DanielSwarrMD

PubMed

• PRDM3/16 Regulate Chromatin Accessibility Required for NKX2-1 Mediated Alveolar Epithelial Differentiation and Function.
  He, H., Bell, S., Davis, A., Zhao, S., Na, C., Guo, M., Xu, Y., Snowball, J., Zacharias, W., Sridharan, A., Swarr, D., Whitsett, J.> ;Biorxiv. 2023 Dec 20
• 1 citations
  Alveolar epithelial progenitor cells require Nkx2-1 to maintain progenitor-specific epigenomic state during lung homeostasis and regeneration.
  Toth, A., Kannan, P., Snowball, J., Kofron, M., Wayman, J., Bridges, J., Miraldi, E., Zacharias, W., Swarr, D.> ;Nature Communications. 2023 Dec 19
• 4 citations
  Sleep Apnea in Children With Down Syndrome.
  Katelyn Seither, Benjamin M Helm, Christine Heubi, Daniel Swarr, Kristen R Suhrie> ;Pediatrics. 2023 Mar 1
• Fetal maturation revealed by amniotic fluid cell-free transcriptome in rhesus macaques.
  Augusto F Schmidt, Daniel J Schnell, Kenneth P Eaton, Kashish Chetal, Paranthaman S Kannan, Lisa A Miller, Claire A Chougnet, Daniel T Swarr, Alan H Jobe, Nathan Salom...> ;JCI Insight. 2022 Sep 22
• 4 citations
  PI3K signaling specifies proximal-distal fate by driving a developmental gene regulatory network in SOX9+ mouse lung progenitors.
  Divya Khattar, Sharlene Fernandes, John Snowball, Minzhe Guo, Matthew C Gillen, Suchi Singh Jain, Debora Sinner, William Zacharias, Daniel T Swarr> ;Elife. 2022 Aug 17
• 5 citations
  Detection and impact of genetic disease in a level IV neonatal intensive care unit.
  Leanne Hagen, Divya Khattar, Katie Whitehead, Hua He, Daniel T Swarr, Kristen Suhrie> ;Journal of Perinatology. 2022 May 1
• 14 citations
  Perinatal Outcomes of Fetuses and Infants Diagnosed with Trisomy 13 or Trisomy 18.
  DonnaMaria E Cortezzo, Leandra K Tolusso, Daniel T Swarr> ;The Journal of Pediatrics. 2022 Aug 1
• 6 citations
  Inflammatory blockade prevents injury to the developing pulmonary gas exchange surface in preterm primates.
  Andrea Toth, Shelby Steinmeyer, Paranthaman Kannan, Jerilyn Gray, Courtney M Jackson, Shibabrata Mukherjee, Martin Demmert, Joshua R Sheak, Daniel Benson, Joseph Kitzm...> ;Science Translational Medicine. 2022 Mar 30
• 1 citations
  Preterm infant with diprosopus and holoprosencephaly.
  Nitya M Nair, Daniel T Swarr, Maria E Barnes-Davis> ;Clinical Case Reports. 2021 Dec 1
• 19 citations
  Beyond diagnostic yield: prenatal exome sequencing results in maternal, neonatal, and familial clinical management changes.
  Leandra K. Tolusso, Paige Hazelton, Beatrix Wong, Daniel T. Swarr> ;Genetics in Medicine. 2021 Jan 13
• "PIK"ing Out New Epigenetic Markers in Lung Disease.
  Daniel T. Swarr, Nirupama Putcha, William J. Zacharias> ;American Journal of Respiratory and Critical Care Medicine. 2020 May 1
• 21 citations
  Making a Genetic Diagnosis in a Level IV Neonatal Intensive Care Unit Population: Who, When, How, and at What Cost?
  Kayleigh A. Swaggart, Daniel T. Swarr, Leandra K. Tolusso, Hua He, D. Brian Dawson, Kristen Suhrie> ;The Journal of Pediatrics. 2019 Jun 27
• 20 citations
  The long noncoding RNA Falcor regulates Foxa2 expression to maintain lung epithelial homeostasis and promote regeneration.
  Daniel T. Swarr, Michael Herriges, Shanru Li, Michael Morley, Sharlene Fernandes, Anusha Sridharan, Su Zhou, Benjamin A. Garcia, Kathleen M. Stewart, Edward E. Morrisey> ;Genes & Development. 2019 Jun 1
• 31 citations
  Novel Molecular and Phenotypic Insights into Congenital Lung Malformations.
