Postinjection delirium/sedation syndrome in patients with schizophrenia receiving olanzapine long-acting injection: Results from a large observational study by Meyers, Kristin J., Upadhyaya, Himanshu P., Landry, John L., Chhabra-Khanna, Rashna, Falk, Deborah M., Seetharama Rao, Balasubramanya, Jones, Meghan E.

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Olanzapine in pregnancy and breastfeeding: a review of data from global safety surveillance by Brunner, Elizabeth, Falk, Deborah M, Jones, Meghan, Dey, Debashish K, Shatapathy, Chetan Chinmaya

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Apicomplexan C-Mannosyltransferases Modify Thrombospondin Type I-containing Adhesins of the TRAP Family by Hoppe, Carolin M, Albuquerque-Wendt, Andreia, Bandini, Giulia, Leon, Deborah R, Shcherbakova, Aleksandra, Buettner, Falk F R, Izquierdo, Luis, Costello, Catherine E, Bakker, Hans, Routier, Françoise H

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Endoscopic approach to eosinophilic esophagitis: American Society for Gastrointestinal Endoscopy Consensus Conference by Aceves, Seema S., Alexander, Jeffrey A., Baron, Todd H., Bredenoord, Arjan J., Day, Lukejohn, Dellon, Evan S., Falk, Gary W., Furuta, Glenn T., Gonsalves, Nirmala, Hirano, Ikuo, Konda, Vani J.A., Lucendo, Alfredo J., Moawad, Fouad, Peterson, Kathryn A., Putnam, Philip E., Richter, Joel, Schoepfer, Alain M., Straumann, Alex, McBride, Deborah L., Sharma, Prateek, Katzka, David A.

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SARS-CoV-2 Receptor ACE2 Is an Interferon-Stimulated Gene in Human Airway Epithelial Cells and Is Detected in Specific Cell Subsets across Tissues by Ziegler, Carly G.K., Allon, Samuel J., Nyquist, Sarah K., Mbano, Ian M., Tzouanas, Constantine N., Cao, Yuming, Hauser, Blake M., Feldman, Jared, Muus, Christoph, Wadsworth, Marc H., Kazer, Samuel W., Hughes, Travis K., Doran, Benjamin, Gatter, G. James, Vukovic, Marko, Taliaferro, Faith, Mead, Benjamin E., Guo, Zhiru, Gras, Delphine, Plaisant, Magali, Ansari, Meshal, Angelidis, Ilias, Adler, Heiko, Sucre, Jennifer M.S., Taylor, Chase J., Lin, Brian, Waghray, Avinash, Mitsialis, Vanessa, Buchheit, Kathleen M., Boyce, Joshua A., Barrett, Nora A., Laidlaw, Tanya M., Carroll, Shaina L., Colonna, Lucrezia, Yu, Alison, Gideon, Hannah P., Lin, Philana Ling, Bingle, Colin D., Snapper, Scott B., Kropski, Jonathan A., Theis, Fabian J., Schiller, Herbert B., Zaragosi, Laure-Emmanuelle, Barbry, Pascal, Leslie, Alasdair, Kiem, Hans-Peter, Flynn, JoAnne L., Fortune, Sarah M., Berger, Bonnie, Finberg, Robert W., Garber, Manuel, Schmidt, Aaron G., Lingwood, Daniel, Shalek, Alex K., Ordovas-Montanes, Jose, Banovich, Nicholas, Barbry, Pascal, Desai, Tushar, Duong, Thu Elizabeth, Eickelberg, Oliver, Falk, Christine, Farzan, Michael, Glass, Ian, Haniffa, Muzlifah, Hung, Deborah, Kaminski, Naftali, Krasnow, Mark, Kuhnemund, Malte, Lafyatis, Robert, Lee, Haeock, Leroy, Sylvie, Lundeberg, Joakim, Meyer, Kerstin, Misharin, Alexander, Nawijn, Martijn, Nikolic, Marko Z., Ordovas-Montanes, Jose, Pe’er, Dana, Quake, Stephen, Rajagopal, Jay, Tata, Purushothama Rao, Regev, Aviv, Reyfman, Paul A., Rosen, Orit, Saeb-Parsy, Kourosh, Samakovlis, Christos, Schiller, Herbert, Schultze, Joachim L., Seibold, Max A., Shalek, Alex K., Shepherd, Douglas, Sun, Xin, Theis, Fabian, Tsankov, Alexander, von Papen, Michael, Whitsett, Jeffrey, Xavier, Ramnik, Xu, Yan, Zaragosi, Laure-Emmanuelle, Zhang, Kun

