Search Results - Swarr, Daniel T.

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  1. 1
    Lung Endoderm Morphogenesis: Gasping for Form and Function

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

    Published 2015
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  2. 2
    “PIK”ing Out New Epigenetic Markers in Lung Disease

    “PIK”ing Out New Epigenetic Markers in Lung Disease by Swarr, Daniel, Putcha, Nirupama, Zacharias, William

    Published 2020
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  3. 3
    Beyond diagnostic yield: prenatal exome sequencing results in maternal, neonatal, and familial clinical management changes

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

    Published 2021
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  4. 4
    Preterm infant with diprosopus and holoprosencephaly

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

    Published 2021
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  5. 5
    Unusual Cardiac “Masses” in a Newborn with Infantile Pompe Disease

    Unusual Cardiac “Masses” in a Newborn with Infantile Pompe Disease by Swarr, Daniel T., Kaufman, Beth, Fogel, Mark A., Finkel, Richard, Ganesh, Jaya

    Published 2011
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  6. 6
    Congenital Cystic Lung Lesions: Redefining the natural distribution of subtypes and assessing the risk of malignancy

    Congenital Cystic Lung Lesions: Redefining the natural distribution of subtypes and assessing the risk of malignancy by Pogoriler, Jennifer, Swarr, Daniel, Kreiger, Portia, Adzick, N Scott, Peranteau, William

    Published 2019
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  7. 7
    Telemedicine for genetic and neurologic evaluation in the Neonatal Intensive Care Unit

    Telemedicine for genetic and neurologic evaluation in the Neonatal Intensive Care Unit by Wenger, Tara L., Gerdes, Jeffrey, Taub, Katherine, Swarr, Daniel T., Deardorff, Matthew A., Abend, Nicholas S.

    Published 2014
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  8. 8
    Accelerating Scientific Advancement for Pediatric Rare Lung Disease Research. Report from a National Institutes of Health–NHLBI Workshop, September 3 and 4, 2015

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

    Published 2016
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  9. 9
    Long noncoding RNAs are spatially correlated with transcription factors and regulate lung development

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

    Published 2014
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  10. 10
    Novel FREM1 Mutations Expand the Phenotypic Spectrum Associated with Manitoba-Oculo-Tricho-Anal (MOTA) Syndrome and Bifid Nose Renal Agenesis Anorectal Malformations (BNAR) Syndrome

    Novel FREM1 Mutations Expand the Phenotypic Spectrum Associated with Manitoba-Oculo-Tricho-Anal (MOTA) Syndrome and Bifid Nose Renal Agenesis Anorectal Malformations (BNAR) Syndrom... by Nathanson, Jared, Swarr, Daniel T., Singer, Amihood, Liu, Mochi, Chinn, Amy, Jones, Wendy, Hurst, Jane, Khalek, Nahla, Zackai, Elaine, Slavotinek, Anne

    Published 2013
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  11. 11
    Expanding the Differential Diagnosis of Fetal Hydrops: An Unusual Prenatal Presentation of Megalencephaly-Capillary Malformation Syndrome

    Expanding the Differential Diagnosis of Fetal Hydrops: An Unusual Prenatal Presentation of Megalencephaly-Capillary Malformation Syndrome by Swarr, Daniel T., Khalek, Nahla, Treat, James, Horton, Margaret A., Mirzaa, Ghayda M., Riviere, Jean-Baptiste, Dobyns, William B, Zackai, Elaine H.

    Published 2013
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  12. 12
    The long noncoding RNA Falcor regulates Foxa2 expression to maintain lung epithelial homeostasis and promote regeneration

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

    Published 2019
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  13. 13
    Novel Molecular and Phenotypic Insights into Congenital Lung Malformations

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

    Published 2018
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  14. 14
    Clinical Features of Three Girls With Mosaic Genome-Wide Paternal Uniparental Isodisomy

    Clinical Features of Three Girls With Mosaic Genome-Wide Paternal Uniparental Isodisomy by 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.

