Stem cell-based treatments for Type 1 diabetes mellitus: bone marrow, embryonic, hepatic, pancreatic and induced pluripotent stem cells von Godfrey, K. J., Mathew, B., Bulman, J. C., Shah, O., Clement, S., Gallicano, G. I.

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“Coopetition” in Practice: Regional Collaborations in Radiology Resident Education von Bulman, JC, McQuiston, SA, Bedi, HS, Rawson, JV

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Stem cell-based treatments for Type1 diabetes mellitus: bone marrow, embryonic, hepatic, pancreatic and induced pluripotent stem cells von Godfrey, K J, Mathew, B, Bulman, J C, Shah, O, Clement, S, Gallicano, GI

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Systematic Analysis of Mobile Genetic Elements Mediating β-Lactamase Gene Amplification in Noncarbapenemase-Producing Carbapenem-Resistant Enterobacterales Bloodstream Infections von Shropshire, W C, Konovalova, A, McDaneld, P, Gohel, M, Strope, B, Sahasrabhojane, P, Tran, C N, Greenberg, D, Kim, J, Zhan, X, Aitken, S, Bhatti, M, Savidge, T C, Treangen, T J, Hanson, B M, Arias, C A, Shelburne, S A

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Utility of whole-exome sequencing for those near the end of the diagnostic odyssey: time to address gaps in care von Sawyer, S.L., Hartley, T., Dyment, D.A., Beaulieu, C.L., Schwartzentruber, J., Smith, A., Bedford, H.M., Bernard, G., Bernier, F.P., Brais, B., Bulman, D.E., Warman Chardon, J., Chitayat, D., Deladoëy, J., Fernandez, B.A., Frosk, P., Geraghty, M.T., Gerull, B., Gibson, W., Gow, R.M., Graham, G.E., Green, J.S., Heon, E., Horvath, G., Innes, A.M., Jabado, N., Kim, R.H., Koenekoop, R.K., Khan, A., Lehmann, O.J., Mendoza-Londono, R., Michaud, J.L., Nikkel, S.M., Penney, L.S., Polychronakos, C., Richer, J., Rouleau, G.A., Samuels, M.E., Siu, V.M., Suchowersky, O., Tarnopolsky, M.A., Yoon, G., Zahir, F.R., Majewski, J., Boycott, K.M.

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Whole‐exome sequencing is a valuable diagnostic tool for inherited peripheral neuropathies: Outcomes from a cohort of 50 families von Hartley, T., Wagner, J.D., Warman‐Chardon, J., Tétreault, M., Brady, L., Baker, S., Tarnopolsky, M., Bourque, P.R., Parboosingh, J.S., Smith, C., McInnes, B., Innes, A.M., Bernier, F., Curry, C.J., Yoon, G., Horvath, G.A., Bareke, E., Gillespie, M., Majewski, J., Bulman, D.E., Dyment, D.A., Boycott, K.M.

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Our Moonlight Revels: "A Midsummer Night's Dream" in the Theatre von Bulman, James C

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Whole-exome sequencing broadens the phenotypic spectrum of rare pediatric epilepsy: a retrospective study von Dyment, D.A., Tétreault, M., Beaulieu, C.L., Hartley, T., Ferreira, P., Chardon, J.W., Marcadier, J., Sawyer, S.L., Mosca, S.J., Innes, A.M., Parboosingh, J.S., Bulman, D.E., Schwartzentruber, J., Majewski, J., Tarnopolsky, M., Boycott, K.M.

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Shakespeare on Television: An Anthology of Essays and Reviews von Berger, Thomas L.

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Comedy from Shakespeare to Sheridan: Change and Continuity in the English and European Dramatic Tradition von Charney, Maurice

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Shakespeare's Imagined Persons: The Psychology of Role-Playing and Acting von Bulman, James C.

