Contemporary retinal imaging techniques in diabetic retinopathy: a review von Cole, Emily Dawn, Novais, Eduardo Amorim, Louzada, Ricardo Noguera, Waheed, Nadia K

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Rare disease patient matchmaking: development and outcomes of an internet case-finding strategy in the Undiagnosed Diseases Network von LeBlanc, Kimberly, Glanton, Emily, Nagy, Anna, Bater, Jorick, Berro, Tala, McGuinness, Molly A, Studwell, Courtney, Might, Matthew

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Toxoplasma gondii protease TgSUB1 is required for cell surface processing of micronemal adhesive complexes and efficient adhesion of tachyzoites von Lagal, Vanessa, Binder, Emily M, Huynh, My‐Hang, Kafsack, Bjorn F.C, Harris, Philippa K, Diez, Roberto, Chen, Dawn, Cole, Robert N, Carruthers, Vern B, Kim, Kami

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The Undiagnosed Diseases Network: Characteristics of solvable applicants and diagnostic suggestions for nonaccepted ones von Mulvihill, John J., Findley, Laura, Newman, John H., Wheeler, Matthew T., Mokry, Jill R., Al-Beshri, Ali, Balasubramanyam, Ashok, Bamshad, Michael, Beck, Anita, Behrens, Edward, Bejerano, Gill, Bellen, Hugo J., Bernstein, Jonathan A., Bonner, Devon, Botto, Lorenzo, Burke, Elizabeth A., Burrage, Lindsay C., Butte, Manish J., Byers, Peter, Cassini, Thomas, Coakley, Terra R., Cobban, Laurel A., Cole, F. Sessions, Dai, Hongzheng, Davis, Joie, Delgado, Margaret, Earl, Dawn, Ezell, Kimberly, Fieg, Elizabeth L., Fisher, Paul G., Gahl, William A., Gonzalez, Joanna M., Gropman, Andrea, Hamid, Rizwan, Hassey, Kelly, Holm, Ingrid A., Hom, Jason, Hurst, Anna, Jarvik, Jeffrey, Jayadev, Suman, Marie, Orpa Jean, Jobanputra, Vaidehi, Karasozen, Yigit, Kilich, Gonench, Kobren, Shilpa N., Korf, Bruce, Krakow, Deborah, Kravets, Elijah, Lam, Christina, Lanza, Ian R., LeBlanc, Kimberly, Lee, Brendan H., Longo, Nicola, Maas, Richard L., Macnamara, Ellen F., Maghiro, Audrey Stephannie, Mao, Rong, Marth, Gabor, McConkie-Rosell, Allyn, McCray, Alexa T., Mikati, Mohamad, Morimoto, Marie, Mulvihill, John J., Novacic, Donna, Oglesbee, Devin, Parker, Neil H., Petcharet, Leoyklang, Posey, Jennifer E., Rao, Deepak A., Raper, Anna, Raskind, Wendy, Rebelo, Adriana, Robertson, Amy K., Rodriguez, Martin, Rosenfeld, Jill A., Ruzhnikov, Maura, Sabaii, Marla, Schedl, Timothy, Seto, Elaine, Shelkowitz, Emily, Sisco, Kathy, Skelton, Tammi, Smith, Carson A., Solnica-Krezel, Lilianna, Sullivan, Kathleen, Sybert, Virginia, Tan, Amelia L.M., Taylor, Herman, Thorson, Willa, Tran, Alyssa A., Vanderver, Adeline, Vogel, Tiphanie P., Wahl, Colleen E., Walker, Melissa, Wangler, Michael F., Ward, Patricia A., Wheeler, Matthew T., Wolfe, Lynne A., Yamamoto, Shinya, Zhang, Zhe

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Advancing Equity in Rare Disease Research: Insights From the Undiagnosed Disease Network von Fernandes, Samuela, Adams, David R., Afzali, Ben, Alvarez, Raquel L., Alvey, Justin, Andrews, Ashley, Ashley, Euan A., Bacino, Carlos A., Bademci, Guney, Baldridge, Dustin, Bale, Jim, Beck, Anita, Beggs, Alan H., Bennett, Jimmy, Berry, Gerard T., Bican, Anna, Bohnsack, John, Borja, Nicholas, Briere, Lauren C., Byers, Peter, Callaway, Kaitlin, Chanprasert, Sirisak, Chinn, Ivan, Clark, Gary D., Corona, Rosario I., Craigen, William J., Crouse, Andrew B., Cunningham, Michael, D’Souza, Precilla, Darr, Kahlen, Dasari, Surendra, Dipple, Katrina, Dorrani, Naghmeh, Douine, Emilie D., Earl, Dawn, Eng, Christine M., Fogel, Brent L., Fu, Jiayu, Goddard, Page C., Gropman, Andrea, Halley, Meghan C., Hanchard, Neal, High, Frances, Hing, Anne, Hisama, Fuki M., Hom, Jason, Horike‐Pyne, Martha, Huang, Alden, Huang, Yan, Hurst, Anna, Introne, Wendy, Jarvik, Gail P., Kanca, Oguz, Kiley, Dana, Korf, Bruce, Krakow, Deborah, Lam, Christina, Lanpher, Brendan C., Lee, Brendan H., Liu, Pengfei, Longo, Nicola, Malicdan, May Christine V., Marth, Gabor, Martínez‐Agosto, Julian A., McCray, Alexa T., Might, Matthew, Mikati, Mohamad, Moretti, Paolo, Morimoto, Marie, Mulvihill, John J., Novacic, Donna, Oglesbee, Devin, Parker, Neil H., Petcharet, Leoyklang, Posey, Jennifer E., Potocki, Lorraine, Rader, Daniel J., Rajagopalan, Ramakrishnan, Reuter, Chloe M., Sabaii, Marla, Sheppeard, Sam, Silverman, Edwin K., Skelton, Tammi, Skraban, Cara, Sutton, Shirley, Tabor, Holly K., Tan, Queenie, Taylor, Herman, Tekin, Mustafa, Tifft, Cynthia J., Toro, Camilo, Vogel, Tiphanie P., Wahl, Colleen E., Walker, Melissa, Wambach, Jennifer, Ward, Patricia A., Hubshman, Monika Weisz, Wenger, Tara, Westerfield, Monte, Wood, Heidi

