(Q37171551)

English

Willingness to participate in genomics research and desire for personal results among underrepresented minority patients: a structured interview study

scientific article published on 22 June 2013

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

Willingness to participate in genomics research and desire for personal results among underrepresented minority patients: a structured interview study (English)

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

0 references

Ethylin Wang Jabs

object named as

Ethylin Wang Jabs

8

0 references

author name string

Saskia C Sanderson

1

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

Michael A Diefenbach

2

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

Randi Zinberg

3

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

Carol R Horowitz

4

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

Margaret Smirnoff

5

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

Micol Zweig

6

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

Samantha Streicher

7

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

Lynne D Richardson

9

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

publication date

22 June 2013

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

Journal of Community Genetics

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

4

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

4

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

469-482

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

Potential bias in the bank: what distinguishes refusers, nonresponders and participants in a clinic-based biobank?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3773313

6 September 2017

Evolving approaches to the ethical management of genomic data

1 reference

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6 September 2017

Identifying personal genomes by surname inference

1 reference

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Why do participants enroll in population biobank studies? A systematic literature review

1 reference

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6 September 2017

Genetic and lifestyle causal beliefs about obesity and associated diseases among ethnically diverse patients: a structured interview study

1 reference

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6 September 2017

Why families choose not to participate in research: feedback from non-responders

1 reference

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Return of research results from pharmacogenomic versus disease susceptibility studies: what's drugs got to do with it?

1 reference

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6 September 2017

Attitudes of African-American parents about biobank participation and return of results for themselves and their children

1 reference

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Recruitment for genetic studies of epilepsy

1 reference

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6 September 2017

Public preferences regarding the return of individual genetic research results: findings from a qualitative focus group study

1 reference

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

1 reference

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6 September 2017

The legal risks of returning results of genomics research

1 reference

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6 September 2017

IRB perspectives on the return of individual results from genomic research

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3773313

6 September 2017

Reasons for participating and genetic information needs among racially and ethnically diverse biobank participants: a focus group study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3773313

6 September 2017

Population biobanks and returning individual research results: mission impossible or new directions?

1 reference

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6 September 2017

Recruitment and retention strategies for minority or poor clinical research participants: lessons from the Healthy Aging in Neighborhoods of Diversity across the Life Span study

1 reference

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6 September 2017

Public perspectives on returning genetics and genomics research results

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3773313

6 September 2017

Interest in genetic testing for modest changes in breast cancer risk: implications for SNP testing.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3773313

6 September 2017

Survey of US public attitudes toward pharmacogenetic testing

1 reference

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6 September 2017

Public and biobank participant attitudes toward genetic research participation and data sharing

1 reference

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6 September 2017

Racial/ethnic differences in association of fasting glucose-associated genomic loci with fasting glucose, HOMA-B, and impaired fasting glucose in the U.S. adult population

1 reference

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6 September 2017

Offering individual genetic research results: context matters

1 reference

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6 September 2017

Prevalence and trends in obesity among US adults, 1999-2008

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3773313

6 September 2017

Access to interpreting services in England: secondary analysis of national data

1 reference

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Association analysis in african americans of European-derived type 2 diabetes single nucleotide polymorphisms from whole-genome association studies

1 reference

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Strategies and stakeholders: minority recruitment in cancer genetics research

1 reference

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Factors associated with enrollment in cancer genetics research

1 reference

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Medical Consequences of Obesity

1 reference

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Genetic testing: psychological aspects and implications

1 reference

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Interest in genetic testing among first-degree relatives of breast cancer patients

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3773313

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Under-representation of minority ethnic groups in cardiovascular research: a semi-structured interview study

1 reference

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14 September 2017

Associations between anticipated reactions to genetic test results and interest in genetic testing: will self-selection reduce the potential for harm?

1 reference

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14 September 2017

Predictors of uptake of obesity genetic testing among affected adults

1 reference

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14 September 2017

Genetic testing for colon cancer among African-Americans in North Carolina

1 reference

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14 September 2017

Self-regulation and the behavioural response to DNA risk information: a theoretical analysis and framework for future research

1 reference

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14 September 2017

Decision-making about genetic testing among women at familial risk for breast cancer

1 reference

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28 September 2017

Interest in genetic testing for colon cancer susceptibility: cognitive and emotional correlates

1 reference

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Interest in learning of personal genetic risk for cancer: a general population survey.

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Factors associated with repeat adherence to breast cancer screening.

1 reference

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1 reference

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1 reference

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1 reference

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1 reference

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1 reference

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1 reference

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1 reference

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Public interest in genetic testing for susceptibility to heart disease and cancer: a population-based survey in the UK

1 reference

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1 reference

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based on heuristic

inferred from PubMed ID database lookup

Risk perception, screening practice and interest in genetic testing among unaffected men in families with hereditary prostate cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/23794263

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Attitudes about genetic testing for breast-ovarian cancer susceptibility

1 reference

https://pubmed.ncbi.nlm.nih.gov/23794263

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Reducing avoidable cancer mortality through prevention and early detection regimens

1 reference

https://pubmed.ncbi.nlm.nih.gov/23794263

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based on heuristic

inferred from PubMed ID database lookup

Impact of limited population diversity of genome-wide association studies

1 reference

https://pubmed.ncbi.nlm.nih.gov/23794263

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based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S12687-013-0154-0

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

ResearchGate publication ID

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