Incorporating linkage information into a common disease/rare variant framework

No abstract is available for this paper.

• Publication year

  2011

• Venue

  Genetic Epidemiology

• Publication date

  Unknown publication date

• Fields of study

  Biology, Medicine, Computer Science

• Identifiers
  DOI 10.1002/gepi.20654PMID 22128063PMCID PMC4558895
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• A method to detect single-nucleotide polymorphisms accounting for a linkage signal using covariate-based affected relative pair linkage analysis

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• Strategies for selection of subjects for sequencing after detection of a linkage peak

  2011cited by this paper
• Identity-by-descent filtering as a tool for the identification of disease alleles in exome sequence data from distant relatives

  2011influential reference
• Different approaches for dealing with rare variants in family-based genetic studies: application of a Genetic Analysis Workshop 17 problem

  2011cited by this paper
• Enriching rare variants using family-specific linkage information

  2011cited by this paper
• Linkage analysis merging replicate phenotypes: an application to three quantitative phenotypes in two African samples

  2011cited by this paper
• A novel method to detect rare variants using both family and unrelated case-control data

  2011cited by this paper
• Old lessons learned anew: family-based methods for detecting genes responsible for quantitative and qualitative traits in the Genetic Analysis Workshop 17 mini-exome sequence data

  2011cited by this paper
• Using linkage analysis of large pedigrees to guide association analyses

  2011influential reference
• On the morphology of the chromosome group in Brachystola magna

  2011cited by this paper
• THE CHROMOSOME NUMBER OF MAN

  2010cited by this paper
• A Groupwise Association Test for Rare Mutations Using a Weighted Sum Statistic

  2009cited by this paper
• An Extension of the Regression of Offspring on Mid‐Parent to Test for Association and Estimate Locus‐Specific Heritability: The Revised ROMP Method

  2007cited by this paper
• Covariate-based linkage analysis: application of a propensity score as the single covariate consistently improves power to detect linkage

  2006cited by this paper
• Merlin—rapid analysis of dense genetic maps using sparse gene flow trees

  2002cited by this paper
• Comparison of Variance Components, ANOVA and Regression of Offspring on Midparent (ROMP) Methods for SNP Markers

  2001cited by this paper
• The significance of not finding a gene.

  2001cited by this paper
• Haseman and Elston revisited

  2000cited by this paper
• A general test of association for quantitative traits in nuclear families.

  2000cited by this paper
• Multilocus linkage analysis by blocked Gibbs sampling

  2000cited by this paper
• Multipoint quantitative-trait linkage analysis in general pedigrees.

  1998cited by this paper
• Linkage and association

  1998cited by this paper
• The Future of Genetic Studies of Complex Human Diseases

  1996cited by this paper
• Avoiding recomputation in linkage analysis.

  1994cited by this paper
• Linkage and association.

  1994cited by this paper
• Faster sequential genetic linkage computations.

  1993cited by this paper
• Construction of a genetic linkage map in man using restriction fragment length polymorphisms.

  1980cited by this paper
• Estimation of the recombination fraction in human pedigrees: efficient computation of the likelihood for human linkage studies.

  1974cited by this paper
• A general model for the genetic analysis of pedigree data.

  1971cited by this paper
• Blood Groups in Man

  1962cited by this paper
• Versuche Uber Pflanzenhybriden

  1960influential reference
• Chromosomes of Man

  1959cited by this paper
• Chromosomes of Man

  1959cited by this paper
• THE CHROMOSOMES IN HEREDITY

  1903cited by this paper
• ON THE MORPHOLOGY OF THE CHROMOSO GROUP IN BRACHYSTOLA MAGNA

  1902cited by this paper

• Genomics in medicine: A new era in medicine

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• Genomic Predictors of Asthma Phenotypes and Treatment Response

  2019cites this paper
• Rediscovering the value of families for psychiatric genetics research

  2018cites this paper
• Family-based approaches: design, imputation, analysis, and beyond

  2016cites this paper
• PBAP: a pipeline for file processing and quality control of pedigree data with dense genetic markers

  2015cites this paper
• Preterm birth: prediction, prevention, care

  2014cites this paper
• Power of Family‐Based Association Designs to Detect Rare Variants in Large Pedigrees Using Imputed Genotypes

  2014cites this paper
• Heritability of type 2 diabetes and related traits

  2014cites this paper
• How next-generation sequencing is transforming complex disease genetics.

  2013cites this paper
• Identification of Rare Variants from Exome Sequence in a Large Pedigree with Autism

  2013cites this paper
• Linkage analysis identifies a locus for plasma von Willebrand factor undetected by genome-wide association

  2012cites this paper
• Genetic heterogeneity in Finnish hereditary prostate cancer using ordered subset analysis

  2012cites this paper
• Population‐based and family‐based designs to analyze rare variants in complex diseases

  2011cites this paper
• Lessons learned from Genetic Analysis Workshop 17: transitioning from genome‐wide association studies to whole‐genome statistical genetic analysis

  2011cites this paper