P704P, P712P, and P775P: A genomic cluster of prostate-specific genes von Stolk, John A., Jiang, Yuqiu, Day, Craig H., Klee, Jennifer I., Zhang, Xinqun, Dillon, Davin C., Houghton, Raymond L., Harlan, Dianne, Reed, Steven G., Xu, Jiangchun

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Compositions and methods for the therapy and diagnosis of lung cancer von KLEE JENNIFER I, HARLOCKER SUSAN L, WANG TONGTONG, SWITZER ANN, BANGUR CHAITANYA S

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Bi-allelic Alterations in AEBP1 Lead to Defective Collagen Assembly and Connective Tissue Structure Resulting in a Variant of Ehlers-Danlos Syndrome von Blackburn, Patrick R., Xu, Zhi, Tumelty, Kathleen E., Zhao, Rose W., Monis, William J., Harris, Kimberly G., Gass, Jennifer M., Cousin, Margot A., Boczek, Nicole J., Mitkov, Mario V., Cappel, Mark A., Francomano, Clair A., Parisi, Joseph E., Klee, Eric W., Faqeih, Eissa, Alkuraya, Fowzan S., Layne, Matthew D., McDonnell, Nazli B., Atwal, Paldeep S.

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Maple syrup urine disease: mechanisms and management von Blackburn, Patrick R, Gass, Jennifer M, Vairo, Filippo Pinto E, Farnham, Kristen M, Atwal, Herjot K, Macklin, Sarah, Klee, Eric W, Atwal, Paldeep S

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Major Impacts of Widespread Structural Variation on Gene Expression and Crop Improvement in Tomato von Alonge, Michael, Wang, Xingang, Benoit, Matthias, Soyk, Sebastian, Pereira, Lara, Zhang, Lei, Suresh, Hamsini, Ramakrishnan, Srividya, Maumus, Florian, Ciren, Danielle, Levy, Yuval, Harel, Tom Hai, Shalev-Schlosser, Gili, Amsellem, Ziva, Razifard, Hamid, Caicedo, Ana L., Tieman, Denise M., Klee, Harry, Kirsche, Melanie, Aganezov, Sergey, Ranallo-Benavidez, T. Rhyker, Lemmon, Zachary H., Kim, Jennifer, Robitaille, Gina, Kramer, Melissa, Goodwin, Sara, McCombie, W. Richard, Hutton, Samuel, Van Eck, Joyce, Gillis, Jesse, Eshed, Yuval, Sedlazeck, Fritz J., van der Knaap, Esther, Schatz, Michael C., Lippman, Zachary B.

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A three-dimensional human neural cell culture model of Alzheimer’s disease von Choi, Se Hoon, Kim, Young Hye, Hebisch, Matthias, Sliwinski, Christopher, Lee, Seungkyu, D’Avanzo, Carla, Chen, Hechao, Hooli, Basavaraj, Asselin, Caroline, Muffat, Julien, Klee, Justin B., Zhang, Can, Wainger, Brian J., Peitz, Michael, Kovacs, Dora M., Woolf, Clifford J., Wagner, Steven L., Tanzi, Rudolph E., Kim, Doo Yeon

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Genome-wide detection of tandem DNA repeats that are expanded in autism von Trost, Brett, Engchuan, Worrawat, Nguyen, Charlotte M., Thiruvahindrapuram, Bhooma, Dolzhenko, Egor, Backstrom, Ian, Mirceta, Mila, Mojarad, Bahareh A., Yin, Yue, Dov, Alona, Chandrakumar, Induja, Prasolava, Tanya, Shum, Natalie, Hamdan, Omar, Pellecchia, Giovanna, Howe, Jennifer L., Whitney, Joseph, Klee, Eric W., Baheti, Saurabh, Amaral, David G., Anagnostou, Evdokia, Elsabbagh, Mayada, Fernandez, Bridget A., Hoang, Ny, Lewis, M. E. Suzanne, Liu, Xudong, Sjaarda, Calvin, Smith, Isabel M., Szatmari, Peter, Zwaigenbaum, Lonnie, Glazer, David, Hartley, Dean, Stewart, A. Keith, Eberle, Michael A., Sato, Nozomu, Pearson, Christopher E., Scherer, Stephen W., Yuen, Ryan K. C.

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Preemptive Genotyping for Personalized Medicine: Design of the Right Drug, Right Dose, Right Time—Using Genomic Data to Individualize Treatment Protocol von Bielinski, Suzette J., PhD, MEd, Olson, Janet E., PhD, Pathak, Jyotishman, PhD, Weinshilboum, Richard M., MD, Wang, Liewei, MD, PhD, Lyke, Kelly J, Ryu, Euijung, PhD, Targonski, Paul V., MD, PhD, Van Norstrand, Michael D., MD, PhD, Hathcock, Matthew A., MS, Takahashi, Paul Y., MD, McCormick, Jennifer B., PhD, MPP, Johnson, Kiley J., MS, CGC, Maschke, Karen J., PhD, Rohrer Vitek, Carolyn R., MS, Ellingson, Marissa S., MS, CGC, Wieben, Eric D., PhD, Farrugia, Gianrico, MD, Morrisette, Jody A., MBA, Kruckeberg, Keri J., BA, Bruflat, Jamie K., MS, Peterson, Lisa M., BS, Blommel, Joseph H., MS, Skierka, Jennifer M., BS, Ferber, Matthew J., PhD, Black, John L., MD, Baudhuin, Linnea M., PhD, Klee, Eric W., PhD, Ross, Jason L., MA, Veldhuizen, Tamra L., BS, Schultz, Cloann G., MS, Caraballo, Pedro J., MD, Freimuth, Robert R., PhD, Chute, Christopher G., MD, DrPH, Kullo, Iftikhar J., MD

