Observations on the association between obstructive sleep apnea and floppy eyelid syndrome: A systematic review and meta-analysis von Chan, Jian S., Lee, Matthew K., Tweedie, Peter J., Tiong, Claudia J., Tsoi, Amy T., Vasanthan, Aadhavi, Maegraith, Jed, Borchert, Grace A., Gunasegaram, James R., Waldie, Anna M., Wilcsek, Geoff, Francis, Ian C.

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Mosaic RBD nanoparticles protect against challenge by diverse sarbecoviruses in animal models von Cohen, Alexander A, van Doremalen, Neeltje, Greaney, Allison J, Andersen, Hanne, Sharma, Ankur, Starr, Tyler N, Keeffe, Jennifer R, Fan, Chengcheng, Schulz, Jonathan E, Gnanapragasam, Priyanthi N P, Kakutani, Leesa M, West, Jr, Anthony P, Saturday, Greg, Lee, Yu E, Gao, Han, Jette, Claudia A, Lewis, Mark G, Tan, Tiong K, Townsend, Alain R, Bloom, Jesse D, Munster, Vincent J, Bjorkman, Pamela J

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Low dose interleukin-2 selectively expands circulating regulatory T cells but fails to promote liver allograft tolerance in humans von Lim, Tiong Y., Perpiñán, Elena, Londoño, Maria-Carlota, Miquel, Rosa, Ruiz, Paula, Kurt, Ada S., Kodela, Elisavet, Cross, Amy R., Berlin, Claudia, Hester, Joanna, Issa, Fadi, Douiri, Abdel, Volmer, Felix H., Taubert, Richard, Williams, Evangelia, Demetris, Anthony J., Lesniak, Andrew, Bensimon, Gilbert, Lozano, Juan José, Martinez-Llordella, Marc, Tree, Tim, Sánchez-Fueyo, Alberto

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Description of a novel subtype of acute myeloid leukemia defined by recurrent CBFB insertions von Ryland, Georgina L., Umeda, Masayuki, Holmfeldt, Linda, Lehmann, Sören, Herlin, Morten Krogh, Ma, Jing, Khanlari, Mahsa, Rubnitz, Jeffrey E., Ries, Rhonda E., Kosasih, Hansen J., Ekert, Paul G., Goh, Hwee Ngee, Tiong, Ing S., Grimmond, Sean M., Haferlach, Claudia, Day, Ryan B., Ley, Timothy J., Meshinchi, Soheil, Ma, Xiaotu, Blombery, Piers, Klco, Jeffery M.

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Variant-specific changes in RAC3 function disrupt corticogenesis in neurodevelopmental phenotypes von Scala, Marcello, Nishikawa, Masashi, Ito, Hidenori, Tabata, Hidenori, Khan, Tayyaba, Accogli, Andrea, Davids, Laura, Ruiz, Anna, Chiurazzi, Pietro, Cericola, Gabriella, Schulte, Björn, Monaghan, Kristin G, Begtrup, Amber, Torella, Annalaura, Pinelli, Michele, Denommé-Pichon, Anne Sophie, Vitobello, Antonio, Racine, Caroline, Mancardi, Maria Margherita, Kiss, Courtney, Guerin, Andrea, Wu, Wendy, Gabau Vila, Elisabeth, Mak, Bryan C, Martinez-Agosto, Julian A, Gorin, Michael B, Duz, Bugrahan, Bayram, Yavuz, Carvalho, Claudia M B, Vengoechea, Jaime E, Chitayat, David, Tan, Tiong Yang, Callewaert, Bert, Kruse, Bernd, Bird, Lynne M, Faivre, Laurence, Zollino, Marcella, Biskup, Saskia, Striano, Pasquale, Nigro, Vincenzo, Severino, Mariasavina, Capra, Valeria, Costain, Gregory, Nagata, Koh Ichi

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Detection of Novel Occult Germline Multi-Exon Deletions in Patients with DDX41 Familial Predisposition to Myeloid Malignancy von Maierhofer, Anna, Fox, Lucy C, Hutter, Stephan, Baer, Constance, Thompson, Ella, Nguyen, Tamia, Den Elzen, Nicole, Filshie, Robin J, Tiong, Ing S, Nadarajah, Niroshan, Meggendorfer, Manja, Kern, Wolfgang, Haferlach, Claudia, Haferlach, Torsten, Blombery, Piers

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Monoallelic BMP2 Variants Predicted to Result in Haploinsufficiency Cause Craniofacial, Skeletal, and Cardiac Features Overlapping Those of 20p12 Deletions von Tan, Tiong Yang, Gonzaga-Jauregui, Claudia, Bhoj, Elizabeth J., Strauss, Kevin A., Brigatti, Karlla, Puffenberger, Erik, Li, Dong, Xie, LiQin, Das, Nanditha, Skubas, Ioanna, Deckelbaum, Ron A., Hughes, Virginia, Brydges, Susannah, Hatsell, Sarah, Siao, Chia-Jen, Dominguez, Melissa G., Economides, Aris, Overton, John D., Mayne, Valerie, Simm, Peter J., Jones, Bryn O., Eggers, Stefanie, Le Guyader, Gwenaël, Pelluard, Fanny, Haack, Tobias B., Sturm, Marc, Riess, Angelika, Waldmueller, Stephan, Hofbeck, Michael, Steindl, Katharina, Joset, Pascal, Rauch, Anita, Hakonarson, Hakon, Baker, Naomi L., Farlie, Peter G.

