Magnitude of type I error when single-locus linkage analysis is maximized over models: a simulation study.
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Linkage analysis in the next-generation sequencing eraIdentification of a new candidate locus for uric acid nephrolithiasis.Genomewide linkage study in 1,176 affected sister pair families identifies a significant susceptibility locus for endometriosis on chromosome 10q26.Centrotemporal sharp wave EEG trait in rolandic epilepsy maps to Elongator Protein Complex 4 (ELP4).Genomewide scan for linkage reveals evidence of several susceptibility loci for alopecia areataAn autosomal dominant genetically heterogeneous variant of rolandic epilepsy and speech disorderUsing linkage analysis to detect gene-gene interaction by stratifying family data on known disease, or disease-associated, alleles.Common and unique susceptibility loci in Graves and Hashimoto diseases: results of whole-genome screening in a data set of 102 multiplex families.Performance comparison of two-point linkage methods using microsatellite markers flanking known disease locationsLinkage analysis of alcohol dependence using MOD scores.Y chromosome lineage- and village-specific genes on chromosomes 1p22 and 6q27 control visceral leishmaniasis in Sudan.All LODs are not created equal.Linkage at 12q24 with systemic lupus erythematosus (SLE) is established and confirmed in Hispanic and European American families.Genomewide linkage scan for myopia susceptibility loci among Ashkenazi Jewish families shows evidence of linkage on chromosome 22q12A major lung cancer susceptibility locus maps to chromosome 6q23-25.Modifier gene study of meconium ileus in cystic fibrosis: statistical considerations and gene mapping resultsEvidence for linkage and association of GABRB3 and GABRA5 to panic disorder.False-positive rates in two-point parametric linkage analysisGenomewide scan and fine-mapping linkage studies in four European samples with bipolar affective disorder suggest a new susceptibility locus on chromosome 1p35-p36 and provides further evidence of loci on chromosome 4q31 and 6q24.Linkage of tuberculosis to chromosome 2q35 loci, including NRAMP1, in a large aboriginal Canadian family.Significant linkage for Tourette syndrome in a large French Canadian family.Reproducibility and complications in gene searches: linkage on chromosome 6, heterogeneity, association, and maternal inheritance in juvenile myoclonic epilepsyLinkage of familial schizophrenia to chromosome 13q32The genetics of reading disability in an often excluded sample: novel loci suggested for reading disability in Rolandic epilepsy.A new Graves disease-susceptibility locus maps to chromosome 20q11.2. International Consortium for the Genetics of Autoimmune Thyroid Disease.Further evidence for the increased power of LOD scores compared with nonparametric methods.The essence of linkage-based imprinting detection: comparing power, type 1 error, and the effects of confounders in two different analysis approaches.Evidence for linkage of adolescent-onset idiopathic generalized epilepsies to chromosome 8-and genetic heterogeneityPower comparison of parametric and nonparametric linkage tests in small pedigrees.Parametric and nonparametric multipoint linkage analysis with imprinting and two-locus-trait models: application to mite sensitizationIdentification of epilepsy genes in human and mouseGenome-wide association studies of adolescent idiopathic scoliosis suggest candidate susceptibility genes.A linkage search for joint panic disorder/bipolar genes.Further genetic evidence for a panic disorder syndrome mapping to chromosome 13q.Genome-wide linkage scan for prostate cancer susceptibility in Finland: evidence for a novel locus on 2q37.3 and confirmation of signal on 17q21-q22.Using Linkage Analysis to Detect Gene-Gene Interactions. 2. Improved Reliability and Extension to More-Complex Models.Linkage Analysis of Genomic Regions Contributing to the Expression of Type 1 Diabetes Microvascular Complications and Interaction with HLA'Linkage analysis of thyroid antibody production: evidence for shared susceptibility to clinical autoimmune thyroid diseaseThe power and robustness of maximum LOD score statisticsAutoimmune thyroiditis and diabetes: dissecting the joint genetic susceptibility in a large cohort of multiplex families.
P2860
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P2860
Magnitude of type I error when single-locus linkage analysis is maximized over models: a simulation study.
description
1997 nî lūn-bûn
@nan
1997 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
1997 թվականի հունվարին հրատարակված գիտական հոդված
@hy
1997年の論文
@ja
1997年論文
@yue
1997年論文
@zh-hant
1997年論文
@zh-hk
1997年論文
@zh-mo
1997年論文
@zh-tw
1997年论文
@wuu
name
Magnitude of type I error when ...... er models: a simulation study.
@ast
Magnitude of type I error when ...... er models: a simulation study.
@en
type
label
Magnitude of type I error when ...... er models: a simulation study.
@ast
Magnitude of type I error when ...... er models: a simulation study.
@en
prefLabel
Magnitude of type I error when ...... er models: a simulation study.
@ast
Magnitude of type I error when ...... er models: a simulation study.
@en
P2093
P2860
P1476
Magnitude of type I error when ...... ver models: a simulation study
@en
P2093
D A Greenberg
P2860
P304
P407
P577
1997-01-01T00:00:00Z