Haplotype analysis in population genetics and association studies.
about
On the use of haplotype phylogeny to detect disease susceptibility lociInferring haplotypes at the NAT2 locus: the computational approach.Association between genetic variations in prostaglandin E2 receptor subtype EP3 gene (Ptger3) and asthma in the Korean populationBeyond race: towards a whole-genome perspective on human populations and genetic variationStatistical Approaches to Combine Genetic Association Data.PKD2 mutation in an Iranian autosomal dominant polycystic kidney disease family with misleading linkage analysis data.Haplotype sharing correlation of alcohol dependence on chromosomes 1-6 in 93 nuclear families.A comparison in association and linkage genome-wide scans for alcoholism susceptibility genes using single-nucleotide polymorphisms.Paraoxonase gene polymorphisms and haplotype analysis in a stroke population.A graphical assessment of p-values from sliding window haplotype tests of association to identify asthma susceptibility loci on chromosome 11q.Empirical vs Bayesian approach for estimating haplotypes from genotypes of unrelated individualsIncorporating single-locus tests into haplotype cladistic analysis in case-control studies.A systematic search for SNPs/haplotypes associated with disease phenotypes using a haplotype-based stepwise procedure.Performance of single nucleotide polymorphisms versus haplotypes for genome-wide association analysis in barley.Haplotype association analyses in resources of mixed structure using Monte Carlo testingAssociation between MFN2 gene polymorphisms and the risk and prognosis of acute liver failure: a case-control study in a Chinese population.Population genetics and comparative genetics of CLDN1, a gene involved in hepatitis C virus entryAssociation of ABCB1, 5-HT3B receptor and CYP2D6 genetic polymorphisms with ondansetron and metoclopramide antiemetic response in Indonesian cancer patients treated with highly emetogenic chemotherapy.Comparative SNP and haplotype analysis reveals a higher genetic diversity and rapider LD decay in tropical than temperate germplasm in maizeOsteoprotegerin CGA haplotype protection against cerebrovascular complications in anti-CCP negative patients with rheumatoid arthritisSequencing genes in silico using single nucleotide polymorphismsAssociation mapping by generalized linear regression with density-based haplotype clusteringGenome-wide association studies using haplotypes and individual SNPs in Simmental cattle.Association of germline variation in CCNE1 and CDK2 with breast cancer risk, progression and survival among Chinese Han womenTesting computational prediction of missense mutation phenotypes: functional characterization of 204 mutations of human cystathionine beta synthaseGenetic association analysis of human longevity in cohort studies of elderly subjects: an example of the PON1 gene in the Danish 1905 birth cohort.The impact of using related individuals for haplotype reconstruction in population studiesA genome-wide scan for breast cancer risk haplotypes among African American womenHaplotypes and the systematic analysis of genetic variation in genes and genomes.Genetic variation and pharmacogenomics: concepts, facts, and challenges.A survey of haplotype variants at several disease candidate genes: the importance of rare variants for complex diseases.Pharmacogenomic approaches to osteoporosis.Practical Consideration of Genotype Imputation: Sample Size, Window Size, Reference Choice, and Untyped Rate.Association mapping via regularized regression analysis of single-nucleotide-polymorphism haplotypes in variable-sized sliding windows.Pharmacogenomics of multigenic diseases: sex-specific differences in disease and treatment outcome.Ethnicity-related polymorphisms and haplotypes in the human ABCB1 geneWill investments in biobanks, prospective cohorts, and markers of common patterns of variation benefit other populations for drug response and disease susceptibility gene discovery?A comprehensive literature review of haplotyping software and methods for use with unrelated individuals.Single Marker and Haplotype-Based Association Analysis of Semolina and Pasta Colour in Elite Durum Wheat Breeding Lines Using a High-Density Consensus Map.Challenges for identifying functionally important genetic variation: the promise of combining complementary research strategies.
P2860
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P2860
Haplotype analysis in population genetics and association studies.
description
2003 nî lūn-bûn
@nan
2003 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի մարտին հրատարակված գիտական հոդված
@hy
2003年の論文
@ja
2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
name
Haplotype analysis in population genetics and association studies.
@ast
Haplotype analysis in population genetics and association studies.
@en
type
label
Haplotype analysis in population genetics and association studies.
@ast
Haplotype analysis in population genetics and association studies.
@en
prefLabel
Haplotype analysis in population genetics and association studies.
@ast
Haplotype analysis in population genetics and association studies.
@en
P2093
P2860
P1433
P1476
Haplotype analysis in population genetics and association studies.
@en
P2093
Hongyu Zhao
Mitchell H Gail
Ruth Pfeiffer
P2860
P304
P356
10.1517/PHGS.4.2.171.22636
P577
2003-03-01T00:00:00Z