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Monoallelic BMP2 Variants Predicted to Result in Haploinsufficiency Cause Craniofacial, Skeletal, and Cardiac Features Overlapping Those of 20p12 Deletions von Tan, Tiong Yang, Gonzaga-Jauregui, Claudia, Bhoj, Elizabeth J, Steindl, Katharina, Joset, Pascal, Rauch, Anita

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MN1 C-terminal truncation syndrome is a novel neurodevelopmental and craniofacial disorder with partial rhombencephalosynapsis von Mak, Christopher C Y, Doherty, Dan, Lin, Angela E, Vegas, Nancy, Cho, Megan T, Viot, Géraldine, Dimartino, Clémantine, Weisfeld-Adams, James D, Lessel, Davor, Joss, Shelagh, Li, Chumei, Gonzaga-Jauregui, Claudia, Zarate, Yuri A, Ehmke, Nadja, Horn, Denise, Troyer, Caitlin, Kant, Sarina G, Lee, Youngha, Ishak, Gisele E, Leung, Gordon, Barone Pritchard, Amanda, Yang, Sandra, Bend, Eric G, Filippini, Francesca, Roadhouse, Chelsea, Lebrun, Nicolas, Mehaffey, Michele G, Martin, Pierre-Marie, Apple, Benjamin, Millan, Francisca, Puk, Oliver, Hoffer, Mariette J V, Henderson, Lindsay B, McGowan, Ruth, Wentzensen, Ingrid M, Pei, Steven, Zahir, Farah R, Yu, Mullin, Gibson, William T, Seman, Ann, Steeves, Marcie, Murrell, Jill R, Luettgen, Sabine, Francisco, Elizabeth, Strom, Tim M, Amlie-Wolf, Louise, Kaindl, Angela M, Wilson, William G, Halbach, Sara, Basel-Salmon, Lina, Lev-El, Noa, Denecke, Jonas, Vissers, Lisenka E L M, Radtke, Kelly, Chelly, Jamel, Zackai, Elaine, Friedman, Jan M, Bamshad, Michael J, Nickerson, Deborah A, Reid, Russell R, Devriendt, Koenraad, Chae, Jong-Hee, Stolerman, Elliot, McDougall, Carey, Powis, Zöe, Bienvenu, Thierry, Tan, Tiong Y, Orenstein, Naama, Dobyns, William B, Shieh, Joseph T, Choi, Murim, Waggoner, Darrel, Gripp, Karen W, Parker, Michael J, Stoler, Joan, Lyonnet, Stanislas, Cormier-Daire, Valérie, Viskochil, David, Hoffman, Trevor L, Amiel, Jeanne, Chung, Brian H Y, Gordon, Christopher T

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MN1 C-terminal truncation syndrome is a novel neurodevelopmental and craniofacial disorder with partial rhombencephalosynapsis von Mak, Christopher C.Y, Doherty, Dan, Lin, Angela E, Vegas, Nancy, Cho, Megan T, Viot, Geraldine, Dimartino, Clemantine, Weisfeld-Adams, James D, Lessel, Davor, Joss, Shelagh, Li, Chumei, Gonzaga-Jauregui, Claudia, Zarate, Yuri A, Ehmke, Nadja, Horn, Denise, Troyer, Caitlin, Kant, Sarina G, Lee, Youngha, Ishak, Gisele E, Leung, Gordon, Pritchard, Amanda Barone, Yang, Sandra, Bend, Eric G, Filippini, Francesca, Roadhouse, Chelsea, Lebrun, Nicolas, Mehaffey, Michele G, Martin, Pierre-Marie, Apple, Benjamin, Millan, Francisca, Puk, Oliver, Hoffer, Mariette J.V, Henderson, Lindsay B, McGowan, Ruth, Wentzensen, Ingrid M, Pei, Steven, Zahir, Farah R, Yu, Mullin, Gibson, William T, Seman, Ann, Steeves, Marcie, Murrell, Jill R, Luettgen, Sabine, Francisco, Elizabeth, Strom, Tim M, Amlie-Wolf, Louise, Kaindl, Angela M, Wilson, William G, Halbach, Sara, Basel-Salmon, Lina, Lev-El, Noa, Denecke, Jonas, Vissers, Lisenka E.L.M, Radtke, Kelly, Chelly, Jamel, Zackai, Elaine, Friedman, Jan M, Bamshad, Michael J, Nickerson, Deborah A, Reid, Russell R, Devriendt, Koenraad, Chae, Jong-Hee, Stolerman, Elliot, McDougall, Carey, Powis, Zoe, Bienvenu, Thierry, Tan, Tiong Y, Orenstein, Naama, Dobyns, William B, Shieh, Joseph T, Choi, Murim, Waggoner, Darrel, Gripp, Karen W, Parker, Michael J, Stoler, Joan, Lyonnet, Stanislas, Cormier-Daire, Valerie, Viskochil, David, Hoffman, Trevor L, Amiel, Jeanne, Chung, Brian H.Y, Gordon, Christopher T

