Reciprocal signaling in honeyguide-human mutualism by Spottiswoode, Claire N., Begg, Keith S., Begg, Colleen M.

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The generality of cryptic dietary niche differences in diverse large-herbivore assemblages by Pansu, Johan, Hutchinson, Matthew C, Anderson, T Michael, Te Beest, Mariska, Begg, Colleen M, Begg, Keith S, Bonin, Aurelie, Chama, Lackson, Chamaillé-Jammes, Simon, Coissac, Eric, Cromsigt, Joris P G M, Demmel, Margaret Y, Donaldson, Jason E, Guyton, Jennifer A, Hansen, Christina B, Imakando, Christopher I, Iqbal, Azwad, Kalima, Davis F, Kerley, Graham I H, Kurukura, Samson, Landman, Marietjie, Long, Ryan A, Munuo, Isaack Norbert, Nutter, Ciara M, Parr, Catherine L, Potter, Arjun B, Siachoono, Stanford, Taberlet, Pierre, Waiti, Eusebio, Kartzinel, Tyler R, Pringle, Robert M

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Effective implementation of age restrictions increases selectivity of sport hunting of the African lion by Begg, Colleen M., Miller, Jennifer R. B., Begg, Keith S.

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Re-assessed molecular phylogeny and evolutionary scenario within genets (Carnivora, Viverridae, Genettinae) by Gaubert, Philippe, Begg, Colleen M.

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The implications of large home range size in a solitary felid, the Leopard (Panthera pardus) by Parker, Daniel M., Nams, Vilis O., Balme, Guy A., Begg, Colleen, Begg, Keith, Bidner, Laura, Bockmuehl, Dirk, Cozzi, Gabriele, Preez, Byron du, Fattebert, Julien, Golabek, Krystyna, Grant, Tanith, Hayward, Matt W., Houser, Ann-Marie, Hunter, Luke T.B., Isbell, Lynne A., Jenny, David, Loveridge, Andrew J., Macdonald, David W., Mann, Gareth K.H., Maputla, Nakedi, Marker, Laurie, Martins, Quinton E., Maruping-Mzileni, Nkabeng, Melzheimer, Joerg, Menges, Vera, Nyoni, Phumuzile, O'Brien, John, Owen, Cailey, Parker, Tim, Pitman, Ross, Power, R. John, Slotow, Rob, Stein, Andrew, Steyn, Villiers, Stratford, Ken, Swanepoel, Lourens H., Vanak, Abi, Van Vuuren, Rudi, Wachter, Bettine, Weise, Florian, Wilmers, Chris C.

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Guidelines for evaluating the conservation value of African lion (Panthera leo) translocations by Becker, Matthew S., Almeida, Joao, Begg, Colleen, Bertola, Laura, Breitenmoser, Christine, Breitenmoser, Urs, Coals, Peter, Funston, Paul, Gaylard, Angela, Groom, Rosemary, Henschel, Philipp, Ikanda, Dennis, Jorge, Agostinho, Kruger, Johan, Lindsey, Peter, Maimbo, Howard, Mandisodza-Chikerema, Roseline, Maude, Glynn, Mbizah, Moreangels, Miller, Susan M., Mudongo, Edwin, Mwape, Henry, Mweetwa, Thandiwe, Naude, Vincent, Nyirenda, Vincent R., Parker, Andrew, Parker, Daniel, Reid, Craig, Robson, Ashley, Sayer, Ed, Selier, SA Jeanetta, Sichande, Mwamba, Simukonda, Chuma, Uiseb, Kenneth, Williams, Vivienne L., Zimba, Dennis, Hunter, Luke

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Telehealth Is Effective in the Evaluation of Individuals With Undiagnosed Rare Disorders: An Undiagnosed Diseases Network Study by Tan, Queenie K-G, McConkie-Rosell, Allyn, Mahoney, Rachel, Spillmann, Rebecca C, Schoch, Kelly, Chanprasert, Sirisak, Acosta, Maria T, Toro, Camilo, Rosenfeld, Jill A, Orengo, James P, Scott, Daryl A, Granadillo, Jorge L, Sisco, Kathleen, Wegner, Daniel J, Tekin, Mustafa, Bivona, Stephanie, Peart, LéShon, Rodan, Lance, Bonner, Devon, Wheeler, Matthew T, Bernstein, Jonathan A, Ruzhnikov, Maura, Adams, David R, Hisama, Fuki M, Shashi, Vandana

