Page last updated: 2024-08-23

s-adenosylmethionine and Genetic Predisposition

s-adenosylmethionine has been researched along with Genetic Predisposition in 19 studies

Research

Studies (19)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	4 (21.05)	29.6817
2010's	11 (57.89)	24.3611
2020's	4 (21.05)	2.80

Authors

Authors	Studies
Chai, JF; Chew, WS; Ching, J; Herr, DR; Khoo, CM; Khor, IW; Kovalik, JP; Raichur, S; Sim, X; Tai, ES; Torta, F; Wenk, MR	1
Chedia, AM; Finegold, DN; McClain, LL; Pan, L; Peters, DG; Rengasamy, M; Sabol, R; Segretti, AM; Shaw, P	1
Cahova, M; Chrastina, P; Drahota, Z; Hansikova, H; Kazdova, L; Malinska, H; Oliyarnyk, O; Palenickova, E; Papackova, Z; Skop, V; Spacilova, J; Trnovska, J	1
Andria, G; Catanzano, F; Di Stefano, C; Frisso, G; Nosari, N; Ombrone, D; Parenti, G; Rossi, A; Ruoppolo, M; Salvatore, F; Scolamiero, E; Tandurella, I	1
Bogas, M; Fonseca, H; Marcão, A; Osório, RV; Rocha, H; Sousa, C; Vilarinho, L	1
Cho, SY; Choi, EW; Ji, S; Jin, DK; Kim, CH; Kim, SH; Kim, SJ; Ko, AR; Paik, KH; Park, HD; Park, SW; Sohn, YB; Yeau, S	1
Chan, AY; Fong, NC; Kwong, NS; Lai, CK; Lam, CW; Lam, DS; Law, CY; Lee, HC; Mak, CM; Ng, HL; Poon, WT; Que, TL; Siu, TS; Siu, WK; Tam, S; Tong, SF; Yuen, YP	1
González-Hormazábal, P; Leiva, N; Pantoja, R; Pardo, R; Recabarren, AS; Recabarren, PA; Salamanca, C; Suazo, J	1
Barbotin, AL; Boutillier, AL; Catteau-Jonard, S; Giacobini, P; Le Gras, S; Mimouni, NEH; Paiva, I; Pigny, P; Plassard, D; Prevot, V; Simon, V; Ternier, G; Timzoura, FE	1
Bain, N; Farkas, M; Ineichen, BV; Kallweit, U; Keskitalo, S; Klotz, L; Linnebank, M; Weller, M	1
Guan, T; Guan, Z; Guo, J; Li, G; Niu, B; Wang, F; Wang, G; Wang, J; Wang, M; Wang, X; Xiang, Q; Xie, Q; Zhang, T; Zhang, Z; Zhu, Z	1
Campbell, MJ; Long, MD; Smiraglia, DJ	1
Hwang, PH; Lian, L; Zavras, AI	1
Christodoulou, J; de Brouwer, AP; Liu, XZ; Xie, D; Yan, D; Yuan, HJ	1
Baurley, J; Crott, JW; Figueiredo, JC; Haile, RW; Levine, AJ	1
Favier, A; Galan, P; Guilland, JC; Hercberg, S; Potier de Courcy, G	1
Bozinov, D; Callaway, ES; Chapkin, RS; Davidson, LA; Finnell, RH; James, J; Kappen, C; Lupton, JR; Ma, DW; Piedrahita, JA; Salbaum, JM; Spiegelstein, O; Weeks, BR	1
Farmand, S; Fliessbach, K; Kleczar, N; Klockgether, T; Linnebank, M; Orlopp, K; Pels, H; Schlegel, U; Schmidt-Wolf, IG; Urbach, H	1
Lorente, S; Montoro, MA	1

