A log-linear approach to case-parent-triad data: assessing effects of disease genes that act either directly or through maternal effects and that may be subject to parental imprinting.
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Maternal genes and facial clefts in offspring: a comprehensive search for genetic associations in two population-based cleft studies from ScandinaviaThe "thermolabile" variant of methylenetetrahydrofolate reductase and neural tube defects: An evaluation of genetic risk and the relative importance of the genotypes of the embryo and the mother.Maternal genetic effects, exerted by genes involved in homocysteine remethylation, influence the risk of spina bifidaA polymorphism, R653Q, in the trifunctional enzyme methylenetetrahydrofolate dehydrogenase/methenyltetrahydrofolate cyclohydrolase/formyltetrahydrofolate synthetase is a maternal genetic risk factor for neural tube defects: report of the Birth DefecCumulative ligand activity of NODAL mutations and modifiers are linked to human heart defects and holoprosencephalyA common variant in MTHFD1L is associated with neural tube defects and mRNA splicing efficiencyFolate and one-carbon metabolism gene polymorphisms and their associations with oral facial cleftsAnalysis of case-parent trios at a locus with a deletion allele: association of GSTM1 with autismExpanding the toolbox of ADHD genetics. How can we make sense of parent of origin effects in ADHD and related behavioral phenotypes?Lack of association between genetic variation in G-protein-coupled receptor for asthma susceptibility and childhood asthma and atopyReview and evaluation of methods correcting for population stratification with a focus on underlying statistical principlesReview 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.Detection of parent-of-origin effects for quantitative traits using general pedigree data.Detection of imprinting and heterogeneous maternal effects on high blood pressure using Framingham Heart Study data.Genetic associations in preterm birth: a primer of marker selection, study design, and data analysis.An evaluation of power and type I error of single-nucleotide polymorphism transmission/disequilibrium-based statistical methods under different family structures, missing parental data, and population stratification.Likelihood-based association analysis for nuclear families and unrelated subjects with missing genotype data.Genetic association analysis using data from triads and unrelated subjectsLinkage and association analysis in pedigrees from different populationsGenetic and epigenetic factors at COL2A1 and ABCA4 influence clinical outcome in congenital toxoplasmosisA new method to account for missing data in case-parent triad studies.Genome-wide association study implicates chromosome 9q21.31 as a susceptibility locus for asthma in mexican childrenThe genetics of preterm birth: using what we know to design better association studiesGenome-wide association study of maternal and inherited loci for conotruncal heart defects.Maternal angiotensinogen (AGT) haplotypes, fetal renin (REN) haplotypes and risk of preeclampsia; estimation of gene-gene interaction from family-triad dataGene-gene interactions in the folate metabolic pathway and the risk of conotruncal heart defectsGenome-wide analysis of parent-of-origin effects in non-syndromic orofacial clefts.A hybrid design: case-parent triads supplemented by control-mother dyadsThe imprinted DLK1-MEG3 gene region on chromosome 14q32.2 alters susceptibility to type 1 diabetes.Evaluation of candidate genes in a genome-wide association study of childhood asthma in MexicansDetecting maternal-fetal genotype interactions associated with conotruncal heart defects: a haplotype-based analysis with penalized logistic regression.Association of combined maternal-fetal TNF-alpha gene G308A genotypes with preterm delivery: a gene-gene interaction study.Differential parental transmission of markers in RUNX2 among cleft case-parent trios from four populations.Entropy-based selection for maternal-fetal genotype incompatibility with application to preterm prelabor rupture of membranes.Variants of folate metabolism genes and risk of left-sided cardiac defects.A statistical design for testing transgenerational genomic imprinting in natural human populations.Detection of parent-of-origin effects based on complete and incomplete nuclear families with multiple affected children.PARP alleles within the linked chromosomal region are associated with systemic lupus erythematosusMI-GWAS: a SAS platform for the analysis of inherited and maternal genetic effects in genome-wide association studies using log-linear models.
P2860
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P2860
A log-linear approach to case-parent-triad data: assessing effects of disease genes that act either directly or through maternal effects and that may be subject to parental imprinting.
description
1998 nî lūn-bûn
@nan
1998 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
1998 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
name
A log-linear approach to case- ...... ubject to parental imprinting.
@ast
A log-linear approach to case- ...... ubject to parental imprinting.
@en
type
label
A log-linear approach to case- ...... ubject to parental imprinting.
@ast
A log-linear approach to case- ...... ubject to parental imprinting.
@en
prefLabel
A log-linear approach to case- ...... ubject to parental imprinting.
@ast
A log-linear approach to case- ...... ubject to parental imprinting.
@en
P2093
P2860
P356
P1476
A log-linear approach to case- ...... ubject to parental imprinting.
@en
P2093
P2860
P304
P356
10.1086/301802
P407
P577
1998-04-01T00:00:00Z