Determination of the in vivo posterior loading environment of the Coflex interlaminar-interspinous implant von Trautwein, Frank T., Dipl-Ing(FH), Lowery, Gary L., MD, PhD, Wharton, Nicholas D., MS, Hipp, John A., PhD, Chomiak, Robert J., MS

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Sagittal alignment after Bryan cervical arthroplasty von Sasso, Rick C, Metcalf, Newton H, Hipp, John A, Wharton, Nicholas D, Anderson, Paul A

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Optimizing success with lumbar disc arthroplasty von Gornet, Matthew F., Schranck, Francine, Wharton, Nicholas D., Beall, Douglas P., Jones, Elizabeth, Myers, Mark E., Hipp, John A.

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Sagittal Alignment After Bryan Cervical Arthroplasty von SASSO, Rick C, METCALF, Newton H, HIPP, John A, WHARTON, Nicholas D, ANDERSON, Paul A

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Asymmetric Motion Distribution Between Components of a Mobile-Core Lumbar Disc Prosthesis: An Explanation of Unequal Wear Distribution in Explanted CHARITÉ Polyethylene Cores von Patwardhan, Avinash G, Havey, Robert M, Wharton, Nicholas D, Tsitsopoulos, Parmenion P, Newman, Patrick, Carandang, Gerard, Voronov, Leonard I

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Development of a novel radiographic measure of lumbar instability and validation using the facet fluid sign von Hipp, John A, Guyer, Richard D, Zigler, Jack E, Ohnmeiss, Donna D, Wharton, Nicholas D

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Optimizing Success with Lumbar Disc Arthroplasty von Gornet, Matthew F., MD, Schranck, Francine W., RN, BSN, Wharton, Nicholas D., MS, Hipp, John A., PhD

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P135. Explanation of Unequal Wear Patterns in the Charité Polyethylene Core: A Quantitative Analysis of Intraprosthesis Motion Distribution von Patwardhan, Avinash G., PhD, Wharton, Nicholas D., MS, Newman, Patrick, MS, Voronov, Leonard I., MD, PhD, Carandang, Gerard, MS, Renner, Susan M., PhD, Havey, Robert M., BS

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Asymmetric Motion Distribution Between Components of a Mobile-Core Lumbar Disc Prosthesis von Patwardhan, Avinash G., PhD, Havey, Robert M., BS, Tsitsopoulos, Parmenion P., MD, PhD, Voronov, Leonard I., MD, PhD, Wharton, Nicholas D., MS, Newman, Patrick, MS, Carandang, Gerard, MS

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INTERACTIVE METHOD TO ASSESS JOINT SPACE NARROWING von WHARTON NICHOLAS D, HIPP JOHN ANDREW, ZIEGLER JAMES M, NEWMAN PATRICK

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First Genotype-Phenotype Study in TBX4 Syndrome: Gain-of-Function Mutations Causative for Lung Disease von Prapa, Matina, Lago-Docampo, Mauro, Swietlik, Emilia M, Montani, David, Eyries, Mélanie, Humbert, Marc, Welch, Carrie L, Chung, Wendy K, Berger, Rolf M F, Bogaard, Harm Jan, Danhaive, Olivier, Escribano-Subías, Pilar, Gall, Henning, Girerd, Barbara, Hernandez-Gonzalez, Ignacio, Holden, Simon, Hunt, David, Jansen, Samara M A, Kerstjens-Frederikse, Wilhelmina, Kiely, David G, Lapunzina, Pablo, McDermott, John, Moledina, Shahin, Pepke-Zaba, Joanna, Polwarth, Gary J, Schotte, Gwen, Tenorio-Castaño, Jair, Thompson, A A Roger, Wharton, John, Wort, Stephen J, Megy, Karyn, Mapeta, Rutendo, Treacy, Carmen M, Martin, Jennifer M, Li, Wei, Swift, Andrew J, Upton, Paul D, Morrell, Nicholas W, Gräf, Stefan, Valverde, Diana

