The DOI matches its Crossref record; 162 of the 162 references it cites were found in a registry or an index.
The Concise Handbook of Family Cancer Syndromes
Abstract
11. Cowden syndrome (gingival multiple hamartoma syndrome) 1051 12. Esophageal cancer, tylosis with (nonepidermolytic palmoplantar keratosis and Howel-Evans’ syndrome) 1052 13. Fanconi’s anemia (includes pancytopenia, Fanconi’s type) 1053 14. Gastric cancer, familial 1054 15. Hodgkin’s disease, familial 1054 16. Li-Fraumeni syndrome 1055 17. Melanoma, familial with or without dysplastic nevi (includes dysplastic nevus syndrome, familial atypical mole–malignant melanoma syndrome, and melanoma–astrocytoma syndrome) 1056
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1 retracted
Nouspikel, T., Lalle, P., Leadon, S. A., Cooper, P. K., & Clarkson, S. G. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.7.3116 · Cited by 163
RetractedGerm Line p53 Mutations in a Familial Syndrome of Breast Cancer, Sarcomas, and Other Neoplasms
Malkin, D., Li, F. P., Strong, L. C., Fraumeni, J. F., Nelson, C. E., Kim, D. H., Kassel, J., Gryka, M. A., Bischoff, F. Z., Tainsky, M. A., et al. (1990) · Science · doi:10.1126/science.1978757 · Cited by 3,765
DPC4 , A Candidate Tumor Suppressor Gene at Human Chromosome 18q21.1
Hahn, S. A., Schutte, M., Shamsul Hoque, A. T. M., Moskaluk, C. A., da Costa, L. T., Rozenblum, E., Weinstein, C. L., Fischer, A., Yeo, C. J., Hruban, R. H., et al. (1996) · Science · doi:10.1126/science.271.5247.350 · Cited by 2,337
The Risk of Cancer Associated with Specific Mutations of BRCA1 and BRCA2 among Ashkenazi Jews
Struewing, J. P., Hartge, P., Wacholder, S., Baker, S. M., Berlin, M., McAdams, M., Timmerman, M. M., Brody, L. C., & Tucker, M. A. (1997) · New England Journal of Medicine · doi:10.1056/nejm199705153362001 · Cited by 2,281
Motzer, R. J., Bander, N. H., & Nanus, D. M. (1996) · New England Journal of Medicine · doi:10.1056/nejm199609193351207 · Cited by 2,219
The International Collaborative Group on Hereditary Non-Polyposis Colorectal Cancer (ICG-HNPCC)
Vasen, H. F. A., Mecklin, J. P., Meera Khan, P., & Lynch, H. T. (1991) · Diseases of the Colon & Rectum · doi:10.1007/bf02053699 · Cited by 2,147
Liaw, D., Marsh, D. J., Li, J., Dahia, P. L. M., Wang, S. I., Zheng, Z., Bose, S., Call, K. M., Tsou, H. C., Peacoke, M., et al. (1997) · Nature Genetics · doi:10.1038/ng0597-64 · Cited by 2,091
Positional Cloning of the Gene for Multiple Endocrine Neoplasia-Type 1
Chandrasekharappa, S. C., Guru, S. C., Manickam, P., Olufemi, S.-E., Collins, F. S., Emmert-Buck, M. R., Debelenko, L. V., Zhuang, Z., Lubensky, I. A., Liotta, L. A., et al. (1997) · Science · doi:10.1126/science.276.5311.404 · Cited by 2,082
Mutations of the Human Homolog of Drosophila patched in the Nevoid Basal Cell Carcinoma Syndrome
Hahn, H., Wicking, C., Zaphiropoulos, P. G., Gailani, M. R., Shanley, S., Chidambaram, A., Vorechovsky, I., Holmberg, E., Unden, A. B., Gillies, S., et al. (1996) · Cell · doi:10.1016/s0092-8674(00)81268-4 · Cited by 2,022
Smith's recognizable patterns of human malformation
Jones, K. L., Jones, M. C., & Campo, M. D. (1997) · Cited by 1,916
Cited by
Pathogenetic mechanisms in thyroid follicular-cell neoplasia
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Nelson, H. D., Huffman, L. H., Fu, R., & Harris, E. L. (2005) · Annals of Internal Medicine · doi:10.7326/0003-4819-143-5-200509060-00012 · Cited by 346
Inherited pancreatic cancer syndromes
Solomon, S., Das, S., Brand, R., & Whitcomb, D. C. (2012) · The Cancer Journal · doi:10.1097/ppo.0b013e318278c4a6 · Cited by 120
Corral, J. E., Mareth, K. F., Riegert-Johnson, D. L., Das, A., & Wallace, M. B. (2019) · Clinical Gastroenterology and Hepatology · doi:10.1016/j.cgh.2018.04.065 · Cited by 113
Metadata
- Authors
- Lindor, N. M., Greene, M. H., & Program, M. F. C.
- Venue
- JNCI: Journal of the National Cancer Institute
- Publisher
- Oxford University Press (OUP)
- Published
- 1998-07-15
- Volume
- 90
- Issue
- 14
- Pages
- 1039-1071
- ISSN
- 0027-8874 (ISSN-L)
- 1460-2105
- OpenAlex
- W2169195868
- Cited by
- 339
- References
- 162
- FWCI
- 10.81
- Type
- journal article
- Language
- en
- Open access
- closed
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- CoChat. (2026). Citation check: The Concise Handbook of Family Cancer Syndromes. https://app.cochat.ai/papers/10.1093/jnci/90.14.1039
- The paper
- Lindor, N. M., Greene, M. H., & Program, M. F. C. (1998). The Concise Handbook of Family Cancer Syndromes. JNCI: Journal of the National Cancer Institute. https://doi.org/10.1093/jnci/90.14.1039
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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.
