The DOI matches its Crossref record.
Handbook of Human Genetic Linkage.
Abstract
In his book Analysis of Human Genetic Linkage Jurg Ott laid out the principles by which geneticists perform studies of genetic linkage in humans. Here, in the Handbook of Human Genetic Linkage, Joseph Terwilliger and Jurg Ott provide a companion piece to the previous work, showing how its principles may be applied in practice. Handbook of Human Genetic Linkage contains detailed instructions on how to carry out linkage analysis, guiding the reader through each process on a step-by-step basis. The chapters are grouped into three main sections: two-point linkage analysis, multi-point linkage analysis, and such advanced topics as mutation rates, gene frequencies, linkage disequilibrium, complex diseases and computer simulation. Each chapter ends with exercises that can be performed on an IBM PC-compatible computer. The solutions are supplied at the end of each section.
Overview
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
Cited by
Gloyn, A. L., Weedon, M. N., Owen, K. R., Turner, M. J., Knight, B. A., Hitman, G., Walker, M., Levy, J. C., Sampson, M., Halford, S., et al. (2003) · Diabetes · doi:10.2337/diabetes.52.2.568 · Cited by 754
Alpha-2 macroglobulin is genetically associated with Alzheimer disease
Blacker, D., Wilcox, M. A., Laird, N. M., Rodes, L., Horvath, S. M., Go, R. C. P., Perry, R., Watson, B., Bassett, S. S., McInnis, M. G., et al. (1998) · Nature Genetics · doi:10.1038/1243 · Cited by 486
Arinami, T. (1997) · Human Molecular Genetics · doi:10.1093/hmg/6.4.577 · Cited by 455
Model-Free Analysis and Permutation Tests for Allelic Associations
Zhao, J. H., Curtis, D., & Sham, P. C. (2000) · Human Heredity · doi:10.1159/000022901 · Cited by 417
Domain-specific mutations in sequestosome 1 (SQSTM1) cause familial and sporadic Paget’s disease.
Hocking, L. J. (2002) · Human Molecular Genetics · doi:10.1093/hmg/11.22.2735 · Cited by 350
Metadata
- Authors
- Edwards, A. W. F., Terwilliger, J. D., & Ott, J.
- Venue
- Biometrics
- Publisher
- JSTOR
- Published
- 1996-09
- Volume
- 52
- Issue
- 3
- Pages
- 1161
- ISSN
- 0006-341X (ISSN-L)
- OpenAlex
- W2066751658
- Cited by
- 869
- References
- 0
- FWCI
- 40.51
- Type
- journal article
- Language
- en
- Open access
- closed
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: Handbook of Human Genetic Linkage. https://app.cochat.ai/papers/10.2307/2533082
- The paper
- Edwards, A. W. F., Terwilliger, J. D., & Ott, J. (1996). Handbook of Human Genetic Linkage. Biometrics. https://doi.org/10.2307/2533082
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.