    Published 2013
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  15. 15
    Mutations in SPECC1L, encoding sperm antigen with calponin homology and coiled-coil domains 1-like, are found in some cases of autosomal dominant Opitz G/BBB syndrome

    Mutations in SPECC1L, encoding sperm antigen with calponin homology and coiled-coil domains 1-like, are found in some cases of autosomal dominant Opitz G/BBB syndrome by Kruszka, Paul, Li, Dong, Harr, Margaret H, Wilson, Nathan R, Swarr, Daniel, McCormick, Elizabeth M, Chiavacci, Rosetta M, Li, Mindy, Martinez, Ariel F, Hart, Rachel A, McDonald-McGinn, Donna M, Deardorff, Matthew A, Falk, Marni J, Allanson, Judith E, Hudson, Cindy, Johnson, John P, Saadi, Irfan, Hakonarson, Hakon, Muenke, Maximilian, Zackai, Elaine H

    Published 2014
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  16. 16
    Inflammatory blockade prevents injury to the developing pulmonary gas exchange surface in preterm primates

    Inflammatory blockade prevents injury to the developing pulmonary gas exchange surface in preterm primates by Toth, Andrea, Steinmeyer, Shelby, Kannan, Paranthaman, Gray, Jerilyn, Jackson, Courtney M., Mukherjee, Shibabrata, Demmert, Martin, Sheak, Joshua R., Benson, Daniel, Kitzmiller, Joseph, Wayman, Joseph A., Presicce, Pietro, Cates, Christopher, Rubin, Rhea, Chetal, Kashish, Du, Yina, Miao, Yifei, Gu, Mingxia, Guo, Minzhe, Kalinichenko, Vladimir V., Kallapur, Suhas G., Miraldi, Emily R., Xu, Yan, Swarr, Daniel, Lewkowich, Ian, Salomonis, Nathan, Miller, Lisa, Sucre, Jennifer S., Whitsett, Jeffrey A., Chougnet, Claire A., Jobe, Alan H., Deshmukh, Hitesh, Zacharias, William J.

    Published 2022
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  17. 17
    Novel FOXF1 mutations in sporadic and familial cases of Alveolar Capillary Dysplasia with Misaligned Pulmonary Veins imply a role for its DNA binding domain

    Novel FOXF1 mutations in sporadic and familial cases of Alveolar Capillary Dysplasia with Misaligned Pulmonary Veins imply a role for its DNA binding domain by Sen, Partha, Yang, Yaping, Navarro, Colby, Silva, Iris, Szafranski, Przemyslaw, Kolodziejska, Katarzyna E., Dharmadhikari, Avinash V., Mostafa, Hasnaa, Kozakewich, Harry, Kearney, Debra, Cahill, John B., Whitt, Merrissa, Bilic, Masha, Margraf, Linda, Charles, Adrian, Goldblatt, Jack, Gibson, Kathleen, Lantz, Patrick, Garvin, Julian, Petty, John, Kiblawi, Zeina, Zuppan, Craig, McConkie-Rosell, Allyn, McDonald, Marie T., Peterson-Carmichael, Stacey L., Gaede, Jane T., Shivanna, Binoy, Schady, Deborah, Friedlich, Philippe S., Hays, Stephen R., Palafoll, Irene Valenzuela, Siebers-Renelt, Ulrike, Bohring, Axel, Finn, Laura S., Siebert, Joseph R., Galambos, Csaba, Nguyen, Lananh, Riley, Melissa, Chassaing, Nicolas, Vigouroux, Adeline, Rocha, Gustavo, Fernandes, Susana, Brumbaugh, Jane, Roberts, Kari, Ho-ming, Luk, Lo, Ivan, Lam, Stephen, Gerychova, Romana, Jezova, Marta, Valaskova, Iveta, Fellmann, Florence, Afshar, Katayoun, Giannoni, Eric, Muhlethaler, Vincent, Liang, Jinlong, Beckmann, Jacques S., Lioy, Janet, Deshmukh, Hitesh, Srinivasan, Lakshmi, Swarr, Daniel T., Sloman, Melissa, Shaw-Smith, Charles, van Loon, Rosa Laura, Hagman, Cecilia, Sznajer, Yves, Barrea, Catherine, Galant, Christine, Detaille, Thierry, Wambach, Jennifer A., Cole, F. Sessions, Hamvas, Aaron, Prince, Lawrence S., Diderich, Karin E.M., Brooks, Alice S., Verdijk, Rob M., Ravindranathan, Hari, Sugo, Ella, Mowat, David, Baker, Michael L., Langston, Claire, Welty, Stephen, Stankiewicz, Pawel

    Published 2013
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