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Multiple Independent Gene Disorders Causing Bardet–Biedl Syndrome, Congenital Hypothyroidism, and Hearing Loss in a Single Indian Patient by Peixoto de Barcelos, Isabella, Li, Dong, Watson, Deborah, M. McCormick, Elizabeth, Elden, Lisa, Aleman, Thomas S, O’Neil, Erin C, J. Falk, Marni, Hakonarson, Hakon

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Myocyte-Specific Upregulation of ACE2 in Cardiovascular Disease: Implications for SARS-CoV-2–Mediated Myocarditis by Tucker, Nathan R., Chaffin, Mark, Bedi, Kenneth C., Papangeli, Irinna, Akkad, Amer-Denis, Arduini, Alessandro, Hayat, Sikander, Eraslan, Gökcen, Muus, Christoph, Bhattacharyya, Roby P., Stegmann, Christian M., Margulies, Kenneth B., Ellinor, Patrick T.

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Open-access quantitative MRI data of the spinal cord and reproducibility across participants, sites and manufacturers by Cohen-Adad, Julien, Alonso-Ortiz, Eva, Abramovic, Mihael, Arneitz, Carina, Atcheson, Nicole, Barlow, Laura, Barry, Robert L., Barth, Markus, Battiston, Marco, Büchel, Christian, Budde, Matthew, Callot, Virginie, Combes, Anna J. E., De Leener, Benjamin, Descoteaux, Maxime, de Sousa, Paulo Loureiro, Dostál, Marek, Doyon, Julien, Dvorak, Adam, Eippert, Falk, Epperson, Karla R., Epperson, Kevin S., Freund, Patrick, Finsterbusch, Jürgen, Foias, Alexandru, Fratini, Michela, Fukunaga, Issei, Gandini Wheeler-Kingshott, Claudia A. M., Germani, Giancarlo, Gilbert, Guillaume, Giove, Federico, Gros, Charley, Grussu, Francesco, Hagiwara, Akifumi, Henry, Pierre-Gilles, Horák, Tomáš, Hori, Masaaki, Joers, James, Kamiya, Kouhei, Karbasforoushan, Haleh, Keřkovský, Miloš, Khatibi, Ali, Kim, Joo-Won, Kinany, Nawal, Kitzler, Hagen H., Kolind, Shannon, Kong, Yazhuo, Kudlička, Petr, Kuntke, Paul, Kurniawan, Nyoman D., Kusmia, Slawomir, Labounek, René, Laganà, Maria Marcella, Laule, Cornelia, Law, Christine S., Lenglet, Christophe, Leutritz, Tobias, Liu, Yaou, Llufriu, Sara, Mackey, Sean, Martinez-Heras, Eloy, Mattera, Loan, Nestrasil, Igor, O’Grady, Kristin P., Papinutto, Nico, Papp, Daniel, Pareto, Deborah, Parrish, Todd B., Pichiecchio, Anna, Prados, Ferran, Rovira, Àlex, Ruitenberg, Marc J., Samson, Rebecca S., Savini, Giovanni, Seif, Maryam, Seifert, Alan C., Smith, Alex K., Smith, Seth A., Smith, Zachary A., Solana, Elisabeth, Suzuki, Y., Tackley, George, Tinnermann, Alexandra, Valošek, Jan, Van De Ville, Dimitri, Yiannakas, Marios C., Weber II, Kenneth A., Weiskopf, Nikolaus, Wise, Richard G., Wyss, Patrik O., Xu, Junqian

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Cryopreservation Changes the Immune Effector Cell Composition of Peripheral Blood Stem Cell Grafts: An Analysis from the DKMS and NMDP Graft Composition Study by Rücker-Braun, Elke, Falk, Bose, Markey, Kate A., Minderman, Hans, Baldauf, Henning, Heymann, Nicole, Uhlemann, Heike, Heiduschke, Lisa, MacMillan, Hugh R., Newell, Evan W., O'Loughlin, Kieran L., Spahn, Ashley, Maguire, Orla, Buk, Deborah, Bornhäuser, Martin, Schmidt, Alexander H., Devine, Steven M., Schetelig, Johannes, Auletta, Jeffery J., van den Brink, Marcel R.M., Spellman, Stephen R., Heidenreich, Falk

