Rurality is associated with lower likelihood of dipeptidyl peptidase 4 inhibitor use for treatment intensification von Nagy, Danielle K., Bresee, Lauren C., Eurich, Dean T., Simpson, Scot H.

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Rural Residence Is Associated With a Delayed Trend Away From Sulfonylurea Use for Treatment Intensification of Type 2 Diabetes von Nagy, Danielle K, Bresee, Lauren C, Eurich, Dean T, Simpson, Scot H

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Professional Fulfillment and Burnout in Fourth-Year Pharmacy Students and Risk Factors for the Future: A Mixed Methods Study von Nagy, Danielle K., Hall, Jill J., Charrois, Theresa L.

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The impact of the COVID-19 pandemic on pharmacy students' personal and professional learning von Nagy, Danielle K., Hall, Jill J., Charrois, Theresa L.

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Are Guideline-concordant Processes of Care Consistent Across the Rural–Urban Continuum? A Retrospective Cohort Study of Adults Newly Treated for Type 2 Diabetes von Nagy, Danielle K., Bresee, Lauren C., Eurich, Dean T., Simpson, Scot H.

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1086-P: Rural Residence Is Associated with a Lower Likelihood of Dipeptidyl Peptidase 4 Inhibitor Use for Treatment Intensification von Nagy, Danielle K, Bresee, Lauren, Eurich, Dean, Simpson, Scot H

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DNA methylation predicts age and provides insight into exceptional longevity of bats von Wilkinson, Gerald S., Adams, Danielle M., Haghani, Amin, Lu, Ake T., Zoller, Joseph, Breeze, Charles E., Arnold, Bryan D., Ball, Hope C., Carter, Gerald G., Cooper, Lisa Noelle, Dechmann, Dina K. N., Devanna, Paolo, Fasel, Nicolas J., Galazyuk, Alexander V., Günther, Linus, Hurme, Edward, Jones, Gareth, Knörnschild, Mirjam, Lattenkamp, Ella Z., Li, Caesar Z., Mayer, Frieder, Reinhardt, Josephine A., Medellin, Rodrigo A., Nagy, Martina, Pope, Brian, Power, Megan L., Ransome, Roger D., Teeling, Emma C., Vernes, Sonja C., Zamora-Mejías, Daniel, Zhang, Joshua, Faure, Paul A., Greville, Lucas J., Herrera M., L. Gerardo, Flores-Martínez, José J., Horvath, Steve

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Interrogating the Genetic Determinants of Tourette’s Syndrome and Other Tic Disorders Through Genome-Wide Association Studies von Yu, Dongmei, Sul, Jae Hoon, Tsetsos, Fotis, Nawaz, Muhammad S, Huang, Alden Y, Zelaya, Ivette, Illmann, Cornelia, Osiecki, Lisa, Darrow, Sabrina M, Hirschtritt, Matthew E, Greenberg, Erica, Muller-Vahl, Kirsten R, Stuhrmann, Manfred, Dion, Yves, Rouleau, Guy, Aschauer, Harald, Stamenkovic, Mara, Schlögelhofer, Monika, Sandor, Paul, Barr, Cathy L, Grados, Marco, Singer, Harvey S, Nöthen, Markus M, Hebebrand, Johannes, Hinney, Anke, King, Robert A, Fernandez, Thomas V, Barta, Csaba, Tarnok, Zsanett, Nagy, Peter, Depienne, Christel, Worbe, Yulia, Hartmann, Andreas, Budman, Cathy L, Rizzo, Renata, Lyon, Gholson J, McMahon, William M, Batterson, James R, Cath, Danielle C, Malaty, Irene A, Okun, Michael S, Berlin, Cheston, Woods, Douglas W, Lee, Paul C, Jankovic, Joseph, Robertson, Mary M, Gilbert, Donald L, Brown, Lawrence W, Coffey, Barbara J, Dietrich, Andrea, Hoekstra, Pieter J, Kuperman, Samuel, Zinner, Samuel H, Luðvigsson, Pétur, Sæmundsen, Evald, Thorarensen, Ólafur, Atzmon, Gil, Barzilai, Nir, Wagner, Michael, Moessner, Rainald, Ophoff, Roel, Pato, Carlos N, Pato, Michele T, Knowles, James A, Roffman, Joshua L, Smoller, Jordan W, Buckner, Randy L, Willsey, A. Jeremy, Tischfield, Jay A, Heiman, Gary A, Stefansson, Hreinn, Stefansson, Kári, Posthuma, Danielle, Cox, Nancy J, Pauls, David L, Freimer, Nelson B, Neale, Benjamin M, Davis, Lea K, Paschou, Peristera, Coppola, Giovanni, Mathews, Carol A, Scharf, Jeremiah M

