Maximum-likelihood estimation of haplotype frequencies in nuclear families.
about
Association of toll-interacting protein gene polymorphisms with atopic dermatitisRXRA gene variations influence Alzheimer's disease risk and cholesterol metabolismPolymorphisms and haplotypes of acid mammalian chitinase are associated with bronchial asthmaThe human GIMAP5 gene has a common polyadenylation polymorphism increasing risk to systemic lupus erythematosusImpact of IL8 and IL8-receptor alpha polymorphisms on the genetics of bronchial asthma and severe RSV infectionsVariation in conserved non-coding sequences on chromosome 5q and susceptibility to asthma and atopy.Accurate haplotype inference for multiple linked single-nucleotide polymorphisms using sibship data.Likelihood-based association analysis for nuclear families and unrelated subjects with missing genotype data.Impact of missing genotype data on Monte-Carlo simulation based haplotype analysis.Surfactant protein B polymorphisms are associated with severe respiratory syncytial virus infection, but not with asthmaHaplotype-based score test for linkage in nuclear families.Catmap: case-control and TDT meta-analysis package.Three microsatellites from the T1DGC MHC data set show highly significant association with type 1 diabetes, independent of the HLA-DRB1, -DQA1 and -DQB1 genesA novel tool for individual haplotype inference using mixed data.A genetic algorithm based method for stringent haplotyping of family data.A novel approach for haplotype-based association analysis using family dataHaplotype association analysis of combining unrelated case-control and triads with consideration of population stratification.The DAOA/G30 locus and affective disorders: haplotype based association study in a polydiagnostic approachAssociation between genes on chromosome 4p16 and non-syndromic oral clefts in four populationsDifferential parental transmission of markers in BCL3 among Korean cleft case-parent triosCombining an evolution-guided clustering algorithm and haplotype-based LRT in family association studies.Is Ankyrin a genetic risk factor for psychiatric phenotypes?Using an uncertainty-coding matrix in Bayesian regression models for haplotype-specific risk detection in family association studies.Evidence that TGFA influences risk to cleft lip with/without cleft palate through unconventional genetic mechanisms.Association of COMT genotypes with S-COMT promoter methylation in growth-discordant monozygotic twins and healthy adults.Influence of a latrophilin 3 (LPHN3) risk haplotype on event-related potential measures of cognitive response control in attention-deficit hyperactivity disorder (ADHD).A novel evolution-based method for detecting gene-gene interactions.Replication analysis confirms the association of ARID5B with childhood B-cell acute lymphoblastic leukemia.The effect of single-nucleotide polymorphism marker selection on patterns of haplotype blocks and haplotype frequency estimatesJoint analysis of tightly linked SNPs in screening step of genome-wide association studies leads to increased power.Transmission disequilibrium of polymorphic variants in the tryptophan hydroxylase-2 gene in attention-deficit/hyperactivity disorder.Detection of parent-of-origin effects in complete and incomplete nuclear families with multiple affected children using multiple tightly linked markers.The chitinase and chitinase-like proteins: a review of genetic and functional studies in asthma and immune-mediated diseases.Evidence for association of DNA sequence variants in the phosphatidylinositol-4-phosphate 5-kinase IIalpha gene (PIP5K2A) with schizophrenia.Genetic variation in the human androgen receptor gene is the major determinant of common early-onset androgenetic alopeciaEvidence for the involvement of genetic variation in the oxytocin receptor gene (OXTR) in the etiology of autistic disorders on high-functioning level.Powerful haplotype-based Hardy-Weinberg equilibrium tests for tightly linked loci.DIRAS2 is associated with adult ADHD, related traits, and co-morbid disorders.HAVCR1 gene haplotypes and infection by different viral hepatitis C virus genotypesContribution of 6p24 to non-syndromic cleft lip and palate in a Malay population: association of variants in OFC1
P2860
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P2860
Maximum-likelihood estimation of haplotype frequencies in nuclear families.
description
2004 nî lūn-bûn
@nan
2004 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2004 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
name
Maximum-likelihood estimation of haplotype frequencies in nuclear families.
@ast
Maximum-likelihood estimation of haplotype frequencies in nuclear families.
@en
Maximum-likelihood estimation of haplotype frequencies in nuclear families.
@nl
type
label
Maximum-likelihood estimation of haplotype frequencies in nuclear families.
@ast
Maximum-likelihood estimation of haplotype frequencies in nuclear families.
@en
Maximum-likelihood estimation of haplotype frequencies in nuclear families.
@nl
prefLabel
Maximum-likelihood estimation of haplotype frequencies in nuclear families.
@ast
Maximum-likelihood estimation of haplotype frequencies in nuclear families.
@en
Maximum-likelihood estimation of haplotype frequencies in nuclear families.
@nl
P356
P1433
P1476
Maximum-likelihood estimation of haplotype frequencies in nuclear families.
@en
P2093
Michael Knapp
Tim Becker
P356
10.1002/GEPI.10323
P577
2004-07-01T00:00:00Z