Use of multivariate linkage analysis for dissection of a complex cognitive trait. - Wikidata - awgldk - TriplyDB

Use of multivariate linkage analysis for dissection of a complex cognitive trait.

Use of multivariate linkage analysis for dissection of a complex cognitive trait.

http://www.wikidata.org/entity/Q33904485

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Genetics of dyslexia: the evolving landscape Strong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia.A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States.Dyslexia and DCDC2: normal variation in reading and spelling is associated with DCDC2 polymorphisms in an Australian population sample Dyslexia and DYX1C1: deficits in reading and spelling associated with a missense mutation Multivariate genomewide linkage scan of neurocognitive traits and ADHD symptoms: suggestive linkage to 3q13.The genetics of reading disabilities: from phenotypes to candidate genes Genome scan for cognitive trait loci of dyslexia: Rapid naming and rapid switching of letters, numbers, and colors Genome-wide linkage scan on estimated breeding values for a quantitative trait Validating endophenotypes for schizophrenia using statistical modeling of twin data.Quantitative trait locus analysis of longitudinal quantitative trait data in complex pedigrees.Multivariate association analysis of the components of metabolic syndrome from the Framingham Heart Study Comparison of univariate and multivariate linkage analysis of traits related to hypertension.Reconsidering the asymptotic null distribution of likelihood ratio tests for genetic linkage in multivariate variance components models under complete pleiotropy.Identification of candidate genes for dyslexia susceptibility on chromosome 18.Pleiotropic effects of a chromosome 3 locus on speech-sound disorder and reading.Highly significant linkage to the SLI1 locus in an expanded sample of individuals affected by specific language impairment.Robust estimation of experimentwise P values applied to a genome scan of multiple asthma traits identifies a new region of significant linkage on chromosome 20q13.The genetics of developmental dyslexia.Subtyping schizophrenia: implications for genetic research.Replication of reported linkages for dyslexia and spelling and suggestive evidence for novel regions on chromosomes 4 and 17.In search of the perfect phenotype: an analysis of linkage and association studies of reading and reading-related processes.Genetics of white matter development: a DTI study of 705 twins and their siblings aged 12 to 29.Linkage to chromosome 1p36 for attention-deficit/hyperactivity disorder traits in school and home settings Genomewide scan for real-word reading subphenotypes of dyslexia: novel chromosome 13 locus and genetic complexity.Evidence for linkage of a new region (11p14) to eczema and allergic diseases.Genomewide scans of red cell indices suggest linkage on chromosome 6q23.The power of linkage analysis of a disease-related endophenotype using asymmetrically ascertained sib pairs.Identification of a major locus, TNF1, that controls BCG-triggered tumor necrosis factor production by leukocytes in an area hyperendemic for tuberculosis.A bivariate genome-wide association study identifies ADAM12 as a novel susceptibility gene for Kashin-Beck disease.A bivariate whole genome linkage study identified genomic regions influencing both BMD and bone structure.Multivariate association test using haplotype trend regression.Calculating asymptotic significance levels of the constrained likelihood ratio test with application to multivariate genetic linkage analysis.Association of reading disabilities with regions marked by acetylated H3 histones in KIAA0319.Genome-wide scan of reading ability in affected sibling pairs with attention-deficit/hyperactivity disorder: unique and shared genetic effects.The University of California, San Francisco Family Alcoholism Study. I. Design, methods, and demographics.Fishing for pleiotropic QTLs in a polygenic sea.Variance components analyses of multiple asthma traits in a large sample of Australian families ascertained through a twin proband.Familial correlations and inter-relationships of four asthma-associated quantitative phenotypes in 320 French EGEA families ascertained through asthmatic probands.Bivariate genome linkage analysis suggests pleiotropic effects on chromosomes 20p and 3p for body fat mass and lean mass.

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Use of multivariate linkage analysis for dissection of a complex cognitive trait.

http://www.wikidata.org/entity/Q33904485

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2003 nî lūn-bûn

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2003 թուականի Փետրուարին հրատարակուած գիտական յօդուած

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2003 թվականի փետրվարին հրատարակված գիտական հոդված

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2003年の論文

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2003年論文

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2003年論文

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2003年論文

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2003年論文

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2003年論文

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2003年论文

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name

Use of multivariate linkage analysis for dissection of a complex cognitive trait.

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Use of multivariate linkage analysis for dissection of a complex cognitive trait.

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type

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Use of multivariate linkage analysis for dissection of a complex cognitive trait.

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Use of multivariate linkage analysis for dissection of a complex cognitive trait.

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Use of multivariate linkage analysis for dissection of a complex cognitive trait.

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Use of multivariate linkage analysis for dissection of a complex cognitive trait.

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American Journal of Human Genetics

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Use of multivariate linkage analysis for dissection of a complex cognitive trait.

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P2093

Alex J Richardson

http://www.w3.org/2001/XMLSchema#string

Angela J Marlow

http://www.w3.org/2001/XMLSchema#string

I Laurence MacPhie

http://www.w3.org/2001/XMLSchema#string

Joel B Talcott

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John F Stein

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Lon R Cardon

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P2860

Evidence for linkage of spelling disability to chromosome 15

Quantitative-trait locus for specific language and reading deficits on chromosome 6p

Susceptibility loci for distinct components of developmental dyslexia on chromosomes 6 and 15

A new gene (DYX3) for dyslexia is located on chromosome 2

Quantitative trait locus for reading disability on chromosome 6

A dominant gene for developmental dyslexia on chromosome 3

A major locus for fasting insulin concentrations and insulin resistance on chromosome 6q with strong pleiotropic effects on obesity-related phenotypes in nondiabetic Mexican Americans

The neurological basis of developmental dyslexia: an overview and working hypothesis.

Evidence for linkage of stature to chromosome 3p26 in a large U.K. Family data set ascertained for type 2 diabetes

A comparison of power to detect a QTL in sib-pair data using multivariate phenotypes, mean phenotypes, and factor scores.

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561-570

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10.1086/368201

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3

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72

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Stacey S. Cherny

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2003-02-13T00:00:00Z

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10900184

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12587094

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1180232

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