Democratizing Strategic Planning in Master-Planned Communities von Allsup, Christopher K, Gabashvili, Irene S

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Modeling the Dynamics of Growth in Master-Planned Communities von Allsup, Christopher K, Gabashvili, Irene S

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Modeling the Dynamics of Growth in Master-Planned Communities von Allsup, Christopher K, Gabashvili, Irene S

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Whole-genome sequencing of a sporadic primary immunodeficiency cohort von Thaventhiran, James E. D., Lango Allen, Hana, Burren, Oliver S., Rae, William, Greene, Daniel, Staples, Emily, Zhang, Zinan, Farmery, James H. R., Simeoni, Ilenia, Rivers, Elizabeth, Maimaris, Jesmeen, Penkett, Christopher J., Stephens, Jonathan, Deevi, Sri V. V., Sanchis-Juan, Alba, Gleadall, Nicholas S., Thomas, Moira J., Sargur, Ravishankar B., Gordins, Pavels, Baxendale, Helen E., Brown, Matthew, Tuijnenburg, Paul, Worth, Austen, Hanson, Steven, Linger, Rachel J., Buckland, Matthew S., Rayner-Matthews, Paula J., Gilmour, Kimberly C., Samarghitean, Crina, Seneviratne, Suranjith L., Sansom, David M., Lynch, Andy G., Megy, Karyn, Ellinghaus, Eva, Ellinghaus, David, Jorgensen, Silje F., Karlsen, Tom H., Stirrups, Kathleen E., Cutler, Antony J., Kumararatne, Dinakantha S., Chandra, Anita, Edgar, J. David M., Herwadkar, Archana, Cooper, Nichola, Grigoriadou, Sofia, Huissoon, Aarnoud P., Goddard, Sarah, Jolles, Stephen, Schuetz, Catharina, Boschann, Felix, Lyons, Paul A., Hurles, Matthew E., Savic, Sinisa, Burns, Siobhan O., Kuijpers, Taco W., Turro, Ernest, Ouwehand, Willem H., Thrasher, Adrian J., Smith, Kenneth G. C.

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Whole-genome sequencing of patients with rare diseases in a national health system von Turro, Ernest, Astle, William J., Megy, Karyn, Gräf, Stefan, Greene, Daniel, Shamardina, Olga, Allen, Hana Lango, Sanchis-Juan, Alba, Frontini, Mattia, Thys, Chantal, Stephens, Jonathan, Mapeta, Rutendo, Burren, Oliver S., Downes, Kate, Haimel, Matthias, Tuna, Salih, Deevi, Sri V. V., Aitman, Timothy J., Bennett, David L., Calleja, Paul, Carss, Keren, Caulfield, Mark J., Chinnery, Patrick F., Dixon, Peter H., Gale, Daniel P., James, Roger, Koziell, Ania, Laffan, Michael A., Levine, Adam P., Maher, Eamonn R., Markus, Hugh S., Morales, Joannella, Morrell, Nicholas W., Mumford, Andrew D., Ormondroyd, Elizabeth, Rankin, Stuart, Rendon, Augusto, Richardson, Sylvia, Roberts, Irene, Roy, Noemi B. A., Saleem, Moin A., Smith, Kenneth G. C., Stark, Hannah, Tan, Rhea Y. Y., Themistocleous, Andreas C., Thrasher, Adrian J., Watkins, Hugh, Webster, Andrew R., Wilkins, Martin R., Williamson, Catherine, Whitworth, James, Humphray, Sean, Bentley, David R., Kingston, Nathalie, Walker, Neil, Bradley, John R., Ashford, Sofie, Penkett, Christopher J., Freson, Kathleen, Stirrups, Kathleen E., Raymond, F. Lucy, Ouwehand, Willem H.

