The DOI matches its Crossref record; 6 of the 6 references it cites were found in a registry or an index.
A Fast, Powerful Method for Detecting Identity by Descent
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Citations
Cites
PLINK: a tool set for whole-genome association and population-based linkage analyses.
Purcell, S., Neale, B., Todd-Brown, K., Thomas, L., Ferreira, M. A. R., Bender, D., Maller, J., Sklar, P., de Bakker, P. I. W., Daly, M. J., et al. (2007) · The American Journal of Human Genetics · doi:10.1086/519795 · Cited by 34,089
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
The Wellcome Trust Case Control Consortium, Management Committee, Burton, P. R., Clayton, D. G., Cardon, L. R., Craddock, N., Deloukas, P., Duncanson, A., Kwiatkowski, D. P., McCarthy, M. I., et al. (2007) · Nature · doi:10.1038/nature05911 · Cited by 9,442
Common polygenic variation contributes to risk of schizophrenia and bipolar disorder
The International Schizophrenia Consortium (2009) · Nature · doi:10.1038/nature08185 · Cited by 4,821
A second generation human haplotype map of over 3.1 million SNPs
The International HapMap Consortium (2007) · Nature · doi:10.1038/nature06258 · Cited by 4,438
Detection of sharing by descent, long-range phasing and haplotype imputation
Kong, A., Masson, G., Frigge, M. L., Gylfason, A., Zusmanovich, P., Thorleifsson, G., Olason, P. I., Ingason, A., Steinberg, S., Rafnar, T., et al. (2008) · Nature Genetics · doi:10.1038/ng.216 · Cited by 447 · cited 1×
“The fastIBD method will also be useful in other applications, such as population-based linkage in founder populations(26) and improving haplotype phase inference and imputation.(14)”
MethodBrowning, B. L., & Browning, S. R. (2007) · Genetic Epidemiology · doi:10.1002/gepi.20216 · Cited by 162
Self-citation
Cited by
Second-generation PLINK: rising to the challenge of larger and richer datasets
Chang, C. C., Chow, C. C., Tellier, L. C., Vattikuti, S., Purcell, S. M., & Lee, J. J. (2015) · Gigascience · doi:10.1186/s13742-015-0047-8 · Cited by 12,709
Altitude adaptation in Tibetans caused by introgression of Denisovan-like DNA
Huerta-Sánchez, E., Jin, X., Asan, Bianba, Z., Peter, B. M., Vinckenbosch, N., Liang, Y., Yi, X., He, M., Somel, M., et al. (2014) · Nature · doi:10.1038/nature13408 · Cited by 1,208
The Genome of the Netherlands Consortium (2014) · Nature Genetics · doi:10.1038/ng.3021 · Cited by 659
Stuart, B. D., Choi, J., Zaidi, S., Xing, C., Holohan, B., Chen, R., Choi, M., Dharwadkar, P., Torres, F., Girod, C. E., et al. (2015) · Nature Genetics · doi:10.1038/ng.3278 · Cited by 469
Fast and accurate long-range phasing in a UK Biobank cohort
Loh, P.-R., Palamara, P. F., & Price, A. L. (2016) · Nature Genetics · doi:10.1038/ng.3571 · Cited by 342
Metadata
- Authors
- Browning, B. L., & Browning, S. R.
- Venue
- The American Journal of Human Genetics
- Publisher
- Elsevier BV
- Published
- 2011-02
- Volume
- 88
- Issue
- 2
- Pages
- 173-182
- ISSN
- 0002-9297 (ISSN-L)
- OpenAlex
- W2151880726
- Cited by
- 374
- References
- 6
- FWCI
- 21.93
- Type
- journal article
- Language
- en
- Open access
- bronze
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- The paper
- Browning, B. L., & Browning, S. R. (2011). A Fast, Powerful Method for Detecting Identity by Descent. The American Journal of Human Genetics. https://doi.org/10.1016/j.ajhg.2011.01.010
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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.