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Impacts of Fishing Low–Trophic Level Species on Marine Ecosystems von Smith, Anthony D. M., Brown, Christopher J., Bulman, Catherine M., Fulton, Elizabeth A., Johnson, Penny, Kaplan, Isaac C., Lozano-Montes, Hector, Mackinson, Steven, Marzloff, Martin, Shannon, Lynne J., Shin, Yunne-Jai, Tam, Jorge

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Political and religious practice in the early modern British world von Bulman, William J, Domínguez, Freddy

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BAFopathies’ DNA methylation epi-signatures demonstrate diagnostic utility and functional continuum of Coffin–Siris and Nicolaides–Baraitser syndromes von Aref-Eshghi, Erfan, Bend, Eric G., Hood, Rebecca L., Schenkel, Laila C., Carere, Deanna Alexis, Chakrabarti, Rana, Nagamani, Sandesh C. S., Cheung, Sau Wai, Campeau, Philippe M., Prasad, Chitra, Siu, Victoria Mok, Brady, Lauren, Tarnopolsky, Mark A., Callen, David J., Innes, A. Micheil, White, Susan M., Meschino, Wendy S., Shuen, Andrew Y., Paré, Guillaume, Bulman, Dennis E., Ainsworth, Peter J., Lin, Hanxin, Rodenhiser, David I., Hennekam, Raoul C., Boycott, Kym M., Schwartz, Charles E., Sadikovic, Bekim

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Effects of climate-driven primary production change on marine food webs: implications for fisheries and conservation von BROWN, C.J, FULTON, E.A, HOBDAY, A.J, MATEAR, R.J, POSSINGHAM, H.P, BULMAN, C, CHRISTENSEN, V, FORREST, R.E, GEHRKE, P.C, GRIBBLE, N.A, GRIFFITHS, S.P, LOZANO-MONTES, H, MARTIN, J.M, METCALF, S, OKEY, T.A, WATSON, R, RICHARDSON, A.J

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The Poetics of English Nationhood, 1590-1612 von Bulman, James C.

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Mutations in PIK3R1 Cause SHORT Syndrome von Dyment, David A., Smith, Amanda C., Alcantara, Diana, Schwartzentruber, Jeremy A., Basel-Vanagaite, Lina, Curry, Cynthia J., Temple, I. Karen, Reardon, William, Mansour, Sahar, Haq, Mushfequr R., Gilbert, Rodney, Lehmann, Ordan J., Vanstone, Megan R., Beaulieu, Chandree L., Majewski, Jacek, Bulman, Dennis E., O’Driscoll, Mark, Boycott, Kym M., Innes, A. Micheil

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XRCC1 mutation is associated with PARP1 hyperactivation and cerebellar ataxia von Hoch, Nicolas C., Hanzlikova, Hana, Rulten, Stuart L., Tétreault, Martine, Komulainen, Emilia, Ju, Limei, Hornyak, Peter, Zeng, Zhihong, Gittens, William, Rey, Stephanie A., Staras, Kevin, Mancini, Grazia M. S., McKinnon, Peter J., Wang, Zhao-Qi, Wagner, Justin D., Yoon, Grace, Caldecott, Keith W.

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Dimethylsulfoniopropionate biosynthesis in marine bacteria and identification of the key gene in this process von Curson, Andrew R. J., Liu, Ji, Bermejo Martínez, Ana, Green, Robert T., Chan, Yohan, Carrión, Ornella, Williams, Beth T., Zhang, Sheng-Hui, Yang, Gui-Peng, Bulman Page, Philip C., Zhang, Xiao-Hua, Todd, Jonathan D.

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Mutations in PNPLA6 are linked to photoreceptor degeneration and various forms of childhood blindness von Kmoch, S., Majewski, J., Ramamurthy, V., Cao, S., Fahiminiya, S., Ren, H., MacDonald, I. M., Lopez, I., Sun, V., Keser, V., Khan, A., Stránecký, V., Hartmannová, H., Přistoupilová, A., Hodaňová, K., Piherová, L., Kuchař, L., Baxová, A., Chen, R., Barsottini, O. G. P., Pyle, A., Griffin, H., Splitt, M., Sallum, J., Tolmie, J. L., Sampson, J. R., Chinnery, P., Banin, E., Sharon, D., Dutta, S., Grebler, R., Helfrich-Foerster, C., Pedroso, J. L., Kretzschmar, D., Cayouette, M., Koenekoop, R. K.

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