Vive la radiorésistance!: converging research in radiobiology and biogerontology to enhance human radioresistance for deep space exploration and colonization

por Cortese, Franco, Klokov, Dmitry, Osipov, Andreyan, Stefaniak, Jakub, Moskalev, Alexey, Schastnaya, Jane, Cantor, Charles, Aliper, Alexander, Mamoshina, Polina, Ushakov, Igor, Sapetsky, Alex, Vanhaelen, Quentin, Alchinova, Irina, Karganov, Mikhail, Kovalchuk, Olga, Wilkins, Ruth, Shtemberg, Andrey, Moreels, Marjan, Baatout, Sarah, Izumchenko, Evgeny, de Magalhães, João Pedro, Artemov, Artem V., Costes, Sylvain V., Beheshti, Afshin, Mao, Xiao Wen, Pecaut, Michael J., Kaminskiy, Dmitry, Ozerov, Ivan V., Scheibye-Knudsen, Morten, Zhavoronkov, Alex
Publicado 2018

How safe are paediatric emergency departments? A national prospective cohort study

por Plint, Amy C, Newton, Amanda S, Stang, Antonia, Cantor, Zach, Hayawi, Lamia, Barrowman, Nick, Boutis, Kathy, Gouin, Serge, Doan, Quynh, Dixon, Andrew, Porter, Robert, Joubert, Gary, Sawyer, Scott, Crawford, Tyrus, Gravel, Jocelyn, Bhatt, Maala, Weldon, Patrick, Millar, Kelly, Tse, Sandy, Neto, Gina, Grewal, Simran, Chan, Melissa, Chan, Kevin, Yung, Grant, Kilgar, Jennifer, Lynch, Tim, Aglipay, Mary, Dalgleish, Dale, Farion, Ken, Klassen, Terry P, Johnson, David W, Calder, Lisa A
Publicado 2022

Serial H3K27M cell-free tumor DNA (cf-tDNA) tracking predicts ONC201 treatment response and progression in diffuse midline glioma

por Cantor, Evan, Wierzbicki, Kyle, Tarapore, Rohinton S, Ravi, Karthik, Thomas, Chase, Cartaxo, Rodrigo, Nand Yadav, Viveka, Ravindran, Ramya, Bruzek, Amy K, Wadden, Jack, John, Vishal, May Babila, Clarissa, Cummings, Jessica R, Rahman Kawakibi, Abed, Ji, Sunjong, Ramos, Johanna, Paul, Alyssa, Walling, Dustin, Leonard, Marcia, Robertson, Patricia, Franson, Andrea, Mody, Rajen, Garton, Hugh J L, Venneti, Sriram, Odia, Yazmin, Kline, Cassie, Vitanza, Nicholas A, Khatua, Soumen, Mueller, Sabine, Allen, Joshua E, Gardner, Sharon L, Koschmann, Carl
Publicado 2022

Amerindian-specific regions under positive selection harbour new lipid variants in Latinos

por Ko, Arthur, Cantor, Rita M., Weissglas-Volkov, Daphna, Nikkola, Elina, Reddy, Prasad M. V. Linga, Sinsheimer, Janet S., Pasaniuc, Bogdan, Brown, Robert, Alvarez, Marcus, Rodriguez, Alejandra, Rodriguez-Guillen, Rosario, Bautista, Ivette C., Arellano-Campos, Olimpia, Muñoz-Hernández, Linda L., Salomaa, Veikko, Kaprio, Jaakko, Jula, Antti, Jauhiainen, Matti, Heliövaara, Markku, Raitakari, Olli, Lehtimäki, Terho, Eriksson, Johan G., Perola, Markus, Lohmueller, Kirk E., Matikainen, Niina, Taskinen, Marja-Riitta, Rodriguez-Torres, Maribel, Riba, Laura, Tusie-Luna, Teresa, Aguilar-Salinas, Carlos A., Pajukanta, Päivi
Publicado 2014

