folic acid has been researched along with Genetic Diseases in 5 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 1 (20.00) | 18.7374 |
1990's | 1 (20.00) | 18.2507 |
2000's | 1 (20.00) | 29.6817 |
2010's | 1 (20.00) | 24.3611 |
2020's | 1 (20.00) | 2.80 |
Authors | Studies |
---|---|
Garg, P; Gecz, J; Jadhav, B; Jain, M; Kooy, RF; Martin-Trujillo, A; Metsu, S; Olsen, H; Patel, N; Paten, B; Ritz, B; Rodriguez, OL; Sharp, AJ | 1 |
Horváth, T; Littvay, L; Métneki, J; Tárnoki, ÁD; Tárnoki, DL | 1 |
Schaapveld, K | 1 |
Grady, J; Hudnall, SD; Kellner, LH; Matalon, RK; Nitowsky, H; Rady, PL; Szucs, S | 1 |
Karlin, R | 1 |
1 review(s) available for folic acid and Genetic Diseases
Article | Year |
---|---|
[Hungarian twin studies: results of four decades].
Topics: Alcohol Drinking; Body Composition; Carotid Intima-Media Thickness; Congenital Abnormalities; Contraceptives, Oral; Diseases in Twins; Fatty Liver; Female; Folic Acid; Gene-Environment Interaction; Genetic Diseases, Inborn; Humans; Hungary; Lactose Intolerance; Mendelian Randomization Analysis; Non-alcoholic Fatty Liver Disease; Pregnancy; Pregnancy, Twin; Psychosexual Development; Registries; Smoking; Twin Studies as Topic; Vascular Stiffness | 2013 |
4 other study(ies) available for folic acid and Genetic Diseases
Article | Year |
---|---|
A Survey of Rare Epigenetic Variation in 23,116 Human Genomes Identifies Disease-Relevant Epivariations and CGG Expansions.
Topics: BRCA1 Protein; DNA Methylation; Epigenesis, Genetic; Female; Folic Acid; Gene Silencing; Genetic Diseases, Inborn; Genetic Loci; Genetic Variation; Genome, Human; High-Throughput Nucleotide Sequencing; Humans; Male; Promoter Regions, Genetic; Receptors, LDL; Trinucleotide Repeat Expansion; Twins, Monozygotic | 2020 |
[Preconception consultation: a good idea?].
Topics: Adult; Female; Folic Acid; Genetic Counseling; Genetic Diseases, Inborn; Humans; Infant, Newborn; Neural Tube Defects; Preconception Care; Pregnancy; Referral and Consultation; Rubella Vaccine | 1995 |
Genetic polymorphism (G80A) of reduced folate carrier gene in ethnic populations.
Topics: Alleles; Black People; Folic Acid; Folic Acid Deficiency; Genetic Diseases, Inborn; Genotype; Heterozygote; Homozygote; Humans; Mutation; Polymorphism, Genetic; White People | 2001 |
[Correlations among the amounts of B 12, methionine and folates in the blood of mothers of hypotrophic infants].
Topics: Biological Assay; Birth Weight; Diet; Female; Folic Acid; Genetic Diseases, Inborn; Humans; Infant, Newborn; Lactobacillus; Leuconostoc; Male; Methionine; Nutritional Requirements; Postpartum Period; Pregnancy; Statistics as Topic; Vitamin B 12 | 1969 |