Fetal Tracheal Occlusion for Congenital Diaphragmatic Hernia von Cole, F. Sessions

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Improving VLBW infant outcomes with big data analytics von Cole, F. Sessions

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Genotype-Phenotype Correlations for Infants and Children with ABCA3 Deficiency von WAMBACH, Jennifer A, CASEY, Alicia M, FISHMAN, Martha P, WEGNER, Daniel J, WERT, Susan E, COLE, F. Sessions, HAMVAS, Aaron, NOGEE, Lawrence M

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Functional characterization of four ATP‐binding cassette transporter A3 gene (ABCA3) variants von Hu, June Y., Yang, Ping, Wegner, Daniel J., Heins, Hillary B., Luke, Cliff J., Li, Fuhai, White, Frances V., Silverman, Gary A., Sessions Cole, F., Wambach, Jennifer A.

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Biologic characterization of ABCA3 variants in lung tissue from infants and children with ABCA3 deficiency von Xu, Kathryn K., Wegner, Daniel J., Geurts, Lucille C., Heins, Hillary B., Yang, Ping, Hamvas, Aaron, Eghtesady, Pirooz, Sweet, Stuart C., Sessions Cole, F., Wambach, Jennifer A.

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NIH Consensus Development Conference Statement: Inhaled Nitric-Oxide Therapy for Premature Infants von SESSIONS COLE, F, ALLEYNE, Claudia, KRAMER, Michael, MITCHELL, Christine, NEU, Josef, PURSLEY, Dewayne M, ROBINSON, Walter M, ROWITCH, David H, BARKS, John D. E, BOYLE, Robert J, CARROLL, John L, DOKKEN, Deborah, EDWARDS, William H, GEORGIEFF, Michael, GREGORY, Katherine, JOHNSTON, Michael V

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Racial disparity in the frequency of recurrence of preterm birth von Kistka, Zachary A.-F, Palomar, Lisanne, Lee, Kirstin A., MD, Boslaugh, Sarah E., PhD, Wangler, Michael F., MD, Cole, F. Sessions, MD, DeBaun, Michael R., MD, MPH, Muglia, Louis J., MD, PhD

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Patient-specific iPSCs carrying an SFTPC mutation reveal the intrinsic alveolar epithelial dysfunction at the inception of interstitial lung disease von Alysandratos, Konstantinos-Dionysios, Russo, Scott J., Petcherski, Anton, Taddeo, Evan P., Acín-Pérez, Rebeca, Villacorta-Martin, Carlos, Jean, J.C., Mulugeta, Surafel, Rodriguez, Luis R., Blum, Benjamin C., Hekman, Ryan M., Hix, Olivia T., Minakin, Kasey, Vedaie, Marall, Kook, Seunghyi, Tilston-Lunel, Andrew M., Varelas, Xaralabos, Wambach, Jennifer A., Cole, F. Sessions, Hamvas, Aaron, Young, Lisa R., Liesa, Marc, Emili, Andrew, Guttentag, Susan H., Shirihai, Orian S., Beers, Michael F., Kotton, Darrell N.

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Outcomes of Lung Transplantation for Infants and Children with Genetic Disorders of Surfactant Metabolism von Eldridge, Whitney B., MD, Zhang, Qunyuan, PhD, Faro, Albert, MD, Sweet, Stuart C., PhD, MD, Eghtesady, Pirooz, MD, PhD, Hamvas, Aaron, MD, Cole, F. Sessions, MD, Wambach, Jennifer A., MD, MS

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A Recurrent Gain-of-Function Mutation in CLCN6, Encoding the ClC-6 Cl−/H+-Exchanger, Causes Early-Onset Neurodegeneration von Polovitskaya, Maya M., Barbini, Carlo, Martinelli, Diego, Harms, Frederike L., Cole, F. Sessions, Calligari, Paolo, Bocchinfuso, Gianfranco, Stella, Lorenzo, Ciolfi, Andrea, Niceta, Marcello, Rizza, Teresa, Shinawi, Marwan, Sisco, Kathleen, Johannsen, Jessika, Denecke, Jonas, Carrozzo, Rosalba, Wegner, Daniel J., Kutsche, Kerstin, Tartaglia, Marco, Jentsch, Thomas J.

