The DOI matches its Crossref record; 187 of the 187 references it cites were found in a registry or an index.
BRCA1 and BRCA2: 1994 and beyond
Abstract
The discovery of the first gene associated with hereditary breast cancer, BRCA1, was anticipated to greatly increase our understanding of both hereditary and sporadic forms of breast cancer, and to lead to therapeutic and preventive breakthroughs. Much has been learned during the past decade about the genetic epidemiology of breast cancer, the ethnic distribution and clinical consequences of BRCA1 and BRCA2 mutations, and the central role of DNA repair in breast cancer susceptibility. The ability to translate this knowledge into novel treatments, however, remains elusive.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“the lifetime risk of developing breast cancer in BRCA1/2 mutation carriers ranges from 45 to 80% [8–11]”
From Fear of cancer recurrence in breast cancer survivors carrying a BRCA1 or 2 genetic mutation : a cross-sectional study (2024) · cites this paper as [11]
In the citing paper
“The tumor suppressor complex BRCA1-BARD1 functions in DNA double-strand break repair by homologous recombination.”
From BRCA1–BARD1 promotes RAD51-mediated homologous DNA pairing (2017) · cites this paper as [1]
Citations
Cites
Molecular portraits of human breast tumours
Perou, C., Sørlie, T., Eisen, M., van de Rijn, M., Jeffrey, S., Rees, C. A., Pollack, J., Ross, D., Johnsen, H., Akslen, L., et al. (2000) · Nature · doi:10.1038/35021093 · Cited by 16,551
Gene expression profiling predicts clinical outcome of breast cancer
van 't Veer, L. J., Dai, H., van de Vijver, M. J., He, Y. D., Hart, A. A. M., Mao, M., Peterse, H. L., van der Kooy, K., Marton, M. J., Witteveen, A. T., et al. (2002) · Nature · doi:10.1038/415530a · Cited by 9,536
A Strong Candidate for the Breast and Ovarian Cancer Susceptibility Gene BRCA1
Miki, Y., Swensen, J. J., Shattuck-Eidens, D. M., Futreal, P. A., Harshman, K., Tavtigian, S. V., Liu, Q., Cochran, C., Bennett, L. M., Ding, W., et al. (1994) · Science · doi:10.1126/science.7545954 · Cited by 6,069
Self-citationRepeated observation of breast tumor subtypes in independent gene expression data sets
Sørlie, T., Tibshirani, R. J., Parker, J. S., Hastie, T. J., Marron, J. S., Nobel, A. B., Deng, S., Johnsen, H., Pesich, R., Geisler, S. B., et al. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0932692100 · Cited by 5,508
Antoniou, A., Pharoah, P. D. P., Narod, S., Risch, H. A., Eyfjord, J. E., Hopper, J. L., Loman, N., Olsson, H., Johannsson, O., Borg, Å., et al. (2003) · The American Journal of Human Genetics · doi:10.1086/375033 · Cited by 3,680
Self-citationIdentification of the breast cancer susceptibility gene BRCA2
Wooster, R., Bignell, G. R., Lancaster, J., Swift, S., Seal, S., Mangion, J., Collins, N., Gregory, S. G., Gumbs, C. E., Micklem, G., et al. (1995) · Nature · doi:10.1038/378789a0 · Cited by 3,645
Self-citationOrita, M., Iwahana, H., Kanazawa, H., Hayashi, K., & Sekiya, T. (1989) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.86.8.2766 · Cited by 3,589
Mutations in the p53 tumor suppressor gene: clues to cancer etiology and molecular pathogenesis.
Greenblatt, M. S., Bennett, W. P., Hollstein, M., & Harris, C. C. (1994) · PubMed · Cited by 3,463
Linkage of Early-Onset Familial Breast Cancer to Chromosome 17q21
Hall, J., Lee, M. K., Newman, B. M., Morrow, J. E., Anderson, L. A., Huey, B., & King, M. (1990) · Science · doi:10.1126/science.2270482 · Cited by 2,544
The risk of cancer associated with specific mutations of BRCA1 and BRCA2 among Ashkenazi Jews.