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Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome von Huang, Alden Y., Yu, Dongmei, Davis, Lea K., Sul, Jae Hoon, Tsetsos, Fotis, Ramensky, Vasily, Zelaya, Ivette, Ramos, Eliana Marisa, Osiecki, Lisa, Chen, Jason A., McGrath, Lauren M., Illmann, Cornelia, Sandor, Paul, Barr, Cathy L., Grados, Marco, Singer, Harvey S., Nöthen, Markus M., Hebebrand, Johannes, King, Robert A., Dion, Yves, Rouleau, Guy, Budman, Cathy L., Depienne, Christel, Worbe, Yulia, Hartmann, Andreas, Müller-Vahl, Kirsten R., Stuhrmann, Manfred, Aschauer, Harald, Stamenkovic, Mara, Schloegelhofer, Monika, Konstantinidis, Anastasios, Lyon, Gholson J., McMahon, William M., Barta, Csaba, Tarnok, Zsanett, Nagy, Peter, Batterson, James R., Rizzo, Renata, Cath, Danielle C., Wolanczyk, Tomasz, Berlin, Cheston, Malaty, Irene A., Okun, Michael S., Woods, Douglas W., Rees, Elliott, Pato, Carlos N., Pato, Michele T., Knowles, James A., Posthuma, Danielle, Pauls, David L., Cox, Nancy J., Neale, Benjamin M., Freimer, Nelson B., Paschou, Peristera, Mathews, Carol A., Scharf, Jeremiah M., Coppola, Giovanni, Bruun, Ruth D., Chouinard, Sylvain, Darrow, Sabrina, Greenberg, Erica, Hirschtritt, Matthew E., Kurlan, Roger, Leckman, James F., Robertson, Mary M., Smit, Jan

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Implementation of next generation sequencing into pediatric hematology-oncology practice: moving beyond actionable alterations von Oberg, Jennifer A, Glade Bender, Julia L, Sulis, Maria Luisa, Pendrick, Danielle, Sireci, Anthony N, Hsiao, Susan J, Turk, Andrew T, Dela Cruz, Filemon S, Hibshoosh, Hanina, Remotti, Helen, Zylber, Rebecca J, Pang, Jiuhong, Diolaiti, Daniel, Koval, Carrie, Andrews, Stuart J, Garvin, James H, Yamashiro, Darrell J, Chung, Wendy K, Emerson, Stephen G, Nagy, Peter L, Mansukhani, Mahesh M, Kung, Andrew L

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Genome-Wide Association Study Meta-Analysis of 9619 Cases With Tic Disorders von Strom, Nora I., Halvorsen, Matthew W., Grove, Jakob, Ásbjörnsdóttir, Bergrún, Thorarensen, Ólafur, de Schipper, Elles, Bäckmann, Julia, Tian, Chao, Sul, Jae Hoon, Tsetsos, Fotis, Zelaya, Ivette, Osiecki, Lisa, Darrow, Sabrina M., Hirschtritt, Matthew E., Greenberg, Erica, Stuhrmann, Manfred, Dion, Yves, Rouleau, Guy, Aschauer, Harald, Stamenkovic, Mara, Schlögelhofer, Monika, Barr, Cathy L., Grados, Marco, Hinney, Anke, King, Robert A., Fernandez, Thomas V., Barta, Csaba, Tarnok, Zsanett, Nagy, Peter, Depienne, Christel, Worbe, Yulia, Hartmann, Andreas, Budman, Cathy L., Lyon, Gholson J., McMahon, William M., Batterson, James R., Malaty, Irene A., Okun, Michael S., Berlin, Cheston, Woods, Douglas W., Lee, Paul C., Jankovic, Joseph, Robertson, Mary M., Gilbert, Donald L., Brown, Lawrence W., Coffey, Barbara J., Hoekstra, Pieter J., Zinner, Samuel H., Luðvigsson, Pétur, Thorarensen, Ólafur, Atzmon, Gil, Barzilai, Nir, Moessner, Rainald, Ophoff, Roel, Pato, Carlos N., Knowles, James A., Buckner, Randy L., Willsey, Jeremy A., Tischfield, Jay A., Heiman, Gary A., Stefansson, Hreinn, Stefansson, Kári, Posthuma, Danielle, Pauls, David L., Freimer, Nelson B., Davis, Lea K., Paschou, Peristera, Coppola, Giovanni, Mathews, Carol A., Scharf, Jeremiah M., Agee, Michelle, Auton, Adam, Elson, Sarah L., Furlotte, Nicholas A., Hicks, Barry, Jewett, Ethan M., Jiang, Yunxuan, Kleinman, Aaron, Lin, Keng-Han, Litterman, Nadia K., McIntyre, Matthew H., McManus, Kimberly F., Mountain, Joanna L., Pitts, Steven J., Poznik, G. David, Sathirapongsasuti, J. Fah, Shelton, Janie F., Shringarpure, Suyash, Tung, Joyce Y., Wang, Xin, Als, Thomas Damm, Meier, Sandra M., Bybjerg-Grauholm, Jonas, Hougaard, David M., Werge, Thomas, Børglum, Anders D., Hinds, David A., Rück, Christian, Mataix-Cols, David, Mattheisen, Manuel

