Efficient multipoint linkage analysis through reduction of inheritance space.
about
Mutations in the formin gene INF2 cause focal segmental glomerulosclerosisA new susceptibility locus for autosomal dominant pancreatic cancer maps to chromosome 4q32-34Identification of a mutation in complement factor H-related protein 5 in patients of Cypriot origin with glomerulonephritisMaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypesComparative linkage analysis and visualization of high-density oligonucleotide SNP array dataGenetic variation in DLG5 is associated with inflammatory bowel diseaseGenotype imputationA novel COL4A1 frameshift mutation in familial kidney disease: the importance of the C-terminal NC1 domain of type IV collagenLinkage analysis of alcohol dependence using MOD scores.An updated meta-analysis approach for genetic linkage.Evaluation of linkage disequilibrium and its effect on non-parametric multipoint linkage analysis using two high density single-nucleotide polymorphism mapping panels.Forward-time simulations of human populations with complex diseasesEstimating genome-wide IBD sharing from SNP data via an efficient hidden Markov model of LD with application to gene mappingA 3.9-centimorgan-resolution human single-nucleotide polymorphism linkage map and screening set.The International Psoriasis Genetics Study: assessing linkage to 14 candidate susceptibility loci in a cohort of 942 affected sib pairs.MDR1 Ala893 polymorphism is associated with inflammatory bowel disease.Sequence-based linkage analysisA genomewide search using an original pairwise sampling approach for large genealogies identifies a new locus for total and low-density lipoprotein cholesterol in two genetically differentiated isolates of Sardinia.Interplay between BRCA1 and RHAMM regulates epithelial apicobasal polarization and may influence risk of breast cancer.Genomewide 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.Quantitative trait loci controlling refractoriness to Plasmodium falciparum in natural Anopheles gambiae mosquitoes from a malaria-endemic region in western Kenya.Dosage transmission disequilibrium test (dTDT) for linkage and association detection.Supervised machine learning and logistic regression identifies novel epistatic risk factors with PTPN22 for rheumatoid arthritis.A survey of current software for linkage analysis.Mutations in mitochondrial DNA causing tubulointerstitial kidney disease.Finding cardiovascular disease genes in the dog.Identification of a prostate cancer susceptibility locus on chromosome 7q11-21 in Jewish families.Searching for epistasis and linkage heterogeneity by correlations of pedigree-specific linkage scoresSpeeding up HMM algorithms for genetic linkage analysis via chain reductions of the state space.Quantitative-trait homozygosity and association mapping and empirical genomewide significance in large, complex pedigrees: fasting serum-insulin level in the HutteritesThe role of pleiotropy vs signaller-receiver gene epistasis in life history trade-offs: dissecting the genomic architecture of organismal design in social systems.Investigation of parent-of-origin effect in comitant strabismus using MOD score analysisExclusion of known corneal dystrophy genes in an autosomal dominant pedigree of a unique anterior membrane corneal dystrophy.Functional annotation of a novel NFKB1 promoter polymorphism that increases risk for ulcerative colitis.Rapid haplotype inference for nuclear families.The IL-10R1 S138G loss-of-function allele and ulcerative colitis.Next-generation genotype imputation service and methodsOnline system for faster multipoint linkage analysis via parallel execution on thousands of personal computers.A highly informative SNP linkage panel for human genetic studies.A missense mutation in ALDH18A1, encoding Delta1-pyrroline-5-carboxylate synthase (P5CS), causes an autosomal recessive neurocutaneous syndrome.
P2860
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P2860
Efficient multipoint linkage analysis through reduction of inheritance space.
description
2001 nî lūn-bûn
@nan
2001 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի մարտին հրատարակված գիտական հոդված
@hy
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
name
Efficient multipoint linkage analysis through reduction of inheritance space.
@ast
Efficient multipoint linkage analysis through reduction of inheritance space.
@en
Efficient multipoint linkage analysis through reduction of inheritance space.
@nl
type
label
Efficient multipoint linkage analysis through reduction of inheritance space.
@ast
Efficient multipoint linkage analysis through reduction of inheritance space.
@en
Efficient multipoint linkage analysis through reduction of inheritance space.
@nl
prefLabel
Efficient multipoint linkage analysis through reduction of inheritance space.
@ast
Efficient multipoint linkage analysis through reduction of inheritance space.
@en
Efficient multipoint linkage analysis through reduction of inheritance space.
@nl
P2860
P356
P1476
Efficient multipoint linkage analysis through reduction of inheritance space.
@en
P2093
K Markianos
L Kruglyak
P2860
P304
P356
10.1086/319507
P407
P577
2001-03-14T00:00:00Z