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Neurological and neuropsychiatric complications of COVID-19 in 153 patients: a UK-wide surveillance study von Varatharaj, Aravinthan, Thomas, Naomi, Ellul, Mark A, Davies, Nicholas W S, Pollak, Thomas A, Tenorio, Elizabeth L, Sultan, Mustafa, Easton, Ava, Zandi, Michael, Coles, Jonathan P, Manji, Hadi, Al-Shahi Salman, Rustam, Menon, David K, Nicholson, Timothy R, Benjamin, Laura A, Carson, Alan, Turner, Martin R, Solomon, Tom, Kneen, Rachel, Pett, Sarah L, Galea, Ian, Thomas, Rhys H, Michael, Benedict D, Allen, Claire, Archibald, Neil, Arkell, James, Arthur-Farraj, Peter, Baker, Mark, Ball, Harriet, Bradley-Barker, Verity, Brown, Zoe, Bruno, Stefania, Carey, Lois, Carswell, Christopher, Chakrabarti, Annie, Choulerton, James, Daher, Mazen, Davies, Ruth, Di Marco Barros, Rafael, Dima, Sofia, Dunley, Rachel, Dutta, Dipankar, Everitt, Alex, Fady, Joseph, Fearon, Patricia, Fisniku, Leonora, Gbinigie, Ivie, Gemski, Alan, Gillies, Emma, Gkrania-Klotsas, Effrossyni, Hamdalla, Hisham, Hubbett, Jack, Hunter, Neil, Ispoglou, Sissi, Jha, Ashwani, Joussi, Ramzi, Khalifeh, Hind, Kooij, Sander, Kumar, Guru, Kyaw, Sandar, Li, Lucia, Littleton, Edward, Macleod, Mary Joan, Madigan, Barbara, Mahadasa, Vikram, Manoharan, Manonmani, Marigold, Richard, Marks, Isaac, Matthews, Paul, Mccormick, Michael, Mcinnes, Caroline, Metastasio, Antonio, Milburn-McNulty, Philip, Mitchell, Duncan, Morgans, Clare, Morris, Huw, Morrow, Jasper, Mubarak Mohamed, Ahmed, Murphy, Louis, Namushi, Robert, Newman, Edward, Phillips, Wendy, Pinto, Ashwin, Price, David Ashley, Proschel, Harald, Ramsey, Deborah, Ross Russell, Amy, Samarasekera, Neshika, Sawcer, Stephen, Sayed, Walee, Sekaran, Lakshmanan, Serra-Mestres, Jordi, Snowdon, Victoria, Strike, Gayle, Vrana, Mark, Wharton, Chris, Wiblin, Lou, Boubriak, Iryna, Herman, Katie, Plant, Gordon

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Genetic determinants of risk in pulmonary arterial hypertension: international genome-wide association studies and meta-analysis von Rhodes, Christopher J, Batai, Ken, Bleda, Marta, Southgate, Laura, Germain, Marine, Pauciulo, Michael W, Aman, Jurjan, Girerd, Barbara, Arora, Amit, Knight, Jo, Hanscombe, Ken B, Karnes, Jason H, Kaakinen, Marika, Harbaum, Lars, Cebola, Inês, Ferrer, Jorge, Lutz, Katie, Swietlik, Emilia M, Ahmad, Ferhaan, Amouyel, Philippe, Archer, Stephen L, Argula, Rahul, Austin, Eric D, Badesch, David, Barnett, Christopher, Benza, Raymond, Bhatt, Nitin, Burger, Charles D, Chakinala, Murali, Church, Colin, Coghlan, John G, Condliffe, Robin, Danesino, Cesare, Debette, Stéphanie, Elliott, C Gregory, Elwing, Jean, Fortin, Terry, Frantz, Robert P, Frost, Adaani, Garcia, Joe G N, Ghio, Stefano, Ghofrani, Hossein-Ardeschir, Gibbs, J Simon R, Harley, John, He, Hua, Hill, Nicholas S, Hirsch, Russel, Houweling, Arjan C, Howard, Luke S, Ivy, Dunbar, Kiely, David G, Klinger, James, Kovacs, Gabor, Lahm, Tim, Machado, Rajiv D, Marsolo, Keith, Martin, Lisa J, Moledina, Shahin, Montani, David, Nathan, Steven D, Olschewski, Andrea, Olschewski, Horst, Oudiz, Ronald J, Pepke-Zaba, Joanna, Rehman, Zia, Robbins, Ivan, Roden, Dan M, Rosenzweig, Erika B, Saydain, Ghulam, Scelsi, Laura, Schilz, Robert, Seeger, Werner, Simms, Robert W, Simon, Marc, Sitbon, Olivier, Suntharalingam, Jay, Tang, Haiyang, Tchourbanov, Alexander Y, Thenappan, Thenappan, Treacy, Carmen M, Vonk Noordegraaf, Anton, Waisfisz, Quinten, Walsworth, Anna K, Walter, Robert E, Wharton, John, White, R James, Wilt, Jeffrey, Wort, Stephen J, Yung, Delphine, Lawrie, Allan, Humbert, Marc, Soubrier, Florent, Trégouët, David-Alexandre, Prokopenko, Inga, Gräf, Stefan, Nichols, William C, Trembath, Richard C, Desai, Ankit A, Morrell, Nicholas W, Wilkins, Martin R

