Intrinsic apurinic/apyrimidinic (AP) endonuclease activity enables Bacillus subtilis DNA polymerase X to recognize, incise, and further repair abasic sites by Baños, Benito, Villar, Laurentino, Salas, Margarita, de Vega, Miguel

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Structural and non-coding variants increase the diagnostic yield of clinical whole genome sequencing for rare diseases by Pagnamenta, Alistair T, Camps, Carme, Giacopuzzi, Edoardo, Taylor, John M, Hashim, Mona, Calpena, Eduardo, Kaisaki, Pamela J, Hashimoto, Akiko, Yu, Jing, Sanders, Edward, Schwessinger, Ron, Hughes, Jim R, Lunter, Gerton, Dreau, Helene, Ferla, Matteo, Lange, Lukas, Kesim, Yesim, Ragoussis, Vassilis, Vavoulis, Dimitrios V, Allroggen, Holger, Ansorge, Olaf, Babbs, Christian, Banka, Siddharth, Baños-Piñero, Benito, Beeson, David, Ben-Ami, Tal, Bennett, David L, Bento, Celeste, Blair, Edward, Brasch-Andersen, Charlotte, Bull, Katherine R, Cario, Holger, Cilliers, Deirdre, Conti, Valerio, Davies, E Graham, Dhalla, Fatima, Dacal, Beatriz Diez, Dong, Yin, Dunford, James E, Guerrini, Renzo, Harris, Adrian L, Hartley, Jane, Hollander, Georg, Javaid, Kassim, Kane, Maureen, Kelly, Deirdre, Kelly, Dominic, Knight, Samantha J L, Kreins, Alexandra Y, Kvikstad, Erika M, Langman, Craig B, Lester, Tracy, Lines, Kate E, Lord, Simon R, Lu, Xin, Mansour, Sahar, Manzur, Adnan, Maroofian, Reza, Marsden, Brian, Mason, Joanne, McGowan, Simon J, Mei, Davide, Mlcochova, Hana, Murakami, Yoshiko, Németh, Andrea H, Okoli, Steven, Ormondroyd, Elizabeth, Ousager, Lilian Bomme, Palace, Jacqueline, Patel, Smita Y, Pentony, Melissa M, Pugh, Chris, Rad, Aboulfazl, Ramesh, Archana, Riva, Simone G, Roberts, Irene, Roy, Noémi, Salminen, Outi, Schilling, Kyleen D, Scott, Caroline, Sen, Arjune, Smith, Conrad, Stevenson, Mark, Thakker, Rajesh V, Twigg, Stephen R F, Uhlig, Holm H, van Wijk, Richard, Vona, Barbara, Wall, Steven, Wang, Jing, Watkins, Hugh, Zak, Jaroslav, Schuh, Anna H, Kini, Usha, Wilkie, Andrew O M, Popitsch, Niko, Taylor, Jenny C

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DNA stabilization at the Bacillus subtilis PolX core--a binding model to coordinate polymerase, AP-endonuclease and 3'-5' exonuclease activities by Baños, Benito, Villar, Laurentino, Salas, Margarita, de Vega, Miguel

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Genome sequencing identifies KMT2E‐disrupting cryptic structural variant in a female with O'Donnell‐Luria‐Rodan syndrome by Hashim, Mona, Stewart, Helen, Yu, Jing, Banos‐Pinero, Benito, Pagnamenta, Alistair T., Taylor, Jenny C.

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Visualization of poly(ADP-ribose) bound to PARG reveals inherent balance between exo- and endo-glycohydrolase activities by Barkauskaite, Eva, Brassington, Amy, Tan, Edwin S., Warwicker, Jim, Dunstan, Mark S., Banos, Benito, Lafite, Pierre, Ahel, Marijan, Mitchison, Timothy J., Ahel, Ivan, Leys, David

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The prevalence and phenotypic range associated with biallelic PKDCC variants by Pagnamenta, Alistair T., Belles, Rebecca S., Salbert, Bonnie Anne, Wentzensen, Ingrid M., Guillen Sacoto, Maria J., Santos, Francis Jeshira Reynoso, Caffo, Alesky, Ferla, Matteo, Banos‐Pinero, Benito, Pawliczak, Karolina, Makvand, Mina, Najmabadi, Hossein, Maroofian, Reza, Lester, Tracy, Yanez‐Felix, Ana Lucia, Villarroel‐Cortes, Camilo E., Xia, Fan, Al Fayez, Khowla, Al Hashem, Amal, Shears, Deborah, Irving, Melita, Offiah, Amaka C., Kariminejad, Ariana, Taylor, Jenny C.

