The evidence is mounting: Insurance coverage disruptions lead to worse outcomes among children diagnosed with cancer by Lupo, Philip J., Magyar, Christina L.

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Dihydroquinazolines enhance 20S proteasome activity and induce degradation of α-synuclein, an intrinsically disordered protein associated with neurodegeneration by Fiolek, Taylor J., Magyar, Christina L., Wall, Tyler J., Davies, Steven B., Campbell, Molly V., Savich, Christopher J., Tepe, Jetze J., Mosey, R. Adam

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An Integrated Phenotypic and Genotypic Approach Reveals a High‐Risk Subtype Association for EBF3 Missense Variants Affecting the Zinc Finger Domain by Deisseroth, Cole A., Lerma, Vanesa C., Magyar, Christina L., Pfliger, Jessica Mae, Nayak, Aarushi, Bliss, Nathan D., LeMaire, Ashley W., Narayanan, Vinodh, Balak, Christopher, Zanni, Ginevra, Valente, Enza Maria, Bertini, Enrico, Benke, Paul J., Wangler, Michael F., Chao, Hsiao‐Tuan

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Triflic anhydride mediated synthesis of 3,4-dihydroquinazolines: a three-component one-pot tandem procedure by Magyar, Christina L, Wall, Tyler J, Davies, Steven B, Campbell, Molly V, Barna, Haven A, Smith, Sydney R, Savich, Christopher J, Mosey, R. Adam

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PRUNE1 c.933G>A synonymous variant induces exon 7 skipping, disrupts the DHHA2 domain, and leads to an atypical NMIHBA syndrome presentation: Case report and review of the literatu... by Magyar, Christina L., Murdock, David R., Burrage, Lindsay C., Dai, Hongzheng, Lalani, Seema R., Lewis, Richard A., Lin, Yuezhen, Astudillo, Marcela F., Rosenfeld, Jill A., Tran, Alyssa A., Gibson, James B., Bacino, Carlos A., Lee, Brendan H., Chao, Hsiao‐Tuan

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Assigning pathogenicity for TAB2 variants using a novel scalable functional assay and expanding TAB2 disease spectrum by Xu, Weiyi, Graves, Andrea, Weisz-Hubshman, Monika, Hegazy, Lamees, Magyar, Christina, Liu, Zian, Nasiotis, Eleni, Samee, Md Abul Hassan, Burris, Thomas, Lalani, Seema, Zhang, Lilei

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One-pot triflic anhydride-mediated synthesis of 1,2-disubstituted 2-imidazolines from N-(2-haloethyl)amides and amines by Ellsworth, Alyssa A., Magyar, Christina L., Hubbell, Grace E., Theisen, Chelsea C., Holmes, Daniel, Mosey, R. Adam

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PRUNE1 c. 933G >A synonymous variant induces exon 7 skipping, disrupts the DHHA2 domain, and leads to an atypical NMIHBA syndrome presentation: Case report and review of the litera... by Magyar, Christina L., Murdock, David R., Burrage, Lindsay C., Dai, Hongzheng, Lalani, Seema R., Lewis, Richard A., Lin, Yuezhen, Astudillo, Marcela F., Rosenfeld, Jill A., Tran, Alyssa A., Gibson, James B., Bacino, Carlos A., Lee, Brendan H., Chao, Hsiao‐Tuan

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Influence of Caring Youth Sport Contexts on Efficacy-Related Beliefs and Social Behaviors by Gano-Overway, Lori A, Newton, Maria, Magyar, T. Michelle, Fry, Mary D, Kim, Mi-Sook, Guivernau, Marta R

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Atonal homolog 7 (ATOH7) loss-of-function mutations in predominant bilateral optic nerve hypoplasia by Atac, David, Koller, Samuel, Hanson, James V M, Feil, Silke, Tiwari, Amit, Bahr, Angela, Baehr, Luzy, Magyar, István, Kottke, Raimund, Gerth-Kahlert, Christina, Berger, Wolfgang

