The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.
The NCBI dbGaP database of genotypes and phenotypes
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Citations
Cites
Genomic Control for Association Studies
Devlin, B., & Roeder, K. (1999) · Biometrics · doi:10.1111/j.0006-341x.1999.00997.x · Cited by 3,162 · cited 1×
“quantile-quantile plots of Cochran-Armitage test statistics (5) and genomic control lambda values ( 6 ), for consideration by the study investigators and advisory committee as they optimize data cleaning thresholds.”
BackgroundClayton, D. G., Walker, N. M., Smyth, D. J., Pask, R., Cooper, J. D., Maier, L. M., Smink, L. J., Lam, A. C., Ovington, N. R., Stevens, H. E., et al. (2005) · Nature Genetics · doi:10.1038/ng1653 · Cited by 526
Cited by
Genome-wide association studies for complex traits: consensus, uncertainty and challenges
McCarthy, M. I., Abecasis, G. R., Cardon, L. R., Goldstein, D. B., Little, J., Ioannidis, J. P. A., & Hirschhorn, J. N. (2008) · Nature Reviews Genetics · doi:10.1038/nrg2344 · Cited by 2,891
The NHGRI GWAS Catalog, a curated resource of SNP-trait associations
Welter, D., MacArthur, J., Morales, J., Burdett, T., Hall, P., Junkins, H., Klemm, A., Flicek, P., Manolio, T., Hindorff, L., et al. (2014) · Nucleic Acids Research · doi:10.1093/nar/gkt1229 · Cited by 2,707
Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program
Taliun, D., Harris, D. N., Kessler, M. D., Carlson, J., Szpiech, Z. A., Torres, R., Taliun, S. A. G., Corvelo, A., Gogarten, S. M., Kang, H. M., et al. (2021) · Nature · doi:10.1038/s41586-021-03205-y · Cited by 2,213
Genome structural variation discovery and genotyping
Alkan, C., Coe, B. P., & Eichler, E. E. (2011) · Nature Reviews Genetics · doi:10.1038/nrg2958 · Cited by 1,630
Rouillard, A. D., Gundersen, G. W., Fernandez, N. F., Wang, Z., Monteiro, C. D., McDermott, M. G., & Ma’ayan, A. (2016) · Database · doi:10.1093/database/baw100 · Cited by 1,515
Self-citation
Metadata
- Authors
- Mailman, M. D., Feolo, M., Jin, Y., Kimura, M., Tryka, K., Bagoutdinov, R., Hao, L., Kiang, A., Paschall, J., Phan, L., Popova, N., Pretel, S., Ziyabari, L., Lee, M., Shao, Y., Wang, Z. Y., Sirotkin, K., Ward, M., Kholodov, M., Zbicz, K., Beck, J., Kimelman, M., Shevelev, S., Preuss, D., Yaschenko, E., Graeff, A., Ostell, J., & Sherry, S. T.
- Venue
- Nature Genetics
- Published
- 2007-10
- Volume
- 39
- Issue
- 10
- Pages
- 1181-1186
- ISSN
- 1061-4036 (ISSN-L)
- 1546-1718
- OpenAlex
- W2102729801
- Cited by
- 1,105
- References
- 2
- FWCI
- 17.92
- Type
- journal article
- Language
- en
- Open access
- green
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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: The NCBI dbGaP database of genotypes and phenotypes. https://app.cochat.ai/papers/10.1038/ng1007-1181
- The paper
- Mailman, M. D., Feolo, M., Jin, Y., Kimura, M., Tryka, K., Bagoutdinov, R., Hao, L., Kiang, A., Paschall, J., Phan, L., Popova, N., Pretel, S., Ziyabari, L., Lee, M., Shao, Y., Wang, Z. Y., Sirotkin, K., Ward, M., Kholodov, M., . . . Sherry, S. T. (2007). The NCBI dbGaP database of genotypes and phenotypes. Nature Genetics. https://doi.org/10.1038/ng1007-1181
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.
