Publications by authors named "Daniel T Swarr"

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The Perspectives and Experiences of Prospective Parents Declining Diagnostic Prenatal Genome Sequencing in Continuing Pregnancies With Fetal Structural Anomalies.
Lisa S Weingarten, Allison Rosenbaum, Jessica de Voest, Stephanie Galloway, Jessica L Giordano, Daniel T Swarr

Prenat Diagn· December 2025

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Differences in Prenatal and Postnatal Phenotypic Evaluations in Patients With Congenital Anomalies and Known Genetic Diagnoses.
Nicole Horton, Leandra Tolusso, Kimberly Widmeyer, Hua He, Daniel T Swarr

Prenat Diagn· September 2025

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Cell fate specification during respiratory development requires ARID1A-containing canonical BAF complex activity.
Hyunwook Lee, Abigail Jaquish, Sharlene Fernandes, Barbara Zhao, Amber Elitz, Daniel T Swarr

bioRxiv· June 2025

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PRDM3/16 regulate chromatin accessibility required for NKX2-1 mediated alveolar epithelial differentiation and function.
Hua He, Sheila M Bell, Ashley Kuenzi Davis, Shuyang Zhao, Anusha Sridharan, Daniel T Swarr

Nat Commun· September 2024

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PRDM3/16 Regulate Chromatin Accessibility Required for NKX2-1 Mediated Alveolar Epithelial Differentiation and Function.
Hua He, Sheila M Bell, Ashley Kuenzi Davis, Shuyang Zhao, Anusha Sridharan, Daniel T Swarr

bioRxiv· December 2023

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Twin-twin transfusion syndrome recipient with arterial calcification and heterozygous variant in ABCC6: Evidence of a gene-environment interaction?
Andrea Springman, Braxton Forde, Leandra Tolusso, Emily DeFranco, Daniel T Swarr

Prenat Diagn· July 2023

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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, Daniel T Swarr

JCI Insight· September 2022

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

J Pediatr· August 2022

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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, Daniel T Swarr

Elife· August 2022

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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

J Perinatol· May 2022

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

Clin Case Rep· December 2021

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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

Genet Med· May 2021

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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

J Pediatr· October 2019

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The long noncoding RNA Falcor regulates Foxa2 expression to maintain lung epithelial homeostasis and promote regeneration.
Daniel T Swarr, Michael Herriges, Shanru Li, Mike Morley, Sharlene Fernandes

Genes Dev· June 2019

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Novel Molecular and Phenotypic Insights into Congenital Lung Malformations.
Daniel T Swarr, William H Peranteau, Jennifer Pogoriler, David B Frank, N Scott Adzick

Am J Respir Crit Care Med· May 2018

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Systematic Review and Meta-analysis: Gene Association Studies in Neonatal Sepsis.
Lakshmi Srinivasan, Daniel T Swarr, Megha Sharma, C Michael Cotten, Haresh Kirpalani

Am J Perinatol· June 2017

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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.
Lisa R Young, Bruce C Trapnell, Kenneth D Mandl, Daniel T Swarr, Jennifer A Wambach

Ann Am Thorac Soc· December 2016

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Lung endoderm morphogenesis: gasping for form and function.
Daniel T Swarr, Edward E Morrisey

Annu Rev Cell Dev Biol· September 2016

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

Genes Dev· June 2014

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Expanding the differential diagnosis of fetal hydrops: an unusual prenatal presentation of megalencephaly-capillary malformation syndrome.
Daniel T Swarr, Nahla Khalek, James Treat, Margaret A Horton, Ghayda M Mirzaa

Prenat Diagn· October 2013

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Clinical features of three girls with mosaic genome-wide paternal uniparental isodisomy.
Jennifer M Kalish, Laura K Conlin, Tricia R Bhatti, Holly A Dubbs, Mary Catherine Harris, Daniel T Swarr

Am J Med Genet A· August 2013

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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, Daniel T Swarr

Hum Mutat· June 2013

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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) syndrome.
Jared Nathanson, Daniel T Swarr, Amihood Singer, Mochi Liu, Amy Chinn

Am J Med Genet A· March 2013

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Unusual cardiac "masses" in a newborn with infantile pompe disease.
Daniel T Swarr, Beth Kaufman, Mark A Fogel, Richard Finkel, Jaya Ganesh

JIMD Rep· February 2013

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

Curr Opin Allergy Clin Immunol· October 2010

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