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Locations

Languages Spoken

  • English
  • Hindi
  • Malay
  • Punjabi
  • Urdu

Education & Training

  • Fellowship Program, Medical Biochemical Genetics, 2018
    Johns Hopkins University School of Medicine
  • Fellowship Program, Medical Genetics Fellowship*, 2017
    Johns Hopkins University School of Medicine
  • Residency Program, Pediatrics, 2014
    Sinai Hospital of Baltimore
  • MBCHB, 2005
    University of Manchester

Board Certifications

  • American Board of Pediatrics
  • American Board of Med. Genetics/Clinical Genetics

National Provider ID: 1699069591


Biography

Tamanna Roshan Lal, M.B.Ch.B., is board-certified in pediatrics and general clinical genetics. She has a special interest in lysosomal storage diseases and the new developments of enzyme replacement therapy, orphan drugs and gene therapy.

Roshan Lal TR, Lopez G, Sidransky E. Glucocerebrosidase gene mutations and parkinsonism. Reference Module in Neuroscience and Biobehavioral Psychology. 2017.

Roshan Lal TR, Sidransky E. The spectrum of neurological manifestations associated with gaucher disease. Diseases. 2017;5(1):10.

Borger DK, McMahon B, Roshan Lal TR, Serra-Vinardell J, Aflaki E, Sidransky E. Induced pluripotent stem cell models of lysosomal storage disorders. Disease Models & Mechanisms2017;10(6):691-704.

Authored 2 chapters for the 5-minute Pediatric Consult Book, Walters Kluwer, 7th Edition, 2017.
─ Metabolic Diseases in Hypoglycemic Newborns.
─ Metabolic Diseases in Hyperammonemic Newborns.

Roshan Lal TR, Kliewer MA, Lopes T, et al. Cornelia de Lange Syndrome: Correlation of Brain MRI Findings with Behavioral Assessment. Am J Med Genet C Semin Med Genet. 2016;172(2):190-197.

Roshan Lal TR, Borger DK, Sidransky E. Once again, rare diseases provide a spotlight. Mol Genet Metab. 2016;118(1):1-2.

Appiah-Sakyi K, Ratti T (Roshan Lal TR). A survey of north-west England obstetric trainees on the management of major perineal trauma. The Internet Journal of Gynecology and Obstetrics. 2008;11(1).