Cardiac-Specific YAP Activation Improves Cardiac Function and Survival in an Experimental Murine MI Model von Lin, Zhiqiang, von Gise, Alexander, Zhou, Pingzhu, Gu, Fei, Ma, Qing, Jiang, Jianming, Yau, Allan L, Buck, Jessica N, Gouin, Katryna A, van Gorp, Pim R.R, Zhou, Bin, Chen, Jinghai, Seidman, Jonathan G, Wang, Da-Zhi, Pu, William T

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Risk Factors for Prolonged Opioid Use Following Spine Surgery, and the Association with Surgical Intensity, Among Opioid-Naive Patients von Schoenfeld, Andrew J., Nwosu, Kenneth, Jiang, Wei, Yau, Allan L., Chaudhary, Muhammad Ali, Scully, Rebecca E., Koehlmoos, Tracey, Kang, James D., Haider, Adil H.

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Utility of Adding Magnetic Resonance Imaging to Computed Tomography Alone in the Evaluation of Cervical Spine Injury: A Propensity-Matched Analysis von Schoenfeld, Andrew J., Tobert, Daniel G., Le, Hai V., Leonard, Dana A., Yau, Allan L., Rajan, Prashant, Cho, Charles H., Kang, James D., Bono, Christopher M., Harris, Mitchel B.

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Characterization of the encoding properties of intraspinal mechanosensory neurons in the lamprey von Massarelli, Nicole, Yau, Allan L., Hoffman, Kathleen A., Kiemel, Tim, Tytell, Eric D.

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The impact of hepatitis C virus infection on 90-day outcomes following major orthopaedic surgery: a propensity-matched analysis von Chowdhury, Ritam, Chaudhary, Muhammad Ali, Sturgeon, Daniel J., Jiang, Wei, Yau, Allan L., Koehlmoos, Tracey P., Haider, Adil H., Schoenfeld, Andrew J.

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Factors influencing success of clinical genome sequencing across a broad spectrum of disorders von Taylor, Jenny C, Martin, Hilary C, Lise, Stefano, Broxholme, John, Cazier, Jean-Baptiste, Rimmer, Andy, Kanapin, Alexander, Lunter, Gerton, Fiddy, Simon, Allan, Chris, Aricescu, A Radu, Attar, Moustafa, Babbs, Christian, Becq, Jennifer, Bento, Celeste, Bignell, Patricia, Blair, Edward, Buckle, Veronica J, Bull, Katherine, Cais, Ondrej, Cario, Holger, Chapel, Helen, Copley, Richard R, Cornall, Richard, Craft, Jude, Dahan, Karin, Davenport, Emma E, Dendrou, Calliope, Devuyst, Olivier, Flint, Jonathan, Fugger, Lars, Gilbert, Rodney D, Goriely, Anne, Greger, Ingo H, Grocock, Russell, Gruszczyk, Anja V, Hastings, Robert, Hatton, Edouard, Higgs, Doug, Hill, Adrian, Holmes, Chris, Howard, Malcolm, Hughes, Linda, Humburg, Peter, Karpe, Fredrik, Kingsbury, Zoya, Kini, Usha, Krohn, Jonathan, Lamble, Sarah, Langman, Craig, Lonie, Lorne, Luck, Joshua, McCarthy, Davis, McGowan, Simon J, McMullin, Mary Frances, Miller, Kerry A, Murray, Lisa, Németh, Andrea H, Nesbit, M Andrew, Nutt, David, Ormondroyd, Elizabeth, Patel, Smita Y, Percy, Melanie, Petousi, Nayia, Piazza, Paolo, Piret, Sian E, Polanco-Echeverry, Guadalupe, Popitsch, Niko, Powrie, Fiona, Pugh, Chris, Quek, Lynn, Robson, Kathryn, Russo, Alexandra, Sahgal, Natasha, van Schouwenburg, Pauline A, Schuh, Anna, Silverman, Earl, Simmons, Alison, Sørensen, Per Soelberg, Sweeney, Elizabeth, Taylor, John, Thakker, Rajesh V, Tomlinson, Ian, Trebes, Amy, Twigg, Stephen R F, Uhlig, Holm H, Vyas, Paresh, Wall, Steven A, Watkins, Hugh, Whyte, Michael P, Witty, Lorna, Wright, Ben, Yau, Chris, Buck, David, Humphray, Sean, Ratcliffe, Peter J, Bell, John I, Wilkie, Andrew O M, Bentley, David, Donnelly, Peter

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Whole-genome sequencing of bladder cancers reveals somatic CDKN1A mutations and clinicopathological associations with mutation burden von Cazier, J. -B., Rao, S. R., McLean, C. M., Walker, A. K., Wright, B. J., Jaeger, E. E. M., Kartsonaki, C., Marsden, L., Yau, C., Camps, C., Kaisaki, P., Taylor, J., Catto, J. W., Tomlinson, I. P. M., Kiltie, A. E., Hamdy, F. C.

