about
DCDC2 is associated with reading disability and modulates neuronal development in the brain.LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophreniaGenetic variation in the 22q11 locus and susceptibility to schizophreniaGenome-wide association study of bipolar disorder in European American and African American individualsDCDC2 genetic variants and susceptibility to developmental dyslexiaAssociations of ADH and ALDH2 gene variation with self report alcohol reactions, consumption and dependence: an integrated analysisGenetic variation in selenoprotein S influences inflammatory responseAssociation of neuropeptide Y receptor Y5 polymorphisms with dyslipidemia in Mexican AmericansThe characterization of Abelson helper integration site-1 in skeletal muscle and its links to the metabolic syndromeFunctional polymorphisms in IL13 are protective against high Schistosoma mansoni infection intensity in a Brazilian populationA transmission disequilibrium test for general pedigrees that is robust to the presence of random genotyping errors and any number of untyped parents.Genome-wide association studies for common diseases and complex traitsGenetic variation in SH3-domain GRB2-like (endophilin)-interacting protein 1 has a major impact on fat mass.Genome-wide linkage scans for type 2 diabetes mellitus in four ethnically diverse populations-significant evidence for linkage on chromosome 4q in African Americans: the Family Investigation of Nephropathy and Diabetes Research Group.A generalized family-based association test for dichotomous traits.Single-nucleotide polymorphisms in corticotropin releasing hormone receptor 1 gene (CRHR1) are associated with quantitative trait of event-related potential and alcohol dependenceReview and evaluation of methods correcting for population stratification with a focus on underlying statistical principlesHandling missing data in transmission disequilibrium test in nuclear families with one affected offspring.An exploration of heterogeneity in genetic analysis of complex pedigrees: linkage and association using whole genome sequencing data in the MAP4 region.Association analysis of whole genome sequencing data accounting for longitudinal and family designs.Family-based bivariate association tests for quantitative traitsApplication of a rank-based genetic association test to age-at-onset data from the Collaborative Study on the Genetics of Alcoholism study.Power calculations using exact data simulation: a useful tool for genetic study designsA new transmission test for affected sib-pair families.The quantitative trait linkage disequilibrium test: a more powerful alternative to the quantitative transmission disequilibrium test for use in the absence of population stratificationPedGenie: an analysis approach for genetic association testing in extended pedigrees and genealogies of arbitrary size.Polymorphisms in the HOXD4 gene are not associated with peak bone mineral density in Chinese nuclear families.Common polymorphisms of calpain-10 and the risk of Type 2 Diabetes in a Tunisian Arab population: a case-control studyDifferences in the heritability of growth and growth velocity during infancy and associations with FTO variants.Polymorphic cis- and trans-regulation of human gene expression.Genetic and molecular functional characterization of variants within TNFSF13B, a positional candidate preeclampsia susceptibility gene on 13qIdentification of candidate genes for dyslexia susceptibility on chromosome 18.Replication of the effect of SLC2A9 genetic variation on serum uric acid levels in American IndiansSCAN: SNP and copy number annotation.Identification of genetic variants associated with capecitabine-induced hand-foot syndrome through integration of patient and cell line genomic analysesAccounting for linkage in family-based tests of association with missing parental genotypesIncreasing the power and efficiency of disease-marker case-control association studies through use of allele-sharing informationParental phenotypes in family-based association analysis.Accuracy of haplotype reconstruction from haplotype-tagging single-nucleotide polymorphisms.Joint modeling of linkage and association: identifying SNPs responsible for a linkage signal
P2860
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P2860
description
2000 nî lūn-bûn
@nan
2000年の論文
@ja
2000年学术文章
@wuu
2000年学术文章
@zh
2000年学术文章
@zh-cn
2000年学术文章
@zh-hans
2000年学术文章
@zh-my
2000年学术文章
@zh-sg
2000年學術文章
@yue
2000年學術文章
@zh-hant
name
Pedigree tests of transmission disequilibrium
@en
Pedigree tests of transmission disequilibrium
@nl
type
label
Pedigree tests of transmission disequilibrium
@en
Pedigree tests of transmission disequilibrium
@nl
prefLabel
Pedigree tests of transmission disequilibrium
@en
Pedigree tests of transmission disequilibrium
@nl
P356
P1476
Pedigree tests of transmission disequilibrium
@en
P2093
P2888
P304
P356
10.1038/SJ.EJHG.5200494
P577
2000-07-01T00:00:00Z