Polygenic disease: methods for mapping complex disease traits.
about
The genetics of inflammatory bowel diseaseGenomewide scans of complex human diseases: true linkage is hard to findSupport for the homeobox transcription factor gene ENGRAILED 2 as an autism spectrum disorder susceptibility locusGenetics and visceral leishmaniasis: of mice and manAn Increased Risk of Osteoporosis during Acquired Immunodeficiency SyndromeUsing single nucleotide polymorphisms as a means to understanding the pathophysiology of asthmaAssociation of the homeobox transcription factor, ENGRAILED 2, 3, with autism spectrum disorderComparison of three methods for single nucleotide polymorphism typing for DNA bank studies: sequence-specific oligonucleotide probe hybridisation, TaqMan liquid phase hybridisation, and microplate array diagonal gel electrophoresis (MADGE).MALDI mass spectrometry analysis of single nucleotide polymorphisms by photocleavage and charge-tagging.Full flexibility genotyping of single nucleotide polymorphisms by the GOOD assayGenetic and functional evidence for a locus controlling otitis media at chromosome 10q26.3.A novel approach to simulate gene-environment interactions in complex diseases.The immunogenetics of resistance to malaria.The role of genetic factors in autoimmune disease: implications for environmental research.ALG: automated genotype calling of Luminex assaysA genomewide scan for attention-deficit/hyperactivity disorder in an extended sample: suggestive linkage on 17p11Three probands with autistic disorder and isodicentric chromosome 15.Linkage mapping for hypertension susceptibility genes.A genomewide screen for autism: strong evidence for linkage to chromosomes 2q, 7q, and 16p.Single nucleotide polymorphisms and the future of genetic epidemiology.Tools for molecular genetic epidemiology: a comparison of MADGE methodology with other systems.Simulating gene-gene and gene-environment interactions in complex diseases: Gene-Environment iNteraction Simulator 2Defining the genetic contribution of type 2 diabetes mellitus.An analysis of linkage disequilibrium in the interleukin-1 gene cluster, using a novel grouping method for multiallelic markers.Familial aggregation of Behçet's disease in Turkey.The association of flowering time quantitative trait loci with duplicated regions and candidate loci in Brassica oleraceaGenetic and nongenetic bases for the L-shaped distribution of quantitative trait loci effects.A tale of two genotypes: consistency between two high-throughput genotyping centers.Genetic susceptibility to tuberculosis in Africans: a genome-wide scan.Genomewide search for genes influencing percent body fat in Pima Indians: suggestive linkage at chromosome 11q21-q22. Pima Diabetes Gene GroupAssociation mapping of disease loci, by use of a pooled DNA genomic screen.Linkage and association studies of atopy and the chromosome 11q13 region.A genomewide scan for loci involved in attention-deficit/hyperactivity disorder.The genetics of complex ophthalmic disorders.Protein set analyses: how could this impact the clinic?eDGAR: a database of Disease-Gene Associations with annotated Relationships among genesGenome-wide association studies in biliary atresia.A search for the gene(s) predisposing to idiopathic clubfoot.DNA variation and the future of human genetics.Genetics of complex disease: approaches, problems, and solutions.
P2860
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P2860
Polygenic disease: methods for mapping complex disease traits.
description
1995 nî lūn-bûn
@nan
1995年の論文
@ja
1995年論文
@yue
1995年論文
@zh-hant
1995年論文
@zh-hk
1995年論文
@zh-mo
1995年論文
@zh-tw
1995年论文
@wuu
1995年论文
@zh
1995年论文
@zh-cn
name
Polygenic disease: methods for mapping complex disease traits.
@en
type
label
Polygenic disease: methods for mapping complex disease traits.
@en
prefLabel
Polygenic disease: methods for mapping complex disease traits.
@en
P1433
P1476
Polygenic disease: methods for mapping complex disease traits.
@en
P2093
P304
P356
10.1016/S0168-9525(00)89163-5
P50
P577
1995-12-01T00:00:00Z