(Q34669217)

3 August 2017

title

CLIA-tested genetic variants on commercial SNP arrays: potential for incidental findings in genome-wide association studies (English)

1 reference

genome-wide association study

3 August 2017

main subject

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3

Emelia J Benjamin

0 references

Gail P. Jarvik

series ordinal

6

object named as

Gail P Jarvik

0 references

Caroline S. Fox

series ordinal

4

object named as

Caroline Fox

1 reference

3 August 2017

Christopher J O'Donnell

series ordinal

7

object named as

Christopher J O'Donnell

1 reference

3 August 2017

1

Andrew D Johnson

1 reference

3 August 2017

5

Daniel Levy

1 reference

3 August 2017

Anupama Bhimavarapu

2

1 reference

3 August 2017

language of work or name

English

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publication date

1 June 2010

1 reference

3 August 2017

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3 August 2017

volume

12

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3 August 2017

issue

6

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3 August 2017

page(s)

355-363

1 reference

Single-nucleotide polymorphism bioinformatics: a comprehensive review of resources

3 August 2017

cites work

1 reference

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Direct to consumer genetic testing: Avoiding a culture war

7 July 2018

1 reference

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Genome-wide QTL mapping for three traits related to teat number in a White Duroc x Erhualian pig resource population

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3056880

SNAP: a web-based tool for identification and annotation of proxy SNPs using HapMap

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3056880

Genomic research and incidental findings

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3056880

Understanding incidental findings in the context of genetics and genomics

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3056880

Managing incidental findings in human subjects research: analysis and recommendations

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3056880

A HapMap harvest of insights into the genetics of common disease

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3056880

Familial Mediterranean Fever in Armenian population.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3056880

A critical appraisal of the scientific basis of commercial genomic profiles used to assess health risks and personalize health interventions

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3056880

A second generation human haplotype map of over 3.1 million SNPs

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3056880

Hereditary chronic pancreatitis

7 July 2018

1 reference

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Best practice guidelines for the molecular genetic diagnosis of Type 1 (HFE-related) hereditary haemochromatosis

7 July 2018

1 reference

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The incidentalome: a threat to genomic medicine

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3056880

Risk of recurrent venous thromboembolism in patients with common thrombophilia: a systematic review

7 July 2018

1 reference

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Hemochromatosis and iron-overload screening in a racially diverse population.

7 July 2018

1 reference

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Informed consent and biobanks: a population-based study of attitudes towards tissue donation for genetic research

7 July 2018

1 reference

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Long-term, low-intensity warfarin therapy for the prevention of recurrent venous thromboembolism

7 July 2018

1 reference

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Prenatal and postnatal prevalence of Klinefelter syndrome: a national registry study

7 July 2018

1 reference

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Clinical utility of factor V leiden (R506Q) testing for the diagnosis and management of thromboembolic disorders

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3056880

The spectrum of Familial Mediterranean Fever (FMF) mutations

7 July 2018

1 reference

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Initial sequencing and analysis of the human genome

7 July 2018

1 reference

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MEFV-Gene analysis in armenian patients with Familial Mediterranean fever: diagnostic value and unfavorable renal prognosis of the M694V homozygous genotype-genetic and therapeutic implications

7 July 2018

1 reference

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Mutation and haplotype studies of familial Mediterranean fever reveal new ancestral relationships and evidence for a high carrier frequency with reduced penetrance in the Ashkenazi Jewish population.

7 July 2018

1 reference

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Both mutations in G6PD A- are necessary to produce the G6PD deficient phenotype

7 July 2018

1 reference

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Reporting genetic results in research studies: summary and recommendations of an NHLBI working group.

7 July 2018

1 reference

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Cystathionine betasynthase and MTHFR deficiencies in adults

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181E1E2A9

A single mutation 202G>A in the human glucose-6-phosphate dehydrogenase gene (G6PD) can cause acute hemolysis by itself

21 January 2018

1 reference

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Not all amino acid substitutions of the common cluster E6 mutation in CYP21 cause congenital adrenal hyperplasia.

21 January 2018

1 reference

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The Third Generation Cohort of the National Heart, Lung, and Blood Institute's Framingham Heart Study: Design, Recruitment, and Initial Examination

21 January 2018

1 reference

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Donors perceptions of consent to and feedback from biobank research: time to acknowledge diversity?

21 January 2018

1 reference

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An investigation of coronary heart disease in families. The Framingham offspring study

26 October 2018

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12 December 2020

Long-term survival in patients with hereditary hemochromatosis

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12 December 2020

An approach to longitudinal studies in a community: the Framingham Study

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12 December 2020

Keeping Pace with the Times — The Genetic Information Nondiscrimination Act of 2008

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12 December 2020

The SPINK1 N34S variant is associated with acute pancreatitis

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12 December 2020

An open access database of genome-wide association results

1 reference

12 December 2020

10.1097/GIM.0B013E3181E1E2A9

Identifiers

DOI

1 reference

Dimensions Publication ID

3 August 2017

0 references

1 reference

3 August 2017

1 reference