The DOI matches its Crossref record; 49 of the 49 references it cites were found in a registry or an index.
Mutational Mechanisms of Williams-Beuren Syndrome Deletions
Open accessOverview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Basic local alignment search tool
Altschul, S. F., Gish, W., Miller, W., Myers, E. W., & Lipman, D. J. (1990) · Journal of Molecular Biology · doi:10.1006/jmbi.1990.9999 · Cited by 98,669
Thompson, J. D., Higgins, D. G., & Gibson, T. J. (1994) · Nucleic Acids Research · doi:10.1093/nar/22.22.4673 · Cited by 64,617
Rozas, J., & Rozas, R. (1999) · Bioinformatics · doi:10.1093/bioinformatics/15.2.174 · Cited by 1,968
Burnside, R. D. (2015) · Cytogenetic and Genome Research · doi:10.1159/000438708 · Cited by 1,946
Alu repeats and human genomic diversity
Batzer, M. A., & Deininger, P. L. (2002) · Nature Reviews Genetics · doi:10.1038/nrg798 · Cited by 1,470
Genome architecture, rearrangements and genomic disorders
Stankiewicz, P., & Lupski, J. R. (2002) · Trends in Genetics · doi:10.1016/s0168-9525(02)02592-1 · Cited by 925
Prevalence Estimation of Williams Syndrome
Strømme, P., Bjømstad, P. G., & Ramstad, K. (2002) · Journal of Child Neurology · doi:10.1177/088307380201700406 · Cited by 779
I. The Neurocognitive Profile of Williams Syndrome: A Complex Pattern of Strengths and Weaknesses
Bellugi, U., Lichtenberger, L., Jones, W., Lai, Z., & St. George, M. (2000) · Journal of Cognitive Neuroscience · doi:10.1162/089892900561959 · Cited by 706
Natural history of Williams syndrome: Physical characteristics
Morris, C. A., Demsey, S. A., Leonard, C. O., Dilts, C., & Blackburn, B. L. (1988) · The Journal of Pediatrics · doi:10.1016/s0022-3476(88)80272-5 · Cited by 672
The origin of interspersed repeats in the human genome
Smit, A. F. (1996) · Current Opinion in Genetics & Development · doi:10.1016/s0959-437x(96)80030-x · Cited by 611
Cited by
Copy number variation in human health, disease, and evolution
Zhang, F., Gu, W., Hurles, M. E., & Lupski, J. R. (2009) · Annual Review of Genomics and Human Genetics · doi:10.1146/annurev.genom.9.081307.164217 · Cited by 1,207
Mechanisms for human genomic rearrangements
Gu, W., Zhang, F., & Lupski, J. R. (2008) · PathoGenetics · doi:10.1186/1755-8417-1-4 · Cited by 710
Vissers, L. E. L. M., de Vries, B. B. A., Osoegawa, K., Janssen, I. M., Feuth, T., Choy, C. O., Straatman, H., van der Vliet, W., Huys, E. H. L. P. G., van Rijk, A., et al. (2003) · The American Journal of Human Genetics · doi:10.1086/379977 · Cited by 469
A common sequence motif associated with recombination hot spots and genome instability in humans
Myers, S., Freeman, C., Auton, A., Donnelly, P., & McVean, G. (2008) · Nature Genetics · doi:10.1038/ng.213 · Cited by 447
Kaminsky, E. B., Kaul, V., Paschall, J., Church, D. M., Bunke, B., Kunig, D., Moreno-De-Luca, D., Moreno-De-Luca, A., Mulle, J. G., Warren, S. T., et al. (2011) · Genetics in Medicine · doi:10.1097/gim.0b013e31822c79f9 · Cited by 437
Metadata
- Authors
- Bayés, M., Magano, L. F., Rivera, N., Flores, R., & A. Pérez Jurado, L.
- Venue
- The American Journal of Human Genetics
- Publisher
- Elsevier BV
- Published
- 2003-07
- Volume
- 73
- Issue
- 1
- Pages
- 131-151
- ISSN
- 0002-9297 (ISSN-L)
- OpenAlex
- W2006455155
- Cited by
- 337
- References
- 49
- FWCI
- 4.99
- Type
- journal article
- Language
- en
- Open access
- bronze
About these checks
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.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review
How to cite
Cite CoChat for the checks on this page, and the paper for its own findings.
- This page
- CoChat. (2026). Citation check: Mutational Mechanisms of Williams-Beuren Syndrome Deletions. https://app.cochat.ai/papers/10.1086/376565
- The paper
- Bayés, M., Magano, L. F., Rivera, N., Flores, R., & A. Pérez Jurado, L. (2003). Mutational Mechanisms of Williams-Beuren Syndrome Deletions. The American Journal of Human Genetics. https://doi.org/10.1086/376565
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.
