A study of urban bicycling accidents von Tucci, James J., Barone, James E.

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Late Acetabular Dysplasia Following Early Successful Pavlik Harness Treatment of Congenital Dislocation of the Hip von Tucci, James J, Kumar, S Jay, Guille, James T, Rubbo, Ernest R

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Slipped Capital Femoral Epiphysis in Black Children: Incidence of Chondrolysis von Spero, Charles R, Masciale, John P, Tornetta, Paul, Star, Michael J, Tucci, James J

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Clinical Practice Guideline: Sudden Hearing Loss von Stachler, Robert J., Chandrasekhar, Sujana S., Archer, Sanford M., Rosenfeld, Richard M., Schwartz, Seth R., Barrs, David M., Brown, Steven R., Fife, Terry D., Ford, Peg, Ganiats, Theodore G., Hollingsworth, Deena B., Lewandowski, Christopher A., Montano, Joseph J., Saunders, James E., Tucci, Debara L., Valente, Michael, Warren, Barbara E., Yaremchuk, Kathleen L., Robertson, Peter J.

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Transfusion Strategies for Patients in Pediatric Intensive Care Units von Lacroix, Jacques, Hébert, Paul C, Hutchison, James S, Hume, Heather A, Tucci, Marisa, Ducruet, Thierry, Gauvin, France, Collet, Jean-Paul, Toledano, Baruch J, Robillard, Pierre, Joffe, Ari, Biarent, Dominique, Meert, Kathleen, Peters, Mark J

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Consensus Recommendations for RBC Transfusion Practice in Critically Ill Children From the Pediatric Critical Care Transfusion and Anemia Expertise Initiative von Valentine, Stacey L, Bembea, Melania M, Muszynski, Jennifer A, Cholette, Jill M, Doctor, Allan, Spinella, Phillip C, Steiner, Marie E, Tucci, Marisa, Hassan, Nabil E, Parker, Robert I, Lacroix, Jacques, Argent, Andrew, Carson, Jeffrey L, Remy, Kenneth E, Demaret, Pierre, Emeriaud, Guillaume, Kneyber, Martin C J, Guzzetta, Nina, Hall, Mark W, Macrae, Duncan, Karam, Oliver, Russell, Robert T, Stricker, Paul A, Vogel, Adam M, Tasker, Robert C, Turgeon, Alexis F, Schwartz, Steven M, Willems, Ariane, Josephson, Cassandra D, Luban, Naomi L C, Lehmann, Leslie E, Stanworth, Simon J, Zantek, Nicole D, Bunchman, Timothy E, Cheifetz, Ira M, Fortenberry, James D, Delaney, Meghan, van de Watering, Leo, Robinson, Karen A, Malone, Sara, Steffen, Katherine M, Bateman, Scot T

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Genome sequencing reveals underdiagnosis of primary ciliary dyskinesia in bronchiectasis von Shoemark, Amelia, Griffin, Helen, Wheway, Gabrielle, Hogg, Claire, Lucas, Jane S, Camps, Carme, Taylor, Jenny, Carroll, Mary, Loebinger, Michael R, Chalmers, James D, Morris-Rosendahl, Deborah, Mitchison, Hannah M, De Soyza, Anthony, Brown, D, Ambrose, J C, Arumugam, P, Bevers, R, Bleda, M, Boardman-Pretty, F, Boustred, C R, Brittain, H, Caulfield, M J, Chan, G C, Fowler, T, Giess, A, Hamblin, A, Henderson, S, Hubbard, T J P, Jackson, R, Jones, L J, Kasperaviciute, D, Kayikci, M, Kousathanas, A, Lahnstein, L, Leigh, S E A, Leong, I U S, Lopez, F J, Maleady-Crowe, F, McEntagart, M, Minneci, F, Moutsianas, L, Mueller, M, Murugaesu, N, Need, A C, O'Donovan, P, Odhams, C A, Patch, C, Perez-Gil, D, Pereira, M B, Pullinger, J, Rahim, T, Rendon, A, Rogers, T, Savage, K, Sawant, K, Scott, R H, Siddiq, A, Sieghart, A, Smith, S C, Sosinsky, A, Stuckey, A, Tanguy, M, Taylor Tavares, A L, Thomas, E R A, Thompson, S R, Tucci, A, Welland, M J, Williams, E, Witkowska, K, Wood, S M