Factors Associated With Hospitalization or Intensive Care Admission in Children With COVID-19 in Latin America

por López-Medina, Eduardo, Camacho-Moreno, German, Brizuela, Martin E., Dávalos, Diana M., Torres, Juan Pablo, Ulloa-Gutierrez, Rolando, López, Pio, Debbag, Roberto, Pérez, Paola, Patiño, Jaime, Norero, Ximena, Mariño, Cristina, Luengas, Miguel A., Ensinck, Gabriela, Daza, Carlos, Luciani, Kathia, Quintana Kuhner, Paola, Rodriguez, Mónica, Rodríguez-Auad, Juan Pablo, Estrada-Villarroel, Alejandra, Carnevale, Mayli, Mantese, Orlando Cesar, Berezin, Eitan N., Castillo, José Iván, Mascareñas, Abiel, Jimenez-Zambrano, Andrea, Dueñas, Lourdes, Melgar, Mario, Galvez, Nancy, Cantor, Erika, Asturias, Edwin J.
Publicado 2022

Rare coding variants in CHRNB2 reduce the likelihood of smoking

por Rajagopal, Veera M., Watanabe, Kyoko, Mbatchou, Joelle, Ayer, Ariane, Quon, Peter, Sharma, Deepika, Kessler, Michael D., Praveen, Kavita, Gelfman, Sahar, Parikshak, Neelroop, Otto, Jacqueline M., Bao, Suying, Chim, Shek Man, Pavlopoulos, Elias, Avbersek, Andreja, Kapoor, Manav, Chen, Esteban, Jones, Marcus B., Leblanc, Michelle, Emberson, Jonathan, Collins, Rory, Torres, Jason, Morales, Pablo Kuri, Tapia-Conyer, Roberto, Alegre, Jesus, Berumen, Jaime, Shuldiner, Alan R., Balasubramanian, Suganthi, Abecasis, Gonçalo R., Kang, Hyun M., Marchini, Jonathan, Stahl, Eli A., Jorgenson, Eric, Sanchez, Robert, Liedtke, Wolfgang, Anderson, Matthew, Cantor, Michael, Lederer, David, Baras, Aris, Coppola, Giovanni
Publicado 2023

Genome-Wide Analyses of Exonic Copy Number Variants in a Family-Based Study Point to Novel Autism Susceptibility Genes

por Bucan, Maja, Abrahams, Brett S., Wang, Kai, Glessner, Joseph T., Herman, Edward I., Sonnenblick, Lisa I., Alvarez Retuerto, Ana I., Imielinski, Marcin, Hadley, Dexter, Bradfield, Jonathan P., Kim, Cecilia, Gidaya, Nicole B., Lindquist, Ingrid, Hutman, Ted, Sigman, Marian, Kustanovich, Vlad, Lajonchere, Clara M., Singleton, Andrew, Kim, Junhyong, Wassink, Thomas H., McMahon, William M., Owley, Thomas, Sweeney, John A., Coon, Hilary, Nurnberger, John I., Li, Mingyao, Cantor, Rita M., Minshew, Nancy J., Sutcliffe, James S., Cook, Edwin H., Dawson, Geraldine, Buxbaum, Joseph D., Grant, Struan F. A., Schellenberg, Gerard D., Geschwind, Daniel H., Hakonarson, Hakon
Publicado 2009

Genetic variation and gene expression across multiple tissues and developmental stages in a non-human primate

por Jasinska, Anna J., Zelaya, Ivette, Service, Susan K., Peterson, Christine B., Cantor, Rita M., Choi, Oi-Wa, DeYoung, Joseph, Eskin, Eleazar, Fairbanks, Lynn A., Fears, Scott, Furterer, Allison E., Huang, Yu S., Ramensky, Vasily, Schmitt, Christopher A., Svardal, Hannes, Jorgensen, Matthew J., Kaplan, Jay R., Villar, Diego, Aken, Bronwen L., Flicek, Paul, Nag, Rishi, Wong, Emily S., Blangero, John, Dyer, Thomas D., Bogomolov, Marina, Benjamini, Yoav, Weinstock, George M., Dewar, Ken, Sabatti, Chiara, Wilson, Richard K., Jentsch, J. David, Warren, Wesley, Coppola, Giovanni, Woods, Roger P., Freimer, Nelson B.
Publicado 2017

Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis

por Gallagher, C. S., Mäkinen, N., Harris, H. R., Rahmioglu, N., Uimari, O., Cook, J. P., Shigesi, N., Ferreira, T., Velez-Edwards, D. R., Edwards, T. L., Mortlock, S., Ruhioglu, Z., Day, F., Becker, C. M., Karhunen, V., Martikainen, H., Järvelin, M.-R., Cantor, R. M., Ridker, P. M., Terry, K. L., Buring, J. E., Gordon, S. D., Medland, S. E., Montgomery, G. W., Nyholt, D. R., Hinds, D. A., Tung, J. Y., Perry, J. R. B., Lind, P. A., Painter, J. N., Martin, N. G., Morris, A. P., Chasman, D. I., Missmer, S. A., Zondervan, K. T., Morton, C. C.
Publicado 2019

HGG-18. CLINICAL EFFICACY OF ONC201 IN THALAMIC H3 K27M-MUTANT GLIOMA

por Kawakibi, Abed Rahman, Tarapore, Rohinton S, Gardner, Sharon, Chi, Andrew, Kurz, Sylvia, Wen, Patrick Y, Arrillaga-Romany, Isabel, Batchelor, Tracy T, Butowski, Nicholas A, Sumrall, Ashley, Shonka, Nicole, Harrison, Rebecca, DeGroot, John, Mehta, Minesh, Odia, Yazmin, Hall, Matthew D, Daghistani, Doured, Cloughesy, Timothy F, Ellingson, Benjamin M, Umemura, Yoshie, Schwartz, Jonathan, Yadav, Vivekanand, Cartaxo, Rodrigo, Siada, Ruby, Miklja, Zachary, Bruzek, Amy, Cantor, Evan, Wierzbicki, Kyle, Paul, Alyssa, Wolfe, Ian, Leaoard, Marcia, Garton, Hugh, Mody, Rajen, Robertson, Patricia L, Lu, Guangrong, Merdinger, Krystal, Venneti, Sriram, Oster, Wolfgang, Allen, Joshua E, Koschmann, Carl
Publicado 2020

LINC-08. Neuro-Oncology tumor board – one-year experience of international collaboration

por Shatara, Margaret, Cantor, Evan, Meyer, Ashley, Ogle, Andrea, Hofmann, Kimberly, Green, Tammy, Beck, Mary, McHugh, Michele, Brossier, Nicole, Cluster, Andrew, Mian, Ali, Dahiya, Sonika, Abdelaziz, Zeyad M, Fadel, Shady, Mobark, Nahla, AlHarbi, Musa, AlJaouni, Soad, Aljunaid, Abrar, Said, Waleed, El-ayadi, Moatasem, Mahmoud, Madeha, Al-Battashi, Abeer, Chabchoub, Imène, Khalifa, Nisreen, Dengler, Nora, Driever, Pablo Hernáiz, Del Río, Nicolás Rojas, Dembowska-Bagińska, Bozenna, Perek-Polnik, Marta, Skoczeń, Szymon, Dholaria, Hetal, Nagabushan, Sumanth, Oliveira, Milena, Hirbe, Angela C, Armstrong, Amy E, Limbrick, David, Gutmann, David H, Abdelbaki, Mohamed S
Publicado 2022

Author Correction: Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis

por Gallagher, C. S., Mäkinen, N., Harris, H. R., Rahmioglu, N., Uimari, O., Cook, J. P., Shigesi, N., Ferreira, T., Velez-Edwards, D. R., Edwards, T. L., Mortlock, S., Ruhioglu, Z., Day, F., Becker, C. M., Karhunen, V., Martikainen, H., Järvelin, M.-R., Cantor, R. M., Ridker, P. M., Terry, K. L., Buring, J. E., Gordon, S. D., Medland, S. E., Montgomery, G. W., Nyholt, D. R., Hinds, D. A., Tung, J. Y., Perry, J. R. B., Lind, P. A., Painter, J. N., Martin, N. G., Morris, A. P., Chasman, D. I., Missmer, S. A., Zondervan, K. T., Morton, C. C.
Publicado 2022

