The DOI matches its Crossref record; 11 of the 11 references it cites were found in a registry or an index.
A Test for Linkage and Association in General Pedigrees: The Pedigree Disequilibrium Test
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Citations
Cites
Spielman, R. S., McGinnis, R. E., & Ewens, W. J. (1993) · PubMed · Cited by 3,651
The TDT and other family-based tests for linkage disequilibrium and association.
(1996) · PubMed Central · Cited by 901
A Sibship Test for Linkage in the Presence of Association: The Sib Transmission/Disequilibrium Test
Spielman, R. S., & Ewens, W. J. (1998) · The American Journal of Human Genetics · doi:10.1086/301714 · Cited by 659
A Discordant-Sibship Test for Disequilibrium and Linkage: No Need for Parental Data
Horvath, S., & Laird, N. M. (1998) · The American Journal of Human Genetics · doi:10.1086/302137 · Cited by 220
Tests for Linkage and Association in Nuclear Families
Martin, E. R., Kaplan, N. L., & Weir, B. S. (1997) · The American Journal of Human Genetics · doi:10.1086/514860 · Cited by 212
Self-citationGenetic Association Mapping Based on Discordant Sib Pairs: The Discordant-Alleles Test
Boehnke, M., & Langefeld, C. D. (1998) · The American Journal of Human Genetics · doi:10.1086/301787 · Cited by 206
Use of siblings as controls in case‐control association studies
CURTIS, D. (1997) · Annals of Human Genetics · doi:10.1046/j.1469-1809.1998.6210089.x · Cited by 189
A note on the application of the transmission disequilibrium test when a parent is missing.
Curtis, D., & Sham, P. C. (1995) · PubMed · Cited by 182
Knapp, M. (1999) · The American Journal of Human Genetics · doi:10.1086/302285 · Cited by 163
Monks, S. A., & Kaplan, N. L. (2000) · The American Journal of Human Genetics · doi:10.1086/302745 · Cited by 116
Self-citation
Cited by
Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease
Hugot, J.-P., Chamaillard, M., Zouali, H., Lesage, S., Cézard, J.-P., Belaiche, J., Almer, S., Tysk, C., O'Morain, C. A., Gassull, M., et al. (2001) · Nature · doi:10.1038/35079107 · Cited by 5,591
Common genetic variants on 5p14.1 associate with autism spectrum disorders
Wang, K., Zhang, H., Ma, D., Bucan, M., Glessner, J. T., Abrahams, B. S., Salyakina, D., Imielinski, M., Bradfield, J. P., Sleiman, P. M. A., et al. (2009) · Nature · doi:10.1038/nature07999 · Cited by 989
Prokunina, L., Castillejo-López, C., Öberg, F., Gunnarsson, I., Berg, L., Magnusson, V., Brookes, A. J., Tentler, D., Kristjansdóttir, H., Gröndal, G., et al. (2002) · Nature Genetics · doi:10.1038/ng1020 · Cited by 769
Edenberg, H. J., Dick, D. M., Xuei, X., Tian, H., Almasy, L., Bauer, L. O., Crowe, R. R., Goate, A., Hesselbrock, V., Jones, K., et al. (2004) · The American Journal of Human Genetics · doi:10.1086/383283 · Cited by 655
for the Multiple Sclerosis Genetics Group, Gregory, S. G., Schmidt, S., Seth, P., Oksenberg, J. R., Hart, J., Prokop, A., Caillier, S. J., Ban, M., Goris, A., et al. (2007) · Nature Genetics · doi:10.1038/ng2103 · Cited by 657
Metadata
- Authors
- Martin, E. R., Monks, S. A., Warren, L. L., & Kaplan, N. L.
- Venue
- The American Journal of Human Genetics
- Publisher
- Elsevier BV
- Published
- 2000-07
- Volume
- 67
- Issue
- 1
- Pages
- 146-154
- ISSN
- 0002-9297 (ISSN-L)
- OpenAlex
- W4247459924
- Cited by
- 538
- References
- 11
- FWCI
- 18.55
- Type
- journal article
- Language
- en
- Open access
- bronze
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- CoChat. (2026). Citation check: A Test for Linkage and Association in General Pedigrees: The Pedigree Disequilibrium Test. https://app.cochat.ai/papers/10.1086/302957
- The paper
- Martin, E. R., Monks, S. A., Warren, L. L., & Kaplan, N. L. (2000). A Test for Linkage and Association in General Pedigrees: The Pedigree Disequilibrium Test. The American Journal of Human Genetics. https://doi.org/10.1086/302957
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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.