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Dominant‐negative variant in SLC1A4 causes an autosomal dominant epilepsy syndrome by Pujol‐Giménez, Jonai, Miller, Danny E., Allworth, Aimee, Chanprasert, Sirisak, Folta, Andrew B., Hing, Anne, Horike‐Pyne, Martha, Leppig, Kathleen A., Parhin, Azma, Rosenthal, Elisabeth A., Schwarze, Ulrike, Strohbehn, Samuel, Sybert, Virginia P., Timms, Andrew, Wener, Mark, Bamshad, Michael J., Bacus, Tamara J., Blue, Elizabeth E., Brower, Katherine, Sánchez, Diana Cornejo, Gomeztagle‐Burgess, Katherine, Hurless, Jameson R., Shively, Kathryn M., Weiss, Jeffrey M., Wheeler, Marsha M., Adam, Margaret, Alvey, Justin, Amendola, Laura, Andrews, Ashley, Ashley, Euan A., Barbouth, Deborah, Bejerano, Gill, Bellen, Hugo J., Bennett, Jimmy, Bivona, Stephanie, Blue, Elizabeth, Bonner, Devon, Byers, Peter, Cassini, Thomas, Chang, Ta Chen Peter, Chanprasert, Sirisak, Clark, Gary D., Cole, F. Sessions, Corona, Rosario, Crouse, Andrew B., Cunningham, Michael, Dasari, Surendra, Dayal, Jyoti G., Emrick, Lisa T., Fisher, Paul G., Gahl, William A., Hadley, Don, Hahn, Sihoun, High, Frances, Hing, Anne, Hisama, Fuki M., Horike‐Pyne, Martha, Hutchison, Sarah, Izumi, Kosuke, Kohane, Isaac S., Kohler, Jennefer N., Lalani, Seema R., Lam, Byron, Lanpher, Brendan C., Lewis, Richard A., Liu, Xue Zhong, Maduro, Valerie V., Manolio, Teri A., McCauley, Jacob, McCray, Alexa T., Mefford, Heather, Moretti, Paolo, Nickerson, Deborah, Nieves‐Rodriguez, Shirley, Orengo, James P., Pak, Stephen, Papp, Jeanette C., Parker, Neil H., Phillips, John A., Rao, Deepak A., Raskind, Wendy, Renteria, Genecee, Rosenfeld, Jill A., Saporta, Mario, Schaechter, Judy, Scott, Daryl A., Sisco, Kathy, Spillmann, Rebecca C., Sullivan, Jennifer A., Tabor, Holly K., Tifft, Cynthia J., Ungar, Rachel A., Walker, Melissa, Wambach, Jennifer, Ward, Patricia A., Wegner, Daniel, Wener, Mark, Yamamoto, Shinya, Dipple, Katrina M., Stergachis, Andrew B.

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Detection of a mosaic CDKL5 deletion and inversion by optical genome mapping ends an exhaustive diagnostic odyssey by Cope, Heidi, Hoppman, Nicole, Rehder, Catherine, Alkelai, Anna, Vilain, Eric, Shashi, Vandana, Acosta, Maria T, Adams, David R, Amendola, Laura, Andrews, Ashley, Bacino, Carlos A., Baker, Eva, Beggs, Alan H., Behrens, Edward, Bejerano, Gill, Bernstein, Jonathan A., Bonner, Devon, Brokamp, Elly, Brown, Gabrielle, Carrasquillo, Olveen, Chao, Hsiao‐Tuan, Cobban, Laurel A., Cogan, Joy D., Crouse, Andrew B., Cunningham, Michael, Dasari, Surendra, Davis, Joie, Dayal, Jyoti G., Deardorff, Matthew, Douine, Emilie D., Draper, David D., Fieg, Elizabeth L., Findley, Laurie C., Fogel, Brent L., Fresard, Laure, Golden‐Grant, Katie, Goldrich, Madison P, Grajewski, Alana, High, Frances, Hisama, Fuki M., Holm, Ingrid A., Isasi, Rosario, Jarvik, Gail P., Jayadev, Suman, Karaviti, Lefkothea, Kohane, Isaac S., Kohler, Jennefer N., Kravets, Elijah, Lam, Byron, Lam, Christina, Lee, Hane, Levitt, Roy, Liu, Pengfei, Longo, Nicola, Majcherska, Marta M., Manolio, Teri A., Mao, Rong, Martínez‐Agosto, Julian A., Marwaha, Shruti, McCauley, Jacob, McCray, Alexa T., McGee, Elisabeth, Mefford, Heather, Mirzaa, Ghayda, Mosbrook‐Davis, Deborah, Newman, John H, Nickerson, Deborah, Nieves‐Rodriguez, Shirley, Orengo, James P., Parker, Neil H., Phillips, John A., Posey, Jennifer E., Potocki, Lorraine, Raskind, Wendy, Raja, Archana N., Rosenfeld, Jill A., Sacco, Ralph, Sampson, Jacinda B., Saporta, Mario, Schaechter, Judy, Schoch, Kelly, Signer, Rebecca, Sisco, Kathy, Smith, Edward C., Spillmann, Rebecca C., Sullivan, Kathleen, Tabor, Holly K., Tifft, Cynthia J., Tucker, Brianna M., Urv, Tiina K., Vogel, Tiphanie P., Walsh, Chris A., Walker, Melissa, Wan, Jijun, Wangler, Michael F., Wener, Mark, Wheeler, Matthew T., Whitlock, Jordan, Yang, John, Zhao, Chunli