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SPTSSA variants alter sphingolipid synthesis and cause a complex hereditary spastic paraplegia by Srivastava, Siddharth, Shaked, Hagar Mor, Gable, Kenneth, Gupta, Sita D, Pan, Xueyang, Somashekarappa, Niranjanakumari, Han, Gongshe, Mohassel, Payam, Gotkine, Marc, Doney, Elizabeth, Goldenberg, Paula, Tan, Queenie K G, Gong, Yi, Kleinstiver, Benjamin, Wishart, Brian, Cope, Heidi, Pires, Claudia Brito, Stutzman, Hannah, Spillmann, Rebecca C, Sadjadi, Reza, Elpeleg, Orly, Lee, Chia-Hsueh, Bellen, Hugo J, Edvardson, Simon, Eichler, Florian, Dunn, Teresa M

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Sitting, physical activity, and serum oestrogen metabolism in postmenopausal women: the Women’s Health Initiative Observational Study by Oh, Hannah, Arem, Hannah, Matthews, Charles E, Wentzensen, Nicolas, Reding, Kerryn W, Brinton, Louise A, Anderson, Garnet L, Coburn, Sally B, Cauley, Jane A, Chen, Chu, Goodman, Deborah, Pfeiffer, Ruth M, Falk, Roni T, Xu, Xia, Trabert, Britton

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Model organisms contribute to diagnosis and discovery in the undiagnosed diseases network: current state and a future vision by 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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Evolution of genes and genomes on the Drosophila phylogeny by Clark, Andrew G, Eisen, Michael B, Smith, Douglas R, Bergman, Casey M, Oliver, Brian, Markow, Therese A, Kaufman, Thomas C, Kellis, Manolis, Gelbart, William, Iyer, Venky N, Pollard, Daniel A, Sackton, Timothy B, Larracuente, Amanda M, Singh, Nadia D, Abad, Jose P, Abt, Dawn N, Adryan, Boris, Aguade, Montserrat, Akashi, Hiroshi, Anderson, Wyatt W, Aquadro, Charles F, Ardell, David H, Arguello, Roman, Artieri, Carlo G, Barbash, Daniel A, Barker, Daniel, Barsanti, Paolo, Batterham, Phil, Batzoglou, Serafim, Begun, Dave, Bhutkar, Arjun, Blanco, Enrico, Bosak, Stephanie A, Bradley, Robert K, Brand, Adrianne D, Brent, Michael R, Brooks, Angela N, Brown, Randall H, Butlin, Roger K, Caggese, Corrado, Calvi, Brian R, Bernardo de Carvalho, A, Caspi, Anat, Castrezana, Sergio, Celniker, Susan E, Chang, Jean L, Chapple, Charles, Chatterji, Sourav, Chinwalla, Asif, Civetta, Alberto, Clifton, Sandra W, Comeron, Josep M, Costello, James C, Coyne, Jerry A, Daub, Jennifer, David, Robert G, Delcher, Arthur L, Delehaunty, Kim, Do, Chuong B, Ebling, Heather, Edwards, Kevin, Eickbush, Thomas, Evans, Jay D, Filipski, Alan, Findeiss, Sven, Freyhult, Eva, Fulton, Lucinda, Fulton, Robert, Garcia, Ana C L, Gardiner, Anastasia, Garfield, David A, Garvin, Barry E, Gibson, Greg, Gilbert, Don, Gnerre, Sante, Godfrey, Jennifer, Good, Robert, Gotea, Valer, Gravely, Brenton, Greenberg, Anthony J, Griffiths-Jones, Sam, Gross, Samuel, Guigo, Roderic, Gustafson, Erik A, Haerty, Wilfried, Hahn, Matthew W, Halligan, Daniel L, Halpern, Aaron L, Halter, Gillian M, Han, Mira V, Heger, Andreas, Hillier, LaDeana, Hinrichs, Angie S, Holmes, Ian, Hoskins, Roger A, Hubisz, Melissa J, Hultmark, Dan, Huntley, Melanie A, Jaffe, David B, Jagadeeshan, Santosh