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Mutations in TCF12, encoding a basic helix-loop-helix partner of TWIST1, are a frequent cause of coronal craniosynostosis von Sharma, Vikram P, Fenwick, Aimée L, Brockop, Mia S, McGowan, Simon J, Goos, Jacqueline A C, Hoogeboom, A Jeannette M, Brady, Angela F, Jeelani, Nu Owase, Lynch, Sally Ann, Mulliken, John B, Murray, Dylan J, Phipps, Julie M, Sweeney, Elizabeth, Tomkins, Susan E, Wilson, Louise C, Bennett, Sophia, Cornall, Richard J, Broxholme, John, Kanapin, Alexander, Johnson, David, Wall, Steven A, van der Spek, Peter J, Mathijssen, Irene M J, Maxson, Robert E, Twigg, Stephen R F, Wilkie, Andrew O M

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NOX1 loss-of-function genetic variants in patients with inflammatory bowel disease von Schwerd, T, Bryant, R V, Pandey, S, Capitani, M, Meran, L, Cazier, J-B, Jung, J, Mondal, K, Parkes, M, Mathew, C G, Fiedler, K, McCarthy, D J, Sullivan, P B, Rodrigues, A, Travis, S P L, Moore, C, Sambrook, J, Ouwehand, W H, Roberts, D J, Danesh, J, Russell, R K, Wilson, D C, Kelsen, J R, Cornall, R, Denson, L A, Kugathasan, S, Knaus, U G, Serra, E G, Anderson, C A, Duerr, R H, McGovern, D PB, Cho, J, Powrie, F, Li, V SW, Muise, A M, Uhlig, H H

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Etiology of White Matter Hyperintensities in Autosomal Dominant and Sporadic Alzheimer Disease von Shirzadi, Zahra, Schultz, Stephanie A, Yau, Wai-Ying W, Joseph-Mathurin, Nelly, Fitzpatrick, Colleen D, Levin, Raina, Kantarci, Kejal, Preboske, Gregory M, Jack, Jr, Clifford R, Farlow, Martin R, Hassenstab, Jason, Jucker, Mathias, Morris, John C, Xiong, Chengjie, Karch, Celeste M, Levey, Allan I, Gordon, Brian A, Schofield, Peter R, Salloway, Stephen P, Perrin, Richard J, McDade, Eric, Levin, Johannes, Cruchaga, Carlos, Allegri, Ricardo F, Fox, Nick C, Goate, Alison, Day, Gregory S, Koeppe, Robert, Chui, Helena C, Berman, Sarah, Mori, Hiroshi, Sanchez-Valle, Raquel, Lee, Jae-Hong, Rosa-Neto, Pedro, Ruthirakuhan, Myuri, Wu, Che-Yuan, Swardfager, Walter, Benzinger, Tammie L S, Sohrabi, Hamid R, Martins, Ralph N, Bateman, Randall J, Johnson, Keith A, Sperling, Reisa A, Greenberg, Steven M, Schultz, Aaron P, Chhatwal, Jasmeer P

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Mutations in GDP-Mannose Pyrophosphorylase B Cause Congenital and Limb-Girdle Muscular Dystrophies Associated with Hypoglycosylation of α-Dystroglycan von Carss, Keren J., Stevens, Elizabeth, Foley, A. Reghan, Cirak, Sebahattin, Riemersma, Moniek, Torelli, Silvia, Hoischen, Alexander, Willer, Tobias, van Scherpenzeel, Monique, Moore, Steven A., Messina, Sonia, Bertini, Enrico, Bönnemann, Carsten G., Abdenur, Jose E., Grosmann, Carla M., Kesari, Akanchha, Punetha, Jaya, Quinlivan, Ros, Waddell, Leigh B., Young, Helen K., Wraige, Elizabeth, Yau, Shu, Brodd, Lina, Feng, Lucy, Sewry, Caroline, MacArthur, Daniel G., North, Kathryn N., Hoffman, Eric, Stemple, Derek L., Hurles, Matthew E., van Bokhoven, Hans, Campbell, Kevin P., Lefeber, Dirk J., Lin, Yung-Yao, Muntoni, Francesco

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Natural history of benign multiple sclerosis: Clinical and HLA correlates in a Western Australian cohort von Fabis-Pedrini, Marzena J., James, Ian, Seewann, Alexandra, Yau, Wai Y., van de Bovenkamp, Arnold A., Sanders, Fay R.K., Qiu, Wei, Burton, Jason, Mastaglia, Frank L., Carroll, William M., Kermode, Allan G.

