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The role of exome sequencing in newborn screening for inborn errors of metabolism

Nature medicine, 2020-09, Vol.26 (9), p.1392-1397

2020

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Managing Incidental Findings in Human Subjects Research: Analysis and Recommendations

The Journal of law, medicine & ethics, 2008-06, Vol.36 (2), p.219-248

2008

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Hopeful and Concerned: Public Input on Building a Trustworthy Medical Information Commons

The Journal of law, medicine & ethics, 2019-03, Vol.47 (1), p.70-87

2019

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A draft human pangenome reference

Nature (London), 2023-05, Vol.617 (7960), p.312-324

2023

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Preferences Regarding Return of Genomic Results to Relatives of Research Participants, Including after Participant Death: Empirical Results from a Cancer Biobank

The Journal of law, medicine & ethics, 2015-09, Vol.43 (3), p.464-475

2015

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Toward better governance of human genomic data

Nature genetics, 2021-01, Vol.53 (1), p.2-8

2021

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Mapping the Ethics of Translational Genomics: Situating Return of Results and Navigating the Research-Clinical Divide

The Journal of law, medicine & ethics, 2015-09, Vol.43 (3), p.486-501

2015

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Characterizing the Biomedical Data-Sharing Landscape

The Journal of law, medicine & ethics, 2019-03, Vol.47 (1), p.21-30

2019

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Returning a Research Participant's Genomic Results to Relatives: Analysis and Recommendations

The Journal of law, medicine & ethics, 2015-09, Vol.43 (3), p.440-463

2015

Volltextzugriff (PDF)

The Role of Participants in a Medical Information Commons

The Journal of law, medicine & ethics, 2019-03, Vol.47 (1), p.51-61

2019

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Importance of Participant-Centricity and Trust for a Sustainable Medical Information Commons

The Journal of law, medicine & ethics, 2019-03, Vol.47 (1), p.12-20

2019

Volltextzugriff (PDF)

Pragmatic Tools for Sharing Genomic Research Results with the Relatives of Living and Deceased Research Participants

The Journal of law, medicine & ethics, 2018-03, Vol.46 (1), p.87-109

2018

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Listening in on difficult conversations: an observational, multi-center investigation of real-time conversations in medical oncology

BMC cancer, 2013-10, Vol.13 (1), p.455-455, Article 455

2013

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

BMC genomics, 2011-01, Vol.4 (1), p.13-13, Article 13

2011

Volltextzugriff (PDF)

Pangenome graph construction from genome alignments with Minigraph-Cactus

Nature biotechnology, 2024-04, Vol.42 (4), p.663-673

2024

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Recombination between heterologous human acrocentric chromosomes

Nature (London), 2023-05, Vol.617 (7960), p.335-343

2023

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Increased mutation and gene conversion within human segmental duplications

Nature (London), 2023-05, Vol.617 (7960), p.325-334

2023

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Collective Fear, Individualized Risk: the social and cultural context of genetic testing forbreast cancer

Nursing ethics, 2000-05, Vol.7 (3), p.237-249

2000

Volltextzugriff (PDF)

Informed Consent in a Multicultural Cancer Patient Population: implications for nursing practice

Nursing ethics, 1998-09, Vol.5 (5), p.412

Barnes, D M

1998

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Informed Consent in a Multicultural Cancer Patient Population: implications for nursing practice

Nursing ethics, 1998-09, Vol.5 (5), p.412-423

1998

Volltextzugriff (PDF)

The thymocyte-specific RNA-binding protein Arpp21 provides TCR repertoire diversity by binding to the 3'-UTR and promoting Rag1 mRNA expression

Nature communications, 2024-03, Vol.15 (1), p.2194-20, Article 2194

2024

Volltextzugriff (PDF)

Lack of astrocytes hinders parenchymal oligodendrocyte precursor cells from reaching a myelinating state in osmolyte-induced demyelination

Acta neuropathologica communications, 2020-12, Vol.8 (1), p.224-224, Article 224

2020

Volltextzugriff (PDF)

Deficiency of PORCN , a regulator of Wnt signaling, is associated with focal dermal hypoplasia

Nature genetics, 2007-07, Vol.39 (7), p.833-835

2007

Volltextzugriff (PDF)

Elucidating mechanisms of genetic cross-disease associations at the PROCR vascular disease locus

Nature communications, 2022-03, Vol.13 (1), p.1222-15, Article 1222

2022

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The role of exome sequencing in newborn screening for inborn errors of metabolism

Managing Incidental Findings in Human Subjects Research: Analysis and Recommendations

Hopeful and Concerned: Public Input on Building a Trustworthy Medical Information Commons

A draft human pangenome reference

Preferences Regarding Return of Genomic Results to Relatives of Research Participants, Including after Participant Death: Empirical Results from a Cancer Biobank

The Human Pangenome Project: a global resource to map genomic diversity

Toward better governance of human genomic data

Mapping the Ethics of Translational Genomics: Situating Return of Results and Navigating the Research-Clinical Divide

Characterizing the Biomedical Data-Sharing Landscape

Returning a Research Participant's Genomic Results to Relatives: Analysis and Recommendations

The Role of Participants in a Medical Information Commons

Importance of Participant-Centricity and Trust for a Sustainable Medical Information Commons

Pragmatic Tools for Sharing Genomic Research Results with the Relatives of Living and Deceased Research Participants

Listening in on difficult conversations: an observational, multi-center investigation of real-time conversations in medical oncology

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

Pangenome graph construction from genome alignments with Minigraph-Cactus

Recombination between heterologous human acrocentric chromosomes

Increased mutation and gene conversion within human segmental duplications

Collective Fear, Individualized Risk: the social and cultural context of genetic testing forbreast cancer

Informed Consent in a Multicultural Cancer Patient Population: implications for nursing practice

Informed Consent in a Multicultural Cancer Patient Population: implications for nursing practice

The thymocyte-specific RNA-binding protein Arpp21 provides TCR repertoire diversity by binding to the 3'-UTR and promoting Rag1 mRNA expression

Lack of astrocytes hinders parenchymal oligodendrocyte precursor cells from reaching a myelinating state in osmolyte-induced demyelination

Deficiency of PORCN , a regulator of Wnt signaling, is associated with focal dermal hypoplasia

Elucidating mechanisms of genetic cross-disease associations at the PROCR vascular disease locus

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