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The All of Us Research Program is an opportunity to enhance the diversity of US biomedical research von Bianchi, Diana W., Brennan, Patricia Flatley, Chiang, Michael F., Criswell, Lindsey A., D’Souza, Rena N., Gibbons, Gary H., Gilman, James K., Gordon, Joshua A., Green, Eric D., Gregurick, Susan, Hodes, Richard J., Kilmarx, Peter H., Koob, George F., Koroshetz, Walter J., Langevin, Helene M., Lorsch, Jon R., Marrazzo, Jeanne M., Pérez-Stable, Eliseo J., Rathmell, W. Kimryn, Rodgers, Griffin P., Rutter, Joni L., Simoni, Jane M., Tromberg, Bruce J., Tucci, Debara L., Volkow, Nora D., Woychik, Rick, Zenk, Shannon N., Kozlowski, Elyse, Peterson, Rachele S., Ginsburg, Geoffrey S., Denny, Joshua C.

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The NHS England 100,000 Genomes Project: feasibility and utility of centralised genome sequencing for children with cancer von Trotman, Jamie, Armstrong, Ruth, Firth, Helen, Trayers, Claire, Watkins, James, Allinson, Kieren, Jacques, Thomas S., Nicholson, James C., Burke, G. A. Amos, Behjati, Sam, Murray, Matthew J., Hook, Catherine E., Tarpey, Patrick

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Increased Survival with Enzalutamide in Prostate Cancer after Chemotherapy von Scher, Howard I, Fizazi, Karim, Saad, Fred, Taplin, Mary-Ellen, Sternberg, Cora N, Miller, Kurt, de Wit, Ronald, Mulders, Peter, Chi, Kim N, Shore, Neal D, Armstrong, Andrew J, Flaig, Thomas W, Fléchon, Aude, Mainwaring, Paul, Fleming, Mark, Hainsworth, John D, Hirmand, Mohammad, Selby, Bryan, Seely, Lynn, de Bono, Johann S

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Widespread genomic influences on phenotype in Dravet syndrome, a ‘monogenic’ condition von Martins Custodio, Helena, Clayton, Lisa M, Bellampalli, Ravishankara, Pagni, Susanna, Silvennoinen, Katri, Caswell, Richard, Brunklaus, Andreas, Guerrini, Renzo, Koeleman, Bobby P C, Lemke, Johannes R, Møller, Rikke S, Scheffer, Ingrid E, Weckhuysen, Sarah, Zara, Federico, Zuberi, Sameer, Kuchenbaecker, Karoline, Balestrini, Simona, Mills, James D, Sisodiya, Sanjay M

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Hypothermia Therapy After Pediatric Cardiac Arrest von DOHERTY, Dermot R, PARSHURAM, Christopher S, HUTCHISON, James S, GABOURY, Isabelle, HOSKOTE, Aparna, LACROIX, Jacques, TUCCI, Marisa, JOFFE, Ari, CHOONG, Karen, FARRELL, Rosemarie, BOHN, Desmond J

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Acute Liver Dysfunction Criteria in Critically Ill Children: The PODIUM Consensus Conference von Squires, James E, McKiernan, Patrick J, Squires, Robert H

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Scoring Systems for Organ Dysfunction and Multiple Organ Dysfunction: The PODIUM Consensus Conference von Schlapbach, Luregn J, Weiss, Scott L, Bembea, Melania M, Carcillo, Joseph A, Leclerc, Francis, Leteurtre, Stephane, Tissieres, Pierre, Wynn, James L, Zimmerman, Jerry, Lacroix, Jacques

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Refining the Pediatric Multiple Organ Dysfunction Syndrome von Weiss, Scott L, Carcillo, Joseph A, Leclerc, Francis, Leteurtre, Stephane, Schlapbach, Luregn J, Tissieres, Pierre, Wynn, James L, Lacroix, Jacques

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Recommendations on the Indications for RBC Transfusion for the Critically Ill Child Receiving Support From Extracorporeal Membrane Oxygenation, Ventricular Assist, and Renal Replac... von Bembea, Melania M, Cheifetz, Ira M, Fortenberry, James D, Bunchman, Timothy E, Valentine, Stacey L, Bateman, Scot T, Steiner, Marie E

