Designing a multistage, SNP-based, genome screen for common diseases. (Q51557878)

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English	Designing a multistage, SNP-based, genome screen for common diseases.	scientific article

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scholarly article

1 reference

Europe PubMed Central

7 April 2018

http://europepmc.org/abstract/MED/15635486

Designing a multistage, SNP-based, genome screen for common diseases. (English)

1 reference

Europe PubMed Central

7 April 2018

http://europepmc.org/abstract/MED/15635486

author name string

Yasunori Sato

1

1 reference

Europe PubMed Central

7 April 2018

http://europepmc.org/abstract/MED/15635486

Hideki Suganami

2

1 reference

Europe PubMed Central

7 April 2018

http://europepmc.org/abstract/MED/15635486

Chikuma Hamada

3

1 reference

Europe PubMed Central

7 April 2018

http://europepmc.org/abstract/MED/15635486

Isao Yoshimura

4

1 reference

Europe PubMed Central

7 April 2018

http://europepmc.org/abstract/MED/15635486

Teruhiko Yoshida

5

1 reference

Europe PubMed Central

7 April 2018

http://europepmc.org/abstract/MED/15635486

Kimio Yoshimura

6

1 reference

Europe PubMed Central

7 April 2018

http://europepmc.org/abstract/MED/15635486

publication date

24 November 2004

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Europe PubMed Central

7 April 2018

http://europepmc.org/abstract/MED/15635486

Journal of Human Genetics

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Europe PubMed Central

7 April 2018

http://europepmc.org/abstract/MED/15635486

49

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Europe PubMed Central

7 April 2018

http://europepmc.org/abstract/MED/15635486

12

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Europe PubMed Central

7 April 2018

http://europepmc.org/abstract/MED/15635486

669-676

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Europe PubMed Central

7 April 2018

http://europepmc.org/abstract/MED/15635486

https://scigraph.springernature.com/pub.10.1007/s10038-004-0205-9

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Population choice in mapping genes for complex diseases

1 reference

https://pubmed.ncbi.nlm.nih.gov/15635486

12 December 2020

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Analysis of the mouse transcriptome based on functional annotation of 60,770 full-length cDNAs

1 reference

https://pubmed.ncbi.nlm.nih.gov/15635486

12 December 2020

based on heuristic

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JSNP: a database of common gene variations in the Japanese population

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https://pubmed.ncbi.nlm.nih.gov/15635486

12 December 2020

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Polygenic susceptibility to breast cancer and implications for prevention

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https://pubmed.ncbi.nlm.nih.gov/15635486

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Cancer genetics.

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https://pubmed.ncbi.nlm.nih.gov/15635486

12 December 2020

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Functional SNPs in the lymphotoxin-alpha gene that are associated with susceptibility to myocardial infarction

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https://pubmed.ncbi.nlm.nih.gov/15635486

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[SNP project in the Millennium Genome Project, Japan].

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https://pubmed.ncbi.nlm.nih.gov/15635486

12 December 2020

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A high-throughput SNP typing system for genome-wide association studies

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https://pubmed.ncbi.nlm.nih.gov/15635486

12 December 2020

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The Sequence of the Human Genome

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https://pubmed.ncbi.nlm.nih.gov/15635486

12 December 2020

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Two-Stage Designs for Gene-Disease Association Studies

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https://pubmed.ncbi.nlm.nih.gov/15635486

12 December 2020

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Complex genetic diseases: controversy over the Croesus code

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https://pubmed.ncbi.nlm.nih.gov/15635486

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gene-based SNP discovery as part of the Japanese Millennium Genome Project: identification of 190,562 genetic variations in the human genome. Single-nucleotide polymorphism

1 reference

https://pubmed.ncbi.nlm.nih.gov/15635486

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S10038-004-0205-9

1 reference

Europe PubMed Central

7 April 2018

http://europepmc.org/abstract/MED/15635486

1 reference

Europe PubMed Central

7 April 2018

http://europepmc.org/abstract/MED/15635486

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