| scholarly article | Q13442814 |
| P50 | author | Richard H. Finnell | Q48454483 |
| Gary M Shaw | Q61783575 | ||
| Andrew F. Olshan | Q89913486 | ||
| Huiping Zhu | Q94959704 | ||
| Philip J Lupo | Q38523984 | ||
| P2093 | author name string | A J Agopian | |
| Laura E Mitchell | |||
| Wei Lu | |||
| Mark A Canfield | |||
| D Kim Waller | |||
| Claudia Chapa | |||
| P2860 | cites work | RETRACTED: Transcription factor 7-like 2 regulates beta-cell survival and function in human pancreatic islets | Q24302717 |
| Decreased TCF7L2 protein levels in type 2 diabetes mellitus correlate with downregulation of GIP- and GLP-1 receptors and impaired beta-cell function | Q24318496 | ||
| Effects of hyperinsulinemia and obesity on risk of neural tube defects among Mexican Americans. | Q43711999 | ||
| Risk factors for neural tube defects: associations between uncoupling protein 2 polymorphisms and spina bifida | Q44471952 | ||
| Risk of neural tube defect-affected pregnancies among obese women | Q46340446 | ||
| Are obese women at higher risk for producing malformed offspring? | Q46457036 | ||
| Prepregnant weight in relation to risk of neural tube defects | Q47333238 | ||
| Guidelines for case classification for the National Birth Defects Prevention Study | Q47847456 | ||
| Maternal obesity and risk for birth defects | Q47937598 | ||
| Cellular-tissue localization and regulation of the GLUT-1 protein in both the embryo and the visceral yolk sac from normal and experimental diabetic rats during the early postimplantation period | Q48177311 | ||
| Glucose transporter gene expression in rat conceptus during high glucose culture | Q48235645 | ||
| Polymorphisms of the UCP2 gene are associated with body fat distribution and risk of abdominal obesity in Spanish population. | Q51535656 | ||
| Impaired neural regulation of insulin secretion related to the leptin receptor gene mutation in Wistar fatty rats. | Q51552292 | ||
| Health care expenditures of children and adults with spina bifida in a privately insured U.S. population. | Q51992861 | ||
| Method for using complete and incomplete trios to identify genes related to a quantitative trait. | Q51996464 | ||
| Integration of DNA sample collection into a multi-site birth defects case-control study. | Q52114352 | ||
| Is maternal obesity a risk factor for anencephaly and spina bifida? | Q52200132 | ||
| Glucose transporter gene expression in rat conceptus during early organogenesis and exposure to insulin-induced hypoglycemic serum. | Q52228456 | ||
| Evaluation of 64 candidate single nucleotide polymorphisms as risk factors for neural tube defects in a large Irish study population. | Q54622641 | ||
| Common variants of FTO and the risk of obesity and type 2 diabetes in Indians | Q57303749 | ||
| UKPDS 19: Heterogeneity in NIDDM: separate contributions of IRS-1 and b3-adrenergic-receptor mutations to insulin resistance and obesity respectively with no evidence for glycogen synthase gene mutations | Q58679006 | ||
| Prepregnancy Obesity as a Risk Factor for Structural Birth Defects | Q60213689 | ||
| Congenital malformations in infants of diabetic mothers | Q67486618 | ||
| Maternal smoking, body mass index, and neural tube defects | Q74725209 | ||
| Haplotypes of transcription factor 7-like 2 (TCF7L2) gene and its upstream region are associated with type 2 diabetes and age of onset in Mexican Americans | Q79678220 | ||
| Human uncoupling protein 2 and 3 genes are associated with obesity in Japanese | Q79713987 | ||
| From fused toes in mice to human obesity | Q80395856 | ||
| Obesity and pregnancy | Q80870223 | ||
| TCF7L2 regulates late events in insulin secretion from pancreatic islet beta-cells | Q24321979 | ||
| A common variant in the FTO gene is associated with body mass index and predisposes to childhood and adult obesity | Q24650037 | ||
| A polymorphism (K121Q) of the human glycoprotein PC-1 gene coding region is strongly associated with insulin resistance | Q28144111 | ||
| Short-Chain Acyl-CoA Dehydrogenase Deficiency: Studies in a Large Family Adding to the Complexity of the Disorder | Q28181473 | ||
| Expression of the gene encoding the high-Km glucose transporter 2 by the early postimplantation mouse embryo is essential for neural tube defects associated with diabetic embryopathy | Q28284049 | ||
| Variation in FTO contributes to childhood obesity and severe adult obesity | Q28301922 | ||
| A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants | Q29547210 | ||
| Genome-wide association scan shows genetic variants in the FTO gene are associated with obesity-related traits | Q29614593 | ||
| A log-linear approach to case-parent-triad data: assessing effects of disease genes that act either directly or through maternal effects and that may be subject to parental imprinting | Q32074789 | ||
| Metabolic syndrome features and risk of neural tube defects | Q33299613 | ||
| Prevalence of loss-of-function FTO mutations in lean and obese individuals | Q33556631 | ||