Struewing, J., Hartge, P., Wacholder, S., Baker, S. M., Berlin, M., McAdams, M., Timmerman, M. M., Brody, L., & Tucker, M. A. (1997) · New England Journal of Medicine · doi:10.1056/nejm199705153362001 · Cited by 2,399
Flagged first, then by citations
Cited by
Sorted by citations
Items 601–700 of 978
Melki, R., Melloul, M., Aissaoui, S., Harroudi, T. E., & Boukhatem, N. (2023) · BMC Cancer · doi:10.1186/s12885-023-10822-5 · Cited by 7
Xue, M., Xu, Z., Wang, X., Chen, J., Kong, X., Zhou, S., Wu, J., Zhang, Y., Li, Y., Christiani, D. C., et al. (2024) · Journal of Advanced Research · doi:10.1016/j.jare.2024.08.015 · Cited by 7
Zheng, J., Zhou, X., Fu, Y., & Chen, Q. (2023) · Cancers · doi:10.3390/cancers15041314 · Cited by 7
The deubiquitinating enzyme USP4 regulates BRCA1 stability and function
Guo, X., Ma, Y., Zhang, T., Liu, R., Chang, F., Yan, X., Yu, T., Wu, P., Li, Q., Xu, L., et al. (2024) · npj Breast Cancer · doi:10.1038/s41523-024-00641-7 · Cited by 7
Genetic Approaches to Human Disease
Lifton, R. P., & Boyden, L. M. (2009) · Elsevier eBooks · doi:10.1016/b978-0-12-449851-8.00001-2 · Cited by 8
Long Non-Coding RNA Neighbor of BRCA1 Gene 2: A Crucial Regulator in Cancer Biology
Wang, T., Li, Z., Yan, L., Yan, F., Shen, H., & Tian, X. (2021) · Frontiers in Oncology · doi:10.3389/fonc.2021.783526 · Cited by 7
Yang, G., Lü, T., Weisenberger, D. J., & Liang, G. (2022) · Genes · doi:10.3390/genes13091555 · Cited by 7
BRCA and Pancreatic Cancer: Selection of Chemotherapy
Kim, R. D., Byer, J., & Saif, M. W. (2012) · PubMed · doi:10.6092/1590-8577/727 · Cited by 7
Structural and Functional Implication of RAP80 ΔGlu81 Mutation
Vikrant, Kumar, R., Yadav, L. R., Nakhwa, P., Waghmare, S. K., Goyal, P., & Varma, A. K. (2013) · PLoS ONE · doi:10.1371/journal.pone.0072707 · Cited by 7
CHEK2 1100 delC mutation in Russian ovarian cancer patients
Krylova, N., Ponomariova, D. N., Sherina, N., Ogorodnikova, N., Logvinov, D. A., Porhanova, N. V., Lobeiko, O. S., Urmancheyeva, A. F., Maximov, S. Y., Togo, A. V., et al. (2007) · Hereditary Cancer in Clinical Practice · doi:10.1186/1897-4287-5-3-153 · Cited by 7
Crump, R., Fitzgerald, R. P., & Legge, M. (2010) · Journal of Primary Health Care · doi:10.1071/hc10311 · Cited by 7
Aging Mouse Models Reveal Complex Tumor-Microenvironment Interactions in Cancer Progression
Mori, H., Cardiff, R. D., & Borowsky, A. D. (2018) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2018.00035 · Cited by 8
Fridriksdottir, A. J., Guðjónsson, Þ., Halldorsson, T. I., Björnsson, J., Steinarsdóttir, M., Jóhannsson, Ó. Þ., & Ogmundsdottir, H. M. (2005) · In Vitro Cellular & Developmental Biology - Animal · doi:10.1290/0505033.1 · Cited by 7
McCullough, S. D., Hu, Y., & Li, R. (2007) · Cancer metastasis · doi:10.1007/978-1-4020-5867-7_3 · Cited by 7