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Bi-allelic variants in INTS11 are associated with a complex neurological disorder by Tepe, Burak, Cogne, Benjamin, Neil, Jennifer E., Walsh, Christopher A., Magal, Nurit, Drasinover, Valerie, Schwab, Tanya, Schmitz, Chris, Clark, Karl, Blanc, Pierre, Bademci, Guney, Balasubramanyam, Ashok, Baldridge, Dustin, Bayrak-Toydemir, Pinar, Beck, Anita, Behrens, Edward, Bican, Anna, Bivona, Stephanie, Blue, Elizabeth, Boyd, Brenna, Briere, Lauren C., Brown, Gabrielle, Byers, Peter, Byrd, William E., Carey, John, Clark, Gary D., Coakley, Terra R., Colley, Heather A., Craigen, William J., Cunningham, Michael, Dasari, Surendra, Dayal, Jyoti G., Deardorff, Matthew, Dipple, Katrina, Doherty, Daniel, Doss, Argenia L., Emrick, Lisa T., Fernandez, Liliana, Forghani, Irman, Glass, Ian, Gochuico, Bernadette, Golden-Grant, Katie, Goldrich, Madison P., Gutierrez, Irma, Hamid, Rizwan, Hayes, Nichole, Hom, Jason, Horike-Pyne, Martha, Isasi, Rosario, Jarvik, Jeffrey, Jobanputra, Vaidehi, Karaviti, Lefkothea, Kiley, Dana, Kobren, Shilpa N., Krasnewich, Donna M., LeBlanc, Kimberly, Levitt, Roy, Mahoney, Rachel, Malicdan, May Christine V., Mamounas, Laura A., Mao, Rong, Maravilla, Kenneth, Marom, Ronit, Martin, Martin G., Martínez-Agosto, Julian A., Merritt, J. Lawrence, Morava, Eva, Newman, John H., Nickerson, Deborah, Novacic, Donna, Oglesbee, Devin, Pace, Laura, Palmer, Christina GS, Papp, Jeanette C., Rao, Deepak A., Renteria, Genecee, Reuter, Chloe M., Robertson, Amy K., Rosenfeld, Jill A., Rossignol, Francis, Ruzhnikov, Maura, Scott, C. Ron, Shin, Jimann, Sinsheimer, Janet S., Sullivan, Jennifer A., Sun, Angela, Tabor, Holly K., Telischi, Fred, Toro, Camilo, Tucker, Brianna M., Urv, Tiina K., Vogel, Tiphanie P., Walker, Melissa, Wangler, Michael F., Perry, Katherine Wesseling, Westerfield, Monte, Wolfe, Lynne A., Worley, Kim, Xiao, Changrui, Zuchner, Stephan

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Effect of Fluconazole Prophylaxis on Candidiasis and Mortality in Premature Infants: A Randomized Clinical Trial by Benjamin, Daniel K, Hudak, Mark L, Duara, Shahnaz, Randolph, David A, Bidegain, Margarita, Mundakel, Gratias T, Natarajan, Girija, Burchfield, David J, White, Robert D, Shattuck, Karen E, Neu, Natalie, Bendel, Catherine M, Kim, M. Roger, Finer, Neil N, Stewart, Dan L, Arrieta, Antonio C, Wade, Kelly C, Kaufman, David A, Manzoni, Paolo, Prather, Kristi O, Testoni, Daniela, Berezny, Katherine Y, Smith, P. Brian

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Laparoscopic sleeve gastrectomy at a new bariatric surgery centre in Canada: 30-day complication rates using the Clavien–Dindo classification by Falk, Vanessa, MD, Twells, Laurie, PhD, Gregory, Deborah, PhD, Murphy, Raleen, Smith, Chris, MD, Boone, Darrell, MD, Pace, David, MD

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Implications of gender differences for human health risk assessment and toxicology by Vahter, Marie, Gochfeld, Michael, Casati, Barbara, Thiruchelvam, Mona, Falk-Filippson, Agneta, Kavlock, Robert, Marafante, Erminio, Cory-Slechta, Deborah

