(Q33775580)

29 July 2017

title

Efficient utilization of rare variants for detection of disease-related genomic regions (English)

1 reference

29 July 2017

Lei Zhang

1

0 references

Hong-Wen Deng

object named as

Hong-Wen Deng

5

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author name string

Yu-Fang Pei

2

1 reference

29 July 2017

Jian Li

3

1 reference

29 July 2017

Christopher J Papasian

4

1 reference

29 July 2017

language of work or name

English

0 references

publication date

10 December 2010

1 reference

29 July 2017

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29 July 2017

volume

5

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29 July 2017

issue

12

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29 July 2017

page(s)

e14288

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Creative Commons Attribution 4.0 International

29 July 2017

copyright license

start time

10 December 2010

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

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4 July 2018

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4 July 2018

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4 July 2018

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4 July 2018

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4 July 2018

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4 July 2018

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4 July 2018

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4 July 2018

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4 July 2018

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Most rare missense alleles are deleterious in humans: implications for complex disease and association studies

4 July 2018

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Population-based resequencing of ANGPTL4 uncovers variations that reduce triglycerides and increase HDL.

4 July 2018

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Overrepresentation of rare variants in a specific ethnic group may confuse interpretation of association analyses

4 July 2018

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Principal components analysis corrects for stratification in genome-wide association studies

4 July 2018

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4 July 2018

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

4 July 2018

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4 July 2018

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Low LDL cholesterol in individuals of African descent resulting from frequent nonsense mutations in PCSK9.

4 July 2018

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4 July 2018

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Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol

4 July 2018

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4 July 2018

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4 July 2018

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4 July 2018

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4 July 2018

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4 July 2018

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4 July 2018

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4 July 2018

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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).

4 July 2018

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https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0014288

Exhaustive allelic transmission disequilibrium tests as a new approach to genome-wide association studies.

21 January 2018

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https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0014288

Improved use of SNP information to detect the role of genes.

21 January 2018

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https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0014288

Population genetics--making sense out of sequence

21 January 2018

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PubMed

https://pubmed.ncbi.nlm.nih.gov/21170328

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

1 reference

https://pubmed.ncbi.nlm.nih.gov/21170328

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1371/JOURNAL.PONE.0014288

1 reference

29 July 2017

0 references

1 reference

29 July 2017

1 reference