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Germline selection shapes human mitochondrial DNA diversity von Wei, Wei, Tuna, Salih, Keogh, Michael J, Smith, Katherine R, Aitman, Timothy J, Beales, Phil L, Bennett, David L, Gale, Daniel P, Bitner-Glindzicz, Maria A K, Black, Graeme C, Brennan, Paul, Elliott, Perry, Flinter, Frances A, Floto, R Andres, Houlden, Henry, Irving, Melita, Koziell, Ania, Maher, Eamonn R, Markus, Hugh S, Morrell, Nicholas W, Newman, William G, Roberts, Irene, Sayer, John A, Smith, Kenneth G C, Taylor, Jenny C, Watkins, Hugh, Webster, Andrew R, Wilkie, Andrew O M, Williamson, Catherine, Ashford, Sofie, Penkett, Christopher J, Stirrups, Kathleen E, Rendon, Augusto, Ouwehand, Willem H, Bradley, John R, Raymond, F Lucy, Caulfield, Mark, Turro, Ernest, Chinnery, Patrick F

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Higher dose corticosteroids in patients admitted to hospital with COVID-19 who are hypoxic but not requiring ventilatory support (RECOVERY): a randomised, controlled, open-label, p... von Abraham, Tizzy, Adcock, Kirsty, Ahmed, Nausheen, Ali, Ali, Ali, Sakina, Allen, Kerry, Alveyn, Edward, Antonina, Zhelyazkova, Arias, Ana-Maria, Arnison-Newgass, Clare, Athorne, Deborah, Austin, Emily, Badhan, Gurpreet R, Bakere, Hugh, Balluz, Ismael, Bancroft, Elizabeth, Billings, Jessica, Chukkambotla, Srikanth, Clarke, Alison, Collier, Dawn, Dales, Jolyon, David, Mini, Davies, Jim, Denton, Elise, Dlouhy, Petr, Edmondson, Mary, Elkaram, Nadia, Eskander, Peter, Ezenduka, Chiamaka, Fathima, Suman, Finan, Shona, Garner, Justin, Georgiou, Domonique, Gillespie, Katherine, Goumalatsou, Charlotte, Griffiths, Sandra, Hassell, Jane, Heath, Angela, Hewertson, John, Hewitson, Nicola, Hilldrith, Annette, Hornby, Nicola, Huah, Chiang O H, Iqbal, Madiha, Iwanikiw, Sophie, James, Nicholas, Johnston, Victoria, Kala Bhushan, Azad, Kamfose, Musaiwale, Kant, Abhinav, Karbasi, Elshad, Keith, Laura, Kennedy, James, Keogan, Lynne, Kitching, Toby, Konar, Niladri, Lam, Alison, Liao, Angela, Lonsdale, Caroline, Martinez Garrido, Jose C, Masters, Joseph, McIntyre, Mhairi, McMinn, Jason, Mellor, Joe S, Millett, Louise, Monika, Tesha, Moramorell, Nuria, Mwaura, Esther, Myint, Yadee, Ng, Sarah, Nisha James, Aksinya, O'Hara, Chloe, Patel, Alkesh, Priest, Anne, Pyart, Eleanor, Quinn, Tom, Roche, Lisa, Samuels, Kevin, Sanz-Cepero, Aureo F, Saralaya, Dinesh, Satchithananthasivam, Krishna, Saunderson, Anne, Sellars, Rachael, Shirley, Kim, Singh, Shivani, Smith, Rachel, Soren, Jennifer, Spencer, Tom, Stephensen, David, Stone, Roisin, Stuart, Carmel, Stubbs, Harrison, Sumardi, Uun, Swinhoe, Sophie, Venn, Richard, Vethanayagam, Natalie, Vlies, Ben, Walsh, Donna, Wittes, Janet, Yang, Freda

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Phenotypic Characterization of EIF2AK4 Mutation Carriers in a Large Cohort of Patients Diagnosed Clinically With Pulmonary Arterial Hypertension von Hadinnapola, Charaka, Bleda, Marta, Haimel, Matthias, Screaton, Nicholas, Swift, Andrew, Dorfmüller, Peter, Preston, Stephen D, Southwood, Mark, Hernandez-Sanchez, Jules, Martin, Jennifer, Treacy, Carmen, Yates, Katherine, Bogaard, Harm, Church, Colin, Coghlan, Gerry, Condliffe, Robin, Corris, Paul A, Gibbs, Simon, Girerd, Barbara, Holden, Simon, Humbert, Marc, Kiely, David G, Lawrie, Allan, Machado, Rajiv, MacKenzie Ross, Robert, Moledina, Shahin, Montani, David, Newnham, Michael, Peacock, Andrew, Pepke-Zaba, Joanna, Rayner-Matthews, Paula, Shamardina, Olga, Soubrier, Florent, Southgate, Laura, Suntharalingam, Jay, Toshner, Mark, Trembath, Richard, Vonk Noordegraaf, Anton, Wilkins, Martin R, Wort, Stephen J, Wharton, John, Gräf, Stefan, Morrell, Nicholas W

