(Q33398062)

English

Application of genome-wide SNP data for uncovering pairwise relationships and quantitative trait loci

scientific article

In more languages

default values for all languages

No label defined

No description defined

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

1 reference

Europe PubMed Central

Application of genome-wide SNP data for uncovering pairwise relationships and quantitative trait loci (English)

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

quantitative trait locus

1 reference

based on heuristic

inferred from title

Stacey S. Cherny

2

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

author name string

P C Sham

1

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

S Purcell

3

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

language of work or name

0 references

publication date

7 January 2009

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

136

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

2

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

237-243

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

The Correlation between Relatives on the Supposition of Mendelian Inheritance

1 reference

https://api.crossref.org/works/10.1007%2FS10709-008-9349-4

21 January 2018

A general test of association for quantitative traits in nuclear families

1 reference

https://pubmed.ncbi.nlm.nih.gov/19127410

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The family based association test method: strategies for studying general genotype--phenotype associations.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19127410

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A second generation human haplotype map of over 3.1 million SNPs

1 reference

https://pubmed.ncbi.nlm.nih.gov/19127410

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A haplotype map of the human genome

1 reference

https://pubmed.ncbi.nlm.nih.gov/19127410

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Selecting a maximally informative set of single-nucleotide polymorphisms for association analyses using linkage disequilibrium

1 reference

https://pubmed.ncbi.nlm.nih.gov/19127410

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The structure of haplotype blocks in the human genome

1 reference

https://pubmed.ncbi.nlm.nih.gov/19127410

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Assumption-free estimation of heritability from genome-wide identity-by-descent sharing between full siblings

1 reference

https://pubmed.ncbi.nlm.nih.gov/19127410

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Robust variance-components approach for assessing genetic linkage in pedigrees

1 reference

https://pubmed.ncbi.nlm.nih.gov/19127410

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Combining functional and linkage disequilibrium information in the selection of tag SNPs.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19127410

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Merlin--rapid analysis of dense genetic maps using sparse gene flow trees

1 reference

https://pubmed.ncbi.nlm.nih.gov/19127410

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multipoint quantitative-trait linkage analysis in general pedigrees

1 reference

https://pubmed.ncbi.nlm.nih.gov/19127410

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pedigree tests of transmission disequilibrium

1 reference

https://pubmed.ncbi.nlm.nih.gov/19127410

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An improved multipoint sib-pair analysis of quantitative traits

1 reference

https://pubmed.ncbi.nlm.nih.gov/19127410

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

PLINK: a tool set for whole-genome association and population-based linkage analyses

1 reference

https://pubmed.ncbi.nlm.nih.gov/19127410

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Complete multipoint sib-pair analysis of qualitative and quantitative traits

1 reference

https://pubmed.ncbi.nlm.nih.gov/19127410

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Combined linkage and association sib-pair analysis for quantitative traits

1 reference

https://pubmed.ncbi.nlm.nih.gov/19127410

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evaluation of coverage variation of SNP chips for genome-wide association studies.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19127410

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rapid multipoint linkage analysis of recessive traits in nuclear families, including homozygosity mapping.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19127410

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S10709-008-9349-4

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q33398062&oldid=2195322226"