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Long-term (180-Day) Outcomes in Critically Ill Patients With COVID-19 in the REMAP-CAP Randomized Clinical Trial by Higgins, Alisa M, Berry, Lindsay R, Lorenzi, Elizabeth, Murthy, Srinivas, McQuilten, Zoe, Mouncey, Paul R, Al-Beidh, Farah, Annane, Djillali, Arabi, Yaseen M, Beane, Abi, van Bentum-Puijk, Wilma, Bhimani, Zahra, Bonten, Marc J. M, Bradbury, Charlotte A, Brunkhorst, Frank M, Burrell, Aiden, Buzgau, Adrian, Buxton, Meredith, Charles, Walton N, Cove, Matthew, Detry, Michelle A, Estcourt, Lise J, Fagbodun, Elizabeth O, Fitzgerald, Mark, Girard, Timothy D, Goligher, Ewan C, Goossens, Herman, Haniffa, Rashan, Hills, Thomas, Horvat, Christopher M, Huang, David T, Ichihara, Nao, Lamontagne, Francois, Marshall, John C, McAuley, Daniel F, McGlothlin, Anna, McGuinness, Shay P, McVerry, Bryan J, Neal, Matthew D, Nichol, Alistair D, Parke, Rachael L, Parker, Jane C, Parry-Billings, Karen, Peters, Sam E. C, Reyes, Luis F, Rowan, Kathryn M, Saito, Hiroki, Santos, Marlene S, Saunders, Christina T, Serpa-Neto, Ary, Seymour, Christopher W, Shankar-Hari, Manu, Stronach, Lucy M, Turgeon, Alexis F, Turner, Anne M, van de Veerdonk, Frank L, Zarychanski, Ryan, Green, Cameron, Lewis, Roger J, Angus, Derek C, McArthur, Colin J, Berry, Scott, Derde, Lennie P. G, Gordon, Anthony C, Webb, Steve A, Lawler, Patrick R

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Deep Sequencing of RNA from Blood and Oral Swab Samples Reveals the Presence of Nucleic Acid from a Number of Pathogens in Patients with Acute Ebola Virus Disease and Is Consistent... by Carroll, Miles W, Haldenby, Sam, Rickett, Natasha Y, Pályi, Bernadett, Garcia-Dorival, Isabel, Liu, Xuan, Barker, Gary, Bore, Joseph Akoi, Koundouno, Fara Raymond, Williamson, E Diane, Laws, Thomas R, Kerber, Romy, Sissoko, Daouda, Magyar, Nóra, Di Caro, Antonino, Biava, Mirella, Fletcher, Tom E, Sprecher, Armand, Ng, Lisa F P, Rénia, Laurent, Magassouba, N'faly, Günther, Stephan, Wölfel, Roman, Stoecker, Kilian, Matthews, David A, Hiscox, Julian A

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Effect of Antiplatelet Therapy on Survival and Organ Support–Free Days in Critically Ill Patients With COVID-19: A Randomized Clinical Trial by Bradbury, Charlotte A, Lawler, Patrick R, Stanworth, Simon J, McVerry, Bryan J, McQuilten, Zoe, Higgins, Alisa M, Mouncey, Paul R, Al-Beidh, Farah, Rowan, Kathryn M, Berry, Lindsay R, Lorenzi, Elizabeth, Zarychanski, Ryan, Arabi, Yaseen M, Annane, Djillali, Beane, Abi, van Bentum-Puijk, Wilma, Bhimani, Zahra, Bihari, Shailesh, Bonten, Marc J. M, Brunkhorst, Frank M, Buzgau, Adrian, Buxton, Meredith, Carrier, Marc, Cheng, Allen C, Cove, Matthew, Detry, Michelle A, Estcourt, Lise J, Fitzgerald, Mark, Girard, Timothy D, Goligher, Ewan C, Goossens, Herman, Haniffa, Rashan, Hills, Thomas, Huang, David T, Horvat, Christopher M, Hunt, Beverley J, Ichihara, Nao, Lamontagne, Francois, Leavis, Helen L, Linstrum, Kelsey M, Litton, Edward, Marshall, John C, McAuley, Daniel F, McGlothlin, Anna, McGuinness, Shay P, Middeldorp, Saskia, Montgomery, Stephanie K, Morpeth, Susan C, Murthy, Srinivas, Neal, Matthew D, Nichol, Alistair D, Parke, Rachael L, Parker, Jane C, Reyes, Luis F, Saito, Hiroki, Santos, Marlene S, Saunders, Christina T, Serpa-Neto, Ary, Seymour, Christopher W, Shankar-Hari, Manu, Singh, Vanessa, Tolppa, Timo, Turgeon, Alexis F, Turner, Anne M, van de Veerdonk, Frank L, Green, Cameron, Lewis, Roger J, Angus, Derek C, McArthur, Colin J, Berry, Scott, Derde, Lennie P. G, Webb, Steve A, Gordon, Anthony C

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Mutations in CABP4, the gene encoding the Ca2+-binding protein 4, cause autosomal recessive night blindness by ZEITZ, Christina, KLOECKENER-GRUISSEM, Barbara, MUNIER, Francis L, BERGER, Wolfgang, FORSTER, Ursula, KOHL, Susanne, MAGYAR, Istvan, WISSINGER, Bernd, MATYAS, Gabor, BORRUAT, Francois-Xavier, SCHORDERET, Daniel F, ZRENNER, Eberhart

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Novel Arylalkenylpropargylamines as Neuroprotective, Potent, and Selective Monoamine Oxidase B Inhibitors for the Treatment of Parkinson’s Disease by Huleatt, Paul B, Khoo, Mui Ling, Chua, Yi Yuan, Tan, Tiong Wei, Liew, Rou Shen, Balogh, Balázs, Deme, Ruth, Gölöncsér, Flóra, Magyar, Kalman, Sheela, David P, Ho, Han Kiat, Sperlágh, Beáta, Mátyus, Péter, Chai, Christina L. L

