Education and Knowledge in Pharmacogenomics: Still a Challenge? by Giri, Jyothsna, Curry, Timothy B., Formea, Christine M., Nicholson, Wayne T., Rohrer Vitek, Carolyn R.

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Pharmacogenomics education and perceptions: is there a gap between internal medicine resident and attending physicians? by Rohrer Vitek, Carolyn R, Giri, Jyothsna, Caraballo, Pedro J, Curry, Timothy B, Nicholson, Wayne T

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Healthcare provider education to support integration of pharmacogenomics in practice: the eMERGE Network experience by Rohrer Vitek, Carolyn R, Abul-Husn, Noura S, Connolly, John J, Hartzler, Andrea L, Kitchner, Terrie, Peterson, Josh F, Rasmussen, Luke V, Smith, Maureen E, Stallings, Sarah, Williams, Marc S, Wolf, Wendy A, Prows, Cynthia A

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Diagnostic yield of exome and genome sequencing after non-diagnostic multi-gene panels in patients with single-system diseases by Wilke, Matheus V M B, Klee, Eric W, Dhamija, Radhika, Fervenza, Fernando C, Thomas, Brittany, Leung, Nelson, Hogan, Marie C, Hager, Megan M, Kolbert, Kayla J, Kemppainen, Jennifer L, Loftus, Elle C, Leitzen, Katie M, Vitek, Carolyn R, McAllister, Tammy, Lazaridis, Konstantinos N, Pinto E Vairo, Filippo

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Implementing individualized medicine into the medical practice by Lazaridis, Konstantinos N., MCAllister, Tammy M., Babovic-Vuksanovic, Dusica, Beck, Scott A., Borad, Mitesh J., Bryce, Alan H., Chanan-Khan, Asher A., Ferber, Matthew J., Fonseca, Rafael, Johnson, Kiley J., Klee, Eric W., Lindor, Noralane M., MCCormick, Jennifer B., MCWilliams, Robert R., Parker, Alexander S., Riegert-Johnson, Douglas L., Rohrer Vitek, Carolyn R., Schahl, Kimberly A., Schultz, Cloann, Stewart, Keith, Then, George C., Wieben, Eric D., Farrugia, Gianrico

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Practical considerations for implementing genomic information resources. Experiences from eMERGE and CSER by Rasmussen, Luke V, Overby, Casey L, Connolly, John, Chute, Christopher G, Denny, Joshua C, Freimuth, Robert, Hartzler, Andrea L, Holm, Ingrid A, Manzi, Shannon, Pathak, Jyotishman, Peissig, Peggy L, Smith, Maureen, Williams, Marc S, Shirts, Brian H, Stoffel, Elena M, Tarczy-Hornoch, Peter, Rohrer Vitek, Carolyn R, Wolf, Wendy A, Starren, Justin

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Cohort Profile: The Right Drug, Right Dose, Right Time: Using Genomic Data to Individualize Treatment Protocol (RIGHT Protocol) by Bielinski, Suzette J, St Sauver, Jennifer L, Olson, Janet E, Larson, Nicholas B, Black, John L, Scherer, Steven E, Bernard, Matthew E, Boerwinkle, Eric, Borah, Bijan J, Caraballo, Pedro J, Curry, Timothy B, Doddapaneni, HarshaVardhan, Formea, Christine M, Freimuth, Robert R, Gibbs, Richard A, Giri, Jyothsna, Hathcock, Matthew A, Hu, Jianhong, Jacobson, Debra J, Jones, Leila A, Kalla, Sara, Koep, Tyler H, Korchina, Viktoriya, Kovar, Christie L, Lee, Sandra, Liu, Hongfang, Matey, Eric T, McGree, Michaela E, McAllister, Tammy M, Moyer, Ann M, Muzny, Donna M, Nicholson, Wayne T, Oyen, Lance J, Qin, Xiang, Raj, Ritika, Roger, Véronique L, Rohrer Vitek, Carolyn R, Ross, Jason L, Sharp, Richard R, Takahashi, Paul Y, Venner, Eric, Walker, Kimberly, Wang, Liwei, Wang, Qiaoyan, Wright, Jessica A, Wu, Tsung-Jung, Wang, Liewei, Weinshilboum, Richard M

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Nine-gene pharmacogenomics profile service: The Mayo Clinic experience by Matey, Eric T., Ragan, Ashley Kate, Oyen, Lance J., Vitek, Carolyn R., Aoudia, Stacy L., Ragab, Ahmed K., Fee-Schroeder, Kelliann C., Black, John L., Moyer, Ann M., Nicholson, Wayne T., Shrestha, Sofia, McAllister, Tammy M., Sinnwell, Jason P., Faubion, Stephanie S., Lazaridis, Konstantinos N.

