Variant Classification Concordance using the ACMG-AMP Variant Interpretation Guidelines across Nine Genomic Implementation Research Studies
Amendola, Laura M., Muenzen, Kathleen, Biesecker, Leslie G., Bowling, Kevin M., Cooper, Greg M., Dorschner, Michael O., Driscoll, Catherine, Foreman, Ann Katherine M., Golden-Grant, Katie, Greally, John M., Hindorff, Lucia, Kanavy, Dona, Jobanputra, Vaidehi, Johnston, Jennifer J., Kenny, Eimear E., McNulty, Shannon, Murali, Priyanka, Ou, Jeffrey, Powell, Bradford C., Rehm, Heidi L., Rolf, Bradley, Roman, Tamara S., Van Ziffle, Jessica, Guha, Saurav, Abhyankar, Avinash, Crosslin, David, Venner, Eric, Yuan, Bo, Zouk, Hana, Jarvik, Gail P.
Published in American journal of human genetics (05.11.2020)
Published in American journal of human genetics (05.11.2020)
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Journal Article
Medical interpreter‐mediated genetic counseling for Spanish preferring adults at risk for a hereditary cancer syndrome
Joseph, Galen, Lindberg, Nangel M., Guerra, Claudia, Hernandez, Cindy, Karliner, Leah S., Gilmore, Marian J., Zepp, Jamilyn, Rolf, Bradley A., Caruncho, Mikaella, Riddle, Leslie, Kauffman, Tia L., Leo, Michael C., Wilfond, Benjamin S.
Published in Journal of genetic counseling (01.08.2023)
Published in Journal of genetic counseling (01.08.2023)
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Journal Article
Spinal cord‐predominant neuropathology in an adult‐onset case of POLR3A‐related spastic ataxia
Sytsma, Trevor M., Chen, Dong‐Hui, Rolf, Bradley, Dorschner, Michael, Jayadev, Suman, Keene, C. Dirk, Zhang, Jing, Bird, Thomas D., Latimer, Caitlin S.
Published in Neuropathology (01.02.2022)
Published in Neuropathology (01.02.2022)
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Journal Article
An accessible, relational, inclusive, and actionable (ARIA) model of genetic counseling compared with usual care: Results of a randomized controlled trial
Joseph, Galen, Leo, Michael C., Riddle, Leslie, Guerra, Claudia, Amendola, Laura M., Gilmore, Marian J., Rolf, Bradley A., Dorschner, Michael O., Zepp, Jamilyn, Biesecker, Barbara B., Caruncho, Mikaella, Hunter, Jessica Ezzell, Keast, Erin, Lewis, Hannah S., Duenas, Devan, Kauffman, Tia, Bulkley, Joanna E., Anderson, Katherine P., Jarvik, Gail P., Goddard, Katrina A.B., Wilfond, Benjamin S.
Published in Genetics in medicine (01.11.2022)
Published in Genetics in medicine (01.11.2022)
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Journal Article
ORCA, a values-based decision aid for selecting additional findings from genomic sequencing in adults: Efficacy results from a randomized trial
Liles, Elizabeth G., Leo, Michael C., Freed, Amanda S., Porter, Kathryn M., Zepp, Jamilyn M., Kauffman, Tia L., Keast, Erin, McMullen, Carmit K., Gruß, Inga, Biesecker, Barbara B., Muessig, Kristin R., Eubanks, Donna J., Amendola, Laura M., Dorschner, Michael O., Rolf, Bradley A., Jarvik, Gail P., Goddard, Katrina A.B., Wilfond, Benjamin S.
