Lista de obras - Stephanie M Fullerton - Dominio Público Uruguay

"Getting off the Bus Closer to Your Destination": Patients' Views about Pharmacogenetic Testing

artículo científico publicado en 2015

A high-resolution HLA reference panel capturing global population diversity enables multi-ancestry fine-mapping in HIV host response

artículo científico publicado en 2021

A review of the key issues associated with the commercialization of biobanks

artículo científico publicado en 2014

Actionable exomic incidental findings in 6503 participants: challenges of variant classification

artículo científico publicado en 2015

Allocation of Resources to Communication of Research Result Summaries

artículo científico publicado en 2016

Awareness of Federal Regulatory Mechanisms Relevant to Community-Engaged Research: Survey of Health Disparities-Oriented NIH-Funded Investigators

artículo científico publicado en 2014

Beneficence, clinical urgency, and the return of individual research results to relatives

artículo científico publicado en 2012

Broad Consent for Research With Biological Samples: Workshop Conclusions

artículo científico publicado en 2015

Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine

artículo científico publicado en 2016

Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine

article

Conducting a large, multi-site survey about patients' views on broad consent: challenges and solutions

artículo científico publicado en 2016

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

artículo científico publicado en 2010

Discordance in selected designee for return of genomic findings in the event of participant death and estate executor

artículo científico publicado en 2017

Dissecting complex disease: the quest for the Philosopher's Stone?

artículo científico publicado en 2006

Engaging Study Participants in Research Dissemination at a Center for Population Health and Health Disparities

artículo científico publicado en 2016

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

artículo científico publicado en 2011

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

artículo científico publicado en 2010

Familial identification: population structure and relationship distinguishability

artículo científico publicado en 2012

Forensic familial searching: scientific and social implications

artículo científico publicado en 2013

From patients to partners: participant-centric initiatives in biomedical research

artículo científico publicado en 2012

Genes, Environment, and Cancer Disparities

article

Genomic research and wide data sharing: views of prospective participants

artículo científico publicado en 2010

Genomics is failing on diversity

scientific article published on 12 October 2016

Geographic and haplotype structure of candidate type 2 diabetes susceptibility variants at the calpain-10 locus

artículo científico publicado en 2002

Glad you asked: participants' opinions of re-consent for dbGap data submission

artículo científico publicado en 2010

Has the biobank bubble burst? Withstanding the challenges for sustainable biobanking in the digital era

artículo científico publicado en 2016

Inferring genetic ancestry: opportunities, challenges, and implications

artículo científico publicado en 2010

Informed Consent in Genome-Scale Research: What Do Prospective Participants Think?

artículo científico publicado en 2012

Informed Consent in Translational Genomics: Insufficient Without Trustworthy Governance

scholarly article by Wylie Burke et al published March 2018 in Journal of Law, Medicine, and Ethics

Looking for Trouble and Finding It.

artículo científico publicado en 2015

Meeting the governance challenges of next-generation biorepository research

artículo científico publicado en 2010

No Panacea: Next-Gen Sequencing Will Not Mitigate Adoptees' Lack of Genetic Family Health History

artículo científico publicado en 2016

Offering aggregate results to participants in genomic research: opportunities and challenges

artículo científico publicado en 2012

Parent perspectives on pediatric genetic research and implications for genotype-driven research recruitment

artículo científico publicado en 2011

Parents' attitudes toward consent and data sharing in biobanks: A multisite experimental survey

scientific article published on 01 July 2018

Patient safety in genomic medicine: an exploratory study

artículo científico publicado en Marzo 2016

Patients' Choices for Return of Exome Sequencing Results to Relatives in the Event of Their Death

artículo científico publicado en 2015

Population description and its role in the interpretation of genetic association

artículo científico publicado en 2010

Practice Implications of Expanded Genetic Testing in Oncology

artículo científico publicado en 2019

Prospective participant selection and ranking to maximize actionable pharmacogenetic variants and discovery in the eMERGE Network ⬇️

artículo científico publicado en 2015

Public Attitudes toward Consent and Data Sharing in Biobank Research: A Large Multi-site Experimental Survey in the US

artículo científico publicado en 2017

Race and ancestry in biomedical research: exploring the challenges

artículo científico publicado en 2009

Race-based medicine and justice as recognition: exploring the phenomenon of BiDil

artículo científico publicado en 2009

Racialized genetics and the study of complex diseases: the thrifty genotype revisited

artículo científico publicado en 2007

Racing around, getting nowhere

Recommendations for ethical approaches to genotype-driven research recruitment

artículo científico publicado en 2012

Refining the structure and content of clinical genomic reports

artículo científico publicado en 2014

Relationships with Test-Tubes: Where's the Reciprocity?

Research guidelines in the era of large-scale collaborations: an analysis of Genome-wide Association Study Consortia

artículo científico publicado en 2012

Return of genomic results to research participants: the floor, the ceiling, and the choices in between

artículo científico publicado en 2014

Return of incidental findings in genomic medicine: measuring what patients value--development of an instrument to measure preferences for information from next-generation testing (IMPRINT).