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Reanalysis of RNA sequencing data ends diagnostic odyssey and expands the phenotypic spectrum of congenital titinopathy von McNamee, Lucy, Huang, Alden, Wang, Lee‐kai, Buckley, Anne F., Adams, David R., Afzali, Ben, Allworth, Aimee, Alvey, Justin, Andrews, Ashley, Bacino, Carlos A., Bademci, Guney, Baldridge, Dustin, Bale, Jim, Barbouth, Deborah, Beck, Anita, Bennett, Jimmy, Berry, Gerard T., Borja, Nicholas, Briere, Lauren C., Callaway, Kaitlin, Chanprasert, Sirisak, Coggins, Matthew, Craigen, William J., Cuddapah, Vishnu, Darr, Kahlen, Dipple, Katrina, Doherty, Daniel, Douglas, Jessica, Emrick, Lisa T., Eng, Christine M., Fogel, Brent L., Fu, Jiayu, Glass, Ian, Gropman, Andrea, Halley, Meghan C., Hassey, Kelly, Hayes, Nichole, Hing, Anne, Horike‐Pyne, Martha, Huang, Alden, Huang, Yan, Karasozen, Yigit, Ketkar, Shamika, Kilich, Gonench, Klee, Eric, Kohler, Jennefer N., Korrick, Susan, Kravets, Elijah, Lalani, Seema R., Latchman, Kumarie, LeBlanc, Kimberly, Liu, Pengfei, Longo, Nicola, MacRae, Calum A., Maghiro, AudreyStephannie, Mahoney, Rachel, Malicdan, May Christine V., Martin, Beth A., Miller, Danny, Moretti, Paolo, Mulvihill, Lindsay, Neumann, Serena, Novacic, Donna, Orengo, James P., Pace, Laura, Pak, Stephen, Parker, Neil H., Pinto e Vairo, Filippo, Posey, Jennifer E., Potocki, Lorraine, Rader, Daniel J., Rosenfeld, Jill A., Ruzhnikov, Maura, Sampson, Jacinda B., Schoch, Kelly, Shashi, Vandana, Shin, Jimann, Silverman, Edwin K., Skelton, Tammi, Spillmann, Rebecca C., Stergachis, Andrew, Stoler, Joan M., Sutton, Shirley, Sweetser, David A., Tabor, Holly K., Tan, Queenie, Tan, Amelia L. M., Tifft, Cynthia J., Viskochil, Dave, Walker, Melissa, Walley, Nicole M., Wambach, Jennifer, Ward, Patricia A., Wegner, Daniel, Hubshman, Monika Weisz, Wener, Mark, Wenger, Tara, Westerfield, Monte, Wood, Heidi, Worley, Kim

