Antineoplastic drugs sulindac sulfide and sulfone inhibit cell growth by inducing apoptosis von PIAZZA, G. A, KULCHAK RAHM, A. L, AHNEN, D. J, KRUTZSCH, M, SPERL, G, PARANKA, N. S, GROSS, P. H, BRENDEL, K, BURT, R. W, ALBERTS, D. S, PAMUKCU, R

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Alternate Service Delivery Models in Cancer Genetic Counseling: A Mini-Review von Buchanan, Adam Hudson, Rahm, Alanna Kulchak, Williams, Janet L

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Barriers, facilitators, and solutions to familial hypercholesterolemia treatment von Jones, Laney K., Sturm, Amy C., Seaton, Terry L., Gregor, Christina, Gidding, Samuel S., Williams, Marc S., Rahm, Alanna Kulchak

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A Model for Genome-First Care: Returning Secondary Genomic Findings to Participants and Their Healthcare Providers in a Large Research Cohort von Schwartz, Marci L.B., McCormick, Cara Zayac, Lazzeri, Amanda L., Lindbuchler, D’Andra M., Hallquist, Miranda L.G., Manickam, Kandamurugu, Buchanan, Adam H., Rahm, Alanna Kulchak, Giovanni, Monica A., Frisbie, Lauren, Flansburg, Carroll N., Davis, F. Daniel, Sturm, Amy C., Nicastro, Christine, Lebo, Matthew S., Mason-Suares, Heather, Mahanta, Lisa Marie, Carey, David J., Williams, Janet L., Williams, Marc S., Ledbetter, David H., Faucett, W. Andrew, Murray, Michael F.

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Clinical outcomes of a genomic screening program for actionable genetic conditions von Buchanan, Adam H., Lester Kirchner, H., Schwartz, Marci L. B., Kelly, Melissa A., Schmidlen, Tara, Jones, Laney K., Hallquist, Miranda L. G., Rocha, Heather, Betts, Megan, Schwiter, Rachel, Butry, Loren, Lazzeri, Amanda L., Frisbie, Lauren R., Rahm, Alanna Kulchak, Hao, Jing, Willard, Huntington F., Martin, Christa L., Ledbetter, David H., Williams, Marc S., Sturm, Amy C.

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Development, Evaluation, and User Testing of a Decision-Making Toolkit to Promote Organizations to Implement Universal Tumor Screening for Lynch Syndrome von Kulchak Rahm, Alanna, Wolfinger, Tara, Salvati, Zachary M, Schneider, Jennifer L, Cragun, Deborah

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A RE-AIM Framework Analysis of DNA-Based Population Screening: Using Implementation Science to Translate Research Into Practice in a Healthcare System von Jones, Laney K, Strande, Natasha T, Calvo, Evan M, Chen, Jingheng, Rodriguez, Gabriela, McCormick, Cara Z, Hallquist, Miranda L G, Savatt, Juliann M, Rocha, Heather, Williams, Marc S, Sturm, Amy C, Buchanan, Adam H, Glasgow, Russell E, Martin, Christa L, Rahm, Alanna Kulchak

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Leukemia Risk in a Cohort of 3.9 Million Children with and without Down Syndrome von Marlow, Emily C., Ducore, Jonathan, Kwan, Marilyn L., Cheng, Stephanie Y., Bowles, Erin J.A., Greenlee, Robert T., Pole, Jason D., Rahm, Alanna Kulchak, Stout, Natasha K., Weinmann, Sheila, Smith-Bindman, Rebecca, Miglioretti, Diana L.

