Influence of rubbing on rotor dynamics, part 2 von Muszynska, Agnes, Bently, Donald E., Franklin, Wesley D., Hayashida, Robert D., Kingsley, Lori M., Curry, Arthur E.

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Influence of rubbing on rotor dynamics, part 1 von Muszynska, Agnes, Bently, Donald E., Franklin, Wesley D., Hayashida, Robert D., Kingsley, Lori M., Curry, Arthur E.

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Randomized Withdrawal Study of Patients With Symptomatic Neurogenic Orthostatic Hypotension Responsive to Droxidopa von Biaggioni, Italo, Freeman, Roy, Mathias, Christopher J, Low, Phillip, Hewitt, L Arthur, Kaufmann, Horacio

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The effect of extending graduated driver licensing to older novice drivers in Indiana von Wang, Yudan Chen, Foss, Robert D., Goodwin, Arthur H., Curry, Allison E., Tefft, Brian C.

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Personal journeys to and in human genetics and dysmorphology von Schwartz, Charles E., Aylsworth, Arthur S., Allanson, Judith, Battaglia, Agatino, Carey, John C., Curry, Cynthia J., Davies, Kay E., Eichler, Evan E., Graham, John M., Hall, Bryan, Hall, Judith G., Holmes, Lewis B., Hoyme, H. Eugene, Hunter, Alasdair, Innis, Jeffrey, Johnson, John, Keppler‐Noreuil, Kim M., Leroy, Jules G., Moore, Cynthia, Nelson, David L., Neri, Giovanni, Opitz, John M., Picketts, David, Raymond, F. Lucy, Shalev, Stavit Allon, Stevenson, Roger E., Stumpel, Connie T. R. M., Sutherland, Grant, Viskochil, David H., Weaver, David D., Zackai, Elaine H.

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Episodic deposition of Illinois Valley Peoria silt in association with Lake Michigan Lobe fluctuations during the last glacial maximum von Nash, Thomas A., Conroy, Jessica L., Grimley, David A., Guenthner, William R., Curry, Ben Brandon

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Mutations in PIEZO2 Cause Gordon Syndrome, Marden-Walker Syndrome, and Distal Arthrogryposis Type 5 von McMillin, Margaret J., Beck, Anita E., Chong, Jessica X., Shively, Kathryn M., Buckingham, Kati J., Gildersleeve, Heidi I.S., Aracena, Mariana I., Aylsworth, Arthur S., Bitoun, Pierre, Carey, John C., Clericuzio, Carol L., Crow, Yanick J., Curry, Cynthia J., Devriendt, Koenraad, Everman, David B., Fryer, Alan, Gibson, Kate, Giovannucci Uzielli, Maria Luisa, Graham, John M., Hall, Judith G., Hecht, Jacqueline T., Heidenreich, Randall A., Hurst, Jane A., Irani, Sarosh, Krapels, Ingrid P.C., Leroy, Jules G., Mowat, David, Plant, Gordon T., Robertson, Stephen P., Schorry, Elizabeth K., Scott, Richard H., Seaver, Laurie H., Sherr, Elliott, Splitt, Miranda, Stewart, Helen, Stumpel, Constance, Temel, Sehime G., Weaver, David D., Whiteford, Margo, Williams, Marc S., Tabor, Holly K., Smith, Joshua D., Shendure, Jay, Nickerson, Deborah A., Bamshad, Michael J.

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SYNTAX Score and Long-Term Outcomes: The BARI-2D Trial von Ikeno, Fumiaki, Brooks, Maria Mori, Nakagawa, Kaori, Kim, Min-Kyu, Kaneda, Hideaki, Mitsutake, Yoshiaki, Vlachos, Helen A, Schwartz, Leonard, Frye, Robert L, Kelsey, Sheryl F, Waseda, Katsuhisa, Hlatky, Mark A

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A Randomized Trial of a Brief Primary-Care-Based Intervention for Reducing At-Risk Drinking Practices von Curry, Susan J, Ludman, Evette J, Grothaus, Louis C, Donovan, Dennis, Kim, Eleanor

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Instrument-based pediatric vision screening policy statement von Miller, Joseph M, Lessin, Herschel R