A deep catalog of protein-coding variation in 985,830 individuals

por Sun, Kathie Y., Bai, Xiaodong, Chen, Siying, Bao, Suying, Kapoor, Manav, Zhang, Chuanyi, Backman, Joshua, Joseph, Tyler, Maxwell, Evan, Mitra, George, Gorovits, Alexander, Mansfield, Adam, Boutkov, Boris, Gokhale, Sujit, Habegger, Lukas, Marcketta, Anthony, Locke, Adam, Kessler, Michael D., Sharma, Deepika, Staples, Jeffrey, Bovijn, Jonas, Gelfman, Sahar, Gioia, Alessandro Di, Rajagopal, Veera, Lopez, Alexander, Varela, Jennifer Rico, Alegre, Jesus, Berumen, Jaime, Tapia-Conyer, Roberto, Kuri-Morales, Pablo, Torres, Jason, Emberson, Jonathan, Collins, Rory, Cantor, Michael, Thornton, Timothy, Kang, Hyun Min, Overton, John, Shuldiner, Alan R., Cremona, M. Laura, Nafde, Mona, Baras, Aris, Abecasis, Goncalo, Marchini, Jonathan, Reid, Jeffrey G., Salerno, William, Balasubramanian, Suganthi
Publicado 2023

Pharmacologic and Genetic Downregulation of Proprotein Convertase Subtilisin/Kexin Type 9 and Survival From Sepsis

por Lawler, Patrick R., Manvelian, Garen, Coppi, Alida, Damask, Amy, Cantor, Michael N., Ferreira, Manuel A. R., Paulding, Charles, Banerjee, Nilanjana, Li, Dadong, Jorgensen, Susan, Attre, Richa, Carey, David J., Krebs, Kristi, Milani, Lili, Hveem, Kristian, Damås, Jan K., Solligård, Erik, Stender, Stefan, Tybjærg-Hansen, Anne, Nordestgaard, Børge G., Hernandez-Beeftink, Tamara, Rogne, Tormod, Flores, Carlos, Villar, Jesús, Walley, Keith R., Liu, Vincent X., Fohner, Alison E., Lotta, Luca A., Kyratsous, Christos A., Sleeman, Mark W., Scemama, Michel, DelGizzi, Richard, Pordy, Robert, Horowitz, Julie E., Baras, Aris, Martin, Greg S., Steg, Philippe Gabriel, Schwartz, Gregory G., Szarek, Michael, Goodman, Shaun G.
Publicado 2023

Contribution of common and rare variants to bipolar disorder susceptibility in extended pedigrees from population isolates

por Sul, Jae Hoon, Service, Susan K., Huang, Alden Y., Ramensky, Vasily, Hwang, Sun-Goo, Teshiba, Terri M., Park, YoungJun, Ori, Anil P. S., Zhang, Zhongyang, Mullins, Niamh, Olde Loohuis, Loes M., Fears, Scott C., Araya, Carmen, Araya, Xinia, Spesny, Mitzi, Bejarano, Julio, Ramirez, Margarita, Castrillón, Gabriel, Gomez-Makhinson, Juliana, Lopez, Maria C., Montoya, Gabriel, Montoya, Claudia P., Aldana, Ileana, Escobar, Javier I., Ospina-Duque, Jorge, Kremeyer, Barbara, Bedoya, Gabriel, Ruiz-Linares, Andres, Cantor, Rita M., Molina, Julio, Coppola, Giovanni, Ophoff, Roel A., Macaya, Gabriel, Lopez-Jaramillo, Carlos, Reus, Victor, Bearden, Carrie E., Sabatti, Chiara, Freimer, Nelson B.
Publicado 2020

The RUNX1 database (RUNX1db): establishment of an expert curated RUNX1 registry and genomics database as a public resource for familial platelet disorder with myeloid malignancy

por Homan, Claire C., King-Smith, Sarah L., Lawrence, David M., Arts, Peer, Feng, Jinghua, Andrews, James, Armstrong, Mark, Ha, Thuong, Dobbins, Julia, Drazer, Michael W., Yu, Kai, Bödör, Csaba, Cantor, Alan, Cazzola, Mario, Degelman, Erin, DiNardo, Courtney D., Duployez, Nicolas, Favier, Remi, Fröhling, Stefan, Fitzgibbon, Jude, Klco, Jeffery M., Krämer, Alwin, Kurokawa, Mineo, Lee, Joanne, Malcovati, Luca, Morgan, Neil V., Natsoulis, Georges, Owen, Carolyn, Patel, Keyur P., Preudhomme, Claude, Raslova, Hana, Rienhoff, Hugh, Ripperger, Tim, Schulte, Rachael, Tawana, Kiran, Velloso, Elvira, Yan, Benedict, Liu, Paul, Godley, Lucy A., Schreiber, Andreas W., Hahn, Christopher N., Scott, Hamish S., Brown, Anna L.
Publicado 2021

