Treffer 1 - 20 von 70 für Suche 'Tucker, Grace K.', Suchdauer: 1,70s Treffer weiter einschränken
  1. 1
  2. 2
  3. 3
  4. 4
  5. 5
  6. 6
  7. 7
  8. 8

    The Atacama Cosmology Telescope: Two-Season ACTPol Spectra and Parameters von Louis, Thibaut, Grace, Emily, Hasselfield, Matthew, Lungu, Marius, Maurin, Loic, Addison, Graeme E., R., Adem Peter A., Aiola, Simone, Allison, Rupert, Amiri, Mandana, Angile, Elio, Battaglia, Nicholas, Beall, James A., De Bernardis, Francesco, Bond, J. Richard, Britton, Joe, Calabrese, Erminia, Cho, Hsiao-mei, Choi, Steve K., Coughlin, Kevin, Crichton, Devin, Crowley, Kevin, Datta, Rahul, Devlin, Mark J., Dicker, Simon R., Dunkley, Joanna, Dunner, Rolando, Ferraro, Simone, Fox, Anna E., Gallardo, Patricio, Gralla, Megan, Halpern, Mark, Henderson, Shawn, Hill, J. Colin, Hilton, Gene C., Hilton, Matt, Hincks, Adam D., Hlozek, Renee, Ho, S. P. Patty, Huang, Zhiqi, Hubmayr, Johannes, Huffenberger, Kevin M., Hughes, John P., Infante, Leopoldo, Irwin, Kent, Kasanda, Simon Muya, Klein, Jeff, Koopman, Brian, Kosowsky, Arthur, Li, Dale, Madhavacheril, Mathew, Marriage, Tobias A., McMahon, Jeff, Menanteau, Felipe, Moodley, Kavilan, Munson, Charles, Naess, Sigurd, Nati, Federico, Newburgh, Laura, Nibarger, John, Niemack, Michael D., Nolta, Michael R., Nunez, Carolina, Pappas, Christine, Partridge, Bruce, Rojas, Felipe, Schaan, Emmanuel, Schmitt, Benjamin L., Sehgal, Neelima, Sherwin, Blake D., Sievers, Jon, Simon, Sara, Spergel, David N., Staggs, Suzanne T., Switzer, Eric R., Thornton, Robert, Trac, Hy, Treu, Jesse, Tucker, Carole, Van Engelen, Alexander, Ward, Jonathan T., Wollack, Edward J.


    Volltext
    Artikel
  9. 9
  10. 10
  11. 11
  12. 12

    The Gravity Collective: A Search for the Electromagnetic Counterpart to the Neutron Star–Black Hole Merger GW190814 von Kilpatrick, Charles D., Coulter, David A., Arcavi, Iair, Brink, Thomas G., Dimitriadis, Georgios, Filippenko, Alexei V., Foley, Ryan J., Howell, D. Andrew, Jones, David O., Kasen, Daniel, Makler, Martin, Piro, Anthony L., Rojas-Bravo, César, Sand, David J., Swift, Jonathan J., Tucker, Douglas, Zheng, WeiKang, Allam, Sahar S., Annis, James T., Antilen, Juanita, Bachmann, Tristan G., Bloom, Joshua S., Bom, Clecio R., Bostroem, K. Azalee, Brout, Dillon, Burke, Jamison, Butler, Robert E., Butner, Melissa, Campillay, Abdo, Clever, Karoli E., Conselice, Christopher J., Cooke, Jeff, Dage, Kristen C., de Carvalho, Reinaldo R., de Jaeger, Thomas, Desai, Shantanu, Garcia, Alyssa, Garcia-Bellido, Juan, Gill, Mandeep S. S., Girish, Nachiket, Hallakoun, Na’ama, Herner, Kenneth, Hiramatsu, Daichi, Holz, Daniel E., Huber, Grace, Kawash, Adam M., McCully, Curtis, Medallon, Sophia A., Metzger, Brian D., Modak, Shaunak, Morgan, Robert, Muñoz, Ricardo R., Muñoz-Elgueta, Nahir, Murakami, Yukei S., E., Felipe Olivares, Palmese, Antonella, Patra, Kishore C., Pereira, Maria E. S., Pessi, Thallis L., Pineda-Garcia, J., Quirola-Vásquez, Jonathan, Ramirez-Ruiz, Enrico, Rembold, Sandro Barboza, Rest, Armin, Rodríguez, Ósmar, Santana-Silva, Luidhy, Sherman, Nora F., Siebert, Matthew R., Smith, Carli, Smith, J. Allyn, Soares-Santos, Marcelle, Stacey, Holland, Stahl, Benjamin E., Strader, Jay, Strasburger, Erika, Sunseri, James, Tinyanont, Samaporn, Tucker, Brad E., Ulloa, Natalie, Valenti, Stefano, Vasylyev, Sergiy S., Wiesner, Matthew P., Zhang, Keto D.

