System and method for fantasy sports gambling von DELEVIE ALAN DAVID, GOLDMAN JUSTIN EDWARD, KEATING SIMON, SHEDD ROBERT DANIEL, BEATTY JONATHAN, MANNING DAIRE, O'MAHONY CATHERINE

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System and Method for Fantasy Sports Gambling von SHEDD, JR. ROBERT DANIEL, DELEVIE ALAN DAVID, GOLDMAN JUSTIN EDWARD

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System and Method for Fantasy Sports Gambling von DELEVIE ALAN DAVID, GOLDMAN JUSTIN EDWARD, KEATING SIMON, SHEDD ROBERT DANIEL, BEATTY JONATHAN, MANNING DAIRE, O'MAHONY CATHERINE

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Cell diversity and network dynamics in photosensitive human brain organoids von Quadrato, Giorgia, Nguyen, Tuan, Macosko, Evan Z., Sherwood, John L., Min Yang, Sung, Berger, Daniel R., Maria, Natalie, Scholvin, Jorg, Goldman, Melissa, Kinney, Justin P., Boyden, Edward S., Lichtman, Jeff W., Williams, Ziv M., McCarroll, Steven A., Arlotta, Paola

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Ultrasound renal denervation for hypertension resistant to a triple medication pill (RADIANCE-HTN TRIO): a randomised, multicentre, single-blind, sham-controlled trial von Azizi, Michel, Sanghvi, Kintur, Gosse, Philippe, Levy, Terry, Rump, Lars C, Daemen, Joost, Lobo, Melvin D, Sharp, Andrew S P, Weber, Michael A, Sapoval, Marc, Fong, Pete, Pathak, Atul, Lantelme, Pierre, Kably, Benjamin, Barman, Neil C, Coleman, Leslie, Williams, Shannon, Jarvis, Maria, Gainer, James, Ducey, Maryanne, DelMastro, Elizabeth, Bangalore, Sripal, Williams, Stephen, Cabos, Stanley, Rodriguez Alvarez, Carolina, Todoran, Thomas, Paladugu, Vijay, Fiebach, Amanda, Merlin, Claudia, Kim, Hyun-Min, Rashid, Mohammad, Abraham, Josephine, Owan, Theophilus, Maddox, William, Oparil, Suzanne, Radhakrishnan, Jai, Zusman, Randy, Rosenfield, Kenneth, Barb, Ilie, Jay, Desmond, Schwartz, Robert, Goldman, Jessie, Katof, Nancy, Potluri, Srinivasa, Biedermann, Scott, Sobieszczky, Piotr, Aseltine, Laura, Hinderliter, Alan, Wade, Tyrone, Effron, Barry, Costa, Marco, Semenec, Terence, Nelson, Priscilla, Giri, Jay, Vo, Thu, Chugh, Atul R, Huang, Pei-Hsiu, Flack, John, Fishman, Robert, Bajzer, Christopher, Saxena, Manish, D'Souza, Richard J, Robinson, Nicholas, Ocampo, Madelaine, Davies, Justin, Burak, Paula, Jadhav, Sachin, Rump, Lars Christian, Potthoff, Sebastian, Köllner, Tanja, Mahfoud, Felix, Kulenthiran, Saarraaken, Lurz, Philipp, Fengler, Karl, Rommel, Karl-Philipp, Trautmann, Kai, Schmieder, Roland E, Heinritz, Ulrike, Grawe, Armin, Kaesberger, Bärbel, Welzel, Markus, Trabitzsch, Barbara, Trillaud, Hervé, Maire, Florent, Gaudissard, Julie, Sapoval, Marc, Pathak, Atul, Honton, Benjamin, Lantelme, Pierre, Berge, Constance, Langevin, Fatou, Longere, Benjamin, van Zwam, W H, Vranken, Jeannique, de Haan, Claudia, Persu, Alexandre, Renkin, Jean, Huyberechts, Dominique, Januszewicz, Andrzej, Owczuk, Radoslaw