Henningson, M., Bågeman, E., Sandberg, T., Borg, Å., Olsson, H. L., & Jernström, H. (2007) · Familial Cancer · doi:10.1007/s10689-007-9141-0 · Cited by 7
DNA damage hypersensitivity in cells lacking BRCA2: a review of in vitro and in vivo data
Hay, T., & Clarke, A. R. (2005) · Biochemical Society Transactions · doi:10.1042/bst0330715 · Cited by 7
BRCA1 and BRCA2 Genetic Testing in Breast and/or Ovarian Cancer Families in Iran
Keshavarzi, F., Javadi, G. R., Nafissi, N., Akbari, M. E., Yassaee, V. R., Farzad, M. S., & Zeinali, S. (2010) · DOAJ (DOAJ: Directory of Open Access Journals) · Cited by 7
BRCA/Fanconi anemia pathway genes in hereditary predisposition to breast cancer
Sólyom, S. (2011) · Cited by 7
Burness, M. L., & Olopade, O. I. (2011) · Journal of Clinical Oncology · doi:10.1200/jco.2010.32.5274 · Cited by 7
Jang, S. Y., Kwak, Y., Choi, J. Y., Shin, D. S., Lee, H., Kim, M., Jung, B. Y., Chae, B. J., Yu, J., Lee, J. E., et al. (2024) · Cancers · doi:10.3390/cancers16101865 · Cited by 6
Haanpää, M. K. (2014) · Cited by 6
Ahmad, H., Ali, A., Ali, R., Khalil, A. T., Khan, I. N., Khan, M. M., & Alorini, M. (2024) · Neoplasia · doi:10.1016/j.neo.2024.100989 · Cited by 6
Identification of Functional Immune Biomarkers in Breast Cancer Patients
Derakhshandeh, R., Zhu, Y., Li, J., Hester, D., Younis, R. H., Koka, R. M., Jones, L. P., Sun, W., Goloubeva, O. G., Tkaczuk, K. H. R., et al. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms252212309 · Cited by 6
Bellè, F., Mercatanti, A., Lodovichi, S., Congregati, C., Guglielmi, C., Tancredi, M., Caligo, M. A., Cervelli, T., & Galli, A. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23074049 · Cited by 6
Estrogen and BRCA1 deficiency synergistically induce breast cancer mutation-related DNA damage
Chen, J., Liu, J., Zeng, P., Zhao, C., Liu, X., Sun, J., Wang, J., Fang, P., Chen, W., & Ding, J. (2022) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2022.04.142 · Cited by 6
Wang, C., Yi, T., Li, X., Cui, J., Li, B., Qin, Y., Tang, S., & Zhang, J. (2023) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.18033 · Cited by 6
Kang, E. K., Jung, J.-J., Lim, C., Kim, H. K., Lee, H., Han, W., & Moon, H. (2024) · Breast Cancer Research · doi:10.1186/s13058-024-01769-x · Cited by 6
Erben, P. B., Brunner, K., Hecht, M., Haderlein, M., Büttner-Herold, M. J., Agaimy, A., Fietkau, R., Hartmann, A., & Distel, L. V. (2015) · PubMed Central · Cited by 6
Direct to consumer genetic testing—law and policy concerns in Ireland
de Paor, A. (2017) · Irish Journal of Medical Science (1971 -) · doi:10.1007/s11845-017-1712-y · Cited by 6
Practical consensus recommendation on when to do BRCA testing
Parikh, P. M., Wadhwa, J., Minhas, S., Gupta, A., Mittal, S., Ranjan, S., Mehta, P., Singh, R. K., Kataria, S. P., Salim, S., et al. (2018) · South Asian Journal of Cancer · doi:10.4103/sajc.sajc_112_18 · Cited by 6
Screening Breast MRI Primer: Indications, Current Protocols, and Emerging Techniques
