| review article | Q7318358 |
| scholarly article | Q13442814 |
| P50 | author | James Cheverud | Q29922075 |
| P2093 | author name string | Patrick Y Jay | |
| Rachel A Magnan | |||
| Yidan Qin | |||
| Ehiole Akhirome | |||
| Julie M Nogee | |||
| Nelson Ugwu | |||
| Lillian Kang | |||
| M Rebecca Zhang | |||
| Suk Dev Regmi | |||
| P2860 | cites work | Recurrence of Congenital Heart Defects in Families | Q63353105 |
| Maternal age and prevalence of isolated congenital heart defects in an urban area of the United States | Q64127646 | ||
| Maternal age and malformations in singleton births | Q73103633 | ||
| Cardiac septal and valvular dysmorphogenesis in mice heterozygous for mutations in the homeobox gene Nkx2-5 | Q73178362 | ||
| Mapping quantitative trait loci for murine growth: a closer look at genetic architecture | Q73481624 | ||
| A mouse model of congenital heart disease: cardiac arrhythmias and atrial septal defect caused by haploinsufficiency of the cardiac transcription factor Csx/Nkx2.5. | Q73665047 | ||
| Contribution of maternal effect QTL to genetic architecture of early growth in mice | Q74813674 | ||
| PROGRESS REPORT ON POSSIBILITIES IN PROGENY-TEST BREEDING | Q80960169 | ||
| The spectrum of cardiovascular anomalies in CHF1/Hey2 deficient mice reveals roles in endocardial cushion, myocardial and vascular maturation | Q81387718 | ||
| Maternal genotype affects adult offspring lipid, obesity, and diabetes phenotypes in LGXSM recombinant inbred strains | Q81753040 | ||
| The Changing Demographics of Congenital Heart Disease Hospitalizations in the United States, 1998 Through 2010 | Q86313303 | ||
| Mutations in the cardiac transcription factor NKX2.5 affect diverse cardiac developmental pathways | Q22010903 | ||
| Mutations in NOTCH1 cause aortic valve disease | Q24307999 | ||
| Congenital heart disease caused by mutations in the transcription factor NKX2-5 | Q24311343 | ||
| Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene family | Q24311501 | ||
| Mutations in human TBX5 [corrected] cause limb and cardiac malformation in Holt-Oram syndrome | Q24311600 | ||
| Missense mutations in CRELD1 are associated with cardiac atrioventricular septal defects | Q24532094 | ||
| Running forward: new frontiers in endurance exercise biology | Q26824141 | ||
| Of mice and men: molecular genetics of congenital heart disease | Q26995476 | ||
| Global genetic analysis in mice unveils central role for cilia in congenital heart disease | Q27316952 | ||
| Impact of Maternal Exercise during Pregnancy on Offspring Chronic Disease Susceptibility | Q28087749 | ||
| Mutations in NOTCH1 cause Adams-Oliver syndrome | Q28246210 | ||
| Physiologic repair of aortic atresia-hypoplastic left heart syndrome | Q28274835 | ||
| Associations between maternal genotypes and metabolites implicated in congenital heart defects | Q28276846 | ||
| Spectrum of heart disease associated with murine and human GATA4 mutation | Q28509800 | ||
| Loss of glypican-3 function causes growth factor-dependent defects in cardiac and coronary vascular development | Q28587262 | ||
| A murine model of Holt-Oram syndrome defines roles of the T-box transcription factor Tbx5 in cardiogenesis and disease | Q28594121 | ||
| The incidence of congenital heart disease | Q29614195 | ||
| Exercise prevents maternal high-fat diet-induced hypermethylation of the Pgc-1α gene and age-dependent metabolic dysfunction in the offspring | Q30457309 | ||
| The epidemiology of cardiovascular defects, part I: a study based on data from three large registries of congenital malformations | Q30776464 | ||
| Cardiovascular malformations caused by NOTCH1 mutations do not keep left: data on 428 probands with left-sided CHD and their families. | Q31040681 | ||
| Evaluation of potential modifiers of the cardiac phenotype in the 22q11.2 deletion syndrome | Q33608633 | ||
| Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study | Q33679532 | ||
| Detecting maternal-fetal genotype interactions associated with conotruncal heart defects: a haplotype-based analysis with penalized logistic regression | Q33705120 | ||
| Comparison of shunt types in the Norwood procedure for single-ventricle lesions | Q33936319 | ||
| The impact of maternal uterine genotype on postnatal growth and adult body size in mice | Q33955324 | ||