Reviews

5 review(s) available for s-adenosylmethionine and Genetic Predisposition

Article	Year
The Genomic Impact of DNA CpG Methylation on Gene Expression; Relationships in Prostate Cancer. Biomolecules, 2017, 02-14, Volume: 7, Issue:1 Topics: CpG Islands; Databases, Genetic; DNA Methylation; Epigenomics; Gene Expression; Gene Expression Regulation, Neoplastic; Gene Regulatory Networks; Genetic Predisposition to Disease; Humans; Male; Prostatic Neoplasms; S-Adenosylmethionine	2017
Hearing loss and PRPS1 mutations: Wide spectrum of phenotypes and potential therapy. International journal of audiology, 2013, Volume: 52, Issue:1 Topics: Dietary Supplements; Female; Genetic Predisposition to Disease; Hearing; Hearing Loss; Heredity; Humans; Male; Mutation; Phenotype; Ribose-Phosphate Pyrophosphokinase; S-Adenosylmethionine; Severity of Illness Index; Sex Factors	2013
Folate-genetics and colorectal neoplasia: what we know and need to know next. Molecular nutrition & food research, 2013, Volume: 57, Issue:4 Topics: 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase; Colorectal Neoplasms; Ferredoxin-NADP Reductase; Folic Acid; Genetic Predisposition to Disease; Genotype; Homocysteine; Humans; Meta-Analysis as Topic; Methylenetetrahydrofolate Reductase (NADPH2); Odds Ratio; Polymorphism, Single Nucleotide; Randomized Controlled Trials as Topic; Risk Factors; S-Adenosylmethionine; Thymidylate Synthase	2013
[Hyperhomocysteinemia: an independent risk factor or a simple marker of vascular disease?. 1. Basic data]. Pathologie-biologie, 2003, Volume: 51, Issue:2 Topics: Animals; Arteriosclerosis; Biomarkers; Cystathionine beta-Synthase; Folic Acid Deficiency; Genetic Predisposition to Disease; Homocysteine; Homocystinuria; Humans; Hyperhomocysteinemia; Methionine; Methylation; Methylenetetrahydrofolate Reductase (NADPH2); Models, Biological; Nitric Oxide; Oxidative Stress; Oxidoreductases Acting on CH-NH Group Donors; Rats; Risk Factors; S-Adenosylmethionine; Signal Transduction; Thrombophilia; Vascular Diseases; Vasodilation; Vitamin B 6 Deficiency	2003
[Cholestasis of pregnancy]. Gastroenterologia y hepatologia, 2007, Volume: 30, Issue:9 Topics: Bile; Cholagogues and Choleretics; Cholestasis, Intrahepatic; Cholestyramine Resin; Dexamethasone; Female; Fetal Distress; Genetic Predisposition to Disease; Gonadal Steroid Hormones; Humans; Incidence; Liver Function Tests; Pregnancy; Pregnancy Complications; Pregnancy Outcome; Pruritus; Risk Factors; S-Adenosylmethionine; Ursodeoxycholic Acid	2007

Other Studies

14 other study(ies) available for s-adenosylmethionine and Genetic Predisposition