artículo científico publicado en 2013

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

artículo científico publicado en 2012

Returning pleiotropic results from genetic testing to patients and research participants

artículo científico publicado en 2014

Rural Mexican-Americans' perceptions of family health history, genetics, and disease risk: implications for disparities-focused research dissemination

artículo científico publicado en 2015

Secondary uses and the governance of de-identified data: lessons from the human genome diversity panel

artículo científico publicado en 2011

Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

artículo científico publicado en 2019

Sharing data and experience: using the Clinical and Translational Science Award (CTSA) "moral community" to improve research ethics consultation

artículo científico publicado en 2008

Stakeholder engagement: a key component of integrating genomic information into electronic health records

artículo científico publicado en 2013

Strategies and stakeholders: minority recruitment in cancer genetics research

artículo científico publicado en 2008

The effects of scale: variation in the APOA1/C3/A4/A5 gene cluster

artículo científico publicado en 2004

Toward better governance of human genomic data

artículo científico publicado en 2021

Transdisciplinary approaches to understanding and eliminating ethnic health disparities: are we on the right track? ⬇️

artículo científico publicado el 1 de enero de 2012

Using Genetic Technologies To Reduce, Rather Than Widen, Health Disparities

artículo científico publicado en 2016

Using genetically informed, randomized prevention trials to test etiological hypotheses about child and adolescent drug use and psychopathology.

artículo científico publicado en 2013

Values in translation: how asking the right questions can move translational science toward greater health impact

artículo científico publicado en 2012

What are our AIMs? Interdisciplinary Perspectives on the Use of Ancestry Estimation in Disease Research

artículo científico publicado en 2012

dbGaP data access requests: a call for greater transparency

artículo científico publicado en 2011

Lista de obras de Stephanie M Fullerton

"Getting off the Bus Closer to Your Destination": Patients' Views about Pharmacogenetic Testing

A high-resolution HLA reference panel capturing global population diversity enables multi-ancestry fine-mapping in HIV host response

A review of the key issues associated with the commercialization of biobanks

Actionable exomic incidental findings in 6503 participants: challenges of variant classification

Allocation of Resources to Communication of Research Result Summaries

Awareness of Federal Regulatory Mechanisms Relevant to Community-Engaged Research: Survey of Health Disparities-Oriented NIH-Funded Investigators

Beneficence, clinical urgency, and the return of individual research results to relatives

Broad Consent for Research With Biological Samples: Workshop Conclusions

Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine

Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine

Conducting a large, multi-site survey about patients' views on broad consent: challenges and solutions

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

Discordance in selected designee for return of genomic findings in the event of participant death and estate executor

Dissecting complex disease: the quest for the Philosopher's Stone?

Engaging Study Participants in Research Dissemination at a Center for Population Health and Health Disparities

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

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

Familial identification: population structure and relationship distinguishability

Forensic familial searching: scientific and social implications

From patients to partners: participant-centric initiatives in biomedical research

Genes, Environment, and Cancer Disparities

Genomic research and wide data sharing: views of prospective participants

Genomics is failing on diversity

Geographic and haplotype structure of candidate type 2 diabetes susceptibility variants at the calpain-10 locus

Glad you asked: participants' opinions of re-consent for dbGap data submission

Has the biobank bubble burst? Withstanding the challenges for sustainable biobanking in the digital era

Inferring genetic ancestry: opportunities, challenges, and implications

Informed Consent in Genome-Scale Research: What Do Prospective Participants Think?

Informed Consent in Translational Genomics: Insufficient Without Trustworthy Governance

Looking for Trouble and Finding It.

Meeting the governance challenges of next-generation biorepository research

No Panacea: Next-Gen Sequencing Will Not Mitigate Adoptees' Lack of Genetic Family Health History

Offering aggregate results to participants in genomic research: opportunities and challenges

Parent perspectives on pediatric genetic research and implications for genotype-driven research recruitment

Parents' attitudes toward consent and data sharing in biobanks: A multisite experimental survey

Patient safety in genomic medicine: an exploratory study

Patients' Choices for Return of Exome Sequencing Results to Relatives in the Event of Their Death

Population description and its role in the interpretation of genetic association

Practice Implications of Expanded Genetic Testing in Oncology

Prospective participant selection and ranking to maximize actionable pharmacogenetic variants and discovery in the eMERGE Network ⬇️

Public Attitudes toward Consent and Data Sharing in Biobank Research: A Large Multi-site Experimental Survey in the US

Race and ancestry in biomedical research: exploring the challenges

Race-based medicine and justice as recognition: exploring the phenomenon of BiDil

Racialized genetics and the study of complex diseases: the thrifty genotype revisited

Racing around, getting nowhere

Recommendations for ethical approaches to genotype-driven research recruitment

Refining the structure and content of clinical genomic reports

Relationships with Test-Tubes: Where's the Reciprocity?

Research guidelines in the era of large-scale collaborations: an analysis of Genome-wide Association Study Consortia

Return of genomic results to research participants: the floor, the ceiling, and the choices in between

Return of incidental findings in genomic medicine: measuring what patients value--development of an instrument to measure preferences for information from next-generation testing (IMPRINT).

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

Returning pleiotropic results from genetic testing to patients and research participants

Rural Mexican-Americans' perceptions of family health history, genetics, and disease risk: implications for disparities-focused research dissemination

Secondary uses and the governance of de-identified data: lessons from the human genome diversity panel

Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

Sharing data and experience: using the Clinical and Translational Science Award (CTSA) "moral community" to improve research ethics consultation

Stakeholder engagement: a key component of integrating genomic information into electronic health records

Strategies and stakeholders: minority recruitment in cancer genetics research

The effects of scale: variation in the APOA1/C3/A4/A5 gene cluster

Toward better governance of human genomic data

Transdisciplinary approaches to understanding and eliminating ethnic health disparities: are we on the right track? ⬇️

Using Genetic Technologies To Reduce, Rather Than Widen, Health Disparities

Using genetically informed, randomized prevention trials to test etiological hypotheses about child and adolescent drug use and psychopathology.

Values in translation: how asking the right questions can move translational science toward greater health impact

What are our AIMs? Interdisciplinary Perspectives on the Use of Ancestry Estimation in Disease Research

dbGaP data access requests: a call for greater transparency