We found 8 genetics specialists who accept Humana Simplicity near Cincinnati, OH.
Dr. Taosheng Huang specializes in genetics. He honors Health Net, Humana HMO, Humana Bronze, and more. He studied medicine at Fujian Medical University. In addition to English, Dr. Huang speaks Mandarin.
Dr. Robert Hopkin's specialty is genetics. Dr. Hopkin is in-network for Humana HMO, Humana Bronze, and Humana Catastrophic, in addition to other insurance carriers. After attending the University of Nevada School of Medicine, he completed his residency training at Phoenix Hospitals Affiliated Pediatric Program.
Dr. Donald Rucknagel is a genetics specialist. He is in-network for Humana HMO, Humana Bronze, Humana Catastrophic, and more. He studied medicine at Washington University in St. Louis School of Medicine.
Dr. Thomas Burrow is a physician who specializes in genetics. He accepts Humana HMO, Humana Bronze, and Humana Catastrophic, in addition to other insurance carriers. He graduated from the University of Arkansas for Medical Sciences College of Medicine.
Dr. Bradley Tinkle practices genetics. He graduated from Indiana University School of Medicine. Humana HMO, Humana Bronze, and Humana Catastrophic are among the insurance carriers that Dr. Tinkle takes.
Dr. Elizabeth Schorry sees patients in Cincinnati, OH. Her medical specialty is genetics. She studied medicine at the University of Michigan Medical School. Dr. Schorry honors several insurance carriers, including Humana HMO, Humana Bronze, and Humana Catastrophic.
Dr. Derek Neilson's medical specialty is genetics. He graduated from Oregon Health & Science University School of Medicine. Humana HMO, Humana Bronze, and Humana Catastrophic are among the insurance carriers that Dr. Neilson honors.
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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.