Methods and systems to avoid unproductive dispatches von RIVES DAVID G, BREWER JASON

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Methods and systems to avoid unproductive dispatches von RIVES DAVID G, BREWER JASON

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Future Surgical Leaders: Resident Perception Of Longitudinal Leadership And Non-Technical Skills Curriculum von Mann, David R., Thomas, Christopher S., Parrado, Raphael H., Rives, G. Tyler, Talley, Cynthia L.

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Harmonizing Clinical Sequencing and Interpretation for the eMERGE III Network von Venner, Eric, Muzny, Donna M., Abrams, Debra, Albertson-Junkans, Ladia, Ames, Darren C., Aronson, Samuel, Babb, Lawrence J., Balasubramanian, Adithya, Bastarache, Lisa, Behr, Meckenzie, Blout, Carrie, Bowser, Mark, Brilliant, Murray, Brodeur, Wendy, Caraballo, Pedro, Castro, Victor, Chisholm, Rex L., Chung, Wendy, Chute, Christopher G., City, Brittany, Connolly, John J., Crane, Paul, Crew, Katherine, De Andrade, Mariza, Denson, Shawn, Denny, Josh, DeSmet, Tim, Dikilitas, Ozan, Fullerton, Stephanie M., Gabriel, Stacey, Gainer, Vivian, Gharavi, Ali, Glazer, Andrew M., Goehringer, Jessica, Gordon, Adam S., Graham, Chet, Dayal, Jyoti, Hakonarson, Hakon, Harden, Maegan V., Harr, Margaret, Hayes, M. Geoffrey, Henrikson, Nora, Howell, Kayla M., Jiang, Yunyun, Joo, Yoonjung Yoonie, Justice, Anne E., Kalla, Sara E., Kalra, Divya, Kelly, Melissa A., Key, Dustin, Kiryluk, Krzysztof, Kullo, Iftikhar J., Larson, Eric B., Lin, Chiao-Feng, Linder, Jodell, Macbeth, Alyssa, Dinsmore, Michael J., Dodge, Sheila, Fasel, David, Fedotov, Alex, Feng, Qiping, McGowan, Michelle L., Meldrim, Jim, Mosley, Jonathan, Muniz, Jesse, Murdock, David R., Murugan, Mullai, Myers, Melanie F., Namjou, Bahram, Ni, Yizhao, Obeng, Aniwaa Owusu, Taylor, Casey Overby, Peterson, Josh F., Pratap, Siddharth, Prows, Cynthia A., Ralston, James D., Ramaprasan, Arvind, Rasmussen-Torvik, Laura, Schaid, Dan, Sengupta, Soumitra, Singh, Rajbir, Sleiman, Patrick M.A., Smoller, Jordan W., Stanaway, Ian B., Stroud, Mary, Tolwinski, Kasia, Van Driest, Sara L., Veenstra, David, Vicente, Gina, Wagner, Michael, Walunas, Theresa, Wells, Quinn, White, Peter S., Wiley, Ken L., Wilson, Michael W., Woolf, Betty, Yi, Victoria, Zhang, Ge, Zhang, Lan, Gibbs, Richard A.

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Identification of rare-disease genes using blood transcriptome sequencing and large control cohorts von Frésard, Laure, Smail, Craig, Ferraro, Nicole M., Teran, Nicole A., Li, Xin, Smith, Kevin S., Bonner, Devon, Kernohan, Kristin D., Marwaha, Shruti, Zappala, Zachary, Balliu, Brunilda, Davis, Joe R., Liu, Boxiang, Prybol, Cameron J., Kohler, Jennefer N., Zastrow, Diane B., Reuter, Chloe M., Fisk, Dianna G., Grove, Megan E., Davidson, Jean M., Hartley, Taila, Joshi, Ruchi, Strober, Benjamin J., Utiramerur, Sowmithri, Lind, Lars, Ingelsson, Erik, Battle, Alexis, Bejerano, Gill, Bernstein, Jonathan A., Ashley, Euan A., Boycott, Kym M., Merker, Jason D., Wheeler, Matthew T., Montgomery, Stephen B.

