Validity of diagnostic coding within the General Practice Research Database: a systematic review by Khan, Nada F, Harrison, Sian E, Rose, Peter W

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Optimal loading dose of warfarin for the initiation of oral anticoagulation by Mahtani, Kamal R, Heneghan, Carl J, Nunan, David, Bankhead, Clare, Keeling, David, Ward, Alison M, Harrison, Sian E, Roberts, Nia W, Hobbs, F D Richard, Perera, Rafael

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Calibration of computational tools for missense variant pathogenicity classification and ClinGen recommendations for PP3/BP4 criteria by Pejaver, Vikas, Byrne, Alicia B., Feng, Bing-Jian, Pagel, Kymberleigh A., Mooney, Sean D., Karchin, Rachel, O’Donnell-Luria, Anne, Harrison, Steven M., Tavtigian, Sean V., Greenblatt, Marc S., Biesecker, Leslie G., Radivojac, Predrag, Brenner, Steven E., Biesecker, Leslie G., Harrison, Steven M., Tayoun, Ahmad A., Berg, Jonathan S., Brenner, Steven E., Cutting, Garry R., Ellard, Sian, Greenblatt, Marc S., Kang, Peter, Karbassi, Izabela, Karchin, Rachel, Mester, Jessica, O’Donnell-Luria, Anne, Pesaran, Tina, Plon, Sharon E., Rehm, Heidi L., Strande, Natasha T., Tavtigian, Sean V., Topper, Scott

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Recommendations for application of the functional evidence PS3/BS3 criterion using the ACMG/AMP sequence variant interpretation framework by Brnich, Sarah E, Abou Tayoun, Ahmad N, Couch, Fergus J, Cutting, Garry R, Greenblatt, Marc S, Heinen, Christopher D, Kanavy, Dona M, Luo, Xi, McNulty, Shannon M, Starita, Lea M, Tavtigian, Sean V, Wright, Matt W, Harrison, Steven M, Biesecker, Leslie G, Berg, Jonathan S

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Using the ACMG/AMP framework to capture evidence related to predicted and observed impact on splicing: Recommendations from the ClinGen SVI Splicing Subgroup by Walker, Logan C., Hoya, Miguel de la, Wiggins, George A.R., Lindy, Amanda, Vincent, Lisa M., Parsons, Michael T., Canson, Daffodil M., Bis-Brewer, Dana, Cass, Ashley, Tchourbanov, Alexander, Zimmermann, Heather, Byrne, Alicia B., Pesaran, Tina, Karam, Rachid, Harrison, Steven M., Spurdle, Amanda B., Biesecker, Leslie G., Harrison, Steven M., Tayoun, Ahmad A., Berg, Jonathan S., Brenner, Steven E., Cutting, Garry R., Ellard, Sian, Greenblatt, Marc S., Kang, Peter, Karbassi, Izabela, Karchin, Rachel, Mester, Jessica, O’Donnell-Luria, Anne, Pesaran, Tina, Plon, Sharon E., Rehm, Heidi L., Strande, Natasha T., Tavtigian, Sean V., Topper, Scott

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Whole exome sequencing identifies genetic variants in inherited thrombocytopenia with secondary qualitative function defects by Johnson, Ben, Lowe, Gillian C, Futterer, Jane, Lordkipanidzé, Marie, MacDonald, David, Simpson, Michael A, Sanchez-Guiú, Isabel, Drake, Sian, Bem, Danai, Leo, Vincenzo, Fletcher, Sarah J, Dawood, Ban, Rivera, José, Allsup, David, Biss, Tina, Bolton-Maggs, Paula Hb, Collins, Peter, Curry, Nicola, Grimley, Charlotte, James, Beki, Makris, Mike, Motwani, Jayashree, Pavord, Sue, Talks, Katherine, Thachil, Jecko, Wilde, Jonathan, Williams, Mike, Harrison, Paul, Gissen, Paul, Mundell, Stuart, Mumford, Andrew, Daly, Martina E, Watson, Steve P, Morgan, Neil V

