(Q33856320)

29 July 2017

title

Genetic tests: clinical validity and clinical utility (English)

1 reference

29 July 2017

1

Wylie Burke

1 reference

29 July 2017

publication date

24 April 2014

1 reference

Current protocols in human genetics / editorial board, Nicholas C, Dracapoli ... [et al.]

29 July 2017

published in

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29 July 2017

volume

81

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29 July 2017

page(s)

9.15.1-8

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Comparative effectiveness research in cancer genomics and precision medicine: current landscape and future prospects

29 July 2017

cites work

1 reference

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5 July 2018

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How can polygenic inheritance be used in population screening for common diseases?

5 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4084965

Revised guidelines for the clinical management of Lynch syndrome (HNPCC): recommendations by a group of European experts

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4084965

Abundant pleiotropy in human complex diseases and traits.

5 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4084965

Natural history and management of HFE-hemochromatosis

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4084965

Inherited mutations in breast cancer genes--risk and response

5 July 2018

1 reference

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Update multiple endocrine neoplasia type 2.

5 July 2018

1 reference

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Iron-overload-related disease in HFE hereditary hemochromatosis

5 July 2018

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Iron storage disease: facts, fiction and progress

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4084965

Cancer risks among BRCA1 and BRCA2 mutation carriers

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4084965

Screening for hemochromatosis: recommendation statement

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4084965

Genetic testing for cardiovascular disease susceptibility: a useful clinical management tool or possible misinformation?

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4084965

Genetic test evaluation: information needs of clinicians, policy makers, and the public

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4084965

Guidelines for diagnosis and therapy of MEN type 1 and type 2.

5 July 2018

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HFE gene and hereditary hemochromatosis: a HuGE review. Human Genome Epidemiology

5 July 2018

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Rare diseases and the assessment of intervention: what sorts of clinical trials can we use?

5 July 2018

1 reference

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Evidence-based medicine and practice guidelines: an overview

5 July 2018

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Sickle hemoglobin (HbS) allele and sickle cell disease: a HuGE review

5 July 2018

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Risks of cancer in BRCA1-mutation carriers. Breast Cancer Linkage Consortium

5 July 2018

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Alpha1-antitrypsin deficiency: a position statement of the Canadian Thoracic Society.

5 July 2018

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Penetrance of the C28Y/C282Y genotype of the HFE gene.

21 January 2018

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On the use of familial aggregation in population-based case probands for calculating penetrance.

21 January 2018

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Prophylactic thyroidectomy in multiple endocrine neoplasia type 2A.

21 January 2018

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Intravenous human plasma-derived augmentation therapy in alpha 1-antitrypsin deficiency: from pharmacokinetic analysis to individualizing therapy

21 January 2018

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Controlled 15-year trial on screening for colorectal cancer in families with hereditary nonpolyposis colorectal cancer

21 January 2018

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Strengthening the reporting of Genetic Risk Prediction Studies: The GRIPS statement

21 January 2018

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12 December 2020

Genetic risk in context: calculating the penetrance of BRCA1 and BRCA2 mutations

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12 December 2020

Alpha 1-antitrypsin deficiency: memorandum from a WHO meeting

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12 December 2020

Testing and reporting ACMG cystic fibrosis mutation panel results

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12 December 2020

Guilt beyond a reasonable doubt

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12 December 2020

Personalized medicine in the era of genomics

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12 December 2020

From human genetics and genomics to pharmacogenetics and pharmacogenomics: past lessons, future directions

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12 December 2020

Promoting safe and effective genetic testing in the United States. Final report of the Task Force on Genetic Testing

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12 December 2020

10.1002/0471142905.HG0915S81

Identifiers

DOI

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29 July 2017

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29 July 2017

1 reference