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EFEMP1 haploinsufficiency causes a Marfan‐like hereditary connective tissue disorder von Forghani, Irman, Adam, Margaret, Azamian, Mahshid S., Baker, Eva, Baldridge, Dustin, Bale, Jim, Beck, Anita, Berg‐Rood, Beverly, Berry, Gerard T., Bican, Anna, Boyd, Brenna, Briere, Lauren C., Burke, Elizabeth A., Burrage, Lindsay C., Byers, Peter, Carey, John, Chang, Ta Chen Peter, Cogan, Joy D., Colley, Heather A., D'Souza, Precilla, Dasari, Surendra, Dell'Angelica, Esteban C., Duncan, Laura, Eckstein, David J., Emrick, Lisa T., Eng, Christine M., Esteves, Cecilia, Fernandez, Liliana, Fieg, Elizabeth L., Forghani, Irman, Gochuico, Bernadette, Grajewski, Alana, Hahn, Sihoun, Hamid, Rizwan, High, Frances, Hing, Anne, Hisama, Fuki M., Holm, Ingrid A., Huang, Yong, Jamal, Fariha, Jayadev, Suman, Kohler, Jennefer N., Krakow, Deborah, Kravets, Elijah, Koziura, Mary, Lam, Byron, Lam, Christina, Lanza, Ian R., LeBlanc, Kimberly, Lee, Brendan H., Lee, Hane, Levitt, Roy, Liu, Pengfei, Maas, Richard L., Macnamara, Ellen F., Maduro, Valerie V., Majcherska, Marta M., Manolio, Teri A., Marth, Gabor, Martínez‐Agosto, Julian A., Marwaha, Shruti, McCauley, Jacob, McConkie‐Rosell, Allyn, McGee, Elisabeth, Might, Matthew, Mirzaa, Ghayda, Moretti, Paolo M., Mosbrook‐Davis, Deborah, Murdock, David R., Nieves‐Rodriguez, Shirley, Parker, Neil H., Phillips, John A., Power, Bradley, Pusey, Barbara N., Quinlan, Aaron, Raskind, Wendy, Sacco, Ralph, Sampson, Jacinda B., Saporta, Mario, Shin, Jimann, Silverman, Edwin K., Sinsheimer, Janet S., Solem, Emily, Stoler, Joan M., Sun, Angela, Tabor, Holly K., Tan, Amelia L. M., Telischi, Fred, Tifft, Cynthia J., Toro, Camilo, Tucker, Brianna M., Vogel, Tiphanie P., Wambach, Jennifer, Wang, Lee‐kai, Wegner, Daniel, Wenger, Tara, Westerfield, Monte, Wolfe, Lynne A., Zein, Wadih, Zuchner, Stephan

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H4C5 missense variant leads to a neurodevelopmental phenotype overlapping with Angelman syndrome von Bivona, Stephanie, Peart, LéShon, Guo, Shengru, Adam, Margaret, Agrawal, Pankaj B., Alvey, Justin, Balasubramanyam, Ashok, Bayrak‐Toydemir, Pinar, Beck, Anita, Bohnsack, John, Bonner, Devon, Botto, Lorenzo, Butte, Manish J., Chanprasert, Sirisak, Clark, Gary D., Coggins, Matthew, Cope, Heidi, Craigen, William J., Dorrani, Naghmeh, Doss, Argenia L., Douine, Emilie D., Earl, Dawn, Eckstein, David J., Emrick, Lisa T., Ferreira, Carlos, Fisher, Paul G., Gahl, William A., Goldman, Alica M., Goldstein, David B., Grajewski, Alana, Groden, Catherine A., Hamid, Rizwan, Hanchard, Neil A., Hassey, Kelly, Hayes, Nichole, Horike‐Pyne, Martha, Huang, Alden, Huang, Yong, Huryn, Laryssa, Isasi, Rosario, Jarvik, Gail P., Kennedy, Jennifer, Kiley, Dana, Kohane, Isaac S., Krakow, Deborah, Krasnewich, Donna M., Kravets, Elijah, Korrick, Susan, Koziura, Mary, Krier, Joel B., Lalani, Seema R., Lam, Christina, LaMoure, Grace L., Lee, Brendan H., Lincoln, Sharyn A., Loo, Sandra K., Maduro, Valerie V., Majcherska, Marta M., Malicdan, May Christine V., Mamounas, Laura A., Mao, Rong, Maravilla, Kenneth, Marom, Ronit, Martin, Beth A., Marwaha, Shruti, Mefford, Heather, Morava, Eva, Mulvihill, John J., Nakano‐Okuno, Mariko, Nath, Avi, Nickerson, Deborah, Nieves‐Rodriguez, Shirley, Pallais, J. Carl, Raskind, Wendy, Renteria, Genecee, Ruzhnikov, Maura, Samson, Susan L., Shashi, Vandana, Silverman, Edwin K., Sisco, Kathy, Solnica‐Krezel, Lilianna, Solomon, Ben, Sun, Angela, Sweetser, David A., Tan, Queenie K.‐G., Thorson, Willa, Thurm, Audrey, Tran, Alyssa A., Vanderver, Adeline, Velinder, Matt, Viskochil, Dave, Wallace, Stephanie, Walsh, Chris A., Wambach, Jennifer, Wan, Jijun, Ward, Patricia A., Wener, Mark, Wenger, Tara, Yang, John, Yousef, Muhammad