Article	Year
Associations with metabolites in Chinese suggest new metabolic roles in Alzheimer's and Parkinson's diseases. Human molecular genetics, 2020, 01-15, Volume: 29, Issue:2 Topics: Alzheimer Disease; Asian People; ATP-Binding Cassette Transporters; Carnitine; China; DNA-Binding Proteins; Female; Galactosyltransferases; Genetic Loci; Genetic Predisposition to Disease; Genome-Wide Association Study; Glutathione Transferase; Glycosphingolipids; Humans; Hydroxymethylglutaryl-CoA Reductase Inhibitors; Liver-Specific Organic Anion Transporter 1; Lysophospholipids; Male; Membrane Proteins; Middle Aged; Parkinson Disease; Phosphoric Monoester Hydrolases; Serine; Serine C-Palmitoyltransferase; Sphingolipids; Sphingosine; Tandem Mass Spectrometry; Transcription Factors	2020
Rare variants and biological pathways identified in treatment-refractory depression. Journal of neuroscience research, 2020, Volume: 98, Issue:7 Topics: Adolescent; Adult; Alleles; Biopterins; Carnitine; Computer Simulation; Depressive Disorder, Treatment-Resistant; Exome Sequencing; Female; Genetic Predisposition to Disease; Humans; Male; Phenotype; Polymorphism, Single Nucleotide; Tetrahydrofolates; Young Adult	2020
Carnitine supplementation alleviates lipid metabolism derangements and protects against oxidative stress in non-obese hereditary hypertriglyceridemic rats. Applied physiology, nutrition, and metabolism = Physiologie appliquee, nutrition et metabolisme, 2015, Volume: 40, Issue:3 Topics: Animals; Carnitine; Dietary Supplements; DNA, Mitochondrial; Gene Expression Regulation; Genetic Predisposition to Disease; Homeostasis; Hypertriglyceridemia; Insulin Resistance; Kidney; Lipid Metabolism; Liver; Male; Muscle, Skeletal; Oxidative Stress; Rats	2015
The first case of mitochondrial acetoacetyl-CoA thiolase deficiency identified by expanded newborn metabolic screening in Italy: the importance of an integrated diagnostic approach. Journal of inherited metabolic disease, 2010, Volume: 33 Suppl 3 Topics: Acetyl-CoA C-Acetyltransferase; Acetyl-CoA C-Acyltransferase; Amino Acid Metabolism, Inborn Errors; Biomarkers; Carnitine; Chromatography, Liquid; DNA Mutational Analysis; Dried Blood Spot Testing; Genetic Predisposition to Disease; Genetic Testing; Heredity; Humans; Infant, Newborn; Italy; Mutation; Neonatal Screening; Pedigree; Phenotype; Predictive Value of Tests; Tandem Mass Spectrometry	2010
Four years of expanded newborn screening in Portugal with tandem mass spectrometry. Journal of inherited metabolic disease, 2010, Volume: 33 Suppl 3 Topics: Amino Acids; Biomarkers; Carnitine; Early Diagnosis; False Positive Reactions; Genetic Predisposition to Disease; Humans; Infant, Newborn; Metabolism, Inborn Errors; Neonatal Screening; Phenotype; Portugal; Predictive Value of Tests; Prevalence; Prognosis; Program Evaluation; Tandem Mass Spectrometry; Time Factors	2010
Mutations of ACADS gene associated with short-chain acyl-coenzyme A dehydrogenase deficiency. Annals of clinical and laboratory science, 2011,Fall, Volume: 41, Issue:1 Topics: Acyl-CoA Dehydrogenase; Base Sequence; Carnitine; DNA Mutational Analysis; Female; Genetic Predisposition to Disease; Homozygote; Humans; Infant, Newborn; Lipid Metabolism, Inborn Errors; Molecular Sequence Data; Mutation	2011
Fatal viral infection-associated encephalopathy in two Chinese boys: a genetically determined risk factor of thermolabile carnitine palmitoyltransferase II variants. Journal of human genetics, 2011, Volume: 56, Issue:8 Topics: Amino Acid Substitution; Base Sequence; Carnitine; Carnitine O-Palmitoyltransferase; Child, Preschool; DNA Mutational Analysis; Encephalitis, Viral; Enzyme Stability; Family Health; Fatal Outcome; Female; Genetic Predisposition to Disease; Genotype; Humans; Influenza, Human; Male; Molecular Sequence Data; Mutation; Pedigree; Risk Factors; Temperature	2011
