Aligning policy to promote cascade genetic screening for prevention and early diagnosis of heritable diseases (Q86507056)

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27 February 2020

title

Aligning policy to promote cascade genetic screening for prevention and early diagnosis of heritable diseases (English)

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1

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author name string

Karen Kovak

series ordinal

2

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Summer L Cox

series ordinal

3

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27 February 2020

publication date

11 January 2015

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Journal of Genetic Counseling

27 February 2020

published in

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volume

24

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issue

3

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page(s)

388-399

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Estimating the efficacy and efficiency of cascade genetic screening

27 February 2020

cites work

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12 December 2020

Duty to warn at‐risk relatives for genetic disease: Genetic counselors' clinical experience

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12 December 2020

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12 December 2020

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What facilitates or impedes family communication following genetic testing for cancer risk? A systematic review and meta-synthesis of primary qualitative research

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A whisper-game perspective on the family communication of DNA-test results: a retrospective study on the communication process of BRCA1/2-test results between proband and relatives

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Learning about a twist in the road: perspectives of at-risk relatives learning of potential for cancer

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The search for unaffected individuals with Lynch syndrome: do the ends justify the means?

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A large health system's approach to utilization of the genetic counselor CPT® 96040 code

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A Pilot study of the Sharing Risk Information Tool (ShaRIT) for Families with Hereditary Breast and Ovarian Cancer Syndrome

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A multidisciplinary clinic for individualizing management of patients at increased risk for breast and gynecologic cancer.

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Adverse events in cancer genetic testing: medical, ethical, legal, and financial implications

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Life events may contribute to family communication about cancer risk following BRCA1/2 testing

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Public health action in genomics is now needed beyond newborn screening

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Patterns of cancer genetic testing: a randomized survey of Oregon clinicians.

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Duty to warn at-risk family members of genetic disease

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Informing family members of individuals with Lynch syndrome: a guideline for clinical geneticists

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Identification of genetic counseling service delivery models in practice: a report from the NSGC Service Delivery Model Task Force

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Family communication of BRCA1/2 results and family uptake of BRCA1/2 testing in a diverse population of BRCA1/2 carriers.

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What's the harm? Genetic counselor perceptions of adverse effects of genetics service provision by non-genetics professionals

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Colorectal cancer: Cascade genetic testing in Lynch syndrome: room for improvement

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Familial hypercholesterolaemia is underdiagnosed and undertreated in the general population: guidance for clinicians to prevent coronary heart disease: consensus statement of the European Atherosclerosis Society

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A time study of cancer genetic counselors using a genetic counselor-only patient care model versus a traditional combined genetic counselor plus medical geneticist care model

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Factors which impact the delivery of genetic risk assessment services focused on inherited cancer genomics: expanding the role and reach of certified genetics professionals.

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12 December 2020

A genetic counseling intervention to facilitate family communication about inherited conditions

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12 December 2020

Patients' perceptions and experiences of familial hypercholesterolemia, cascade genetic screening and treatment

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12 December 2020

Improving family communication after a new genetic diagnosis: a randomised controlled trial of a genetic counselling intervention.

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12 December 2020

Evaluating the utilization of educational materials in communicating about Lynch syndrome to at-risk relatives.

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12 December 2020

ASHG statement. Professional disclosure of familial genetic information. The American Society of Human Genetics Social Issues Subcommittee on Familial Disclosure

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12 December 2020

10.1007/S10897-014-9805-5

Identifiers

DOI

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27 February 2020

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