Factors associated with preimplantation genetic diagnosis acceptance among women concerned about hereditary breast and ovarian cancer
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Summary
It is important to understand existing levels of awareness and attitudes toward preimplantation genetic diagnosis to provide optimal counseling and support among women concerned about hereditary breast and ovarian cancer.
- Type
- article
- Published
- 2009-10-01
- Cited by
- 39
- References
- 32
- Access
- Open access
- OpenAlex
- https://openalex.org/W2021595331
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:9501801
Keywords
Preimplantation genetic diagnosis, Genetic counseling, Genetic testing, Breast cancer, Medicine
References
- Prenatal diagnosis of Down syndrome: Ten year experience in the Israeli population
- Decisions About Testing and Termination of Pregnancy for Different Fetal Conditions: A Qualitative Study of European White and Pakistani Mothers of Affected Children
- Decisions regarding pregnancy termination among Bedouin couples referred to third level ultrasound clinic.
- Identification of the breast cancer susceptibility gene BRCA2
- Attitudes of high-risk women toward preimplantation genetic diagnosis.
- Evaluating Online Direct-to-Consumer Marketing of Genetic Tests: Informed Choices or Buyers Beware?
- Characteristics of women who refuse an offer of prenatal diagnosis: data from the California maternal serum alpha fetoprotein blood test experience.
- Genetic testing of embryos: practices and perspectives of US in vitro fertilization clinics.
- Cancer risk reduction and reproductive concerns in female BRCA1/2 mutation carriers
- Breast and Ovarian Cancer Risks Due to Inherited Mutations in BRCA1 and BRCA2
- Cancer genetic testing and assisted reproduction.
- Cancer risk estimates for BRCA1 mutation carriers identified in a risk evaluation program.
- Fertility intentions following testing for a BRCA1 gene mutation.
- A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1.
- Views of BRCA gene mutation carriers on preimplantation genetic diagnosis as a reproductive option for hereditary breast and ovarian cancer.
- Prenatal diagnosis and genetic screening--integration into prenatal care.
- A Mechanism for Cox-2 Inhibitor Anti-Inflammatory Activity in Chemoprevention of Epithelial Cancers
- Opinion about reproductive decision making among individuals undergoing BRCA1/2 genetic testing in a multicentre Spanish cohort.
- Preimplantation genetic diagnosis for BRCA1/2—a novel clinical experience
- Preimplantation Genetic Diagnosis—An Overview
Cited by
- BRCA carriers' thoughts on risk management in relation to preimplantation genetic diagnosis and childbearing: when too many choices are just as difficult as none.
- Knowledge, attitudes, and clinical experience of physicians regarding preimplantation genetic diagnosis for hereditary cancer predisposition syndromes
- Hereditary breast cancer and genetic counseling in young women
- 100 years lynch syndrome: what have we learned about psychosocial issues?
- Comparison of Attitudes Regarding Preimplantation Genetic Diagnosis Among Patients with Hereditary Cancer Syndromes
- High-risk consumers’ perceptions of preimplantation genetic diagnosis for hereditary cancers: a systematic review and meta-analysis
- ‘My funky genetics’: BRCA1/2 mutation carriers’ understanding of genetic inheritance and reproductive merger in the context of new repro-genetic technologies
- BRCA1/2 carriers: their childbearing plans and theoretical intentions about having preimplantation genetic diagnosis and prenatal diagnosis
- Genetic/familial high-risk assessment: breast and ovarian.
- Expanding indications for preimplantation genetic diagnosis
- High risk men's perceptions of pre-implantation genetic diagnosis for hereditary breast and ovarian cancer.
- Essential Genetic and Genomic Nursing Competencies for the Oncology Nurse
- Reproductive Endocrinologists’ Utilization of Genetic Counselors for Oncofertility and Preimplantation Genetic Diagnosis (PGD) Treatment of BRCA1/2 Mutation Carriers
- “I Do Not Want My Baby to Suffer as I Did”; Prenatal and Preimplantation Genetic Diagnosis for BRCA1/2 Mutations: A Case Report and Genetic Counseling Considerations
- Waiting for Cancer to Come: Women’s Experiences with Genetic Testing and Medical Decision Making for Breast and Ovarian Cancer
- REPRODUCTIVE DECISION-MAKING IN WOMEN WITH BRCA1/2 MUTATIONS
- Awareness and attitude regarding reproductive options of persons carrying a BRCA mutation and their partners
- “It was an Emotional Baby”: Previvors’ Family Planning Decision-Making Styles about Hereditary Breast and Ovarian Cancer Risk
- Performing and Declining PGD: Accounts of Jewish Israeli Women Who Carry a BRCA1/2 Mutation or Partners of Male Mutation Carriers
- How Can Contingent Valuation Inform the Bioethics Debate? Evidence from a Survey on Hereditary Cancers in France
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