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Identification and molecular characterization of a new ovarian cancer susceptibility locus at 17q21.31 by Shen, Howard C., Velkova, Aneliya, Chen, Zhihua, Lin, Hui-Yi, Ann Chen, Y, Qu, Xiaotao, Ramus, Susan J., Lee, Janet, Lee, Nathan, Larson, Melissa C., Anton-Culver, Hoda, Antoniou, Antonis C., Armasu, Sebastian M., Bacot, François, Baglietto, Laura, Bandera, Elisa V., Bogdanova, Natalia, Brooks-Wilson, Angela, Butzow, Ralf, Cai, Qiuyin, Campbell, Ian, Chang-Claude, Jenny, Chanock, Stephen, Cheng, Jin Q., Cook, Linda S., Couch, Fergus J., Cunningham, Julie M., Dansonka-Mieszkowska, Agnieszka, Doherty, Jennifer A., Easton, Douglas F., Fasching, Peter A., Flanagan, James M., Giles, Graham G., Gonzalez-Bosquet, Jesus, Gore, Martin, Halle, Mari K., Harter, Philipp, Hillemanns, Peter, Hoatlin, Maureen, Høgdall, Claus K., Høgdall, Estrid, Hosono, Satoyo, Jensen, Allan, Jim, Heather, Karlan, Beth Y., Kaye, Stanley B., Kiemeney, Lambertus A., Kikkawa, Fumitaka, Konecny, Gottfried E., Krüger Kjaer, Susanne, Lambrechts, Sandrina, Lancaster, Johnathan M., Leminen, Arto, Levine, Douglas A., Liang, Dong, Kiong Lim, Boon, Lissowska, Jolanta, Lubiński, Jan, McLaughlin, John R., Moysich, Kirsten B., Nakanishi, Toru, Narod, Steven A., Ness, Roberta B., Nickels, Stefan, Noushmehr, Houtan, Odunsi, Kunle, Olson, Sara H., Orlow, Irene, Paul, James, Pelttari, Liisa M., Pike, Malcolm C., Poole, Elizabeth M., Renner, Stefan P., Risch, Harvey A., Rodriguez-Rodriguez, Lorna, Anne Rossing, Mary, Rudolph, Anja, Rzepecka, Iwona K., Salvesen, Helga B., Shu, Xiao-Ou, Shvetsov, Yurii B., Southey, Melissa C., Spiewankiewicz, Beata, Sutphen, Rebecca, van Altena, Anne M., Vincent, Daniel, Vitonis, Allison F., Wentzensen, Nicolas, Wik, Elisabeth, Winterhoff, Boris, Ling Woo, Yin, Yang, Hannah P., Zulkifli, Famida, Schildkraut, Joellen M., Berchuck, Andrew, Goode, Ellen L., Pharoah, Paul D.P., Monteiro, Alvaro N.A., Sellers, Thomas A., Gayther, Simon A.

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Biallelic MADD variants cause a phenotypic spectrum ranging from developmental delay to a multisystem disorder by Schneeberger, Pauline E, Kortüm, Fanny, Korenke, Georg Christoph, Alawi, Malik, Santer, René, Woidy, Mathias, Buhas, Daniela, Fox, Stephanie, Juusola, Jane, Alfadhel, Majid, Webb, Bryn D, Coci, Emanuele G, Abou Jamra, Rami, Siekmeyer, Manuela, Biskup, Saskia, Heller, Corina, Maier, Esther M, Javaher-Haghighi, Poupak, Bedeschi, Maria F, Ajmone, Paola F, Iascone, Maria, Peeters, Hilde, Ballon, Katleen, Jaeken, Jaak, Rodríguez Alonso, Aroa, Palomares-Bralo, María, Santos-Simarro, Fernando, Meuwissen, Marije E C, Beysen, Diane, Kooy, R Frank, Houlden, Henry, Murphy, David, Doosti, Mohammad, Karimiani, Ehsan G, Mojarrad, Majid, Maroofian, Reza, Noskova, Lenka, Kmoch, Stanislav, Honzik, Tomas, Cope, Heidi, Sanchez-Valle, Amarilis, Gelb, Bruce D, Kurth, Ingo, Hempel, Maja, Kutsche, Kerstin

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The microRNA processor DROSHA is a candidate gene for a severe progressive neurological disorder by 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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