Identifying disease polymorphisms from case–control genetic association data (Q33719613)

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scientific article published on October 14, 2010

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English	Identifying disease polymorphisms from case–control genetic association data	scientific article published on October 14, 2010

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instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

20949309

retrieved

28 July 2017

title

Identifying disease polymorphisms from case-control genetic association data (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

20949309

retrieved

28 July 2017

Identifying disease polymorphisms from case–control genetic association data (English)

1 reference

stated in

Crossref

DOI

10.1007/S10709-010-9505-5

reference URL

https://api.crossref.org/works/10.1007/S10709-010-9505-5

retrieved

3 August 2024

main subject

genetic predisposition to disease

1 reference

stated in

Europe PubMed Central

PubMed publication ID

20949309

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A20949309

retrieved

3 August 2024

gene frequency

1 reference

stated in

Europe PubMed Central

PubMed publication ID

20949309

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A20949309

retrieved

3 August 2024

linkage disequilibrium

1 reference

stated in

Europe PubMed Central

PubMed publication ID

20949309

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A20949309

retrieved

3 August 2024

single-nucleotide polymorphism

1 reference

stated in

Europe PubMed Central

PubMed publication ID

20949309

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A20949309

retrieved

3 August 2024

genetic model

1 reference

stated in

Europe PubMed Central

PubMed publication ID

20949309

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A20949309

retrieved

3 August 2024

author name string

L. Park

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

20949309

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A20949309

retrieved

3 August 2024

language of work or name

English

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publication date

14 October 2010

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stated in

Europe PubMed Central

PubMed publication ID

20949309

retrieved

28 July 2017

full work available at URL

http://link.springer.com/content/pdf/10.1007/s10709-010-9505-5.pdf

file format

Portable Document Format

1 reference

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Crossref

DOI

10.1007/S10709-010-9505-5

reference URL

https://api.crossref.org/works/10.1007/S10709-010-9505-5

retrieved

3 August 2024

http://link.springer.com/article/10.1007/s10709-010-9505-5/fulltext.html

file format

HTML

1 reference

stated in

Crossref

DOI

10.1007/S10709-010-9505-5

reference URL

https://api.crossref.org/works/10.1007/S10709-010-9505-5

retrieved

3 August 2024

http://link.springer.com/content/pdf/10.1007/s10709-010-9505-5

1 reference

stated in

Crossref

DOI

10.1007/S10709-010-9505-5

reference URL

https://api.crossref.org/works/10.1007/S10709-010-9505-5

retrieved

3 August 2024

published in

Genetica

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stated in

Europe PubMed Central

PubMed publication ID

20949309

retrieved

28 July 2017

volume

138

1 reference

stated in

Europe PubMed Central

PubMed publication ID

20949309

retrieved

28 July 2017

issue

11-12

1 reference

stated in

Europe PubMed Central

PubMed publication ID

20949309

retrieved

28 July 2017

page(s)

1147-1159

1 reference

stated in

Europe PubMed Central

PubMed publication ID

20949309

retrieved

28 July 2017

cites work

Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry

1 reference

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Crossref

reference URL

https://api.crossref.org/works/10.1007%2FS10709-010-9505-5

retrieved

21 January 2018

Chromosome 6p22 locus associated with clinically aggressive neuroblastoma

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/20949309

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A unified stepwise regression procedure for evaluating the relative effects of polymorphisms within a gene using case/control or family data: application to HLA in type 1 diabetes

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/20949309

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genome-wide association study identifies novel breast cancer susceptibility loci

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/20949309

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Joint linkage and association analysis for identification of potentially causal polymorphisms in GAW15 data

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/20949309

retrieved

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

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/20949309

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A haplotype map of the human genome

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/20949309

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genomewide association studies and human disease

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/20949309

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genome-wide association study identifies five susceptibility loci for glioma

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/20949309

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Partition-ligation-expectation-maximization algorithm for haplotype inference with single-nucleotide polymorphisms

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/20949309

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Machine learning in genome-wide association studies.

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/20949309

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Variants in the CDKN2B and RTEL1 regions are associated with high-grade glioma susceptibility

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/20949309

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A composite-likelihood approach for identifying polymorphisms that are potentially directly associated with disease

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/20949309

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic mapping in human disease

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/20949309

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Variants in KCNQ1 are associated with susceptibility to type 2 diabetes mellitus.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/20949309

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A genome-wide association study identifies a new ovarian cancer susceptibility locus on 9p22.2.

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/20949309

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

New susceptibility locus for coronary artery disease on chromosome 3q22.3.

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/20949309

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Haploview: analysis and visualization of LD and haplotype maps

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/20949309

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/20949309

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

SNPs in KCNQ1 are associated with susceptibility to type 2 diabetes in East Asian and European populations

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/20949309

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sequence diversity and large-scale typing of SNPs in the human apolipoprotein E gene

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/20949309

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Comprehensive association analysis of APOE regulatory region polymorphisms in Alzheimer disease.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/20949309

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/20949309

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Finding the missing heritability of complex diseases

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/20949309

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage and association analysis of GAW15 simulated data: fine-mapping of chromosome 6 region

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/20949309

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rare variants create synthetic genome-wide associations

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/20949309

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Score tests for association between traits and haplotypes when linkage phase is ambiguous

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/20949309

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/20949309

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sequential haplotype scan methods for association analysis.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/20949309

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Comprehensive analysis of APOE and selected proximate markers for late-onset Alzheimer's disease: patterns of linkage disequilibrium and disease/marker association

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/20949309

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1007/S10709-010-9505-5

1 reference

stated in

Europe PubMed Central

PubMed publication ID

20949309

retrieved

28 July 2017

Dimensions Publication ID

1034628923

0 references

PubMed publication ID

20949309

1 reference

stated in

Europe PubMed Central

PubMed publication ID

20949309

retrieved

28 July 2017

 

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