Cantilever bridges by C.F. Findley von Findley, C. F

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Sniff-synchronized, gradient-guided olfactory search by freely moving mice von Findley, Teresa M., Wyrick, David G., Cramer, Jennifer L., Brown, Morgan A., Holcomb, Blake, Attey, Robin, Yeh, Dorian, Monasevitch, Eric, Nouboussi, Nelly, Cullen, Isabelle, Songco, Jeremea O., King, Jared F., Ahmadian, Yashar, Smear, Matthew C.

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The Dimensional Yale-Brown Obsessive-Compulsive Scale (DY-BOCS): an instrument for assessing obsessive-compulsive symptom dimensions von ROSARIO-CAMPOS, M. C, MIGUEL, E. C, TOLIN, D, HOLLANDER, E, KANO, Y, LECKMAN, J. F, QUATRANO, S, CHACON, P, FERRAO, Y, FINDLEY, D, KATSOVICH, L, SCAHILL, L, KING, R. A, WOODY, S. R

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A broadly implementable research course in phage discovery and genomics for first-year undergraduate students von Jordan, Tuajuanda C, Burnett, Sandra H, Carson, Susan, Caruso, Steven M, Clase, Kari, DeJong, Randall J, Dennehy, John J, Denver, Dee R, Dunbar, David, Elgin, Sarah C R, Findley, Ann M, Gissendanner, Chris R, Golebiewska, Urszula P, Guild, Nancy, Hartzog, Grant A, Grillo, Wendy H, Hollowell, Gail P, Hughes, Lee E, Johnson, Allison, King, Rodney A, Lewis, Lynn O, Li, Wei, Rosenzweig, Frank, Rubin, Michael R, Saha, Margaret S, Sandoz, James, Shaffer, Christopher D, Taylor, Barbara, Temple, Louise, Vazquez, Edwin, Ware, Vassie C, Barker, Lucia P, Bradley, Kevin W, Jacobs-Sera, Deborah, Pope, Welkin H, Russell, Daniel A, Cresawn, Steven G, Lopatto, David, Bailey, Cheryl P, Hatfull, Graham F

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The Paleozoic Origin of Enzymatic Lignin Decomposition Reconstructed from 31 Fungal Genomes von Flundas, Dimitrios, Binder, Manfred, Riley, Robert, Barry, Kerrie, Blanchette, Robert A., Henrissat, Bernard, Martínez, Angel T., Otillar, Robert, Spatafora, Joseph W., Yadav, Jagjit S., Aerts, Andrea, Benoit, Isabelle, Boyd, Alex, Carlson, Alexis, Copeland, Alex, Coutinho, Pedro M., de Vries, Ronald P., Ferreira, Patricia, Findley, Keisha, Foster, Brian, Gaskell, Jill, Glotzer, Dylan, Górecki, Paweł, Heitman, Joseph, Hesse, Cedar, Hori, Chiaki, Igarashi, Kiyohiko, Jurgens, Joel A., Kallen, Nathan, Kersten, Phil, Kohler, Annegret, Kües, Ursula, Kumar, T. K. Arun, Kuo, Alan, LaButti, Kurt, Larrondo, Luis F., Lindquist, Erika, Ling, Albee, Lombard, Vincent, Lucas, Susan, Lundell, Taina, Martin, Rachael, McLaughlin, David J., Morgenstern, Ingo, Morin, Emanuelle, Murat, Claude, Nagy, Laszlo G., Nolan, Matt, Ohm, Robin A., Patyshakuliyeva, Aleksandrina, Rokas, Antonis, Ruiz-Dueñas, Francisco J., Sabat, Grzegorz, Salamov, Asaf, Samejima, Masahiro, Schmutz, Jeremy, Slot, Jason C., St. John, Franz, Stenlid, Jan, Sun, Hui, Sun, Sheng, Syed, Khajamohiddin, Tsang, Adrian, Wiebenga, Ad, Young, Darcy, Pisabarro, Antonio, Eastwood, Daniel C., Martin, Francis, Cullen, Dan, Grigoriev, Igor V., Hibbett, David S.

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Habitually sleepy drivers have a high frequency of automobile crashes associated with respiratory disorders during sleep von Masa, J F, Rubio, M, Findley, L J

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Model organisms contribute to diagnosis and discovery in the undiagnosed diseases network: current state and a future vision von Baldridge, Dustin, Wangler, Michael F., Bowman, Angela N., Yamamoto, Shinya, Schedl, Tim, Pak, Stephen C., Postlethwait, John H., Shin, Jimann, Solnica-Krezel, Lilianna, Bellen, Hugo J., Westerfield, Monte

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New Capabilities and Methods of the X-12-ARIMA Seasonal-Adjustment Program von Findley, David F., Monsell, Brian C., Bell, William R., Otto, Mark C., Chen, Bor-Chung

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Lamotrigine Monotherapy in Newly Diagnosed Untreated Epilepsy: A Double‐Blind Comparison with Phenytoin von Steiner, T. J., Dellaportas, C. I., Findley, L. J., Gross, M., Gibberd, F. B., Perkin, G. D., Park, D. M., Abbott, R.