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An autosomal dominant neurological disorder caused by de novo variants in FAR1 resulting in uncontrolled synthesis of ether lipids von Ruiter, Jos P.N., van Lint, Alida E.M., Pras-Raves, Mia, Wever, Eric, Guillen Sacoto, Maria J., Begtrup, Amber, Tarnopolsky, Mark, Sell, Susan L., Nowak, Catherine B., Douglas, Jessica, Perlman, Seth, Martin, Nicole, Brault, Jennifer, Gahl, William A., Alejandro, Mercedes E., Dai, Hongzheng, Dhar, Shweta U., Hanchard, Neil A., Lee, Brendan H., Moretti, Paolo M., Murdock, David R., Nicholas, Sarah K., Potocki, Lorraine, Scott, Daryl A., Eng, Christine M., Deardorff, Matthew, Hassey, Kelly, Sullivan, Kathleen, Tan, Queenie K.-G., Beggs, Alan H., Berry, Gerard T., Cooper, Cynthia M., Pallais, J. Carl, Rodan, Lance H., Kelley, Emily G., Morava, Eva, Forghani, Irman, Lam, Byron, Levitt, Roy, Liu, Xue Zhong, McCauley, Jacob, Tekin, Mustafa, Thorson, Willa, Findley, Laurie C., Krasnewich, Donna M., Manolio, Teri A., Goldrich, Madison P., Draper, David D., Nath, Avi, Pusey, Barbara N., Toro, Camilo, Baker, Eva, Gochuico, Bernadette, Mosbrook-Davis, Deborah, Rossignol, Francis, Adam, Margaret, Amendola, Laura, Cunningham, Michael, Jarvik, Gail P., Jarvik, Jeffrey, Lam, Christina, Raskind, Wendy, Sybert, Virginia, Ashley, Euan A., Coakley, Terra R., Hom, Jason, Majcherska, Marta M., Martin, Beth A., Marwaha, Shruti, Ruzhnikov, Maura, Tabor, Holly K., Tucker, Brianna M., Zastrow, Diane B., Byrd, William E., Dell’Angelica, Esteban C., Douine, Emilie D., Mak, Bryan C., Martin, Martin G., Martínez-Agosto, Julian A., McGee, Elisabeth, Nelson, Stanley F., Parker, Neil H., Sinsheimer, Janet S., Wang, Lee-kai, Perry, Katherine Wesseling, Woods, Jeremy D., Pace, Laura, Marth, Gabor, Viskochil, Dave, Bayrak-Toydemir, Pinar, Duncan, Laura, Robertson, Amy K., Solem, Emily, Schedl, Timothy, Shin, Jimann, Solnica-Krezel, Lilianna, Waisfisz, Quinten, Zwijnenburg, Petra J.G., Wanders, Ronald J.A., Vaz, Frédéric M.

