
Jeff Mark Milunsky MD
Clinical Genetics, Clinical Molecular Genetics
Co-Director, Center for Human Genetics
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840 Memorial DrSuite 101Cambridge, MA 02139
Phone+1 617-492-7083
Fax+1 617-492-7092
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Summary
- Dr. Jeff Milunsky is a medical geneticist based in Cambridge, MA, specializing in clinical genetics and clinical molecular genetics. He completed his medical training at the Boston University School of Medicine in 1992 and pursued a residency in pediatrics at Tufts Medical Center until 1995, followed by fellowships in clinical genetics and clinical molecular genetics at Boston University School of Medicine. Dr. Milunsky has expertise in evaluating the genetic etiology of autism/intellectual disability/congenital anomalies and his research is well-documented with multiple publications. Notable works include studies on microdeletion syndromes,Waardenburg syndrome, BOF syndrome , Ladd syndrome, Snijders Blok-Campeau syndrome, and Coffin-Siris syndrome, with several of his papers cited extensively in related research. He co-directs the Center for Human Genetics. One of his main clinical interests is in the diagnosis and management of connective tissue disorders.
Education & Training
Boston Medical CenterMedical Genetics, 1995 - 1998
Tufts Medical CenterResidency, Pediatrics, 1992 - 1995
Boston University School of MedicineClass of 1992
Certifications & Licensure
MA State Medical License 1995 - 2027
American Board of Medical Genetics and Genomics Clinical Genetics and Genomics
American Board of Medical Genetics and Genomics Clinical Molecular Genetics and Genomics
Publications & Presentations
PubMed
- Shared autonomic phenotype of long COVID and myalgic encephalomyelitis/chronic fatigue syndrome.Peter Novak, David M Systrom, Alexandra Witte, Sadie P Marciano, Donna Felsenstein
Plos One. 2026-01-01 - Abdominal Compression Syndromes in the Hypermobile Ehlers-Danlos Syndrome.Aubrey Milunsky, Jeff M Milunsky, Richard Hsu
American Journal of Medical Genetics. Part A. 2025-12-01 - Correction to: A contiguous microdeletion syndrome at Xp22.13 with non-obstructive azoospermia and congenital cataracts.Aubrey Milunsky, Jeff M. Milunsky, Weilai Dong, Hayk Hovhannisyan, Robert D. Oates
Journal of Assisted Reproduction and Genetics. 2021-06-19
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