Accounting for linkage in family-based tests of association with missing parental genotypes
about
Identification of significant association and gene-gene interaction of GABA receptor subunit genes in autismCigarette smoking strongly modifies the association of LOC387715 and age-related macular degenerationInteraction between interleukin 3 and dystrobrevin-binding protein 1 in schizophreniaTapasin gene polymorphism in systemic onset juvenile rheumatoid arthritis: a family-based case-control study.A dinucleotide deletion in CD24 confers protection against autoimmune diseasesGenome-wide scan linkage analysis for Parkinson's disease: the European genetic study of Parkinson's diseaseCandidate-gene screening and association analysis at the autism-susceptibility locus on chromosome 16p: evidence of association at GRIN2A and ABATPolymorphic variants in tenascin-C (TNC) are associated with atherosclerosis and coronary artery disease.Review and evaluation of methods correcting for population stratification with a focus on underlying statistical principlesFamily-based association test using both common and rare variants and accounting for directions of effects for sequencing data.An evaluation of power and type I error of single-nucleotide polymorphism transmission/disequilibrium-based statistical methods under different family structures, missing parental data, and population stratification.Likelihood-based association analysis for nuclear families and unrelated subjects with missing genotype data.GATA2 is associated with familial early-onset coronary artery disease.The Fangshan/Family-based Ischemic Stroke Study In China (FISSIC) protocol.Genetic and functional association of FAM5C with myocardial infarctionAn association analysis of Alzheimer disease candidate genes detects an ancestral risk haplotype clade in ACE and putative multilocus association between ACE, A2M, and LRRTM3.Interleukin 12B (IL12B) genetic variation and pulmonary tuberculosis: a study of cohorts from The Gambia, Guinea-Bissau, United States and ArgentinaCAPL: an efficient association software package using family and case-control data and accounting for population stratification.Association testing in a linked region using large pedigreesAging-related atherosclerosis is exacerbated by arterial expression of tumor necrosis factor receptor-1: evidence from mouse models and human association studies.TDT-HET: a new transmission disequilibrium test that incorporates locus heterogeneity into the analysis of family-based association data.Fine mapping of a linkage peak with integration of lipid traits identifies novel coronary artery disease genes on chromosome 5Investigation of the PARK10 gene in Parkinson disease.Dosage transmission disequilibrium test (dTDT) for linkage and association detection.Dissection of chromosome 16p12 linkage peak suggests a possible role for CACNG3 variants in age-related macular degeneration susceptibilityKIAA1462, a coronary artery disease associated gene, is a candidate gene for late onset Alzheimer disease in APOE carriersFamily-based gene-by-environment interaction studies: revelations and remediesNeural tube defects and folate pathway genes: family-based association tests of gene-gene and gene-environment interactions.X-APL: an improved family-based test of association in the presence of linkage for the X chromosomePeakwide mapping on chromosome 3q13 identifies the kalirin gene as a novel candidate gene for coronary artery disease.Molecular genetics of autism spectrum disorder.Case-sibling studies that acknowledge unstudied parents and permit the inclusion of unmatched individualsVariation in the miRNA-433 binding site of FGF20 confers risk for Parkinson disease by overexpression of alpha-synucleinAssociation mapping of the high-grade myopia MYP3 locus reveals novel candidates UHRF1BP1L, PTPRR, and PPFIA2.Ordered-subset analysis (OSA) for family-based association mapping of complex traitsMolecular genetics of human myopia: an update.Nitric oxide synthase genes and their interactions with environmental factors in Parkinson's diseaseComprehensive genetic analysis of the platelet activating factor acetylhydrolase (PLA2G7) gene and cardiovascular disease in case-control and family datasets.Polymorphisms of the tumor suppressor gene LSAMP are associated with left main coronary artery disease.Genomic convergence to identify candidate genes for Alzheimer disease on chromosome 10.
P2860
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P2860
Accounting for linkage in family-based tests of association with missing parental genotypes
description
2003 nî lūn-bûn
@nan
2003 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2003年の論文
@ja
2003年学术文章
@wuu
2003年学术文章
@zh-cn
2003年学术文章
@zh-hans
2003年学术文章
@zh-my
2003年学术文章
@zh-sg
2003年學術文章
@yue
name
Accounting for linkage in fami ...... ith missing parental genotypes
@ast
Accounting for linkage in fami ...... ith missing parental genotypes
@en
type
label
Accounting for linkage in fami ...... ith missing parental genotypes
@ast
Accounting for linkage in fami ...... ith missing parental genotypes
@en
prefLabel
Accounting for linkage in fami ...... ith missing parental genotypes
@ast
Accounting for linkage in fami ...... ith missing parental genotypes
@en
P2093
P2860
P356
P1476
Accounting for linkage in fami ...... ith missing parental genotypes
@en
P2093
Eden R Martin
Elizabeth R Hauser
Meredyth P Bass
Norman L Kaplan
P2860
P304
P356
10.1086/378779
P407
P577
2003-10-09T00:00:00Z