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Public Health Genomics and Precision Health Knowledge Base (v9.0)
PHGKB
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Public Health Genomics Branch
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Precision Health Database|Search|Public Health Genomics and Precision Health Knowledge Base (PHGKB)
Last data update: May 08, 2024
. (Total: 63790 Documents since 2012)
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Addressing Barriers and Facilitators to African Americans' and Hispanics' Participation in Clinical and Genomic Research Through a Bioethical Sensitive Video.
Victoria Churchill et al. J Cancer Educ 2024
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On the Hunt for the Missed Genetic Causes of Multiple Primary Tumors.
Fiona Chan-Pak-Choon et al. Cancer Prev Res (Phila) 2024 17(5) 193-195
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CDH1 Genotype Exploration in Women With Hereditary Lobular Breast Cancer Phenotype.
Giovanni Corso et al. JAMA Netw Open 2024 7(4) e247862
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Eating Behaviors and Physical Activity versus the Big Five Personality Traits in Women with a Hereditary Predisposition to Breast or Ovarian Cancer.
Beata Pieta et al. Nutrients 2024 16(8)
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ChatGPT accurately performs genetic counseling for gynecologic cancers.
Jharna M Patel et al. Gynecol Oncol 2024 183115-119
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Enhancing clinical decision support with genomic tools in breast cancer: A Scottish perspective.
A L Peters et al. Breast 2024 75103728
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Women's Knowledge of Genomic Testing and Precision Medicine in Breast Cancer Treatment Decision-Making.
Evelyn Robles-Rodriguez et al. Oncol Nurs Forum 2024 51(3) 199-208
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Endometrioid Endometrial RNA Index Predicts Recurrence in Stage I Patients.
Corrine A Nief et al. Clin Cancer Res 2024
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Psychosocial barriers and facilitators for cascade genetic testing in hereditary breast and ovarian cancer: a scoping review.
Agani Afaya et al. Fam Cancer 2024
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Profiling the molecular and clinical landscape of glioblastoma utilizing the Oncology Research Information Exchange Network brain cancer database.
Alexandra N Demetriou et al. Neurooncol Adv 2024 6(1) vdae046
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Real-world utilization, patient characteristics, and treatment patterns among men with localized prostate cancer tested with the 17-gene genomic prostate score® (GPS) assay.
Amy M Nguyen et al. Prostate 2024
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Role of Breast Cancer Risk Estimation Models to Identify Women Eligible for Genetic Testing and Risk-Reducing Surgery.
Azzurra Irelli et al. Biomedicines 2024 12(4)
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National Experiences from 30 Years of Provider-Mediated Cascade Testing in Lynch Syndrome Families-The Danish Model.
Lars Joachim Lindberg et al. Cancers (Basel) 2024 16(8)
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No Racial Disparities Observed Using Point-of-Care Genetic Counseling and Testing for Endometrial and Ovarian Cancer in a Diverse Patient Population: A Retrospective Cohort Study.
Michael Kim et al. Cancers (Basel) 2024 16(8)
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TTSBBC: triplex target site biomarkers and barcodes in cancer.
Maya Ylagan et al. Nucleic Acids Res 2024
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Correlation between NGS panel-based mutation results and clinical information in colorectal cancer patients.
Bo Cheng et al. Heliyon 2024 10(7) e29299
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A Study on the Retrospective Reinterpretation of BRCA1 and BRCA2 Variants.
Jin Ju Kim et al. Clin Lab 2024 70(4)
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Cost-effectiveness of BRCA1 testing at time of obstetrical prenatal carrier screening for cancer prevention.
Shayan M Dioun et al. Am J Obstet Gynecol 2024
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Assessing the value of incorporating a polygenic risk score with non-genetic factors for predicting breast cancer diagnosis in the UK Biobank.
Jennifer A Collister et al. Cancer Epidemiol Biomarkers Prev 2024
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Uptake of Risk-Reducing Measures, Cascade Testing, and Related Challenges Among Carriers of Breast Cancer-Associated Germline Pathogenic Variants in Mexico.
Fernanda Mesa-Chavez et al. JCO Glob Oncol 2024 10e2300417
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Germline Testing in Patients With Breast Cancer: ASCO-Society of Surgical Oncology Guideline.
Isabelle Bedrosian et al. J Clin Oncol 2024 42(5) 584-604
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Postpartum Breast Cancer and Survival in Women With Germline BRCA Pathogenic Variants.
Zhenzhen Zhang et al. JAMA Netw Open 2024 7(4) e247421
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Medicolegal and insurance issues regarding BRCA1 and BRCA2 gene tests in high income countries.
Riccardo Oliva et al. Int J Gynecol Cancer 2024
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Prevalence of Homologous Recombination Deficiency Among Patients With Germline RAD51C/D Breast or Ovarian Cancer.
Sara Torres-Esquius et al. JAMA Netw Open 2024 7(4) e247811
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Evolving assessment pathways for precision oncology medicines to improve patient access: a tumor-agnostic lens.
Priscila Radu et al. Oncologist 2024
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Development and Validation of an 18-Gene Urine Test for High-Grade Prostate Cancer
Postpartum Breast Cancer and Survival in Women With Germline BRCA Pathogenic Variants
Somatic Tumor Testing in Prostate Cancer: Experience of a Tertiary-Care Center Including Pathologist-Driven Reflex Testing of Localized Tumors at Diagnosis.
Susan Prendeville et al. Mod Pathol 2024 100489
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Impact of Family History and Germline Genetic Risk Single Nucleotide Polymorphisms on Long-Term Outcomes of Favorable-Risk Prostate Cancer.
Florian Rumpf et al. J Urol 2024 101097JU0000000000003927
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Uptake of screening and risk-reducing recommendations among women with hereditary breast and ovarian cancer syndrome due to pathogenic BRCA1/2 variants evaluated at a large urban comprehensive cancer center.
Hadeel Assad et al. Breast Cancer Res Treat 2024
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Page last reviewed:
Feb 1, 2024
Page last updated:
May 08, 2024
Content source:
Public Health Genomics Branch in the Division of Blood Disorders and Public Health Genomics
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National Center on Birth Defects and Developmental Disabilities
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