Return of individual research results from genome-wide association studies: experience of the Electronic Medical Records and Genomics (eMERGE) Network (Q28673413)

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scientific article (publication date: April 2012)

Language	Label	Description	Also known as
English	Return of individual research results from genome-wide association studies: experience of the Electronic Medical Records and Genomics (eMERGE) Network	scientific article (publication date: April 2012)

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scholarly article

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Return of individual research results from genome-wide association studies: experience of the Electronic Medical Records and Genomics (eMERGE) Network (English)

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genome-wide association study

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Ellen Wright Clayton

4

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Stephanie M Fullerton

1

object named as

Stephanie M Fullerton

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19

object named as

Wylie Burke

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20

object named as

Gail P Jarvik

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Barbara A Koenig

8

object named as

Barbara A Koenig

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Catherine A. McCarty

object named as

Catherine A McCarty

11

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12

object named as

Amy L McGuire

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Marylyn D. Ritchie

16

object named as

Marylyn D Ritchie

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5

object named as

Dana C Crawford

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Joshua C. Denny

6

object named as

Joshua C Denny

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Noralane Lindor

10

object named as

Noralane M Lindor

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Kathleen A Leppig

9

object named as

Kathleen A Leppig

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15

object named as

Erin M Ramos

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14

object named as

Daniel B Mirel

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2

object named as

Wendy A Wolf

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3

object named as

Kyle B Brothers

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Maureen E Smith

17

object named as

Maureen E Smith

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18

object named as

Carol J Waudby

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Philip Greenland

7

object named as

Philip Greenland

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author name string

Eugenia R McPeek Hinz

13

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language of work or name

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publication date

April 2012

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Genetics in Medicine

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14

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4

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424-31

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Ethical and practical challenges of sharing data from genome-wide association studies: the eMERGE Consortium experience

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3723451

17 March 2017

The eMERGE Network: a consortium of biorepositories linked to electronic medical records data for conducting genomic studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3723451

17 March 2017

Iron-overload-related disease in HFE hereditary hemochromatosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3723451

17 March 2017

Causes of death in X chromatin positive males (Klinefelter's syndrome).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3723451

17 March 2017

Electronic medical records for genetic research: results of the eMERGE consortium

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3723451

3 June 2018

Klinefelter syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3723451

3 June 2018

Breast cancer risk among patients with Klinefelter syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3723451

3 June 2018

Disclosure of individual genetic data to research participants: the debate reconsidered

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3723451

3 June 2018

Ethical and practical guidelines for reporting genetic research results to study participants: updated guidelines from a National Heart, Lung, and Blood Institute working group

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3723451

3 June 2018

Recommendations from the EGAPP Working Group: routine testing for Factor V Leiden (R506Q) and prothrombin (20210G>A) mutations in adults with a history of idiopathic venous thromboembolism and their adult family members

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3723451

3 June 2018

Factor V Leiden thrombophilia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3723451

3 June 2018

Confronting real time ethical, legal, and social issues in the Electronic Medical Records and Genomics (eMERGE) Consortium

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3723451

3 June 2018

How do you monitor the patient with Turner's syndrome in adulthood?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3723451

3 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3723451

3 June 2018

Genetics of venous thrombosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3723451

3 June 2018

Autoimmunity and Klinefelter's syndrome: when men have two X chromosomes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3723451

3 June 2018

Loss of the Y chromosome: an age-related or clonal phenomenon in acute myelogenous leukemia/myelodysplastic syndrome?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3723451

3 June 2018

Managing incidental findings in human subjects research: analysis and recommendations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3723451

3 June 2018

Development of a large-scale de-identified DNA biobank to enable personalized medicine.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3723451

3 June 2018

Hereditary hemochromatosis: pathophysiology, diagnosis, and management

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3723451

3 June 2018

Turner syndrome and clinical treatment.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3723451

3 June 2018

Duty to disclose what? Querying the putative obligation to return research results to participants

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3723451

3 June 2018

Klinefelter syndrome in clinical practice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3723451

3 June 2018

X chromosome loss and ageing

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3723451

3 June 2018

Informed consent and subject motivation to participate in a large, population-based genomics study: the Marshfield Clinic Personalized Medicine Research Project

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3723451

3 June 2018

Disclosing individual genetic results to research participants

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3723451

3 June 2018

Screening for hereditary hemochromatosis: a systematic review for the U.S. Preventive Services Task Force

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3723451

3 June 2018

Trends in age at diagnosis of Turner syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3723451

3 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3723451

3 June 2018

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

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2012.15

21 January 2018

Medicine. Reestablishing the researcher-patient compact.

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2012.15

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2012.15

21 January 2018

Dementia and Alzheimer disease incidence: a prospective cohort study.

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2012.15

21 January 2018

Assessing the understanding of biobank participants.

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2012.15

21 January 2018

Smoking increases the risk of venous thrombosis and acts synergistically with oral contraceptive use.

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2012.15

21 January 2018

The emergence of an ethical duty to disclose genetic research results: international perspectives

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3723451

27 November 2018

HFE-associated hereditary hemochromatosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/22361898

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Determinants of medical care for young women with Turner syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/22361898

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dissection of the aorta in Turner syndrome: two cases and review of 85 cases in the literature

1 reference

https://pubmed.ncbi.nlm.nih.gov/22361898

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic risk estimation in the Coriell Personalized Medicine Collaborative

1 reference

https://pubmed.ncbi.nlm.nih.gov/22361898

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1038/GIM.2012.15

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

PMC publication ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

PubMed publication ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

ResearchGate publication ID

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