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Lysosomal Storage and Albinism Due to Effects of a De Novo CLCN7 Variant on Lysosomal Acidification von Becerril, Alissa, Larson, Austin, Zerfas, Patricia M., Acosta, Maria T., Agrawal, Pankaj, Alejandro, Mercedes E., Andrews, Ashley, Bacino, Carlos A., Bademci, Guney, Baker, Eva, Baldridge, Dustin, Bale, Jim, Barbouth, Deborah, Batzli, Gabriel F., Bayrak-Toydemir, Pinar, Bernstein, Jonathan A., Birch, Camille L., Bivona, Stephanie, Bohnsack, John, Bonnenmann, Carsten, Bostwick, Bret L., Brokamp, Elly, Burrage, Lindsay C., Carey, John, Clark, Gary D., Cope, Heidi, Dasari, Surendra, Dayal, Jyoti G., Dorset, Daniel C., Eng, Christine M., Esteves, Cecilia, Fresard, Laure, Goldman, Alica M., Goldstein, David B., Groden, Catherine A., Haendel, Melissa, Hayes, Nichole, Holm, Ingrid A., Jiang, Yong-hui, Johnston, Jean M., Jones, Angela L., Kohane, Isaac S., Krakow, Deborah, Krasnewich, Donna M., Korrick, Susan, Krier, Joel B., Lalani, Seema R., Lam, Byron, Lazar, Jozef, Levy, Shawn E., Liu, Xue Zhong, Malicdan, May Christine V., Mamounas, Laura A., Markello, Thomas C., Marom, Ronit, Martínez-Agosto, Julian A., McCormack, Colleen E., McCray, Alexa T., Might, Matthew, Morava-Kozicz, Eva, Murdock, David R., Nath, Avi, Nelson, Stan F., Newman, John H., Orengo, James P., Pace, Laura, Papp, Jeanette C., Parker, Neil H., Potocki, Lorraine, Raja, Archana N., Reuter, Chloe M., Rives, Lynette, Rowley, Robb K., Sampson, Jacinda B., Saporta, Mario, Schedl, Timothy, Shields, Kathleen, Signer, Rebecca, Sillari, Catherine H., Sisco, Kathy, Spillmann, Rebecca C., Stoler, Joan M., Stong, Nicholas, Sullivan, Jennifer A., Tekin, Mustafa, Thorson, Willa, Tran, Alyssa A., Wahl, Colleen E., Wan, Jijun, Wang, Lee-kai, Wangler, Michael F., Westerfield, Monte, Wheeler, Matthew T., Wolfe, Lynne A., Woods, Jeremy D., Worthey, Elizabeth A., Yamamoto, Shinya, Zuchner, Stephan, Day-Salvatore, Debra L., Mindell, Joseph A.

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Comparative genome sequencing of Drosophila pseudoobscura: chromosomal, gene, and cis-element evolution von Richards, Stephen, Liu, Yue, Bettencourt, Brian R, Hradecky, Pavel, Letovsky, Stan, Nielsen, Rasmus, Thornton, Kevin, Hubisz, Melissa J, Chen, Rui, Meisel, Richard P, Couronne, Olivier, Hua, Sujun, Smith, Mark A, Zhang, Peili, Liu, Jing, Bussemaker, Harmen J, van Batenburg, Marinus F, Howells, Sally L, Scherer, Steven E, Sodergren, Erica, Matthews, Beverly B, Crosby, Madeline A, Schroeder, Andrew J, Ortiz-Barrientos, Daniel, Rives, Catharine M, Metzker, Michael L, Muzny, Donna M, Scott, Graham, Steffen, David, Wheeler, David A, Worley, Kim C, Havlak, Paul, Durbin, K James, Egan, Amy, Gill, Rachel, Hume, Jennifer, Morgan, Margaret B, Miner, George, Hamilton, Cerissa, Huang, Yanmei, Waldron, Lenée, Verduzco, Daniel, Clerc-Blankenburg, Kerstin P, Dubchak, Inna, Noor, Mohamed A F, Anderson, Wyatt, White, Kevin P, Clark, Andrew G, Schaeffer, Stephen W, Gelbart, William, Weinstock, George M, Gibbs, Richard A

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SPTSSA variants alter sphingolipid synthesis and cause a complex hereditary spastic paraplegia von Srivastava, Siddharth, Shaked, Hagar Mor, Gable, Kenneth, Gupta, Sita D, Pan, Xueyang, Somashekarappa, Niranjanakumari, Han, Gongshe, Mohassel, Payam, Gotkine, Marc, Doney, Elizabeth, Goldenberg, Paula, Tan, Queenie K G, Gong, Yi, Kleinstiver, Benjamin, Wishart, Brian, Cope, Heidi, Pires, Claudia Brito, Stutzman, Hannah, Spillmann, Rebecca C, Sadjadi, Reza, Elpeleg, Orly, Lee, Chia-Hsueh, Bellen, Hugo J, Edvardson, Simon, Eichler, Florian, Dunn, Teresa M

