The DOI matches its Crossref record; 4 of the 4 references it cites were found in a registry or an index.
Dark matter in the genome: evidence of widespread transcription detected by microarray tiling experiments
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Citations
Cites
The sequence of the human genome
Venter, J. C., Adams, M. D., Myers, E. W., Li, P. W., Mural, R. J., Sutton, G. G., Smith, H. O., Yandell, M., Evans, C. A., Holt, R. A., et al. (2001) · Science · doi:10.1126/science.1058040 · Cited by 13,909
Self-citationCawley, S., Bekiranov, S., Ng, H. H., Kapranov, P., Sekinger, E. A., Kampa, D., Piccolboni, A., Sementchenko, V., Cheng, J., Williams, A. J., et al. (2004) · Cell · doi:10.1016/s0092-8674(04)00127-8 · Cited by 1,095
Complete sequencing and characterization of 21,243 full-length human cDNAs
Ota, T., Suzuki, Y., Nishikawa, T., Otsuki, T., Sugiyama, T., Irie, R., Wakamatsu, A., Hayashi, K., Sato, H., Nagai, K., et al. (2004) · Nature Genetics · doi:10.1038/ng1285 · Cited by 925
Using the transcriptome to annotate the genome
Saha, S., Sparks, A. B., Rago, C., Akmaev, V., Wang, C. J., Vogelstein, B., Kinzler, K. W., & Velculescu, V. E. (2002) · Nature Biotechnology · doi:10.1038/nbt0502-508 · Cited by 630
Cited by
Interpretation of Shotgun Proteomic Data
Nesvizhskii, A. I., & Aebersold, R. (2005) · Molecular & Cellular Proteomics · doi:10.1074/mcp.r500012-mcp200 · Cited by 1,025
Dynamic genome architecture in the nuclear space: regulation of gene expression in three dimensions
Lanctôt, C., Cheutin, T., Cremer, M., Cavalli, G., & Cremer, T. (2007) · Nature Reviews Genetics · doi:10.1038/nrg2041 · Cited by 781
The Antisense Transcriptomes of Human Cells
He, Y., Vogelstein, B., Velculescu, V. E., Papadopoulos, N., & Kinzler, K. W. (2008) · Science · doi:10.1126/science.1163853 · Cited by 531
The biology of intron gain and loss
Jeffares, D. C., Mourier, T., & Penny, D. (2006) · Trends in Genetics · doi:10.1016/j.tig.2005.10.006 · Cited by 296
Antisense artifacts in transcriptome microarray experiments are resolved by actinomycin D
Perocchi, F., Xu, Z., Clauder-Münster, S., & Steinmetz, L. M. (2007) · Nucleic Acids Research · doi:10.1093/nar/gkm683 · Cited by 193
Li, L., Zhu, Q., He, X., Sinha, S., & Halfon, M. S. (2007) · Genome Biology · doi:10.1186/gb-2007-8-6-r101 · Cited by 69
Bliim, N., Leshchyns'ka, I., Keable, R., Chen, B. J., Curry-Hyde, A., Gray, L., Sytnyk, V., & Janitz, M. (2019) · Genomics · doi:10.1016/j.ygeno.2018.11.019 · Cited by 17
Metadata
- Authors
- Johnson, J. M., Edwards, S., Shoemaker, D., & Schadt, E. E.
- Venue
- Trends in Genetics
- Publisher
- Elsevier BV
- Published
- 2005-02
- Volume
- 21
- Issue
- 2
- Pages
- 93-102
- ISSN
- 0168-9525 (ISSN-L)
- OpenAlex
- W2123067735
- Cited by
- 386
- References
- 4
- FWCI
- 11.15
- Type
- journal article
- Language
- en
- Open access
- closed
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Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
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Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.
