A Fine-Scale Chimpanzee Genetic Map from Population Sequencing von Auton, Adam, Fledel-Alon, Adi, Pfeifer, Susanne, Venn, Oliver, Ségurel, Laure, Street, Teresa, Leffler, Ellen M., Bowden, Rory, Aneas, Ivy, Broxholme, John, Humburg, Peter, Iqbal, Zamin, Lunter, Gerton, Maller, Julian, Hernandez, Ryan D., Melton, Cord, Venkat, Aarti, Nobrega, Marcelo A., Bontrop, Ronald, Myers, Simon, Donnelly, Peter, Przeworski, Molly, McVean, Gil

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A practical solution for preserving single cells for RNA sequencing von Attar, Moustafa, Sharma, Eshita, Li, Shuqiang, Bryer, Claire, Cubitt, Laura, Broxholme, John, Lockstone, Helen, Kinchen, James, Simmons, Alison, Piazza, Paolo, Buck, David, Livak, Kenneth J., Bowden, Rory

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Distinct regulation of hippocampal neuroplasticity and ciliary genes by corticosteroid receptors von Mifsud, Karen R., Kennedy, Clare L. M., Salatino, Silvia, Sharma, Eshita, Price, Emily M., Haque, Samantha N., Gialeli, Andriana, Goss, Hannah M., Panchenko, Polina E., Broxholme, John, Engledow, Simon, Lockstone, Helen, Cordero Llana, Oscar, Reul, Johannes M. H. M.

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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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Next-generation sequencing (NGS) as a diagnostic tool for retinal degeneration reveals a much higher detection rate in early-onset disease von Shanks, Morag E, Downes, Susan M, Copley, Richard R, Lise, Stefano, Broxholme, John, Hudspith, Karl Az, Kwasniewska, Alexandra, Davies, Wayne Il, Hankins, Mark W, Packham, Emily R, Clouston, Penny, Seller, Anneke, Wilkie, Andrew Om, Taylor, Jenny C, Ragoussis, Jiannis, Németh, Andrea H

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Genomic regulation of Krüppel-like-factor family members by corticosteroid receptors in the rat brain von Kennedy, Clare L M, Price, Emily M, Mifsud, Karen R, Salatino, Silvia, Sharma, Eshita, Engledow, Simon, Broxholme, John, Goss, Hannah M, Reul, Johannes M H M

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Coexpression network analysis in abdominal and gluteal adipose tissue reveals regulatory genetic loci for metabolic syndrome and related phenotypes von Min, Josine L, Nicholson, George, Halgrimsdottir, Ingileif, Almstrup, Kristian, Petri, Andreas, Barrett, Amy, Travers, Mary, Rayner, Nigel W, Mägi, Reedik, Pettersson, Fredrik H, Broxholme, John, Neville, Matt J, Wills, Quin F, Cheeseman, Jane, Allen, Maxine, Holmes, Chris C, Spector, Tim D, Fleckner, Jan, McCarthy, Mark I, Karpe, Fredrik, Lindgren, Cecilia M, Zondervan, Krina T

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Host genetic factors and vaccine-induced immunity to hepatitis B virus infection von Hennig, Branwen J, Fielding, Katherine, Broxholme, John, Diatta, Mathurin, Mendy, Maimuna, Moore, Catrin, Pollard, Andrew J, Rayco-Solon, Pura, Sirugo, Giorgio, van der Sande, Marianne A, Waight, Pauline, Whittle, Hilton C, Zaman, Syed M, Hill, Adrian V, Hall, Andrew J

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The use of genome-wide eQTL associations in lymphoblastoid cell lines to identify novel genetic pathways involved in complex traits von Min, Josine L, Taylor, Jennifer M, Richards, J Brent, Watts, Tim, Pettersson, Fredrik H, Broxholme, John, Ahmadi, Kourosh R, Surdulescu, Gabriela L, Lowy, Ernesto, Gieger, Christian, Newton-Cheh, Chris, Perola, Markus, Soranzo, Nicole, Surakka, Ida, Lindgren, Cecilia M, Ragoussis, Jiannis, Morris, Andrew P, Cardon, Lon R, Spector, Tim D, Zondervan, Krina T

