Associated Papers
Genotype Combinations and Genetic Risk Score Analyses of MTHFR, MTRR, and MTR Polymorphisms in Hypothyroidism Susceptibility: A Case-Control Study.
Tabakoglu NT et al.
Current Issues in Molecular Biology, 2025
41150742 (PubMed )
Supplement: cimb-47-00794-s001.zip › Supplementary_File_S6_PCR_and_RFLP_Product_Lengths.pdf
Combined Genetic Biomarkers Confer Susceptibility to Risk of Urothelial Bladder Carcinoma in a Saudi Population.
Elhawary NA et al.
Disease Markers, 2017
Systematic meta-analyses and field synopsis of genetic association studies in colorectal adenomas.
Montazeri Z et al.
International Journal of Epidemiology, 2016
Folate and vitamin B12-related genes and risk for omphalocele.
Mills JL et al.
Human Genetics, 2012
Association between selected folate pathway polymorphisms and nonsyndromic limb reduction defects: a case-parental analysis.
Cleves MA et al.
Paediatric and Perinatal Epidemiology, 2011
Folate-mediated one-carbon metabolism and its effect on female fertility and pregnancy viability.
Laanpere M et al.
Nutrition Reviews, 2010
The search for genetic polymorphisms in the homocysteine/folate pathway that contribute to the etiology of human neural tube defects.
Molloy AM et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology, 2009
Polymorphic background of methionine synthase reductase modulates the phenotype of a disease-causing mutation.
Gherasim C et al.
Human Mutation, 2007
Are the betaine-homocysteine methyltransferase (BHMT and BHMT2) genes risk factors for spina bifida and orofacial clefts?
Zhu H et al.
American Journal of Medical Genetics. Part A, 2005
cblE type of homocystinuria due to methionine synthase reductase deficiency: functional correction by minigene expression.
Zavadáková P et al.
Human Mutation, 2005
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