Search Results - Fox, Samantha K

Refine Results
  1. 1
  2. 2
  3. 3
  4. 4
  5. 5

    Justify your alpha by Lakens, Daniel, Adolfi, Federico G., Albers, Casper J., Anvari, Farid, Apps, Matthew A. J., Argamon, Shlomo E., Baguley, Thom, Becker, Raymond B., Benning, Stephen D., Bradford, Daniel E., Buchanan, Erin M., Caldwell, Aaron R., Van Calster, Ben, Carlsson, Rickard, Chen, Sau-Chin, Chung, Bryan, Colling, Lincoln J., Collins, Gary S., Crook, Zander, Cross, Emily S., Daniels, Sameera, Danielsson, Henrik, DeBruine, Lisa, Dunleavy, Daniel J., Earp, Brian D., Feist, Michele I., Ferrell, Jason D., Field, James G., Fox, Nicholas W., Friesen, Amanda, Gomes, Caio, Gonzalez-Marquez, Monica, Grange, James A., Grieve, Andrew P., Guggenberger, Robert, Grist, James, van Harmelen, Anne-Laura, Hasselman, Fred, Hochard, Kevin D., Hoffarth, Mark R., Holmes, Nicholas P., Ingre, Michael, Isager, Peder M., Isotalus, Hanna K., Johansson, Christer, Juszczyk, Konrad, Kenny, David A., Khalil, Ahmed A., Konat, Barbara, Lao, Junpeng, Larsen, Erik Gahner, Lodder, Gerine M. A., Lukavský, Jiří, Madan, Christopher R., Manheim, David, Martin, Stephen R., Martin, Andrea E., Mayo, Deborah G., McCarthy, Randy J., McConway, Kevin, McFarland, Colin, Nio, Amanda Q. X., Nilsonne, Gustav, de Oliveira, Cilene Lino, de Xivry, Jean-Jacques Orban, Parsons, Sam, Pfuhl, Gerit, Quinn, Kimberly A., Sakon, John J., Saribay, S. Adil, Schneider, Iris K., Selvaraju, Manojkumar, Sjoerds, Zsuzsika, Smith, Samuel G., Smits, Tim, Spies, Jeffrey R., Sreekumar, Vishnu, Steltenpohl, Crystal N., Stenhouse, Neil, Świątkowski, Wojciech, Vadillo, Miguel A., Van Assen, Marcel A. L. M., Williams, Matt N., Williams, Samantha E., Williams, Donald R., Yarkoni, Tal, Ziano, Ignazio, Zwaan, Rolf A.

    Published in Nature human behaviour
    Get full text
    Article
  6. 6
  7. 7
  8. 8
  9. 9
  10. 10

    Evaluation of the US COVID-19 Scenario Modeling Hub for informing pandemic response under uncertainty by Howerton, Emily, Contamin, Lucie, Mullany, Luke C, Qin, Michelle, Reich, Nicholas G, Bents, Samantha, Borchering, Rebecca K, Jung, Sung-Mok, Loo, Sara L, Smith, Claire P, Levander, John, Kerr, Jessica, Espino, J, van Panhuis, Willem G, Hochheiser, Harry, Galanti, Marta, Yamana, Teresa, Pei, Sen, Shaman, Jeffrey, Rainwater-Lovett, Kaitlin, Kinsey, Matt, Tallaksen, Kate, Wilson, Shelby, Shin, Lauren, Lemaitre, Joseph C, Kaminsky, Joshua, Hulse, Juan Dent, Lee, Elizabeth C, McKee, Clifton D, Hill, Alison, Karlen, Dean, Chinazzi, Matteo, Davis, Jessica T, Mu, Kunpeng, Xiong, Xinyue, Pastore Y Piontti, Ana, Vespignani, Alessandro, Rosenstrom, Erik T, Ivy, Julie S, Mayorga, Maria E, Swann, Julie L, España, Guido, Cavany, Sean, Moore, Sean, Perkins, Alex, Hladish, Thomas, Pillai, Alexander, Ben Toh, Kok, Longini, Jr, Ira, Chen, Shi, Paul, Rajib, Janies, Daniel, Thill, Jean-Claude, Bouchnita, Anass, Bi, Kaiming, Lachmann, Michael, Fox, Spencer J, Meyers, Lauren Ancel, Srivastava, Ajitesh, Porebski, Przemyslaw, Venkatramanan, Srini, Adiga, Aniruddha, Lewis, Bryan, Klahn, Brian, Outten, Joseph, Hurt, Benjamin, Chen, Jiangzhuo, Mortveit, Henning, Wilson, Amanda, Marathe, Madhav, Hoops, Stefan, Bhattacharya, Parantapa, Machi, Dustin, Cadwell, Betsy L, Healy, Jessica M, Slayton, Rachel B, Johansson, Michael A, Biggerstaff, Matthew, Truelove, Shaun, Runge, Michael C, Shea, Katriona, Viboud, Cécile, Lessler, Justin

