The DOI matches its Crossref record; 9 of the 9 references it cites were found in a registry or an index.
Reconciling the analysis of IBD and IBS in complex trait studies
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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
Finding the missing heritability of complex diseases
Manolio, T. A., Collins, F. S., Cox, N. J., Goldstein, D. B., Hindorff, L. A., Hunter, D. J., McCarthy, M. I., Ramos, E. M., Cardon, L. R., Chakravarti, A., et al. (2009) · Nature · doi:10.1038/nature08494 · Cited by 8,336
Self-citationEfficient Methods to Compute Genomic Predictions
VanRaden, P. M. (2008) · Journal of Dairy Science · doi:10.3168/jds.2007-0980 · Cited by 6,050
Population Structure and Eigenanalysis
Patterson, N., Price, A. L., & Reich, D. (2006) · PLoS Genetics · doi:10.1371/journal.pgen.0020190 · Cited by 5,280
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
Heritability in the genomics era — concepts and misconceptions
Visscher, P. M., Hill, W. G., & Wray, N. R. (2008) · Nature Reviews Genetics · doi:10.1038/nrg2322 · Cited by 1,921 · cited 1×
“However, the relationship matrix can also be estimated from genome-wide genetic marker”
BackgroundSelf-citationPersonal genomes: The case of the missing heritability
Maher, B. (2008) · Nature · doi:10.1038/456018a · Cited by 1,737
Genealogical trees, coalescent theory and the analysis of genetic polymorphisms
Rosenberg, N. A., & Nordborg, M. (2002) · Nature Reviews Genetics · doi:10.1038/nrg795 · Cited by 750
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×
“This fundamental concept has many uses in genetics, including predicting genotype frequencie”
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The mystery of missing heritability: Genetic interactions create phantom heritability
Zuk, O., Hechter, E., Sunyaev, S. R., & Lander, E. S. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1119675109 · Cited by 1,542
Estimating Missing Heritability for Disease from Genome-wide Association Studies
Lee, S. H., Wray, N. R., Goddard, M. E., & Visscher, P. M. (2011) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2011.02.002 · Cited by 1,064
Self-citationEstimating the proportion of variation in susceptibility to schizophrenia captured by common SNPs
The Schizophrenia Psychiatric Genome-Wide Association Study Consortium (PGC-SCZ), Lee, S. H., The International Schizophrenia Consortium (ISC), The Molecular Genetics of Schizophrenia Collaboration (MGS), DeCandia, T. R., Ripke, S., Yang, J., Sullivan, P. F., Goddard, M. E., Keller, M. C., et al. (2012) · Nature Genetics · doi:10.1038/ng.1108 · Cited by 579
Self-citationThe Tohoku Medical Megabank Project: Design and Mission
Kuriyama, S., Yaegashi, N., Nagami, F., Arai, T., Kawaguchi, Y., Osumi, N., Sakaida, M., Suzuki, Y., Nakayama, K., Hashizume, H., et al. (2016) · Journal of Epidemiology · doi:10.2188/jea.je20150268 · Cited by 359
Relatedness in the post-genomic era: is it still useful?
Speed, D., & Balding, D. J. (2015) · Nature Reviews Genetics · doi:10.1038/nrg3821 · Cited by 316
Metadata
- Authors
- Powell, J. E., Visscher, P. M., & Goddard, M. E.
- Venue
- Nature Reviews Genetics
- Published
- 2010-09-28
- Volume
- 11
- Issue
- 11
- Pages
- 800-805
- ISSN
- 1471-0056 (ISSN-L)
- 1471-0064
- OpenAlex
- W2025865441
- Cited by
- 389
- References
- 9
- FWCI
- 1.92
- Type
- journal article
- Language
- en
- Open access
- closed
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- CoChat. (2026). Citation check: Reconciling the analysis of IBD and IBS in complex trait studies. https://app.cochat.ai/papers/10.1038/nrg2865
- The paper
- Powell, J. E., Visscher, P. M., & Goddard, M. E. (2010). Reconciling the analysis of IBD and IBS in complex trait studies. Nature Reviews Genetics. https://doi.org/10.1038/nrg2865
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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.