Samreen, N., Mercado, C. L., Heacock, L. C., Chacko, C., Partridge, S. C., & Chhor, C. M. (2021) · Journal of Breast Imaging · doi:10.1093/jbi/wbaa116 · Cited by 6
Zhou, Q., Katano, M., Zhang, J.-H., Liu, X., Wang, K., Iinuma, M., Kubo, K., & Azuma, K. (2021) · Brain Sciences · doi:10.3390/brainsci11040479 · Cited by 6
Sinha, S., Qin, Z., Tam, B., & Wang, S. M. (2022) · Briefings in Functional Genomics · doi:10.1093/bfgp/elac003 · Cited by 6
Influence of cellular models and individual factor in the biological response to chest CT scan exams
Devic, C., Bodgi, L., Sonzogni, L., Pilleul, F., Ribot, H., Charry, C. D., Moigne, F. L., Paul, D., Carbillet, F., Munier, M., et al. (2022) · European Radiology Experimental · doi:10.1186/s41747-022-00266-0 · Cited by 6
Balleine, R. L., Provan, P. J., Pupo, G. M., Pathmanathan, N., Cummings, M. C., Farshid, G., Salisbury, E., Bilous, A. M., Byth, K., & Mann, G. J. (2010) · Genes Chromosomes and Cancer · doi:10.1002/gcc.20816 · Cited by 6
BRCA1: A locus‐specific “liaison” in gene expression and genetic integrity
Aiyar, S. E., Sun, J., & Li, R. (2005) · Journal of Cellular Biochemistry · doi:10.1002/jcb.20386 · Cited by 6
Molecular Characterization of a Human BRCA2 Homolog in Leishmania donovani
Misra, S., Hall, M., & Chaudhuri, G. (2005) · Journal of Parasitology · doi:10.1645/ge-579r.1 · Cited by 6
DNA repair and replicative stress addiction in neuroblastoma
Durinck, K., & Irwin, M. S. (2024) · EJC Paediatric Oncology · doi:10.1016/j.ejcped.2024.100177 · Cited by 5
Liu, Q., Fan, Y., Huang, C., Wu, M., Jin, Y., Tao, L., Liu, Y., Song, J., Wang, S., Kong, W., et al. (2026) · ESMO Open · doi:10.1016/j.esmoop.2026.106060 · Cited by 5
Hietala, M., Henningson, M., Törngren, T., Olsson, H. L., & Jernström, H. (2010) · Molecular Genetics and Metabolism · doi:10.1016/j.ymgme.2010.09.006 · Cited by 5
Cancer diagnosis by biosensor-based devices: types and challenges
Manna, K., Mukherjee, N., Chatterjee, N., & Saha, K. D. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-823424-2.00017-x · Cited by 5
Universal genetic testing of patients with newly diagnosed breast cancer — ready for prime time?
Silva, D. L. D., James, P. A., Mann, G. B., & Lindeman, G. J. (2021) · The Medical Journal of Australia · doi:10.5694/mja2.51317 · Cited by 5
Li, Y., Zhang, S.-W., Xie, M., & Zhang, T. (2023) · Briefings in Bioinformatics · doi:10.1093/bib/bbad291 · Cited by 5
Cerne, J. Z., Zong, L., Jelı́nek, J., Hilsenbeck, S. G., Wang, T., Oesterreich, S., & McGuire, S. E. (2012) · Breast Cancer Research and Treatment · doi:10.1007/s10549-012-2117-2 · Cited by 5
Breast Cancer Detection Using Surface Plasmon Resonance-Based Biosensors
ABSTRACT, C.-W. L. A. C.-C. C. (2012) · CRC Press eBooks · doi:10.1201/b12737-17 · Cited by 5
Breast and ovarian cancer referrals to the ACT Genetic Service: are we meeting guidelines?