| Advanced intercross lines, an experimental population for fine genetic mapping | Q33966112 | ||
| Quantitative trait loci for murine growth | Q33967063 | ||
| Analysis of Quantitative Inheritance of Body Size in Mice. I. Hybridization and Maternal Influence | Q33976317 | ||
| Analysis of Quantitative Inheritance of Body Size in Mice. II. Gene Action and Segregation. | Q33976324 | ||
| Fine-mapping QTLs in advanced intercross lines and other outbred populations | Q34019187 | ||
| The adaptive significance of maternal effects | Q34159255 | ||
| Heterogeneity of genetic modifiers ensures normal cardiac development | Q34193363 | ||
| Metabolic signatures of exercise in human plasma | Q34441396 | ||
| Uterine and postnatal maternal effects in mice selected for differential rate of early development | Q34607805 | ||
| Quantitative trait loci for maternal performance for offspring survival in mice | Q34616395 | ||
| Rapid 3D phenotyping of cardiovascular development in mouse embryos by micro-CT with iodine staining | Q34691626 | ||
| Identification of genetic regions of importance for reproductive performance in female mice | Q34895251 | ||
| Exercise before and during pregnancy prevents the deleterious effects of maternal high-fat feeding on metabolic health of male offspring | Q35004320 | ||
| The incidence of congenital heart defects in the first year of life | Q44422241 | ||
| UTERINE EFFECTS, EPIGENETICS, AND POSTNATAL SKELETAL DEVELOPMENT IN THE MOUSE. | Q44872767 | ||
| Effect of long-term selection for early postnatal growth rate on survival and prenatal development of transferred mouse embryos | Q44873124 | ||
| Maternal obesity and infant heart defects | Q44997692 | ||
| Programmed changes in the adult rat offspring caused by maternal protein restriction during gestation and lactation are attenuated by maternal moderate-low physical training | Q45021012 | ||
| ENU induced mutations causing congenital cardiovascular anomalies | Q45153465 | ||
| Maternal age and birth defects: a population study | Q45268766 | ||
| Maternal age and non-chromosomal birth defects, Atlanta--1968-2000: teenager or thirty-something, who is at risk? | Q46282270 | ||
| Descriptive epidemiology of selected congenital heart defects, Hawaii, 1986-1999. | Q46345636 | ||
| Identification of serum analytes and metabolites associated with aerobic capacity. | Q46576290 | ||
| Cardiovascular phenotyping of fetal mice by noninvasive high-frequency ultrasound facilitates recovery of ENU-induced mutations causing congenital cardiac and extracardiac defects | Q46713408 | ||
| Mice lacking sister chromatid cohesion protein PDS5B exhibit developmental abnormalities reminiscent of Cornelia de Lange syndrome. | Q48096157 | ||
| Chromosomal Imbalances in Patients with Congenital Cardiac Defects: A Meta-analysis Reveals Novel Potential Critical Regions Involved in Heart Development | Q48318063 | ||
| Cardiac and skeletal muscle adaptations to voluntary wheel running in the mouse. | Q48921159 | ||
| Association between prepregnancy body mass index and congenital heart defects. | Q51925328 | ||
| The prostaglandin receptor EP4 triggers remodelling of the cardiovascular system at birth. | Q53963048 | ||
| Prepregnancy Body Mass Index and Congenital Heart Defects among Offspring: A Population-based Study | Q54975843 | ||
| Wheel running in the wild. | Q55546608 | ||
| NKX2.5mutations in patients with congenital heart disease | Q55671009 | ||
| Ethnicity, sex, and the incidence of congenital heart defects: a report from the National Down Syndrome Project | Q57315750 | ||
| Genome-wide association study of maternal and inherited effects on left-sided cardiac malformations | Q35078632 | ||
| Effects of maternal diet and exercise during pregnancy on glucose metabolism in skeletal muscle and fat of weanling rats | Q35324087 | ||
| The maternal-age-associated risk of congenital heart disease is modifiable | Q35365452 | ||
| Distinct metabolomic signatures are associated with longevity in humans | Q35411463 | ||
| Contribution of copy-number variation to Down syndrome-associated atrioventricular septal defects. | Q35533264 | ||
| Disentangling prenatal and postnatal maternal genetic effects reveals persistent prenatal effects on offspring growth in mice | Q35541971 | ||
