(Q37806780)

23 August 2017

title

Rare variant association analysis methods for complex traits (English)

1 reference

23 August 2017

Rare Variant Association Analysis Methods for Complex Traits (English)

1 reference

https://api.crossref.org/works/10.1146/ANNUREV-GENET-102209-163421

19 August 2024

1 reference

2

1 reference

23 August 2017

1

0 references

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=21047260

19 August 2024

publication date

1 January 2010

1 reference

full work available at URL

23 August 2017

http://arjournals.annualreviews.org/doi/abs/10.1146/annurev-genet-102209-163421

online access status

open access

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A21047260

https://www.annualreviews.org/doi/pdf/10.1146/annurev-genet-102209-163421

19 August 2024

1 reference

https://api.crossref.org/works/10.1146/ANNUREV-GENET-102209-163421

Annual Review of Genetics

19 August 2024

published in

1 reference

23 August 2017

volume

44

1 reference

23 August 2017

page(s)

293-308

1 reference

Common and rare variants in multifactorial susceptibility to common diseases

23 August 2017

cites work

2

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Rapid and accurate haplotype phasing and missing-data inference for whole-genome association studies by use of localized haplotype clustering

19 August 2024

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Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol

19 August 2024

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Multiple rare variants in NPC1L1 associated with reduced sterol absorption and plasma low-density lipoprotein levels

19 August 2024

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https://api.crossref.org/works/10.1146/ANNUREV-GENET-102209-163421

Shifting paradigm of association studies: value of rare single-nucleotide polymorphisms

19 August 2024

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A data-adaptive sum test for disease association with multiple common or rare variants

19 August 2024

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A flexible and accurate genotype imputation method for the next generation of genome-wide association studies

19 August 2024

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Rare independent mutations in renal salt handling genes contribute to blood pressure variation

19 August 2024

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Methods for detecting associations with rare variants for common diseases: application to analysis of sequence data

19 August 2024

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https://api.crossref.org/works/10.1146/ANNUREV-GENET-102209-163421

Discovery of rare variants via sequencing: implications for the design of complex trait association studies

19 August 2024

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An evolutionary trace method defines binding surfaces common to protein families

19 August 2024

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A new statistic to evaluate imputation reliability

19 August 2024

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A groupwise association test for rare mutations using a weighted sum statistic

19 August 2024

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A new multipoint method for genome-wide association studies by imputation of genotypes

19 August 2024

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A strategy to discover genes that carry multi-allelic or mono-allelic risk for common diseases: a cohort allelic sums test (CAST).

19 August 2024

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An evaluation of statistical approaches to rare variant analysis in genetic association studies

19 August 2024

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On the advantage of haplotype analysis in the presence of multiple disease susceptibility alleles

19 August 2024

21

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Association tests using kernel-based measures of multi-locus genotype similarity between individuals

19 August 2024

22

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Rare variants of IFIH1, a gene implicated in antiviral responses, protect against type 1 diabetes

19 August 2024

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SIFT: Predicting amino acid changes that affect protein function

19 August 2024

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The allelic architecture of human disease genes: common disease-common variant... or not?

19 August 2024

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Human non-synonymous SNPs: server and survey

19 August 2024

26

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Nonparametric tests of association of multiple genes with human disease

19 August 2024

27

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Common vs. rare allele hypotheses for complex diseases

19 August 2024

28

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GENE SEQUENCING: The Race for the $1000 Genome

19 August 2024

29

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Imputation-based analysis of association studies: candidate regions and quantitative traits

19 August 2024

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Case-control studies of genetic markers: power and sample size approximations for Armitage's test for trend

19 August 2024

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Genome-wide comparisons of variation in linkage disequilibrium

19 August 2024

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Generalized T2 test for genome association studies

19 August 2024

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Mathematical properties of the r2 measure of linkage disequilibrium

19 August 2024

34

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Improved power by use of a weighted score test for linkage disequilibrium mapping

19 August 2024

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Generalized genomic distance-based regression methodology for multilocus association analysis

19 August 2024

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An evaluation of HapMap sample size and tagging SNP performance in large-scale empirical and simulated data sets

19 August 2024

37

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https://api.crossref.org/works/10.1146/ANNUREV-GENET-102209-163421

19 August 2024

Identifiers

1 reference

23 August 2017

1 reference