(Q35194662)

7 August 2017

title

Why is genetic screening for autosomal dominant disorders underused in families? The case of hereditary hemorrhagic telangiectasia (English)

1 reference

hereditary hemorrhagic telangiectasia

7 August 2017

main subject

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1

Barbara A Bernhardt

1 reference

7 August 2017

Cara Zayac

2

1 reference

7 August 2017

Reed E Pyeritz

series ordinal

3

1 reference

7 August 2017

language of work or name

English

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publication date

1 September 2011

1 reference

7 August 2017

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7 August 2017

volume

13

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7 August 2017

issue

9

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7 August 2017

page(s)

812-820

1 reference

Hereditary hemorrhagic telangiectasia: an overview of diagnosis, management, and pathogenesis

7 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166421

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

13 July 2018

1 reference

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Evaluation of the Validity and Utility of Genetic Testing for Rare Diseases

13 July 2018

1 reference

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Impediments to DNA Testing and Cascade Screening for Hypertrophic Cardiomyopathy and Long QT syndrome: A Qualitative Study of Patient Experiences

13 July 2018

1 reference

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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

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166421

DNA testing for hypertrophic cardiomyopathy: a cost-effectiveness model

13 July 2018

1 reference

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Uptake of genetic testing and long-term tumor surveillance in von Hippel-Lindau disease

13 July 2018

1 reference

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International guidelines for the diagnosis and management of hereditary haemorrhagic telangiectasia.

13 July 2018

1 reference

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Physicians' attitudes toward race, genetics, and clinical medicine

13 July 2018

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Online focus groups as a tool to collect data in hard-to-include populations: examples from paediatric oncology

13 July 2018

1 reference

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Factors determining dissemination of results and uptake of genetic testing in families with known BRCA1/2 mutations

13 July 2018

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Delivery of genomic medicine for common chronic adult diseases: a systematic review

13 July 2018

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13 July 2018

1 reference

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Clinical and analytical sensitivities in hereditary hemorrhagic telangiectasia testing and a report of de novo mutations

13 July 2018

1 reference

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SMAD4 mutations found in unselected HHT patients.

13 July 2018

1 reference

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Genetic counseling for fragile x syndrome: updated recommendations of the national society of genetic counselors

13 July 2018

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Regret in cancer-related decisions

13 July 2018

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Barriers to translating emerging genetic research on smoking into clinical practice. Perspectives of primary care physicians

13 July 2018

1 reference

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Hereditary breast/ovarian and colorectal cancer genetics knowledge in a national sample of US physicians

13 July 2018

1 reference

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Texas physicians' perceptions of genomic medicine as an innovation

13 July 2018

1 reference

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Barriers to the provision of genetic services by primary care physicians: a systematic review of the literature

13 July 2018

1 reference

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Carrier screening for cystic fibrosis among Maryland obstetricians before and after the 1997 NIH Consensus Conference

13 July 2018

1 reference

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Primary care physicians' perceptions of barriers to genetic testing and their willingness to participate in research

13 July 2018

1 reference

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Diagnostic criteria for hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber syndrome).

13 July 2018

1 reference

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Impact of genetic testing for Huntington disease on the family system

13 July 2018

1 reference

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Physician knowledge and attitudes towards molecular genetic (DNA) testing of their patients.

13 July 2018

1 reference

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Incorporation of genetics in primary care practice. Will physicians do the counseling and will they be directive?

13 July 2018

1 reference

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Characteristics of health information gatherers, disseminators, and blockers within families at risk of hereditary cancer: implications for family health communication interventions.

13 July 2018

1 reference

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Update on molecular diagnosis of hereditary hemorrhagic telangiectasia

28 July 2018

1 reference

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Evolving perspectives on genetic discrimination in health insurance among health care providers

27 September 2018

1 reference

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Family-based detection for hereditary hemochromatosis

27 September 2018

1 reference

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Patient acceptability of genotypic testing for hemochromatosis in primary care.

27 September 2018

1 reference

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Genetic discrimination: the clinician perspective

27 September 2018

1 reference

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Genetic counseling and testing in families with hereditary nonpolyposis colorectal cancer.

27 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166421

Providers' knowledge of genetics: A survey of 5915 individuals and families with genetic conditions

27 September 2018

1 reference

12 December 2020

Cancer genetics evaluation: barriers to and improvements for referral

1 reference

12 December 2020

Uptake of genetic counselling and predictive DNA testing in hypertrophic cardiomyopathy

1 reference

12 December 2020

Family letters are an effective way to inform relatives about inherited cardiac disease

1 reference

12 December 2020

Comment on the impact of gene patents and licensing practices on access to genetic testing: lessons from hereditary hemorrhagic telangiectasia

1 reference

12 December 2020

The patient with hypertrophic cardiomyopathy has a family

1 reference

12 December 2020

Primary care physicians' utilization and perceptions of genetics services

1 reference

12 December 2020

Survey of physician knowledge about hemochromatosis

1 reference

12 December 2020

Fostering applications of genetics in primary care: what will it take?

1 reference

12 December 2020

How families communicate about HNPCC genetic testing: Findings from a qualitative study

1 reference

12 December 2020

Participation by clinical geneticists in genetic advocacy groups

1 reference

12 December 2020

Medical Geneticists' duty to warn at-risk relatives for genetic disease

1 reference

12 December 2020

Attitudes about and psychosocial outcomes of HFE genotyping for hemochromatosis

1 reference

12 December 2020

Genetic testing in families with hereditary nonpolyposis colon cancer

1 reference

12 December 2020

Perceptions of genetic discrimination among at-risk relatives of colorectal cancer patients

1 reference

12 December 2020

Impact of self-reported familiarity with guidelines for cystic fibrosis carrier screening

1 reference

12 December 2020

Facilitating family communication about predictive genetic testing: probands' perceptions

1 reference

12 December 2020

Life expectancy in patients with hereditary haemorrhagic telangiectasia

1 reference

12 December 2020

Doing synchronous online focus groups with young people: methodological reflections

1 reference

12 December 2020

10.1097/GIM.0B013E31821D2E6D

Identifiers

DOI

1 reference

Dimensions Publication ID

7 August 2017

0 references

1 reference

7 August 2017

1 reference