Bio

Clinical Focus


  • Clinical Genetics

Academic Appointments


Professional Education


  • Board Certification: Pediatrics, American Board of Pediatrics (2018)
  • Board Certification, American Board of Pediatrics, Pediatrics (2018)
  • Board Certification: Clinical Genetics, American Board of Medical Genetics and Genomics (2017)
  • Fellowship:Children's Hospital of Philadelphia (2017) PA
  • Residency:Children's Hospital of Philadelphia (2016) PA
  • Internship:Children's Hospital of Philadelphia (2014) PA
  • Medical Education:Jefferson Medical College (2013) PA

Publications

All Publications


  • ClinPhen extracts and prioritizes patient phenotypes directly from medical records to expedite genetic disease diagnosis GENETICS IN MEDICINE Deisseroth, C. A., Birgmeier, J., Bodle, E. E., Kohler, J. N., Matalon, D. R., Nazarenko, Y., Genetti, C. A., Brownstein, C. A., Schmitz-Abe, K., Schoch, K., Cope, H., Signer, R., Network, U., Martinez-Agosto, J. A., Shashi, V., Beggs, A. H., Wheeler, M. T., Bernstein, J. A., Bejerano, G. 2019; 21 (7): 1585–93
  • LOCALIZING NEUROLOGIC FEATURES AT PRESENTATION OF VLCAD DEFICIENCY Leahy, P., Matalon, D., Ruzhnikov, M., Cowan, T., Enns, G. ACADEMIC PRESS INC ELSEVIER SCIENCE. 2019: 282
  • Paraspinal Atrophy Suggesting Underlying Genetic Etiology Schwartz, D., Fong, J., Matalon, D., Wong, J., Greene, M. LIPPINCOTT WILLIAMS & WILKINS. 2019
  • LOCALIZING NEUROLOGIC FEATURES AT PRESENTATION OF VLCAD DEFICIENCY Leahy, P., Matalon, D., Ruzhnikov, M., Cowan, T., Enns, G. ACADEMIC PRESS INC ELSEVIER SCIENCE. 2019: 311
  • THE DIAGNOSIS AND NATURAL HISTORY OF THE MUCOPOLYSACCHARIDOSIS IVA IN ONE FAMILY Matalon, D. R., Dougherty, P., Lulis, L., Medne, L., Krantz, I., Yum, S., Ficicioglu, C. ACADEMIC PRESS INC ELSEVIER SCIENCE. 2018: 249–50
  • The diagnosis and natural history of mucopolysaccharidosis type IVA in one family Matalon, D., Dougherty, P., Lulis, L., Medne, L., Krantz, I., Yum, S., Ficicioglu, C. ACADEMIC PRESS INC ELSEVIER SCIENCE. 2018: S92
  • ClinPhen extracts and prioritizes patient phenotypes directly from medical records to expedite genetic disease diagnosis. Genetics in medicine : official journal of the American College of Medical Genetics Deisseroth, C. A., Birgmeier, J., Bodle, E. E., Kohler, J. N., Matalon, D. R., Nazarenko, Y., Genetti, C. A., Brownstein, C. A., Schmitz-Abe, K., Schoch, K., Cope, H., Signer, R., Martinez-Agosto, J. A., Shashi, V., Beggs, A. H., Wheeler, M. T., Bernstein, J. A., Bejerano, G. 2018

    Abstract

    Diagnosing monogenic diseases facilitates optimal care, but can involve the manual evaluation of hundreds of genetic variants per case. Computational tools like Phrank expedite this process by ranking all candidate genes by their ability to explain the patient's phenotypes. To use these tools, busy clinicians must manually encode patient phenotypes from lengthy clinical notes. With 100 million human genomes estimated to be sequenced by 2025, a fast alternative to manual phenotype extraction from clinical notes will become necessary.We introduce ClinPhen, a fast, high-accuracy tool that automatically converts clinical notes into a prioritized list of patient phenotypes using Human Phenotype Ontology (HPO) terms.ClinPhen shows superior accuracy and 20× speedup over existing phenotype extractors, and its novel phenotype prioritization scheme improves the performance of gene-ranking tools.While a dedicated clinician can process 200 patient records in a 40-hour workweek, ClinPhen does the same in 10 minutes. Compared with manual phenotype extraction, ClinPhen saves an additional 3-5 hours per Mendelian disease diagnosis. Providers can now add ClinPhen's output to each summary note attached to a filled testing laboratory request form. ClinPhen makes a substantial contribution to improvements in efficiency critically needed to meet the surging demand for clinical diagnostic sequencing.

    View details for PubMedID 30514889