Henry Joel Mroczkowski, MD, PhD

Assistant Professor
Department of Pediatrics
Division of Medical Genetics and Genomics

Office: 49 N. DUNLAP FACILITY OFFICE BUILDING
SUITE 144
MEMPHIS TN 38105
Tel: (901) 287-6472
hmroczko@uthsc.edu

Research Description

 Study of the underlying metabolic and immunological mechanism of genetic disorders related to fatty acid oxidation and aging.  Previous research experience in bone metabolism as related to osteoporosis and bone mineral density.

Research Interest/Specialty

ImmunoMetabolics of Fatty Acid Oxidation Disorders

Research Keywords

Fatty Acid Oxidation Disorders

Genetics and Genomics

Bone Metabolism

Metabolism

Aging

Clinical Care Specialty/Interest

Medical Genetics and Genomics

Inborn Errors of Metabolism

Publications

  1. Mroczkowski, HJ, Arnold, G, Schneck, FX, Rajkovic, A, Yatsenko, SA. Interstitial 10p11.23-p12.1 microdeletions associated with developmental delay, craniofacial abnormalities, and cryptorchidism. Am J Med Genet A, 164A (10), 2623-6, 2014.
  2. Buterbaugh, A, Mroczkowski, HJ, Shankar, SP, Visootsak, J. Contribution of Family History in Co-occurring Down Syndrome and Ehlers-Danlos Syndrome. Ann Paediatr Rheumatol, 2 (4), 165-167, 2013.
  3. Parsons, CA, Mroczkowski, HJ, McGuigan, FE, Albagha, OM, Manolagas, S, Reid, DM, Ralston, SH, Shmookler Reis, RJ. Interspecies synteny mapping identifies a quantitative trait locus for bone mineral density on human chromosome Xp22. Hum Mol Genet, 14 (21), 3141-8, 2005.