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Do research participants share genomic screening results with family members? von Wynn, Julia, Milo Rasouly, Hila, Vasquez‐Loarte, Tania, Saami, Akilan M., Weiss, Robyn, Ziniel, Sonja I., Appelbaum, Paul S., Wright Clayton, Ellen, Christensen, Kurt D., Fasel, David, Green, Robert C., Hain, Heather S., Harr, Margaret, Hoell, Christin, Kullo, Iftikhar J, Leppig, Kathleen A., Myers, Melanie F., Pacyna, Joel E., Perez, Emma F., Prows, Cynthia A., Kulchak Rahm, Alanna, Campbell‐Salome, Gemme, Sharp, Richard R., Smith, Maureen E, Wiesner, Georgia L., Williams, Janet L., Blout Zawatsky, Carrie L., Gharavi, Ali G., Chung, Wendy K., Holm, Ingrid A.

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Identifying factors and causal chains associated with optimal implementation of Lynch syndrome tumor screening: An application of coincidence analysis von Cragun, Deborah, Salvati, Zachary M., Schneider, Jennifer L., Burnett-Hartman, Andrea N., Epstein, Mara M., Hunter, Jessica Ezzell, Liang, Su-Ying, Lowery, Jan, Lu, Christine Y., Pawloski, Pamala A., Schlieder, Victoria, Sharaf, Ravi N., Williams, Marc S., Rahm, Alanna Kulchak

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“Go ahead and screen” - advice to healthcare systems for routine lynch syndrome screening from interviews with newly diagnosed colorectal cancer patients von Schneider, Jennifer L, Firemark, Alison J, Gille, Sara, Davis, James, Pawloski, Pamala A, Liang, Su-Ying, Epstein, Mara M, Lowery, Jan, Lu, Christine Y, Sharaf, Ravi N, Burnett-Hartman, Andrea N, Schlieder, Victoria, Salvati, Zachary M, Cragun, Deborah, Rahm, Alanna Kulchak, Hunter, Jessica Ezzell

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Developing Pharmacogenomic Reports: Insights from Patients and Clinicians von Jones, Laney K., Kulchak Rahm, Alanna, Gionfriddo, Michael R., Williams, Janet L., Fan, Audrey L., Pulk, Rebecca A., Wright, Eric A., Williams, Marc S.

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Returning Results in the Genomic Era: Initial Experiences of the eMERGE Network von Wiesner, Georgia L., Rahm, Alanna Kulchak, Appelbaum, Paul, Aufox, Sharon, Bland, Sarah T., Blout, Carrie L., Christensen, Kurt D., Chung, Wendy K., Clayton, Ellen Wright, Green, Robert C., Harr, Margaret H., Henrikson, Nora, Hoell, Christin, Holm, Ingrid A., Jarvik, Gail P., Kullo, Iftikhar J., Lammers, Philip E., Larson, Eric B., Lindor, Noralane M., Marasa, Maddalena, Myers, Melanie F., Peterson, Josh F., Prows, Cynthia A., Ralston, James D., Rasouly, Hila Milo, Sharp, Richard R., Smith, Maureen E., Van Driest, Sara L., Williams, Janet L., Williams, Marc S., Wynn, Julia, Leppig, Kathleen A.

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Applying theories, models, and frameworks to help genetic counselors and students achieve clinical and professional goals von Cragun, Deborah, Victoria, Lindsey, Bradbury, Angela R, Dean, Marleah, Hamilton, Jada G, Katz, Mira L, Rahm, Alanna Kulchak, Mack, Jennifer W, Resnicow, Ken, Kaphingst, Kimberly A

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Positive impact of genetic counseling assistants on genetic counseling efficiency, patient volume, and cost in a cancer genetics clinic von Hallquist, Miranda L. G., Tricou, Eric P., Hallquist, Michael N., Savatt, Juliann M., Rocha, Heather, Evans, Alyson E., Deckard, Nicole, Hu, Yirui, Kirchner, H. Lester, Pervola, Josie, Rahm, Alanna Kulchak, Rashkin, Misha, Schmidlen, Tara J., Schwartz, Marci L. B., Williams, Janet L., Williams, Marc S., Buchanan, Adam H.

