Extending rare-variant testing strategies: analysis of noncoding sequence and imputed genotypes (Q34300842)

1 August 2017

Extending rare-variant testing strategies: analysis of noncoding sequence and imputed genotypes (English)

1 reference

1 August 2017

2

Shyam Gopalakrishnan

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1 August 2017

Matthew Zawistowski

1

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1 August 2017

Jun Ding

3

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1 August 2017

Yun Li

4

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1 August 2017

Sara Grimm

5

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1 August 2017

Sebastian Zöllner

6

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1 August 2017

language of work or name

English

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publication date

1 November 2010

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American Journal of Human Genetics

1 August 2017

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1 August 2017

87

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1 August 2017

604-617

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1 August 2017

5

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describes a project that uses

1 August 2017

Bayes' theorem

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18 June 2022

https://europepmc.org/article/PMC/2978957

based on heuristic

inferred from PubMed Central ID database lookup

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6 July 2018

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Rare variants create synthetic genome-wide associations

6 July 2018

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Human genetic variation recognizes functional elements in noncoding sequence

6 July 2018

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Sequencing the IL4 locus in African Americans implicates rare noncoding variants in asthma susceptibility

6 July 2018

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6 July 2018

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

6 July 2018

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6 July 2018

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Genome-wide scan reveals association of psoriasis with IL-23 and NF-kappaB pathways

6 July 2018

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

6 July 2018

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

6 July 2018

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6 July 2018

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Widely distributed noncoding purifying selection in the human genome

6 July 2018

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

6 July 2018

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Calibrating a coalescent simulation of human genome sequence variation

6 July 2018

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A common sex-dependent mutation in a RET enhancer underlies Hirschsprung disease risk.

6 July 2018

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6 July 2018

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6 July 2018

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6 July 2018

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6 July 2018

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6 July 2018

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6 July 2018

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The future of genetic studies of complex human diseases

6 July 2018

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A functional haplotype variant in the TBX22 promoter is associated with cleft palate and ankyloglossia

6 July 2018

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12 December 2020

based on heuristic

Identifiers

DOI

10.1016/J.AJHG.2010.10.012

1 reference

1 August 2017

1 reference

1 August 2017

1 reference