    Veröffentlicht in The Astrophysical journal

    Volltext
    Artikel
  13. 13
  14. 14
  15. 15

    Phenotypic expansion of CACNA1C-associated disorders to include isolated neurological manifestations von Kurata, Harley T., Jamra, Rami Abou, Alkelai, Anna, Antonarakis, Stylianos E., Bolkier, Yoav, Dickson, Patricia, Donald, Kirsten A., Eliyahu, Aviva, Emrick, Lisa, Odent, Sylvie, Ortiz-Gonzalez, Xilma, Rosenfeld, Jill A., Skraban, Cara, Alejandro, Mercedes E., Azamian, Mahshid S., Chao, Hsiao-Tuan, Dai, Hongzheng, Dhar, Shweta U., Karaviti, Lefkothea, Lee, Brendan H., Rosenfeld, Jill A., Scott, Daryl A., Wangler, Michael F., Eng, Christine M., Sullivan, Kathleen, Goldstein, David B., McConkie-Rosell, Allyn, Schoch, Kelly, Shashi, Vandana, Beggs, Alan H., Cobban, Laurel A., Cooper, Cynthia M., Fieg, Elizabeth L., Korrick, Susan, Loscalzo, Joseph, Maas, Richard L., MacRae, Calum A., Stoler, Joan M., Nagy, Anna, Dasari, Surendra, Lanpher, Brendan C., Bivona, Stephanie, Isasi, Rosario, Levitt, Roy, Tekin, Mustafa, Thorson, Willa, Eckstein, David J., Mamounas, Laura A., D’Souza, Precilla, Ferreira, Carlos, Godfrey, Rena A., Groden, Catherine A., Macnamara, Ellen F., Maduro, Valerie V., Nath, Avi, Baker, Eva, Power, Bradley, Mosbrook-Davis, Deborah, Rossignol, Francis, Yousef, Muhammad, Amendola, Laura, Bamshad, Michael, Beck, Anita, Bennett, Jimmy, Blue, Elizabeth, Chanprasert, Sirisak, Glass, Ian, Jarvik, Gail P., Jarvik, Jeffrey, Mefford, Heather, Merritt, J. Lawrence, Raskind, Wendy, Sybert, Virginia, Wener, Mark, Wenger, Tara, Fisher, Paul G., Reuter, Chloe M., Smith, Kevin S., Zastrow, Diane B., Nakano-Okuno, Mariko, Whitlock, Jordan, Butte, Manish J., Fogel, Brent L., Krakow, Deborah, Lee, Hane, Palmer, Christina G.S., Papp, Jeanette C., Woods, Jeremy D., Andrews, Ashley, Pace, Laura, Viskochil, Dave, Bican, Anna, Kennedy, Jennifer, Cogan, Joy D., Cole, F. Sessions, Kiley, Dana, Sisco, Kathy, Schedl, Timothy, Solnica-Krezel, Lilianna, Pitt, Geoffrey S.

    Veröffentlicht in Genetics in medicine

    Volltext
    Artikel
  16. 16

    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.

    Veröffentlicht in Genetics in medicine

    Volltext
    Artikel
  17. 17
  18. 18

    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

    Veröffentlicht in Genetics in medicine

    Volltext
    Artikel
  19. 19

    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

    Veröffentlicht in Genetics in medicine

    Volltext
    Artikel
  20. 20