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Alliance of Genome Resources Portal: unified model organism research platform by Agapite, Julie, Albou, Laurent-Philippe, Aleksander, Suzi, Argasinska, Joanna, Arnaboldi, Valerio, Attrill, Helen, Bello, Susan M, Blake, Judith A, Blodgett, Olin, Bradford, Yvonne M, Bult, Carol J, Cain, Scott, Calvi, Brian R, Carbon, Seth, Chan, Juancarlos, Chen, Wen J, Cherry, J Michael, Cho, Jaehyoung, Christie, Karen R, Crosby, Madeline A, Pons, Jeff De, Dolan, Mary E, Santos, Gilberto dos, Dunn, Barbara, Dunn, Nathan, Eagle, Anne, Ebert, Dustin, Engel, Stacia R, Fashena, David, Frazer, Ken, Gao, Sibyl, Gondwe, Felix, Goodman, Josh, Gramates, L Sian, Grove, Christian A, Harris, Todd, Harrison, Marie-Claire, Howe, Douglas G, Howe, Kevin L, Jha, Sagar, Kadin, James A, Kaufman, Thomas C, Kalita, Patrick, Karra, Kalpana, Kishore, Ranjana, Laulederkind, Stan, Lee, Raymond, MacPherson, Kevin A, Marygold, Steven J, Matthews, Beverley, Millburn, Gillian, Miyasato, Stuart, Moxon, Sierra, Mueller, Hans-Michael, Mungall, Christopher, Muruganujan, Anushya, Mushayahama, Tremayne, Nash, Robert S, Ng, Patrick, Paulini, Michael, Perrimon, Norbert, Pich, Christian, Raciti, Daniela, Richardson, Joel E, Russell, Matthew, Gelbart, Susan Russo, Ruzicka, Leyla, Schaper, Kevin, Shimoyama, Mary, Simison, Matt, Smith, Cynthia, Shaw, David R, Shrivatsav, Ajay, Skrzypek, Marek, Smith, Jennifer R, Sternberg, Paul W, Tabone, Christopher J, Thomas, Paul D, Thota, Jyothi, Toro, Sabrina, Tomczuk, Monika, Tutaj, Marek, Tutaj, Monika, Urbano, Jose-Maria, Auken, Kimberly Van, Slyke, Ceri E Van, Wang, Shur-Jen, Weng, Shuai, Westerfield, Monte, Williams, Gary, Wong, Edith D, Wright, Adam, Yook, Karen

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Kinship and social organization in Copper Age Europe. A cross-disciplinary analysis of archaeology, DNA, isotopes, and anthropology from two Bell Beaker cemeteries by Sjögren, Karl-Göran, Olalde, Iñigo, Carver, Sophie, Allentoft, Morten E, Knowles, Tim, Kroonen, Guus, Pike, Alistair W G, Schröter, Peter, Brown, Keri A, Brown, Kate Robson, Harrison, Richard J, Bertemes, Francois, Reich, David, Kristiansen, Kristian, Heyd, Volker

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Assessing transmissibility of SARS-CoV-2 lineage B.1.1.7 in England by Volz, Erik, Mishra, Swapnil, Chand, Meera, Barrett, Jeffrey C., Johnson, Robert, Geidelberg, Lily, Hinsley, Wes R., Laydon, Daniel J., Dabrera, Gavin, O’Toole, Áine, Amato, Robert, Ragonnet-Cronin, Manon, Harrison, Ian, Jackson, Ben, Ariani, Cristina V., Boyd, Olivia, Loman, Nicholas J., McCrone, John T., Gonçalves, Sónia, Jorgensen, David, Myers, Richard, Hill, Verity, Jackson, David K., Gaythorpe, Katy, Groves, Natalie, Sillitoe, John, Kwiatkowski, Dominic P., Flaxman, Seth, Ratmann, Oliver, Bhatt, Samir, Hopkins, Susan, Gandy, Axel, Rambaut, Andrew, Ferguson, Neil M.

