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2009 1
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2019 1
2021 0
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Breast cancer: The translation of big genomic data to cancer precision medicine.
Low SK, Zembutsu H, Nakamura Y. Low SK, et al. Cancer Sci. 2018 Mar;109(3):497-506. doi: 10.1111/cas.13463. Epub 2017 Dec 30. Cancer Sci. 2018. PMID: 29215763 Free PMC article. Review.
Cancer is a complex genetic disease that develops from the accumulation of genomic alterations in which germline variations predispose individuals to cancer and somatic alterations initiate and trigger the progression of cancer. For the past 2 decades, genomic research has …
Cancer is a complex genetic disease that develops from the accumulation of genomic alterations in which germline variations predispos …
Genome-wide association database developed in the Japanese Integrated Database Project.
Koike A, Nishida N, Inoue I, Tsuji S, Tokunaga K. Koike A, et al. J Hum Genet. 2009 Sep;54(9):543-6. doi: 10.1038/jhg.2009.68. Epub 2009 Jul 24. J Hum Genet. 2009. PMID: 19629137
The establishment of high-throughput single-nucleotide polymorphism (SNP)-typing technologies has enabled astonishing progress to be made in genome-wide association studies (GWAS), and various novel genetic factors associated with complex diseases have …
The establishment of high-throughput single-nucleotide polymorphism (SNP)-typing technologies has enabled astonishing progress to be made in …
MGeND: an integrated database for Japanese clinical and genomic information.
Kamada M, Nakatsui M, Kojima R, Nohara S, Uchino E, Tanishima S, Sugiyama M, Kosaki K, Tokunaga K, Mizokami M, Okuno Y. Kamada M, et al. Hum Genome Var. 2019 Dec 6;6:53. doi: 10.1038/s41439-019-0084-4. eCollection 2019. Hum Genome Var. 2019. PMID: 31839973 Free PMC article.
To promote the implementation of genomic medicine, we developed an integrated database, the Medical Genomics Japan Variant Database (MGeND). ...These variations consist of curated SNV/INDEL variants and susceptibility variants for diseases established …
To promote the implementation of genomic medicine, we developed an integrated database, the Medical Genomics Japan Vari …
Validation of genotype imputation in Southeast Asian populations and the effect of single nucleotide polymorphism annotation on imputation outcome.
Lert-Itthiporn W, Suktitipat B, Grove H, Sakuntabhai A, Malasit P, Tangthawornchaikul N, Matsuda F, Suriyaphol P. Lert-Itthiporn W, et al. BMC Med Genet. 2018 Feb 13;19(1):23. doi: 10.1186/s12881-018-0534-8. BMC Med Genet. 2018. PMID: 29439659 Free PMC article.
BACKGROUND: Imputation involves the inference of untyped single nucleotide polymorphisms (SNPs) in genome-wide association studies. The haplotypic reference of choice for imputation in Southeast Asian populations is unclear. ...In the first part, we ap …
BACKGROUND: Imputation involves the inference of untyped single nucleotide polymorphisms (SNPs) in genome-wide association