The use of pedigree, sib-pair and association studies of common diseases for genetic mapping and epidemiology.
about
Generation Scotland: the Scottish Family Health Study; a new resource for researching genes and heritabilityLinkage analysis in the next-generation sequencing eraRuns of homozygosity in European populationsMolecular genetics of coronary artery diseaseAdvances in the genetic basis of coronary artery diseaseCognitive ontologies for neuropsychiatric phenomics researchPowerful bivariate genome-wide association analyses suggest the SOX6 gene influencing both obesity and osteoporosis phenotypes in malesGenome-wide association analyses suggested a novel mechanism for smoking behavior regulated by IL15Lack of association between the Trp719Arg polymorphism in kinesin-like protein-6 and coronary artery disease in 19 case-control studiesAccurate haplotype inference for multiple linked single-nucleotide polymorphisms using sibship data.Merging microsatellite data: enhanced methodology and software to combine genotype data for linkage and association analysisA case-control study of rheumatoid arthritis identifies an associated single nucleotide polymorphism in the NCF4 gene, supporting a role for the NADPH-oxidase complex in autoimmunity.Identification of PLCL1 gene for hip bone size variation in females in a genome-wide association study.Genomic convergence analysis of schizophrenia: mRNA sequencing reveals altered synaptic vesicular transport in post-mortem cerebellum.The genetic aspects of multiple sclerosis.The endophenotype concept in psychiatric genetics.Genome-wide association studies: progress and potential for drug discovery and development.A comparison of linkage disequilibrium patterns and estimated population recombination rates across multiple populationsLocalization of a type 1 diabetes locus in the IL2RA/CD25 region by use of tag single-nucleotide polymorphisms.Population-based proband-oriented pedigree information system: application to hypertension with population-based screening data (KCIS No. 25).Neurocognitive phenotypes and genetic dissection of disorders of brain and behavior.Contribution of regulatory and structural variations in APOE to predicting dyslipidemia.Genetic contributions to clinical pain and analgesia: avoiding pitfalls in genetic researchGenetics and epidemiology of Tourette syndrome.Polymorphisms of the IL12B and IL23R genes are associated with psoriasis.Genetic analyses of interferon pathway-related genes reveal multiple new loci associated with systemic lupus erythematosus.Discovery and replication of dopamine-related gene effects on caudate volume in young and elderly populations (N=1198) using genome-wide search.IL21R and PTH may underlie variation of femoral neck bone mineral density as revealed by a genome-wide association study.Nonlinear tests for genomewide association studies.Examining impulsivity as an endophenotype using a behavioral approach: a DRD2 TaqI A and DRD4 48-bp VNTR association study.Genome scan for Tourette disorder in affected-sibling-pair and multigenerational families.Assessing the quality of published genetic association studies in meta-analyses: the quality of genetic studies (Q-Genie) toolMolecular genetic studies of gene identification for osteoporosis: a 2004 update.Most rare missense alleles are deleterious in humans: implications for complex disease and association studies.Children of persons with Alzheimer disease: what does the future hold?The search for genenotype/phenotype associations and the phenome scan.Variation in 5' promoter region of the APOE gene contributes to predicting ischemic heart disease (IHD) in the population at large: the Copenhagen City Heart StudyTechniques for the identification of genes involved in psychiatric disorders.Cerebral vasospasm after sub-arachnoid hemorrhage as a clinical predictor and phenotype for genetic association studyCatechol-O-methyltransferase contributes to genetic susceptibility shared among anxiety spectrum phenotypes
P2860
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P2860
The use of pedigree, sib-pair and association studies of common diseases for genetic mapping and epidemiology.
description
2004 nî lūn-bûn
@nan
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
2004年论文
@zh
2004年论文
@zh-cn
name
The use of pedigree, sib-pair ...... etic mapping and epidemiology.
@ast
The use of pedigree, sib-pair ...... etic mapping and epidemiology.
@en
type
label
The use of pedigree, sib-pair ...... etic mapping and epidemiology.
@ast
The use of pedigree, sib-pair ...... etic mapping and epidemiology.
@en
prefLabel
The use of pedigree, sib-pair ...... etic mapping and epidemiology.
@ast
The use of pedigree, sib-pair ...... etic mapping and epidemiology.
@en
P2860
P356
P1433
P1476
The use of pedigree, sib-pair ...... etic mapping and epidemiology.
@en
P2093
Chiara Sabatti
Nelson Freimer
P2860
P2888
P304
P356
10.1038/NG1433
P407
P577
2004-10-01T00:00:00Z