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Evaluating the Effects of SARS-CoV-2 Spike Mutation D614G on Transmissibility and Pathogenicity by Shepherd, James, Koshy, Cherian, Wise, Emma, Curran, Tanya, Adams, Helen, Moore, Catrin, Khokhar, Fahad A., Reynolds, Nicola, Afifi, Safiah, Price, Anna, Kitchen, Christine, Merrick, Ian, Connor, Thomas R., Bresner, Catherine, Robson, Samuel C., Menegazzo, Mirko, Clark, Gemma, Fleming, Vicki M., Howson-Wells, Hannah C., Bird, Paul, Helmer, Thomas, Fallon, Karlie, du Plessis, Louis, Attwood, Stephen, Vasylyeva, Tetyana, Chaudhry, Yasmin, Moses, Samuel, Ryan, Felicity, Brown, Julianne Rose, Lee, Jack C.D., Alcolea-Medina, Adela, Moore, Nathan, Cortes, Nicholas, Williams, Rebecca, Smith, Darren L., Holmes, Alison, Price, James, Rowan, Aileen, Taylor, Graham P., Watts, Joanne, Ludden, Catherine, George, Ryan P., Li, Kathy K., Carmichael, Stephen N., Johnson, Natasha, Orton, Richard J., Hale, Antony D., Harper, Katherine L., Eltringham, Gary, Coupland, Lindsay J., Barton, Edward, Scott, Garren, Yew, Wen C., Resende Silva, Paola C., Justice, Anita, Chand, Meera, Williams, David, Harrison, Ian, Chalker, Vicki, Heyburn, David, Downing, Fatima, Watkins, Joanne, Howe, Robin, Taylor, Sarah, Wain, John, Rudder, Steven, Gilroy, Rachel A.J., Alikhan, Nabil-Fareed, Casey, Anna, Liggett, Steven, Caller, Laura G., Panchbhaya, Yasmin N., Forrest, Leysa M., Findlay, Jacqueline, Beggs, Andrew, Hesketh, Andrew R., Higginson, Ellen E., Aggarwal, Dinesh, Colquhoun, Rachel, Ashworth, Jordan, McCrone, J.T., Michell, Stephen L., Hughes, Margaret, Rainbow, Lucille, Haldenby, Sam T., Green, Luke R., Parker, Matthew D., Bridgewater, Hannah E., Alam, Mohammad T., Quail, Mike, Thurston, Scott, Beaver, Charlotte, McMinn, Liz, Puethe, Christoph, Tonkin-Hill, Gerry, Smith, Christen, Jamrozy, Dorota, Patel, Minal, Drury, Eleanor, Loman, Nicholas J.

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Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls by Craddock, Nick, Hurles, Matthew E, Cardin, Niall, Pearson, Richard D, Plagnol, Vincent, Robson, Samuel, Vukcevic, Damjan, Barnes, Chris, Conrad, Donald F, Giannoulatou, Eleni, Holmes, Chris, Marchini, Jonathan L, Stirrups, Kathy, Tobin, Martin D, Wain, Louise V, Yau, Chris, Aerts, Jan, Ahmad, Tariq, Andrews, T Daniel, Arbury, Hazel, Attwood, Anthony, Auton, Adam, Ball, Stephen G, Balmforth, Anthony J, Barrett, Jeffrey C, Barroso, Inês, Barton, Anne, Bennett, Amanda J, Bhaskar, Sanjeev, Blaszczyk, Katarzyna, Bowes, John, Brand, Oliver J, Braund, Peter S, Bredin, Francesca, Breen, Gerome, Brown, Morris J, Bruce, Ian N, Bull, Jaswinder, Burren, Oliver S, Burton, John, Byrnes, Jake, Caesar, Sian, Clee, Chris M, Coffey, Alison J, Connell, John M C, Cooper, Jason D, Dominiczak, Anna F, Downes, Kate, Drummond, Hazel E, Dudakia, Darshna, Dunham, Andrew, Ebbs, Bernadette, Eccles, Diana, Edkins, Sarah, Edwards, Cathryn, Elliot, Anna, Emery, Paul, Evans, David M, Evans, Gareth, Eyre, Steve, Farmer, Anne, Ferrier, I Nicol, Feuk, Lars, Fitzgerald, Tomas, Flynn, Edward, Forbes, Alistair, Forty, Liz, Franklyn, Jayne A, Freathy, Rachel M, Gibbs, Polly, Gilbert, Paul, Gokumen, Omer, Gordon-Smith, Katherine, Gray, Emma, Green, Elaine, Groves, Chris J, Grozeva, Detelina, Gwilliam, Rhian, Hall, Anita, Hammond, Naomi, Hardy, Matt, Harrison, Pile, Hassanali, Neelam, Hebaishi, Husam, Hines, Sarah, Hinks, Anne, Hitman, Graham A, Hocking, Lynne, Howard, Eleanor, Howard, Philip, Howson, Joanna M M, Hughes, Debbie, Hunt, Sarah, Isaacs, John D, Jain, Mahim, Jewell, Derek P, Johnson, Toby, Jolley, Jennifer D, Jones, Ian R, Jones, Lisa A