Aitken, L., Warwick, L., & Davis, A. J. (2016) · Internal Medicine Journal · doi:10.1111/imj.13357 · Cited by 5
(2011) · Elsevier eBooks · doi:10.1016/b978-0-323-06969-4.00029-5 · Cited by 5
Ductal Carcinoma In Situ (DCIS) Diagnosed by MRI-Guided Biopsy among BRCA1/BRCA2 Mutation Carriers
Faermann, R., Friedman, E., Kaidar‐Person, O., Weidenfeld, J., Brodsky, M., Shalmon, A., Neiman, O. H., Gotlieb, M., Yagil, Y., Samoocha, D., et al. (2022) · The Breast Journal · doi:10.1155/2022/4317693 · Cited by 5
Non-random genomic instability in cancer: A fact, not an illusion
Mai, S., & Imreh, S. (2006) · Seminars in Cancer Biology · doi:10.1016/j.semcancer.2006.11.002 · Cited by 5
Olsen, B. B., Niefind, K., & Issinger, O. (2006) · Springer eBooks · doi:10.1007/7050_002 · Cited by 5
Tracking profiles of genomic instability in spontaneous transformation and tumorigenesis
Lawrenson, L. (2010) · Human Biology · Cited by 5
Familial Pancreatic Cancer Research: Bridging Gaps in Basic Research and Clinical Application
Archasappawat, S., Al-Musawi, F., Liu, P., Lee, E., & Hwang, C. (2024) · Biomolecules · doi:10.3390/biom14111381 · Cited by 4
Gautam, N., Kaur, S., Kaur, K., & Kumar, N. (2019) · Meta Gene · doi:10.1016/j.mgene.2019.01.003 · Cited by 4
Diagnosis and treatment of patients with breast cancer and mutation in the BRCA1/2 genes
Kufel-Grabowska, J., & Wasąg, B. (2023) · Oncology in Clinical Practice · doi:10.5603/ocp.2023.0035 · Cited by 4
Screening in Women With BRCA Mutations Revisited
Greenwood, H. I., & Dodelzon, K. (2023) · Journal of Breast Imaging · doi:10.1093/jbi/wbad093 · Cited by 4
Liu, T., Liu, C., Wei, Y., Song, M., Zhang, Q., Song, Y., Chen, P., Liu, L., Wang, B., & Shi, H. (2024) · International Journal of Cancer · doi:10.1002/ijc.35043 · Cited by 4
$k$-Shape Clustering Enhances Group Lasso for Gene Selection and Sample Classification
Chen, S., Wang, P., & Lü, J. (2025) · IEEE Transactions on Computational Biology and Bioinformatics · doi:10.1109/tcbbio.2025.3551675 · Cited by 4
Discussion on the use of taxanes for treatment of breast cancers in BRCA1 mutations carriers
Elsakov, P., Foretová, L., Goetz, P., de Groot, J. W. B., van der Graaf, W. T. A., Guler, G., Huebner, K., Kingsbury, N., Hamann, U., Ho, J. W. C., et al. (2007) · Hereditary Cancer in Clinical Practice · doi:10.1186/1897-4287-5-3-119 · Cited by 3
What drives breast cancer heterogeneity: oncogenic events or cell of origin?