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The incidence and significance of anti-natalizumab antibodies : Results from AFFIRM and SENTINEL von CALABRESI, P. A, GIOVANNONI, G, POLMAN, C. H, RADUE, E.-W, RUDICK, R. A, STUART, W. H, LUBLIN, F. D, WAJGT, A, WEINSTOCK-GUTTMAN, B, WYNN, D. R, LYNN, F, PANZARA, M. A, CONFAVREUX, C, GALETTA, S. L, HAVRDOVA, E, HUTCHINSON, M, KAPPOS, L, MILLER, D. H, O'CONNOR, P. W, PHILLIPS, J. T

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Prophage-mediated defence against viral attack and viral counter-defence von Dedrick, Rebekah M., Jacobs-Sera, Deborah, Bustamante, Carlos A. Guerrero, Garlena, Rebecca A., Mavrich, Travis N., Pope, Welkin H., Reyes, Juan C. Cervantes, Russell, Daniel A., Adair, Tamarah, Alvey, Richard, Bonilla, J. Alfred, Bricker, Jerald S., Brown, Bryony R., Byrnes, Deanna, Cresawn, Steven G., Davis, William B., Dickson, Leon A., Edgington, Nicholas P., Findley, Ann M., Golebiewska, Urszula, Grose, Julianne H., Hayes, Cory F., Hughes, Lee E., Hutchison, Keith W., Isern, Sharon, Johnson, Allison A., Kenna, Margaret A., Klyczek, Karen K., Mageeney, Catherine M., Michael, Scott F., Molloy, Sally D., Montgomery, Matthew T., Neitzel, James, Page, Shallee T., Pizzorno, Marie C., Poxleitner, Marianne K., Rinehart, Claire A., Robinson, Courtney J., Rubin, Michael R., Teyim, Joseph N., Vazquez, Edwin, Ware, Vassie C., Washington, Jacqueline, Hatfull, Graham F.

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Adaptive, Emotional, and Family Functioning of Children With Obsessive-Compulsive Disorder and Comorbid Attention Deficit Hyperactivity Disorder von Sukhodolsky, Denis G., do Rosario-Campos, Maria C., Scahill, Lawrence, Katsovich, Lily, Pauls, David L., Peterson, Bradley S., King, Robert A., Lombroso, Paul J., Findley, Diane B., Leckman, James F.

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An autosomal dominant neurological disorder caused by de novo variants in FAR1 resulting in uncontrolled synthesis of ether lipids von Ruiter, Jos P.N., van Lint, Alida E.M., Pras-Raves, Mia, Wever, Eric, Guillen Sacoto, Maria J., Begtrup, Amber, Tarnopolsky, Mark, Sell, Susan L., Nowak, Catherine B., Douglas, Jessica, Perlman, Seth, Martin, Nicole, Brault, Jennifer, Gahl, William A., Alejandro, Mercedes E., Dai, Hongzheng, Dhar, Shweta U., Hanchard, Neil A., Lee, Brendan H., Moretti, Paolo M., Murdock, David R., Nicholas, Sarah K., Potocki, Lorraine, Scott, Daryl A., Eng, Christine M., Deardorff, Matthew, Hassey, Kelly, Sullivan, Kathleen, Tan, Queenie K.-G., Beggs, Alan H., Berry, Gerard T., Cooper, Cynthia M., Pallais, J. Carl, Rodan, Lance H., Kelley, Emily G., Morava, Eva, Forghani, Irman, Lam, Byron, Levitt, Roy, Liu, Xue Zhong, McCauley, Jacob, Tekin, Mustafa, Thorson, Willa, Findley, Laurie C., Krasnewich, Donna M., Manolio, Teri A., Goldrich, Madison P., Draper, David D., Nath, Avi, Pusey, Barbara N., Toro, Camilo, Baker, Eva, Gochuico, Bernadette, Mosbrook-Davis, Deborah, Rossignol, Francis, Adam, Margaret, Amendola, Laura, Cunningham, Michael, Jarvik, Gail P., Jarvik, Jeffrey, Lam, Christina, Raskind, Wendy, Sybert, Virginia, Ashley, Euan A., Coakley, Terra R., Hom, Jason, Majcherska, Marta M., Martin, Beth A., Marwaha, Shruti, Ruzhnikov, Maura, Tabor, Holly K., Tucker, Brianna M., Zastrow, Diane B., Byrd, William E., Dell’Angelica, Esteban C., Douine, Emilie D., Mak, Bryan C., Martin, Martin G., Martínez-Agosto, Julian A., McGee, Elisabeth, Nelson, Stanley F., Parker, Neil H., Sinsheimer, Janet S., Wang, Lee-kai, Perry, Katherine Wesseling, Woods, Jeremy D., Pace, Laura, Marth, Gabor, Viskochil, Dave, Bayrak-Toydemir, Pinar, Duncan, Laura, Robertson, Amy K., Solem, Emily, Schedl, Timothy, Shin, Jimann, Solnica-Krezel, Lilianna, Waisfisz, Quinten, Zwijnenburg, Petra J.G., Wanders, Ronald J.A., Vaz, Frédéric M.

