The DOI matches its Crossref record; 45 of the 45 references it cites were found in a registry or an index.
Genetics of retinoblastoma
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Citations
Cites
Mutation and cancer: statistical study of retinoblastoma
Knudson, A. G. (1971) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.68.4.820 · Cited by 7,612
Human Genetics. Problems and Approaches.
(1980) · Annals of Internal Medicine · doi:10.7326/0003-4819-93-1-163_3 · Cited by 991
Worthen, D. M. (1972) · Archives of Ophthalmology · doi:10.1001/archopht.1972.01000030236034 · Cited by 798
The rate of spontaneous mutation of a human gene
Haldane, J. B. S. (2004) · Journal of Genetics · doi:10.1007/bf02717892 · Cited by 472
Retinoblastoma and Subband Deletion of Chromosome 13
Yunis, J. J. (1978) · Archives of Pediatrics & Adolescent Medicine · doi:10.1001/archpedi.1978.02120270059012 · Cited by 445
SVEJGAARD, A. (1977) · Revue Francaise de Transfusion et Immuno-hématologie · doi:10.1016/s0338-4535(77)80006-8 · Cited by 422
Vogel, F., Schalt, E., Kr�ger, J., Propping, P., & Lehnert, K. F. (1979) · Human Genetics · doi:10.1007/bf00295569 · Cited by 385
Self-citationMutation and childhood cancer: a probabilistic model for the incidence of retinoblastoma.
Knudson, A. G., Hethcote, H. W., & Brown, B. W. (1975) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.72.12.5116 · Cited by 348
PENROSE, L. (1955) · The Lancet · doi:10.1016/s0140-6736(55)92305-9 · Cited by 345
Regional Assignment of Genes for Human Esterase D and Retinoblastoma to Chromosome Band 13q14
Sparkes, R. S., Sparkes, M. C., Wilson, M. G., Towner, J. W., Benedict, W., Murphree, A. L., & Yunis, J. J. (1980) · Science · doi:10.1126/science.7375916 · Cited by 342
Vogel, F., & Rathenberg, R. (1975) · Advances in Human Genetics · doi:10.1007/978-1-4615-9068-2_4 · Cited by 341
Self-citationCharacteristics of an Established Cell Line of Retinoblastoma2
Reid, T. W., Albert, D. M., Rabson, A. S., Russell, P., Craft, J., Chu, E. W., Tralka, T. S., & Wilcox, J. L. (1974) · JNCI: Journal of the National Cancer Institute · doi:10.1093/jnci/53.2.347 · Cited by 340
THE MOLECULAR BASIS OF MUTATION
Drake, J. W., & Flamm, W. G. (1972) · Mutagenic Effects of Environmental Contaminants · doi:10.1016/b978-0-12-677950-9.50008-8 · Cited by 312
Chromosomal Deletion and Retinoblastoma
Knudson, A. G., Meadows, A. T., Nichols, W. W., & Hill, R. (1976) · New England Journal of Medicine · doi:10.1056/nejm197611112952007 · Cited by 281
Methodology in medical genetics
Emery, A. E. H. (1976) · Cited by 266
LEVAN, A., LEVAN, G., & MITELMAN, F. (2009) · Hereditas · doi:10.1111/j.1601-5223.1977.tb01208.x · Cited by 263
Older paternal age and fresh gene mutation: Data on additional disorders
Jones, K. L., Smith, D. W., Harvey, M. A. S., Hall, B. D., & Quan, L. (1975) · The Journal of Pediatrics · doi:10.1016/s0022-3476(75)80709-8 · Cited by 263
RADIATION INDUCED NEOPLASIA FOLLOWING EXTERNAL BEAM THERAPY FOR CHILDREN WITH RETINOBLASTOMA
SAGERMAN, R. H., CASSADY, J. R., TRETTER, P., & ELLSWORTH, R. M. (1969) · American Journal of Roentgenology · doi:10.2214/ajr.105.3.529 · Cited by 222
Chromosome deletion in a case of retinoblastoma
LELE, K. P., PENROSE, L. S., & STALLARD, H. B. (1963) · Annals of Human Genetics · doi:10.1111/j.1469-1809.1963.tb00209.x · Cited by 215
The Incidence of Retinoblastoma
Devesa, S. S. (1975) · American Journal of Ophthalmology · doi:10.1016/0002-9394(75)90143-9 · Cited by 172
The two “hit” and multiple “hit” theories of carcinogenesis.
Ashley, D. J. B. (1969) · British Journal of Cancer · doi:10.1038/bjc.1969.41 · Cited by 170
Allderdice, P. W., Davis, J. G., Miller, O. J., Klinger, H. P., Warburton, D., Miller, D., Allen, F. H., Abrams, C. A., & Mcgilvray, E. T. (1969) · Europe PMC (PubMed Central) · Cited by 152
Falls, H. F., & Neel, J. V. (1951) · Archives of Ophthalmology · doi:10.1001/archopht.1951.01700020378002 · Cited by 141
Retinoblastoma and chromosome 13
Francke, U. (2008) · Cytogenetics and Cell Genetics · doi:10.1159/000130573 · Cited by 133
Epidemiology of Bone Cancer in Children
Glass, A. G., & Joseph F. Fraumeni, Jr. (1970) · JNCI Journal of the National Cancer Institute · doi:10.1093/jnci/44.1.187 · Cited by 132
Schroeder, T. M., & KURTH, R. (1971) · Blood · doi:10.1182/blood.v37.1.96.96 · Cited by 131
Genetics and Etiology of Human Cancer
Knudson, A. G. (1977) · Springer eBooks · doi:10.1007/978-1-4615-8267-0_1 · Cited by 119
The occurrence of new mutants in the X-linked recessive Lesch-Nyhan disease.