Exome sequencing and analysis of 454,787 UK Biobank participants

por Backman, Joshua D., Li, Alexander H., Marcketta, Anthony, Sun, Dylan, Mbatchou, Joelle, Kessler, Michael D., Benner, Christian, Liu, Daren, Locke, Adam E., Balasubramanian, Suganthi, Yadav, Ashish, Banerjee, Nilanjana, Gillies, Christopher E., Damask, Amy, Liu, Simon, Bai, Xiaodong, Hawes, Alicia, Maxwell, Evan, Gurski, Lauren, Watanabe, Kyoko, Kosmicki, Jack A., Rajagopal, Veera, Mighty, Jason, Jones, Marcus, Mitnaul, Lyndon, Stahl, Eli, Coppola, Giovanni, Jorgenson, Eric, Habegger, Lukas, Salerno, William J., Shuldiner, Alan R., Lotta, Luca A., Overton, John D., Cantor, Michael N., Reid, Jeffrey G., Yancopoulos, George, Kang, Hyun M., Marchini, Jonathan, Baras, Aris, Abecasis, Gonçalo R., Ferreira, Manuel A. R.
Publicado 2021

MicroRNA-3148 Modulates Allelic Expression of Toll-Like Receptor 7 Variant Associated with Systemic Lupus Erythematosus

por Deng, Yun, Zhao, Jian, Sakurai, Daisuke, Kaufman, Kenneth M., Edberg, Jeffrey C., Kimberly, Robert P., Kamen, Diane L., Gilkeson, Gary S., Jacob, Chaim O., Scofield, R. Hal, Langefeld, Carl D., Kelly, Jennifer A., Ramsey-Goldman, Rosalind, Petri, Michelle A., Reveille, John D., Vilá, Luis M., Alarcón, Graciela S., Vyse, Timothy J., Pons-Estel, Bernardo A., Freedman, Barry I., Gaffney, Patrick M., Sivils, Kathy Moser, James, Judith A., Gregersen, Peter K., Anaya, Juan-Manuel, Niewold, Timothy B., Merrill, Joan T., Criswell, Lindsey A., Stevens, Anne M., Boackle, Susan A., Cantor, Rita M., Chen, Weiling, Grossman, Jeniffer M., Hahn, Bevra H., Harley, John B., Alarcόn-Riquelme, Marta E., Brown, Elizabeth E., Tsao, Betty P.
Publicado 2013

Common and rare variant associations with clonal haematopoiesis phenotypes

por Kessler, Michael D., Damask, Amy, O’Keeffe, Sean, Banerjee, Nilanjana, Li, Dadong, Watanabe, Kyoko, Marketta, Anthony, Van Meter, Michael, Semrau, Stefan, Horowitz, Julie, Tang, Jing, Kosmicki, Jack A., Rajagopal, Veera M., Zou, Yuxin, Houvras, Yariv, Ghosh, Arkopravo, Gillies, Christopher, Mbatchou, Joelle, White, Ryan R., Verweij, Niek, Bovijn, Jonas, Parikshak, Neelroop N., LeBlanc, Michelle G., Jones, Marcus, Glass, David J., Lotta, Luca A., Cantor, Michael N., Atwal, Gurinder S., Locke, Adam E., Ferreira, Manuel A. R., Deering, Raquel, Paulding, Charles, Shuldiner, Alan R., Thurston, Gavin, Ferrando, Adolfo A., Salerno, Will, Reid, Jeffrey G., Overton, John D., Marchini, Jonathan, Kang, Hyun M., Baras, Aris, Abecasis, Gonçalo R., Jorgenson, Eric
Publicado 2022

Revisitar los géneros teatrales

por Vincent, Nidia
Publicado 2018