Genetic variants in S-adenosyl-methionine synthesis pathway and nonsyndromic cleft lip with or without cleft palate in Chile. Pediatric research, 2021, Volume: 89, Issue:4 Topics: 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase; Adenosylhomocysteinase; Alleles; Chile; Cleft Lip; Cleft Palate; Female; Ferredoxin-NADP Reductase; Gene Frequency; Genes, Dominant; Genes, Recessive; Genetic Predisposition to Disease; Genotype; Haplotypes; Humans; Male; Methionine; Methionine Adenosyltransferase; Odds Ratio; Polymorphism, Single Nucleotide; S-Adenosylmethionine	2021
Polycystic ovary syndrome is transmitted via a transgenerational epigenetic process. Cell metabolism, 2021, 03-02, Volume: 33, Issue:3 Topics: Animals; Anti-Mullerian Hormone; Case-Control Studies; Disease Models, Animal; DNA Methylation; Epigenesis, Genetic; Female; Genetic Predisposition to Disease; Humans; Luteinizing Hormone; Male; Mice; Mice, Inbred C57BL; Mixed Function Oxygenases; Ovary; Polycystic Ovary Syndrome; Prenatal Care; Proto-Oncogene Proteins; S-Adenosylmethionine; Transcriptome	2021
Genetic variants of homocysteine metabolism and multiple sclerosis: a case-control study. Neuroscience letters, 2014, Mar-06, Volume: 562 Topics: 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase; Adult; Case-Control Studies; Cystathionine beta-Synthase; Female; Genetic Predisposition to Disease; Genetic Testing; Genotype; Homocysteine; Humans; Male; Methionine; Methylenetetrahydrofolate Reductase (NADPH2); Middle Aged; Multiple Sclerosis; Polymorphism, Genetic; S-Adenosylmethionine	2014
Analyses of copy number variation reveal putative susceptibility loci in MTX-induced mouse neural tube defects. Developmental neurobiology, 2014, Volume: 74, Issue:9 Topics: Animals; Chromatography, Liquid; Comparative Genomic Hybridization; Disease Models, Animal; DNA Copy Number Variations; Folic Acid; Gene Expression Profiling; Genetic Predisposition to Disease; Leucovorin; Methotrexate; Mice, Inbred C57BL; MicroRNAs; Neural Tube Defects; Real-Time Polymerase Chain Reaction; S-Adenosylmethionine; Tandem Mass Spectrometry; Tetrahydrofolate Dehydrogenase; Tetrahydrofolates	2014
Alcohol intake and folate antagonism via CYP2E1 and ALDH1: effects on oral carcinogenesis. Medical hypotheses, 2012, Volume: 78, Issue:2 Topics: Alcohol Drinking; Aldehyde Dehydrogenase 1 Family; Carcinogenesis; Cytochrome P-450 CYP2E1; DNA; Ethanol; Folic Acid Antagonists; Folic Acid Deficiency; Gene Expression Regulation, Neoplastic; Genetic Predisposition to Disease; Humans; Isoenzymes; Mouth Neoplasms; Nucleotides; Retinal Dehydrogenase; Risk; S-Adenosylmethionine	2012
Folate transport gene inactivation in mice increases sensitivity to colon carcinogenesis. Cancer research, 2005, Feb-01, Volume: 65, Issue:3 Topics: Animals; Azoxymethane; Carcinogens; Carrier Proteins; Cell Cycle; Cell Transformation, Neoplastic; Colon; Colonic Neoplasms; Folate Receptors, GPI-Anchored; Gene Expression Profiling; Gene Silencing; Genetic Predisposition to Disease; Kidney; Male; Membrane Transport Modulators; Membrane Transport Proteins; Mice; Mice, Inbred C57BL; Mice, Knockout; Oligonucleotide Array Sequence Analysis; Precancerous Conditions; Receptors, Cell Surface; Reduced Folate Carrier Protein; Reverse Transcriptase Polymerase Chain Reaction; S-Adenosylhomocysteine; S-Adenosylmethionine	2005
MTX-induced white matter changes are associated with polymorphisms of methionine metabolism. Neurology, 2005, Mar-08, Volume: 64, Issue:5 Topics: Aged; Brain; Central Nervous System Neoplasms; Demyelinating Diseases; DNA Mutational Analysis; Drug Resistance; Female; Folic Acid; Folic Acid Antagonists; Gene Frequency; Genetic Predisposition to Disease; Genetic Testing; Haplotypes; Humans; Lymphoma; Male; Methionine; Methotrexate; Middle Aged; Myelin Sheath; Nerve Fibers, Myelinated; Neurotoxins; Polymorphism, Genetic; Risk Factors; S-Adenosylmethionine	2005