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Cited by in F6Publishing
For: Eslami Rasekh M, Hernández Y, Drinan SD, Fuxman Bass JI, Benson G. Genome-wide characterization of human minisatellite VNTRs: population-specific alleles and gene expression differences. Nucleic Acids Res 2021;49:4308-24. [PMID: 33849068 DOI: 10.1093/nar/gkab224] [Cited by in Crossref: 4] [Cited by in F6Publishing: 5] [Article Influence: 2.0] [Reference Citation Analysis]
Number Citing Articles
1 Mukamel RE, Handsaker RE, Sherman MA, Barton AR, Hujoel MLA, Mccarroll SA, Loh P. Repeat polymorphisms in non-coding DNA underlie top genetic risk loci for glaucoma and colorectal cancer.. [DOI: 10.1101/2022.10.11.22280955] [Reference Citation Analysis]
2 Garg P, Jadhav B, Lee W, Rodriguez OL, Martin-Trujillo A, Sharp AJ. A phenome-wide association study identifies effects of copy-number variation of VNTRs and multicopy genes on multiple human traits. Am J Hum Genet 2022;109:1065-76. [PMID: 35609568 DOI: 10.1016/j.ajhg.2022.04.016] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
3 Garg P, Jadhav B, Lee W, Rodriguez OL, Martin-trujillo A, Sharp AJ. A phenome-wide association study identifies effects of copy number variation of VNTRs and multicopy genes on multiple human traits.. [DOI: 10.1101/2022.01.26.22269891] [Reference Citation Analysis]
4 Ghamari R, Yazarlou F, Khosravizadeh Z, Moradkhani A, Abdollahi E, Alizadeh F. Serotonin transporter functional polymorphisms potentially increase risk of schizophrenia separately and as a haplotype. Sci Rep 2022;12:1336. [PMID: 35079035 DOI: 10.1038/s41598-022-05206-x] [Reference Citation Analysis]
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