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Detailed Analysis of ITPR1 Missense Variants Guides Diagnostics and Therapeutic Design by Tolonen, Jussi Pekka, Parolin Schnekenberg, Ricardo, McGowan, Simon, Sims, David, McEntagart, Meriel, Elmslie, Frances, Shears, Debbie, Stewart, Helen, Tofaris, George K., Dabir, Tabib, Morrison, Patrick J., Johnson, Diana, Hadjivassiliou, Marios, Ellard, Sian, Shaw‐Smith, Charles, Znaczko, Anna, Dixit, Abhijit, Suri, Mohnish, Sarkar, Ajoy, Harrison, Rachel E., Jones, Gabriela, Houlden, Henry, Ceravolo, Giorgia, Jarvis, Joanna, Williams, Jonathan, Shanks, Morag E., Clouston, Penny, Rankin, Julia, Blumkin, Lubov, Lerman‐Sagie, Tally, Ponger, Penina, Raskin, Salmo, Granath, Katariina, Uusimaa, Johanna, Conti, Hector, McCann, Emma, Joss, Shelagh, Blakes, Alexander J.M., Metcalfe, Kay, Kingston, Helen, Bertoli, Marta, Kneen, Rachel, Lynch, Sally Ann, Martínez Albaladejo, Inmaculada, Moore, Austen Peter, Jones, Wendy D., Becker, Esther B.E., Németh, Andrea H.

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An immune dysfunction score for stratification of patients with acute infection based on whole-blood gene expression by Cano-Gamez, Eddie, Burnham, Katie L, Goh, Cyndi, Allcock, Alice, Malick, Zunaira H, Overend, Lauren, Kwok, Andrew, Smith, David A, Peters-Sengers, Hessel, Antcliffe, David, McKechnie, Stuart, Scicluna, Brendon P, van der Poll, Tom, Gordon, Anthony C, Hinds, Charles J, Davenport, Emma E, Knight, Julian C, Webster, Nigel, Galley, Helen, Taylor, Jane, Hall, Sally, Addison, Jenni, Roughton, Sian, Tennant, Heather, Guleri, Achyut, Waddington, Natalia, Arawwawala, Dilshan, Durcan, John, Short, Alasdair, Swan, Karen, Williams, Sarah, Smolen, Susan, Mitchell-Inwang, Christine, Gordon, Tony, Errington, Emily, Templeton, Maie, Venatesh, Pyda, Ward, Geraldine, McCauley, Marie, Baudouin, Simon, Higham, Charley, Soar, Jasmeet, Grier, Sally, Hall, Elaine, Brett, Stephen, Kitson, David, Wilson, Robert, Mountford, Laura, Moreno, Juan, Hall, Peter, Hewlett, Jackie, McKechnie, Stuart, Garrard, Christopher, Millo, Julian, Young, Duncan, Hutton, Paula, Parsons, Penny, Smiths, Alex, Faras-Arraya, Roser, Raymode, Parizade, Thompson, Jonathan, Bowrey, Sarah, Kazembe, Sandra, Rich, Natalie, Andreou, Prem, Hales, Dawn, Roberts, Emma, Fletcher, Simon, Rosbergen, Melissa, Glister, Georgina, Cuesta, Jeronimo Moreno, Bion, Julian, Millar, Joanne, Perry, Elsa Jane, Willis, Heather, Mitchell, Natalie, Ruel, Sebastian, Carrera, Ronald, Wilde, Jude, Nilson, Annette, Lees, Sarah, Kapila, Atul, Jacques, Nicola, Atkinson, Jane, Brown, Abby, Prowse, Heather, Krige, Anton, Bland, Martin, Bullock, Lynne, Harrison, Donna, Mills, Gary, Humphreys, John, Armitage, Kelsey, Laha, Shond, Baldwin, Jacqueline, Walsh, Angela, Doherty, Nicola, Drage, Stephen, Ortiz-Ruiz de Gordoa, Laura

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Prostate-Specific Antigen Screening and 15-Year Prostate Cancer Mortality: A Secondary Analysis of the CAP Randomized Clinical Trial by Martin, Richard M, Turner, Emma L, Young, Grace J, Metcalfe, Chris, Walsh, Eleanor I, Lane, J Athene, Sterne, Jonathan A C, Noble, Sian, Holding, Peter, Ben-Shlomo, Yoav, Williams, Naomi J, Pashayan, Nora, Bui, Mai Ngoc, Albertsen, Peter C, Seibert, Tyler M, Zietman, Anthony L, Oxley, Jon, Adolfsson, Jan, Mason, Malcolm D, Davey Smith, George, Neal, David E, Hamdy, Freddie C, Donovan, Jenny L

