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Times Cited: 52
Times Cited
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Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing.
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Analysis of protein-coding genetic variation in 60,706 humans.
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Inherited Mutations in Women With Ovarian Carcinoma.
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ColoSeq provides comprehensive lynch and polyposis syndrome mutational analysis using massively parallel sequencing.
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Clinical evaluation of a multiple-gene sequencing panel for hereditary cancer risk assessment.
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Hereditary predisposition to ovarian cancer, looking beyond BRCA1/BRCA2.
Lindsey E Minion, Jill S Dolinsky, Dana M Chase, Charles L Dunlop, Elizabeth C Chao, Bradley J Monk. Gynecol Oncol 2015
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PD-1 Blockade in Tumors with Mismatch-Repair Deficiency.
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NCCN Guidelines Insights: Genetic/Familial High-Risk Assessment: Breast and Ovarian, Version 2.2017.
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Screening for the Lynch syndrome (hereditary nonpolyposis colorectal cancer).
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Targeted massively parallel sequencing of a panel of putative breast cancer susceptibility genes in a large cohort of multiple-case breast and ovarian cancer families.
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Germline mutations in breast and ovarian cancer pedigrees establish RAD51C as a human cancer susceptibility gene.
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Mutations in BRIP1 confer high risk of ovarian cancer.
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Germline Mutations in the BRIP1, BARD1, PALB2, and NBN Genes in Women With Ovarian Cancer.
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Multi-gene panel testing for hereditary cancer predisposition in unsolved high-risk breast and ovarian cancer patients.
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Prevalence and Spectrum of Germline Cancer Susceptibility Gene Mutations Among Patients With Early-Onset Colorectal Cancer.
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Integrative clinical genomics of advanced prostate cancer.
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7
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.