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Genome Capture Sequencing Selectively Enriches Bacterial DNA and Enables Genome-Wide Measurement of Intrastrain Genetic Diversity in Human Infections von Hayden, Hillary S, Joshi, Snehal, Radey, Matthew C, Vo, Anh T, Forsberg, Cara, Morgan, Sarah J, Waalkes, Adam, Holmes, Elizabeth A, Klee, Sara M, Emond, Mary J, Singh, Pradeep K, Salipante, Stephen J

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Diagnostic yield of exome and genome sequencing after non-diagnostic multi-gene panels in patients with single-system diseases von 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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Outcome of Whole Exome Sequencing for Diagnostic Odyssey Cases of an Individualized Medicine Clinic: The Mayo Clinic Experience von Lazaridis, Konstantinos N, Schahl, Kimberly A, Cousin, Margot A, Babovic-Vuksanovic, Dusica, Riegert-Johnson, Douglas L, Gavrilova, Ralitza H, McAllister, Tammy M, Lindor, Noralane M, Abraham, Roshini S, Ackerman, Michael J, Pichurin, Pavel N, Deyle, David R, Gavrilov, Dimitar K, Hand, Jennifer L, Klee, Eric W, Stephens, Michael C, Wick, Myra J, Atkinson, Elizabeth J, Linden, David R, Ferber, Matthew J, Wieben, Eric D, Farrugia, Gianrico

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Development and Verification of an RNA Sequencing (RNA-Seq) Assay for the Detection of Gene Fusions in Tumors von Winters, Jennifer L., Davila, Jaime I., McDonald, Amber M., Nair, Asha A., Fadra, Numrah, Wehrs, Rebecca N., Thomas, Brittany C., Balcom, Jessica R., Jin, Long, Wu, Xianglin, Voss, Jesse S., Klee, Eric W., Oliver, Gavin R., Graham, Rondell P., Neff, Jadee L., Rumilla, Kandelaria M., Aypar, Umut, Kipp, Benjamin R., Jenkins, Robert B., Jen, Jin, Halling, Kevin C.

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Preemptive Pharmacogenomic Testing for Precision Medicine: A Comprehensive Analysis of Five Actionable Pharmacogenomic Genes Using Next-Generation DNA Sequencing and a Customized C... von Ji, Yuan, Skierka, Jennifer M, Blommel, Joseph H, Moore, Brenda E, VanCuyk, Douglas L, Bruflat, Jamie K, Peterson, Lisa M, Veldhuizen, Tamra L, Fadra, Numrah, Peterson, Sandra E, Lagerstedt, Susan A, Train, Laura J, Baudhuin, Linnea M, Klee, Eric W, Ferber, Matthew J, Bielinski, Suzette J, Caraballo, Pedro J, Weinshilboum, Richard M, Black, 3rd, John L

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Perceived Barriers and Facilitators to Implementation of Peer Support in Veterans Health Administration Primary Care-Mental Health Integration Settings von Shepardson, Robyn L., Johnson, Emily M., Possemato, Kyle, Arigo, Danielle, Funderburk, Jennifer S.

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εγ-Thalassemia, a New Hemoglobinopathy Category von Oliveira, Jennifer L, Thompson, Christineil H, Saravanaperumal, Siva Arumugam, Koganti, Tejaswi, Jenkinson, Garrett, Hein, Molly S, Kohorst, Mira A, Hasadsri, Linda, Nguyen, Phuong L, Matern, Dietrich, Kipp, Benjamin R, Klee, Eric W, Wieben, Eric D, Hoyer, James D, Rangan, Aruna

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Cultural Adaptations of Motivational Interviewing: A Systematic Review von Self, Kyle J., Borsari, Brian, Ladd, Benjamin O., Nicolas, Guerda, Gibson, Carolyn J., Jackson, Kristina, Manuel, Jennifer K.

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Parallel recovery of chromatin accessibility and gene expression dynamics from frozen human regulatory T cells von Wong, Ying Y., Harbison, Jessica E., Hope, Christopher M., Gundsambuu, Batjargal, Brown, Katherine A., Wong, Soon W., Brown, Cheryl Y, Couper, Jennifer J., Breen, Jimmy, Liu, Ning, Pederson, Stephen M., Köhne, Maren, Klee, Kathrin, Schultze, Joachim, Beyer, Marc, Sadlon, Timothy, Barry, Simon C.

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Abstract 4145039: Prevalence, Penetrance, and Phenotypic Manifestation of Incidental Cardiomyopathy-Associated Genetic Variants in a Quaternary Medical Center-based Population von Figueiral, Marta, Fazzini, Luca, Tan-Arroyo, Jennifer, Olson, Rory, Bublitz, Josh, Olson, Janet, Klee, Eric, Pereira, Naveen

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Prevalence, Penetrance, and Phenotypic Manifestation of Cardiomyopathy-Associated Genetic Variants in the General Population: Insights from a Mayo Clinic Biobank Study von Figueiral, Marta, Paldino, Alessia, Wilke, Matheus Vernet Machado Bressan, Farris, Joseph D., Verheijen, Jan, Giudicessi, John R., Ackerman, Michael J., Olson, Janet E., Arroyo, Jennifer, Olson, Rory J., Klee, Eric W., Pereira, Naveen L.

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ClinGen — The Clinical Genome Resource von Rehm, Heidi L, Berg, Jonathan S, Brooks, Lisa D, Bustamante, Carlos D, Evans, James P, Landrum, Melissa J, Ledbetter, David H, Maglott, Donna R, Martin, Christa Lese, Nussbaum, Robert L, Plon, Sharon E, Ramos, Erin M, Sherry, Stephen T, Watson, Michael S

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