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Expanding the genetics and phenotypes of ocular congenital cranial dysinnervation disorders von Jurgens, Julie A., Barry, Brenda J., Chan, Wai-Man, MacKinnon, Sarah, Matos Ruiz, Paola M., England, Eleina M., Pais, Lynn, Groopman, Emily, Russell, Kathryn A., Di Gioia, Silvio Alessandro, Lee, Arthur S., Shaaban, Sherin, Bekele, Sarah, Toffoloni, Melissa, Foster, Emma E., Berube, Lindsay, Rivera-Quiles, Cristina, Mensching, Fiona M., Sanchis-Juan, Alba, Fu, Jack M., Wong, Isaac, Zhao, Xuefang, Wilson, Michael W., Lek, Monkol, Abarca-Barriga, Hugo, Al-Haddad, Christiane, Chacon-Camacho, Oscar Francisco, Chang, Lan, Christiansen, Stephen P., Ciccarelli, Maria Laura, Cordonnier, Monique, Cox, Gerald F., Curry, Cynthia J., Lee Dahm, Thomas, David, Karen L., De Berardinis, Teresa, Demer, Joseph L., Drack, Arlene V., Eggenberger, Eric, Elder, James E., Elliott, Alexandra T., Epley, K. David, Feldman, Hagit Baris, Ferreira, Carlos R., Gerth-Kahlert, Christina, Halliday, Dorothy J., Hanisch, Frank, Hay, Eleanor, Holder, Christopher, Iannaccone, Alessandro, Isenberg, Sherwin J., Kahana, Alon, Kazlas, Melanie, Kerr, Natalie C., Ko, Melissa W., Koc, Feray, Larsen, Dorte Ancher, Lay-Son, Guillermo, Ledoux, Danielle M., Levin, Alex V., Levy, Richard L., Mackey, David A., Mantagos, Iason S., Marti, Candice, Menezes, Manoj P., Mikail, Claudia N., Miller, Kathryn Bisceglia, Miyana, Kaori, Mullineaux, Lisa, Nishimura, Julie K., Noble, A. Gwendolyn, Pavone, Piero, Phalen, James A., Poduri, Annapurna, Polo, Claudia R., Prasov, Lev, Ramos, Feliciano J., Ramos-Caceres, Maria, Robb, Richard M., Rossillion, Béatrice, Smith, Lois E.H., Sorkin, Jeffrey A., Soul, Janet S., Stalker, Heather J., Stasheff, Steven F., Strassberg, Sonya, Thomas, Ioan Talfryn, VanderVeen, Deborah K., Vincent, Andrea L., Wabbels, Bettina, Wong, Agnes M.F., Wu, Carolyn, Yeung, Alison, Young, Terri L., Zwaan, Johan, Brand, Harrison, Talkowski, Michael E., MacArthur, Daniel G., Robson, Caroline D., Engle, Elizabeth C.

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The duplication 17p13.3 phenotype: Analysis of 21 families delineates developmental, behavioral and brain abnormalities, and rare variant phenotypes von Curry, Cynthia J., Rosenfeld, Jill A., Grant, Erica, Gripp, Karen W., Anderson, Carol, Aylsworth, Arthur S., Saad, Taha Ben, Chizhikov, Victor V., Dybose, Giedre, Fagerberg, Christina, Falco, Michelle, Fels, Christina, Fichera, Marco, Graakjaer, Jesper, Greco, Donatella, Hair, Jennifer, Hopkins, Elizabeth, Huggins, Marlene, Ladda, Roger, Li, Chumei, Moeschler, John, Nowaczyk, Malgorzata J.M., Ozmore, Jillian R., Reitano, Santina, Romano, Corrado, Roos, Laura, Schnur, Rhonda E., Sell, Susan, Suwannarat, Pim, Svaneby, Dea, Szybowska, Marta, Tarnopolsky, Mark, Tervo, Raymond, Tsai, Anne Chun-Hui, Tucker, Megan, Vallee, Stephanie, Wheeler, Ferrin C, Zand, Dina J., Barkovich, A. James, Aradhya, Swaroop, Shaffer, Lisa G., Dobyns, William B.

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LUMINOS-101: Phase 2 study of PVSRIPO with pembrolizumab in recurrent glioblastoma von Sloan, Andrew E., Buerki, Robin Arthur, Murphy, Christopher, Kelly, Andrea True, Ambady, Prakash, Brown, Michael, Butowski, Nicholas A., Cavaliere, Robert, Curry, William T., Desjardins, Annick, Franklin, Lisa, Friedman, Henry S., Gromeier, Matthias, Jackson, LeAnn, Mixson, Lori, Ong, Shirley S., Randazzo, Dina, Wen, Patrick Y., Nichols, Garrett

