Challenges in the Use of Direct-to-Consumer Personal Genome Testing in Children

द्वारा Tabor, Holly K., Kelley, Maureen
प्रकाशित 2009

Ethical implications of array comparative genomic hybridization in complex phenotypes: points to consider in research

द्वारा Tabor, Holly K., Cho, Mildred K.
प्रकाशित 2007

“Before Facebook and before social media…we did not know anybody else that had this”: parent perspectives on internet and social media use during the pediatric clinical genetic tes...

द्वारा Barton, Krysta S., Wingerson, Andrew, Barzilay, Julie R., Tabor, Holly K.
में प्रकाशित J Community Genet (2018)

“We don’t know her history, her background”: Adoptive parents’ perspectives on whole genome sequencing results

द्वारा Crouch, Julia, Yu, Joon-Ho, Shankar, Aditi G., Tabor, Holly K.
में प्रकाशित J Genet Couns (2014)

Self-guided management of exome and whole genome sequencing results: changing the results return model

द्वारा Yu, Joon-Ho, Jamal, Seema M., Tabor, Holly K., Bamshad, Michael J.
प्रकाशित 2013

Genomics Really Gets Personal: How Exome and Whole Genome Sequencing Challenge the Ethical Framework of Human Genetics Research

द्वारा Tabor, Holly K., Berkman, Benjamin E., Hull, Sara Chandros, Bamshad, Michael J.
में प्रकाशित Am J Med Genet A (2011)

Attitudes of African Americans toward Return of Results from Exome and Whole Genome Sequencing

द्वारा Yu, Joon-Ho, Crouch, Julia, Jamal, Seema M., Tabor, Holly K., Bamshad, Michael J.
प्रकाशित 2013

Attitudes of Non-African American Focus Group Participants Toward Return of Results from Exome and Whole Genome Sequencing

द्वारा Yu, Joon-Ho, Crouch, Julia, Jamal, Seema M., Bamshad, Michael J., Tabor, Holly K.
में प्रकाशित Am J Med Genet A (2014)

Pathways from Autism Spectrum Disorder (ASD) Diagnosis to Genetic Testing

द्वारा Barton, Krysta S., Tabor, Holly K., Starks, Helene, Garrison, Nanibaa’ A., Laurino, Mercy, Burke, Wylie
में प्रकाशित Genet Med (2017)

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

द्वारा Yu, Joon-Ho, Harrell, Tanya M., Jamal, Seema M., Tabor, Holly K., Bamshad, Michael J.
प्रकाशित 2014

Parent Perspectives on Pediatric Genetic Research and Implications for Genotype-driven Research Recruitment

द्वारा Tabor, Holly K., Brazg, Tracy, Crouch, Julia, Namey, Emily E., Fullerton, Stephanie M., Beskow, Laura M., Wilfond, Benjamin S.
प्रकाशित 2011

“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

द्वारा Halley, Meghan C., Stanley, Talia, Maturi, Jay, Goldenberg, Aaron J., Bernstein, Jonathan A., Wheeler, Matthew T., Tabor, Holly K.
में प्रकाशित Genet Med (2021)

Single Nucleotide Polymorphism (SNP) Arrays and Unexpected Consanguinity: Considerations for Clinicians When Returning Results to Families

द्वारा Delgado, Fernanda, Tabor, Holly K., Chow, Penny M., Conta, Jessie H., Feldman, Kenneth W., Tsuchiya, Karen D., Beck, Anita E.
में प्रकाशित Genet Med (2014)

Practices and Policies of Clinical Exome Sequencing Providers: Analysis and Implications

द्वारा Jamal, Seema M., Yu, Joon-Ho, Chong, Jessica X., Dent, Karin M., Conta, Jessie H., Tabor, Holly K., Bamshad, Michael J.
प्रकाशित 2013

Informed Consent for Whole Genome Sequencing: A Qualitative Analysis of Participant Expectations and Perceptions of Risks, Benefits, and Harms

द्वारा Tabor, Holly K., Stock, Jacquie, Brazg., Tracy, McMillin, Margaret J., Dent., Karin M., Yu, Joon-Ho, Shendure, Jay, Bamshad, Michael J.
प्रकाशित 2012

RESEARCH PARTICIPANTS’ PERSPECTIVES ON GENOTYPE-DRIVEN RESEARCH RECRUITMENT

द्वारा Beskow, Laura M., Namey, Emily E., Cadigan, R. Jean, Brazg, Tracy, Crouch, Julia, Henderson, Gail E., Michie, Marsha, Nelson, Daniel K., Tabor, Holly K., Wilfond, Benjamin S.
प्रकाशित 2011

My46: a web-based tool for self-guided management of genomic test results in research and clinical settings

द्वारा Tabor, Holly K., Jamal, Seema M., Yu, Joon-Ho, Crouch, Julia M., Shankar, Aditi G., Dent, Karin M., Anderson, Nick, Miller, Damon A., Futral, Brett T., Bamshad, Michael J.
में प्रकाशित Genet Med (2016)

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

द्वारा Tabor, Holly K., Auer, Paul L., Jamal, Seema M., Chong, Jessica X., Yu, Joon-Ho, Gordon, Adam S., Graubert, Timothy A., O’Donnell, Christopher J., Rich, Stephen S., Nickerson, Deborah A., Bamshad, Michael J.
प्रकाशित 2014

Exome sequencing identifies the cause of a Mendelian disorder

द्वारा Ng, Sarah B., Buckingham, Kati J., Lee, Choli, Bigham, Abigail W., Tabor, Holly K., Dent, Karin M., Huff, Chad D., Shannon, Paul T., Jabs, Ethylin Wang, Nickerson, Deborah A., Shendure, Jay, Bamshad, Michael J.
प्रकाशित 2009

Gene discovery for Mendelian conditions via social networking: de novo variants in KDM1A cause developmental delay and distinctive facial features

द्वारा Chong, Jessica X., Yu, Joon-Ho, Lorentzen, Peter, Park, Karen M., Jamal, Seema M., Tabor, Holly K., Rauch, Anita, Saenz, Margarita Sifuentes, Boltshauser, Eugen, Patterson, Karynne E., Nickerson, Deborah A., Bamshad, Michael J.
में प्रकाशित Genet Med (2015)