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Publisher Correction: Whole-genome sequencing of a sporadic primary immunodeficiency cohort von Thaventhiran, James E. D., Lango Allen, Hana, Burren, Oliver S., Rae, William, Greene, Daniel, Staples, Emily, Zhang, Zinan, Farmery, James H. R., Simeoni, Ilenia, Rivers, Elizabeth, Maimaris, Jesmeen, Penkett, Christopher J., Stephens, Jonathan, Deevi, Sri V. V., Sanchis-Juan, Alba, Gleadall, Nicholas S., Thomas, Moira J., Sargur, Ravishankar B., Gordins, Pavels, Baxendale, Helen E., Brown, Matthew, Tuijnenburg, Paul, Worth, Austen, Hanson, Steven, Linger, Rachel J., Buckland, Matthew S., Rayner-Matthews, Paula J., Gilmour, Kimberly C., Samarghitean, Crina, Seneviratne, Suranjith L., Sansom, David M., Lynch, Andy G., Megy, Karyn, Ellinghaus, Eva, Ellinghaus, David, Jorgensen, Silje F., Karlsen, Tom H., Stirrups, Kathleen E., Cutler, Antony J., Kumararatne, Dinakantha S., Chandra, Anita, Edgar, J. David M., Herwadkar, Archana, Cooper, Nichola, Grigoriadou, Sofia, Huissoon, Aarnoud P., Goddard, Sarah, Jolles, Stephen, Schuetz, Catharina, Boschann, Felix, Lyons, Paul A., Hurles, Matthew E., Savic, Sinisa, Burns, Siobhan O., Kuijpers, Taco W., Turro, Ernest, Ouwehand, Willem H., Thrasher, Adrian J., Smith, Kenneth G. C.

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Next‐generation sequencing for the diagnosis of MYH9‐RD: Predicting pathogenic variants von Bury, Loredana, Megy, Karyn, Stephens, Jonathan C., Grassi, Luigi, Greene, Daniel, Gleadall, Nick, Althaus, Karina, Allsup, David, Bariana, Tadbir K., Bonduel, Mariana, Butta, Nora V., Collins, Peter, Curry, Nicola, Deevi, Sri V. V., Downes, Kate, Duarte, Daniel, Elliott, Kim, Falcinelli, Emanuela, Furie, Bruce, Keeling, David, Lambert, Michele P., Linger, Rachel, Mangles, Sarah, Mapeta, Rutendo, Millar, Carolyn M., Penkett, Christopher, Perry, David J., Stirrups, Kathleen E., Turro, Ernest, Westbury, Sarah K., Wu, John, BioResource, NIHR, Gomez, Keith, Freson, Kathleen, Ouwehand, Willem H., Gresele, Paolo, Simeoni, Ilenia

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Telomerecat: A ploidy-agnostic method for estimating telomere length from whole genome sequencing data von Farmery, James H. R., Smith, Mike L., Lynch, Andy G.