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Reliability and Validity of Smartphone Cognitive Testing for Frontotemporal Lobar Degeneration von Staffaroni, Adam M, Clark, Annie L, Taylor, Jack C, Heuer, Hilary W, Sanderson-Cimino, Mark, Wise, Amy B, Dhanam, Sreya, Cobigo, Yann, Wolf, Amy, Manoochehri, Masood, Forsberg, Leah, Mester, Carly, Rankin, Katherine P, Appleby, Brian S, Bayram, Ece, Bozoki, Andrea, Clark, David, Darby, R Ryan, Domoto-Reilly, Kimiko, Fields, Julie A, Galasko, Douglas, Geschwind, Daniel, Ghoshal, Nupur, Graff-Radford, Neill, Grossman, Murray, Hsiung, Ging-Yuek, Huey, Edward D, Jones, David T, Lapid, Maria I, Litvan, Irene, Masdeu, Joseph C, Massimo, Lauren, Mendez, Mario F, Miyagawa, Toji, Pascual, Belen, Pressman, Peter, Ramanan, Vijay K, Ramos, Eliana Marisa, Rascovsky, Katya, Roberson, Erik D, Tartaglia, M Carmela, Wong, Bonnie, Miller, Bruce L, Kornak, John, Kremers, Walter, Hassenstab, Jason, Kramer, Joel H, Boeve, Bradley F, Rosen, Howard J, Boxer, Adam L

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Clinical application of a scale to assess genomic healthcare empowerment (GEmS): Process and illustrative case examples von Tan, Queenie K.‐G., Palmer, Christina G. S., Adams, David R., Azamian, Mahshid S., Bademci, Guney, Balasubramanyam, Ashok, Baldridge, Dustin, Bayrak‐Toydemir, Pinar, Beck, Anita, Berg‐Rood, Beverly, Berry, Gerard T., Bican, Anna, Bohnsack, John, Boyd, Brenna, Briere, Lauren C., Burke, Elizabeth A., Burrage, Lindsay C., Byrd, William E., Carey, John, Sessions Cole, F., Craigen, William J., Davids, Mariska, Dorrani, Naghmeh, Earl, Dawn, Ferreira, Carlos, Fisher, Paul G., Gahl, William A., Godfrey, Rena A., Goldman, Alica M., Gutierrez, Irma, Hassey, Kelly, Hayes, Nichole, Hom, Jason, Horike‐Pyne, Martha, Huang, Alden, Isasi, Rosario, Johnston, Jean M., Kennedy, Jennifer, Kiley, Dana, Krasnewich, Donna M., Krier, Joel B., Lee, Hane, Lincoln, Sharyn A., Liu, Xue Zhong, Maas, Richard L., Macnamara, Ellen F., MacRae, Calum A., Maduro, Valerie V., Mak, Bryan, Markello, Thomas C., Marom, Ronit, Marth, Gabor, Martínez‐Agosto, Julian A., McGee, Elisabeth, Lawrence Merritt, J., Might, Matthew, Mirzaa, Ghayda, Moretti, Paolo M., Morimoto, Marie, Murdock, David R., Newman, John H., Nickerson, Deborah, Nieves‐Rodriguez, Shirley, Novacic, Donna, Oglesbee, Devin, Carl Pallais, J., Papp, Jeanette C., Phillips, John A., Posey, Jennifer E., Raskind, Wendy, Renteria, Genecee, Rives, Lynette, Rodan, Lance H., Rosenfeld, Jill A., Sampson, Jacinda B., Ron Scott, C., Schedl, Timothy, Scott, Daryl A., Sillari, Catherine H., Sinsheimer, Janet S., Stoler, Joan M., Sullivan, Jennifer A., Sun, Angela, Sutton, Shirley, Tabor, Holly K., Tamburro, Cecelia P., Thorson, Willa, Tran, Alyssa A., Tucker, Brianna M., Velinder, Matt, Viskochil, Dave, Vogel, Tiphanie P., Walsh, Chris A., Wang, Lee‐kai, Wangler, Michael F., Wener, Mark, Perry, Katherine Wesseling, Wheeler, Matthew T., Whitlock, Jordan, Woods, Jeremy D.

