26744-Durbin, Matthew
Faculty

Matthew D. Durbin, MD

Assistant Professor of Clinical Pediatrics

Bio

Dr. Durbin is an Assistant Professor of Clinical Pediatrics at Indiana University School of Medicine.  He received his undergraduate degree from Indiana University and did his medical training at Wright State University. After medical school, Dr. Durbin completed a residency in pediatrics at the Loyola University Chicago and a fellowship in Neonatal-Perinatal Medicine at Vanderbilt University in Nashville.  He is an attending neonatologist providing clinical service in the ICU and CVICU at the Riley Hospital for Children, Eskenazi Hospital, and St. Francis Hospital in Indianapolis.  He is also a basic scientist at the Wells Center for Pediatric Research, focusing on the genomics and developmental defects leading to congenital heart disease

 

Key Publications

1)  Denver D, Feinberg S, Steding C, Durbin M, and  Lynch, M.  The relative roles of three DNA repair pathways in preventing Caenorhabditis elegans mutation accumulation. Genetics 174.1 (2006): 57-65.

 

 2)  Michail S, Durbin M, Turner D, Griffiths A, Mack D, Hyams J, Leleiko N, Kenche H, Stolfi A, Wine E. Alterations in the gut microbiome of children with severe ulcerative colitis. Inflammatory Bowel Diseases 18.10 (2012): 1799-1808.

 

 3)  Durbin, M. D., Cadar, A. G., Williams, C. H., Guo, Y., Bichell, D. P., Su, Y. R., & Hong, C. C. (2017). Hypoplastic Left Heart Syndrome Sequencing Reveals a Novel NOTCH1 Mutation in a Family with Single Ventricle Defects. Pediatric Cardiology, 1-9.

 

4)  Cadar, A. G.*, Feaster, T. K.*, Durbin, M. D.*, & Hong, C. C. (2017). Production of Single Contracting Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes: Matrigel Mattress Technique. Current Protocols in Stem Cell Biology, 4A-14.  *Authors contributed equally to publication.


Titles & Appointments

  • Assistant Professor of Clinical Pediatrics
  • Education
    2016 FEL Vanderbilt University Medical Center
    2013 RES Loyola University Medical Center
    2010 MD Wright State University
    2006 BA&BS Indiana University
  • Research

    Congenital heart disease is the most common birth defect, and a leading cause of death in the newborn period, yet etiology remains mostly unknown. During Neonatology Fellowship he used next generation sequencing and disease modeling with patient derived induced pluripotent stem cells to study the genetics and mechanism of congenital heart disease. After Fellowship Dr. Durbin joined the faculty at Indiana University and the lab of Dr. Stephanie Ware. He is using genomics, gene editing, animal models, and cell culture models to elucidate the developmental pathways and molecular mechanisms altered in structural heart disease. He is currently exploring the role of a gene called SHROOM3 in structural heart disease. He is also exploring the optimal clinical evaluation for newborns with heart disease in the ICU, including diagnostic testing using next generation sequencing, and whole exome sequencing.

  • Professional Organizations
    American Academy of Pediatrics
    Society for Pediatric Research
  • Board Certifications
    American Board of Pediatrics - Pediatrics
  • Clinical Interests

    Pediatrics, Neonatal-Perinatal Medicine, Congenital Heart Disease

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