Impact of PEG sensitization on the efficacy of PEG hydrogel-mediated tissue engineering by Isaac, Alisa H., Recalde Phillips, Sarea Y., Ruben, Elizabeth, Estes, Matthew, Rajavel, Varsha, Baig, Talia, Paleti, Carol, Landsgaard, Kirsten, Lee, Ryang Hwa, Guda, Teja, Criscitiello, Michael F., Gregory, Carl, Alge, Daniel L.

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Impact of Annealing Chemistry on the Properties and Performance of Microporous Annealed Particle Hydrogels by Recalde Phillips, Sarea Y., Perez-Ponce, Kiara D., Ruben, Elizabeth, Baig, Talia, Poux, Emily, Gregory, Carl A., Alge, Daniel L.

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Aberrant splicing due to a novel RPS7 variant causes Diamond-Blackfan Anemia associated with spontaneous remission and meningocele by Akram, Talia, Fatima, Ambrin, Klar, Joakim, Hoeber, Jan, Zakaria, Muhammad, Tariq, Muhammad, Baig, Shahid M., Schuster, Jens, Dahl, Niklas

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Mutations of KIF14 cause primary microcephaly by impairing cytokinesis by Moawia, Abubakar, Shaheen, Ranad, Rasool, Sajida, Waseem, Syeda Seema, Ewida, Nour, Budde, Birgit, Kawalia, Amit, Motameny, Susanne, Khan, Kamal, Fatima, Ambrin, Jameel, Muhammad, Ullah, Farid, Akram, Talia, Ali, Zafar, Abdullah, Uzma, Irshad, Saba, Höhne, Wolfgang, Noegel, Angelika Anna, Al‐Owain, Mohammed, Hörtnagel, Konstanze, Stöbe, Petra, Baig, Shahid Mahmood, Nürnberg, Peter, Alkuraya, Fowzan Sami, Hahn, Andreas, Hussain, Muhammad Sajid

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Monoallelic and bi-allelic variants in NCDN cause neurodevelopmental delay, intellectual disability, and epilepsy by Fatima, Ambrin, Hoeber, Jan, Schuster, Jens, Koshimizu, Eriko, Maya-Gonzalez, Carolina, Keren, Boris, Mignot, Cyril, Akram, Talia, Ali, Zafar, Miyatake, Satoko, Tanigawa, Junpei, Koike, Takayoshi, Kato, Mitsuhiro, Murakami, Yoshiko, Abdullah, Uzma, Ali, Muhammad Akhtar, Fadoul, Rein, Laan, Loora, Castillejo-López, Casimiro, Liik, Maarika, Jin, Zhe, Birnir, Bryndis, Matsumoto, Naomichi, Baig, Shahid M., Klar, Joakim, Dahl, Niklas

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Monoallelic and bi-allelic variants in NCDN cause neurodevelopmental delay, intellectual disability, and epilepsy by Fatima, Ambrin, Hoeber, Jan, Schuster, Jens, Koshimizu, Eriko, Maya-Gonzalez, Carolina, Keren, Boris, Mignot, Cyril, Akram, Talia, Ali, Zafar, Miyatake, Satoko, Tanigawa, Junpei, Koike, Takayoshi, Kato, Mitsuhiro, Murakami, Yoshiko, Abdullah, Uzma, Ali, Muhammad Akhtar, Fadoul, Rein, Laan, Loora, Castillejo-López, Casimiro, Liik, Maarika, Jin, Zhe, Birnir, Bryndis, Matsumoto, Naomichi, Baig, Shahid M., Klar, Joakim, Dahl, Niklas

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OUTCOMES OF NEW PERMANENT PACEMAKER IMPLANTATION FOLLOWING TRANSCATHETER AND SURGICAL AORTIC VALVE REPLACEMENT by Lanfear, Allison, Beveridge, Stephanie, Meidan, Talia, Shih, Emily, Hamandi, Mohanad, Baig, Imran, Lee, Arthur J., Aldrich, Allison, Hale, Sarah, Potluri, Srinivasa P., Szerlip, Molly, Harrington, Katherine, Schaffer, Justin Michael, Brinkman, William, DiMaio, J Michael, Mack, Michael J., Al-Azizi, Karim

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A recurrent rare intronic variant in CAPN3 alters mRNA splicing and causes autosomal recessive limb‐girdle muscular dystrophy‐1 in three Pakistani pedigrees by Khan, Kamal, Mehmood, Sarmad, Liu, Chunyu, Siddiqui, Maimoona, Ahmad, Arsalan, Faiz, Belqees Yawar, Chioza, Barry A., Baple, Emma A., Ullah, Muhammad I., Akram, Zaineb, Satti, Humayoon S., Khan, Raees, Harlalka, Gaurav V., Jameel, Muhammad, Akram, Talia, Baig, Shahid M., Crosby, Andrew H., Hassan, Muhammad J., Zhang, Feng, Davis, Erica E., Khan, Tahir N.

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Mono-allelic and bi-allelic variants in NCDN cause neurodevelopmental delay, intellectual disability, and epilepsy by Fatima, Ambrin, Hoeber, Jan, Schuster, Jens, Koshimizu, Eriko, Maya-Gonzalez, Carolina, Keren, Boris, Mignot, Cyril, Akram, Talia, Ali, Zafar, Miyatake, Satoko, Tanigawa, Junpei, Koike, Takayoshi, Kato, Mitsuhiro, Murakami, Yoshiko, Abdullah, Uzma, Ali, Muhammad Akhtar, Fadoul, Rein, Laan, Loora, Castillejo-López, Casimiro, Liik, Maarika, Jin, Zhe, Birnir, Bryndis, Matsumoto, Naomichi, Baig, Shahid M, Klar, Joakim, Dahl, Niklas

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