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Congenital hallux valgus occurs in Fibrodysplasia Ossificans Progressiva and BMPR1B-associated dysplasia: an important distinction by Shirodkar, Diksha, Smithson, Sarah Francesca, Keen, Richard, Lester, Tracy, Banos-Pinero, Benito, Burren, Christine Pamela

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Characterization of a Bacillus subtilis 64-kDa DNA Polymerase X Potentially Involved in DNA Repair by Baños, Benito, Lázaro, José M., Villar, Laurentino, Salas, Margarita, de Vega, Miguel

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Characterization of Bacillus subtilis uracil‐DNA glycosylase and its inhibition by phage φ29 protein p56 by Pérez‐Lago, Laura, Serrano‐Heras, Gemma, Baños, Benito, Lázaro, José M., Alcorlo, Martín, Villar, Laurentino, Salas, Margarita

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Editing of misaligned 3'-termini by an intrinsic 3'-5' exonuclease activity residing in the PHP domain of a family X DNA polymerase by Baños, Benito, Lázaro, José M, Villar, Laurentino, Salas, Margarita, de Vega, Miguel

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Characterization of Bacillus subtilis uracil-DNA glycosylase and its inhibition by phage [straight phi]29 protein p56 by Pérez-Lago, Laura, Serrano-Heras, Gemma, Baños, Benito, Lázaro, José M, Alcorlo, Martín, Villar, Laurentino, Salas, Margarita

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An HNRNPK-specific DNA methylation signature makes sense of missense variants and expands the phenotypic spectrum of Au-Kline syndrome by Choufani, Sanaa, McNiven, Vanda, Cytrynbaum, Cheryl, Jangjoo, Maryam, Adam, Margaret P., Bjornsson, Hans T., Harris, Jacqueline, Dyment, David A., Graham, Gail E., Nezarati, Marjan M., Aul, Ritu B., Castiglioni, Claudia, Breckpot, Jeroen, Devriendt, Koen, Stewart, Helen, Banos-Pinero, Benito, Mehta, Sarju, Sandford, Richard, Dunn, Carolyn, Mathevet, Remi, van Maldergem, Lionel, Piard, Juliette, Brischoux-Boucher, Elise, Vitobello, Antonio, Faivre, Laurence, Bournez, Marie, Tran-Mau, Frederic, Maystadt, Isabelle, Fernández-Jaén, Alberto, Alvarez, Sara, García-Prieto, Irene Díez, Alkuraya, Fowzan S., Alsaif, Hessa S., Rahbeeni, Zuhair, El-Akouri, Karen, Al-Mureikhi, Mariam, Spillmann, Rebecca C., Shashi, Vandana, Sanchez-Lara, Pedro A., Graham, John M., Roberts, Amy, Chorin, Odelia, Evrony, Gilad D., Kraatari-Tiri, Minna, Dudding-Byth, Tracy, Richardson, Anamaria, Hunt, David, Hamilton, Laura, Dyack, Sarah, Mendelsohn, Bryce A., Rodríguez, Nicolás, Sánchez-Martínez, Rosario, Tenorio-Castaño, Jair, Nevado, Julián, Lapunzina, Pablo, Tirado, Pilar, Carminho Amaro Rodrigues, Maria-Teresa, Quteineh, Lina, Innes, A. Micheil, Kline, Antonie D., Au, P.Y. Billie, Weksberg, Rosanna