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ATP13A3 variants promote pulmonary arterial hypertension by disrupting polyamine transport von Liu, Bin, Azfar, Mujahid, Legchenko, Ekaterina, West, James A, Martin, Shaun, Van den Haute, Chris, Baekelandt, Veerle, Wharton, John, Howard, Luke, Wilkins, Martin R, Vangheluwe, Peter, Morrell, Nicholas W, Upton, Paul D

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Identification of rare sequence variation underlying heritable pulmonary arterial hypertension von Gräf, Stefan, Haimel, Matthias, Bleda, Marta, Hadinnapola, Charaka, Southgate, Laura, Li, Wei, Hodgson, Joshua, Liu, Bin, Salmon, Richard M., Southwood, Mark, Machado, Rajiv D., Martin, Jennifer M., Treacy, Carmen M., Yates, Katherine, Daugherty, Louise C., Shamardina, Olga, Whitehorn, Deborah, Holden, Simon, Aldred, Micheala, Bogaard, Harm J., Church, Colin, Coghlan, Gerry, Condliffe, Robin, Corris, Paul A., Danesino, Cesare, Eyries, Mélanie, Gall, Henning, Ghio, Stefano, Ghofrani, Hossein-Ardeschir, Gibbs, J. Simon R., Girerd, Barbara, Houweling, Arjan C., Howard, Luke, Humbert, Marc, Kiely, David G., Kovacs, Gabor, MacKenzie Ross, Robert V., Moledina, Shahin, Montani, David, Newnham, Michael, Olschewski, Andrea, Olschewski, Horst, Peacock, Andrew J., Pepke-Zaba, Joanna, Prokopenko, Inga, Rhodes, Christopher J., Scelsi, Laura, Seeger, Werner, Soubrier, Florent, Stein, Dan F., Suntharalingam, Jay, Swietlik, Emilia M., Toshner, Mark R., van Heel, David A., Vonk Noordegraaf, Anton, Waisfisz, Quinten, Wharton, John, Wort, Stephen J., Ouwehand, Willem H., Soranzo, Nicole, Lawrie, Allan, Upton, Paul D., Wilkins, Martin R., Trembath, Richard C., Morrell, Nicholas W.