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Cannabis use a co-existing condition in admitted first episode bipolar patients von Currie, Terrence T., Hamilton, Jane E, Weaver, Michael F, Findley, Chase J, Soares, Jair C, Selek, Salih

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Macrocephaly and developmental delay caused by missense variants in RAB5C von Koop, Klaas, Yuan, Weimin, Tessadori, Federico, Rodriguez-Polanco, Wilmer R, Grubbs, Jeremy, Zhang, Bo, Osmond, Matt, Graham, Gail, Sawyer, Sarah, Conboy, Erin, Vetrini, Francesco, Treat, Kayla, Płoski, Rafal, Pienkowski, Victor Murcia, Kłosowska, Anna, Fieg, Elizabeth, Krier, Joel, Mallebranche, Coralie, Alban, Ziegler, Aldinger, Kimberly A, Ritter, Deborah, Macnamara, Ellen, Sullivan, Bonnie, Herriges, John, Alaimo, Joseph T, Helbig, Catherine, Ellis, Colin A, van Eyk, Clare, Gecz, Jozef, Farrugia, Daniel, Osei-Owusu, Ikeoluwa, Adès, Lesley, van den Boogaard, Marie-Jose, Fuchs, Sabine, Bakker, Jeroen, Duran, Karen, Dawson, Zachary D, Lindsey, Anika, Huang, Huiyan, Baldridge, Dustin, Silverman, Gary A, Grant, Barth D, Raizen, David, van Haaften, Gijs, Pak, Stephen C, Rehmann, Holger, Schedl, Tim, van Hasselt, Peter

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Heterozygous loss-of-function variants significantly expand the phenotypes associated with loss of GDF11 von Ravenscroft, Thomas A., Fieg, Elizabeth, Zirin, Jonathan, Kanca, Oguz, Adam, Margaret, Agrawal, Pankaj B., Alejandro, Mercedes E., Alvey, Justin, Andrews, Ashley, Azamian, Mahshid S., Bademci, Guney, Balasubramanya, Ashok, Behrens, Edward, Bican, Anna, Bohnsack, John, Botto, Lorenzo, Brown, Gabrielle, Byers, Peter, Chanprasert, Sirisak, Chao, Hsiao-Tuan, Cobban, Laurel A., Cogan, Joy D., Colley, Heather A., Cope, Heidi, Craigen, William J., Crouse, Andrew B., Dai, Hongzheng, Dayal, Jyoti G., Dipple, Katrina, Dorrani, Naghmeh, Draper, David D., Emrick, Lisa T., Falk, Marni, Fernandez, Liliana, Fieg, Elizabeth L., Findley, Laurie C., Gahl, William A., Godfrey, Rena A., Goldman, Alica M., Goldstein, David B., Hamid, Rizwan, Hanchard, Neil A., Hassey, Kelly, Hayes, Nichole, High, Frances, Hing, Anne, Hisama, Fuki M., Holm, Ingrid A., Huang, Yong, Huryn, Laryssa, Isasi, Rosario, Jarvik, Gail P., Jarvik, Jeffrey, Jayadev, Suman, Kiley, Dana, Krasnewich, Donna M., Lam, Christina, Lee, Hane, MacDowall, John, Majcherska, Marta M., Mak, Bryan C., Mamounas, Laura A., Martínez-Agosto, Julian A., McCauley, Jacob, Mulvihill, John J., Newman, John H., Oglesbee, Devin, Pace, Laura, Pallais, J. Carl, Palmer, Christina GS, Posey, Jennifer E., Potocki, Lorraine, Power, Bradley, Pusey, Barbara N., Rives, Lynette, Sacco, Ralph, Sampson, Jacinda B., Samson, Susan L., Scott, C. Ron, Schedl, Timothy, Shashi, Vandana, Tan, Queenie K.-G., Toro, Camilo, Viskochil, Dave, Wahl, Colleen E., Wambach, Jennifer, Wang, Lee-kai, Wener, Mark, Perry, Katherine Wesseling, Westerfield, Monte, Whitlock, Jordan, Yamamoto, Shinya, Yang, John, Yousef, Muhammad, Zastrow, Diane B., Zhao, Chunli, Osmond, Matthew, Postlethwait, John H., Krier, Joel, Bellen, Hugo J.

