Gerald Feldman, MD, PhD

Gerald Feldman, MD, PhD
Professor of Molecular Medicine and Genetics, Pathology and Pediatrics
Division Director for Clinical Genetics, CMMG
Director, Clinical Genetics Services
Medical Director, Division of Laboratory Genetics and Molecular Pathology, Detroit Medical Center-University Laboratories
Scott Hall, Rm 2375
540 E. Canfield Avenue
Detroit, MI 48201
313-577-6298
gfeldman@med.wayne.edu

Education

PhD: Virginia Commonwealth University/Medical College of Virginia, 1982
MD:  Virginia Commonwealth University/Medical College of Virginia, 1984

Research Focus

Use of molecular technologies in the diagnosis of genetic diseases, clinical genetics, and dysmorphology; educational programs in medical genetics residency training, Newborn screening and inborn errors of metabolism

Recent Publications

Abdulfatah E, Wakeling E, Sakr S, Al-Obaidy K, Bandyopadhyay S, Morris R, Feldman G and Ali-Fehmi R.  Molecular classification of endometrial carcinoma applied to endometrial biopsy specimens: towards early personalized patient management.  Gynecol Oncol. 2019 Jun 24. pii: S0090-8258(19)31323-X. doi: 10.1016/j.ygyno.2019.06.012. [Epub ahead of print]

Fabie, NAV, Pappas, KB and Feldman, GL.  The current state of newborn screening in the United States.  Pediatr Clin N Am 66 (2019): 369–386.  https://doi.org/10.1016/j.pcl.2018.12.007

Majumdar R, Yori A, Rush P, Raymond K; Gavrilov D, Tortorelli S, Matern D, Rinaldo P, Feldman GL, and Oglesbee D. Allelic Spectrum of Formiminotransferase-Cyclodeaminase Gene Variants in Individuals with Formiminoglutamic Aciduria.   Molecular Genetics and Genomic Medicine.  doi: 10.1002/mgg3.333.   2017. 

Putra M, Idler J, Dai J, Blitzer MG, Feldman GL and Sokol, RJ.  Medical Genetics and Genomics Training in Obstetrics and Gynecology Residencies:  Are We Ready for The Future?  J Assist Reprod Genet. 2018 Jan;35(1):3-16. doi: 10.1007/s10815-017-1039-7. Epub 2017

Smith J, Kean V, Bianchi DW, Feldman GL, Petrucelli N, Simon M and Gonik B.  Cell-free DNA Results Lead to Unexpected Diagnosis. Clin Case Rep. 2017 Aug; 5(8): 1323–1326; doi: 10.1002/ccr3.1051. 

Thakur M, Feldman GL and Puscheck EE.  Primary ovarian insufficiency in classic galactosemia: Current understanding and future research opportunities.  Journal of Assisted Reproduction and Genetics.  J Assist Reprod Genet. 2018 Jan;35(1):3-16. doi: 10.1007/s10815-017-1039-7. Epub 2017 Sep 20

Korf BR, Blitzer MG, Demmer LA, Feldman GL and Watson MS.  Report on the Banbury Summit Meeting on Medical Genetics Training in the Genomic Era, February 23-26, 2014.  Genetics in Medicine doi:10.1038/gim.2017.38.  [Epub ahead of print June 22, 2017]. 

Bowdin S, Gilbert A, Bedoukian E, Carew C, Adam, MP, Belmont J, Bernhardt, B, Biesecker L,  Bjornsson, HT, Blitzer M, D’Alessandro L, Deardorff, MA, Demmer, L, Elliott A, Feldman GL, Glass IA,  Herman, G, Hindorff, L, Hisama F, Hudgins L, Innes AM, Jackson, L, Jarvik G, Kim R, Korf  B, Ledbetter DH, Li M, Liston, E, Marshall C, Medne L, Meyn MS, Monfared N, Morton C, Mulvihill JJ, Plon SE, Rehm H, Roberts A, Shuman C, Spinner NB, Stavropoulos, DJ, Valverde K, Waggoner DJ, Wilkens A, Cohn RD and Krantz ID.  Recommendations for the Integration of Genomics into Medical Practice.  Genetics in Medicine 2016 May 12. doi: 10.1038/gim.2016.17. [Epub ahead of print]

Bentler K, Zhai S, Elsbecker SA, Arnold GL, Burton BK, Vockley J, Cameron CA, Hiner SJ, Edick MJ, Berry SA and Inborn Errors of Metabolism Collaborative.  221 Newborn-Screened Neonates with Medium Chain Acyl CoA Dehydrogenase Deficiency:  Findings from the Inborn Errors of Metabolism Collaborative.  Molecular Genetics and Metabolism 2016. 119:75-82 (doi.org/10.1016/j.ymgme.2016.07.002).