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Commonalities across computational workflows for uncovering explanatory variants in undiagnosed cases von Krier, Joel B., Züchner, Stephan, Huang, Alden, Bastarache, Lisa, Bican, Anna, Liu, Pengfei, Adam, Margaret, Alejandro, Mercedes E., Alvey, Justin, Azamian, Mahshid S., Bademci, Guney, Baker, Eva, Balasubramanyam, Ashok, Bale, Jim, Beck, Anita, Bennett, Jimmy, Berry, Gerard T., Bican, Anna, Bohnsack, John, Bonner, Devon, Boyd, Brenna, Brown, Gabrielle, Burrage, Lindsay C., Butte, Manish J., Coakley, Terra R., Cobban, Laurel A., Cogan, Joy D., Cole, F. Sessions, Cunningham, Michael, Dorrani, Naghmeh, Doss, Argenia L., Douine, Emilie D., Eng, Christine M., Falk, Marni, Ferreira, Carlos, Findley, Laurie C., Fogel, Brent L., Forghani, Irman, Gahl, William A., Glass, Ian, Godfrey, Rena A., Hanchard, Neil A., Hing, Anne, Huryn, Laryssa, Isasi, Rosario, Kiley, Dana, Korrick, Susan, Krakow, Deborah, Lalani, Seema R., LeBlanc, Kimberly, Liu, Xue Zhong, MacDowall, John, MacRae, Calum A., Mamounas, Laura A., Maravilla, Kenneth, Markello, Thomas C., Martin, Beth A., Martin, Martin G., Marwaha, Shruti, McCauley, Jacob, Merritt, J. Lawrence, Might, Matthew, Moretti, Paolo, Murdock, David R., Nakano-Okuno, Mariko, Nickerson, Deborah, Oglesbee, Devin, Pace, Laura, Pallais, J. Carl, Papp, Jeanette C., Phillips, John A., Power, Bradley, Pusey, Barbara N., Raja, Archana N., Renteria, Genecee, Rosenwasser, Natalie, Rossignol, Francis, Ruzhnikov, Maura, Sampson, Jacinda B., Schedl, Timothy, Shin, Jimann, Smith, Edward C., Sun, Angela, Sutton, Shirley, Sweetser, David A., Sybert, Virginia, Toro, Camilo, Tucker, Brianna M., Velinder, Matt, Viskochil, Dave, Wambach, Jennifer, Wang, Lee-kai, Ward, Patricia A., Wener, Mark, Westerfield, Monte, Whitlock, Jordan, Woods, Jeremy D., Yamamoto, Shinya, Yang, John, Zein, Wadih