Published in Genetics in medicine (01.08.2022)
Published in Genetics in medicine (01.08.2022)
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Journal Article
The motivation and process for developing a consortium‐wide time and motion study to estimate resource implications of innovations in the use of genome sequencing to inform patient care
Hoban, Hannah G., Yip, Tiffany A., Chau, Joanna C., Bensen, Jeannette T., Desrosiers, Lauren R., Finnila, Candice R., Hindorff, Lucia A., Kelly, Nicole R., Lynch, Frances L., Rolf, Bradley A., Smith, Hadley S., Wasserstein, Melissa P., Hassmiller Lich, Kristen
Published in Clinical and translational science (01.01.2024)
Published in Clinical and translational science (01.01.2024)
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Journal Article
Cancer Health Assessments Reaching Many (CHARM): A clinical trial assessing a multimodal cancer genetics services delivery program and its impact on diverse populations
Mittendorf, Kathleen F., Kauffman, Tia L., Amendola, Laura M., Anderson, Katherine P., Biesecker, Barbara B., Dorschner, Michael O., Duenas, Devan M., Eubanks, Donna J., Feigelson, Heather Spencer, Gilmore, Marian J., Hunter, Jessica Ezzell, Joseph, Galen, Kraft, Stephanie A., Lee, Sandra Soo Jin, Leo, Michael C., Liles, Elizabeth G., Lindberg, Nangel M., Muessig, Kristin R., Okuyama, Sonia, Porter, Kathryn M., Riddle, Leslie S., Rolf, Bradley A., Rope, Alan F., Zepp, Jamilyn M., Jarvik, Gail P., Wilfond, Benjamin S., Goddard, Katrina A.B.
Published in Contemporary clinical trials (01.07.2021)
Published in Contemporary clinical trials (01.07.2021)
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Journal Article
Improving Care for Marginalized Populations at Risk for Hereditary Cancer Syndromes: Innovations that Expanded Reach in the CHARM Study
Gilmore, Marian J., Knerr, Sarah, Kraft, Stephanie A., Bulkley, Joanna E., Biesecker, Barbara B., Feigelson, Heather Spencer, Hunter, Jessica Ezzell, Jenkins, Charisma L., Kauffman, Tia L., Lee, Sandra Soo-Jin, Liles, Elizabeth G., Mittendorf, Kathleen F., Muessig, Kristin R., Porter, Kathryn M., Rolf, Bradley A., Rope, Alan F., Zepp, Jamilyn M., Anderson, Katherine Patrice, Devine, Beth, Joseph, Galen, Leo, Michael C., Goddard, Katrina, Wilfond, Benjamin S.
Published in Public health genomics (01.01.2024)
Published in Public health genomics (01.01.2024)
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Journal Article
A review and definition of ‘usual care’ in genetic counseling trials to standardize use in research
Biesecker, Barbara B., Lillie, Sarah E., Amendola, Laura M., Donohue, Katherine E., East, Kelly M., Foreman, Ann Katherine M., Gilmore, Marian J., Greve, Veronica, Liangolou, Billie, O'Daniel, Julianne M., Odgis, Jacqueline A., Rego, Shannon, Rolf, Bradley, Scollon, Sarah, Suckiel, Sabrina A., Zepp, Jamilyn, Joseph, Galen
Published in Journal of genetic counseling (01.02.2021)
Published in Journal of genetic counseling (01.02.2021)
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Journal Article
Barriers to family history knowledge and family communication among LGBTQ+ individuals in the context of hereditary cancer risk assessment
Rolf, Bradley A., Schneider, Jennifer L., Amendola, Laura M., Davis, James V., Mittendorf, Kathleen F., Schmidt, Mark A., Jarvik, Gail P., Wilfond, Benjamin S., Goddard, Katrina A. B., Ezzell Hunter, Jessica