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Human and mouse essentiality screens as a resource for disease gene discovery von Cacheiro, Pilar, Muñoz-Fuentes, Violeta, Murray, Stephen A., Dickinson, Mary E., Bucan, Maja, Nutter, Lauryl M. J., Peterson, Kevin A., Haselimashhadi, Hamed, Flenniken, Ann M., Morgan, Hugh, Westerberg, Henrik, Konopka, Tomasz, Hsu, Chih-Wei, Christiansen, Audrey, Lanza, Denise G., Beaudet, Arthur L., Heaney, Jason D., Fuchs, Helmut, Gailus-Durner, Valerie, Sorg, Tania, Prochazka, Jan, Novosadova, Vendula, Lelliott, Christopher J., Wardle-Jones, Hannah, Wells, Sara, Teboul, Lydia, Cater, Heather, Stewart, Michelle, Hough, Tertius, Wurst, Wolfgang, Sedlacek, Radislav, Adams, David J., Seavitt, John R., Tocchini-Valentini, Glauco, Mammano, Fabio, Braun, Robert E., McKerlie, Colin, Herault, Yann, de Angelis, Martin Hrabě, Mallon, Ann-Marie, Lloyd, K. C.  Kent, Brown, Steve D. M., Parkinson, Helen, Meehan, Terrence F., Smedley, Damian

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Whole-genome sequencing of chronic lymphocytic leukemia identifies subgroups with distinct biological and clinical features von Robbe, Pauline, Ridout, Kate E., Vavoulis, Dimitrios V., Dréau, Helene, Kinnersley, Ben, Denny, Nicholas, Chubb, Daniel, Appleby, Niamh, Cutts, Anthony, Cornish, Alex J., Lopez-Pascua, Laura, Clifford, Ruth, Burns, Adam, Stamatopoulos, Basile, Cabes, Maite, Alsolami, Reem, Antoniou, Pavlos, Oates, Melanie, Cavalieri, Doriane, Gibson, Jane, Prabhu, Anika V., Schwessinger, Ron, Jennings, Daisy, James, Terena, Maheswari, Uma, Duran-Ferrer, Martí, Carninci, Piero, Knight, Samantha J. L., Månsson, Robert, Hughes, Jim, Davies, James, Ross, Mark, Bentley, David, Strefford, Jonathan C., Devereux, Stephen, Pettitt, Andrew R., Hillmen, Peter, Caulfield, Mark J., Houlston, Richard S., Martín-Subero, José I., Schuh, Anna

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A gene pathogenicity tool “GenePy” identifies missed biallelic diagnoses in the 100,000 Genomes Project von Seaby, Eleanor G., Leggatt, Gary, Cheng, Guo, Thomas, N. Simon, Ashton, James J., Stafford, Imogen, Baralle, Diana, Rehm, Heidi L., O’Donnell-Luria, Anne, Ennis, Sarah, Ambrose, J.C., Arumugam, P., Bevers, R., Bleda, M., Boardman-Pretty, F., Boustred, C.R., Brittain, H., Brown, M.A., Caulfield, M.J., Chan, G.C., Giess, A., Griffin, J.N., Hamblin, A., Henderson, S., Hubbard, T.J.P., Jackson, R., Jones, L.J., Kasperaviciute, D., Kayikci, M., Kousathanas, A., Lahnstein, L., Lakey, A., Leigh, S.E.A., Leong, I.U.S., Lopez, F.J., Maleady-Crowe, F., McEntagart, M., Minneci, F., Mitchell, J., Moutsianas, L., Mueller, M., Murugaesu, N., Need, A.C., O‘Donovan, P., Odhams, C.A., Patch, C., Perez-Gil, D., Pereira, M.B., Pullinger, J., Rahim, T., Rendon, A., Rogers, T., Savage, K., Sawant, K., Scott, R.H., Siddiq, A., Sieghart, A., Smith, S.C., Sosinsky, A., Stuckey, A., Tanguy, M., Taylor Tavares, A.L., Thomas, E.R.A., Thompson, S.R., Tucci, A., Welland, M.J., Williams, E., Witkowska, K., Wood, S.M., Zarowiecki, M.

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Adaptive Long‐Read Sequencing Reveals GGC Repeat Expansion in ZFHX3 Associated with Spinocerebellar Ataxia Type 4 von Chen, Zhongbo, Gustavsson, Emil K., Macpherson, Hannah, Anderson, Claire, Clarkson, Chris, Rocca, Clarissa, Self, Eleanor, Alvarez Jerez, Pilar, Scardamaglia, Annarita, Pellerin, David, Montgomery, Kylie, Lee, Jasmaine, Gagliardi, Delia, Luo, Huihui, Hardy, John, Polke, James, Singleton, Andrew B., Blauwendraat, Cornelis, Mathews, Katherine D., Tucci, Arianna, Fu, Ying‐Hui, Houlden, Henry, Ryten, Mina, Ptáček, Louis J.

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