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Semiautomated approach focused on new genomic information results in time and effort-efficient reannotation of negative exome data by Ferrer, Alejandro, Duffy, Patrick, Olson, Rory J., Meiners, Michael A., Schultz-Rogers, Laura, Macke, Erica L., Safgren, Stephanie, Morales-Rosado, Joel A., Cousin, Margot A., Oliver, Gavin R., Rider, David, Williams, Megan, Pichurin, Pavel N., Deyle, David R., Morava, Eva, Gavrilova, Ralitza H., Dhamija, Radhika, Wierenga, Klass J., Lanpher, Brendan C., Babovic-Vuksanovic, Dusica, Kaiwar, Charu, Vitek, Carolyn R., McAllister, Tammy M., Wick, Myra J., Schimmenti, Lisa A., Lazaridis, Konstantinos N., Vairo, Filippo Pinto e, Klee, Eric W.

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Evaluation of the use of clinical decision support and online resources for pharmacogenomics education by Rohrer Vitek, Carolyn R, Nicholson, Wayne T, Schultz, Cloann, Caraballo, Pedro J

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An assessment of patient perspectives on pharmacogenomics educational materials by Asiedu, Gladys B, Finney Rutten, Lila J, Agunwamba, Amenah, Bielinski, Suzette J, St Sauver, Jennifer L, Olson, Janet E, Rohrer Vitek, Carolyn R

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Return of Genomic Results to Research Participants: The Floor, the Ceiling, and the Choices In Between by Berg, Jonathan S., Brothers, Kyle, Clayton, Ellen W., Chung, Wendy, Evans, Barbara J., Evans, James P., Fullerton, Stephanie M., Gallego, Carlos J., Garrison, Nanibaa’ A., Gray, Stacy W., Holm, Ingrid A., Kullo, Iftikhar J., Lehmann, Lisa Soleymani, McCarty, Cathy, Prows, Cynthia A., Rehm, Heidi L., Sharp, Richard R., Salama, Joseph, Sanderson, Saskia, Wolf, Wendy A., Myers, Melanie, Vinks, Sander, Crosslin, David, Leppig, Kathy, Wicklund, Cathy, Chute, Christopher, Lynch, John, De Andrade, Mariza, Heit, John, Brilliant, Murray, Kitchner, Terrie, Ritchie, Marylyn, Persell, Stephen, Rasmussen-Torvik, Laura, McGregor, Tracy, Antommaria, Armand, Chiavacci, Rosetta, Ledbetter, David, Williams, Janet, Hartzler, Andrea, Vitek, Carolyn R. Rohrer, Frost, Norm, Ferryman, Kadija, Horowitz, Carol, Zinberg, Randi, Pan, Vivian, Long, Rochelle, Ramos, Erin, Odgis, Jackie, Wise, Anastasia, Hull, Sara, Gitlin, Jonathan, Green, Robert, Metterville, Danielle, McGuire, Amy, Kong, Sek Won, Trinidad, Sue, Veenstra, David, Roche, Myra, Skinner, Debra, Raspberry, Kelly, O’Daniel, Julianne, Parsons, Will, Eng, Christine, Hilsenbeck, Susan, Karavite, Dean, Conlin, Laura, Spinner, Nancy, Krantz, Ian, Falk, Marni, Santani, Avni, Dechene, Elizabeth, Bernhardt, Barbara, Schuetze, Scott, Everett, Jessica, Gornick, Michele Caroline, Wilfond, Ben, Tabor, Holly, Lemke, Amy A., Goddard, Katrina, East, Kelly, Barsh, Greg, Koenig, Barbara, Van Allen, Eliezer, Garber, Judy, Zawati, Ma’n, Lewis, Michelle, Savage, Sarah, Smith, Maureen, Roychowdhury, Sameek, Anan, Charlisse Caga, Hindorff, Lucia, Hutter, Carolyn, King, Rosalind, Li, Rongling, Lockhart, Nicole, McEwen, Jean, Scholes, Derek, Sun, Kathie, Burke, Wylie

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Distribution of Chromosome-Arm Specific Telomere Length in Patients with Telomere Biology Disorders by Ferrer, Alejandro, Stephens, Zachary D, Geyer, Susan M., Simon, Rachel A, Lasho, Terra L, Finke, Christy M, Burnap, Brittany, Mulvihill, Lindsay A, McAllister, Tammy M, Rohrer Vitek, Carolyn R., Lazaridis, Konstantinos N, Jain, Angita, Klee, Eric W, Kocher, Jean-Pierre A, Patnaik, Mrinal M.

