Francis White

St. Louis Children's Hospital — United States

Medicine · Health Sciences

35h-index4.7kcitations94works0.02yr avg
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Research Topics

Neonatal Respiratory Health Research(16), Pediatric Hepatobiliary Diseases and Treatments(10), Congenital Diaphragmatic Hernia Studies(9), Gallbladder and Bile Duct Disorders(6), Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis(6)

Publications92 total

Lentiviral-mediated gene complementation rescues pathogenic <i>ABCA3</i> variants
2025Open Access
Yolk Sac Tumor of the Liver: An Important Differential for Liver Mass with Elevated Serum Alpha-Fetoprotein in the Pediatric Population
Fetal and Pediatric Pathology·2025
Contributors
Elsevier eBooks·2024Open Access
Lung Neoplasms in Infants and Children
Elsevier eBooks·2024
Homozygous, Intragenic Tandem Duplication of <i>SFTPB</i> Causes Neonatal Respiratory Failure
American Journal of Respiratory Cell and Molecular Biology·2023· 2 citedOpen Access
Lethal neonatal respiratory failure due to biallelic variants in BBS1 and monoallelic variant in TTC21B
Pediatric Nephrology·2022· 3 citedOpen Access
Lysoptosis is an evolutionarily conserved cell death pathway moderated by intracellular serpins
Communications Biology·2022· 29 citedOpen Access
The common ABCA3<sup>E292V</sup> variant disrupts AT2 cell quality control and increases susceptibility to lung injury and aberrant remodeling
American Journal of Physiology-Lung Cellular and Molecular Physiology·2021· 30 citedOpen Access
Biallelic <scp><i>ASCC1</i></scp> variants including a novel intronic variant result in expanded phenotypic spectrum of spinal muscular atrophy with congenital bone fractures 2 (<scp>SMABF2</scp>)
American Journal of Medical Genetics Part A·2021· 8 citedOpen Access
Functional Genomics of <i>ABCA3</i> Variants
American Journal of Respiratory Cell and Molecular Biology·2020· 27 citedOpen Access
Functional characterization of four ATP‐binding cassette transporter A3 gene (<i>ABCA3</i>) variants
Human Mutation·2020· 18 citedOpen Access
Phenotypic expansion of <i>KMT2D‐</i>related disorder: Beyond Kabuki syndrome
American Journal of Medical Genetics Part A·2020· 36 citedOpen Access
Inflammation, Active Fibroplasia, and End-stage Fibrosis in 172 Biliary Atresia Remnants Correlate Poorly With Age at Kasai Portoenterostomy, Visceral Heterotaxy, and Outcome
2018
Lung Neoplasms in Infants and Children
Elsevier eBooks·2018
Contributors
Elsevier eBooks·2018
Infants with Atypical Presentations of Alveolar Capillary Dysplasia with Misalignment of the Pulmonary Veins Who Underwent Bilateral Lung Transplantation
The Journal of Pediatrics·2017· 62 citedOpen Access
Differentiation of Human Pluripotent Stem Cells into Functional Lung Alveolar Epithelial Cells
Cell stem cell·2017· 573 citedOpen Access
Hepatic Hilar Lymph Node Reactivity at Kasai Portoenterostomy for Biliary Atresia: Correlations With Age, Outcome, and Histology of Proximal Biliary Remnant
Pediatric and Developmental Pathology·2017· 16 citedOpen Access
Key Histopathologic Features of Liver Biopsies That Distinguish Biliary Atresia From Other Causes of Infantile Cholestasis and Their Correlation With Outcome
The American Journal of Surgical Pathology·2016· 126 citedOpen Access
The role of post-mortem MRI in the neonatal intensive care unit
Journal of Perinatology·2016· 15 citedOpen Access
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Frequent Co-authors

F. Sessions Cole(9), Jennifer Wambach(8), Aaron Hamvas(8), Daniel Wegner(6), Gail Deutsch(5), Lawrence M. Nogee(5), Susan E. Wert(5), Hillary B. Heins(4), Megan K. Dishop(4), Jeffrey A. Whitsett(3), Michael F. Beers(3), Lisa R. Young(3), Robin R. Deterding(3), Claire Langston(3), Mary M. Davis(3), Csaba Galambos(3), Charles B. Huddleston(3), Stuart C. Sweet(3), Ping Yang(3), Dorothy K. Grange(3)