Ginestier, C., Charafe‐Jauffret, E., & Birnbaum, D. (2012) · The Journal of Pathology · doi:10.1002/path.4028 · Cited by 4
Gynaecological cancers in genetically susceptible women: new thoughts on tubal pathology
Khoo, U., Shen, D., Wong, R. W.-C., & Cheung, A. (2009) · Diagnostic histopathology · doi:10.1016/j.mpdhp.2009.09.001 · Cited by 4
Genetics of common complex diseases: a view from Iceland
Arnar, D. O., & Pálsson, R. (2017) · European Journal of Internal Medicine · doi:10.1016/j.ejim.2017.03.018 · Cited by 7
A narrative review of biomarkers in advanced triple negative breast cancer
Chehade, R., Awan, A. A., & Fernandes, R. (2021) · Precision Cancer Medicine · doi:10.21037/pcm-20-76 · Cited by 4
Epidemiology, Risk Factors, and Prevention
Bayraktar, S., & Arun, B. (2019) · Springer eBooks · doi:10.1007/978-3-030-04606-4_4 · Cited by 4
Breast Cancer Screening and Optimizing Recommendations
Lancaster, R. B., Gulla, S., Santos, J. D. L., & Umphrey, H. R. (2018) · Seminars in Roentgenology · doi:10.1053/j.ro.2018.08.002 · Cited by 4
MEDICAL AND GENETIC COUNSELING OF HEREDITARY BREAST AND OVARIAN CANCER
Laptiev, S. A., Korzhenevskaia, M. A., Соколенко, А. П., Iyevleva, A. G., & Имянитов, Е. Н. (2018) · The Scientific Notes of the Pavlov University · doi:10.24884/1607-4181-2018-25-2-7-18 · Cited by 4
DNA Repair Perspectives in Thyroid and Breast Cancer: The Role of DNA Repair Polymorphisms
Susana, N., Costa, B., Rueff, J., & Francisco, J. (2011) · InTech eBooks · doi:10.5772/22944 · Cited by 5
Effect of Excess Body Weight on the Genetic Susceptibility to Cancer
Burza, M. A., Spagnuolo, R., Montalcini, T., Doldo, P., Pujia, A., & Romeo, S. (2014) · Journal of Clinical Gastroenterology · doi:10.1097/mcg.0000000000000237 · Cited by 4
Frech, M. S., Jones, L. P., & Furth, P. A. (2005) · Breast Cancer Online · doi:10.1017/s1470903105003135 · Cited by 4
Earlier Age of Breast Cancer Onset in Israeli BRCA Carriers-Is it a Real Phenomenon?
Agranat, S., Baris, H. N., Kedar, I., Shochat, M., Rizel, S., Perry, S., Margel, D., Sulkes, A., & Yerushalmi, R. (2016) · The Breast Journal · doi:10.1111/tbj.12653 · Cited by 4
MOLECULAR-GENETIC «PORTRAIT» OF BREAST CANCER
Laptiev, S. A., Korzhenevskaia, M. A., & Imyanitov, E. N. (2017) · The Scientific Notes of the Pavlov University · doi:10.24884/1607-4181-2017-24-2-12-22 · Cited by 4
BRCA mutation in breast cancer patients: Prognostic impact and implications on clinical management
Loi, M., Desideri, I., Olmetto, E., Francolini, G., Greto, D., Bonomo, P., Simontacchi, G., Brina, L. D., Meattini, I., & Livi, L. (2018) · The Breast Journal · doi:10.1111/tbj.13100 · Cited by 4
Benson, K. F., & Horwitz, M. S. (2006) · Best Practice & Research Clinical Haematology · doi:10.1016/j.beha.2005.11.002 · Cited by 5
Effects of genetic testing on insurance : pedigree analysis and ascertainment adjustment
MacCalman, L. (2009) · Cited by 4
Hereditary Breast Cancer Syndromes: Molecular Pathogenesis and Diagnostics
Vos, S., van Diest, P. J., van der Wall, E., & van Diest, P. J. (2015) · Wiley eBooks · doi:10.1002/9780470015902.a0005375 · Cited by 4
