We found 8 genetics specialists who accept Humana Simplicity HMO Open Access Silver 04/100 near Cincinnati, OH.
Dr. Taosheng Huang's medical specialty is genetics. He honors Health Net, Humana HMO, and Humana Bronze, in addition to other insurance carriers. He graduated from Fujian Medical University. Dr. Huang speaks Mandarin.
Dr. Robert Hopkin is a genetics specialist in Cincinnati, OH. Dr. Hopkin honors several insurance carriers, including Humana HMO, Humana Bronze, and Humana Catastrophic. He attended the University of Nevada School of Medicine and then went on to complete his residency at Phoenix Hospitals Affiliated Pediatric Program.
Dr. Donald Rucknagel's specialty is genetics. He is an in-network provider for several insurance carriers, including Humana HMO, Humana Bronze, and Humana Catastrophic. Dr. Rucknagel is a graduate of Washington University in St. Louis School of Medicine.
Dr. Thomas Burrow's area of specialization is genetics. Humana HMO, Humana Bronze, and Humana Catastrophic are among the insurance carriers that Dr. Burrow accepts. He is a graduate of the University of Arkansas for Medical Sciences College of Medicine.
Dr. Bradley Tinkle's area of specialization is genetics. He is a graduate of Indiana University School of Medicine. Dr. Tinkle is in-network for several insurance carriers, including Humana HMO, Humana Bronze, and Humana Catastrophic.
Dr. Elizabeth Schorry's area of specialization is genetics. Humana HMO, Humana Bronze, and Humana Catastrophic are among the insurance carriers that Dr. Schorry honors. Dr. Schorry studied medicine at the University of Michigan Medical School.
Dr. Derek Neilson is a genetics specialist. He is in-network for several insurance carriers, including Humana HMO, Humana Bronze, and Humana Catastrophic. Dr. Neilson is a graduate of Oregon Health & Science University School of Medicine.
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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.