A new human genetic resource: a DNA bank established as part of the Avon longitudinal study of pregnancy and childhood (ALSPAC).
about
WNT16 influences bone mineral density, cortical bone thickness, bone strength, and osteoporotic fracture riskGenetic epidemiology: some special contributions of birth cohortsThe fat mass- and obesity-associated locus and dietary intake in childrenA non-synonymous variant in ADH1B is strongly associated with prenatal alcohol use in a European sample of pregnant womenPrenatal alcohol exposure and childhood balance ability: findings from a UK birth cohort studyALSPAC--the Avon Longitudinal Study of Parents and Children. I. Study methodologyPrevalence and audiological features in carriers of GJB2 mutations, c.35delG and c.101T>C (p.M34T), in a UK population study.Refining associations between TAS2R38 diplotypes and the 6-n-propylthiouracil (PROP) taste test: findings from the Avon Longitudinal Study of Parents and Children.How does body fat influence bone mass in childhood? A Mendelian randomization approachCarrier status for the common R501X and 2282del4 filaggrin mutations is not associated with hearing phenotypes in 5,377 children from the ALSPAC cohort.Glutathione-S-transferase genes and asthma phenotypes: a Human Genome Epidemiology (HuGE) systematic review and meta-analysis including unpublished data.Traits contributing to the autistic spectrum.Genome-wide association meta-analysis of cortical bone mineral density unravels allelic heterogeneity at the RANKL locus and potential pleiotropic effects on bone.Maternal prenatal anxiety and child COMT genotype predict working memory and symptoms of ADHD.Cis and trans effects of human genomic variants on gene expression.The Association Between Peer and own Aggression is Moderated by the BDNF Val-met Polymorphism.Maternal smoking during pregnancy and offspring smoking initiation: assessing the role of intrauterine exposureOPG and RANK polymorphisms are both associated with cortical bone mineral density: findings from a metaanalysis of the Avon longitudinal study of parents and children and gothenburg osteoporosis and obesity determinants cohorts.Perinatal folate-related exposures and risk of psychotic symptoms in the ALSPAC birth cohort.Association between a high-risk autism locus on 5p14 and social communication spectrum phenotypes in the general populationDependence of deodorant usage on ABCC11 genotype: scope for personalized genetics in personal hygieneTwo British women studies replicated the association between the Val66Met polymorphism in the brain-derived neurotrophic factor (BDNF) and BMI.Maternal and offspring fasting glucose and type 2 diabetes-associated genetic variants and cognitive function at age 8: a Mendelian randomization study in the Avon Longitudinal Study of Parents and Children.Vitamin B-12 status during pregnancy and child's IQ at age 8: a Mendelian randomization study in the Avon longitudinal study of parents and children.Genetic determinants of trabecular and cortical volumetric bone mineral densities and bone microstructure.Stressing the system.Effects of stressful life events, maternal depression and 5-HTTLPR genotype on emotional symptoms in pre-adolescent childrenPostnatal growth and DNA methylation are associated with differential gene expression of the TACSTD2 gene and childhood fat mass.Maternal inheritance of a promoter variant in the imprinted PHLDA2 gene significantly increases birth weightGermline melanocortin-1-receptor genotype is associated with severity of cutaneous phenotype in congenital melanocytic nevi: a role for MC1R in human fetal development.The Generation R Study Biobank: a resource for epidemiological studies in children and their parentsCognitive effects of genetic variation in monoamine neurotransmitter systems: a population-based study of COMT, MAOA, and 5HTTLPR.New germline mutations in the hypervariable minisatellite CEB1 in the parents of children with leukaemia.Umbilical cord PUFA are determined by maternal and child fatty acid desaturase (FADS) genetic variants in the Avon Longitudinal Study of Parents and Children (ALSPAC).Lack of association between COMT and working memory in a population-based cohort of healthy young adultsGenome-wide prediction of childhood asthma and related phenotypes in a longitudinal birth cohort.Ghrelin receptor gene polymorphisms and body size in children and adultsCMIP and ATP2C2 modulate phonological short-term memory in language impairment.Next-gen sequencing identifies non-coding variation disrupting miRNA-binding sites in neurological disorders.Smoking and caffeine consumption: a genetic analysis of their association.
P2860
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P2860
A new human genetic resource: a DNA bank established as part of the Avon longitudinal study of pregnancy and childhood (ALSPAC).
description
2000 nî lūn-bûn
@nan
2000 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2000 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2000年の論文
@ja
2000年論文
@yue
2000年論文
@zh-hant
2000年論文
@zh-hk
2000年論文
@zh-mo
2000年論文
@zh-tw
2000年论文
@wuu
name
A new human genetic resource: ...... gnancy and childhood (ALSPAC).
@ast
A new human genetic resource: ...... gnancy and childhood (ALSPAC).
@en
type
label
A new human genetic resource: ...... gnancy and childhood (ALSPAC).
@ast
A new human genetic resource: ...... gnancy and childhood (ALSPAC).
@en
prefLabel
A new human genetic resource: ...... gnancy and childhood (ALSPAC).
@ast
A new human genetic resource: ...... gnancy and childhood (ALSPAC).
@en
P2093
P356
P1476
A new human genetic resource: ...... gnancy and childhood (ALSPAC).
@en
P2093
ALSPAC Study Team
P2888
P304
P356
10.1038/SJ.EJHG.5200502
P50
P577
2000-09-01T00:00:00Z