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Heterozygous loss-of-function variants significantly expand the phenotypes associated with loss of GDF11 von Ravenscroft, Thomas A., Fieg, Elizabeth, Zirin, Jonathan, Kanca, Oguz, Adam, Margaret, Agrawal, Pankaj B., Alejandro, Mercedes E., Alvey, Justin, Andrews, Ashley, Azamian, Mahshid S., Bademci, Guney, Balasubramanya, Ashok, Behrens, Edward, Bican, Anna, Bohnsack, John, Botto, Lorenzo, Brown, Gabrielle, Byers, Peter, Chanprasert, Sirisak, Chao, Hsiao-Tuan, Cobban, Laurel A., Cogan, Joy D., Colley, Heather A., Cope, Heidi, Craigen, William J., Crouse, Andrew B., Dai, Hongzheng, Dayal, Jyoti G., Dipple, Katrina, Dorrani, Naghmeh, Draper, David D., Emrick, Lisa T., Falk, Marni, Fernandez, Liliana, Fieg, Elizabeth L., Findley, Laurie C., Gahl, William A., Godfrey, Rena A., Goldman, Alica M., Goldstein, David B., Hamid, Rizwan, Hanchard, Neil A., Hassey, Kelly, Hayes, Nichole, High, Frances, Hing, Anne, Hisama, Fuki M., Holm, Ingrid A., Huang, Yong, Huryn, Laryssa, Isasi, Rosario, Jarvik, Gail P., Jarvik, Jeffrey, Jayadev, Suman, Kiley, Dana, Krasnewich, Donna M., Lam, Christina, Lee, Hane, MacDowall, John, Majcherska, Marta M., Mak, Bryan C., Mamounas, Laura A., Martínez-Agosto, Julian A., McCauley, Jacob, Mulvihill, John J., Newman, John H., Oglesbee, Devin, Pace, Laura, Pallais, J. Carl, Palmer, Christina GS, Posey, Jennifer E., Potocki, Lorraine, Power, Bradley, Pusey, Barbara N., Rives, Lynette, Sacco, Ralph, Sampson, Jacinda B., Samson, Susan L., Scott, C. Ron, Schedl, Timothy, Shashi, Vandana, Tan, Queenie K.-G., Toro, Camilo, Viskochil, Dave, Wahl, Colleen E., Wambach, Jennifer, Wang, Lee-kai, Wener, Mark, Perry, Katherine Wesseling, Westerfield, Monte, Whitlock, Jordan, Yamamoto, Shinya, Yang, John, Yousef, Muhammad, Zastrow, Diane B., Zhao, Chunli, Osmond, Matthew, Postlethwait, John H., Krier, Joel, Bellen, Hugo J.

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Biallelic MADD variants cause a phenotypic spectrum ranging from developmental delay to a multisystem disorder von Schneeberger, Pauline E, Kortüm, Fanny, Korenke, Georg Christoph, Alawi, Malik, Santer, René, Woidy, Mathias, Buhas, Daniela, Fox, Stephanie, Juusola, Jane, Alfadhel, Majid, Webb, Bryn D, Coci, Emanuele G, Abou Jamra, Rami, Siekmeyer, Manuela, Biskup, Saskia, Heller, Corina, Maier, Esther M, Javaher-Haghighi, Poupak, Bedeschi, Maria F, Ajmone, Paola F, Iascone, Maria, Peeters, Hilde, Ballon, Katleen, Jaeken, Jaak, Rodríguez Alonso, Aroa, Palomares-Bralo, María, Santos-Simarro, Fernando, Meuwissen, Marije E C, Beysen, Diane, Kooy, R Frank, Houlden, Henry, Murphy, David, Doosti, Mohammad, Karimiani, Ehsan G, Mojarrad, Majid, Maroofian, Reza, Noskova, Lenka, Kmoch, Stanislav, Honzik, Tomas, Cope, Heidi, Sanchez-Valle, Amarilis, Gelb, Bruce D, Kurth, Ingo, Hempel, Maja, Kutsche, Kerstin

