(Q86507056)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25577298%20AND%20SRC:MED&resulttype=core&format=json

27 February 2020

title

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

1 reference

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27 February 2020

1

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27 February 2020

author name string

Karen Kovak

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25577298%20AND%20SRC:MED&resulttype=core&format=json

27 February 2020

Summer L Cox

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25577298%20AND%20SRC:MED&resulttype=core&format=json

27 February 2020

publication date

11 January 2015

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25577298%20AND%20SRC:MED&resulttype=core&format=json

Journal of Genetic Counseling

27 February 2020

published in

1 reference

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27 February 2020

volume

24

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25577298%20AND%20SRC:MED&resulttype=core&format=json

27 February 2020

issue

3

1 reference

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27 February 2020

page(s)

388-399

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25577298%20AND%20SRC:MED&resulttype=core&format=json

Estimating the efficacy and efficiency of cascade genetic screening

27 February 2020

cites work

1 reference

12 December 2020

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

1 reference

12 December 2020

Review article: targeted screening for hereditary haemochromatosis in high-risk groups

1 reference

12 December 2020

The "duty to warn" a patient's family members about hereditary disease risks

1 reference

12 December 2020

Genetic risk assessment and BRCA mutation testing for breast and ovarian cancer susceptibility: recommendation statement

1 reference

12 December 2020

Return on investment in disease management: a review

1 reference

12 December 2020

Interviews with primary care physicians regarding taking and interpreting the cancer family history

1 reference

12 December 2020

Clinical genetics provider real-time workflow study

1 reference

12 December 2020

Billing for medical genetics and genetic counseling services: a national survey

1 reference

12 December 2020

Assessment of clinical practices among cancer genetic counselors

1 reference

12 December 2020

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

1 reference

12 December 2020

Genetic health professionals and the communication of genetic information in families: Practice during and after a genetic consultation

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Awareness and utilization of BRCA1/2 testing among U.S. primary care physicians

1 reference

12 December 2020

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

1 reference

12 December 2020

Reported referral for genetic counseling or BRCA 1/2 testing among United States physicians: a vignette-based study

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Public health action in genomics is now needed beyond newborn screening

1 reference

12 December 2020

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

1 reference

12 December 2020

Duty to warn at-risk family members of genetic disease

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Uptake of genetic testing by relatives of lynch syndrome probands: a systematic review.

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

A genetic counseling intervention to facilitate family communication about inherited conditions

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

10.1007/S10897-014-9805-5

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25577298%20AND%20SRC:MED&resulttype=core&format=json

27 February 2020

1 reference