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Pathogenic variants in SMARCA5 , a chromatin remodeler, cause a range of syndromic neurodevelopmental features von Li, Dong, Wang, Qin, Gong, Naihua N, Kurolap, Alina, Feldman, Hagit Baris, Boy, Nikolas, Brugger, Melanie, Grand, Katheryn, McWalter, Kirsty, Guillen Sacoto, Maria J, Wakeling, Emma, Hurst, Jane, March, Michael E, Bhoj, Elizabeth J, Nowaczyk, Małgorzata J M, Gonzaga-Jauregui, Claudia, Mathew, Mariam, Dava-Wala, Ashita, Siemon, Amy, Bartholomew, Dennis, Huang, Yue, Lee, Hane, Martinez-Agosto, Julian A, Schwaibold, Eva M C, Brunet, Theresa, Choukair, Daniela, Pais, Lynn S, White, Susan M, Christodoulou, John, Brown, Dana, Lindstrom, Kristin, Grebe, Theresa, Tiosano, Dov, Kayser, Matthew S, Tan, Tiong Yang, Deardorff, Matthew A, Song, Yuanquan, Hakonarson, Hakon

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A Model of the Spatiotemporal Dynamics of Soil Carbon Following Coastal Wetland Loss Applied to a Louisiana Salt Marsh in the Mississippi River Deltaic Plain von Schoolmaster, Donald R., Stagg, Camille L., Creamer, Courtney, Laurenzano, Claudia, Ward, Eric J., Waldrop, Mark P., Baustian, Melissa M., Aw, Tiong, Merino, Sergio, Villani, Rachel, Scott, Laura

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Measures of success von Barz, Claudia S., Benford, Melodie Elane, Mishra, Manoj Kumar, Chia, Tiong Sun, Cooper, Endymion, Newton, Kate, Bonel, Nicolás, de Bock, Charles, Farenhem, Kelsey, Zupanc, Jernej, Elsanadidy, Esraa, Gopinath, Suchitra D., Winter, Marten, Kemp, K. Christian, Nieuwenhuis, Rense, Hoyer, J. Steen, Li, Rosa, Lindsay, Grace, Li, Dayuan, O'Mullane, Anthony, Schuenemann, Keah C., Ramirez, Daniel, Yu, Shann S., Pun, Matiram, Li, Catherine Y.

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KAT6A Syndrome: genotype–phenotype correlation in 76 patientswith pathogenic KAT6A variants von Kennedy, Joanna, Goudie, David, Blair, Edward, Chandler, Kate, Joss Shelagh, McKay, Victoria, Green, Andrew, Armstrong, Ruth, Lees, Melissa, Kamien, Benjamin, Hopper, Bruce, Yang, Tan Tiong, Yap, Patrick, Stark Zornitza, Okamoto Nobuhiko, Miyake Noriko, Matsumoto Naomichi, Macnamara, Ellen, Murphy, Jennifer L, McCormick, Elizabeth, Hakonarson Hakon, Falk, Marni J, Li, Dong, Blackburn, Patrick, Klee, Eric, Babovic-Vuksanovic Dusica, Schelley, Susan, Hudgins Louanne, Kant Sarina, Bertrand, Isidor, Cogne, Benjamin, Bradbury, Kimberley, Williams, Mark, Patel, Chirag, Heussler Helen, Duff-Farrier, Celia, Lakeman Phillis, Scurr, Ingrid, Kini Usha, Elting Mariet, Reijnders Margot, Schuurs-Hoeijmakers Janneke, Wafik, Mohamed, Blomhoff, Anne, Ruivenkamp Claudia A L, Nibbeling Esther, Dingemans Alexander J M, Douine, Emilie D, Nelson, Stanley F, Hempel Maja, Bierhals Tatjana, Lessel Davor, Johannsen Jessika, Arboleda, Valerie A, Newbury-Ecob Ruth

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