methionine has been researched along with Abnormality, Heart in 10 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (10.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 4 (40.00) | 29.6817 |
| 2010's | 4 (40.00) | 24.3611 |
| 2020's | 1 (10.00) | 2.80 |
| Authors | Studies |
|---|---|
| Bahado Singh, R; Friedman, P; Graham, S; Jafar, F; Turkoglu, O; Ugur, Z; Ustun, I; Whitten, A; Yilmaz, A | 1 |
| Aylsworth, AS; Botto, LD; Carmichael, SL; Correa, A; Gilboa, SM; Langlois, PH; Luben, TJ; Nembhard, WN; Olshan, AF; Richmond-Bryant, J; Shaw, GM; Stingone, JA | 1 |
| Chen, YQ; Guo, WY; Li, T; Su, FJ; Zhang, YX | 1 |
| Cleves, MA; Hobbs, CA; Jill James, S; MacLeod, SL | 1 |
| Chowdhury, S; Cleves, MA; Erickson, SW; Hobbs, CA; Hu, P; James, SJ; MacLeod, SL; Melnyk, S | 1 |
| Cleves, MA; Hobbs, CA; James, SJ; Melnyk, S; Zhao, W | 1 |
| Cohn, JS; Li, D; Liu, Y; Pickell, L; Rozen, R; Wu, Q | 1 |
| Abdulsabur, N; Antshel, KM; Colgan, D; Fremont, W; Funke, B; Higgins, AM; Kates, WR; Kucherlapati, R; Shprintzen, RJ | 1 |
| Eskes, TK | 1 |
| Doszpod, J; Fekete, M; Gáti, I; Járai, I; Mestyán, J; Preisz, J; Soltész, G | 1 |
1 review(s) available for methionine and Abnormality, Heart
| Article | Year |
|---|---|
Clotting disorders and placental abruption: homocysteine--a new risk factor.
Topics: Abruptio Placentae; Blood Coagulation Disorders; Endothelium, Vascular; Female; Fetal Growth Retardation; Folic Acid; Heart Defects, Congenital; Humans; Hyperhomocysteinemia; Methionine; Methylenetetrahydrofolate Reductase (NADPH2); Mutation; Oxidoreductases Acting on CH-NH Group Donors; Pregnancy; Pregnancy Complications, Hematologic; Risk Factors | 2001 |
9 other study(ies) available for methionine and Abnormality, Heart
| Article | Year |
|---|---|
Urine metabolomic biomarkers for prediction of isolated fetal congenital heart defect.
Topics: Biomarkers; Female; Fetal Diseases; Heart Defects, Congenital; Humans; Lipids; Metabolomics; Methionine; Pregnancy; Prospective Studies; Tandem Mass Spectrometry | 2022 |
Maternal Exposure to Nitrogen Dioxide, Intake of Methyl Nutrients, and Congenital Heart Defects in Offspring.
Topics: Adult; Air Pollutants; Air Pollution; Case-Control Studies; Choline; Diet Records; Eating; Female; Folic Acid; Food Analysis; Heart Defects, Congenital; Humans; Infant, Newborn; Maternal Exposure; Methionine; Nitrogen Dioxide; Odds Ratio; Pregnancy; Prenatal Nutritional Physiological Phenomena; Risk Factors; United States; Vitamin B 12; Vitamin B 6 | 2017 |
Identification of altered pathways in Down syndrome-associated congenital heart defects using an individualized pathway aberrance score.
Topics: Case-Control Studies; Dioxygenases; Down Syndrome; Gene Regulatory Networks; Heart Defects, Congenital; Humans; Membrane Glycoproteins; Metabolic Networks and Pathways; Methionine; NADPH Oxidase 2; NADPH Oxidases; Phagosomes | 2016 |
Congenital heart defects and maternal genetic, metabolic, and lifestyle factors.
Topics: Adult; Arkansas; Biomarkers; Case-Control Studies; Female; Folic Acid; Genetic Variation; Genotype; Glutathione Disulfide; Heart Defects, Congenital; Humans; Life Style; Linear Models; Logistic Models; Methionine; Multivariate Analysis; Polymorphism, Single Nucleotide; Pregnancy; Risk Factors | 2011 |
Associations between maternal genotypes and metabolites implicated in congenital heart defects.
Topics: Adult; Asymptomatic Diseases; Carbon-Nitrogen Ligases; Case-Control Studies; Catalase; DNA (Cytosine-5-)-Methyltransferases; DNA Modification Methylases; DNA Repair Enzymes; Female; Folic Acid; Genotype; Glutathione; Glutathione Peroxidase; Heart Defects, Congenital; Homocysteine; Humans; Life Style; Male; Methionine; Methionine Adenosyltransferase; Polymorphism, Single Nucleotide; Risk; Tumor Suppressor Proteins | 2012 |
Congenital heart defects and abnormal maternal biomarkers of methionine and homocysteine metabolism.
Topics: Adult; Arkansas; Biomarkers; Case-Control Studies; Female; Heart Defects, Congenital; Homocysteine; Humans; Infant, Newborn; Life Style; Methionine; Pregnancy; Registries; Risk Factors; S-Adenosylhomocysteine | 2005 |
Maternal methylenetetrahydrofolate reductase deficiency and low dietary folate lead to adverse reproductive outcomes and congenital heart defects in mice.
Topics: Animals; Diet; Female; Fetal Growth Retardation; Folic Acid; Folic Acid Deficiency; Heart Defects, Congenital; Homocysteine; Methionine; Methylenetetrahydrofolate Reductase (NADPH2); Mice; Pregnancy | 2005 |
A gender-moderated effect of a functional COMT polymorphism on prefrontal brain morphology and function in velo-cardio-facial syndrome (22q11.2 deletion syndrome).
Topics: Abnormalities, Multiple; Adolescent; Alleles; Brain; Catechol O-Methyltransferase; Child; Chromosome Deletion; Chromosomes, Human, Pair 22; Cognition; DNA Mutational Analysis; Face; Female; Gene Frequency; Genotype; Heart Defects, Congenital; Humans; Magnetic Resonance Imaging; Male; Methionine; Neuropsychological Tests; Polymorphism, Genetic; Sex Factors; Syndrome; Task Performance and Analysis; Valine; Velopharyngeal Insufficiency | 2006 |
The postnatal changes in the circulating free amino acid pool in the newborn infant. 3. The plasma amino acid ratio in infants born after pregnancies complicated by toxaemia, placental infarction, impaired umbilical circulation and chronic maternal diseas
Topics: Amino Acids; Chronic Disease; Female; Glutamine; Glycine; Heart Defects, Congenital; Heart Failure; Humans; Infant, Newborn; Infarction; Isoleucine; Leucine; Maternal-Fetal Exchange; Methionine; Placenta; Pre-Eclampsia; Pregnancy; Pregnancy Complications, Cardiovascular; Pyelonephritis; Serine; Taurine; Torsion Abnormality; Umbilical Cord; Valine | 1971 |