Pages that link to "Q42669163"

The following pages link to Comparison of nonparametric statistics for detection of linkage in nuclear families: single-marker evaluation (Q42669163):

Displaying 42 items.

• Tests and estimates of allelic association in complex inheritance (Q22337189) (← links)
• Genomewide linkage study in 1,176 affected sister pair families identifies a significant susceptibility locus for endometriosis on chromosome 10q26. (Q24533776) (← links)
• Genome-wide scan linkage analysis for Parkinson's disease: the European genetic study of Parkinson's disease (Q28764371) (← links)
• Are there mappable genes for family resemblance for the magnitude of intra-individual variation in systolic blood pressure? (Q33198439) (← links)
• A SAGE study of apolipoprotein E3/3, E3/4 and E4/4 allele-specific gene expression in hippocampus in Alzheimer disease (Q33297839) (← links)
• Development of molecular genetics (Q33746321) (← links)
• Haseman-Elston regression in ascertained samples: importance of dependent variable and mean correction factor selection (Q33802260) (← links)
• Recent advances in human quantitative-trait-locus mapping: comparison of methods for discordant sibling pairs (Q33906066) (← links)
• Linkage and associated studies of schizophrenia (Q33920492) (← links)
• A survey of affected-sibship statistics for nonparametric linkage analysis (Q34020388) (← links)
• Overview of model-free methods for linkage analysis (Q34064007) (← links)
• Genomewide search for type 2 diabetes-susceptibility genes in French whites: evidence for a novel susceptibility locus for early-onset diabetes on chromosome 3q27-qter and independent replication of a type 2-diabetes locus on chromosome 1q21-q24. (Q34144320) (← links)
• Two loci on chromosomes 2 and X for premature coronary heart disease identified in early- and late-settlement populations of Finland (Q34144326) (← links)
• A genome screen of multiplex sibships with prostate cancer. (Q34145438) (← links)
• Linkage analysis in the presence of errors IV: joint pseudomarker analysis of linkage and/or linkage disequilibrium on a mixture of pedigrees and singletons when the mode of inheritance cannot be accurately specified (Q34145564) (← links)
• A genomewide screen for schizophrenia genes in an isolated Finnish subpopulation, suggesting multiple susceptibility loci (Q34145757) (← links)
• Genome scan for human obesity and linkage to markers in 20q13. (Q34388612) (← links)
• Further evidence for the increased power of LOD scores compared with nonparametric methods (Q34388663) (← links)
• Sib-pairs in multifactorial disorders: the sib-similarity problem (Q35041698) (← links)
• Genetics of diabetic nephropathy in the Pima Indians (Q35087689) (← links)
• Statistical tools for linkage analysis and genetic association studies (Q36252211) (← links)
• Family-based designs for genome-wide association studies (Q37883023) (← links)
• Gene-dropping vs. empirical variance estimation for allele-sharing linkage statistics (Q42595653) (← links)
• The power and statistical behaviour of allele-sharing statistics when applied to models with two disease loci (Q42597984) (← links)
• Direct power comparisons between simple LOD scores and NPL scores for linkage analysis in complex diseases (Q43218606) (← links)
• An evaluation of affected-sib-pair methods and transmission/disequilibrium tests for detecting genes underlying a complex trait (Q43540837) (← links)
• Two tests of association for a susceptibility locus for families of variable size: an example using two sampling strategies (Q44872333) (← links)
• A schizophrenia locus may be located in region 10p15-p11. (Q45112693) (← links)
• Reply to niermeijer (Q46903118) (← links)
• Xq27 FRAXA locus is a strong candidate for dyslexia: evidence from a genome-wide scan in French families (Q48216718) (← links)
• Model-free tests for genetic linkage (Q51309366) (← links)
• A study comparing precision of the maximum multipoint heterogeneity LOD statistic to three model-free multipoint linkage methods. (Q52049789) (← links)
• Evidence for genetic linkage to alcohol dependence on chromosomes 4 and 11 from an autosome-wide scan in an American Indian population. (Q54136978) (← links)
• Detection of a cystic fibrosis modifier locus for meconium ileus on human chromosome 19q13. (Q55033106) (← links)
• Genomewide linkage scan for obsessive-compulsive disorder: evidence for susceptibility loci on chromosomes 3q, 7p, 1q, 15q and 6q (Q61875942) (← links)
• The impact of redefining affection status for alcoholism on affected-sib-pair analysis (Q73271067) (← links)
• A simple allele sharing statistic for multiple locus systems (Q73271179) (← links)
• Alternative strategies for uncovering genes contributing to alcoholism risk: unpredictable findings in a genetic wonderland (Q74743908) (← links)
• To type or not to type: the use of unaffected siblings in nonparametric linkage analysis (Q77496098) (← links)
• Update on the Genetics of Inflammatory Bowel Disease (Q79176920) (← links)
• Efficient intermediate fine mapping: confidence set inference with likelihood ratio test statistic (Q80577034) (← links)
• Pedigree Selection and Information Content (Q90439430) (← links)