The DOI matches its Crossref record; 21 of the 21 references it cites were found in a registry or an index.
Continuum of overlapping clones spanning the entire human chromosome 21q
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Citations
Cites
Construction of a genetic linkage map in man using restriction fragment length polymorphisms.
Botstein, D., White, R. L., Skolnick, M. H., & Davis, R. W. (1980) · Europe PMC (PubMed Central) · Cited by 8,327
Cloning of Large Segments of Exogenous DNA into Yeast by Means of Artificial Chromosome Vectors
Burke, D. T., Carle, G. F., & Olson, M. V. (1987) · Science · doi:10.1126/science.3033825 · Cited by 1,501
A Common Language for Physical Mapping of the Human Genome
Olson, M., Hood, L., Cantor, C., & Botstein, D. (1989) · Science · doi:10.1126/science.2781285 · Cited by 857
Toward a physical map of the genome of the nematode Caenorhabditis elegans
Coulson, A., Sulston, J., Brenner, S., & Karn, J. (1986) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.83.20.7821 · Cited by 625
Cox, D. R., Burmeister, M., Price, E. R., Kim, S., & Myers, R. M. (1990) · Science · doi:10.1126/science.2218528 · Cited by 621
Self-citationHuman genome organization: Alu, LINES, and the molecular structure of metaphase chromosome bands
Korenberg, J. R., & Rykowski, M. C. (1988) · Cell · doi:10.1016/0092-8674(88)90159-6 · Cited by 557
Random-clone strategy for genomic restriction mapping in yeast.
Olson, M. V., Dutchik, J. E., Graham, M. Y., Brodeur, G. M., Helms, C., Frank, M., MacCollin, M., Scheinman, R., & Frank, T. (1986) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.83.20.7826 · Cited by 416
Albertsen, H. M., Abderrahim, H., Cann, H. M., Dausset, J., Le Paslier, D., & Cohen, D. (1990) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.87.11.4256 · Cited by 399
Self-citationYeast artificial chromosome libraries containing large inserts from mouse and human DNA.
Larin, Z., Monaco, A. P., & Lehrach, H. (1991) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.88.10.4123 · Cited by 327
Gardiner, K., Horisberger, M., Kraus, J., Tantravahi, U., Korenberg, J., Rao, V., Reddy, S., & Patterson, D. (1990) · The EMBO Journal · doi:10.1002/j.1460-2075.1990.tb08076.x · Cited by 186
Self-citation
Cited by
Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease
Sherrington, R., Rogaev, E. I., Liang, Y., Rogaeva, E. A., Levesque, G., Ikeda, M., Chi, H., Lin, C., Li, G., Holman, K., et al. (1995) · Nature · doi:10.1038/375754a0 · Cited by 4,051
Self-citationAn STS-Based Map of the Human Genome
Hudson, T. J., Stein, L. D., Gerety, S. S., Ma, J., Castle, A. B., Silva, J., Slonim, D. K., Baptista, R., Kruglyak, L., Xu, S.-H., et al. (1995) · Science · doi:10.1126/science.270.5244.1945 · Cited by 773
Self-citationThe t(12;21) of acute lymphoblastic leukemia results in a tel-AML1 gene fusion
Romana, S., Mauchauffe, M., Le Coniat, M., Chumakov, I., Le Paslier, D., Berger, R., & Bernard, O. (1995) · Blood · doi:10.1182/blood.v85.12.3662.bloodjournal85123662 · Cited by 530
Self-citationLitt, M. (1998) · Human Molecular Genetics · doi:10.1093/hmg/7.3.471 · Cited by 447
High frequency of t(12;21) in childhood B-lineage acute lymphoblastic leukemia
Romana, S., Poirel, H., Leconiat, M., Flexor, M., Mauchauffe, M., Jonveaux, P., Macintyre, E., Berger, R., & Bernard, O. (1995) · Blood · doi:10.1182/blood.v86.11.4263.bloodjournal86114263 · Cited by 427
Metadata
- Authors
- Chumakov, I., Rigault, P., Guillou, S., Ougen, P., Billaut, A., Guasconi, G., Gervy, P., LeGall, I., Soularue, P., Grinas, L., Bougueleret, L., Bellanné-Chantelot, C., Lacroix, B., Barillot, E., Gesnouin, P., Pook, S., Vaysseix, G., Frelat, G., Schmitz, A., Sambucy, J.-L., Bosch, A., Estivill, X., Weissenbach, J., Vignal, A., Riethman, H., Cox, D., Patterson, D., Gardiner, K., Hattori, M., Sakaki, Y., Ichikawa, H., Ohki, M., Paslier, D. L., Heilig, R., Antonarakis, S., & Cohen, D.
- Venue
- Nature
- Published
- 1992-10
- Volume
- 359
- Issue
- 6394
- Pages
- 380-387
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- OpenAlex
- W2026884566
- Cited by
- 388
- References
- 21
- FWCI
- 36.77
- 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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- This page
- CoChat. (2026). Citation check: Continuum of overlapping clones spanning the entire human chromosome 21q. https://app.cochat.ai/papers/10.1038/359380a0
- The paper
- Chumakov, I., Rigault, P., Guillou, S., Ougen, P., Billaut, A., Guasconi, G., Gervy, P., LeGall, I., Soularue, P., Grinas, L., Bougueleret, L., Bellanné-Chantelot, C., Lacroix, B., Barillot, E., Gesnouin, P., Pook, S., Vaysseix, G., Frelat, G., Schmitz, A., . . . Cohen, D. (1992). Continuum of overlapping clones spanning the entire human chromosome 21q. Nature. https://doi.org/10.1038/359380a0
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.