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Variants in PRKAR1B cause a neurodevelopmental disorder with autism spectrum disorder, apraxia, and insensitivity to pain von Erger, Florian, Settas, Nikolaos, London, Edra, Torti, Erin, Nelson, Stanley F., Acosta, Maria T., Adams, David R., Balasubramanyam, Ashok, Baldridge, Dustin, Bale, Jim, Bamshad, Michael, Bayrak-Toydemir, Pinar, Beck, Anita, Bennett, Jimmy, Bernstein, Jonathan A., Blue, Elizabeth, Bohnsack, John, Bonnenmann, Carsten, Boyd, Brenna, Brokamp, Elly, Burke, Elizabeth A., Byrd, William E., Carrasquillo, Olveen, Chanprasert, Sirisak, Chao, Hsiao-Tuan, Coggins, Matthew, Cole, F. Sessions, Crouse, Andrew B., Cunningham, Michael, D’Souza, Precilla, Dai, Hongzheng, Dipple, Katrina, Doherty, Daniel, Earl, Dawn, Eckstein, David J., Eng, Christine M., Ferreira, Carlos, Glass, Ian, Gochuico, Bernadette, Goldman, Alica M., Goldstein, David B., Hassey, Kelly, Hom, Jason, Huang, Yong, Jarvik, Gail P., Jarvik, Jeffrey, Krasnewich, Donna M., LaMoure, Grace L., Lalani, Seema R., Lanpher, Brendan C., Latham, Lea, Liu, Pengfei, Liu, Xue Zhong, Macnamara, Ellen F., Malicdan, May Christine V., Manolio, Teri A., Maravilla, Kenneth, Marom, Ronit, Martin, Beth A., Marwaha, Shruti, McCormack, Colleen E., McGee, Elisabeth, Might, Matthew, Nakano-Okuno, Mariko, Nath, Avi, Nicholas, Sarah K., Novacic, Donna, Orengo, James P., Pallais, J. Carl, Palmer, Christina G.S., Parker, Neil H., Posey, Jennifer E., Quinlan, Aaron, Reuter, Chloe M., Robertson, Amy K., Ruzhnikov, Maura, Samson, Susan L., Saporta, Mario, Schaechter, Judy, Signer, Rebecca H., Smith, Kevin S., Ben Solomon, Stoler, Joan M., Sullivan, Jennifer A., Sullivan, Kathleen, Sun, Angela, Tabor, Holly K., Tucker, Brianna M., Vanderver, Adeline, Wallace, Stephanie, Wangler, Michael F., Ward, Patricia A., Whitlock, Jordan, Wolfe, Lynne A., Woods, Jeremy D., Zastrow, Diane B., Grange, Dorothy K., Willaert, Rebecca, Theiß, Susanne, Stocco, Amber

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Coronal Heating as Determined by the Solar Flare Frequency Distribution Obtained by Aggregating Case Studies von Youngblood, Allison, Peck, Courtney L., Chaparro, David, Nelson, Emma E, Osborne, Andrew, Aaron, James Holland, Abrashoff, Riley, Al-Ghazwi, Adel, Albaum, Jonathan, Alhamli, Dania, Alqabani, Emeen, Altenbern, Ava L., Amos, Meggan, Andrew, Carter, Beattie, Ryan, Behr, Braden, Billman, Jayce A., Bisacca, Gabrielle E., Bodzianowski, Michal, Bowen, Troy, Boyne, Tom, Brown, Gabriel T., Burritt, John J., Busch, Celeste, Chandler, Olivia M., Chen, Lily, Collins, Nathaniel A., Curnow, Tyler L., Curry, Riley T., Das, Swagatam, Deng, Tianyue, Desai, Om, Ehrlich, Lauren, Enrich, Andrew, Evans, Nathan, D. Figueirinhas, John Alfred, Furney, Sebastian, Gale, Skylar, Ghaith, Bandar Abu, Gilpatrick, Connor B., Gjini, Michael, Haines, Jessica, Hicks, Imari R., Hill, Paula, Houck, Timothy J, Huebsch, Tyler J., Hull, Owen, Huynh, Leslie, Samour Ii, Antonio E., Ingram, Julia A., Iovan, Taro, Ji, Soo Yeun, Ketterer, Marilyn, Kim, Brian T., Kim, Matthew M., Kubiak, Bartlomiej, Kuester, Chrisanne, Kuybus, Connor, Kwiatkowski, Daniel, Lantz, Maxwell B., Liu, Steven Y., Macdonald, William, Maly, Blake, Martinez, Hazelia K., Mcconvey, Rowan, Mulcahy, Owen T., Murphy, Maxwell J., Nelson, Maya Li, Norris, Cooper, Ort, Althea E., Otto, Grant, Patton, Catherine, Payne, Matthew P., Pham, Alexander V., Quinn, Megan S., Rahn, Anna L., Ramachandra, Nidhi, Reynolds, Alexander, Robert, Amanda M., Rosasco, Ryan, Rouse, Charlotte, Routledge, Allie C., Rule, Ian C., Salindeho, Adam D., Shannahan, Callie D., Siles, Nathan, Solt, Lincoln, Spangler, Ava A, Steward, Ellie N., Szabo, Emi, Trautwein, Emily D., Vadayar, Shreenija, Venegas, Nancy Ortiz, Vinson, Jessica, Wallace, Steven P., White, Jamison R., White, Zachary, Wood, Travis M., Yang, Zhanchao, Ziegler, Lucas J.

