全部文献期刊学位论文会议报纸专利标准年鉴图书|学者科研项目
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作者:Wendy R. Uhlmann , Katie Schwalm , Victoria M. Raymond
来源:[J].Journal of Genetic Counseling(IF 1.454), 2017, Vol.26 (4), pp.657-668Springer
摘要:Obtaining genetic testing insurance authorizations for patients is a complex, time-involved process often requiring genetic counselor (GC) and physician involvement. In an effort to mitigate this complexity and meet the increasing number of genetic testing insurance authoriz...
作者:... Nancie Petrucelli , Victoria M. Raymond , on behalf of the BRCA Clinical Network Partners
来源:[J].Journal of Genetic Counseling(IF 1.454), 2017, Vol.26 (4), pp.859-865Springer
摘要:Genetic counseling (GC) and genetic testing (GT) identifies high-risk individuals who benefit from enhanced medical management. Not all individuals undergo GT following GC and understanding the reasons why can impact clinical efficiency, reduce GT costs through appropriate identi...
作者:Victoria M. Raymond , Yukimasa Shiotsu ...
来源:[J].Clinical Lung Cancer(IF 2.038), 2018Elsevier
摘要:Abstract(#br)Background(#br)Genomic profiling of cell-free circulating tumor DNA (ctDNA) is a potential alternative to repeat invasive biopsy in patients with advanced cancer. We report the first real-world cohort of comprehensive genomic assessments of patients with non–sma...
作者:Victoria M. Raymond , Richard B. Lanman ...
来源:[J].Annals of Surgical Oncology(IF 4.12), 2018, Vol.25 (8), pp.2400-2408Springer
摘要:Abstract(#br) Background(#br)Next-generation sequencing (NGS) is a useful tool for detecting genomic alterations in circulating tumor DNA (ctDNA). To date, most ctDNA tests have been performed on patients with widely metastatic disease. Patients with peritoneal carcinomatosi...
作者:Victoria M. Raymond , Jordan Garst ...
来源:[J].Lung Cancer(IF 3.392), 2017, Vol.108, pp.22-28Elsevier
摘要:Abstract(#br)Targetable, somatic EGFR mutations are highly prevalent in patients with non-small cell lung cancer (NSCLC), making them eligible for tyrosine kinase inhibitor (TKI) therapy. Circulating tumor DNA (ctDNA), isolated from blood or urine, has been demonstrated to reliab...
作者:Victoria M. Raymond , Arden M. Morris ...
来源:[J].Familial Cancer(IF 1.935), 2015, Vol.14 (1), pp.77-80Springer
摘要:Abstract(#br)There are approximately 136,830 new colorectal cancer (CRC) cases diagnosed annually in the United States. In an effort to identify those at highest risk for Lynch Syndrome, an inherited CRC predisposition syndrome, several professional guidelines advocate for r...
作者:Victoria M. Raymond , Monica L. Marvin ...
来源:[J].Familial Cancer(IF 1.935), 2015, Vol.14 (1), pp.167-174Springer
摘要:Abstract(#br)Genetic testing (GT) for inherited cancer predisposition is most informative when initiated in individuals with cancer, thus standard practice recommends GT start in an affected individual. This strategy can be frustrating for unaffected consultands and providers. Re...

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