Published in Journal of genetic counseling (01.02.2022)
Published in Journal of genetic counseling (01.02.2022)
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Journal Article
Assessment of a Peer Physician Coaching Partnership Between a Designated Cancer Center Genetics Service and a Community Cancer Network Hospital
Santos, Lauren G, Buzdnitskaya, Tatyana, Rolf, Bradley A, Souza, William, Sienko, Mark, Ruiz-Bonilla, Jose Alberto, Shah, Binay, Jewell, Patrick, Jensen, Lindsay, Horike-Pyne, Martha, Elrod, Jo Ann, Crews, Jennie, Laurino, Mercy, Weeks, Kevin Austin, Dubard-Gault, Marianne E
Published in JAMA network open (01.03.2023)
Published in JAMA network open (01.03.2023)
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Journal Article
Corrigendum to “Cancer Health Assessments Reaching Many (CHARM): A clinical trial assessing a multimodal cancer genetics services delivery program and its impact on diverse populations” [Contemporary Clinical Trials 106 (2021) 106432]
Mittendorf, Kathleen F., Kauffman, Tia L., Amendola, Laura M., Anderson, Katherine P., Biesecker, Barbara B., Dorschner, Michael O., Duenas, Devan M., Eubanks, Donna J., Feigelson, Heather Spencer, Gilmore, Marian J., Hunter, Jessica Ezzell, Joseph, Galen, Kraft, Stephanie A., Lee, Sandra Soo Jin, Leo, Michael C., Liles, Elizabeth G., Lindberg, Nangel M., Muessig, Kristin R., Okuyama, Sonia, Porter, Kathryn M., Riddle, Leslie S., Rolf, Bradley A., Rope, Alan F., Zepp, Jamilyn M., Jarvik, Gail P., Wilfond, Benjamin S., Goddard, Katrina A.B.
Published in Contemporary clinical trials (01.03.2022)
Published in Contemporary clinical trials (01.03.2022)
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Journal Article
Most people share genetic test results with relatives even if the findings are normal: Family communication in a diverse population
Hunter, Jessica E., Riddle, Leslie, Joseph, Galen, Amendola, Laura M., Gilmore, Marian J., Zepp, Jamilyn M., Shuster, Elizabeth, Bulkley, Joanna E., Muessig, Kristin R., Anderson, Katherine P., Goddard, Katrina A.B., Wilfond, Benjamin S., Leo, Michael C., Allen, Jake, Angelo, Frank, Arnold, Briana L., Bellcross, Cecelia, Bendelow, Tiffany, B, Barbara, Biesecker, Breslin, Kristin D., Booker, Kristina F., Caruncho, Mikaella, Davis, James V., Deutsch, Sonia, Devine, Beth, Dorschner, Michael O., Duenas, Devan, Eubanks, Donna J., Feigelson, Heather Spencer, Freed, Amanda S., Greaney, Clay, Gruß, Inga, Guerra, Claudia, Guo, Boya, Holup, Joan, Ingphakorn, Chalinya L., Jackson, Paige, Jarvik, Gail P., Jenkins, Charisma L., Karliner, Leah S., Kaufmann, Tia, Keast, Erin, Knerr, Sarah, Koomas, Alyssa H., Kraft, Stephanie A., Lee, Mi H., Lee, Robin, Soo-Jin Lee, Sandra, Lewis, Hannah S., Liles, Elizabeth G., Lindberg, Nangel M., Lynch, Frances, McMullen, Carmit K., Medina, Elizabeth, Mittendorf, Kathleen F., Muessig, Kristin R., Okuyama, Sonia, Peterson, C. Samuel, Paolucci, Angela R., Perez, Rosse Rodriguez, Porter, Kathryn M., Ransom, Chelese L., Reyes, Ana, Robinson, Sperry, Rolf, Bradley A., Rope, Alan F., Schield, Emily, Schneider, Jennifer L., Shipman, Kelly J., Shirts, Brian H., Shuster, Elizabeth, Syngal, Sapna, Torgrimson-Ojerio, Britta N., Ukaegbu, Chinedu, Vandermeer, Meredith L., Varga, Alexandra M., Veenstra, David L., Whitebirch, W. Chris, Lee White, Larissa
