Improved use of SNP information to detect the role of genes. (Q47693211)

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scientific article published in September 2003

Language	Label	Description	Also known as
English	Improved use of SNP information to detect the role of genes.	scientific article published in September 2003

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12916024%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

Improved use of SNP information to detect the role of genes (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12916024%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

Anne-Sophie Jannot

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12916024%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

Françoise Clerget-Darpoux

4

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12916024%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

author name string

Essioux L

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12916024%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

Reese MG

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12916024%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

publication date

1 September 2003

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12916024%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

Genetic Epidemiology

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12916024%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

25

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12916024%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12916024%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

158-167

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12916024%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

Haplotypes vs single marker linkage disequilibrium tests: what do we gain?

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.10256

7 January 2021

based on heuristic

inferred from DOI database lookup

The relative power of SNPs and haplotype as genetic markers for association tests.

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.10256

7 January 2021

based on heuristic

inferred from DOI database lookup

A perspective on epistasis: limits of models displaying no main effect

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.10256

7 January 2021

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A variation in 3' UTR of hPTP1B increases specific gene expression and associates with insulin resistance

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.10256

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Genetic analysis of case/control data using estimated haplotype frequencies: application to APOE locus variation and Alzheimer's disease

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.10256

7 January 2021

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Complex interactions of new quantitative trait loci, Sluc1, Sluc2, Sluc3, and Sluc4, that influence the susceptibility to lung cancer in the mouse

1 reference

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7 January 2021

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Allegro, a new computer program for multipoint linkage analysis

1 reference

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Complexity and power in case-control association studies

1 reference

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A combinatorial partitioning method to identify multilocus genotypic partitions that predict quantitative trait variation

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.10256

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A new type of mutation causes a splicing defect in ATM.

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Investigation of the mode of inheritance of the HLA associated diseases by the method of antigen genotype frequencies among diseased individuals.

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.10256

7 January 2021

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inferred from DOI database lookup

Heterogeneity of linkage disequilibrium in human genes has implications for association studies of common diseases

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.10256

7 January 2021

based on heuristic

inferred from DOI database lookup

Gene interaction and single gene effects in colon tumour susceptibility in mice

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.10256

7 January 2021

based on heuristic

inferred from DOI database lookup

Use of haplotype information to test involvement of the LRP gene in Alzheimer's disease in the French population

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.10256

7 January 2021

based on heuristic

inferred from DOI database lookup

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