Francke, U., Felsenstein, J., Gartler, S. M., Migeon, B. R., Dancis, J., Seegmiller, J. E., Bakay, F., & Nyhan, W. L. (1976) · Europe PMC (PubMed Central) · Cited by 112
The Heredity of Retinoblastoma
Schappert-Kimmijser, J. S., Hemmes, G. D., & Nijland, R. (2010) · Ophthalmologica · doi:10.1159/000304891 · Cited by 107
Radiation-induced neoplasms following curative therapy for retinoblastoma
Soloway, H. B. (1966) · Cancer · Cited by 102
Sporadic bilateral retinoblastoma and 13q‐chromosomal deletion
Francke, U., & Kung, F. (1976) · Medical and Pediatric Oncology · doi:10.1002/mpo.2950020404 · Cited by 95
Skin fibroblasts from a D-deletion type retinoblastoma patient are abnormally X-ray sensitive
Weichselbaum, R. R., Nove, J., & Little, J. B. (1977) · Nature · doi:10.1038/266726a0 · Cited by 91
Chromosomal anomalies in patients with retinoblastoma
Wilson, M. G., Ebbin, A. J., Towner, J. W., & Spencer, W. H. (1977) · Clinical Genetics · doi:10.1111/j.1399-0004.1977.tb00894.x · Cited by 87
Retinoblastoma with 13q- Chromosomal Deletion Associated with Maternal Paracentric Inversion of 13q
Sparkes, R. S., Muller, H. M., Klisak, I. J., & Abram, J. A. (1979) · Science · doi:10.1126/science.424728 · Cited by 86
A study of retinoblastoma in Ohio.
Macklin, M. T. (1960) · PubMed · Cited by 84
Letter: Half chromatid mutations may explain incontinentia pigmenti in males.
Lenz, W. (1975) · PubMed · Cited by 75
Retinoblastoma and osteogenic sarcoma in siblings
Schimke, R. N., Lowman, J. T., & Cowan, G. A. (1974) · Cancer · Cited by 64
Retinoblastoma and deletion D (14) syndrome.
Wilson, M. G., Melnyk, J., & Towner, J. W. (1969) · Journal of Medical Genetics · doi:10.1136/jmg.6.3.322 · Cited by 59
Hereditary retinoblastoma: Penetrance, expressivity and age of onset
Matsunaga, E. (1976) · Human Genetics · doi:10.1007/bf00447281 · Cited by 51
Retinoblastoma in a Patient with a 13qxp Translocation
Cross, H. E., Hansen, R. C., Morrow, G., et al. (1977) · American Journal of Ophthalmology · doi:10.1016/0002-9394(77)90450-0 · Cited by 49
Retinoblastoma and Chromosome Abnormality
Howard, R. O. (1974) · Archives of Ophthalmology · doi:10.1001/archopht.1974.01010010504007 · Cited by 47
A POSSIBLE CASE OF DELAYED MUTATION IN MAN
AUERBACH, B. C. (1956) · Annals of Human Genetics · doi:10.1111/j.1469-1809.1955.tb01281.x · Cited by 46
Chromosome studies in twelve patients with retinoblastoma
Czeizel, A. E., Csősz, L., Gárdonyi, J., Remenár, L., & Ruziscka, P. (1974) · Human Genetics · doi:10.1007/bf00278455 · Cited by 33
RETINOBLASTOMA: SOME GENETIC ASPECTS
SMITH, S. M., & Sorsby, A. (1958) · Annals of Human Genetics · doi:10.1111/j.1469-1809.1958.tb01441.x · Cited by 22
[New studies on the genetics of retinoblastoma; glioma retinae].
VOGEL, F. (1957) · PubMed · Cited by 18
Self-citation
Cited by
A human DNA segment with properties of the gene that predisposes to retinoblastoma and osteosarcoma
Friend, S. H., Bernards, R., Rogelj, S., Weinberg, R. A., Rapaport, J. M., Albert, D. M., & Dryja, T. P. (1986) · Nature · doi:10.1038/323643a0 · Cited by 2,948
Whyte, P., Buchkovich, K. J., Horowitz, J. M., Friend, S. H., Raybuck, M., Weinberg, R. A., & Harlow, E. (1988) · Nature · doi:10.1038/334124a0 · Cited by 1,403
Risk of Second Malignancies in Survivors of Retinoblastoma: More Than 40 Years of Follow-up
Marees, T., Moll, A. C., Imhof, S. M., de Boer, M. R., Ringens, P. J., & van Leeuwen, F. E. (2008) · JNCI: Journal of the National Cancer Institute · doi:10.1093/jnci/djn394 · Cited by 286
Metadata
- Authors
- Vogel, F.
- Venue
- Human Genetics
- Published
- 1979
- Volume
- 52
- Issue
- 1
- Pages
- 1-54
- ISSN
- 0018-7348 (ISSN-L)
- 0340-6717
- 1432-1203
- OpenAlex
- W2058454398
- Cited by
- 438
- References
- 45
- FWCI
- 25.34
- Type
- journal article
- Language
- en
- Open access
- closed
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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.