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Molecular and Clinical Analyses of Greig Cephalopolysyndactyly and Pallister-Hall Syndromes: Robust Phenotype Prediction from the Type and Position of GLI3 Mutations von Johnston, Jennifer J., Olivos-Glander, Isabelle, Killoran, Christina, Elson, Emma, Turner, Joyce T., Peters, Kathryn F., Abbott, Margaret H., Aughton, David J., Aylsworth, Arthur S., Bamshad, Michael J., Booth, Carol, Curry, Cynthia J., David, Albert, Dinulos, Mary Beth, Flannery, David B., Fox, Michelle A., Graham, John M., Grange, Dorothy K., Guttmacher, Alan E., Hannibal, Mark C., Henn, Wolfram, Hennekam, RaoulC.M., Holmes, Lewis B., Hoyme, H. Eugene, Leppig, Kathleen A., Lin, Angela E., MacLeod, Patrick, Manchester, David K., Marcelis, Carlo, Mazzanti, Laura, McCann, Emma, McDonald, Marie T., Mendelsohn, Nancy J., Moeschler, John B., Moghaddam, Billur, Neri, Giovanni, Newbury-Ecob, Ruth, Pagon, Roberta A., Phillips III, John A., Sadler, Laurie S., Stoler, Joan M., Tilstra, David, Walsh Vockley, Catherine M., Zackai, Elaine H., Zadeh, Touran M., Brueton, Louise, Black, Graeme Charles M., Biesecker, Leslie G.

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4-Phenyl tetrahydroisoquinolines as dual norepinephrine and dopamine reuptake inhibitors von Pechulis, Anthony D., Beck, James P., Curry, Matt A., Wolf, Mark A., Harms, Arthur E., Xi, Ning, Opalka, Chet, Sweet, Mark P., Yang, Zhicai, Vellekoop, A. Samuel, Klos, Andrew M., Crocker, Peter J., Hassler, Carla, Laws, Mia, Kitchen, Douglas B., Smith, Mark A., Olson, Richard E., Liu, Shuang, Molino, Bruce F.

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Profile of infants born to drug-using mothers: A state-wide audit von Abdel-Latif, Mohamed E, Oei, Julee, Craig, Fiona, Lui, Kei

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Development of an Accessible Audio Computer-Assisted Self-Interview (A-CASI) to Screen for Abuse and Provide Safety Strategies for Women With Disabilities von Oschwald, Mary, Renker, Paula, Hughes, Rosemary B., Arthur, Anne, Powers, Laurie E., Curry, Mary Ann

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Pediatric Chronic Illness (Cancer, Cystic Fibrosis) Effects On Well Siblings: Parents' Voices von Williams, Phoebe Dauz, Ridder, E. Lavonne, Setter, Robyn Karlin, Liebergen, Adrienne, Curry, Heather, Piamjariyakul, Ubolrat, Williams, Arthur R.

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Mutations in PIEZO2 Cause Gordon Syndrome, Marden-Walker Syndrome, and Distal Arthrogryposis Type 5 von McMillin, Margaret J, Beck, Anita E, Chong, Jessica X, Shively, Kathryn M, Buckingham, Kati J, Gildersleeve, Heidi I.S, Aracena, Mariana I, Aylsworth, Arthur S, Bitoun, Pierre, Carey, John C, Clericuzio, Carol L, Crow, Yanick J, Curry, Cynthia J, Devriendt, Koenraad, Everman, David B, Fryer, Alan, Gibson, Kate, Giovannucci Uzielli, Maria Luisa, Graham, John M, Hall, Judith G, Hecht, Jacqueline T, Heidenreich, Randall A, Hurst, Jane A, Irani, Sarosh, Krapels, Ingrid P.C, Leroy, Jules G, Mowat, David, Plant, Gordon T, Robertson, Stephen P, Schorry, Elizabeth K, Scott, Richard H, Seaver, Laurie H, Sherr, Elliott, Splitt, Miranda, Stewart, Helen, Stumpel, Constance, Temel, Sehime G, Weaver, David D, Whiteford, Margo, Williams, Marc S, Tabor, Holly K, Smith, Joshua D, Shendure, Jay, Nickerson, Deborah A, University of Washington Center for Mendelian Genomics, Bamshad, Michael J

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Detection of a de novo interstitial 2q microdeletion by CGH microarray analysis in a patient with limb malformations, microcephaly and mental retardation von Svensson, Annika M., Curry, Cynthia J., South, Sarah T., Whitby, Heidi, Maxwell, Teresa M., Aston, Emily, Fisher, Jamie, Carmack, C.E., Scheffer, Alicia, Abu‐Shamsieh, Aimee, Brothman, Arthur R.

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