Parametric and nonparametric multipoint linkage analysis with imprinting and two-locus-trait models: application to mite sensitization
about
Exome capture reveals ZNF423 and CEP164 mutations, linking renal ciliopathies to DNA damage response signalingCandidate exome capture identifies mutation of SDCCAG8 as the cause of a retinal-renal ciliopathyMutations in TPRN cause a progressive form of autosomal-recessive nonsyndromic hearing lossLRP4 mutations alter Wnt/beta-catenin signaling and cause limb and kidney malformations in Cenani-Lenz syndromeDCDC2 mutations cause a renal-hepatic ciliopathy by disrupting Wnt signalingMutations in the gene encoding gap junction protein alpha 12 (connexin 46.6) cause Pelizaeus-Merzbacher-like diseaseMutations in the tight-junction gene claudin 19 (CLDN19) are associated with renal magnesium wasting, renal failure, and severe ocular involvementCrisponi syndrome is caused by mutations in the CRLF1 gene and is allelic to cold-induced sweating syndrome type 1Phenotypic and genetic heterogeneity in a genome-wide linkage study of asthma familiesA transition zone complex regulates mammalian ciliogenesis and ciliary membrane composition.Mutation of the Mg2+ transporter SLC41A1 results in a nephronophthisis-like phenotypeMutations in nuclear pore genes NUP93, NUP205 and XPO5 cause steroid-resistant nephrotic syndromeSkeletal dysplasia in a consanguineous clan from the island of Nias/Indonesia is caused by a novel mutation in B3GAT3Mutations in TRAF3IP1/IFT54 reveal a new role for IFT proteins in microtubule stabilizationGenomewide linkage screen for Waldenstrom macroglobulinemia susceptibility loci in high-risk familiesMutations in MRAP, encoding a new interacting partner of the ACTH receptor, cause familial glucocorticoid deficiency type 2Genetic imprinting analysis for alcoholism genes using variance components approachReview of statistical methodologies for the detection of parent-of-origin effects in family trio genome-wide association data with binary disease traits.A powerful association test for qualitative traits incorporating imprinting effects using general pedigree data.Linkage analysis of alcohol dependence using MOD scores.Y chromosome lineage- and village-specific genes on chromosomes 1p22 and 6q27 control visceral leishmaniasis in Sudan.A novel approach to detect parent-of-origin effects from pedigree data with application to Beckwith-Wiedemann syndrome.Joint linkage and imprinting analyses of GAW15 rheumatoid arthritis and gene expression dataDetection of parent-of-origin effects using general pedigree dataParent-of-origin effects in autism identified through genome-wide linkage analysis of 16,000 SNPs.Detection of parent-of-origin effects based on complete and incomplete nuclear families with multiple affected children.Genetics of Hereditary Ataxia in Scottish Terriers.Genomic imprinting and linkage test for quantitative-trait Loci in extended pedigreesInvestigating parent of origin effects in studies of type 2 diabetes and obesityGenomewide linkage scan for bipolar-disorder susceptibility loci among Ashkenazi Jewish familiesMapping of a new locus for congenital anomalies of the kidney and urinary tract on chromosome 8q24.A powerful test of parent-of-origin effects for quantitative traits using haplotypesAssessment of parent-of-origin effects in linkage analysis of quantitative traitsGenomewide 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.Genome scans for susceptibility genes in bipolar affective disorder.FAN1 mutations cause karyomegalic interstitial nephritis, linking chronic kidney failure to defective DNA damage repair.Mutations in RDH12 encoding a photoreceptor cell retinol dehydrogenase cause childhood-onset severe retinal dystrophy.Temtamy preaxial brachydactyly syndrome is caused by loss-of-function mutations in chondroitin synthase 1, a potential target of BMP signalingThe essence of linkage-based imprinting detection: comparing power, type 1 error, and the effects of confounders in two different analysis approaches.Detection of parent-of-origin effects in complete and incomplete nuclear families with multiple affected children using multiple tightly linked markers.
P2860
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P2860
Parametric and nonparametric multipoint linkage analysis with imprinting and two-locus-trait models: application to mite sensitization
description
2000 nî lūn-bûn
@nan
2000 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2000 թվականի մայիսին 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
Parametric and nonparametric m ...... lication to mite sensitization
@ast
Parametric and nonparametric m ...... lication to mite sensitization
@en
Parametric and nonparametric m ...... lication to mite sensitization
@nl
type
label
Parametric and nonparametric m ...... lication to mite sensitization
@ast
Parametric and nonparametric m ...... lication to mite sensitization
@en
Parametric and nonparametric m ...... lication to mite sensitization
@nl
prefLabel
Parametric and nonparametric m ...... lication to mite sensitization
@ast
Parametric and nonparametric m ...... lication to mite sensitization
@en
Parametric and nonparametric m ...... lication to mite sensitization
@nl
P2093
P2860
P356
P1476
Parametric and nonparametric m ...... lication to mite sensitization
@en
P2093
P2860
P304
P356
10.1086/302911
P407
P577
2000-05-04T00:00:00Z