Savignoni, A., Kirova, Y., Fourquet, A., & Sigal‐Zafrani, B. (2006) · American Journal of Immunology · doi:10.3844/ajisp.2006.61.63 · Cited by 4
Michel, A., Dorval, M., Chiquette, J., & Savard, J. (2024) · Hereditary Cancer in Clinical Practice · doi:10.1186/s13053-024-00285-5 · Cited by 3
“Depending on the study, the lifetime risk of developing breast cancer in BRCA1/2 mutation carriers ranges from 45 to 80% [8–11], which is much higher than in the general population (13”
BackgroundLi, P., Ye, J., Yang, Q., Wang, N., Li, C., Zou, X., Luo, H.-Y., Pan, Y., Jiang, L., Shen, B., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-62295-8 · Cited by 3
Genetic Basis of Familial Cancer Risk: A Narrative Review
Sabik, E. F. (2026) · DNA · doi:10.3390/dna6010005 · Cited by 3
Torres, S., Peleteiro, B., Magalhães, A., Garrido, L., Costa, S., & Fougo, J. L. (2023) · Journal of Cancer Research and Clinical Oncology · doi:10.1007/s00432-023-04663-9 · Cited by 4
Li, Y., Xu, G., Zhang, L., Zhao, K., Zhao, Y., & Han, D. (2025) · Frontiers in Oncology · doi:10.3389/fonc.2025.1602870 · Cited by 3
Epigenetic tumor suppression by BRCA1
Velkova, A., & Monteiro, Á. N. A. (2011) · Nature Medicine · doi:10.1038/nm.2493 · Cited by 3
Соколенко, А. П., Voskresenskiy, D. A., Iyevleva, A. G., Бит-Сава, Е. М., Gutkina, N. I., Anisimenko, M. S., Sherina, N., Mitiushkina, N. V., Ulibina, Y. M., Yatsuk, O. S., et al. (2009) · Hereditary Cancer in Clinical Practice · doi:10.1186/1897-4287-7-2 · Cited by 3
Eisenbraun, A. J., WENSTRUP, R. J., Hellerstedt, B. A., Patton, J., Reid, J., Sailer, L. M., Copeland, K., Brunger, J. W., Hamilton, S., FRYE, C. A., et al. (2010) · Community Oncology · doi:10.1016/s1548-5315(11)70558-7 · Cited by 3
MEME KANSERLİ HASTALARDA BRCA1 VE BRCA2 GEN MUTASYONLARININ DEĞERLENDİRİLMESİ
Karakuş, N., Kara, N., Yığıt, S., & Okan, İ. (2017) · Cumhuriyet Tıp Dergisi/Cumhuriyet Üniversitesi Tıp Fakültesi dergisi · doi:10.7197/cmj.v39i1.5000187135 · Cited by 3
Kotsopoulos, J., Kim, S. J., Armel, S. R., Bordeleau, L. J., Foulkes, W. D., McKinnon, W. C., Panchal, S., Cohen, S. A., Sun, S. B., Sun, P., et al. (2021) · Cancer · doi:10.1002/cncr.33654 · Cited by 3
Self-citationGliniewicz, K., Kluźniak, W., Wokołorczyk, D., Huzarski, T., Stempa, K., Rudnicka, H., Jakubowska, A., Szwiec, M., Jarkiewicz‐Tretyn, J., Naczk, M., et al. (2023) · Genes · doi:10.3390/genes14071329 · Cited by 3
Self-citationSellars, E., Savguira, M., Wu, J., Cancelliere, S., Jen, M., Krishnan, R., Hakem, A., Baršytė-Lovejoy, D., Hakem, R., Narod, S. A., et al. (2024) · iScience · doi:10.1016/j.isci.2024.110180 · Cited by 4
Self-citationFadebi, O. O., Miya, T. V., Khanyile, R., Dlamini, Z., & Marima, R. M. (2025) · Non-Coding RNA · doi:10.3390/ncrna11010009 · Cited by 4
Empowering protein single-molecule sequencing: nanopore technology toward sensing gene sequences
Gao, S., Huang, X., Zhang, X., Yuan, Z., Chen, H., Li, Z., El‐Mesery, H. S., Shi, J., & Zou, X. (2025) · Analytical Methods · doi:10.1039/d5ay00572h · Cited by 4
Amendola, L. C., & Vieira, R. J. D. S. (2005) · Cited by 3
Environmental impact on carcinogenesis under BRCA1 haploinsufficiency
Toyokuni, S., Kong, Y., Motooka, Y., & Akatsuka, S. (2023) · Genes and Environment · doi:10.1186/s41021-023-00258-5 · Cited by 3
