scholarly article | Q13442814 |
P6179 | Dimensions Publication ID | 1103468504 |
P356 | DOI | 10.1186/S13148-018-0489-9 |
P932 | PMC publication ID | 5909239 |
P698 | PubMed publication ID | 29713392 |
P50 | author | Marie-Pierre Belot | Q56556686 |
Catherine Le Stunff | Q61041678 | ||
Alexandra Benachi | Q61859720 | ||
Pierre Bougnères | Q87031059 | ||
Delphine Fradin | Q42834913 | ||
P2093 | author name string | Sylvie Brailly-Tabard | |
Anne-Laure Castell | |||
Clémence Mille | |||
Nathalie Frament | |||
Nicolas Todd | |||
P2860 | cites work | Prenatal Programming of Insulin Secretion in Intrauterine Growth Restriction | Q26998568 |
DNA methylation differences at growth related genes correlate with birth weight: a molecular signature linked to developmental origins of adult disease? | Q28729719 | ||
Association of the CpG methylation pattern of the proximal insulin gene promoter with type 1 diabetes | Q28730163 | ||
Role of insulin-like growth factors in embryonic and postnatal growth | Q29620034 | ||
DNA methylation arrays as surrogate measures of cell mixture distribution | Q30530775 | ||
Genetic and environmental influences on birth weight, birth length, head circumference, and gestational age by use of population-based parent-offspring data | Q31101849 | ||
Continuous growth reference from 24th week of gestation to 24 months by gender | Q33321722 | ||
Insulin gene expression is regulated by DNA methylation | Q33501742 | ||
Influence of maternal nutrition on outcome of pregnancy: prospective cohort study | Q33638040 | ||
Genome-wide associations for birth weight and correlations with adult disease | Q34678968 | ||
The IGF1 P2 promoter is an epigenetic QTL for circulating IGF1 and human growth. | Q35186243 | ||
Genetic and environmental influences on human birth weight | Q35199106 | ||
The insulin-like growth factors and feto-placental growth | Q35226316 | ||
The insulin gene VNTR is associated with fasting insulin levels and development of juvenile obesity | Q51552396 | ||
Lack of support for a role of the insulin gene variable number of tandem repeats minisatellite (INS-VNTR) locus in fetal growth or type 2 diabetes-related intermediate traits in United Kingdom populations | Q53906332 | ||
IGF-I receptor mutations resulting in intrauterine and postnatal growth retardation | Q55671011 | ||
Conflicting results on variation in the IGFI gene highlight methodological considerations in the design of genetic association studies | Q57920412 | ||
Effects of insulin-like growth factor I (IGF-I) therapy on body composition and insulin resistance in IGF-I gene deletion | Q73687495 | ||
Polymorphism in the IGF-I gene: clinical relevance for short children born small for gestational age (SGA) | Q74245274 | ||
Association between insulin-like growth factor I (IGF-I) polymorphisms, circulating IGF-I, and pre- and postnatal growth in two European small for gestational age populations | Q79161550 | ||
Expression and protein content of IGF-I and IGF-I receptor in placentas from small, adequate and large for gestational age newborns | Q84056707 | ||
Higher methylation of the IGF1 P2 promoter is associated with idiopathic short stature | Q85664338 | ||
Insulin gene mutations as a cause of permanent neonatal diabetes | Q36002587 | ||
Neonatal DNA methylation profile in human twins is specified by a complex interplay between intrauterine environmental and genetic factors, subject to tissue-specific influence | Q36130833 | ||
450K epigenome-wide scan identifies differential DNA methylation in newborns related to maternal smoking during pregnancy | Q36379902 | ||
Insulin-like growth factor axis in pregnancies affected by fetal growth disorders | Q36513691 | ||
Neonatal genome-wide methylation patterns in relation to birth weight in the Norwegian Mother and Child Cohort | Q37671909 | ||
Global and gene-specific DNA methylation across multiple tissues in early infancy: implications for children's health research | Q37702944 | ||
Paternally Inherited IGF2 Mutation and Growth Restriction | Q40758391 | ||
Partial primary deficiency of insulin-like growth factor (IGF)-I activity associated with IGF1 mutation demonstrates its critical role in growth and brain development. | Q41937526 | ||
A novel mutation in a patient with insulin-like growth factor 1 (IGF1) deficiency | Q43074382 | ||
Parental determinants of birth weight. | Q47233870 | ||
Causes of variation in birth weight: a study of offspring of twins | Q47244779 | ||
Association of the INS VNTR with size at birth. ALSPAC Study Team. Avon Longitudinal Study of Pregnancy and Childhood | Q47289282 | ||
Famine, third-trimester pregnancy weight gain, and intrauterine growth: the Dutch Famine Birth Cohort Study. | Q47360622 | ||
Epimutation of the telomeric imprinting center region on chromosome 11p15 in Silver-Russell syndrome | Q48126284 | ||
P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
P6216 | copyright status | copyrighted | Q50423863 |
P304 | page(s) | 57 | |
P577 | publication date | 2018-04-19 | |
P1433 | published in | Clinical Epigenetics | Q18620113 |
P1476 | title | Fetal growth is associated with the CpG methylation of the P2 promoter of the IGF1 gene. | |
P478 | volume | 10 |
Q55489825 | Correction to: Fetal growth is associated with CpG methylation in the P2 promoter of the IGF1 gene. | cites work | P2860 |
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