Latent class model with familial dependence to address heterogeneity in complex diseases: adapting the approach to family-based association studies.
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Haploinsufficiency of two histone modifier genes on 6p22.3, ATXN1 and JARID2, is associated with intellectual disability.TDT-HET: a new transmission disequilibrium test that incorporates locus heterogeneity into the analysis of family-based association data.Haplotype structure enables prioritization of common markers and candidate genes in autism spectrum disorderChromatin-bound RNA and the neurobiology of psychiatric disease.Family-based association analysis of alcohol dependence criteria and severity.The NeuroIMAGE study: a prospective phenotypic, cognitive, genetic and MRI study in children with attention-deficit/hyperactivity disorder. Design and descriptives.
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Latent class model with familial dependence to address heterogeneity in complex diseases: adapting the approach to family-based association studies.
description
article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on 09 February 2011
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
Latent class model with famili ...... ily-based association studies.
@en
Latent class model with famili ...... ily-based association studies.
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type
label
Latent class model with famili ...... ily-based association studies.
@en
Latent class model with famili ...... ily-based association studies.
@nl
prefLabel
Latent class model with famili ...... ily-based association studies.
@en
Latent class model with famili ...... ily-based association studies.
@nl
P2093
P2860
P356
P1433
P1476
Latent class model with famili ...... ily-based association studies.
@en
P2093
Arafat Tayeb
Aurélie Labbe
Chantal Mérette
Jordie Croteau
P2860
P304
P356
10.1002/GEPI.20566
P577
2011-02-09T00:00:00Z