The TDT and other family-based tests for linkage disequilibrium and association
about
High-density SNP screening of the major histocompatibility complex in systemic lupus erythematosus demonstrates strong evidence for independent susceptibility regionsAssociation between the DTNBP1 gene and intelligence: a case-control study in young patients with schizophrenia and related disorders and unaffected siblingsAssociation study in the 5q31-32 linkage region for schizophrenia using pooled DNA genotypingAllelic heterogeneity at the serotonin transporter locus (SLC6A4) confers susceptibility to autism and rigid-compulsive behaviorsVariations in GABRA2, encoding the alpha 2 subunit of the GABA(A) receptor, are associated with alcohol dependence and with brain oscillations.A sibship test for linkage in the presence of association: the sib transmission/disequilibrium testAssociation of MSX1 and TGFB3 with nonsyndromic clefting in humansA fifth locus for Bardet-Biedl syndrome maps to chromosome 2q31Functional variant in a bitter-taste receptor (hTAS2R16) influences risk of alcohol dependence.Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia.Genetics of Parkinson diseaseMaternal genetic effects, exerted by genes involved in homocysteine remethylation, influence the risk of spina bifidaVariations in the vesicular monoamine transporter 1 gene (VMAT1/SLC18A1) are associated with bipolar i disorderThe role of the CD58 locus in multiple sclerosisVariants in estrogen-biosynthesis genes CYP17 and CYP19 and breast cancer risk: a family-based genetic association studyAssociation studies for asthma and atopic diseases: a comprehensive review of the literatureTapasin gene polymorphism in systemic onset juvenile rheumatoid arthritis: a family-based case-control study.Statistical distribution of blood serotonin as a predictor of early autistic brain abnormalities.Assessing the power of tag SNPs in the mapping of quantitative trait loci (QTL) with extremal and random samples.Rheumatoid arthritis seropositive for the rheumatoid factor is linked to the protein tyrosine phosphatase nonreceptor 22-620W alleleThe genetic basis of female reproductive disorders: etiology and clinical testingGenetic Association Studies of Suicidal Behavior: A Review of the Past 10 Years, Progress, Limitations, and Future DirectionsThe disruption of Celf6, a gene identified by translational profiling of serotonergic neurons, results in autism-related behaviors.A transmission disequilibrium test for general pedigrees that is robust to the presence of random genotyping errors and any number of untyped parents.Trend-TDT - a transmission/disequilibrium based association test on functional mini/microsatellites.Differences in candidate gene association between European ancestry and African American asthmatic children.Single-nucleotide polymorphisms in corticotropin releasing hormone receptor 1 gene (CRHR1) are associated with quantitative trait of event-related potential and alcohol dependenceAssociation of single nucleotide polymorphisms in a glutamate receptor gene (GRM8) with theta power of event-related oscillations and alcohol dependenceReview and evaluation of methods correcting for population stratification with a focus on underlying statistical principlesHandling missing data in transmission disequilibrium test in nuclear families with one affected offspring.A test of transmission/disequilibrium for quantitative traits in pedigree data, by multiple regressionLinkage detection adaptive to linkage disequilibrium: the disequilibrium maximum-likelihood-binomial test for affected-sibship data.Detection of disease genes by use of family data. I. Likelihood-based theoryDetection of disease genes by use of family data. II. Application to nuclear families.Identification of two independent risk factors for lupus within the MHC in United Kingdom families.Likelihood-based association analysis for nuclear families and unrelated subjects with missing genotype data.Joint modeling of linkage and association using affected sib-pair data.A log-linear approach to case-parent-triad data: assessing effects of disease genes that act either directly or through maternal effects and that may be subject to parental imprinting.Variation in the interleukin 4-receptor alpha gene confers susceptibility to asthma and atopy in ethnically diverse populations.Genome-wide linkage analysis of inguinal hernia in pigs using affected sib pairs.
