HUMAN HEREDITY

HUMAN HEREDITY(英文缩写 HUM HERED),ISSN 0001-5652,eISSN 1423-0062 是一本学术期刊。本页汇总该期刊的最新影响因子、分区信息以及最新收录于 PubMed 的文献,帮助您快速了解期刊全貌。

指标来源：jcr_cas_ifqb

历年影响因子趋势

HUMAN HEREDITY 最新收录文献

1. Association analysis of population-based quantitative trait data: an assessment of ANOVA.
   Saurabh Ghosh, Gourab De
   Human heredity 2007 IF: 1.10 Q4 PMID: 17483600

   The classical analysis of variance (ANOVA) compares the means of different groups under the assumption that the variances within each of the groups are equal. However, for genetic studies of complex d…

   查看详情 DOI
2. Data acquisition for meta-analysis of genome-wide linkage studies using the genome search meta-analysis method.
   Paola Forabosco, Mandy Y M Ng, Emmanuelle Bouzigon, Sheila A Fisher, Douglas F Levinson, Cathryn M Lewis
   Human heredity 2007 IF: 1.10 Q4 PMID: 17483599

   The Genome Search Meta-Analysis (GSMA) method enables researchers to pool results across genome-wide linkage studies, to increase the power to detect linkage. RESULTS from individual studies must be e…

   查看详情 DOI
3. Detailed analysis of the relative power of direct and indirect association studies and the implications for their interpretation.
   V Moskvina, M C O'Donovan
   Human heredity 2007 IF: 1.10 Q4 PMID: 17483598

   Genetic association studies are usually based upon restricted sets of 'tag' markers selected to represent the total sequence variation. Tag selection is often determined by some threshold for the r(2)…

   查看详情 DOI
4. Relative efficiency of haplotype frequency estimation in sibships and nuclear families compared to unrelated individuals.
   H Putter, I Meulenbelt, J C van Houwelingen
   Human heredity 2007 IF: 1.10 Q4 PMID: 17483597

   The problem of estimating haplotype frequencies from unphased single nucleotide polymorphism (SNP) genotype data in sibships with and without parents is considered. We focus on the Fisher information …

   查看详情 DOI
5. An R package for analysis of whole-genome association studies.
   David Clayton, Hin-Tak Leung
   Human heredity 2007 IF: 1.10 Q4 PMID: 17483596

   To provide data classes and methods to facilitate the analysis of whole genome association studies in the R language for statistical computing. We have implemented data classes in which each genotype …

   查看详情 DOI
6. Statistical models for haplotype sharing in case-parent trio data.
   Andrew S Allen, Glen A Satten
   Human heredity 2007 IF: 1.10 Q4 PMID: 17483595

   Haplotype sharing statistics have been introduced in an ad-hoc way, often relying heavily on permutation testing. As a result, applying these approaches to whole genome association studies or to evalu…

   查看详情 DOI
7. Comparative assessment of the association information captured by SNP tagging.
   Michael Nothnagel, Andreas Wollstein, Michael Krawczak
   Human heredity 2007 IF: 1.10 Q4 PMID: 17483594

   Exploiting the association between single nucleotide polymorphisms (SNP) can potentially reduce the costs of association mapping of common disease genes. Different methods have been proposed for defin…

   查看详情 DOI
8. Towards linkage analysis with markers in linkage disequilibrium by graphical modelling.
   Alun Thomas
   Human heredity 2007 IF: 1.10 Q4 PMID: 17483593

   We review recent developments of MCMC integration methods for computations on graphical models for two applications in statistical genetics: modelling allelic association and pedigree based linkage an…

   查看详情 DOI
9. Score test for linkage in generalized linear models.
   J J P Lebrec, H C van Houwelingen
   Human heredity 2007 IF: 1.10 Q4 PMID: 17483592

   We derive a test for linkage in a Generalized Linear Mixed Model (GLMM) framework which provides a natural adjustment for marginal covariate effects. The method boils down to the score test of a quasi…

   查看详情 DOI
10. Family based studies and genetic epidemiology: theory and practice.
    J H Barrett, N A Sheehan, A Cox, J Worthington, C Cannings, M D Teare
    Human heredity 2007 IF: 1.10 Q4 PMID: 17476114

    Family based studies have underpinned many successes in uncovering the causes of monogenic and oligogenic diseases. Now research is focussing on the identification and characterisation of genes underl…

    查看详情 DOI