We found 70 genetics specialists near Washington, DC.
Dr. Andrea Gropman's medical specialty is neurodevelopmental disabilities and genetics. She is affiliated with Children's National Health System. She obtained her medical school training at the University of Massachusetts Medical School and performed her residency at George Washington University Medical Center and a hospital affiliated with Johns Hopkins University. Dr. Gropman takes Medicaid and Medicare insurance.
Clinical interests: Neurogenetics, w/sp Quals in Child Neur, Fragile X Syndrome
Dr. Melissa Fries practices maternal and fetal medicine (perinatology) and genetics. She graduated from Uniformed Services University of the Health Sciences, F. Edward Hébert School of Medicine and then she performed her residency at Wilford Hall Medical Center. Clinical interests for Dr. Fries include prenatal diagnosis. MAMSI, Blue Cross/Blue Shield, and Coventry are among the insurance carriers that Dr. Fries honors. She has received distinctions including Alpha Omega Alpha Honor Society, Uniformed Services University of the Health Sciences; APGO Outstanding Educator Award, Association of Professors of Gynecology and Obstetrics; and Outstanding Staff Educator, Keesler Medical Center. In addition to English, she speaks Spanish. Dr. Fries is professionally affiliated with MedStar Georgetown University Hospital. Dr. Fries is accepting new patients.
Clinical interests: Prenatal Diagnosis, Obstetrical Genetics
Dr. Kenneth Rosenbaum's area of specialization is pediatric genetics. In Dr. Rosenbaum's practice, he is particularly interested in down syndrome. He is professionally affiliated with Holy Cross Hospital, Children's National Health System, and Shady Grove Adventist Hospital. His education and training includes medical school at the University of Louisville School of Medicine and residency at Children's National Medical Center. Dr. Rosenbaum's average rating from his patients is 5.0 stars out of 5. He takes Medicaid and Medicare insurance. New patients are welcome to contact his office for an appointment.
Clinical interests: Down Syndrome, Skeletal Dysplasias
Dr. Kimberly Chapman is a pediatric genetics and clinical biochemical genetics specialist in Washington, DC. She is especially interested in genetic issues. Dr. Chapman accepts Medicaid and Medicare insurance. She graduated from the University of Nebraska College of Medicine. Her residency was performed at the University of Pittsburgh Medical Center (UPMC). In addition to English, Dr. Chapman (or staff) speaks Telephone Interpretation and Spanish. Her hospital/clinic affiliations include Holy Cross Hospital, Children's National Health System, and Inova Fairfax Hospital. She has an open panel.
Clinical interests: Pediatric Genetics
Dr. Kristina Cusmano-Ozog specializes in genetics. She is professionally affiliated with Children's National Health System and Lucile Packard Children's Hospital Stanford. Dr. Cusmano-Ozog graduated from the University of South Florida (USF) College of Medicine. For her professional training, Dr. Cusmano-Ozog completed residency programs at Stanford Hospital & Clinics and a hospital affiliated with the University of South Florida (USF). Dr. Cusmano-Ozog takes Medicaid insurance.
Dr. Pranoot Tanpaiboon works as a clinical biochemical geneticist. Areas of expertise for Dr. Tanpaiboon include lysosomal storage disease. She is in-network for Medicare insurance. Dr. Tanpaiboon is a graduate of ChiangMai University Faculty of Medicine. Her medical residency was performed at National Institutes of Health (NIH) and a hospital affiliated with ChiangMai University. Dr. Tanpaiboon is conversant in Thai. Her professional affiliations include Holy Cross Hospital, Children's National Health System, and Shady Grove Adventist Hospital. New patients are welcome to contact her office for an appointment.
Clinical interests: Lysosomal Storage Disorders, Pediatric Genetics
Dr. Marshall Summar is a specialist in genetics. Before performing his residency at Vanderbilt University Medical Center, Dr. Summar attended the University of Tennessee Health Science Center College of Medicine for medical school. In his practice, he is particularly interested in cleft lip and palate, down syndrome, and diaphragmatic hernia. Dr. Summar is affiliated with Children's National Health System.
Clinical interests: Angelman Syndrome, Biotinidase Deficiency, Birth Defects, Carpenter Syndrome, Cleft Lip/Cleft ... (Read more)
Dr. Amy Lewanda is a medical specialist in pediatric genetics. She is affiliated with Holy Cross Hospital, Inova Fair Oaks Hospital, and Children's National Health System. She accepts the following insurance: Medicaid and Medicare. Dr. Lewanda is open to new patients. Before completing her residency at The Mount Sinai Medical Center, New York, Dr. Lewanda attended medical school at Mount Sinai School of Medicine. Dr. Lewanda speaks Spanish.