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GLIDERS--a web-based search engine for genome-wide linkage disequilibrium between HapMap SNPs von Lawrence, Robert, Day-Williams, Aaron G, Mott, Richard, Broxholme, John, Cardon, Lon R, Zeggini, Eleftheria

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A blood atlas of COVID-19 defines hallmarks of disease severity and specificity von Ai, Zhichao, Ainsworth, Mark, Arancibia-Cárcamo, Carolina V., Attar, Moustafa, Baillie, J. Kenneth, Bashford-Rogers, Rachael, Bicanic, Tihana, Bowness, Paul, Brent, Andrew, Buck, David, Camara, Susana, Clutterbuck, Elizabeth A., Coles, Mark, Conlon, Christopher P., Cribbs, Adam P., Curion, Fabiola, Davenport, Emma E., Davidson, Neil, Davis, Simon, Dendrou, Calliope A., Dequaire, Julie, Docker, James, Dold, Christina, Downes, Damien, Drakesmith, Hal, Dunachie, Susanna J., Espinosa, Alexis, Felle, Sally, Fernandez Mendoza, Maria, Forrow, Aden, Frater, John, Fries, Anastasia, Garner, Lucy C., Godfrey, Leila, Gomez Vazquez, Maria, Green, Angie, Harper, Hong, Heilig, Raphael, Hester, Svenja, Hill, Jennifer, Hinds, Charles, Hird, Clare, Hutton, Paula, Jainarayanan, Ashwin, Jansen, Kathrin, Jones, Elizabeth, Klenerman, Paul, Knight, Julian C., Kumar Sharma, Piyush, Kurupati, Prathiba, Kwok, Andrew, Lee, Angela, Lonie, Lorne, Luo, Jian, Marsden, Brian, Martinez, Jose, Matthews, Philippa C., Mazurczyk, Michalina, McGowan, Simon, Mi, Yuxin, Montadon, Ruddy, O'Brien, Darragh P., Ogg, Graham, Overend, Lauren, Pereira Pinho, Mariana, Perez, Elena, Pollard, Andrew J., Quan, T. Phuong, Revale, Santiago, Silva-Reyes, Laura, Richard, Jean-Baptiste, Rich-Griffin, Charlotte, Salio, Mariolina, Sansom, Stephen Nicholas, Sauka-Spengler, Tatjana, Schwessinger, Ron, Sobrinodiaz, Alberto, Stockdale, Lisa, Strickland, Marie, Sun, Bo, Taylor, Chelsea, Taylor, Stephen, Taylor, Adan, Tomic, Adriana, Tong, Orion, Trebes, Amy, Uhlig, Holm, van Grinsven, Erinke, Vendrell, Iolanda, Verheul, Marije, Wang, Guanlin, Wang, Lihui, Wang, Dapeng, Watkinson, Peter, Watson, Robert, Witty, Lorna, Wray, Katherine, Xue, Luzheng, Young, Rebecca K., Zhang, Ping

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Germline mutations affecting the proofreading domains of POLE and POLD1 predispose to colorectal adenomas and carcinomas von Palles, Claire, Cazier, Jean-Baptiste, Howarth, Kimberley M, Domingo, Enric, Jones, Angela M, Broderick, Peter, Kemp, Zoe, Spain, Sarah L, Guarino, Estrella, Salguero, Israel, Sherborne, Amy, Chubb, Daniel, Carvajal-Carmona, Luis G, Ma, Yusanne, Kaur, Kulvinder, Dobbins, Sara, Barclay, Ella, Gorman, Maggie, Martin, Lynn, Kovac, Michal B, Humphray, Sean, Lucassen, Anneke, Holmes, Christopher C, Bentley, David, Donnelly, Peter, Taylor, Jenny, Petridis, Christos, Roylance, Rebecca, Sawyer, Elinor J, Kerr, David J, Clark, Susan, Grimes, Jonathan, Kearsey, Stephen E, Thomas, Huw J W, McVean, Gilean, Houlston, Richard S, Tomlinson, Ian

