Student or educator? Sign up with your school email and get 6 months of Pro free.
CoChat
Sign Up
Cited by 1,736

The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.

A high-resolution recombination map of the human genome

Kong, Augustine, Gudbjartsson, Daniel F., Sainz, Jesus, Jonsdottir, Gudrun M., Gudjonsson, Sigurjon A., Richardsson, Bjorgvin, Sigurdardottir, Sigrun, Barnard, John, Hallbeck, Bjorn, Masson, Gisli, Shlien, Adam, Palsson, Stefan T., Frigge, Michael L., Thorgeirsson, Thorgeir E., Gulcher, Jeffrey R., Stefansson, Kari·2002·Nature Genetics
DOI 10.1038/ng917
Open this paper in CoChat — free account

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.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1038/ng917

Cites

1 of 1 references verified0 citation errors · 0 not checkable

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.

A few free checks a day · papers already verified open instantly · results are public

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

Cites

Show all 1 references

Research works printed but not linked: 23

  1. Initial sequencing and analysis of the human genome. Nature 409, 860–921 (2001). · DOI · Paper page
  2. Dib, C. et al. A comprehensive genetic map of the human genome based on 5,264 microsatellites. Nature 380, 152–154 (1996). · DOI
  3. Murray, J.C. et al. A comprehensive human linkage map with centimorgan density. Science 265, 2049–2054 (1994). · DOI
  4. Broman, K.W., Murray, J.C., Sheffield, V.C., White, R.L. & Weber, J.L. Comprehensive human genetic map: individual and sex-specific variation in recombination. Am. J. Hum. Genet. 63, 861–869 (1998). · DOI · Paper page
  5. Sheffield, V.C. et al. A collection of tri- and tetranucleotide repeat markers used to generate high quality, high resolution human genome-wide linkage maps. Hum. Mol. Genet. 4, 1837–1844 (1995). · DOI
  6. Sunden, S.L. et al. Chromosomal assignment of 2900 tri- and tetranucleotide repeat markers using NIGMS somatic cell hybrid panel 2. Genomics 32, 15–20 (1996). · DOI
  7. Rosenberg, M. et al. Characterization of short tandem repeats from thirty-one human telomeres. Genome Res. 7, 917–923 (1996). · DOI
  8. DeWan, A.T., Parrado, A.R., Matise, T.C. & Leal, S.M. The map problem: a comparison of genetic and sequence-based physical maps. Am. J. Hum. Genet. 70, 101–107 (2002). · DOI
  9. Gudbjartsson, D.F., Jonasson, K., Frigge, M.L. & Kong, A. Allegro, a new computer program for multipoint linkage analysis. Nature Genet. 25, 12–14 (2000). · DOI · Paper page
  10. Giglio, S. et al. Olfactory receptor-gene clusters, genomic-inversion polymorphisms, and common chromosome rearrangements. Am. J. Hum. Genet. 68, 874–883 (2001). · DOI · Paper page
  11. Yu, A. et al. Comparison of human genetic and sequence-based physical maps. Nature 409, 951–953 (2001). · DOI · Paper page
  12. Halpern, J. & Whittemore, A.S. Multipoint linkage analysis. A cautionary note. Hum. Hered. 49, 194–196 (1999). · DOI
  13. Gretarsdottir, S. et al. Localization of a susceptibility gene for common forms of stroke to chromosome 5q12. Am. J. Hum. Genet. 70, 593–603 (2002). · DOI
  14. Daw, E.W., Thompson, E.A. & Wijsman, E.M. Bias in multipoint linkage analysis arising from map misspecification. Genet. Epidemiol. 19, 366–380 (2000). · DOI
  15. Thompson, E.A. Crossover counts and likelihood in multipoint linkage analysis. IMA J. Math. Appl. Med. Biol. 4, 93–108 (1987). · DOI
  16. The International SNP Map Working Group. A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms. Nature 409, 928–933 (2001). · DOI · Paper page
  17. Mohrenweiser, H.W., Tsujimoto, S., Gordon, L. & Olsen, A. Regions of sex-specific hypo- and hyper-recombination identified through integration of 180 genetic markers into the metric physical map of the human chromosome 19. Genomics 47, 153–162 (1998). · DOI
  18. Laurie, D.A. & Hulten, M.A. Further studies on bivalent chiasma frequency in human males with normal karyotypes. Ann. Hum. Genet. 49, 189–201 (1985). · DOI
  19. Ji, Y., Stelly, D.M., DeDonato, M., Goodman, M.M. & Williams, C.G. A candidate recombination modifier gene for Zea mays L. Genetics 151, 821–830 (1999). · DOI
  20. Jeffreys, A.J., Kauppi, L. & Neuman, R. Intensely punctuate meiotic recombination in the class II region of the major histocompatibility complex. Nature Genet. 29, 217–222 (2001). · DOI · Paper page
  21. Daly, M.J., Rioux, J.D., Schaffner, S.F., Hudson, T.J. & Lander, E.S. High-resolution haplotype structure in the human genome. Nature Genet. 29, 229–232 (2001). · DOI · Paper page
  22. Gulcher, J.R., Kristjansson, K., Gudbjartsson, H. & Stefansson, K. Protection of privacy by third-party encryption in genetic research in Iceland. Eur. J. Hum. Genet. 8, 739–742 (2000). · DOI
  23. Venables, W.N. & and Ripley, B.D. Modern Applied Statistics with S-plus (Springer, New York, 1994). · DOI

Cited by

Metadata

Authors
Kong, A., Gudbjartsson, D. F., Sainz, J., Jonsdottir, G. M., Gudjonsson, S. A., Richardsson, B., Sigurdardottir, S., Barnard, J., Hallbeck, B., Masson, G., Shlien, A., Palsson, S. T., Frigge, M. L., Thorgeirsson, T. E., Gulcher, J. R., & Stefansson, K.
Venue
Nature Genetics
Publisher
Springer Science and Business Media LLC
Published
2002-06-10
Volume
31
Issue
3
Pages
241-247
ISSN
  • 1061-4036 (ISSN-L)
  • 1546-1718
DOI
10.1038/ng917
OpenAlex
W2104743461
Cited by
1,736
References
1
FWCI
84.71
Type
journal article
Language
en
Open access
closed
Licence
www.springer.com/tdm (tdm)

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

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.