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Whole-Blood RNA Profiles Associated with Pulmonary Arterial Hypertension and Clinical Outcome von Rhodes, Christopher J, Otero-Núñez, Pablo, Wharton, John, Swietlik, Emilia M, Kariotis, Sokratis, Harbaum, Lars, Dunning, Mark J, Elinoff, Jason M, Errington, Niamh, Thompson, A A Roger, Iremonger, James, Coghlan, J Gerry, Corris, Paul A, Howard, Luke S, Kiely, David G, Church, Colin, Pepke-Zaba, Joanna, Toshner, Mark, Wort, Stephen J, Desai, Ankit A, Humbert, Marc, Nichols, William C, Southgate, Laura, Trégouët, David-Alexandre, Trembath, Richard C, Prokopenko, Inga, Gräf, Stefan, Morrell, Nicholas W, Wang, Dennis, Lawrie, Allan, Wilkins, Martin R

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ETA and ETB Receptors Modulate the Proliferation of Human Pulmonary Artery Smooth Muscle Cells von DAVIE, NEIL, HALEEN, STEPHEN J, UPTON, PAUL D, POLAK, JULIA M, YACOUB, MAGDI H, MORRELL, NICHOLAS W, WHARTON, JOHN

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Characterization of GDF2 Mutations and Levels of BMP9 and BMP10 in Pulmonary Arterial Hypertension von Hodgson, Joshua, Swietlik, Emilia M, Salmon, Richard M, Hadinnapola, Charaka, Nikolic, Ivana, Wharton, John, Guo, Jingxu, Liley, James, Haimel, Matthias, Bleda, Marta, Southgate, Laura, Machado, Rajiv D, Martin, Jennifer M, Treacy, Carmen M, Yates, Katherine, Daugherty, Louise C, Shamardina, Olga, Whitehorn, Deborah, Holden, Simon, Bogaard, Harm J, Church, Colin, Coghlan, Gerry, Condliffe, Robin, Corris, Paul A, Danesino, Cesare, Eyries, Mélanie, Gall, Henning, Ghio, Stefano, Ghofrani, Hossein-Ardeschir, Gibbs, J Simon R, Girerd, Barbara, Houweling, Arjan C, Howard, Luke, Humbert, Marc, Kiely, David G, Kovacs, Gabor, Lawrie, Allan, MacKenzie Ross, Robert V, Moledina, Shahin, Montani, David, Olschewski, Andrea, Olschewski, Horst, Ouwehand, Willem H, Peacock, Andrew J, Pepke-Zaba, Joanna, Prokopenko, Inga, Rhodes, Christopher J, Scelsi, Laura, Seeger, Werner, Soubrier, Florent, Suntharalingam, Jay, Toshner, Mark R, Trembath, Richard C, Vonk Noordegraaf, Anton, Wort, Stephen J, Wilkins, Martin R, Yu, Paul B, Li, Wei, Gräf, Stefan, Upton, Paul D, Morrell, Nicholas W

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Rare variant analysis of 4241 pulmonary arterial hypertension cases from an international consortium implicates FBLN2, PDGFD, and rare de novo variants in PAH von Zhu, Na, Swietlik, Emilia M, Welch, Carrie L, Pauciulo, Michael W, Hagen, Jacob J, Zhou, Xueya, Guo, Yicheng, Karten, Johannes, Pandya, Divya, Tilly, Tobias, Lutz, Katie A, Martin, Jennifer M, Treacy, Carmen M, Rosenzweig, Erika B, Krishnan, Usha, Coleman, Anna W, Gonzaga-Jauregui, Claudia, Lawrie, Allan, Trembath, Richard C, Wilkins, Martin R, Morrell, Nicholas W, Shen, Yufeng, Gräf, Stefan, Nichols, William C, Chung, Wendy K

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Deficiency of Axl aggravates pulmonary arterial hypertension via BMPR2 von Novoyatleva, Tatyana, Rai, Nabham, Kojonazarov, Baktybek, Veeroju, Swathi, Ben-Batalla, Isabel, Caruso, Paola, Shihan, Mazen, Presser, Nadine, Götz, Elsa, Lepper, Carina, Herpel, Sebastian, Manaud, Grégoire, Perros, Frédéric, Gall, Henning, Ghofrani, Hossein Ardeschir, Weissmann, Norbert, Grimminger, Friedrich, Wharton, John, Wilkins, Martin, Upton, Paul D., Loges, Sonja, Morrell, Nicholas W., Seeger, Werner, Schermuly, Ralph T.

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