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

Bằng Yu, Joon-Ho, Jamal, Seema M., Tabor, Holly K., Bamshad, Michael J.
Được phát hành 2013

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

Bằng Yu, Joon-Ho, Crouch, Julia, Jamal, Seema M., Tabor, Holly K., Bamshad, Michael J.
Được phát hành 2013

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

Bằng Yu, Joon-Ho, Crouch, Julia, Jamal, Seema M., Bamshad, Michael J., Tabor, Holly K.
Xuất bản năm Am J Med Genet A (2014)

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

Bằng Yu, Joon-Ho, Harrell, Tanya M., Jamal, Seema M., Tabor, Holly K., Bamshad, Michael J.
Được phát hành 2014

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

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

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

Bằng 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.
Xuất bản năm Genet Med (2016)

Genotype Prediction of Adult Type 2 Diabetes From Adolescence in a Multiracial Population

Bằng Vassy, Jason L., DasMahapatra, Pronabesh, Meigs, James B., Schork, Nicholas J., Magnussen, Costan G., Chen, Wei, Raitakari, Olli T., Pencina, Michael J., Jamal, Seema M., Berenson, Gerald S., Goodman, Elizabeth
Được phát hành 2012

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

Bằng 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.
Được phát hành 2014

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

Bằng 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.
Xuất bản năm Genet Med (2015)

Reappraisal of Reported Genes for Sudden Arrhythmic Death: Evidence-Based Evaluation of Gene Validity for Brugada Syndrome

Bằng Hosseini, S. Mohsen, Kim, Raymond, Udupa, Sharmila, Costain, Gregory, Jobling, Rebekah, Liston, Eriskay, Jamal, Seema M., Szybowska, Marta, Morel, Chantal F., Bowdin, Sarah, Garcia, John, Care, Melanie, Sturm, Amy C., Novelli, Valeria, Ackerman, Michael J., Ware, James S., Hershberger, Ray E., Wilde, Arthur A.M., Gollob, Michael H.
Xuất bản năm Circulation (2018)

Approaches to carrier testing and results disclosure in translational genomics research: The clinical sequencing exploratory research consortium experience

Bằng Porter, Kathryn M., Kauffman, Tia L., Koenig, Barbara A., Lewis, Katie L., Rehm, Heidi L., Richards, Carolyn Sue, Strande, Natasha T., Tabor, Holly K., Wolf, Susan M., Yang, Yaping, Amendola, Laura M., Azzariti, Danielle R., Berg, Jonathan S., Bergstrom, Katie, Biesecker, Leslie G., Biswas, Sawona, Bowling, Kevin M., Chung, Wendy K., Clayton, Ellen W., Conlin, Laura K., Cooper, Gregory M., Dulik, Matthew C., Garraway, Levi A., Ghazani, Arezou A., Green, Robert C., Hiatt, Susan M., Jamal, Seema M., Jarvik, Gail P., Goddard, Katrina A. B., Wilfond, Benjamin S.
Xuất bản năm Mol Genet Genomic Med (2018)

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

Bằng Amendola, Laura M., Dorschner, Michael O., Robertson, Peggy D., Salama, Joseph S., Hart, Ragan, Shirts, Brian H., Murray, Mitzi L., Tokita, Mari J., Gallego, Carlos J., Kim, Daniel Seung, Bennett, James T., Crosslin, David R., Ranchalis, Jane, Jones, Kelly L., Rosenthal, Elisabeth A., Jarvik, Ella R., Itsara, Andy, Turner, Emily H., Herman, Daniel S., Schleit, Jennifer, Burt, Amber, Jamal, Seema M., Abrudan, Jenica L., Johnson, Andrew D., Conlin, Laura K., Dulik, Matthew C., Santani, Avni, Metterville, Danielle R., Kelly, Melissa, Foreman, Ann Katherine M., Lee, Kristy, Taylor, Kent D., Guo, Xiuqing, Crooks, Kristy, Kiedrowski, Lesli A., Raffel, Leslie J., Gordon, Ora, Machini, Kalotina, Desnick, Robert J., Biesecker, Leslie G., Lubitz, Steven A., Mulchandani, Surabhi, Cooper, Greg M., Joffe, Steven, Richards, C. Sue, Yang, Yaoping, Rotter, Jerome I., Rich, Stephen S., O’Donnell, Christopher J., Berg, Jonathan S., Spinner, Nancy B., Evans, James P., Fullerton, Stephanie M., Leppig, Kathleen A., Bennett, Robin L., Bird, Thomas, Sybert, Virginia P., Grady, William M., Tabor, Holly K., Kim, Jerry H., Bamshad, Michael J., Wilfond, Benjamin, Motulsky, Arno G., Scott, C. Ronald, Pritchard, Colin C., Walsh, Tom D., Burke, Wylie, Raskind, Wendy H., Byers, Peter, Hisama, Fuki M., Rehm, Heidi, Nickerson, Debbie A., Jarvik, Gail P.
Xuất bản năm Genome Res (2015)