homocysteine has been researched along with Cardiac Septal Defect in 5 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (20.00) | 29.6817 |
2010's | 4 (80.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Li, J; Li, PQ; Li, Y; Wang, YZ; Xie, DX; Xie, HH; Xie, XD; Zhang, AA | 1 |
Dong, X; Wei, Y; Wu, X; Yang, R; Yang, Y | 1 |
Duan, WY; Gong, XH; Gu, ZY; Hou, J; Huang, GY; Jin, L; Qiao, B; Shen, HB; Shi, KH; Wang, HY; Wang, J; Yang, XY; Ye, ZZ; Zhao, JY | 1 |
Duan, WY; Gu, ZY; Huang, GY; Qiao, B; Sun, JW; Wang, EL; Wang, HY; Wang, J; Yang, XY; Zhao, JY | 1 |
Cheng, J; Dao, J; Zhao, R; Zhu, W | 1 |
5 other study(ies) available for homocysteine and Cardiac Septal Defect
Article | Year |
---|---|
A genetic variant in a homocysteine metabolic gene that increases the risk of congenital cardiac septal defects in Han Chinese populations.
Topics: Alleles; Female; Gene Expression; Genetic Association Studies; Genetic Predisposition to Disease; Genotype; Heart Septal Defects; Homocysteine; Humans; Male; Polymorphism, Single Nucleotide; Risk Factors; Synaptotagmins | 2017 |
[Correlation between endogenous sulfur dioxide and homocysteine in children with pulmonary arterial hypertension associated with congenital heart disease].
Topics: Biomarkers; Case-Control Studies; Child, Preschool; Ductus Arteriosus, Patent; Familial Primary Pulmonary Hypertension; Female; Heart Defects, Congenital; Heart Septal Defects; Hemodynamics; Homocysteine; Humans; Infant; Male; Sulfur Dioxide | 2014 |
Functional variant in methionine synthase reductase intron-1 significantly increases the risk of congenital heart disease in the Han Chinese population.
Topics: Adult; Animals; Asian People; Case-Control Studies; Cells, Cultured; Child; China; Ferredoxin-NADP Reductase; Genetic Variation; Genotype; Heart Septal Defects; HEK293 Cells; Homocysteine; Humans; Introns; Myocytes, Cardiac; Polymorphism, Single Nucleotide; Rats; Risk Factors; Transcriptional Activation | 2012 |
Genetic polymorphisms of the TYMS gene are not associated with congenital cardiac septal defects in a Han Chinese population.
Topics: Case-Control Studies; Catalysis; Child; Child, Preschool; China; DNA; Female; Gene Expression Regulation; Genetic Variation; Heart Septal Defects; Homocysteine; Humans; Male; Polymorphism, Genetic; Polymorphism, Single Nucleotide; Purines; Pyrimidines; Thymidylate Synthase | 2012 |
[Relations of methionine synthase gene variation with congenital heart disease].
Topics: 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase; Adolescent; Adult; Child; Child, Preschool; Female; Folic Acid; Genetic Predisposition to Disease; Genetic Variation; Genotype; Glutathione; Heart Defects, Congenital; Heart Septal Defects; Homocysteine; Humans; Infant; Male; Polymorphism, Genetic; Vitamin B 12 | 2004 |