Lung Endoderm Morphogenesis: Gasping for Form and Function von Swarr, Daniel T, Morrisey, Edward E

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PRDM3/16 regulate chromatin accessibility required for NKX2-1 mediated alveolar epithelial differentiation and function von He, Hua, Bell, Sheila M., Davis, Ashley Kuenzi, Zhao, Shuyang, Sridharan, Anusha, Na, Cheng-Lun, Guo, Minzhe, Xu, Yan, Snowball, John, Swarr, Daniel T., Zacharias, William J., Whitsett, Jeffrey A.

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Making a Genetic Diagnosis in a Level IV Neonatal Intensive Care Unit Population: Who, When, How, and at What Cost? von Swaggart, Kayleigh A., Swarr, Daniel T., Tolusso, Leandra K., He, Hua, Dawson, D. Brian, Suhrie, Kristen R.

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PI3K signaling specifies proximal-distal fate by driving a developmental gene regulatory network in SOX9+ mouse lung progenitors von Khattar, Divya, Fernandes, Sharlene, Snowball, John, Guo, Minzhe, Gillen, Matthew C, Jain, Suchi Singh, Sinner, Debora, Zacharias, William, Swarr, Daniel T

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Preterm infant with diprosopus and holoprosencephaly von Nair, Nitya M., Swarr, Daniel T., Barnes‐Davis, Maria E.

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Beyond diagnostic yield: prenatal exome sequencing results in maternal, neonatal, and familial clinical management changes von Tolusso, Leandra K., Hazelton, Paige, Wong, Beatrix, Swarr, Daniel T.

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Fetal maturation revealed by amniotic fluid cell-free transcriptome in rhesus macaques von Schmidt, Augusto F, Schnell, Daniel J, Eaton, Kenneth P, Chetal, Kashish, Kannan, Paranthaman S, Miller, Lisa A, Chougnet, Claire A, Swarr, Daniel T, Jobe, Alan H, Salomonis, Nathan, Kamath-Rayne, Beena D

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Perinatal Outcomes of Fetuses and Infants Diagnosed with Trisomy 13 or Trisomy 18 von Cortezzo, DonnaMaria E., Tolusso, Leandra K., Swarr, Daniel T.

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Long noncoding RNAs are spatially correlated with transcription factors and regulate lung development von Herriges, Michael J, Swarr, Daniel T, Morley, Michael P, Rathi, Komal S, Peng, Tien, Stewart, Kathleen M, Morrisey, Edward E

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Detection and impact of genetic disease in a level IV neonatal intensive care unit von Hagen, Leanne, Khattar, Divya, Whitehead, Katie, He, Hua, Swarr, Daniel T., Suhrie, Kristen

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The long noncoding RNA Falcor regulates Foxa2 expression to maintain lung epithelial homeostasis and promote regeneration von Swarr, Daniel T, Herriges, Michael, Li, Shanru, Morley, Mike, Fernandes, Sharlene, Sridharan, Anusha, Zhou, Su, Garcia, Benjamin A, Stewart, Kathleen, Morrisey, Edward E

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Twin‐twin transfusion syndrome recipient with arterial calcification and heterozygous variant in ABCC6: Evidence of a gene‐environment interaction? von Springman, Andrea, Forde, Braxton, Tolusso, Leandra, DeFranco, Emily, Swarr, Daniel T., Wright, E. Deah, Habli, Mounira

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Novel Molecular and Phenotypic Insights into Congenital Lung Malformations von Swarr, Daniel T, Peranteau, William H, Pogoriler, Jennifer, Frank, David B, Adzick, N Scott, Hedrick, Holly L, Morley, Mike, Zhou, Su, Morrisey, Edward E

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Potocki-Shaffer syndrome: Comprehensive clinical assessment, review of the literature, and proposals for medical management von Swarr, Daniel T., Bloom, Douglas, Lewis, Richard Alan, Elenberg, Ewa, Friedman, Ellen M., Glotzbach, Caron, Wissman, Scott D., Shaffer, Lisa G., Potocki, Lorraine

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Accelerating Scientific Advancement for Pediatric Rare Lung Disease Research. Report from a National Institutes of Health-NHLBI Workshop, September 3 and 4, 2015 von Young, Lisa R, Trapnell, Bruce C, Mandl, Kenneth D, Swarr, Daniel T, Wambach, Jennifer A, Blaisdell, Carol J

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Clinical features of three girls with mosaic genome-wide paternal uniparental isodisomy von Kalish, Jennifer M., Conlin, Laura K., Bhatti, Tricia R., Dubbs, Holly A., Harris, Mary Catherine, Izumi, Kosuke, Mostoufi-Moab, Sogol, Mulchandani, Surabhi, Saitta, Sulagna, States, Lisa J., Swarr, Daniel T., Wilkens, Alisha B., Zackai, Elaine H., Zelley, Kristin, Bartolomei, Marisa S., Nichols, Kim E., Palladino, Andrew A., Spinner, Nancy B., Deardorff, Matthew A.

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Novel FREM1 mutations expand the phenotypic spectrum associated with manitoba-oculo-tricho-anal (MOTA) syndrome and bifid nose renal agenesis anorectal malformations (BNAR) syndrom... von Nathanson, Jared, Swarr, Daniel T., Singer, Amihood, Liu, Mochi, Chinn, Amy, Jones, Wendy, Hurst, Jane, Khalek, Nahla, Zackai, Elaine, Slavotinek, Anne

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Unraveling the complex genetic underpinnings of asthma and allergic disorders von Swarr, Daniel T, Hakonarson, Hakon

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Expanding the differential diagnosis of fetal hydrops: an unusual prenatal presentation of megalencephaly-capillary malformation syndrome von Swarr, Daniel T., Khalek, Nahla, Treat, James, Horton, Margaret A., Mirzaa, Ghayda M., Riviere, Jean-Baptiste, Dobyns, William B., Zackai, Elaine H.

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Telemedicine for genetic and neurologic evaluation in the neonatal intensive care unit von Wenger, T L, Gerdes, J, Taub, K, Swarr, D T, Deardorff, M A, Abend, N S

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