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Variable clinical severity in TANGO2 deficiency: Case series and literature review von Schymick, Jennifer, Leahy, Peter, Cowan, Tina, Ruzhnikov, Maura R. Z., Gates, Ryan, Fernandez, Liliana, Pramanik, Gopal, Yarlagadda, Vamsi, Wheeler, Matthew, Bernstein, Jonathan A., Enns, Gregory M., Lee, Chung

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Commonalities across computational workflows for uncovering explanatory variants in undiagnosed cases von Krier, Joel B., Züchner, Stephan, Huang, Alden, Bastarache, Lisa, Bican, Anna, Liu, Pengfei, Adam, Margaret, Alejandro, Mercedes E., Alvey, Justin, Azamian, Mahshid S., Bademci, Guney, Baker, Eva, Balasubramanyam, Ashok, Bale, Jim, Beck, Anita, Bennett, Jimmy, Berry, Gerard T., Bican, Anna, Bohnsack, John, Bonner, Devon, Boyd, Brenna, Brown, Gabrielle, Burrage, Lindsay C., Butte, Manish J., Coakley, Terra R., Cobban, Laurel A., Cogan, Joy D., Cole, F. Sessions, Cunningham, Michael, Dorrani, Naghmeh, Doss, Argenia L., Douine, Emilie D., Eng, Christine M., Falk, Marni, Ferreira, Carlos, Findley, Laurie C., Fogel, Brent L., Forghani, Irman, Gahl, William A., Glass, Ian, Godfrey, Rena A., Hanchard, Neil A., Hing, Anne, Huryn, Laryssa, Isasi, Rosario, Kiley, Dana, Korrick, Susan, Krakow, Deborah, Lalani, Seema R., LeBlanc, Kimberly, Liu, Xue Zhong, MacDowall, John, MacRae, Calum A., Mamounas, Laura A., Maravilla, Kenneth, Markello, Thomas C., Martin, Beth A., Martin, Martin G., Marwaha, Shruti, McCauley, Jacob, Merritt, J. Lawrence, Might, Matthew, Moretti, Paolo, Murdock, David R., Nakano-Okuno, Mariko, Nickerson, Deborah, Oglesbee, Devin, Pace, Laura, Pallais, J. Carl, Papp, Jeanette C., Phillips, John A., Power, Bradley, Pusey, Barbara N., Raja, Archana N., Renteria, Genecee, Rosenwasser, Natalie, Rossignol, Francis, Ruzhnikov, Maura, Sampson, Jacinda B., Schedl, Timothy, Shin, Jimann, Smith, Edward C., Sun, Angela, Sutton, Shirley, Sweetser, David A., Sybert, Virginia, Toro, Camilo, Tucker, Brianna M., Velinder, Matt, Viskochil, Dave, Wambach, Jennifer, Wang, Lee-kai, Ward, Patricia A., Wener, Mark, Westerfield, Monte, Whitlock, Jordan, Woods, Jeremy D., Yamamoto, Shinya, Yang, John, Zein, Wadih

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New Capabilities and Methods of the X-12-ARIMA Seasonal-Adjustment Program von Findley, David F., Monsell, Brian C., Bell, William R., Otto, Mark C., Chen, Bor-Chung

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The microRNA processor DROSHA is a candidate gene for a severe progressive neurological disorder von Barish, Scott, Senturk, Mumine, Schoch, Kelly, Minogue, Amanda L, Lopergolo, Diego, Fallerini, Chiara, Harland, Jake, Seemann, Jacob H, Stong, Nicholas, Kranz, Peter G, Kansagra, Sujay, Mikati, Mohamad A, Jasien, Joan, El-Dairi, Mays, Galluzzi, Paolo, Ariani, Francesca, Renieri, Alessandra, Mari, Francesca, Wangler, Michael F, Arur, Swathi, Jiang, Yong-Hui, Yamamoto, Shinya, Shashi, Vandana, Bellen, Hugo J

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