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Germline mutations in a G protein identify signaling cross-talk in T cells by Ham, Hyoungjun, Jing, Huie, Lamborn, Ian T, Kober, Megan M, Koval, Alexey, Berchiche, Yamina A, Anderson, D Eric, Druey, Kirk M, Mandl, Judith N, Isidor, Bertrand, Ferreira, Carlos R, Freeman, Alexandra F, Ganesan, Sundar, Karsak, Meliha, Mustillo, Peter J, Teo, Juliana, Zolkipli-Cunningham, Zarazuela, Chatron, Nicolas, Lecoquierre, François, Oler, Andrew J, Schmid, Jana Pachlopnik, Kuhns, Douglas B, Xu, Xuehua, Hauck, Fabian, Al-Herz, Waleed, Wagner, Matias, Terhal, Paulien A, Muurinen, Mari, Barlogis, Vincent, Cruz, Phillip, Danielson, Jeffrey, Stewart, Helen, Loid, Petra, Rading, Sebastian, Keren, Boris, Pfundt, Rolph, Zarember, Kol A, Vill, Katharina, Potocki, Lorraine, Olivier, Kenneth N, Lesca, Gaetan, Faivre, Laurence, Wong, Melanie, Puel, Anne, Chou, Janet, Tusseau, Maud, Moutsopoulos, Niki M, Matthews, Helen F, Simons, Cas, Taft, Ryan J, Soldatos, Ariane, Masle-Farquhar, Etienne, Pittaluga, Stefania, Brink, Robert, Fink, Danielle L, Kong, Heidi H, Kabat, Juraj, Kim, Woo Sung, Bierhals, Tatjana, Meguro, Kazuyuki, Hsu, Amy P, Gu, Jingwen, Stoddard, Jennifer, Banos-Pinero, Benito, Slack, Maria, Trivellin, Giampaolo, Mazel, Benoît, Soomann, Maarja, Li, Samuel, Watts, Val J, Stratakis, Constantine A, Rodriguez-Quevedo, Maria F, Bruel, Ange-Line, Lipsanen-Nyman, Marita, Saultier, Paul, Jain, Rashmi, Lehalle, Daphne, Torres, Daniel, Sullivan, Kathleen E, Barbarot, Sébastien, Neu, Axel, Duffourd, Yannis, Similuk, Morgan, McWalter, Kirsty, Blanc, Pierre, Bézieau, Stéphane, Jin, Tian, Geha, Raif S, Casanova, Jean-Laurent, Makitie, Outi M, Kubisch, Christian, Edery, Patrick, Christodoulou, John, Germain, Ronald N, Goodnow, Christopher C, Sakmar, Thomas P, Billadeau, Daniel D, Küry, Sébastien, Katanaev, Vladimir L, Zhang, Yu

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A syndromic neurodevelopmental disorder caused by rare variants in PPFIA3 by Paul, Maimuna S., Michener, Sydney L., Pan, Hongling, Chan, Hiuling, Pfliger, Jessica M., Rosenfeld, Jill A., Lerma, Vanesa C., Tran, Alyssa, Longley, Megan A., Lewis, Richard A., Weisz-Hubshman, Monika, Bekheirnia, Mir Reza, Bekheirnia, Nasim, Massingham, Lauren, Zech, Michael, Wagner, Matias, Engels, Hartmut, Cremer, Kirsten, Mangold, Elisabeth, Peters, Sophia, Trautmann, Jessica, Perne, Claudia, Mester, Jessica L., Guillen Sacoto, Maria J., Person, Richard, McDonnell, Pamela P., Cohen, Stacey R., Lusk, Laina, Cohen, Ana S.A., Le Pichon, Jean-Baptiste, Pastinen, Tomi, Zhou, Dihong, Engleman, Kendra, Racine, Caroline, Faivre, Laurence, Moutton, Sébastien, Denommé-Pichon, Anne-Sophie, Koh, Hyun Yong, Poduri, Annapurna, Bolton, Jeffrey, Knopp, Cordula, Julia Suh, Dong Sun, Maier, Andrea, Toosi, Mehran Beiraghi, Karimiani, Ehsan Ghayoor, Maroofian, Reza, Schaefer, Gerald Bradley, Ramakumaran, Vijayalakshmi, Vasudevan, Pradeep, Banos-Pinero, Benito, Pagnamenta, Alistair T., Prasad, Chitra, Osmond, Matthew, Schuhmann, Sarah, Vasileiou, Georgia, Russ-Hall, Sophie, Scheffer, Ingrid E., Carvill, Gemma L., Mefford, Heather, Bacino, Carlos A., Lee, Brendan H., Chao (趙孝端), Hsiao-Tuan

