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Mega2: validated data-reformatting for linkage and association analysesCRYBA4, a novel human cataract gene, is also involved in microphthalmiaCombined analysis of three genome-wide association studies on vWF and FVIII plasma levelsGenome-wide association study identifies variants in the ABO locus associated with susceptibility to pancreatic cancerBivariate genetic association of KIAA1797 with heart rate in American Indians: the Strong Heart Family StudyA human type 1 diabetes susceptibility locus maps to chromosome 21q22.3Using familial information for variant filtering in high-throughput sequencing studiesA comprehensive genetic study on left atrium size in Caribbean Hispanics identifies potential candidate genes in 17p10Heritability and preliminary genome-wide linkage analysis of arsenic metabolites in urineGenomewide linkage scan of schizophrenia in a large multicenter pedigree sample using single nucleotide polymorphismsALDH2 is associated to alcohol dependence and is the major genetic determinant of "daily maximum drinks" in a GWAS study of an isolated rural Chinese sampleA multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility lociGenetic Modifiers of Age at Onset in Carriers of the G206A Mutation in PSEN1 With Familial Alzheimer Disease Among Caribbean Hispanics.Tests for genetic interactions in type 1 diabetes: linkage and stratification analyses of 4,422 affected sib-pairs.The genetic architecture of lipoprotein subclasses in Gullah-speaking African American families enriched for type 2 diabetes: the Sea Islands Genetic African American Registry (Project SuGAR).Genome-wide scan for linkage to type 1 diabetes in 2,496 multiplex families from the Type 1 Diabetes Genetics ConsortiumGenome-wide linkage scan in Gullah-speaking African American families with type 2 diabetes: the Sea Islands Genetic African American Registry (Project SuGAR).A genome-wide linkage scan identifies multiple chromosomal regions influencing serum lipid levels in the population on the Samoan islandsMultiple genetic variant association testing by collapsing and kernel methods with pedigree or population structured dataPREST-plus identifies pedigree errors and cryptic relatedness in the GAW18 sample using genome-wide SNP data.PBAP: a pipeline for file processing and quality control of pedigree data with dense genetic markersThe impact of data quality on the identification of complex disease genes: experience from the Family Blood Pressure Program.Pedigree and genotype errors in the Framingham Heart StudyY chromosome lineage- and village-specific genes on chromosomes 1p22 and 6q27 control visceral leishmaniasis in Sudan.Linkage study of fibrinogen levels: the Strong Heart Family StudyDiabetes-specific genetic effects on obesity traits in American Indian populations: the Strong Heart Family StudyNovel quantitative trait locus is mapped to chromosome 12p11 for left ventricular mass in Dominican families: the Family Study of Stroke Risk and Carotid AtherosclerosisOtitis media: a genome-wide linkage scan with evidence of susceptibility loci within the 17q12 and 10q22.3 regions.Suggestive linkage detected for blood pressure related traits on 2q and 22q in the population on the Samoan islands.Genome-wide linkage analysis of carotid artery lumen diameter: the strong heart family study.Ancestral informative marker selection and population structure visualization using sparse Laplacian eigenfunctions.Genetic variation within the HLA class III influences T1D susceptibility conferred by high-risk HLA haplotypes.Consanguinity around the world: what do the genomic data of the HGDP-CEPH diversity panel tell us?Genome-wide association of familial late-onset Alzheimer's disease replicates BIN1 and CLU and nominates CUGBP2 in interaction with APOEGenome-wide linkage and peak-wide association study of obesity-related quantitative traits in Caribbean HispanicsAssessment of the effect of age at onset on linkage to bipolar disorder: evidence on chromosomes 18p and 21qGenomewide linkage and peakwide association analyses of carotid plaque in Caribbean HispanicsPRIMUS: rapid reconstruction of pedigrees from genome-wide estimates of identity by descent.New complexities in the genetics of stuttering: significant sex-specific linkage signals.Mapping of a blood pressure QTL on chromosome 17 in American Indians of the strong heart family study
P2860
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P2860
description
2002 nî lūn-bûn
@nan
2002 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2002年の論文
@ja
2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
@wuu
name
Enhanced pedigree error detection.
@ast
Enhanced pedigree error detection.
@en
Enhanced pedigree error detection.
@nl
type
label
Enhanced pedigree error detection.
@ast
Enhanced pedigree error detection.
@en
Enhanced pedigree error detection.
@nl
prefLabel
Enhanced pedigree error detection.
@ast
Enhanced pedigree error detection.
@en
Enhanced pedigree error detection.
@nl
P2093
P356
P1433
P1476
Enhanced pedigree error detection.
@en
P2093
Kenneth Wilder
Mary Sara McPeek
P304
P356
10.1159/000067666
P577
2002-01-01T00:00:00Z