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DYRK1A pathogenic variants in two patients with syndromic intellectual disability and a review of the literature by Macnamara, Ellen F., D'Souza, Precilla, Vezina, Gilbert, Tifft, Cynthia J., Adams, David R., Azamian, Mahshid S., Baldridge, Dustin, Bayrak‐Toydemir, Pinar, Beck, Anita, Berry, Gerard T., Bican, Anna, Bohnsack, John, Boyd, Brenna, Briere, Lauren C., Burke, Elizabeth A., Burrage, Lindsay C., Byrd, William E., Carey, John, Craigen, William J., Cunningham, Michael, Dayal, Jyoti G., Deardorff, Matthew, Doherty, Daniel, Dorrani, Naghmeh, Douine, Emilie D., Earl, Dawn, Eckstein, David J., Emrick, Lisa T., Ferreira, Carlos, Fieg, Elizabeth L., Forghani, Irman, Fresard, Laure, Gahl, William A., Glass, Ian, Goldman, Alica M., Goldstein, David B., Groden, Catherine A., Hassey, Kelly, Horike‐Pyne, Martha, Huang, Alden, Huang, Yong, Jarvik, Gail P., Jarvik, Jeffrey, Johnston, Jean M., Kohane, Isaac S., Krakow, Deborah, Kravets, Elijah, Korrick, Susan, Koziura, Mary, Krier, Joel B., Lalani, Seema R., Lam, Christina, Lanpher, Brendan C., Lincoln, Sharyn A., Loo, Sandra K., Loscalzo, Joseph, MacRae, Calum A., Malicdan, May Christine V., Mamounas, Laura A., Markello, Thomas C., Martin, Martin G., McCormack, Colleen E., McGee, Elisabeth, Merritt, J. Lawrence, Might, Matthew, Mulvihill, John J., Nelson, Stan F., Nicholas, Sarah K., Orengo, James P., Pace, Laura, Pak, Stephen, Pusey, Barbara N., Quinlan, Aaron, Raskind, Wendy, Sacco, Ralph, Saporta, Mario, Ron Scott, C., Schaechter, Judy, Schoch, Kelly, Sharma, Prashant, Shin, Jimann, Sillari, Catherine H., Sisco, Kathy, Smith, Kevin S., Stoler, Joan M., Stong, Nicholas, Tamburro, Cecelia P., Tekin, Mustafa, Tifft, Cynthia J., Toro, Camilo, Tucker, Brianna M., Vogel, Tiphanie P., Wambach, Jennifer, Wang, Lee‐kai, Wegner, Daniel, Wenger, Tara, Wesseling Perry, Katherine, Westerfield, Monte, Wolfe, Lynne A., Zuchner, Stephan

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IgG4‐related disease: Association with a rare gene variant expressed in cytotoxic T cells by Sheehan, Jonathan H., Bastarache, Lisa, Stone, William M., Perugino, Cory, Pilkinton, Mark, McDonnell, Wyatt J., Cogan, Joy, Mattoo, Hamid, Hamid, Rizwan, Allard, Patrick, Bacino, Carlos A., Beggs, Alan H., Behnam, Babak, Bican, Anna, Birch, Camille L., Bonner, Devon, Boone, Braden E., Brown, Donna M., Brush, Matthew, Chen, Shan, Cope, Heidi, Craigen, William J., D'Souza, Precilla, Davidson, Jean M., Dayal, Jyoti G., Dell'Angelica, Esteban C., Dipple, Katrina M., Donnell‐Fink, Laurel A., Dorrani, Naghmeh, Draper, David D., Dries, Annika M., Eckstein, David J., Emrick, Lisa T., Enns, Gregory M., Esteves, Cecilia, Estwick, Tyra, Fernandez, Liliana, Ferreira, Carlos, Fisher, Paul G., Fogel, Brent L., Friedman, Noah D., Gahl, William A., Goldman, Alica M., Gourdine, Jean‐Philippe F., Groden, Catherine A., Gropman, Andrea L., Haendel, Melissa, Handley, Lori H., Herzog, Matthew R., Jamal, Fariha, Jiang, Yong‐hui, Johnston, Jean M., Karaviti, Lefkothea, Koeller, David M., Kohane, Isaac S., Korrick, Susan, Kyle, Jennifer E., Lalani, Seema R., LeBlanc, Kimberly, Lee, Brendan H., Lewis, Richard A., Loo, Sandra K., Loscalzo, Joseph, Maas, Richard L., Macnamara, Ellen F., MacRae, Calum A., Manolio, Teri A., Marom, Ronit, Martin, Martin G., Marwaha, Shruti, McConkie‐Rosell, Allyn, McCormack, Colleen E., Merker, Jason D., Might, Matthew, Murdock, David R., Scott Newberry, J., Nicholas, Sarah K., Novacic, Donna, Orange, Jordan S., Papp, Jeanette C., Reuter, Chloe M., Rodan, Lance H., Rosenfeld, Jill A., Scott, Daryl A., Sharma, Prashant, Spillmann, Rebecca C., Stoler, Joan M., Sweetser, David A., Tran, Alyssa A., Valivullah, Zaheer M., Vogel, Tiphanie P., Waggott, Daryl M., Walker, Melissa, Waters, Katrina M., Wheeler, Matthew T., Wise, Anastasia L., Worthey, Elizabeth A., Yang, Yaping, Zastrow, Diane B., Zheng, Allison

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