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Mosaic PPM1D mutations are associated with predisposition to breast and ovarian cancer by Ruark, Elise, Snape, Katie, Humburg, Peter, Loveday, Chey, Bajrami, Ilirjana, Brough, Rachel, Rodrigues, Daniel Nava, Renwick, Anthony, Seal, Sheila, Ramsay, Emma, Duarte, Silvana Del Vecchio, Rivas, Manuel A., Warren-Perry, Margaret, Zachariou, Anna, Campion-Flora, Adriana, Hanks, Sandra, Murray, Anne, Pour, Naser Ansari, Douglas, Jenny, Gregory, Lorna, Rimmer, Andrew, Walker, Neil M., Yang, Tsun-Po, Adlard, Julian W., Barwell, Julian, Berg, Jonathan, Brady, Angela F., Brewer, Carole, Brice, Glen, Chapman, Cyril, Cook, Jackie, Davidson, Rosemarie, Donaldson, Alan, Douglas, Fiona, Eccles, Diana, Evans, D. Gareth, Greenhalgh, Lynn, Henderson, Alex, Izatt, Louise, Kumar, Ajith, Lalloo, Fiona, Miedzybrodzka, Zosia, Morrison, Patrick J., Paterson, Joan, Porteous, Mary, Rogers, Mark T., Shanley, Susan, Walker, Lisa, Gore, Martin, Houlston, Richard, Brown, Matthew A., Caufield, Mark J., Deloukas, Panagiotis, McCarthy, Mark I., Todd, John A., Turnbull, Clare, Reis-Filho, Jorge S., Ashworth, Alan, Antoniou, Antonis C., Lord, Christopher J., Donnelly, Peter, Rahman, Nazneen

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Genome‐Wide Association Study of Dermatomyositis Reveals Genetic Overlap With Other Autoimmune Disorders by Miller, Frederick W., Cooper, Robert G., Vencovský, Jiří, Rider, Lisa G., Danko, Katalin, Wedderburn, Lucy R., Lundberg, Ingrid E., Pachman, Lauren M., Reed, Ann M., Ytterberg, Steven R., Padyukov, Leonid, Selva‐O'Callaghan, Albert, Radstake, Timothy R. D. J., Isenberg, David A., Chinoy, Hector, Ollier, William E. R., O'Hanlon, Terrance P., Peng, Bo, Lee, Annette, Lamb, Janine A., Chen, Wei, Amos, Christopher I., Gregersen, Peter K.

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Assessing behavioural and social responses to an eco-mooring trial for Zostera marina conservation management in Torbay, Southwest England by Parry-Wilson, Hannah M., Rees, Sian E., Leather, Harrison, Cole, Rachel, Rugg, Clare, Attrill, Martin J.

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High-throughput mass spectrometry maps the sepsis plasma proteome and differences in patient response by Mi, Yuxin, Burnham, Katie L, Charles, Philip D, Heilig, Raphael, Vendrell, Iolanda, Whalley, Justin, Torrance, Hew D, Antcliffe, David B, May, Shaun M, Neville, Matt J, Berridge, Georgina, Hutton, Paula, Geoghegan, Cyndi G, Radhakrishnan, Jayachandran, Nesvizhskii, Alexey I, Yu, Fengchao, Davenport, Emma E, McKechnie, Stuart, Davies, Roger, O'Callaghan, David J P, Patel, Parind, Del Arroyo, Ana G, Karpe, Fredrik, Gordon, Anthony C, Ackland, Gareth L, Hinds, Charles J, Fischer, Roman, Knight, Julian C

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Genomic assessment of quarantine measures to prevent SARS-CoV-2 importation and transmission by Aggarwal, Dinesh, Page, Andrew J., Schaefer, Ulf, Savva, George M., Myers, Richard, Volz, Erik, Ellaby, Nicholas, Platt, Steven, Groves, Natalie, Gallagher, Eileen, Tumelty, Niamh M., Le Viet, Thanh, Hughes, Gareth J., Chen, Cong, Turner, Charlie, Logan, Sophie, Harrison, Abbie, Peacock, Sharon J., Chand, Meera, Harrison, Ewan M.

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Combined effects of three independent SNPs greatly increase the risk estimate for RA at 6q23 by Orozco, Gisela, Hinks, Anne, Eyre, Steve, Ke, Xiayi, Gibbons, Laura J., Bowes, John, Flynn, Edward, Martin, Paul, Wilson, Anthony G., Bax, Deborah E., Morgan, Ann W., Emery, Paul, Steer, Sophia, Hocking, Lynne, Reid, David M., Wordsworth, Paul, Harrison, Pille, Thomson, Wendy, Barton, Anne, Worthington, Jane

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