JessicaLeaPatrick-EsteveMD

PubMed

• 2 citations
  Parents' Perspectives on the Utility of Genomic Sequencing in the Neonatal Intensive Care Unit.
  Amy A Lemke, Michelle L Thompson, Emily C Gimpel, Katelyn C McNamara, Carla A Rich, Candice R Finnila, Meagan E Cochran, James M J Lawlor, Kelly M East, Kevin M Bowlin...> ;Journal of Personalized Medicine. 2023 Jun 21
• 1 citations
  Extracorporeal membrane oxygenation in the care of a preterm infant with COVID-19 infection: Case report.
  Jessica Patrick-Esteve, Christy Mumphrey, David Yu, Emily Masoumy, Jeremy Lawson, David Hebert, Brian Barkemeyer> ;Frontiers in Pediatrics. 2022 Jan 1
• 20 citations
  Genome sequencing as a first-line diagnostic test for hospitalized infants
  Kevin M. Bowling, Michelle L. Thompson, Candice R. Finnila, Susan M. Hiatt, Donald R. Latner, Michelle D. Amaral, James M.J. Lawlor, Kelly M. East, Meagan Cochran, Ver...> ;Genetics in Medicine. 2021 Nov 1
• A novel missense variant in CHD7, a rare cause of CHARGE syndrome.
  Peter Joslyn, Hannah Meddaugh, Jairo I. Torres, Jessica Patrick-Esteve, Staci Olister, Christy Mumphrey, Regina M. Zambrano> ;Clinical Dysmorphology. 2020 Jul 1
• 5 citations
  Neonatal Intensive Care Unit Boot Camp: A Preparatory Curriculum for Pediatric Residents.
  Jeffrey W. Surcouf, Christy Mumphrey, Brian M. Barkemeyer, Marlene Buis, Raegan W. Gupta, Staci Olister, Jessica Patrick-Esteve, Dana Rivera, Amy Zeringue, Sheila W. C...> ;Mededportal. 2018 Jun 1
• 13 citations
  RAF1 variants causing biventricular hypertrophic cardiomyopathy in two preterm infants: further phenotypic delineation and review of literature.
  Danielle Thompson, Jessica Patrick-Esteve, Jeffrey W. Surcouf, Dana Rivera, Bianca Castellanos, Pooja Desai, Christian Lilje, Michael Marble, Regina Zambrano> ;Clinical Dysmorphology. 2017 Oct 1
• Neonatal severe hyperparathyroidism caused by homozygous mutation in CASR: A rare cause of life-threatening hypercalcemia.
  Murphy, H.,Patrick, J.,Báez-Irizarry, E.,Lacassie, Y.,Gómez, R.,Vargas, A.,Barkemeyer, B.,Kanotra, S.,Zambrano, R. M.> ;Eur J Med Genet. 2016 Feb 09
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