Ocular Brachytherapy (Interventional Radiotherapy): Preserving the Vision von Fionda, B., Pagliara, M.M., Chyrek, A.J., Guix, B., O'Day, R.F.J., Fog, L.S., Martínez-Monge, R., Tagliaferri, L.

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A single-cell time-lapse of mouse prenatal development from gastrula to birth von Qiu, Chengxiang, Martin, Beth K., Welsh, Ian C., Daza, Riza M., Le, Truc-Mai, Huang, Xingfan, Nichols, Eva K., Taylor, Megan L., Fulton, Olivia, O’Day, Diana R., Gomes, Anne Roshella, Ilcisin, Saskia, Srivatsan, Sanjay, Deng, Xinxian, Disteche, Christine M., Noble, William Stafford, Hamazaki, Nobuhiko, Moens, Cecilia B., Kimelman, David, Cao, Junyue, Schier, Alexander F., Spielmann, Malte, Murray, Stephen A., Trapnell, Cole, Shendure, Jay

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A human cell atlas of fetal gene expression von Cao, Junyue, O'Day, Diana R., Pliner, Hannah A., Kingsley, Paul D., Deng, Mei, Daza, Riza M., Zager, Michael A., Aldinger, Kimberly A., Blecher-Gonen, Ronnie, Zhang, Fan, Spielmann, Malte, Palis, James, Doherty, Dan, Steemers, Frank J., Glass, Ian A., Trapnell, Cole, Shendure, Jay

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Mutations in LAMA1 Cause Cerebellar Dysplasia and Cysts with and without Retinal Dystrophy von Aldinger, Kimberly A., Mosca, Stephen J., Tétreault, Martine, Dempsey, Jennifer C., Ishak, Gisele E., Hartley, Taila, Phelps, Ian G., Lamont, Ryan E., O’Day, Diana R., Basel, Donald, Gripp, Karen W., Baker, Laura, Stephan, Mark J., Bernier, Francois P., Boycott, Kym M., Majewski, Jacek, Parboosingh, Jillian S., Innes, A. Micheil, Doherty, Dan

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A human cell atlas of fetal chromatin accessibility von Domcke, Silvia, Hill, Andrew J., Daza, Riza M., Cao, Junyue, O'Day, Diana R., Pliner, Hannah A., Aldinger, Kimberly A., Pokholok, Dmitry, Zhang, Fan, Milbank, Jennifer H., Zager, Michael A., Glass, Ian A., Steemers, Frank J., Doherty, Dan, Trapnell, Cole, Cusanovich, Darren A., Shendure, Jay

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Marijuana use differentially affects cannabinoid receptor expression in early gestational human endometrium and placenta von Neradugomma, Naveen K., Drafton, Kaitlyn, O'Day, Diana R., Liao, Michael Z., Han, Lyrialle W., Glass, Ian A., Mao, Qingcheng

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Multiplex Targeted Sequencing Identifies Recurrently Mutated Genes in Autism Spectrum Disorders von O'Roak, Brian J., Vives, Laura, Fu, Wenqing, Egertson, Jarrett D., Stanaway, Ian B., Phelps, Ian G., Carvill, Gemma, Kumar, Akash, Lee, Choli, Ankenman, Katy, Munson, Jeff, Hiatt, Joseph B., Turner, Emily H., Levy, Roie, O'Day, Diana R., Krumm, Niklas, Coe, Bradley P., Martin, Beth K., Borenstein, Elhanan, Nickerson, Deborah A., Mefford, Heather C., Doherty, Dan, Akey, Joshua M., Bernier, Raphael, Eichler, Evan E., Shendure, Jay

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Hypomorphism for RPGRIP1L, a Ciliary Gene Vicinal to the FTO Locus, Causes Increased Adiposity in Mice von Stratigopoulos, George, Martin Carli, Jayne F., O’Day, Diana R., Wang, Liheng, LeDuc, Charles A., Lanzano, Patricia, Chung, Wendy K., Rosenbaum, Michael, Egli, Dieter, Doherty, Daniel A., Leibel, Rudolph L.

