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"Women Who Don't Give a Crap"

PLoS genetics, 2015-12, Vol.11 (12), p.e1005736-e1005736

Tabor, Holly

2015

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The Impact of Inclusion: Improving Medical Student Confidence in Caring for Adults with Intellectual Disabilities through an Interactive, Narrative-Based Session

Journal of intellectual & developmental disability, 2023-07, Vol.48 (3), p.340-344

2023

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Exome sequencing as a tool for Mendelian disease gene discovery

Nature reviews. Genetics, 2011-11, Vol.12 (11), p.745-755

2011

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How are students learning to care for people with disabilities?: exploring the curriculum design of a sample of disability electives offered by US health professions schools

Disability and rehabilitation, 2024-07, Vol.46 (16), p.3749-3759

2024

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Attitudes of Genetics Professionals Toward the Return of Incidental Results from Exome and Whole-Genome Sequencing

American journal of human genetics, 2014-07, Vol.95 (1), p.77-84

2014

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Noninvasive whole-genome sequencing of a human fetus

Science translational medicine, 2012-06, Vol.4 (137), p.137ra76

2012

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Civic Engagement, Autism and Deliberative Democracy: Prioritizing the Inclusion of Marginalized Perspectives

American journal of bioethics, 2020-04, Vol.20 (4), p.41-43

Tabor, Holly K.

2020

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Ventilator Triage Policies During the COVID-19 Pandemic at U.S. Hospitals Associated With Members of the Association of Bioethics Program Directors

Annals of internal medicine, 2020-08, Vol.173 (3), p.188-194

2020

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Supporting undiagnosed participants when clinical genomics studies end

Nature genetics, 2022-08, Vol.54 (8), p.1063-1065

2022

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Exome sequencing identifies the cause of a mendelian disorder

Nature genetics, 2010-01, Vol.42 (1), p.30-35

2010

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A call for an integrated approach to improve efficiency, equity and sustainability in rare disease research in the United States

Nature genetics, 2022-03, Vol.54 (3), p.219-222

2022

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Perspectives of Rare Disease Social Media Group Participants on Engaging With Genetic Counselors: Mixed Methods Study

Journal of medical Internet research, 2022-12, Vol.24 (12), p.e42084-e42084

2022

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Pathogenic Variants for Mendelian and Complex Traits in Exomes of 6,517 European and African Americans: Implications for the Return of Incidental Results

American journal of human genetics, 2014-08, Vol.95 (2), p.183-193

2014

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Exome sequencing identifies MLL2 mutations as a cause of Kabuki syndrome

Nature genetics, 2010-09, Vol.42 (9), p.790-793

2010

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Ethical Challenges Confronted When Providing Nusinersen Treatment for Spinal Muscular Atrophy

JAMA pediatrics, 2018-02, Vol.172 (2), p.188

2018

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Genetic counseling and testing for Asian Americans: a systematic review

Genetics in medicine, 2021-08, Vol.23 (8), p.1424-1437

2021

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Genomics really gets personal: How exome and whole genome sequencing challenge the ethical framework of human genetics research

American journal of medical genetics. Part A, 2011-12, Vol.155A (12), p.2916-2924

2011

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Patient and family social media use surrounding a novel treatment for a rare genetic disease: a qualitative interview study

Genetics in medicine, 2020-11, Vol.22 (11), p.1830-1837

2020

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Ribosomal mutations cause p53-mediated dark skin and pleiotropic effects

Nature genetics, 2008-08, Vol.40 (8), p.963-970

2008

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Perceived utility and disutility of genomic sequencing for pediatric patients: Perspectives from parents with diverse sociodemographic characteristics

American journal of medical genetics. Part A, 2022-04, Vol.188 (4), p.1088-1101

2022

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Rare Disease, Advocacy and Justice: Intersecting Disparities in Research and Clinical Care

American journal of bioethics, 2023-07, Vol.23 (7), p.17-26

2023

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Candidate-gene approaches for studying complex genetic traits: practical considerations

Nature reviews. Genetics, 2002-05, Vol.3 (5), p.391-397

2002

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"It seems like COVID-19 now is the only disease present on Earth": living with a rare or undiagnosed disease during the COVID-19 pandemic

Genetics in medicine, 2021-05, Vol.23 (5), p.837-844

2021

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Opportunities and pitfalls of social media research in rare genetic diseases: a systematic review

Genetics in medicine, 2021-12, Vol.23 (12), p.2250-2259

2021

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Exome Sequencing of Phenotypic Extremes Identifies CAV2 and TMC6 as Interacting Modifiers of Chronic Pseudomonas aeruginosa Infection in Cystic Fibrosis

PLoS genetics, 2015-06, Vol.11 (6), p.e1005273-e1005273

2015

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"Women Who Don't Give a Crap"

The Impact of Inclusion: Improving Medical Student Confidence in Caring for Adults with Intellectual Disabilities through an Interactive, Narrative-Based Session

Exome sequencing as a tool for Mendelian disease gene discovery

How are students learning to care for people with disabilities?: exploring the curriculum design of a sample of disability electives offered by US health professions schools

Attitudes of Genetics Professionals Toward the Return of Incidental Results from Exome and Whole-Genome Sequencing

Noninvasive whole-genome sequencing of a human fetus

Civic Engagement, Autism and Deliberative Democracy: Prioritizing the Inclusion of Marginalized Perspectives

Ventilator Triage Policies During the COVID-19 Pandemic at U.S. Hospitals Associated With Members of the Association of Bioethics Program Directors

Supporting undiagnosed participants when clinical genomics studies end

Exome sequencing identifies the cause of a mendelian disorder

A call for an integrated approach to improve efficiency, equity and sustainability in rare disease research in the United States

Perspectives of Rare Disease Social Media Group Participants on Engaging With Genetic Counselors: Mixed Methods Study

Pathogenic Variants for Mendelian and Complex Traits in Exomes of 6,517 European and African Americans: Implications for the Return of Incidental Results

Exome sequencing identifies MLL2 mutations as a cause of Kabuki syndrome

Ethical Challenges Confronted When Providing Nusinersen Treatment for Spinal Muscular Atrophy

Genetic counseling and testing for Asian Americans: a systematic review

Genomics really gets personal: How exome and whole genome sequencing challenge the ethical framework of human genetics research

Patient and family social media use surrounding a novel treatment for a rare genetic disease: a qualitative interview study

Ribosomal mutations cause p53-mediated dark skin and pleiotropic effects

Perceived utility and disutility of genomic sequencing for pediatric patients: Perspectives from parents with diverse sociodemographic characteristics

Rare Disease, Advocacy and Justice: Intersecting Disparities in Research and Clinical Care

Candidate-gene approaches for studying complex genetic traits: practical considerations

"It seems like COVID-19 now is the only disease present on Earth": living with a rare or undiagnosed disease during the COVID-19 pandemic

Opportunities and pitfalls of social media research in rare genetic diseases: a systematic review

Exome Sequencing of Phenotypic Extremes Identifies CAV2 and TMC6 as Interacting Modifiers of Chronic Pseudomonas aeruginosa Infection in Cystic Fibrosis

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