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De Novo Truncating Mutations in WASF1 Cause Intellectual Disability with Seizures von Duarte, Sofia T., Charles, Perinne, Pfundt, Rolph, van Bokhoven, Hans, van Ravenswaaij-Arts, Conny, Morrell, Nicholas W., Thrasher, Adrian, Fletcher, Debra, Veltman, Marijke, Davis, John, Frary, Amy, Martin, Jennifer M., Collins, Janine, Favier, Remi, Hart, Daniel, Heemskerk, Johan W.M., Liesner, Ri, Mangles, Sarah, Roughley, Catherine, Tait, R. Campbell, Thachil, Jecko, Van Geet, Chris, De Vries, Minka, Warner, Timothy Q., Furnell, Abigail, Mapeta, Rutendo, Whitehorn, Deborah, Daugherty, Louise, Deevi, Sri V.V., Hu, Fengyuan, Matser, Vera, Megy, Karyn, Tuna, Salih, von Ziegenweldt, Julie, Haimel, Matthias, Richardson, Sylvia, Rankin, Stuart, Anderson, Julie, Stock, Sophie, Armstrong, Ruth, Bitner-Glindzicz, Maria, Brady, Angie, Clement, Emma, Firth, Helen, Flinter, Frances, French, Courtney, Holder, Muriel, Hurst, Jane, Josifova, Dragana, Krishnakumar, Deepa, Kurian, Manju A., Mehta, Sarju, Moore, Anthony, Rankin, Julia, Reid, Evan, Scott, Richard, Thomas, Ellen, Wassmer, Evangeline, Creaser-Myers, Amanda, Gall, Henning, Ghataorhe, Pavandeep K., Houweling, Arjan C., in’t Veld, Anna Huis, Ross, Rob V. Mackenzie, Rhodes, Christopher J., Soubrier, Florent, Treacy, Carmen M., Vonk Noordegraaf, Anton, Antrobus, Richard, Arumugakani, Gururaj, Bibi, Shahnaz, Devlin, Lisa, Ghurye, Rohit, Grigoriadou, Sofia, Harper, Lorraine, Herwadkar, Archana, Jolles, Stephen, Kumararatne, Dinakantha, Lorenzo, Lorena, Murng, Sai, Nejentsev, Sergey, Quinti, Isabella, Samarghitean, Crina, Savic, Sinisa, Yong, Patrick, Ancliff, Phil, Layton, Mark, Mead, Adam, Roy, Noémi, Chambers, Jenny, Estiu, Cecelia, Simpson, Michael, Emmerson, Ingrid, McCarthy, Mark, Van Zuydam, Natalie, Afzal, Maryam, Colby, Elizabeth, Boycott, Kym M., Majewski, Jacek, Dyment, David

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Bayesian Inference Associates Rare KDR Variants With Specific Phenotypes in Pulmonary Arterial Hypertension von Swietlik, Emilia M., Greene, Daniel, Zhu, Na, Megy, Karyn, Cogliano, Marcella, Rajaram, Smitha, Pandya, Divya, Tilly, Tobias, Lutz, Katie A., Welch, Carrie C.L., Pauciulo, Michael W., Southgate, Laura, Martin, Jennifer M., Treacy, Carmen M., Penkett, Christopher J., Stephens, Jonathan C., Bogaard, Harm J., Church, Colin, Coghlan, Gerry, Coleman, Anna W., Condliffe, Robin, Eichstaedt, Christina A., Eyries, Mélanie, Gall, Henning, Ghio, Stefano, Girerd, Barbara, Grünig, Ekkehard, Holden, Simon, Howard, Luke, Humbert, Marc, Kiely, David G., Kovacs, Gabor, Lordan, Jim, Machado, Rajiv D., MacKenzie Ross, Robert V., McCabe, Colm, Moledina, Shahin, Montani, David, Olschewski, Horst, Pepke-Zaba, Joanna, Price, Laura, Rhodes, Christopher J., Seeger, Werner, Soubrier, Florent, Suntharalingam, Jay, Toshner, Mark R., Vonk Noordegraaf, Anton, Wharton, John, Wild, James M., Wort, Stephen John, Lawrie, Allan, Wilkins, Martin R., Trembath, Richard C., Shen, Yufeng, Chung, Wendy K., Swift, Andrew J., Nichols, William C., Morrell, Nicholas W., Gräf, Stefan

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Next-generation sequencing for the diagnosis of MYH9-RD: Predicting pathogenic variants von Bury, Loredana, Megy, Karyn, Stephens, Jonathan C, Grassi, Luigi, Greene, Daniel, Gleadall, Nick, Althaus, Karina, Allsup, David, Bariana, Tadbir K, Bonduel, Mariana, Butta, Nora, Collins, Peter, Curry, Nicola, Deevi, Sri V.V, Downes, Kate, Duarte, Daniel, Elliott, Kim, Falcinelli, Emanuela, Furie, Bruce, Keeling, David, Lambert, Michele P, Linger, Rachel, Mangles, Sarah, Mapeta, Rutendo, Millar, Carolyn M, Penkett, Christopher, Perry, David J, Stirrups, Kathleen E, Turro, Ernest, Westbury, Sarah K, Wu, John, Gomez, Keith, Freson, Kathleen, Ouwehand, Willem H, Gresele, Paolo, Simeoni, Ilenia