| Impaired mesenchymal cell function in Gata4 mutant mice leads to diaphragmatic hernias and primary lung defects | Q35659827 | ||
| The genetics of folate metabolism and maternal risk of birth of a child with Down syndrome and associated congenital heart defects | Q35778122 | ||
| Detecting maternal-effect loci by statistical cross-fostering | Q35917369 | ||
| 3-D volumetric MRI evaluation of the placenta in fetuses with complex congenital heart disease | Q36011650 | ||
| Copy-Number Variation of the Glucose Transporter Gene SLC2A3 and Congenital Heart Defects in the 22q11.2 Deletion Syndrome | Q36060851 | ||
| Genetic modifiers predisposing to congenital heart disease in the sensitized Down syndrome population | Q36068173 | ||
| Hyperglycemia impairs left-right axis formation and thereby disturbs heart morphogenesis in mouse embryos | Q36103084 | ||
| Genome-Wide Association Study of Down Syndrome-Associated Atrioventricular Septal Defects. | Q36119845 | ||
| Human cardiac development in the first trimester: a high-resolution magnetic resonance imaging and episcopic fluorescence image capture atlas | Q36137844 | ||
| Hypoplastic left heart syndrome is associated with structural and vascular placental abnormalities and leptin dysregulation | Q36173712 | ||
| Perinatal exercise improves glucose homeostasis in adult offspring | Q36312410 | ||
| An excess of deleterious variants in VEGF-A pathway genes in Down-syndrome-associated atrioventricular septal defects | Q36358093 | ||
| Histone Modifier Genes Alter Conotruncal Heart Phenotypes in 22q11.2 Deletion Syndrome | Q36369962 | ||
| Complex trait analysis of ventricular septal defects caused by Nkx2-5 mutation | Q36464752 | ||
| A metabolic signature predicts biological age in mice | Q36553679 | ||
| Metabolomic Profiling of Submaximal Exercise at a Standardised Relative Intensity in Healthy Adults. | Q36741623 | ||
| Maternal exercise improves insulin sensitivity in mature rat offspring. | Q36741705 | ||
| Individual variability in human blood metabolites identifies age-related differences. | Q36831445 | ||
| De novo mutations in congenital heart disease with neurodevelopmental and other congenital anomalies | Q36959752 | ||
| Prepregnancy Diabetes and Offspring Risk of Congenital Heart Disease: A Nationwide Cohort Study | Q36961872 | ||
| Congenital Heart Defects in the United States: Estimating the Magnitude of the Affected Population in 2010. | Q37088620 | ||
| In silico QTL mapping of maternal nurturing ability with the mouse diversity panel. | Q37175776 | ||
| Maternal Midpregnancy Glucose Levels and Risk of Congenital Heart Disease in Offspring | Q37201277 | ||
| Achievements in congenital heart defect surgery: a prospective, 40-year study of 7038 patients | Q39068545 | ||
| microMRI-HREM pipeline for high-throughput, high-resolution phenotyping of murine embryos | Q39798860 | ||
| Multifactorial inheritance hypothesis for the etiology of congenital heart diseases. The genetic-environmental interaction | Q39973975 | ||
| Periconceptional Folic Acid Supplementation and Infant Risk of Congenital Heart Defects in Norway 1999-2009. | Q41546198 | ||
| Parental age as a risk factor for isolated congenital malformations in a Polish population. | Q41938234 | ||
| The fetal and infant origins of adult disease | Q43172631 | ||
| Congenital heart disease in maternal phenylketonuria: report from the Maternal PKU Collaborative Study | Q43592447 | ||
| Maternal age-specific risk of non-chromosomal anomalies | Q43812688 | ||
| P921 | main subject | maternal health | Q6786626 |
| P304 | page(s) | 94-102 | |
| P577 | publication date | 2016-08-20 | |
| P1433 | published in | Molecular and Cellular Endocrinology | Q1573600 |
| P1476 | title | Transgenerational cardiology: One way to a baby's heart is through the mother | |
| P478 | volume | 435 |
| Q89855892 | Associations of Assisted Reproductive Technology and Twin Pregnancy With Risk of Congenital Heart Defects |
| Q90697209 | Maternal hyperglycemia and fetal cardiac development: Clinical impact and underlying mechanisms |
| Q39223050 | The Complex Genetic Basis of Congenital Heart Defects |
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