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Clinical whole-genome sequencing in severe early-onset epilepsy reveals new genes and improves molecular diagnosis von Martin, Hilary C, Kim, Grace E, Pagnamenta, Alistair T, Murakami, Yoshiko, Carvill, Gemma L, Meyer, Esther, Copley, Richard R, Rimmer, Andrew, Barcia, Giulia, Fleming, Matthew R, Kronengold, Jack, Brown, Maile R, Hudspith, Karl A, Broxholme, John, Kanapin, Alexander, Cazier, Jean-Baptiste, Kinoshita, Taroh, Nabbout, Rima, Bentley, David, McVean, Gil, Heavin, Sinéad, Zaiwalla, Zenobia, McShane, Tony, Mefford, Heather C, Shears, Deborah, Stewart, Helen, Kurian, Manju A, Scheffer, Ingrid E, Blair, Edward, Donnelly, Peter, Kaczmarek, Leonard K, Taylor, Jenny C

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Impact of spliceosome mutations on RNA splicing in myelodysplasia: dysregulated genes/pathways and clinical associations von Pellagatti, Andrea, Armstrong, Richard N., Steeples, Violetta, Sharma, Eshita, Repapi, Emmanouela, Singh, Shalini, Sanchi, Andrea, Radujkovic, Aleksandar, Horn, Patrick, Dolatshad, Hamid, Roy, Swagata, Broxholme, John, Lockstone, Helen, Taylor, Stephen, Giagounidis, Aristoteles, Vyas, Paresh, Schuh, Anna, Hamblin, Angela, Papaemmanuil, Elli, Killick, Sally, Malcovati, Luca, Hennrich, Marco L., Gavin, Anne-Claude, Ho, Anthony D., Luft, Thomas, Hellström-Lindberg, Eva, Cazzola, Mario, Smith, Christopher W.J., Smith, Stephen, Boultwood, Jacqueline

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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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Correction: Host Genetic Factors and Vaccine-Induced Immunity to Hepatitis B Virus Infection von Hennig, Branwen J., Fielding, Katherine, Broxholme, John, Diatta, Mathurin, Mendy, Maimuna, Moore, Catrin, Pollard, Andrew J., Rayco-Solon, Pura, Sirugo, Giorgio, van der Sande, Marianne A., Waight, Pauline, Whittle, Hilton C., Zaman, Syed M., Hill, Adrian V., Hall, Andrew J.

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Nuclear-mitochondrial DNA segments resemble paternally inherited mitochondrial DNA in humans von Wei, Wei, Pagnamenta, Alistair T., Gleadall, Nicholas, Sanchis-Juan, Alba, Stephens, Jonathan, Broxholme, John, Tuna, Salih, Odhams, Christopher A., Fratter, Carl, Turro, Ernest, Caulfield, Mark J., Taylor, Jenny C., Rahman, Shamima, Chinnery, Patrick F.

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AICAR confers prophylactic cardioprotection in doxorubicin-induced heart failure in rats von Choksey, Anurag, Carter, Ryan D., Thackray, Benjamin D., Ball, Vicky, Kennedy, Brett W.C., Ha, Lea Hong Tuan, Sharma, Eshita, Broxholme, John, Castro-Guarda, Marcos, Murphy, Michael P., Heather, Lisa C., Tyler, Damian J., Timm, Kerstin N.

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miR-3156-5p is downregulated in serum of MEN1 patients and regulates expression of MORF4L2 von Kooblall, Kreepa G, Stokes, Victoria J, Shariq, Omair A, English, Katherine A, Stevenson, Mark, Broxholme, John, Wright, Benjamin, Lockstone, Helen E, Buck, David, Grozinsky-Glasberg, Simona, Yates, Christopher J, Thakker, Rajesh V, Lines, Kate E

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Phenotypic and transcriptomic characterization of canine myeloid-derived suppressor cells von Goulart, Michelle R., Hlavaty, Sabina I., Chang, Yu-Mei, Polton, Gerry, Stell, Anneliese, Perry, James, Wu, Ying, Sharma, Eshita, Broxholme, John, Lee, Avery C., Szladovits, Balazs, Turmaine, Mark, Gribben, John, Xia, Dong, Garden, Oliver A.

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