    Published in Nature communications
    Get full text
    Article
  11. 11

    Comprehensive Rare Variant Analysis via Whole-Genome Sequencing to Determine the Molecular Pathology of Inherited Retinal Disease by Stephens, Jonathan, Dewhurst, Eleanor, Malka, Samantha, Plagnol, Vincent, Rizzo, Roberta, Scott, Richard H., Henderson, Robert H.H., MacLaren, Robert E., Paterson, Joan, Aitman, Timothy, Ali, Sonia, Ambegaonkar, Gautum, Arno, Gavin, Astle, William, Attwood, Antony, Bennett, David, Bitner-Glindzicz, Maria, Bleda, Marta, Boggard, Harm, Carss, Keren, Clements-Brod, Naomi, DaCosta, Rosa, De Vries, Minka, Dewhurst, Eleanor, Drewe, Elizabeth, Egner, William, Erber, Wendy N., Everington, Tamara, Fletcher, Debra, Freson, Kathleen, Gale, Daniel, Ghali, Neeti, Ghurye, Rohit, Gräf, Stefan, Greene, Daniel, Grigoriadou, Sofia, Grozeva, Detelina, Hackett, Scott, Hadinnapola, Charaka, Hague, Rosie, Hammerton, Tracey, Heemskerk, Johan W.M., Holder, Muriel, Holder, Susan, Huissoon, Aarnoud, Hurst, Jane, Jolles, Stephen, Keeling, David, Kennedy, Fiona, Kiely, David, Lawrie, Allan, Lear, Sara, Lees, Melissa, Lentaigne, Claire, Lorenzo, Lorena, Mangles, Sarah, Mapeta, Rutendo, Masati, Larahmie, Mathias, Mary, Michaelides, Michel, Millar, Carolyn M., Moledina, Shahin, Moore, Anthony, Murng, Sai, Oksenhendler, Eric, Park, Soo-Mi, Patch, Chris, Paterson, Joan, Penkett, Christopher J., Pepke-Zaba, Joanna, Pollock, Val, Qasim, Waseem, Quinti, Isabella, Reid, Evan, Rondina, Matthew, Rosser, Elisabeth, Santra, Saikat, Sargur, Ravishankar, Savic, Sinisa, Scully, Marie, Sewell, Carrock, Smith, Kenneth, Southgate, Laura, Stauss, Hans, Stein, Penelope, Talks, Kate, Thomas, Ellen, Thrasher, Adrian, Tischkowitz, Marc, Titterton, Catherine, Turro, Ernest, von Ziegenweldt, Julie, Vonk Noordegraaf, Anton, Wakeling, Emma, Wanjiku, Ivy, Welch, Steve, Westbury, Sarah, Woods, Geoffrey, Yong, Patrick, Webster, Andrew R.

    Get full text
    Article
  12. 12

    Clinical spectrum of individuals with pathogenic NF1 missense variants affecting p.Met1149, p.Arg1276, and p.Lys1423: genotype–phenotype study in neurofibromatosis type 1 by Koczkowska, Magdalena, Callens, Tom, Chen, Yunjia, Gomes, Alicia, Hicks, Alesha D., Sharp, Angela, Johns, Eric, Uhas, Kim Armfield, Armstrong, Linlea, Bosanko, Katherine Armstrong, Babovic‐Vuksanovic, Dusica, Baker, Laura, Basel, Donald G., Bennett, James T., Chambers, Chelsea, Clarkson, Lola K., Clementi, Maurizio, Cortés, Fanny M., Cunningham, Mitch, D'Agostino, M. Daniela, Delatycki, Martin B., Digilio, Maria C., Dosa, Laura, Esposito, Silvia, Fox, Stephanie, Freckmann, Mary‐Louise, Fauth, Christine, Giugliano, Teresa, Giustini, Sandra, Goetsch, Allison, Greenwood, Robert S., Griffis, Cristin, Gripp, Karen W., Gupta, Punita, Haan, Eric, Hachen, Rachel K., Haygarth, Tamara L., Hernández‐Chico, Concepción, Hodge, Katelyn, Hopkin, Robert J., Hudgins, Louanne, Janssens, Sandra, Keller, Kory, Kelly‐Mancuso, Geraldine, Kochhar, Aaina, Korf, Bruce R., Lewis, Andrea M., Liebelt, Jan, Lichty, Angie, Listernick, Robert H., Lyons, Michael J., Maystadt, Isabelle, Martinez Ojeda, Mayra, McDougall, Carey, McGregor, Lesley K., Melis, Daniela, Mendelsohn, Nancy, Nowaczyk, Malgorzata J.M., Ortenberg, June, Panzer, Karin, Pierpont, Mary Ella, Piluso, Giulio, Pinna, Valentina, Pivnick, Eniko K., Pond, Dinel A., Powell, Cynthia M., Rogers, Caleb, Ruhrman Shahar, Noa, Rutledge, S. Lane, Saletti, Veronica, Sandaradura, Sarah A., Schatz, Ulrich A., Scott, Daryl A., Sellars, Elizabeth A., Sheffer, Ruth, Siqveland, Elizabeth, Slopis, John M., Smith, Rosemarie, Spalice, Alberto, Stockton, David W., Streff, Haley, Theos, Amy, Tomlinson, Gail E., Tran, Grace, Trapane, Pamela L., Trevisson, Eva, Ullrich, Nicole J., Van den Ende, Jenneke, Schrier Vergano, Samantha A., Wallace, Stephanie E., Wangler, Michael F., Yohay, Kaleb H., Zackai, Elaine, Zonana, Jonathan, Claes, Kathleen B. M., Eoli, Marica, Wimmer, Katharina, De Luca, Alessandro, Legius, Eric, Messiaen, Ludwine M.

    Published in Human mutation
    Get full text
    Article
  13. 13
  14. 14
  15. 15
  16. 16
  17. 17
  18. 18
  19. 19
  20. 20