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Prospective, multi-site study of healthcare utilization after actionable monogenic findings from clinical sequencing von Linder, Jodell E., Tao, Ran, Chung, Wendy K., Kiryluk, Krzysztof, Liu, Cong, Weng, Chunhua, Connolly, John J., Hakonarson, Hakon, Harr, Margaret, Leppig, Kathleen A., Jarvik, Gail P., Veenstra, David L., Aufox, Sharon, Chisholm, Rex L., Gordon, Adam S., Hoell, Christin, Rasmussen-Torvik, Laura J., Smith, Maureen E., Holm, Ingrid A., Miller, Erin M., Prows, Cynthia A., Elskeally, Omar, Kullo, Iftikhar J., Lee, Christopher, Jose, Sheethal, Manolio, Teri A., Rowley, Robb, Padi-Adjirackor, Nana Addo, Wilmayani, Ni Ketut, City, Brittany, Wei, Wei-Qi, Wiesner, Georgia L., Rahm, Alanna Kulchak, Williams, Janet L., Williams, Marc S., Peterson, Josh F.

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Exome Sequencing-Based Screening for BRCA1/2 Expected Pathogenic Variants Among Adult Biobank Participants von Manickam, Kandamurugu, Buchanan, Adam H, Schwartz, Marci L B, Hallquist, Miranda L G, Williams, Janet L, Rahm, Alanna Kulchak, Rocha, Heather, Savatt, Juliann M, Evans, Alyson E, Butry, Loren M, Lazzeri, Amanda L, Lindbuchler, D'Andra M, Flansburg, Carroll N, Leeming, Rosemary, Vogel, Victor G, Lebo, Matthew S, Mason-Suares, Heather M, Hoskinson, Derick C, Abul-Husn, Noura S, Dewey, Frederick E, Overton, John D, Reid, Jeffrey G, Baras, Aris, Willard, Huntington F, McCormick, Cara Z, Krishnamurthy, Sarath B, Hartzel, Dustin N, Kost, Korey A, Lavage, Daniel R, Sturm, Amy C, Frisbie, Lauren R, Person, T Nate, Metpally, Raghu P, Giovanni, Monica A, Lowry, Lacy E, Leader, Joseph B, Ritchie, Marylyn D, Carey, David J, Justice, Anne E, Kirchner, H Lester, Faucett, W Andrew, Williams, Marc S, Ledbetter, David H, Murray, Michael F

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A picture is worth a thousand words: advancing the use of visualization tools in implementation science through process mapping and matrix heat mapping von Salvati, Zachary M, Rahm, Alanna Kulchak, Williams, Marc S, Ladd, Ilene, Schlieder, Victoria, Atondo, Jamie, Schneider, Jennifer L, Epstein, Mara M, Lu, Christine Y, Pawloski, Pamala A, Sharaf, Ravi N, Liang, Su-Ying, Burnett-Hartman, Andrea N, Hunter, Jessica Ezzell, Burton-Akright, Jasmine, Cragun, Deborah

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IMPACT-FH Study for Implementing Innovative Family Communication and Cascade Testing Strategies for Familial Hypercholesterolemia von Jones, Laney K., Campbell-Salome, Gemme, Walters, Nicole L., Brangan, Andrew, Morgan, Kelly M., Tricou, Eric P., Lindsey Mills, Zoe T., McGowan, Mary P., Gidding, Samuel S., Johns, Alicia M., Kirchner, H. Lester, Rahm, Alanna Kulchak, Sturm, Amy C.

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Should Health Systems Share Genetic Findings With At-Risk Relatives When the Proband Is Deceased? Interviews With Individuals Diagnosed With Lynch Syndrome von Hunter, Jessica Ezzell, Schneider, Jennifer L, Firemark, Alison J, Davis, James V, Gille, Sara, Pawloski, Pamala A, Liang, Su-Ying, Schlieder, Victoria, Rahm, Alanna Kulchak

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