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Dexamethasone induces dysferlin in myoblasts and enhances their myogenic differentiation by Belanto, Joseph J, Diaz-Perez, Silvia V, Magyar, Clara E, Maxwell, Michele M, Yilmaz, Yasemin, Topp, Kasey, Boso, Guney, Jamieson, Catriona H, Cacalano, Nicholas A, Jamieson, Christina A.M

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Accelerated Allograft Vasculopathy With Rituximab After Cardiac Transplantation by Starling, Randall C., Armstrong, Brian, Bridges, Nancy D., Eisen, Howard, Givertz, Michael M., Kfoury, Abdallah G., Kobashigawa, Jon, Ikle, David, Morrison, Yvonne, Pinney, Sean, Stehlik, Josef, Tripathi, Sudipta, Sayegh, Mohamed H., Chandraker, Anil, Gus, Barbara, Keslar, Karen, Magyar, Bill, Petrich, John, Starling, Randall C., Tang, W. H. Wilson, Brooks, Kimberly, Givertz, Michael, Kelly, Charles, Klein, Katie, Crisalli, Kerry, DeBronkart, Sandra, Madsen, Joren, Semigran, Marc, Vetrano, John, DeMarco, Teresa, Fields, Scott, Gordon, Robert, Anderson, Allen, Warzecha, Anna, Goldberg, Lee, Olt, Caroline, Rockwell, Kenneth, Harris, Ashley, Johnson, Maryl, Johnston, Susan, Roginski, Chris, Ahmed, Rashid, Cohen, Ivy, Peace, Denise, Pinney, Sean, Yao, Tina, Araujo, Gloria, Bhimaraj, Arvind, Patel, Varsha, Chait, Julie, Fonarow, Gregg, Shin, Christina, Gibbs, Charles, Hunt, Judson, Johnson, Melissa, Worley, Tina, Gibbs, Jeff, Kirk, John, Redd, Winter, Stehlik, Josef, Bryan, Julia, French, Anna, Kfoury, A.G., Konery, Kristin, Feller, Erika, Lee, Myounghee, Pierson, Richard, Young, Cindi, Hollifield, Theodora, Porter, Kimberley, Schulz, Mariann, VanBakel, Adrian, Khush, Kiran, Nguyen, Son, Pham, Michael, DeNofrio, David, O’Kelly, Ryan, Garcia, Lucilla, Kobashigawa, Jon, Sana, Sean, Starks, Brandy, Thottam, Maria, Yi, Annie, Cabuay, Barry, Olson, Rachel, Tucker, Larry, Uppgaard, Laura, Eisen, Howard, Lai, Denise, Poisker, Colleen, Dragicevic, Klaudija, Kelner, Harrison, Luke, Darlette, Nelson, Jennifer, Raveendran, Ganesh, Kleissas, Nick, Murali, Srinivas, Rayl, Kenneth, Sherry, Sarah, Cosgrove, Michele

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C2orf71 Mutations as a Frequent Cause of Autosomal-Recessive Retinitis Pigmentosa: Clinical Analysis and Presentation of 8 Novel Mutations by Gerth-Kahlert, Christina, Tiwari, Amit, Hanson, James V M, Batmanabane, Vaishnavi, Traboulsi, Elias, Pennesi, Mark E, Al-Qahtani, Abdullah A, Lam, Byron L, Heckenlively, John, Zweifel, Sandrine A, Vincent, Ajoy, Fierz, Fabienne, Barthelmes, Daniel, Branham, Kari, Khan, Naheed, Bahr, Angela, Baehr, Luzy, Magyar, István, Koller, Samuel, Azzarello-Burri, Silvia, Niedrist, Dunja, Heon, Elise, Berger, Wolfgang

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Youth sport participation by Theokas, Christina, Gaudreau, Patrick, Amiot, Catherine E, Vallerand, Robert J, Coatsworth, J Douglas, Conroy, David E, Gano-Overway, Lori A, Newton, Maria, Magyar, T Michelle, Fry, Mary D, Kim, Mi-Sook, Guivernau, Marta R, Gardner, Margo, Roth, Jodie, Brooks-Gunn, Jeanne, Linver, Miriam R, Roth, Jodie L, Zarrett, Nicole, Fay, Kristen, Li, Yibing, Carrano, Jennifer, Phelps, Erin, Lerner, Richard M

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Mutations in CABP4, the Gene Encoding the Ca 2+-Binding Protein 4, Cause Autosomal Recessive Night Blindness by Zeitz, Christina, Kloeckener-Gruissem, Barbara, Forster, Ursula, Kohl, Susanne, Magyar, István, Wissinger, Bernd, Mátyás, Gábor, Borruat, François-Xavier, Schorderet, Daniel F., Zrenner, Eberhart, Munier, Francis L., Berger, Wolfgang

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