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Phenotypic expansion of KMT2D‐related disorder: Beyond Kabuki syndrome von Baldridge, Dustin, Spillmann, Rebecca C., Wegner, Daniel J., Wambach, Jennifer A., White, Frances V., Sisco, Kathleen, Toler, Tomi L., Dickson, Patricia I., Cole, F. Sessions, Shashi, Vandana, Grange, Dorothy K.

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Functional Characterization of ATP-Binding Cassette Transporter A3 Mutations from Infants with Respiratory Distress Syndrome von Wambach, Jennifer A, Yang, Ping, Wegner, Daniel J, Heins, Hillary B, Kaliberova, Lyudmila N, Kaliberov, Sergey A, Curiel, David T, White, Frances V, Hamvas, Aaron, Hackett, Brian P, Cole, F Sessions

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Heterogeneous Pulmonary Phenotypes Associated With Mutations in the Thyroid Transcription Factor Gene NKX2-1 von Hamvas, Aaron, MD, Deterding, Robin R., MD, Wert, Susan E., PhD, White, Frances V., MD, Dishop, Megan K., MD, Alfano, Danielle N., MD, Halbower, Ann C., MD, Planer, Benjamin, MD, Stephan, Mark J., MD, Uchida, Derek A., MD, Williames, Lee D., MD, Rosenfeld, Jill A., MS, Lebel, Robert Roger, MD, Young, Lisa R., MD, Cole, F. Sessions, MD, Nogee, Lawrence M., MD

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Mutations in the thyroid transcription factor gene NKX2-1 result in decreased expression of SFTPB and SFTPC von Attarian, Stephanie J, Leibel, Sandra L, Yang, Ping, Alfano, Danielle N, Hackett, Brian P, Cole, F Sessions, Hamvas, Aaron

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Measuring BMI change among children and adolescents von Freedman, David S., Goodwin Davies, Amy J., Phan, Thao‐Ly Tam, Cole, F. Sessions, Pajor, Nathan, Rao, Suchitra, Eneli, Ihuoma, Kompaniyets, Lyudmyla, Lange, Samantha J., Christakis, Dimitri A., Forrest, Christopher B.

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Functional characterization of biallelic RTTN variants identified in an infant with microcephaly, simplified gyral pattern, pontocerebellar hypoplasia, and seizures von Wambach, Jennifer A., Wegner, Daniel J., Yang, Ping, Shinawi, Marwan, Baldridge, Dustin, Betleja, Ewelina, Shimony, Joshua S., Spencer, David, Hackett, Brian P., Andrews, Marisa V., Ferkol, Thomas, Dutcher, Susan K., Mahjoub, Moe R., Cole, F. Sessions

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Rare recessive loss-of-function methionyl-tRNA synthetase mutations presenting as a multi-organ phenotype von van Meel, Eline, Wegner, Daniel J, Cliften, Paul, Willing, Marcia C, White, Frances V, Kornfeld, Stuart, Cole, F Sessions

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The Role of Genome Sequencing in Neonatal Intensive Care Units von Kingsmore, Stephen F, Cole, F. Sessions

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An intronic ABCA3 mutation that is responsible for respiratory disease von Agrawal, Amit, Hamvas, Aaron, Cole, F. Sessions, Wambach, Jennifer A., Wegner, Daniel, Coghill, Carl, Harrison, Keith, Nogee, Lawrence M.

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Survival among children with “Lethal” congenital contracture syndrome 11 caused by novel mutations in the gliomedin gene (GLDN) von Wambach, Jennifer A., Stettner, Georg M., Haack, Tobias B., Writzl, Karin, Škofljanec, Andreja, Maver, Aleš, Munell, Francina, Ossowski, Stephan, Bosio, Mattia, Wegner, Daniel J., Shinawi, Marwan, Baldridge, Dustin, Alhaddad, Bader, Strom, Tim M., Grange, Dorothy K., Wilichowski, Ekkehard, Troxell, Robin, Collins, James, Warner, Barbara B., Schmidt, Robert E., Pestronk, Alan, Cole, F. Sessions, Steinfeld, Robert

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