A general test of association for quantitative traits in nuclear families.
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Congenital sensorineural deafness in Australian stumpy-tail cattle dogs is an autosomal recessive trait that maps to CFA10Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffnessMusical aptitude is associated with AVPR1A-haplotypesMega2: validated data-reformatting for linkage and association analysesTrait-associated SNPs are more likely to be eQTLs: annotation to enhance discovery from GWASDNA methylation age of blood predicts all-cause mortality in later lifeThe ongoing adaptive evolution of ASPM and Microcephalin is not explained by increased intelligenceFunctional genetic screen of human diversity reveals that a methionine salvage enzyme regulates inflammatory cell deathA functional genetic link between distinct developmental language disordersIdentification of risk and age-at-onset genes on chromosome 1p in Parkinson disease.A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States.Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia.Genetic variation in the 22q11 locus and susceptibility to schizophreniaFOXP2 is not a major susceptibility gene for autism or specific language impairmentDyslexia and DCDC2: normal variation in reading and spelling is associated with DCDC2 polymorphisms in an Australian population sampleReplication of association between working memory and Reelin, a potential modifier gene in schizophreniaGenome-wide association scan for five major dimensions of personalityGenetic advances in the study of speech and language disordersIn vivo and in vitro genetic evidence of involvement of neuregulin 1 in immune system dysregulationIdentification of IFRD1 as a modifier gene for cystic fibrosis lung diseaseCorrelated genotypes in friendship networksChemotherapeutic drug susceptibility associated SNPs are enriched in expression quantitative trait lociInvestigation of variants identified in caucasian genome-wide association studies for plasma high-density lipoprotein cholesterol and triglycerides levels in Mexican dyslipidemic study samplesFine mapping on chromosome 10q22-q23 implicates Neuregulin 3 in schizophreniaCandidate genes and neuropsychological phenotypes in children with ADHD: review of association studiesThe sepiapterin reductase gene region reveals association in the PARK3 locus: analysis of familial and sporadic Parkinson's disease in European populationsAssociations of ADH and ALDH2 gene variation with self report alcohol reactions, consumption and dependence: an integrated analysisHDC gene polymorphisms are associated with age at natural menopause in Caucasian womenPLINK: a tool set for whole-genome association and population-based linkage analysesAmino acid variant in the kinase binding domain of dual-specific A kinase-anchoring protein 2: a disease susceptibility polymorphismCatechol-O-methyltransferase (COMT) Val108/158 Met polymorphism does not modulate executive function in children with ADHDAssessing the power of tag SNPs in the mapping of quantitative trait loci (QTL) with extremal and random samples.Association of ENPP1 gene polymorphisms with hand osteoarthritis in a Chuvasha population.A quantitative linkage score for an association study following a linkage analysis.Shared genetic control of expression and methylation in peripheral bloodInsertion/deletion coding polymorphisms in hHAVcr-1 are not associated with atopic asthma in the Japanese populationReplication of linkage on chromosome 7q22 and association of the regional Reelin gene with working memory in schizophrenia familiesVariants of the serotonin transporter gene (SLC6A4) significantly contribute to hyperserotonemia in autismDyslexia and DYX1C1: deficits in reading and spelling associated with a missense mutationNewly identified loci that influence lipid concentrations and risk of coronary artery disease
P2860
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P2860
A general test of association for quantitative traits in nuclear families.
description
2000 nî lūn-bûn
@nan
2000 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2000 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2000年の論文
@ja
2000年論文
@yue
2000年論文
@zh-hant
2000年論文
@zh-hk
2000年論文
@zh-mo
2000年論文
@zh-tw
2000年论文
@wuu
name
A general test of association for quantitative traits in nuclear families.
@ast
A general test of association for quantitative traits in nuclear families.
@en
A general test of association for quantitative traits in nuclear families.
@en-gb
A general test of association for quantitative traits in nuclear families.
@nl
type
label
A general test of association for quantitative traits in nuclear families.
@ast
A general test of association for quantitative traits in nuclear families.
@en
A general test of association for quantitative traits in nuclear families.
@en-gb
A general test of association for quantitative traits in nuclear families.
@nl
prefLabel
A general test of association for quantitative traits in nuclear families.
@ast
A general test of association for quantitative traits in nuclear families.
@en
A general test of association for quantitative traits in nuclear families.
@en-gb
A general test of association for quantitative traits in nuclear families.
@nl
P2860
P356
P1476
A general test of association for quantitative traits in nuclear families.
@en
P2093
P2860
P304
P356
10.1086/302698
P407
P577
2000-01-01T00:00:00Z