Dr. Dina Zand's specialty is genetics. She studied medicine at Northwestern University, Feinberg School of Medicine. For her residency, Dr. Zand trained at St. Louis Children's Hospital. In addition to English, Dr. Zand speaks Spanish. Dr. Zand's professional affiliations include Children's National Health System and Shady Grove Adventist Hospital.
Clinical interests: Skeletal Dysplasias
Dr. Nicholas Ah Mew is a physician who specializes in genetics. Before completing his residency at a hospital affiliated with McGill University, Dr. Ah Mew attended medical school at McGill University Faculty of Medicine. Dr. Ah Mew honors Medicaid and Medicare insurance. He is conversant in French. He is affiliated with Children's National Health System.
Dr. Susan Black is a genetics specialist. Dr. Black attended McGill University Faculty of Medicine for medical school and subsequently trained at Ochsner Medical Center for residency. She takes MAMSI, MultiPlan, Blue Cross/Blue Shield, and more. She has received professional recognition including the following: the University Entrance Scholar; McGill Red Wing Honor Society; and J. F. Williams Prize in Clinical Medicine. Dr. Black (or staff) is conversant in Mandarin, Filipino, and Arabic.
Dr. Gregory Ray practices molecular genetic pathology. Dr. Ray is professionally affiliated with Virginia Hospital Center. He attended Duke University School of Medicine and subsequently trained at Duke University Medical Center for residency. He honors Medicare insurance.
Dr. Ayne Iafolla specializes in pediatric genetics and neonatology. Dr. Iafolla is in-network for Medicaid insurance. Before performing her residency at Dartmouth-Hitchcock Medical Center, Dr. Iafolla attended the University of Pittsburgh School of Medicine. She is affiliated with Western Maryland Health System, Shady Grove Adventist Hospital, and Washington Adventist Hospital.
Dr. Eyby Leon Janampa's specialty is clinical biochemical genetics. Her areas of expertise include down syndrome. Before completing her residency at Boston Medical Center, Harlem Hospital Center, and a hospital affiliated with the University of Utah, Dr. Leon Janampa attended medical school at Cayetano Heredia University. Dr. Leon Janampa speaks Spanish. She is professionally affiliated with Children's National Health System and Inova Fairfax Hospital.
Clinical interests: Ambiguous Genitalia, Disorders of Sex Development, Down Syndrome
Dr. Celeste Riley is a specialist in molecular genetic pathology, pediatric pathology, and cytopathology. Dr. Riley (or staff) speaks the following languages: Spanish, French, and Cantonese. Dr. Riley is a graduate of Penn State College of Medicine. She is an in-network provider for Medicare insurance.
Dr. Brendan Lanpher's specialty is clinical biochemical genetics. He is affiliated with Inova Fairfax Hospital and Mayo Clinic. Dr. Lanpher is an in-network provider for Medicaid and Medicare insurance. He attended the University of Virginia School of Medicine and then went on to complete his residency at Mayo Clinic and a hospital affiliated with Baylor College of Medicine. He speaks Spanish.
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- Single gene disorders, the result of a single mutated gene. Examples include Huntington’s disease, which causes jerky movements, and sickle-cell anemia, where red blood cells have an abnormal, rigid shape.
- Inborn metabolic disorders, which are a specific type of single gene disorder that results in abnormalities in the way the body chemically processes proteins, carbohydrates or fats. Some examples are Urea Cycle Disorder (where ammonia builds up in the body) and Gaucher’s Disease (where fatty substances build up in cells and organs).
- Chromosomal disorders, where gene-carrying chromosomes do not pair up correctly or are missing. Some examples are Klinefelter Syndrome, a sex-chromosome disorder, and Down Syndrome.
- Congenital abnormalities (commonly known as birth defects), which can be caused by genetic abnormalities. They also can happen because of illness or environmental exposure during pregnancy (such as with rubella), or for unknown reasons.
- Other common diseases that have hereditary traits, such diabetes, autism, and some types of cancer.
- Clinical Genetics: This overarching branch of medical genetics deals with the treatment and management of hereditary diseases.
- Biomechanical Genetics: This branch deals with metabolic disorders, such as galactosemia and phenylketonuria.
- Cytogenetics: This specialty deals with chromosomes and their associated diseases, as well as testing their structure and number.
- Molecular Genetics: This specialty focuses on DNA, interpreting DNA sequencing and other tests, and relating DNA information to specific diseases.