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Family genetic result communication in rare and undiagnosed disease communities: Understanding the practice von LeBlanc, Kimberly, Acosta, Maria T, Adams, David R., Bacino, Carlos A., Bademci, Guney, Bale, Jim, Bamshad, Michael, Barbouth, Deborah, Beggs, Alan H., Bejerano, Gill, Bivona, Stephanie, Blue, Elizabeth, Bonnenmann, Carsten, Brokamp, Elly, Butte, Manish J., Byrd, William E., Chang, Ta Chen Peter, Coakley, Terra R., Cobban, Laurel A., Cogan, Joy D., Coggins, Matthew, Colley, Heather A., Cooper, Cynthia M., Cunningham, Michael, Dasari, Surendra, Dayal, Jyoti G., Deardorff, Matthew, Dell'Angelica, Esteban C., Duncan, Laura, Eckstein, David J., Emrick, Lisa T., Eng, Christine M., Esteves, Cecilia, Estwick, Tyra, Fieg, Elizabeth L., Findley, Laurie C., Fresard, Laure, Goldstein, David B., Grajewski, Alana, Gropman, Andrea L., Hahn, Sihoun, Hamid, Rizwan, High, Frances, Hing, Anne, Hisama, Fuki M., Holm, Ingrid A., Huang, Yong, Jarvik, Jeffrey, Kohane, Isaac S., Kohler, Jennefer N., Krakow, Deborah, Kravets, Elijah, Koziura, Mary, Lam, Byron, Lam, Christina, Lanpher, Brendan C., Lau, C. Christopher, Lee, Brendan H., Lewis, Richard A., Maduro, Valerie V., Mamounas, Laura A., Maravilla, Kenneth, Marom, Ronit, McCormack, Colleen E., McCray, Alexa T., Mefford, Heather, Merritt, J. Lawrence, Nicholas, Sarah K., Pak, Stephen, Pallais, J. Carl, Palmer, Christina G.S., Parker, Neil H., Raskind, Wendy, Rao, Deepak A., Sacco, Ralph, Scott, C. Ron, Schaechter, Judy, Schedl, Timothy, Schoch, Kelly, Sharma, Prashant, Shin, Jimann, Sillari, Catherine H., Sinsheimer, Janet S., Smith, Kevin S., Stoler, Joan M., Sullivan, Jennifer A., Sun, Angela, Tamburro, Cecelia P., Telischi, Fred, Toro, Camilo, Vogel, Tiphanie P., Wahl, Colleen E., Perry, Katherine Wesseling, Westerfield, Monte, Wheeler, Matthew T., Whitlock, Jordan, Woods, Jeremy D., Yamamoto, Shinya, Yu, Guoyun, Zhao, Chunli

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Genome sequencing reveals novel noncoding variants in PLA2G6 and LMNB1 causing progressive neurologic disease von Adams, David R., Bademci, Guney, Baker, Eva, Baldridge, Dustin, Bale, Jim, Barbouth, Deborah, Beck, Anita, Berg‐Rood, Beverly, Berry, Gerard T., Brokamp, Elly, Burke, Elizabeth A., Burrage, Lindsay C., Byers, Peter, Carey, John, Chang, Ta Chen Peter, Coakley, Terra R., Colley, Heather A., Cooper, Cynthia M., Dasari, Surendra, Dayal, Jyoti G., Duncan, Laura, Eng, Christine M., Esteves, Cecilia, Fernandez, Liliana, Fieg, Elizabeth L., Forghani, Irman, Glass, Ian, Gochuico, Bernadette, Golden‐Grant, Katie, Goldrich, Madison P., Grajewski, Alana, Hahn, Sihoun, Hamid, Rizwan, Hing, Anne, Holm, Ingrid A., Huang, Yong, Jamal, Fariha, Jayadev, Suman, Kohane, Isaac S., Kohler, Jennefer N., Kravets, Elijah, Lam, Byron, Lam, Christina, Lee, Hane, Levitt, Roy, Liu, Pengfei, Liu, Xue Zhong, Longo, Nicola, Maas, Richard L., Macnamara, Ellen F., Maduro, Valerie V., Manolio, Teri A., Marth, Gabor, Martínez‐Agosto, Julian A., McCauley, Jacob, McConkie‐Rosell, Allyn, McGee, Elisabeth, Might, Matthew, Moretti, Paolo M., Mosbrook‐Davis, Deborah, Nagy, Anna, Nelson, Stan F., Nicholas, Sarah K., Orengo, James P., Pace, Laura, Pallais, J. Carl, Parker, Neil H., Phillips, John A., Power, Bradley, Pusey, Barbara N., Quinlan, Aaron, Rao, Deepak A., Robertson, Amy K., Rosenwasser, Natalie, Rossignol, Francis, Sacco, Ralph, Sampson, Jacinda B., Saporta, Mario, Scott, C. Ron, Scott, Daryl A., Shin, Jimann, Silverman, Edwin K., Sinsheimer, Janet S., Solem, Emily, Stoler, Joan M., Sullivan, Jennifer A., Tifft, Cynthia J., Toro, Camilo, Vanderver, Adeline, Vogel, Tiphanie P., Walker, Melissa, Wambach, Jennifer, Wang, Lee‐kai, Ward, Patricia A., Wegner, Daniel, Wenger, Tara, Westerfield, Monte, Wolfe, Lynne A., Woods, Jeremy D., Yang, John

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