P2860
Q21092448-1EA2A9CD-1D37-4BDD-93C3-1379DB2FFF77Q21203814-17E3EDF8-9EF9-413B-88CF-D754AF3C29E1Q21260266-BD24AC49-C793-43F6-8061-0DC774F3FF25Q24531235-EC64BAFD-497A-48BB-914D-CC764B9DEBE9Q24533346-5B1B7637-4616-4791-BB31-58F384D19BD4Q24538716-89D5FF01-EA8A-42C4-A2F5-D8BDCE018791Q24539140-AD297096-B3FA-48B7-9504-185D9B30A281Q24540164-AE550172-0AA0-4680-9404-E2B2C5812206Q24540485-2216BBEC-584B-45E2-9FE5-53012C2E3CB3Q24540508-CE6D543F-873F-4C01-BC5F-3A2C3359E177Q24558967-42161CA7-C650-4E53-891B-D29C7E5C4BAEQ24632031-09CC5FC2-551F-42F2-89FE-71F4D965B818Q24645725-C6BE4341-871E-4999-9B23-57D7EF010515Q24649291-3B03DDC4-C266-4327-8A18-27BAF14BFB5CQ24796616-45639211-B455-4C64-B2B5-AB64D0B5A248Q24802474-B5981C42-5233-4758-BBA6-B23087D878AFQ24803735-E06FBAFE-B0F6-4AAE-8CCC-AC29B4A3340AQ24811773-50695C1E-2EB4-475A-A58B-0A5C06EF1028Q24812013-21D2E8C5-E8A9-48C4-9543-C0083778176BQ24812738-9D6D2FE4-D345-45B3-97D2-7AD80E31E1B6Q26865875-6C83A59F-C8D1-49CF-A52C-561341FD3D88Q28074917-F47C2393-BA02-4191-9C28-8424D1AF2F8FQ28508280-910BD487-25E3-4AFD-AC4B-B15F955C21C8Q28768577-A7107883-2FCC-4117-A112-D43E6807D459Q30365530-98F6296E-D08E-4F20-B52A-727950EC921DQ30432974-E12D7551-1C0A-433F-8D34-64C21DEDF124Q30471884-3DD89B23-D23F-4C99-9EAD-AF4B85C8A3BBQ30482193-19F0DF43-7351-47B5-BC23-7DB5630528F8Q30492697-485A68CE-14F3-4527-9AD5-C2D54CD76261Q30573014-240EC5C0-29FD-4682-B33C-3D794FC29B99Q30578160-B627A552-50D6-4A8C-8B6B-95AA86789F83Q30584895-4338BAA1-75DD-4B32-92E6-81CEE3C38E52Q30588489-07D96A06-402F-425D-BF9C-C4DD1A064531Q30588493-390E6A4E-46FA-4895-8695-A3F7195CB119Q30837981-EF039B38-B49A-40D3-B938-8A5786EEF864Q31151241-4C1ACF24-6C4A-402F-A424-29ED0BF42D1EQ31154910-061AED00-2D04-46E5-AD67-A5B4261134C8Q32074789-F6A54B38-C2B5-4322-800B-1981D08B1562Q33179741-EFE5939D-DD0F-4909-AEAB-31E63514FDA5Q33242094-C4191171-8EC1-4A08-8736-5A9B08EFA4EE
P2860
The TDT and other family-based tests for linkage disequilibrium and association
description
1996 nî lūn-bûn
@nan
1996 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
1996 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
1996年の論文
@ja
1996年論文
@yue
1996年論文
@zh-hant
1996年論文
@zh-hk
1996年論文
@zh-mo
1996年論文
@zh-tw
1996年论文
@wuu
name
The TDT and other family-based tests for linkage disequilibrium and association
@ast
The TDT and other family-based tests for linkage disequilibrium and association
@en
The TDT and other family-based tests for linkage disequilibrium and association
@nl
type
label
The TDT and other family-based tests for linkage disequilibrium and association
@ast
The TDT and other family-based tests for linkage disequilibrium and association
@en
The TDT and other family-based tests for linkage disequilibrium and association
@nl
prefLabel
The TDT and other family-based tests for linkage disequilibrium and association
@ast
The TDT and other family-based tests for linkage disequilibrium and association
@en
The TDT and other family-based tests for linkage disequilibrium and association
@nl
P2860
P3181
P1476
The TDT and other family-based tests for linkage disequilibrium and association
@en
P2093
R S Spielman
P2860
P3181
P407
P577
1996-11-01T00:00:00Z