80G) polymorphism and other risk factors of neural tube defects].
Pei LJ et al.
Beijing Da Xue Xue Bao. Yi Xue Ban = Journal of Peking University. Health Sciences, 2005
Pharmacogenetics for individualized cancer chemotherapy.
Efferth T et al.
Pharmacology & Therapeutics, 2005
Studies of reduced folate carrier 1 (RFC1) A80G and 5,10-methylenetetrahydrofolate reductase (MTHFR) C677T polymorphisms with neural tube and orofacial cleft defects.
Vieira AR et al.
American Journal of Medical Genetics. Part A, 2005
Interaction between maternal periconceptional supplementation of folic acid and reduced folate carrier gene polymorphism of neural tube defects.
Pei LJ et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics, 2005
Genetic variation of infant reduced folate carrier (A80G) and risk of orofacial and conotruncal heart defects.
Shaw GM et al.
American Journal of Epidemiology, 2003
G80A Single Nucleotide Polymorphism in Reduced Folate Carrier-1 Gene in a Mexican Population and its Impact on Survival in Patients with Acute Lymphoblastic Leukemia.
Candelaria M et al.
Revista De Investigacion Clinica; Organo Del Hospital De Enfermedades De La Nutricion, 0
Association between PTCH1 and RAD54B Single-Nucleotide Polymorphisms and Non-syndromic Orofacial Clefts in the Northeast Population of Iran.
Morvaridi Farimani R et al.
Avicenna Journal of Medical Biotechnology, 0