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Functional Testing of Variants of Uncertain Significance in TERC, TERT,and RTEL1 from Adult Patients with Telomere Biology Disorders by Simon, Rachel A, Finke, Christy M, Lasho, Terra L, Schmitz, Christopher T., Fernandez, Jenna A, Carmona-Porquera, Eva M, Wylam, Mark E, Witzig, Thomas E., McAllister, Tammy M, Rohrer Vitek, Carolyn R., Lazaridis, Konstantinos N, Mangaonkar, Abhishek A, Patnaik, Mrinal M., Ferrer, Alejandro

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Implementation of genomic medicine for rare disease in a tertiary healthcare system: Mayo Clinic Program for Rare and Undiagnosed Diseases (PRaUD) by Pinto E Vairo, Filippo, Kemppainen, Jennifer L, Vitek, Carolyn R Rohrer, Whalen, Denise A, Kolbert, Kayla J, Sikkink, Kaitlin J, Kroc, Sarah A, Kruisselbrink, Teresa, Shupe, Gabrielle F, Knudson, Alyssa K, Burke, Elizabeth M, Loftus, Elle C, Bandel, Lorelei A, Prochnow, Carri A, Mulvihill, Lindsay A, Thomas, Brittany, Gable, Dale M, Graddy, Courtney B, Garzon, Giovanna G Moreno, Ekpoh, Idara U, Porquera, Eva M Carmona, Fervenza, Fernando C, Hogan, Marie C, El Ters, Mireille, Warrington, Kenneth J, Davis, 3rd, John M, Koster, Matthew J, Orandi, Amir B, Basiaga, Matthew L, Vella, Adrian, Kumar, Seema, Creo, Ana L, Lteif, Aida N, Pittock, Siobhan T, Tebben, Peter J, Abate, Ejigayehu G, Joshi, Avni Y, Ristagno, Elizabeth H, Patnaik, Mrinal S, Schimmenti, Lisa A, Dhamija, Radhika, Sabrowsky, Sonia M, Wierenga, Klaas J, Keddis, Mira T, Samadder, Niloy Jewel J, Presutti, Richard J, Robinson, Steven I, Stephens, Michael C, Roberts, Lewis R, Faubion, Jr, William A, Driscoll, Sherilyn W, Wong-Kisiel, Lily C, Selcen, Duygu, Flanagan, Eoin P, Ramanan, Vijay K, Jackson, Lauren M, Mauermann, Michelle L, Ortega, Victor E, Anderson, Sarah A, Aoudia, Stacy L, Klee, Eric W, McAllister, Tammy M, Lazaridis, Konstantinos N

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Are patients willing to incur out-of-pocket costs for pharmacogenomic testing? by Bielinski, S J, St Sauver, J L, Olson, J E, Wieland, M L, Vitek, C R, Bell, E J, Mc Gree, M E, Jacobson, D J, McCormick, J B, Takahashi, P Y, Black, J L, Caraballo, P J, Sharp, R R, Beebe, T J, Weinshilboum, R M, Wang, L, Roger, V L

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Correction: Implementation of genomic medicine for rare disease in a tertiary healthcare system: Mayo Clinic Program for Rare and Undiagnosed Diseases (PRaUD) by Pinto E Vairo, Filippo, Kemppainen, Jennifer L, Vitek, Carolyn R Rohrer, Whalen, Denise A, Kolbert, Kayla J, Sikkink, Kaitlin J, Kroc, Sarah A, Kruisselbrink, Teresa, Shupe, Gabrielle F, Knudson, Alyssa K, Burke, Elizabeth M, Loftus, Elle C, Bandel, Lorelei A, Prochnow, Carri A, Mulvihill, Lindsay A, Thomas, Brittany, Gable, Dale M, Graddy, Courtney B, Garzon, Giovanna G Moreno, Ekpoh, Idara U, Porquera, Eva M Carmona, Fervenza, Fernando C, Hogan, Marie C, El Ters, Mireille, Warrington, Kenneth J, Davis, 3rd, John M, Koster, Matthew J, Orandi, Amir B, Basiaga, Matthew L, Vella, Adrian, Kumar, Seema, Creo, Ana L, Lteif, Aida N, Pittock, Siobhan T, Tebben, Peter J, Abate, Ejigayehu G, Joshi, Avni Y, Ristagno, Elizabeth H, Patnaik, Mrinal S, Schimmenti, Lisa A, Dhamija, Radhika, Sabrowsky, Sonia M, Wierenga, Klaas J, Keddis, Mira T, Samadder, Niloy Jewel J, Presutti, Richard J, Robinson, Steven I, Stephens, Michael C, Roberts, Lewis R, Faubion, Jr, William A, Driscoll, Sherilyn W, Wong-Kisiel, Lily C, Selcen, Duygu, Flanagan, Eoin P, Ramanan, Vijay K, Jackson, Lauren M, Mauermann, Michelle L, Ortega, Victor E, Anderson, Sarah A, Aoudia, Stacy L, Klee, Eric W, McAllister, Tammy M, Lazaridis, Konstantinos N

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Practical considerations for implementing genomic information resources by Rasmussen, Luke V., Overby, Casey L., Connolly, John, Chute, Christopher G., Denny, Joshua C., Freimuth, Robert R., Hartzler, Andrea L., Holm, Ingrid A., Manzi, Shannon, Pathak, Jyotishman, Peissig, Peggy L., Smith, Maureen, Williams, Marc S., Shirts, Brian H., Stoffel, Elena M., Tarczy-Hornoch, Peter, Vitek, Carolyn R. Rohrer, Wolf, Wendy A., Starren, Justin

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