| Analysis of FTO gene variants with obesity and glucose homeostasis measures in the multiethnic Insulin Resistance Atherosclerosis Study cohort | Q33797333 | ||
| FTO gene polymorphisms and obesity risk: a meta-analysis | Q33926033 | ||
| The genetics of obesity: FTO leads the way. | Q34005975 | ||
| Allowing for missing parents in genetic studies of case-parent triads | Q34389420 | ||
| Diabetes mellitus and birth defects | Q34803469 | ||
| FTO polymorphisms are associated with adult body mass index (BMI) and colorectal adenomas in African-Americans | Q34913822 | ||
| Genetic Variance in Uncoupling Protein 2 in Relation to Obesity, Type 2 Diabetes, and Related Metabolic Traits: Focus on the Functional -866G>A Promoter Variant (rs659366) | Q34974646 | ||
| Sixteen years and counting: an update on leptin in energy balance | Q35015746 | ||
| TCF7L2: the biggest story in diabetes genetics since HLA? | Q35566632 | ||
| The National Birth Defects Prevention Study | Q35879923 | ||
| Investigations into the etiology of neural tube defects | Q36016069 | ||
| Teratology Public Affairs Committee position paper: maternal obesity and pregnancy | Q36389426 | ||
| Maternal obesity, metabolism, and pregnancy outcomes | Q36480499 | ||
| ESCI Award 2006. Mitochondrial function and endocrine diseases | Q36764954 | ||
| Genes in glucose metabolism and association with spina bifida | Q36992673 | ||
| Uncoupling protein 2 polymorphisms as risk factors for NTDs. | Q37299596 | ||
| Molecular function of TCF7L2: Consequences of TCF7L2 splicing for molecular function and risk for type 2 diabetes | Q37793987 | ||
| Prepregnancy obesity: a complex risk factor for selected birth defects | Q37802813 | ||
| From GWAS to biology: lessons from FTO. | Q37851176 | ||
| Neural tube defects: a review of human and animal studies on the etiology of neural tube defects | Q39747006 | ||
| Analysis of PGC-1alpha variants Gly482Ser and Thr612Met concerning their PPARgamma2-coactivation function | Q40190687 | ||
| Body mass index and serum folate in childbearing age women. | Q40454699 | ||
| Abnormal metabolism and the risk for birth defects with emphasis on diabetes | Q40908094 | ||
| Microsatellites proximal to leptin and leptin receptor as risk factors for spina bifida | Q41717917 | ||
| Spina bifida phenotypes in infants or fetuses of obese mothers | Q41731742 | ||
| The obesity-associated SNPs in intron 1 of the FTO gene affect primary transcript levels | Q41734681 | ||
| P433 | issue | 12 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | obesity | Q12174 |
| P304 | page(s) | 1101-1109 | |
| P577 | publication date | 2012-11-06 | |
| P1433 | published in | American Journal of Epidemiology | Q4744243 |
| P1476 | title | Diabetes and obesity-related genes and the risk of neural tube defects in the national birth defects prevention study | |
| P478 | volume | 176 |
| Q54311714 | Association between maternal single nucleotide polymorphisms in genes regulating glucose metabolism and risk for neural tube defects in offspring. |
| Q35772757 | Association of facilitated glucose transporter 2 gene variants with the myelomeningocele phenotype |
| Q92474229 | Ceramide: a novel inducer for neural tube defects |
| Q35957563 | Detecting gene-environment interactions in human birth defects: Study designs and statistical methods |
| Q34213531 | Genetic association analyses of nitric oxide synthase genes and neural tube defects vary by phenotype |
| Q40528191 | Genetic association of the glycine cleavage system genes and myelomeningocele. |
| Q50071717 | Genetic epidemiology of neural tube defects |
| Q27015138 | Genetic, epigenetic, and environmental contributions to neural tube closure |
| Q35078632 | Genome-wide association study of maternal and inherited effects on left-sided cardiac malformations |
| Q47102970 | Impact of sample collection participation on the validity of estimated measures of association in the National Birth Defects Prevention Study when assessing gene-environment interactions |
| Q37695522 | Intersection of complex genetic traits affecting maternal metabolism, fetal metabolism, and neural tube defect risk: looking for needles in multiple haystacks |
| Q30431444 | Is LMNB1 a susceptibility gene for neural tube defects in humans? |
| Q35384441 | Maternal-fetal metabolic gene-gene interactions and risk of neural tube defects |
| Q87405864 | Neural tube defects |
| Q33620909 | Neural tube defects: recent advances, unsolved questions, and controversies |
| Q38785854 | Original Findings and Updated Meta-Analysis for the Association Between Maternal Diabetes and Risk for Congenital Heart Disease Phenotypes |
| Q38176281 | Perinatal outcomes in type 2 diabetes |
| Q54976624 | Population-based case-control study of the association between weather-related extreme heat events and neural tube defects. |
| Q35311051 | Replication and exploratory analysis of 24 candidate risk polymorphisms for neural tube defects |
| Q58327950 | Risk of birth defects associated with maternal pregestational diabetes |
Search more.