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Author Correction: DNA methylation predicts age and provides insight into exceptional longevity of bats von Wilkinson, Gerald S., Adams, Danielle M., Haghani, Amin, Lu, Ake T., Zoller, Joseph, Breeze, Charles E., Arnold, Bryan D., Ball, Hope C., Carter, Gerald G., Cooper, Lisa Noelle, Dechmann, Dina K. N., Devanna, Paolo, Fasel, Nicolas J., Galazyuk, Alexander V., Günther, Linus, Hurme, Edward, Jones, Gareth, Knörnschild, Mirjam, Lattenkamp, Ella Z., Li, Caesar Z., Mayer, Frieder, Reinhardt, Josephine A., Medellin, Rodrigo A., Nagy, Martina, Pope, Brian, Power, Megan L., Ransome, Roger D., Teeling, Emma C., Vernes, Sonja C., Zamora-Mejías, Daniel, Zhang, Joshua, Faure, Paul A., Greville, Lucas J., Horvath, Steve, Herrera M., L. Gerardo, Flores-Martínez, José J.

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Genetic association signal near NTN4 in Tourette syndrome von Paschou, Peristera, Yu, Dongmei, Gerber, Gloria, Evans, Patrick, Tsetsos, Fotis, Davis, Lea K., Karagiannidis, Iordanis, Chaponis, Jonathan, Gamazon, Eric, Mueller-Vahl, Kirsten, Stuhrmann, Manfred, Schloegelhofer, Monika, Stamenkovic, Mara, Hebebrand, Johannes, Noethen, Markus, Nagy, Peter, Barta, Csaba, Tarnok, Zsanett, Rizzo, Renata, Depienne, Christel, Worbe, Yulia, Hartmann, Andreas, Cath, Danielle C., Budman, Cathy L., Sandor, Paul, Barr, Cathy, Wolanczyk, Thomas, Singer, Harvey, Chou, I-Ching, Grados, Marco, Posthuma, Danielle, Rouleau, Guy A., Aschauer, Harald, Freimer, Nelson B., Pauls, David L., Cox, Nancy J., Mathews, Carol A., Scharf, Jeremiah M.

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Author Correction: DNA methylation predicts age and provides insight into exceptional longevity of bats von Wilkinson, Gerald S., Adams, Danielle M., Haghani, Amin, Lu, Ake T., Zoller, Joseph, Breeze, Charles E., Arnold, Bryan D., Ball, Hope C., Carter, Gerald G., Cooper, Lisa Noelle, Dechmann, Dina K. N., Devanna, Paolo, Fasel, Nicolas J., Galazyuk, Alexander V., Günther, Linus, Hurme, Edward, Jones, Gareth, Knörnschild, Mirjam, Lattenkamp, Ella Z., Li, Caesar Z., Mayer, Frieder, Reinhardt, Josephine A., Medellin, Rodrigo A., Nagy, Martina, Pope, Brian, Power, Megan L., Ransome, Roger D., Teeling, Emma C., Vernes, Sonja C., Zamora-Mejías, Daniel, Zhang, Joshua, Faure, Paul A., Greville, Lucas J., Herrera M., L. Gerardo, Flores-Martínez, José J., Horvath, Steve

