Entropy-based SNP selection for genetic association studies (Q47611187)

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scientific article published on September 18, 2003

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English	Entropy-based SNP selection for genetic association studies	scientific article published on September 18, 2003

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scholarly article

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Europe PubMed Central

PubMed publication ID

14505034

retrieved

4 February 2018

reference URL

http://europepmc.org/abstract/MED/14505034

title

Entropy-based SNP selection for genetic association studies (English)

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Crossref

DOI

10.1007/S00439-003-1017-2

reference URL

https://api.crossref.org/works/10.1007/S00439-003-1017-2

retrieved

13 March 2024

main subject

human genome

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stated in

Europe PubMed Central

PubMed publication ID

14505034

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14505034

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13 March 2024

genetics

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Crossref

DOI

10.1007/S00439-003-1017-2

reference URL

https://api.crossref.org/works/10.1007/S00439-003-1017-2

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13 March 2024

author

Michael Krawczak

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Michael Krawczak

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Europe PubMed Central

PubMed publication ID

14505034

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4 February 2018

Stefan Schreiber

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2

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Stefan Schreiber

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Europe PubMed Central

PubMed publication ID

14505034

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4 February 2018

reference URL

http://europepmc.org/abstract/MED/14505034

Jochen Hampe

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Jochen Hampe

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Europe PubMed Central

PubMed publication ID

14505034

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14505034

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13 March 2024

language of work or name

English

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National Center for Biotechnology Information

PubMed publication ID

14505034

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=14505034

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13 March 2024

publication date

18 September 2003

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stated in

Europe PubMed Central

PubMed publication ID

14505034

retrieved

4 February 2018

reference URL

http://europepmc.org/abstract/MED/14505034

full work available at URL

http://link.springer.com/content/pdf/10.1007/s00439-003-1017-2.pdf

file format

Portable Document Format

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Crossref

DOI

10.1007/S00439-003-1017-2

reference URL

https://api.crossref.org/works/10.1007/S00439-003-1017-2

retrieved

13 March 2024

http://link.springer.com/article/10.1007/s00439-003-1017-2/fulltext.html

file format

HTML

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Crossref

DOI

10.1007/S00439-003-1017-2

reference URL

https://api.crossref.org/works/10.1007/S00439-003-1017-2

retrieved

13 March 2024

http://link.springer.com/content/pdf/10.1007/s00439-003-1017-2

1 reference

stated in

Crossref

DOI

10.1007/S00439-003-1017-2

reference URL

https://api.crossref.org/works/10.1007/S00439-003-1017-2

retrieved

13 March 2024

published in

Human Genetics

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stated in

Europe PubMed Central

PubMed publication ID

14505034

retrieved

4 February 2018

reference URL

http://europepmc.org/abstract/MED/14505034

volume

114

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Europe PubMed Central

PubMed publication ID

14505034

retrieved

4 February 2018

reference URL

http://europepmc.org/abstract/MED/14505034

issue

1

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Europe PubMed Central

PubMed publication ID

14505034

retrieved

4 February 2018

reference URL

http://europepmc.org/abstract/MED/14505034

page(s)

36-43

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Europe PubMed Central

PubMed publication ID

14505034

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4 February 2018

reference URL

http://europepmc.org/abstract/MED/14505034

cites work

Beyond Mendel: an evolving view of human genetic disease transmission

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/14505034

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Parametric and nonparametric linkage analysis: a unified multipoint approach

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/14505034

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Efficiency of estimation of haplotype frequencies: use of marker phenotypes of unrelated individuals versus counting of phase-known gametes

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/14505034

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A dynamic programming algorithm for haplotype block partitioning

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/14505034

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Family-based analysis using a dense single-nucleotide polymorphism-based map defines genetic variation at PSORS1, the major psoriasis-susceptibility locus

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/14505034

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The allelic architecture of human disease genes: common disease-common variant... or not?

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/14505034

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Haplotype structure and association to Crohn's disease of CARD15 mutations in two ethnically divergent populations.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/14505034

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Relative efficiency of ambiguous vs. directly measured haplotype frequencies.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/14505034

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The structure of haplotype blocks in the human genome

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/14505034

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Haplotype block structure and its applications to association studies: power and study designs

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/14505034

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The future of genetic studies of complex human diseases

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/14505034

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Selection of single nucleotide polymorphisms for association studies in candidate genes

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/14505034

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A non-organic and non-enzymatic extraction method gives higher yields of genomic DNA from whole-blood samples than do nine other methods tested

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/14505034

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Allelic association of the cystic fibrosis locus and two DNA markers, XV2c and KM19, in 55 German families

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/14505034

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic variation in the 5q31 cytokine gene cluster confers susceptibility to Crohn disease

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/14505034

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Experimentally-derived haplotypes substantially increase the efficiency of linkage disequilibrium studies

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/14505034

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Efficiency of haplotype frequency estimation when nuclear family information is included

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/14505034

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The optimal measure of allelic association

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/14505034

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Detecting recent positive selection in the human genome from haplotype structure

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/14505034

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High-resolution haplotype structure in the human genome

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/14505034

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Blocks of limited haplotype diversity revealed by high-resolution scanning of human chromosome 21.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/14505034

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Haplotype tagging for the identification of common disease genes

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/14505034

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1007/S00439-003-1017-2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

14505034

retrieved

4 February 2018

reference URL

http://europepmc.org/abstract/MED/14505034

PubMed publication ID

14505034

1 reference

stated in

Europe PubMed Central

PubMed publication ID

14505034

retrieved

4 February 2018

reference URL

http://europepmc.org/abstract/MED/14505034

ResearchGate publication ID

9084396

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