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Measurements of CP asymmetries in charmless four-body Λb0 and Ξb0 decays von Badalov, Alexey, Calvo Gómez, Míriam, Camboni, Alessandro, Coquereau, Samuel, Fernandez, G, Garrido Beltrán, Lluís, Gascón Fora, David, Graciani Díaz, Ricardo, Graugés Pous, Eugeni, Marín Benito, Carla, Picatoste Olloqui, Eduardo, Rives Molina, Vicente José, Vilasis-Cardona, Xavier, Alfonso Albero, Alejandro, LHCb Collaboration

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Measurement of the Y(nS) polarizations in pp collisions at √{s}=7 and 8 TeV von LHCb Collaboration, Coquereau, Samuel, Fernandez, G, Garrido Beltrán, Lluís, Gascón Fora, David, Graciani Díaz, Ricardo, Graugés Pous, Eugeni, Marin Benito, Carla, Picatoste Olloqui, Eduardo, Rives Molina, Vicente José

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Measurement of the shape of the Λb0→Λc+μ-ν¯μ differential decay rate von Alfonso Albero, Alejandro, Camboni, Alessandro, Coquereau, Samuel, Fernandez, G, Garrido Beltrán, Lluís, Gascón Fora, David, Graciani Diaz, Ricardo, Graugés Pous, Eugeni, Marin Benito, Carla, Picatoste Olloqui, Eduardo, Rives Molina, Vicente José, Sánchez Gonzalo, David, LHCb Collaboration

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Amplitude Analysis of the Decay B 0 → KS0 π+π- and First Observation of the CP Asymmetry in B 0 →k∗ (892)-π von Alfonso Albero, Alejandro, Badalov, Alexey, Calvo Gómez, Míriam, Camboni, Alessandro, Coquereau, Samuel, Fernandez, G, Garrido Beltrán, Lluís, Gascón Fora, David, Graciani Díaz, Ricardo, Graugés Pous, Eugeni, Marin Benito, Carla, Picatoste Olloqui, Eduardo, Rives Molina, Vicente José, Vilasis-Cardona, Xavier, LHCb Collaboration

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Amplitude Analysis of the Decay B 0 → KS0 π+π- and First Observation of the CP Asymmetry in B 0 →k∗ (892)-π von Alfonso Albero, Alejandro, Badalov, Alexey, Calvo Gómez, Míriam, Camboni, Alessandro, Coquereau, Samuel, Fernandez, G, Garrido Beltrán, Lluís, Gascón Fora, David, Graciani Díaz, Ricardo, Graugés Pous, Eugeni, Marin Benito, Carla, Picatoste Olloqui, Eduardo, Rives Molina, Vicente José, Vilasis-Cardona, Xavier, LHCb Collaboration

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Amplitude Analysis of the Decay B 0 → KS0 π+π- and First Observation of the CP Asymmetry in B 0 →k∗ (892)-π von Alfonso Albero, Alejandro, Badalov, Alexey, Calvo Gómez, Míriam, Camboni, Alessandro, Coquereau, Samuel, Fernandez, G, Garrido Beltrán, Lluís, Gascón Fora, David, Graciani Díaz, Ricardo, Graugés Pous, Eugeni, Marin Benito, Carla, Picatoste Olloqui, Eduardo, Rives Molina, Vicente José, Vilasis-Cardona, Xavier, LHCb Collaboration

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