Published in Genetics in medicine (01.11.2023)
Published in Genetics in medicine (01.11.2023)
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Journal Article
Laboratory-related outcomes from integrating an accessible delivery model for hereditary cancer risk assessment and genetic testing in populations with barriers to access
Amendola, Laura M., Shuster, Elizabeth, Leo, Michael C., Dorschner, Michael O., Rolf, Bradley A., Shirts, Brian H., Gilmore, Marian J., Okuyama, Sonia, Zepp, Jamilyn M., Kauffman, Tia L., Mittendorf, Kathleen F., Bellcross, Cecilia, Jenkins, Charisma L., Joseph, Galen, Riddle, Leslie, Syngal, Sapna, Ukaegbu, Chinedu, Goddard, Katrina A.B., Wilfond, Benjamin S., Jarvik, Gail P., Allen, Jake, Amendola, Laura M., Anderson, Katherine P., Angelo, Frank, Arnold, Briana L., Bellcross, Cecelia, Bendelow, Tiffany, Biesecker, Barbara B., Breslin, Kristin D., Bulkley, Joanna E., Booker, Kristina F., Caruncho, Mikaella, Davis, James V., Deutsch, Sonia, Devine, Beth, Dorschner, Michael O., Duenas, Devan M., Eubanks, Donna J., Feigelson, Heather Spencer, Freed, Amanda S., Gilmore, Marian J., Goddard, Katrina A.B., Greaney, Clay, Gruß, Inga, Guerra, Claudia, Guo, Boya, Holup, Joan, Hunter, Jessica Ezzell, Ingphakorn, Chalinya L., Jackson, Paige, Jarvik, Gail P., Jenkins, Charisma L., Joseph, Galen, Karliner, Leah S., Kauffman, Tia L., Keast, Erin, Knerr, Sarah, Koomas, Alyssa H., Kraft, Stephanie A., Lee, Mi H., Lee, Robin, Soo-Jin Lee, Sandra, Leo, Michael C., Lewis, Hannah S., Liles, Elizabeth G., Lindberg, Nangel M., Lynch, Frances, McMullen, Carmit K., Medina, Elizabeth, Mittendorf, Kathleen F., Muessig, Kristin R., Okuyama, Sonia, Peterson, C. Samuel, Paolucci, Angela R., Perez, Rosse Rodriguez, Porter, Kathryn M., Ransom, Chelese L., Reyes, Ana, Riddle, Leslie S., Robinson, Sperry, Rolf, Bradley A., Rope, Alan F., Schield, Emily, Schneider, Jennifer L., Shipman, Kelly J., Shirts, Brian H., Shuster, Elizabeth, Syngal, Sapna, Torgrimson-Ojerio, Britta N., Ukaegbu, Chinedu, Vandermeer, Meredith L., Varga, Alexandra M., Veenstra, David L., Whitebirch, W. Chris, Lee White, Larissa, Wilfond, Benjamin S., Zepp, Jamilyn M.
Published in Genetics in medicine (01.06.2022)
Published in Genetics in medicine (01.06.2022)
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Journal Article
Evaluation of mailed results versus telephone disclosure of normal cancer genetic test results in a low-risk underserved population
Gilmore, Marian J, Leo, Michael C, Amendola, Laura M, Goddard, Katrina A B, Hunter, Jessica Ezzell, Joseph, Galen, Kauffman, Tia L, Rolf, Bradley, Shuster, Elizabeth, Zepp, Jamilyn M, Wilfond, Benjamin S, Biesecker, Barbara B
Published in Translational behavioral medicine (01.07.2024)
Published in Translational behavioral medicine (01.07.2024)
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Journal Article
Spinal cord-predominant neuropathology in an adult-onset case of POLR3A-related spastic ataxia
Sytsma, Trevor M, Chen, Dong-Hui, Rolf, Bradley, Dorschner, Michael, Jayadev, Suman, Keene, C Dirk, Zhang, Jing, Bird, Thomas D, Latimer, Caitlin S
Published in Neuropathology : official journal of the Japanese Society of Neuropathology (01.02.2022)
Published in Neuropathology : official journal of the Japanese Society of Neuropathology (01.02.2022)
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