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The impact of inversions across 33,924 families with rare disease from a national genome sequencing project by Pagnamenta, Alistair T., Yu, Jing, Walker, Susan, Noble, Alexandra J., Lord, Jenny, Dutta, Prasun, Hashim, Mona, Camps, Carme, Green, Hannah, Devaiah, Smrithi, Nashef, Lina, Parr, Jason, Fratter, Carl, Ibnouf Hussein, Rana, Lindsay, Sarah J., Lalloo, Fiona, Banos-Pinero, Benito, Evans, David, Mallin, Lucy, Waite, Adrian, Evans, Julie, Newman, Andrew, Allen, Zoe, Perez-Becerril, Cristina, Ryan, Gavin, Hart, Rachel, Taylor, John, Bedenham, Tina, Clement, Emma, Blair, Ed, Hay, Eleanor, Forzano, Francesca, Higgs, Jenny, Canham, Natalie, Majumdar, Anirban, McEntagart, Meriel, Lahiri, Nayana, Stewart, Helen, Smithson, Sarah, Calpena, Eduardo, Jackson, Adam, Banka, Siddharth, Titheradge, Hannah, McGowan, Ruth, Rankin, Julia, Shaw-Smith, Charles, Evans, D. Gareth, Burghel, George J., Smith, Miriam J., Anderson, Emily, Madhu, Rajesh, Firth, Helen, Ellard, Sian, Brennan, Paul, Anderson, Claire, Taupin, Doug, Rogers, Mark T., Cook, Jackie A., Durkie, Miranda, East, James E., Fowler, Darren, Wilson, Louise, Igbokwe, Rebecca, Gardham, Alice, Tomlinson, Ian, Baralle, Diana, Uhlig, Holm H., Taylor, Jenny C.

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A syndromic neurodevelopmental disorder caused by rare variants in PPFIA3 by Paul, Maimuna S., Michener, Sydney L., Pan, Hongling, Chan, Hiuling, Pfliger, Jessica M., Rosenfeld, Jill A., Lerma, Vanesa C., Tran, Alyssa, Longley, Megan A., Lewis, Richard A., Weisz-Hubshman, Monika, Bekheirnia, Mir Reza, Bekheirnia, Nasim, Massingham, Lauren, Zech, Michael, Wagner, Matias, Engels, Hartmut, Cremer, Kirsten, Mangold, Elisabeth, Peters, Sophia, Trautmann, Jessica, Perne, Claudia, Mester, Jessica L., Guillen Sacoto, Maria J., Person, Richard, McDonnell, Pamela P., Cohen, Stacey R., Lusk, Laina, Cohen, Ana S.A., Le Pichon, Jean-Baptiste, Pastinen, Tomi, Zhou, Dihong, Engleman, Kendra, Racine, Caroline, Faivre, Laurence, Moutton, Sébastien, Denommé-Pichon, Anne-Sophie, Koh, Hyun Yong, Poduri, Annapurna, Bolton, Jeffrey, Knopp, Cordula, Julia Suh, Dong Sun, Maier, Andrea, Toosi, Mehran Beiraghi, Karimiani, Ehsan Ghayoor, Maroofian, Reza, Schaefer, Gerald Bradley, Ramakumaran, Vijayalakshmi, Vasudevan, Pradeep, Banos-Pinero, Benito, Pagnamenta, Alistair T., Prasad, Chitra, Osmond, Matthew, Schuhmann, Sarah, Vasileiou, Georgia, Russ-Hall, Sophie, Scheffer, Ingrid E., Carvill, Gemma L., Mefford, Heather, Bacino, Carlos A., Lee, Brendan H., Chao, Hsiao-Tuan

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Characterization of Bacillus subtilis uracil-DNA glycosylase and its inhibition by phage phi 29 protein p56 by Perez-Lago, Laura, Serrano-Heras, Gemma, Banos, Benito, Lazaro, Jose M, Alcorlo, Martin, Villar, Laurentino, Salas, Margarita

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A novel time-saving multiplex PCR assay for detecting and discriminating the most common canine Babesia species in Europe by Remesar, S., Méndez, A., Benito, A., Prieto, A., García-Dios, D., López, C.M., Panadero, R., Díez-Baños, P., Morrondo, P., Díaz, P.

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Microbiota-based markers predictive of development of Clostridioides difficile infection by Berkell, Matilda, Mysara, Mohamed, Xavier, Basil Britto, van Werkhoven, Cornelis H., Monsieurs, Pieter, Lammens, Christine, Ducher, Annie, Vehreschild, Maria J. G. T., Goossens, Herman, de Gunzburg, Jean, Bonten, Marc J. M., Malhotra-Kumar, Surbhi

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LMIC-17. DIAGNOSTIC DELAY IN CHILDREN WITH CNS TUMORS IN A TERTIARY HOSPITAL IN MEXICO by de la Peña-Hernández, Beth Sainz, Arreguín-González, Farina, Valdéz-Orduño, Ricardo, Almazán-García, Blanca, Sandoval-de Jesús, San Juanita, Baños-Rodríguez, Eduardo, López-Azcárraga, Alejandra, García-Ramos, Jeannie, Sebastian-Barajas, Ruben, Ochoa-Madrigal, Georgina, Moreira, Daniel, Benito-Reséndiz, Alma

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