Ovarian Cancer
What's New
Last Posted: Oct 04, 2024
- Screening Familial Risk for Hereditary Breast and Ovarian Cancer
- BRCA1 and friends 30 years on
- Healthcare Professionals' Learning Needs and Perspectives on Essential Information in Genetic Cancer Care: A Systematic Review.
Sun-Young Park et al. Cancers (Basel) 2024 16(11) - Cost-Effectiveness of Unselected Multigene Germline and Somatic Genetic Testing for Epithelial Ovarian Cancer.
Ranjit Manchanda et al. J Natl Compr Canc Netw 2024 22(2D) - Decision aids for female BRCA mutation carriers: a scoping review.
Sarah A McGarrigle et al. BMJ Open 2024 14(6) e076876 - Recommendations of Health Care Professionals on the Issue of Breastfeeding in BRCA Carriers.
Moran Echar et al. Breastfeed Med 2024 - Genetic Testing Utilization: Discrepancies Between Somatic and Germline Results in Patients With Cancer Reviewed at the UW Health Precision Medicine Molecular Tumor Board.
Isaac P Horn et al. JCO Precis Oncol 2024 8e2300466 - Results from the Delivery of a Community Health Worker Training to Advance Competencies in Cancer Genomics.
Caitlin G Allen et al. Public Health Genomics 2024 - Current practices and challenges in genetic testing and counseling for women with breast and ovarian cancer in Asia.
Ava Kwong et al. Asia Pac J Clin Oncol 2024 - Clients' experiences of empathy in genetic counseling for hereditary breast and ovarian cancer: A qualitative study in Japan.
Chikako Tomozawa et al. J Genet Couns 2024
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About Rare Diseases PHGKB
Rare Disease PHGKB is an online, continuously updated, searchable database of published scientific literature, CDC and NIH resources, and other information that address the public health impact and translation of genomic and other precision health discoveries into improved health outcomes related to rare diseases...more
Content Summary
Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Eclampsia
- Erythema Multiforme
- Familial Mediterranean Fever
- Fragile X Syndrome
- Gaucher Disease
- Glomerulonephritis
- Graves Disease
- Hemophilia
- Huntington Disease
- Microcephaly
- Myasthenia Gravis
- Phenylketonuria
- Retinitis Pigmentosa
- Severe Combined Immunodeficiency
Disclaimer: Articles listed in the Public Health Knowledge Base are selected by Public Health Genomics Branch to provide current awareness of the literature and news. Inclusion in the update does not necessarily represent the views of the Centers for Disease Control and Prevention nor does it imply endorsement of the article's methods or findings. CDC and DHHS assume no responsibility for the factual accuracy of the items presented. The selection, omission, or content of items does not imply any endorsement or other position taken by CDC or DHHS. Opinion, findings and conclusions expressed by the original authors of items included in the update, or persons quoted therein, are strictly their own and are in no way meant to represent the opinion or views of CDC or DHHS. References to publications, news sources, and non-CDC Websites are provided solely for informational purposes and do not imply endorsement by CDC or DHHS.
- Page last reviewed:Feb 1, 2024
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