Masayuki Sekine, Koji Nishino, Takayuki Enomoto. Cancers (Basel) 2021
Times Cited: 3
Times Cited: 3
Times Cited
Times Co-cited
Similarity
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Localization of a novel susceptibility gene for familial ovarian cancer to chromosome 3p22-p25.
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Association of type and location of BRCA1 and BRCA2 mutations with risk of breast and ovarian cancer.
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Association of gBRCA1/2 mutation locations with ovarian cancer risk in Japanese patients from the CHARLOTTE study.
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Mutational analysis of BRCA1 and BRCA2 and clinicopathologic analysis of ovarian cancer in 82 ovarian cancer families: two common founder mutations of BRCA1 in Japanese population.
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Phase II study of single-agent cabozantinib in patients with recurrent clear cell ovarian, primary peritoneal or fallopian tube cancer (NRG-GY001).
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Mutations in context: implications of BRCA testing in diverse populations.
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Variation in BRCA1 cancer risks by mutation position.
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Risk-reducing salpingo-oophorectomy for the prevention of BRCA1- and BRCA2-associated breast and gynecologic cancer: a multicenter, prospective study.
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Prevalence and clinical correlations of BRCA1/BRCA2 unclassified variant carriers among unselected primary ovarian cancer cases - preliminary report.
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Inherited Mutations in Women With Ovarian Carcinoma.
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The association of BRCA1 and BRCA2 mutations with prostate cancer risk, frequency, and mortality: A meta-analysis.
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Cancer risks for BRCA1 and BRCA2 mutation carriers: results from prospective analysis of EMBRACE.
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Ovarian cancer in BRCA1/2 mutation carriers: The impact of mutation position and family history on the cancer risk.
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Analysis of BRCA1 and BRCA2 genes in Spanish breast/ovarian cancer patients: a high proportion of mutations unique to Spain and evidence of founder effects.
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BRCA2 Polymorphic Stop Codon K3326X and the Risk of Breast, Prostate, and Ovarian Cancers.
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BRCA mutated pancreatic cancer: A change is coming.
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Frequency of mutations in individuals with breast cancer referred for BRCA1 and BRCA2 testing using next-generation sequencing with a 25-gene panel.
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Is uterine papillary serous adenocarcinoma a manifestation of the hereditary breast-ovarian cancer syndrome?
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The first Japanese nationwide multicenter study of BRCA mutation testing in ovarian cancer: CHARacterizing the cross-sectionaL approach to Ovarian cancer geneTic TEsting of BRCA (CHARLOTTE).
Takayuki Enomoto, Daisuke Aoki, Kana Hattori, Masahisa Jinushi, Junzo Kigawa, Nobuhiro Takeshima, Hitoshi Tsuda, Yoh Watanabe, Kosuke Yoshihara, Toru Sugiyama. Int J Gynecol Cancer 2019
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BRCA1 and BRCA2 mutation prevalence and clinical characteristics of a population-based series of ovarian cancer cases from Denmark.
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Risks of Breast, Ovarian, and Contralateral Breast Cancer for BRCA1 and BRCA2 Mutation Carriers.
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BRCA1 genomic deletions are major founder mutations in Dutch breast cancer patients.
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Population BRCA1 and BRCA2 mutation frequencies and cancer penetrances: a kin-cohort study in Ontario, Canada.
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The risk of endometrial cancer in women with BRCA1 and BRCA2 mutations. A prospective study.
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A study of over 35,000 women with breast cancer tested with a 25-gene panel of hereditary cancer genes.
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Predictors of contralateral breast cancer in BRCA1 and BRCA2 mutation carriers.
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BRCA1 and BRCA2 mutations and clinical interpretation in 398 ovarian cancer patients: comparison with breast cancer variants in a similar population.
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Cancer Incidence in BRCA1 mutation carriers.
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Prevalence of deleterious germline variants in risk genes including BRCA1/2 in consecutive ovarian cancer patients (AGO-TR-1).
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Reclassification of BRCA1 and BRCA2 variants found in ovarian epithelial, fallopian tube, and primary peritoneal cancers.
Hyeong In Ha, Jin Sun Ryu, Hyoeun Shim, Sun Young Kong, Myong Cheol Lim. J Gynecol Oncol 2020
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The Icelandic founder mutation BRCA2 999del5: analysis of expression.
Evgenia K Mikaelsdottir, Sigridur Valgeirsdottir, Jorunn E Eyfjord, Thorunn Rafnar. Breast Cancer Res 2004
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One in 10 ovarian cancer patients carry germ line BRCA1 or BRCA2 mutations: results of a prospective study in Southern Sweden.
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Decreased prostate cancer-specific survival of men with BRCA2 mutations from multiple breast cancer families.
Heather Thorne, Amber J Willems, Eveline Niedermayr, Ivan M Y Hoh, Jason Li, David Clouston, Gillian Mitchell, Stephen Fox, John L Hopper, Damien Bolton. Cancer Prev Res (Phila) 2011
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Treatment of endometriosis in different ethnic populations: a meta-analysis of two clinical trials.
Christoph Gerlinger, Thomas Faustmann, Jeffrey J Hassall, Christian Seitz. BMC Womens Health 2012
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Multigene Panels to Evaluate Hereditary Cancer Risk: Reckless or Relevant?
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Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.