  Daniel T. Swarr, William H. Peranteau, Jennifer Pogoriler, David B. Frank, N. Scott Adzick, Holly L. Hedrick, Michael Morley, Su Zhou, Edward E. Morrisey> ;American Journal of Respiratory and Critical Care Medicine. 2018 May 15
• 33 citations
  Congenital Cystic Lung Lesions: Redefining the Natural Distribution of Subtypes and Assessing the Risk of Malignancy.
  Jennifer Pogoriler, Daniel T. Swarr, Portia A. Kreiger, N. Scott Adzick, William H. Peranteau> ;The American Journal of Surgical Pathology. 2017 Dec 1
• 15 citations
  Systematic Review and Meta-analysis: Gene Association Studies in Neonatal Sepsis.
  Lakshmi Srinivasan, Daniel T. Swarr, Megha Sharma, C. Michael Cotten, Haresh Kirpalani> ;American Journal of Perinatology. 2016 Dec 13
• 8 citations
  Accelerating Scientific Advancement for Pediatric Rare Lung Disease Research. Report from a National Institutes of Health–NHLBI Workshop, September 3 and 4, 2015
  Lisa R. Young, Bruce C. Trapnell, Kenneth D. Mandl, Daniel T. Swarr, Jennifer A. Wambach, Carol J. Blaisdell> ;Annals of the American Thoracic Society. 2016 Dec 7
• 5 citations
  Detection of mutually exclusive mosaicism in a girl with genotype‐phenotype discrepancies
  Minjie Luo, Surabhi Mulchandani, Holly Dubbs, Daniel T. Swarr, Louise C. Pyle, Elaine H. Zackai, Nancy B. Spinner, Laura K. Conlin> ;American Journal of Medical Genetics. Part A. 2015 Dec 1
• 52 citations
  Lung Endoderm Morphogenesis: Gasping for Form and Function
  Daniel T. Swarr, Edward E. Morrisey> ;Annual Review of Cell and Developmental Biology. 2015 Nov 13
• 39 citations
  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
  Paul Kruszka, Dong Li, Margaret Harr, Nathan R. Wilson, Daniel T. Swarr, Elizabeth M. McCormick, Rosetta M. Chiavacci, Mindy H. Li, Ariel F. Martinez, Rachel A. Hart, ...> ;Journal of Medical Genetics. 2015 Feb 1
• 118 citations
  Long noncoding RNAs are spatially correlated with transcription factors and regulate lung development.
  Michael J. Herriges, Daniel T. Swarr, Michael Morley, Komal S. Rathi, Tien Peng, Kathleen M. Stewart, Edward E. Morrisey> ;Genes & Development. 2014 Jun 15
• 35 citations
  Telemedicine for genetic and neurologic evaluation in the neonatal intensive care unit.
  Tara L. Wenger, Jeffrey Gerdes, Katherine S. Taub, Daniel T. Swarr, Matthew A. Deardorff, Nicholas S. Abend> ;Journal of Perinatology. 2014 Jan 9
• 6 citations
  Expanding the differential diagnosis of fetal hydrops: an unusual prenatal presentation of megalencephaly-capillary malformation syndrome.
  Daniel T. Swarr, Nahla Khalek, James R. Treat, Margaret A. Horton, Ghayda M. Mirzaa, Jean Baptiste Riviere, William B. Dobyns, Elaine H. Zackai> ;Prenatal Diagnosis. 2013 Oct 1
• 81 citations
  Novel FOXF1 mutations in sporadic and familial cases of alveolar capillary dysplasia with misaligned pulmonary veins imply a role for its DNA binding domain
  Partha Sen, Yaping Yang, Colby Navarro, Iris Silva, Przemyslaw Szafranski, Katarzyna E. Kolodziejska, Avinash V. Dharmadhikari, Hasnaa Mostafa, Harry P.W. Kozakewich, ...> ;Human Mutation. 2013 Jun 1
• 18 citations
  Novel FREM1 mutations expand the phenotypic spectrum associated with manitoba‐oculo‐tricho‐anal (MOTA) syndrome and bifid nose renal agenesis anorectal malformations (...
  Jared Nathanson, Daniel T. Swarr, Amihood Singer, Mochi Liu, Amy Chinn, Wendy D Jones, Jane A. Hurst, Nahla Khalek, Elaine H. Zackai, Anne Slavotinek> ;American Journal of Medical Genetics. Part A. 2013 Feb 8
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