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Synaptic processes and immune-related pathways implicated in Tourette syndrome von Yu, Dongmei, Sul, Jae Hoon, Huang, Alden Y., Illmann, Cornelia, Osiecki, Lisa, Darrow, Sabrina M., Hirschtritt, Matthew E., Greenberg, Erica, Stuhrmann, Manfred, Dion, Yves, Rouleau, Guy A., Aschauer, Harald, Barr, Cathy L., Grados, Marco A., Singer, Harvey S., Nöthen, Markus M., Hebebrand, Johannes, King, Robert A., Fernandez, Thomas V., Barta, Csaba, Tarnok, Zsanett, Depienne, Christel, Worbe, Yulia, Hartmann, Andreas, Budman, Cathy L., Rizzo, Renata, McMahon, William M., Batterson, James R., Cath, Danielle C., Malaty, Irene A., Okun, Michael S., Berlin, Cheston, Lee, Paul C., Robertson, Mary M., Gilbert, Donald L., Brown, Lawrence W., Coffey, Barbara J., Dietrich, Andrea, Hoekstra, Pieter J., Kuperman, Samuel, Wagner, Michael, Knowles, James A., Jeremy Willsey, A., Tischfield, Jay A., Heiman, Gary A., Cox, Nancy J., Freimer, Nelson B., Davis, Lea K., Mathews, Carol A., Scharf, Jeremiah M., Paschou, Peristera, Coppola, Giovanni, Darrow, Sabrina, Davis, Lea K., Dion, Yves, Freimer, Nelson B., Greenberg, Erica, Kurlan, Roger, Leckman, James F., Malaty, Irene A., Neale, Benjamin M., Okun, Michael S., Rouleau, Guy A., Smit, Jan H., Aschauer, Harald Aschauer Harald, Barta, Csaba, Depienne, Christel, Konstantinidis, Anastasios, Müller-Vahl, Kirsten, Paschou, Peristera, Wolanczyk, Tomasz, Brown, Lawrence, Fernandez, Thomas V., Garcia-Delgar, Blanca, Gilbert, Donald, Grice, Dorothy E., Hedderly, Tammy, Heiman, Gary A., Heyman, Isobel, Kim, Young Key, Kim, Young-Shin, Koh, Yun-Joo, Kook, Sodahm, Leventhal, Bennett L., Madruga-Garrido, Marcos, Mir, Pablo, Morer, Astrid, Münchau, Alexander, Plessen, Kerstin J., Roessner, Veit, Shin, Eun-Young, Song, Dong-Ho, Song, Jungeun, Willsey, A. Jeremy, Zinner, Samuel, Aschauer, Harald, Fernandez, Thomas, Heiman, Gary, Hoekstra, Pieter, Tischfield, Jay

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Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome von Huang, Alden Y, Yu, Dongmei, Davis, Lea K, Sul, Jae Hoon, Tsetsos, Fotis, Ramensky, Vasily, Zelaya, Ivette, Ramos, Eliana Marisa, Osiecki, Lisa, Chen, Jason A, McGrath, Lauren M, Illmann, Cornelia, Sandor, Paul, Barr, Cathy L, Grados, Marco A, Singer, Harvey S, Nöthen, Markus M, Hebebrand, Johannes, King, Robert A, Dion, Yves, Rouleau, Guy A, Budman, Cathy L, Depienne, Christel, Worbe, Yulia, Hartmann, Andreas, Müller-Vahl, Kirsten R, Stuhrmann, Manfred, Aschauer, Harald, Stamenkovic, Mara, Schloegelhofer, Monika, Konstantinidis, Anastasios, Lyon, Gholson J, McMahon, William M, Barta, Csaba, Tarnok, Zsanett, Nagy, Peter, Batterson, James R, Rizzo, Renata, Cath, Danielle C, Wolanczyk, Tomasz, Berlin, Cheston, Malaty, Irene A, Okun, Michael S, Woods, Douglas W, Rees, Elliott, Pato, Carlos N, Pato, Michele T, Knowles, James A, Posthuma, Danielle, Smit, Jan, The Tourette Syndrome Association International Consortium for Genetics (TSAICG), The Gilles de la Tourette Syndrome GWAS Replication Initiative (GGRI)

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Abstract PR01: Precision in Pediatric Sequencing (PIPseq): Clinical implementation of genomic sequencing into pediatric hematology-oncology practice von Bender, Julia L. Glade, Oberg, Jennifer A., Sulis, Maria Luisa, Cruz, Filamon Dela, Sireci, Anthony N., Hsiao, Susan J., Yamashiro, Darrell J., Koval, Carrie, Chung, Wendy K., Emerson, Stephen G., Zylber, Rebecca, Cano, Samantha, Denney, Danielle P., Andrews, Stuart, Nagy, Peter L., Mansukhani, Mahesh M., Kung, Andrew L.

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Genetic association signal near NTN 4 in T ourette syndrome von Paschou, Peristera, Yu, Dongmei, Gerber, Gloria, Evans, Patrick, Tsetsos, Fotis, Davis, Lea K., Karagiannidis, Iordanis, Chaponis, Jonathan, Gamazon, Eric, Mueller‐Vahl, Kirsten, Stuhrmann, Manfred, Schloegelhofer, Monika, Stamenkovic, Mara, Hebebrand, Johannes, Noethen, Markus, Nagy, Peter, Barta, Csaba, Tarnok, Zsanett, Rizzo, Renata, Depienne, Christel, Worbe, Yulia, Hartmann, Andreas, Cath, Danielle C., Budman, Cathy L., Sandor, Paul, Barr, Cathy, Wolanczyk, Thomas, Singer, Harvey, Chou, I‐Ching, Grados, Marco, Posthuma, Danielle, Rouleau, Guy A., Aschauer, Harald, Freimer, Nelson B., Pauls, David L., Cox, Nancy J., Mathews, Carol A., Scharf, Jeremiah M.

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