Investigation of maternal effects, maternal-fetal interactions and parent-of-origin effects (imprinting), using mothers and their offspring.
about
Expanding the toolbox of ADHD genetics. How can we make sense of parent of origin effects in ADHD and related behavioral phenotypes?Genome-wide association study identifies loci on 12q24 and 13q32 associated with tetralogy of FallotReview of statistical methodologies for the detection of parent-of-origin effects in family trio genome-wide association data with binary disease traits.Nonparametric method for detecting imprinting effect using all members of general pedigrees with missing data.A powerful association test for qualitative traits incorporating imprinting effects using general pedigree data.A unified framework integrating parent-of-origin effects for association study.Detecting maternal-fetal genotype interactions associated with conotruncal heart defects: a haplotype-based analysis with penalized logistic regression.Entropy-based selection for maternal-fetal genotype incompatibility with application to preterm prelabor rupture of membranes.The Gene Variants of Maternal/Fetal Renin-Angiotensin System in Preeclampsia: A Hybrid Case-Parent/Mother-Control Study.Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment.PREMIM and EMIM: tools for estimation of maternal, imprinting and interaction effects using multinomial modelling.Placental genome and maternal-placental genetic interactions: a genome-wide and candidate gene association study of placental abruptionA genome-wide survey of transgenerational genetic effects in autism.Methods for detecting interactions between imprinted genes and environmental exposures using birth cohort designs with mother-offspring pairsMaternal filaggrin mutations increase the risk of atopic dermatitis in children: an effect independent of mutation inheritanceA multi-locus likelihood method for assessing parent-of-origin effects using case-control mother-child pairs.Detecting gene-environment interactions in human birth defects: Study designs and statistical methods.Epigenetics and microRNAs in preeclampsia.Environmental epigenetics: prospects for studying epigenetic mediation of exposure-response relationships.Analysis of genetic interactions involving maternal and offspring genotypes at different Loci: power simulation and application to testicular cancer.The role of genetics in pre-eclampsia and potential pharmacogenomic interventions.Efficient simulation of epistatic interactions in case-parent trios.Joint detection of association, imprinting and maternal effects using all children and their parents.Investigation of maternal genotype effects in autism by genome-wide association.Variants in the fetal genome near FLT1 are associated with risk of preeclampsia.Human Birth Weight and Reproductive Immunology: Testing for Interactions between Maternal and Offspring KIR and HLA-C Genes.A genome-wide investigation into parent-of-origin effects in autism spectrum disorder identifies previously associated genes including SHANK3.A powerful parent-of-origin effects test for qualitative traits incorporating control children in nuclear families.Interaction between MTHFR 677C>T and periconceptional folic acid supplementation in the risk of Hypospadias.Analysis of case-parent trios for imprinting effect using a loglinear model with adjustment for sex-of-parent-specific transmission ratio distortion.Genome-Wide Association Studies and Meta-Analyses for Congenital Heart Defects.Increased Power for Detection of Parent-of-Origin Effects via the Use of Haplotype Estimation.Family-based exome-wide assessment of maternal genetic effects on susceptibility to childhood B-cell acute lymphoblastic leukemia in hispanics.Family-based exome-wide association study of childhood acute lymphoblastic leukemia among Hispanics confirms role of ARID5B in susceptibility.Genome-Wide Studies of Specific Language Impairment.Likelihood approach for detecting imprinting and in utero maternal effects using general pedigrees from prospective family-based association studies.Genome-wide detection and characterization of mating asymmetry in human populations.Genetic Association Family-Based Studies and Preeclampsia.No major role for periconceptional folic acid use and its interaction with the MTHFR C677T polymorphism in the etiology of congenital anorectal malformations.Genome-wide association study of maternal genetic effects and parent-of-origin effects on food allergy.
P2860
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P2860
Investigation of maternal effects, maternal-fetal interactions and parent-of-origin effects (imprinting), using mothers and their offspring.
description
2011 nî lūn-bûn
@nan
2011 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Investigation of maternal effe ...... g mothers and their offspring.
@ast
Investigation of maternal effe ...... g mothers and their offspring.
@en
Investigation of maternal effe ...... g mothers and their offspring.
@nl
type
label
Investigation of maternal effe ...... g mothers and their offspring.
@ast
Investigation of maternal effe ...... g mothers and their offspring.
@en
Investigation of maternal effe ...... g mothers and their offspring.
@nl
prefLabel
Investigation of maternal effe ...... g mothers and their offspring.
@ast
Investigation of maternal effe ...... g mothers and their offspring.
@en
Investigation of maternal effe ...... g mothers and their offspring.
@nl
P2093
P2860
P356
P1433
P1476
Investigation of maternal effe ...... g mothers and their offspring.
@en
P2093
Deborah L Jamison
Heather J Cordell
Holly F Ainsworth
Jennifer Unwin
P2860
P356
10.1002/GEPI.20547
P577
2011-01-01T00:00:00Z