Dr. Gabriel M Cohn MD
Geneticist | Clinical Genetics (M.D.)
759 CHESTNUT ST SPRINGFIELD MA, 01199About
Dr. Gabriel Cohn practices Genetic Medicine in SPRINGFIELD, MA. As a geneticist, Dr. Cohn performs experiments and analyzes data to interpret the inheritance of different traits in patients. A geneticist evaluates, diagnoses, and manages patients with hereditary conditions or congenital malformations, genetic risk calculations, and mutation analysis. Dr. Cohn carries out studies, tests, and counsels patients with genetic diseases.
Education and Training
Suny-Hlth Sci Ctr At Syracuse, Coll of Med, Syracuse Ny 1986
Upstate Medical University/ College of Health Professions 1986
Board Certification
Medical GeneticsAmerican Board of Medical GeneticsABMG
Provider Details
Expert Publications
Data provided by the National Library of Medicine- Spontaneous conversion to estrogen receptor expression by the human breast epithelial cell line, MCF-10A.
- An antibody assay predictive of BRCA1 mutations in ovarian tumors and normal tissue.
- Immunohistochemical analysis of BRCA2 expression in normal human buccal cells.
- A rapid immunoassay predicts BRCA1 and BRCA2 mutations in buccal cells.
- Differences in clinical expression of hypertrophic cardiomyopathy associated with two distinct mutations in the beta-myosin heavy chain gene. A 908Leu----Val mutation and a 403Arg----Gln mutation.
- Efficacy of rectal misoprostol as second-line therapy for the treatment of primary postpartum hemorrhage.
- Osteopathies encountered in the endocrine clinic.
- Testosterone therapy in a case of fibrous dysplasia of bone with hypogenitalism.
- The oral administration of methyl testosterone in a male castrate.
- Testosterone therapy in a case of fibrous dysplasia of bone with hypogenitalism.
- Phase 1/2 and extension study of velaglucerase alfa replacement therapy in adults with type 1 Gaucher disease: 48-month experience.
- Testosterone in a case of polyostotic fibrous dysplasia.
- Early achievement and maintenance of the therapeutic goals using velaglucerase alfa in type 1 Gaucher disease.
- Significant and continuous improvement in bone mineral density among type 1 Gaucher disease patients treated with velaglucerase alfa: 69-month experience, including dose reduction.
- Development of a mnemonic screening tool for identifying subjects with Hunter syndrome.
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Nearest Hospitals
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759 CHESTNUT STREET SPRINGFIELD MA 1199SHRINERS' HOSPITAL FOR CHILDREN (THE)l
516 CAREW STREET SPRINGFIELD MA 1104