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Undiagnosed Disease Network collaborative approach in diagnosing rare disease in a patient with a mosaic CACNA1D variant von Gulsevin, Alican, Hamid, Rizwan, Neumann, Serena, Phillips, John A., Adams, David R., Afzali, Ben, Andrews, Ashley, Bademci, Guney, Balasubramanyam, Ashok, Baldridge, Dustin, Bayrak‐Toydemir, Pinar, Beck, Anita, Bennett, Jimmy, Berry, Gerard T., Bican, Anna, Bohnsack, John, Bonner, Devon, Borja, Nicholas, Butte, Manish J., Byrd, William E., Callaway, Kaitlin, Carvalho, George, Chanprasert, Sirisak, Chinn, Ivan, Clark, Gary D., Cogan, Joy D., Coggins, Matthew, Corner, Brian, Dipple, Katrina, Doherty, Daniel, Douglas, Jessica, Emrick, Lisa T., Eng, Christine M., Fogel, Brent L., Fu, Jiayu, Glass, Ian, Gropman, Andrea, Halley, Meghan C., Hassey, Kelly, Hayes, Nichole, Hing, Anne, Horike‐Pyne, Martha, Huang, Alden, Huang, Yan, Kaitryn, Emerald, Kanca, Oguz, Kohler, Jennefer N., Krakow, Deborah, Lam, Christina, Lanpher, Brendan C., Lanza, Ian R., Liu, Pengfei, Longo, Nicola, Mahoney, Rachel, Marth, Gabor, McCray, Alexa T., Might, Matthew, Miller, Danny, Moretti, Paolo, Mulvihill, John J., Mulvihill, Lindsay, Neumann, Serena, Novacic, Donna, Orengo, James P., Pace, Laura, Pak, Stephen, Parker, Neil H., Pinto e Vairo, Filippo, Posey, Jennifer E., Potocki, Lorraine, Rader, Daniel J., Rosenfeld, Jill A., Ruzhnikov, Maura, Sampson, Jacinda B., Schoch, Kelly, Shashi, Vandana, Shin, Jimann, Silverman, Edwin K., Skelton, Tammi, Spillmann, Rebecca C., Stergachis, Andrew, Stoler, Joan M., Sutton, Shirley, Sweetser, David A., Tabor, Holly K., Tan, Queenie, Tan, Amelia L. M., Tifft, Cynthia J., Viskochil, Dave, Walker, Melissa, Walley, Nicole M., Wambach, Jennifer, Ward, Patricia A., Wegner, Daniel, Hubshman, Monika Weisz, Wener, Mark, Wenger, Tara, Westerfield, Monte, Wood, Heidi, Worley, Kim

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Manic fringe is not required for embryonic development, and fringe family members do not exhibit redundant functions in the axial skeleton, limb, or hindbrain von Moran, Jennifer L., Shifley, Emily T., Levorse, John M., Mani, Shyamala, Ostmann, Kristin, Perez‐Balaguer, Ariadna, Walker, Dawn M., Vogt, Thomas F., Cole, Susan E.

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Bi-allelic ATG4D variants are associated with a neurodevelopmental disorder characterized by speech and motor impairment von Morimoto, Marie, Bhambhani, Vikas, Gazzaz, Nour, Davids, Mariska, Sathiyaseelan, Paalini, Macnamara, Ellen F., Lange, Jennifer, Lehman, Anna, Zerfas, Patricia M., Murphy, Jennifer L., Acosta, Maria T., Wang, Camille, Alderman, Emily, Reichert, Sara, Thurm, Audrey, Adams, David R., Introne, Wendy J., Gorski, Sharon M., Boerkoel, Cornelius F., Gahl, William A., Tifft, Cynthia J., Malicdan, May Christine V.

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Assessment of Corticosteroid Therapy and Death or Disability According to Pretreatment Risk of Death or Bronchopulmonary Dysplasia in Extremely Preterm Infants von Jensen, Erik A, Wiener, Laura Elizabeth, Rysavy, Matthew A, Dysart, Kevin C, Gantz, Marie G, Eichenwald, Eric C, Greenberg, Rachel G, Harmon, Heidi M, Laughon, Matthew M, Watterberg, Kristi L, Walsh, Michele C, Yoder, Bradley A, Lorch, Scott A, DeMauro, Sara B

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Thanks to reviewers

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Defining an ageing-related pathology, disease or syndrome: International Consensus Statement von Short, Emma, Calimport, Stuart, Bentley, Barry

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Demographic and Clinical Characteristics of Mpox in Persons Who Had Previously Received 1 Dose of JYNNEOS Vaccine and in Unvaccinated Persons - 29 U.S. Jurisdictions, May 22-Septem... von Farrar, Jennifer L, Lewis, Nathaniel M, Houck, Kennedy, Canning, Michelle, Fothergill, Amy, Payne, Amanda B, Cohen, Adam L, Vance, Joshua, Brassil, Bridget, Youngkin, Erin, Glenn, Bailey, Mangla, Anil, Kupferman, Nikki, Saunders, Katharine, Meza, Cristina, Nims, Dawn, Soliva, Susan, Blouse, Brandon, Henderson, Tiffany, Banerjee, Emily, White, Brooklyn, Birn, Rachael, Stadelman, Anna M, Abrego, Meaghan, McLafferty, Meagan, Eberhart, Michael G, Pietrowski, Michael, De León, Sandra Miranda, Creegan, Emma, Diedhiou, Abdoulaye, Wiedeman, Caleb, Murray-Thompson, Jade, McCarty, Elizabeth, Marcinkevage, Jessica, Kocharian, Anna, Torrone, Elizabeth A, Ray, Logan C, Payne, Daniel C

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Examining the roles of Lunatic fringe during secondary body formation von Cole, Susan E., Shifley, Emily T., Walker, Dawn

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Toxoplasma gondii protease TgSUB1 is required for cell surface processing of micronemal adhesive complexes and efficient adhesion of tachyzoites: TgSUB1 microneme protein processin... von Lagal, Vanessa, Binder, Emily M., Huynh, My-Hang, Kafsack, Bjorn F. C., Harris, Philippa K., Diez, Roberto, Chen, Dawn, Cole, Robert N., Carruthers, Vern B., Kim, Kami

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