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Homozygous mutations in a predicted endonuclease are a novel cause of congenital dyserythropoietic anemia type I von Babbs, C., Roberts, N. A., Sanchez-Pulido, L., McGowan, S. J., Ahmed, M. R., Brown, J. M., Sabry, M. A., Bentley, D. R., McVean, G. A., Donnelly, P., Gileadi, O., Ponting, C. P., Higgs, D. R., Buckle, V. J.

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Burkholderia pseudomallei infection in a cystic fibrosis patient from the Caribbean: a case report von Corral, Dimas Mateos, Coates, Allan L, Yau, Yvonne C W, Tellier, Raymond, Glass, Mindy, Jones, Steven M, Waters, Valerie J

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Erythrocytosis associated with a novel missense mutation in the BPGM gene von Petousi, Nayia, Copley, Richard R, Lappin, Terence R J, Haggan, Sally E, Bento, Celeste M, Cario, Holger, Percy, Melanie J, Ratcliffe, Peter J, Robbins, Peter A, McMullin, Mary Frances

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REMEMBRANCES OF LI XUEQIN (1933–2019)

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Patients Experiencing Early Virologic Failure on a Protease Inhibitor- or Nonnucleoside Reverse Transcriptase Inhibitor-Based Initial Regimen Containing a Thymidine Analogue and La... von Rodriguez, Allan, Hill-Zabala, Christina, Sloan, Louis, Jefferson, Thomas, Yau, Linda, Watson, Maria, Irlbeck, David, Shaefer, Mark

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Factors influencing success of clinical genome sequencing across a broad spectrum of disorders von Taylor, JC, Martin, HC, Lise, S, Broxholme, J, Cazier, J-B, Rimmer, A, Kanapin, A, Lunter, G, Fiddy, S, Allan, C, Aricescu, AR, Attar, M, Babbs, C, Becq, J, Beeson, D, Bento, C, Bignell, P, Blair, E, Buckle, VJ, Bull, K, Cario, H, Chapel, H, Copley, RR, Cornall, R, Craft, J, Dahan, K, Davenport, EE, Dendrou, C, Devuyst, O, Fenwick, AL, Flint, J, Fugger, L, Gilbert, RD, Goriely, A, Green, A, Greger, IH, Grocock, R, Gruszczyk, AV, Hastings, R, Higgs, D, Holmes, C, Howard, M, Hughes, L, Humburg, P, Johnson, D, Karpe, F, Kingsbury, Z, Kini, U, Knight, JC, Krohn, J, Lamble, S, Langman, C, Lonie, L, Luck, J, McCarthy, D, McGowan, SJ, McMullin, MF, Miller, KA, Murray, L, Nemeth, AH, Nesbit, MA, Nutt, D, Ormondroyd, E, Oturai, AB, Pagnamenta, A, Patel, SY, Percy, M, Petousi, N, Piazza, P, Piret, SE, Polanco-Echeverry, G, Powrie, F, Pugh, C, Quek, L, Robbins, PA, Robson, K, Russo, A, Schuh, A, Silverman, E, Simmons, A, Sorensen, PS, Sweeney, E, Taylor, J, Thakker, RV, Tomlinson, I, Trebes, A, Twigg, SRF, Vyas, P, Vyse, T, Watkins, H, Whyte, MP, Witty, L, Wright, B, Buck, D, Humphray, S, Ratcliffe, PJ, Bell, JI, Bentley, D, Donnelly, P, McVean, G

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Initial Clinical Experience with a Single Pass VDDR Pacing System von LAU, CHU-PAK, TAI, YAU-TING, LI, JOHN PO-SHAN, CHUNG, FELSA LAI-WAH, SUNG, STELLA, YAMAMGTO, ALLAN

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REMEMBRANCES OF LI XUEQIN (1933-2019) von Allan, Sarah, Barman, Genevieve, Cook, C.A, Defoort, Carine, von Falkenhausen, Lothar, Feng, Li, Loewe, Michael, Marechal, Chrystelle, Rea, Christopher, Ryden, Edmund, Shaughnessy, Edward L, Sisci, Francesco, Wang, Helen, Tao, Wang, Wood, Frances, McKillop, Beth, Shun-chiu, Yau, Williams, Crispin, Yates, Robin D.S

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