about
Large-scale evidence for the effect of the COLIA1 Sp1 polymorphism on osteoporosis outcomes: the GENOMOS study.Role of the neurotrophin network in eating disorders' subphenotypes: body mass index and age at onset of the diseaseEarly life environment, neurodevelopment and the interrelation with atopyPrenatal exposure to mixtures of xenoestrogens and repetitive element DNA methylation changes in human placentaStorage conditions and stability of global DNA methylation in placental tissueThe human early-life exposome (HELIX): project rationale and designA genome-wide association meta-analysis identifies new childhood obesity loci.A pooling-based genome-wide analysis identifies new potential candidate genes for atopy in the European Community Respiratory Health Survey (ECRHS).Interaction between airborne copper exposure and ATP7B polymorphisms on inattentiveness in scholar children.Polymorphisms in ABC transporter genes and concentrations of mercury in newborns--evidence from two Mediterranean birth cohortsGenetic variants of the FADS gene cluster and ELOVL gene family, colostrums LC-PUFA levels, breastfeeding, and child cognitionGenome-wide association study of sexual maturation in males and females highlights a role for body mass and menarche loci in male puberty.Genotoxic effects in swimmers exposed to disinfection by-products in indoor swimming pools.Short-term changes in respiratory biomarkers after swimming in a chlorinated pool.Genome-wide associations for birth weight and correlations with adult diseaseGene expression of desaturase (FADS1 and FADS2) and Elongase (ELOVL5) enzymes in peripheral blood: association with polyunsaturated fatty acid levels and atopic eczema in 4-year-old children.Case-control genome-wide association study of persistent attention-deficit hyperactivity disorder identifies FBXO33 as a novel susceptibility gene for the disorder.A novel common variant in DCST2 is associated with length in early life and height in adulthoodAncient Haplotypes at the 15q24.2 Microdeletion Region Are Linked to Brain Expression of MAN2C1 and Children's Intelligence.A Genome-Wide Association Study of Attention Function in a Population-Based Sample of Children.DNA methylation levels and long-term trihalomethane exposure in drinking water: an epigenome-wide association study.The emerging landscape of dynamic DNA methylation in early childhood.Multi-ancestry genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitisNew loci associated with birth weight identify genetic links between intrauterine growth and adult height and metabolismDNA Methylation in Newborns and Maternal Smoking in Pregnancy: Genome-wide Consortium Meta-analysisPrenatal Ambient Air Pollution, Placental Mitochondrial DNA Content, and Birth Weight in the INMA (Spain) and ENVIRONAGE (Belgium) Birth CohortsHeritability and Genome-Wide Association Analyses of Sleep Duration in Children: The EAGLE Consortium.Dietary benzo(a)pyrene and fetal growth: effect modification by vitamin C intake and glutathione S-transferase P1 polymorphism.Epigenome-Wide Meta-Analysis of Methylation in Children Related to Prenatal NO2 Air Pollution ExposureA common 16p11.2 inversion underlies the joint susceptibility to asthma and obesity.Risk Model for Colorectal Cancer in Spanish Population Using Environmental and Genetic Factors: Results from the MCC-Spain study.In vitro functional assay of alleles and haplotypes of two COL1A1-promoter SNPs.A genome-wide association meta-analysis of diarrhoeal disease in young children identifies FUT2 locus and provides plausible biological pathways.Fruit and vegetable intake and vitamin C transporter gene (SLC23A2) polymorphisms in chronic lymphocytic leukaemia.Large-scale analysis of association between polymorphisms in the transforming growth factor beta 1 gene (TGFB1) and osteoporosis: the GENOMOS study.Functional analysis of the I.3, I.6, pII and I.4 promoters of CYP19 (aromatase) gene in human osteoblasts and their role in vitamin D and dexamethasone stimulation.Prenatal exposure to mixtures of xenoestrogens and genome-wide DNA methylation in human placenta.New suggestive genetic loci and biological pathways for attention function in adult attention-deficit/hyperactivity disorder.Analysis of three functional polymorphisms in relation to osteoporosis phenotypes: replication in a Spanish cohort.Maternal C-reactive protein levels in pregnancy are associated with wheezing and lower respiratory tract infections in the offspring.
P50
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P50
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hulumtuese
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հետազոտող
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Mariona Bustamante
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Mariona Bustamante
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Mariona Bustamante
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Mariona Bustamante
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P1053
M-7277-2015
P106
P1153
10539367000
P21
P2798
P31
P3829
P496
0000-0003-0127-2860