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A single-cell multi-omic atlas spanning the adult rhesus macaque brain von Chiou, Kenneth L, Huang, Xingfan, Bohlen, Martin O, Tremblay, Sébastien, DeCasien, Alex R, O'Day, Diana R, Spurrell, Cailyn H, Gogate, Aishwarya A, Zintel, Trisha M, Andrews, Madeline G, Martínez, Melween I, Starita, Lea M, Montague, Michael J, Platt, Michael L, Shendure, Jay, Snyder-Mackler, Noah

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Keratinocytes produce IL-17c to protect peripheral nervous systems during human HSV-2 reactivation von Peng, Tao, Chanthaphavong, R Savanh, Sun, Sijie, Trigilio, James A, Phasouk, Khamsone, Jin, Lei, Layton, Erik D, Li, Alvason Z, Correnti, Colin E, De van der Schueren, Willem, Vazquez, Julio, O'Day, Diana R, Glass, Ian A, Knipe, David M, Wald, Anna, Corey, Lawrence, Zhu, Jia

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Abnormal glycosylation in Joubert syndrome type 10 von Kane, Megan S, Davids, Mariska, Bond, Michelle R, Adams, Christopher J, Grout, Megan E, Phelps, Ian G, O'Day, Diana R, Dempsey, Jennifer C, Li, Xeuli, Golas, Gretchen, Vezina, Gilbert, Gunay-Aygun, Meral, Hanover, John A, Doherty, Dan, He, Miao, Malicdan, May Christine V, Gahl, William A, Boerkoel, Cornelius F

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PO-2163 The effect of eccentric plaque placement on tumour dose in Ruthenium plaque brachytherapy von Flanagan, J.P.M., Udovenya, W.H.F., Astrahan, M.A., McKay, D., Phillips, C., McKenzie, J.D., O'Day, R., Fog, L.S.

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Whole-Genome and RNA Sequencing Reveal Variation and Transcriptomic Coordination in the Developing Human Prefrontal Cortex von Werling, Donna M., Pochareddy, Sirisha, Choi, Jinmyung, An, Joon-Yong, Sheppard, Brooke, Peng, Minshi, Li, Zhen, Dastmalchi, Claudia, Santpere, Gabriel, Sousa, André M.M., Tebbenkamp, Andrew T.N., Kaur, Navjot, Gulden, Forrest O., Breen, Michael S., Liang, Lindsay, Gilson, Michael C., Zhao, Xuefang, Dong, Shan, Klei, Lambertus, Cicek, A. Ercument, Buxbaum, Joseph D., Adle-Biassette, Homa, Thomas, Jean-Leon, Aldinger, Kimberly A., O’Day, Diana R., Glass, Ian A., Zaitlen, Noah A., Talkowski, Michael E., Roeder, Kathryn, State, Matthew W., Devlin, Bernie, Sanders, Stephan J., Sestan, Nenad

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John 12:20–33 von O’Day, Gail R.

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Smoking history, and not depression, is related to deficits in detection of happy and sad faces von Meyers, K.K, Crane, N.A, O'Day, R, Zubieta, J.K, Giordani, B, Pomerleau, C.S, Horowitz, J.C, Langenecker, S.A

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Optometric use of a teleophthalmology service in rural Western Australia: comparison of two prospective audits von O'day, Roderick, Smith, Constance, Muir, Josephine, Turner, Angus

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Jesus as Friend in the Gospel of John von O'Day, Gail R.

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Mutations in CSPP1 Cause Primary Cilia Abnormalities and Joubert Syndrome with or without Jeune Asphyxiating Thoracic Dystrophy von Tuz, Karina, Bachmann-Gagescu, Ruxandra, O’Day, Diana R., Hua, Kiet, Isabella, Christine R., Phelps, Ian G., Stolarski, Allan E., O’Roak, Brian J., Dempsey, Jennifer C., Lourenco, Charles, Alswaid, Abdulrahman, Bönnemann, Carsten G., Medne, Livija, Nampoothiri, Sheela, Stark, Zornitza, Leventer, Richard J., Topçu, Meral, Cansu, Ali, Jagadeesh, Sujatha, Done, Stephen, Ishak, Gisele E., Glass, Ian A., Shendure, Jay, Neuhauss, Stephan C.F., Haldeman-Englert, Chad R., Doherty, Dan, Ferland, Russell J.

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Reporting of harms by randomised controlled trials in ophthalmology von O'Day, R, Walton, R, Blennerhassett, R, Gillies, M C, Barthelmes, D

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Mutations in LAMA1 Cause Cerebellar Dysplasia and Cysts with and without Retinal Dystrophy von Aldinger, Kimberly A., Mosca, Stephen J., Tétreault, Martine, Dempsey, Jennifer C., Ishak, Gisele E., Hartley, Taila, Phelps, Ian G., Lamont, Ryan E., O’Day, Diana R., Basel, Donald, Gripp, Karen W., Baker, Laura, Stephan, Mark J., Bernier, Francois P., Boycott, Kym M., Majewski, Jacek, Parboosingh, Jillian S., Innes, A. Micheil, Doherty, Dan

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