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Germline selection shapes human mitochondrial DNA diversity von Wei, Wei, Tuna, Salih, Keogh, Michael J, Smith, Katherine R, Aitman, Timothy J, Beales, Phil L, Bennett, David L, Gale, Daniel P, Bitner-Glindzicz, Maria A.K, Black, Graeme C, Brennan, Paul, Elliott, Perry, Flinter, Frances A, Floto, R. Andres, Houlden, Henry, Irving, Melita, Koziell, Ania, Maher, Eamonn R, Markus, Hugh S, Morrell, Nicholas W, Newman, William G, Roberts, Irene, Sayer, John A, Smith, Kenneth G.C, Taylor, Jenny C, Watkins, Hugh, Webster, Andrew R, Wilkie, Andrew O.M, Williamson, Catherine, Attwood, Anthony, Brown, Matthew, Brod, Naomi Clements, Crisp-Hihn, Abigail, Davis, John, Deevi, Sri V.V, Dewhurst, Eleanor F, Edwards, Karen, Erwood, Marie, Fox, James, Frary, Amy J, Hu, Fengyuan, Jolley, Jennifer, Kingston, Nathalie, Linger, Rachel, Mapeta, Rutendo, Martin, Jennifer, Meacham, Stuart, Papadia, Sofia, Rayner-Matthews, Paula J, Samarghitean, Crina, Shamardina, Olga, Simeoni, Ilenia, Staines, Simon, Staples, Emily, Stark, Hannah, Stephens, Jonathan, Titterton, Catherine, von Ziegenweidt, Julie, Watt, Christopher, Whitehorn, Deborah, Wood, Yvette, Yates, Katherine, Yu, Ping, James, Roger, Ashford, Sofie, Penkett, Christopher J, Stirrups, Kathleen E, Bariana, Tadbir, Lentaigne, Claire, Sivapalaratnam, Suthesh, Westbury, Sarah K, Allsup, David J, Bakchoul, Tamam, Biss, Tina, Boyce, Sara, Collins, Janine, Collins, Peter W, Curry, Nicola S, Downes, Kate, Dutt, Tina, Erber, Wendy N, Evans, Gillian, Everington, Tamara, Favier, Remi, Gomez, Keith, Greene, Daniel, Gresele, Paolo, Hart, Daniel, Kazmi, Rashid, Kelly, Anne M, Lambert, Michele, Madan, Bella, Mangles, Sarah, Mathias, Mary, Millar, Carolyn, Obaji, Samya, Peerlinck, Kathelijne, Roughley, Catherine, Schulman, Sol, Scully, Marie

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Publisher Correction: Telomerecat: A ploidy-agnostic method for estimating telomere length from whole genome sequencing data von Farmery, James H. R., Smith, Mike L., Lynch, Andy G.

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Next-generation sequencing for the diagnosis of MYH9-RD: Predicting pathogenic variants von Bury, Loredana, Megy, Karyn, Stephens, Jonathan C, Grassi, Luigi, Greene, Daniel, Gleadall, Nick, Althaus, Karina, Allsup, David, Bariana, Tadbir K, Bonduel, Mariana, Butta, Nora V, Collins, Peter, Curry, Nicola, Deevi, Sri VV, Downes, Kate, Duarte, Daniel, Elliott, Kim, Falcinelli, Emanuela, Furie, Bruce, Keeling, David, Lambert, Michele P, Linger, Rachel, Mangles, Sarah, Mapeta, Rutendo, Millar, Carolyn M, Penkett, Christopher, Perry, David J, Stirrups, Kathleen E, Turro, Ernest, Westbury, Sarah K, Wu, John, BioResource, Nihr, Gomez, Keith, Freson, Kathleen, Ouwehand, Willem H, Gresele, Paolo, Simeoni, Ilenia

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