Analysis and Classification of Breast Cancer Disease Via Different Datasets and Classifier Models
Barwal, R. K., Raheja, N., Mohan, B. R., Yamuna, U., Gadde, S. S., & Patil, M. (2023) · International Journal on Recent and Innovation Trends in Computing and Communication · doi:10.17762/ijritcc.v11i3s.6174 · Cited by 3
Erblicher Brust- und Eierstockkrebs
Gadzicki, D., Meindl, A., & Schlegelberger, B. (2007) · Medizinische Genetik · doi:10.1007/s11825-007-0019-1 · Cited by 3
DNA Repair and Cell Cycle Regulation After Ionizing Irradiation
Iliakis, G. E., Dahm‐Daphi, J., & Dikomey, E. (2009) · Medical radiology · doi:10.1007/978-3-540-74386-6_14 · Cited by 3
Sivarajasingham, N. S., Cawkwell, L., Baker, R. P., O’Kane, S. L., Smyth, E. F., Tilsed, J., Watson, M. B., Greenman, J., & Monson, J. R. T. (2006) · Annals of Surgical Oncology · doi:10.1245/aso.2006.05.021 · Cited by 3
Korean Hereditary Breast Cancer
Kim, S. (2009) · Journal of Korean Medical Association · doi:10.5124/jkma.2009.52.10.952 · Cited by 3
Interaction of p14ARF with Brca1 in cancer cell lines and primary breast cancer
He, L., Fan, C., Ning, X., Feng, X., Liu, Y., Chen, B., & Tang, D. (2008) · Cell Biology International · doi:10.1016/j.cellbi.2008.07.018 · Cited by 3
Lu, Y., Kang, T., & Hu, Y. (2010) · The Journal of Steroid Biochemistry and Molecular Biology · doi:10.1016/j.jsbmb.2010.11.006 · Cited by 3
Differences in Us Healthcare Coverage Policies in BRCA Testing and Potential Implications
Beattie, M. S., Wang, G., & Phillips, K. A. (2011) · Personalized Medicine · doi:10.2217/pme.11.85 · Cited by 3
Heranças familiares: entre os genes e os afetos
Valle, F. A. A. L., Trivellato, I. O., Shikasho, L., Filgueiras, M. S. T., da Silva, N. C., & de Almeida, T. R. (2012) · Saúde e Sociedade · doi:10.1590/s0104-12902012000200018 · Cited by 3
Metadata
- Authors
- Narod, S. A., & Foulkes, W. D.
- Affiliations
- Sunnybrook Health Science Centre (CA)
- McGill University (CA)
- Corresponding author
- Narod, Steven A.
- Venue
- Nature Reviews Cancer
- Published
- 2004-09
- Volume
- 4
- Issue
- 9
- Pages
- 665-676
- ISSN
- 1474-175X (ISSN-L)
- 1474-1768
- OpenAlex
- W2091961739
- Cited by
- 967
- References
- 187
- Citations by year
- 2026: 13 · 2025: 29 · 2024: 30 · 2023: 37 · 2022: 36 · 2021: 40 · 2020: 30 · 2019: 31 · 2018: 33 · 2017: 35 · 2016: 38 · 2015: 53 · 2014: 38 · 2013: 43 · 2012: 59
- FWCI
- 6.57
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature reviews. Cancer (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › BRCA gene mutations in cancer
- Health Sciences › Medicine › Pathology and Forensic Medicine › Genetic factors in colorectal cancer
- Health Sciences › Medicine › Oncology › PARP inhibition in cancer therapy
- Keywords
- BRCA1, BRCA2, hereditary breast cancer, genetic susceptibility, DNA repair, genetic epidemiology, breast cancer prevention, breast cancer treatment
- MeSH terms
- Breast Neoplasms, DNA Damage, DNA Repair, Female, Humans, Mutation, Molecular Epidemiology, Genes, BRCA1, Genetic Predisposition to Disease, Genes, BRCA2
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