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Cancer

Last data update: Oct 02, 2022. (Total: 49793 Documents since 2012)
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Query Trace: all[original query]>>Original Studies[Product Type]
Characterization of lung cancers in patients with BRCA germline variants: A multicenter series.
Sanchis-Borja Mateo et al. Lung cancer (Amsterdam, Netherlands) 2022 17367-70
Prevalence and breakdown of non-small cell lung cancer BRAF driver mutations in a large UK cohort.
Lim Guan Hui Tricia et al. Lung cancer (Amsterdam, Netherlands) 2022 17371-74
A comprehensive genomic and transcriptomic dataset of triple-negative breast cancers.
Chen Qingwang et al. Scientific data 2022 9(1) 587
Comparison of psychological distress for breast, ovarian and colorectal cancer predisposition in a Spanish sample at high risk of hereditary cancer.
Costa-Requena Gema et al. European journal of cancer prevention : the official journal of the European Cancer Prevention Organisation (ECP) 2022 31(5) 482-486
Targeted molecular profiling of epithelial ovarian cancer from Italian BRCA wild-type patients with a BRCA and PARP pathways gene panel.
Salvati Annamaria et al. Experimental and molecular pathology 2022 128104833
Multiple primary cancers in men with sporadic or familial prostate cancer: Its clinical implications.
Kim Myong et al. Urologic oncology 2022
Landscape of EGFR mutations in lung adenocarcinoma: a single institute experience with comparison of PANAMutyper testing and targeted next-generation sequencing.
Lee Jeonghyo et al. Journal of pathology and translational medicine 2022 56(5) 249-259
Somatic tumor mutations in moderate risk cancer genes: Targets for germline confirmatory testing.
Llorin Hannah et al. Cancer genetics 2022 268-26922-27
Clinical Utility of Universal Germline Genetic Testing for Patients With Breast Cancer.
Whitworth Pat W et al. JAMA network open 2022 5(9) e2232787
Does the 21-gene recurrence score have clinical utility in HR+/HER2+ breast cancer?
Bilani Nadeem et al. Breast (Edinburgh, Scotland) 2022 6649-53
Clinical applicability of the Polygenic Risk Score for breast cancer risk prediction in familial cases.
Lakeman Inge M M et al. Journal of medical genetics 2022
Breast cancer polygenic risk scores are associated with short-term risk of poor prognosis breast cancer.
McCarthy Anne Marie et al. Breast cancer research and treatment 2022
Combined Focused Next-Generation Sequencing Assays to Guide Precision Oncology in Solid Tumors: A Retrospective Analysis from an Institutional Molecular Tumor Board.
Tarawneh Thomas S et al. Cancers 2022 14(18)
Circulating Methylated SEPT9 DNA Analyses to Predict Recurrence Risk and Adjuvant Chemotherapy Benefit in Stage II to III Colorectal Cancer.
Yuan Zhen et al. Medical science monitor : international medical journal of experimental and clinical research 2022 28e937757
Implementation and outcome evaluations of a multi-site improvement program in cancer genetics.
Bednar Erica M et al. Journal of genetic counseling 2022
Analysis of rare disruptive germline mutations in 2,135 enriched BRCA-negative breast cancers excludes additional high-impact susceptibility genes.
Loveday C et al. Annals of oncology : official journal of the European Society for Medical Oncology 2022
Effect of comprehensive cancer genomic profiling on therapeutic strategies and clinical outcomes in patients with advanced biliary tract cancer: A prospective multicenter study.
Takada Kohichi et al. Frontiers in oncology 2022 12988527
Ultrasonography screening in children and adolescents who have one parent with familial non-medullary thyroid carcinoma.
Rosario Pedro W et al. Journal of paediatrics and child health 2022
Usefulness of Genetic Aberration and Shorter Telomere Length in Myelodysplastic Syndrome: A Pilot Study.
Park Hee Sue et al. Laboratory medicine 2022
Differences in Prostate Cancer Transcriptomes by Age at Diagnosis: Are Primary Tumors from Older Men Inherently Different?
Zhou Charlie D et al. Cancer prevention research (Philadelphia, Pa.) 2022 OF1-OF11
Ten-year follow-up of the observational RASTER study, prospective evaluation of the 70-gene signature in ER-positive, HER2-negative, node-negative, early breast cancer.
Vliek Sonja B et al. European journal of cancer (Oxford, England : 1990) 2022 175169-179
Assessing Oncologists' Adoption of Biomarker Testing in Metastatic Colorectal Cancer Using Real World Data.
Iyer Pritish et al. JNCI cancer spectrum 2022
Patient Understanding of Tumor Genomic Testing: A Quality Improvement Effort.
Senter Leigha et al. JCO oncology practice 2022 OP2200316
What can we learn from more than 1,000 Brazilian patients at risk of hereditary cancer?
Leite Ana Carolina Rathsam et al. Frontiers in oncology 2022 12963910
Breast Cancer Risk and Screening Mammography Frequency Among Multiethnic Women.
Zhang Jingwen et al. American journal of preventive medicine 2022
Clinical Significance of Germline Pathogenic Variants among 51 Cancer Predisposition Genes in an Unselected Cohort of Italian Pancreatic Cancer Patients.
Puccini Alberto et al. Cancers 2022 14(18)
Circulating EGFR Mutations in Patients with Lung Adenocarcinoma by Circulating Tumor Cell Isolation Systems: A Concordance Study.
Li Shih-Hong et al. International journal of molecular sciences 2022 23(18)
Mutation of breast cancer susceptibility genes increases cerebral microbleeds: A pilot study.
Pope Brandon et al. Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association 2022 31(11) 106729
Susceptibility Loci in SLC15A1, UGT1A3, and CWC27 Genes Associated with Bladder Cancer in the Northeast Chinese Population.
Wu Peihong et al. BioMed research international 2022 20222988159
Clinical implementation of genetic testing in adults for hereditary hematologic malignancy syndromes.
Ansar Safa et al. Genetics in medicine : official journal of the American College of Medical Genetics 2022
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