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by Newton-Cheh, Christopher and Johnson, Toby and Gateva, Vesela and Tobin, Martin D and Bochud, Murielle and Coin, Lachlan and Najjar, Samer S and Zhao, Jing Hua and Heath, Simon C and Eyheramendy, Susana and Papadakis, Konstantinos and Voight, Benjamin F and Scott, Laura J and Zhang, Feng and Farrall, Martin and Tanaka, Toshiko and Wallace, Chris and Chambers, John C and Khaw, Kay-Tee and Nilsson, Peter and van der Harst, Pim and Polidoro, Silvia and Grobbee, Diederick E and Onland-Moret, N. Charlotte and Bots, Michiel L and Wain, Louise V and Elliott, Katherine S and Teumer, Alexander and Luan, Jian'an and Lucas, Gavin and Kuusisto, Johanna and Burton, Paul R and Hadley, David and McArdle, Wendy L and Brown, Morris and Dominiczak, Anna and Newhouse, Stephen J and Samani, Nilesh J and Webster, John and Zeggini, Eleftheria and Beckmann, Jacques S and Bergmann, Sven and Lim, Noha and Song, Kijoung and Vollenweider, Peter and Waeber, Gerard and Waterworth, Dawn M and Yuan, Xin and Groop, Leif and Orho-Melander, Marju and Allione, Alessana and Di Gregorio, Alessana and Guarrera, Simonetta and Panico, Salvatore and Ricceri, Fulvio and Romanazzi, Valeria and Sacerdote, Carlotta and Vineis, Paolo and Barroso, Ines and Sandhu, Manjinder S and Luben, Robert N and Crawford, Gabriel J and Jousilahti, Pekka and Perola, Markus and Boehnke, Michael and Bonnycastle, Lori L and Collins, Francis S and Jackson, Anne U and Mohlke, Karen L and Stringham, Heather M and Valle, Timo T and Willer, Cristen J and Bergman, Richard N and Morken, Mario A and Doering, Angela and Gieger, Christian and Illig, Thomas and Meitinger, Thomas and Org, Elin and Pfeufer, Arne and Wichmann, H. Erich and Kathiresan, Sekar and Marrugat, Jaume and O'Donnell, Christopher J and Schwartz, Stephen M and Siscovick, David S and Subirana, Isaac and Freimer, Nelson B and Hartikainen, Anna-Liisa and McCarthy, Mark I and O'Reilly, Paul F and Peltonen, Leena and Pouta, Anneli and de Jong, Paul E and Snieder, Harold and van Gilst, Wiek H and Clarke, Robert and Goel, Anuj and Hamsten, Anders and Peden, John F and ... and Wellcome Trust Case Control Consor and Wellcome Trust Case Control Consortium and Medicinska fakulteten and Medicinska och farmaceutiska vetenskapsområdet and Molekylär medicin and Uppsala universitet and Institutionen för medicinska vetenskaper
Nature Genetics, ISSN 1061-4036, 06/2009, Volume 41, Issue 6, pp. 666 - 676
Journal Article
American Journal of Clinical Nutrition, ISSN 0002-9165, 07/2012, Volume 96, Issue 1, pp. 80 - 89
Background: Periconceptional folate is essential for proper neurodevelopment. Objective: Maternal folic acid intake was examined in relation to the risk of... 
UNITED-STATES | NEURODEVELOPMENT | NUTRITION & DIETETICS | DNA METHYLATION | EARLY-PREGNANCY | DIAGNOSTIC INTERVIEW | NEURAL-TUBE DEFECTS | SUPPLEMENT USE | SELECTION | CEREBRAL FOLATE-DEFICIENCY | CHILDREN | Maternal Nutritional Physiological Phenomena | Diet - adverse effects | Humans | Child, Preschool | Child Development Disorders, Pervasive - etiology | Infant | Male | Risk | Developmental Disabilities - genetics | Methylenetetrahydrofolate Reductase (NADPH2) - metabolism | Folic Acid - administration & dosage | Pregnancy Trimester, First | Case-Control Studies | Dietary Supplements - analysis | Methylenetetrahydrofolate Reductase (NADPH2) - genetics | Female | Food, Fortified - analysis | Child Development Disorders, Pervasive - epidemiology | Genetic Association Studies | California - epidemiology | Developmental Disabilities - etiology | Pregnancy Complications - physiopathology | Folic Acid Deficiency - physiopathology | Developmental Disabilities - epidemiology | Pregnancy | Confounding Factors (Epidemiology) | Child Development Disorders, Pervasive - genetics | Polymorphism, Single Nucleotide | Folic acid deficiency | Research | Developmental delay | Risk factors | Pervasive developmental disorders | Autism | Maternal & child health | Nutrition | Metabolism | Vitamin B | Index Medicus | Abridged Index Medicus
Journal Article
American Journal of Clinical Nutrition, ISSN 0002-9165, 03/2015, Volume 101, Issue 3, pp. 646 - 658
Background: Increased consumption of folic acid is prevalent, leading to concerns about negative consequences. The effects of folic acid on the liver, the... 
Methylenetetrahydrofolate reductase | Lipid metabolism | Liver | Choline metabolism | Folic acid | PORCINE LIVER | EMBRYONIC-DEVELOPMENT | liver | lipid metabolism | choline metabolism | NONALCOHOLIC STEATOHEPATITIS | 5,10-METHYLENETETRAHYDROFOLATE REDUCTASE | COMMON MUTATION | MASS-SPECTROMETRY | methylenetetrahydrofolate reductase | NUTRITION & DIETETICS | RISK-FACTOR | MOUSE MODEL | folic acid | DIETARY-FOLATE | Liver - pathology | Enzyme Inhibitors - poisoning | Folic Acid - poisoning | Non-alcoholic Fatty Liver Disease - etiology | Homocystinuria - etiology | Male | Methylenetetrahydrofolate Reductase (NADPH2) - metabolism | Homocystinuria - metabolism | Liver - physiopathology | Homocystinuria - physiopathology | Psychotic Disorders - physiopathology | Methylenetetrahydrofolate Reductase (NADPH2) - genetics | Mice, Mutant Strains | Psychotic Disorders - pathology | Lipogenesis | Methylenetetrahydrofolate Reductase (NADPH2) - deficiency | Dietary Supplements - poisoning | Methylenetetrahydrofolate Reductase (NADPH2) - antagonists & inhibitors | Specific Pathogen-Free Organisms | Liver - metabolism | Gene Expression Regulation | Organ Size | Lipid Metabolism | Muscle Spasticity - metabolism | Muscle Spasticity - pathology | Homocystinuria - pathology | Muscle Spasticity - etiology | Psychotic Disorders - metabolism | Animals | Heterozygote | Mice, Inbred BALB C | Muscle Spasticity - physiopathology | Mutation | Methylation | Psychotic Disorders - etiology | Fetal alcohol syndrome | Liver diseases | RNA | Cytochrome P-450 | Effect of alcohol on | Gene expression | S-adenosylmethionine | Metabolites | Choline | Physiological aspects | Fetus | Protein binding | Metabolism | Health aspects | Risk factors | Lipids | Vitamin B | Rodents | Index Medicus | Abridged Index Medicus
Journal Article
JAMA, ISSN 0098-7484, 04/2015, Volume 313, Issue 13, pp. 1325 - 1335
Journal Article
Journal Article
Lancet, The, ISSN 0140-6736, 2011, Volume 378, Issue 9791, pp. 584 - 594
Journal Article
Human Mutation, ISSN 1059-7794, 06/2015, Volume 36, Issue 6, pp. 611 - 621
Journal Article