The DOI matches its Crossref record; 22 of the 22 references it cites were found in a registry or an index.
Susceptible chiasmate configurations of chromosome 21 predispose to non–disjunction in both maternal meiosis I and meiosis II
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
Cites
Construction of multilocus genetic linkage maps in humans.
Lander, E. S., & Green, P. (1987) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.84.8.2363 · Cited by 1,428
ZIP1 is a synaptonemal complex protein required for meiotic chromosome synapsis
Sym, M., Engebrecht, J., & Roeder, G. S. (1993) · Cell · doi:10.1016/0092-8674(93)90114-6 · Cited by 598
Centre d'Etude du polymorphisme humain (CEPH): Collaborative genetic mapping of the human genome
Dausset, J., Cann, H., Cohen, D., Lathrop, M., Lalouel, J.-M., & White, R. (1990) · Genomics · doi:10.1016/0888-7543(90)90491-c · Cited by 575
NON-DISJUNCTION AS PROOF OF THE CHROMOSOME THEORY OF HEREDITY
Bridges, C. B. (1916) · Genetics · doi:10.1093/genetics/1.1.1 · Cited by 557
Chiasma Frequency and Maternal Age in Mammals
HENDERSON, S. A., & EDWARDS, R. G. (1968) · Nature · doi:10.1038/218022a0 · Cited by 443
Parental Origin of the Extra Chromosome in Trisomy 21 as Indicated by Analysis of DNA Polymorphisms
Antonarakis, S. E. (1991) · New England Journal of Medicine · doi:10.1056/nejm199103283241302 · Cited by 281
Sherman, S. L., Petersen, M. B., Freeman, S. B., Hersey, J., Pettay, D., Taft, L., Frantzen, M., Mikkelsen, M., & Hassold, T. J. (1994) · Human Molecular Genetics · doi:10.1093/hmg/3.9.1529 · Cited by 237
Self-citationMacDonald, M., Hassold, T., Harvey, J., Wang, L. H., Morton, N. E., & Jacobs, P. (1994) · Human Molecular Genetics · doi:10.1093/hmg/3.8.1365 · Cited by 230
Self-citationRecombination and maternal age-dependent nondisjunction: molecular studies of trisomy 16.
Hassold, T. J., Merrill, M. C., Adkins, K., Freeman, S. B., & Sherman, S. L. (1995) · PubMed Central · Cited by 229
Self-citationAntonarakis, S. E., Avramopoulos, D., Blouin, J.-L., Conover Talbot, C., & Schinzel, A. A. (1993) · Nature Genetics · doi:10.1038/ng0293-146 · Cited by 217
Self-citation
Cited by
An evolutionary view of human recombination
Coop, G., & Przeworski, M. (2007) · Nature Reviews Genetics · doi:10.1038/nrg1947 · Cited by 344
Chromosome mosaicism in cleavage-stage human embryos: evidence of a maternal age effect
Munné, S., Sandalinas, M., Escudero, T., Márquez, C., & Cohen, J. (2002) · Reproductive BioMedicine Online · doi:10.1016/s1472-6483(10)61810-x · Cited by 278
Meiosis in oocytes: predisposition to aneuploidy and its increased incidence with age
Jones, K. T. (2008) · Human Reproduction Update · doi:10.1093/humupd/dmm043 · Cited by 228
DNA damage in aging, the stem cell perspective
McNeely, T., Leone, M., Yanai, H., & Beerman, I. (2020) · Human Genetics · doi:10.1007/s00439-019-02047-z · Cited by 52
Metadata
- Authors
- Lamb, N. E., Freeman, S. B., Savage-Austin, A., Pettay, D., Taft, L., Hersey, J., Gu, Y., Shen, J., Saker, D., May, K. M., Avramopoulos, D., Petersen, M. B., Hallberg, A., Mikkelsen, M., Hassold, T. J., & Sherman, S. L.
- Venue
- Nature Genetics
- Published
- 1996-12
- Volume
- 14
- Issue
- 4
- Pages
- 400-405
- ISSN
- 1061-4036 (ISSN-L)
- 1546-1718
- OpenAlex
- W2021647091
- Cited by
- 386
- References
- 22
- FWCI
- 31.30
- 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: Susceptible chiasmate configurations of chromosome 21 predispose to non–disjunction in both maternal meiosis I and meiosis II. https://app.cochat.ai/papers/10.1038/ng1296-400
- The paper
- Lamb, N. E., Freeman, S. B., Savage-Austin, A., Pettay, D., Taft, L., Hersey, J., Gu, Y., Shen, J., Saker, D., May, K. M., Avramopoulos, D., Petersen, M. B., Hallberg, A., Mikkelsen, M., Hassold, T. J., & Sherman, S. L. (1996). Susceptible chiasmate configurations of chromosome 21 predispose to non–disjunction in both maternal meiosis I and meiosis II. Nature Genetics. https://doi.org/10.1038/ng1296-400
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.