The DOI matches its Crossref record; 22 of the 22 references it cites were found in a registry or an index.
Evidence for at least four Fanconi anaemia genes including FACC on chromosome 9
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
Variable Number of Tandem Repeat (VNTR) Markers for Human Gene Mapping
Nakamura, Y., Leppert, M., O'Connell, P., Wolff, R., Holm, T., Culver, M., Martin, C., Fujimoto, E., Hoff, M., Kumlin, E., et al. (1987) · Science · doi:10.1126/science.3029872 · Cited by 1,654
Localization of single copy DNA sequences on G-banded human chromosomes by in situ hybridization
Harper, M. E., & Saunders, G. F. (1981) · Chromosoma · doi:10.1007/bf00327364 · Cited by 825
A high susceptibility of Fanconi's anemia to chromosome breakage by DNA cross-linking agents.
Sasaki, M. S., & Tonomura, A. (1973) · PubMed · Cited by 530
Repair deficient human disorders and cancer
Setlow, R. B. (1978) · Nature · doi:10.1038/271713a0 · Cited by 482
Tanaka, K., Miura, N., Satokata, I., Miyamoto, I., Yoshida, M. C., Satoh, Y., Kondo, S., Yasui, A., Okayama, H., & Okada, Y. (1990) · Nature · doi:10.1038/348073a0 · Cited by 388
International Fanconi Anemia Registry: relation of clinical symptoms to diepoxybutane sensitivity
Auerbach, A., Rogatko, A., & Schroeder-Kurth, T. (1989) · Blood · doi:10.1182/blood.v73.2.391.391 · Cited by 345
Spontane Chromosomenaberrationen bei famili�rer Panmyelopathie
Schroeder, T. M., Ansch�tz, F., & Knopp, A. (1964) · Human Genetics · doi:10.1007/bf00389636 · Cited by 309
Familial constitutional panmyelocytopathy, Fanconi's anemia (F.A.). I. Clinical aspects.
Fanconi, G. (1967) · PubMed · Cited by 306
Susceptibility of Fanconi's anemia lymphoblasts to DNA-cross-linking and alkylating agents.
Ishida, R., & Buchwald, M. (1982) · PubMed · Cited by 200
Self-citationSpectrum of anomalies in Fanconi anaemia.
Glanz, A., & Fraser, F. C. (1982) · Journal of Medical Genetics · doi:10.1136/jmg.19.6.412 · Cited by 192
Cited by
Biallelic Inactivation of BRCA2 in Fanconi Anemia
Howlett, N. G., Taniguchi, T., Olson, S., Cox, B., Waisfisz, Q., de Die-Smulders, C., Persky, N., Grompe, M., Joenje, H., Pals, G., et al. (2002) · Science · doi:10.1126/science.1073834 · Cited by 1,149
Emergence of a DNA-damage response network consisting of Fanconi anaemia and BRCA proteins
Wang, W. (2007) · Nature Reviews Genetics · doi:10.1038/nrg2159 · Cited by 663
A 20-year perspective on the International Fanconi Anemia Registry (IFAR)
Kutler, D. I., Singh, B., Satagopan, J., Batish, S. D., Berwick, M., Giampietro, P. F., Hanenberg, H., & Auerbach, A. D. (2003) · Blood · doi:10.1182/blood-2002-07-2170 · Cited by 618
The emerging genetic and molecular basis of Fanconi anaemia
Joenje, H., & Patel, K. J. (2001) · Nature Reviews Genetics · doi:10.1038/35076590 · Cited by 572
The Fanconi anaemia group G gene FANCG is identical with XRCC9
de Winter, J. P., Waisfisz, Q., Rooimans, M. A., van Berkel, C. G. M., Bosnoyan-Collins, L., Alon, N., Carreau, M., Bender, O., Demuth, I., Schindler, D., et al. (1998) · Nature Genetics · doi:10.1038/3093 · Cited by 335
Self-citation
Metadata
- Authors
- Strathdee, C. A., Duncan, A. M. V., & Buchwald, M.
- Venue
- Nature Genetics
- Published
- 1992-06
- Volume
- 1
- Issue
- 3
- Pages
- 196-198
- ISSN
- 1061-4036 (ISSN-L)
- 1546-1718
- OpenAlex
- W2029026115
- Cited by
- 289
- References
- 22
- FWCI
- 7.76
- 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: Evidence for at least four Fanconi anaemia genes including FACC on chromosome 9. https://app.cochat.ai/papers/10.1038/ng0692-196
- The paper
- Strathdee, C. A., Duncan, A. M. V., & Buchwald, M. (1992). Evidence for at least four Fanconi anaemia genes including FACC on chromosome 9. Nature Genetics. https://doi.org/10.1038/ng0692-196
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.
