We found 8 genetics specialists who accept Humana Simplicity near Cincinnati, OH.
Dr. Taosheng Huang is a genetics specialist in Cincinnati, OH. In addition to English, Dr. Huang speaks Mandarin. He attended medical school at Fujian Medical University. He is an in-network provider for Health Net, Humana HMO, and Humana Bronze, as well as other insurance carriers.
Dr. Robert Hopkin works as a genetics specialist in Cincinnati, OH. Dr. Hopkin takes Humana HMO, Humana Bronze, Humana Catastrophic, and more. He attended the University of Nevada School of Medicine and subsequently trained at Phoenix Hospitals Affiliated Pediatric Program for residency.
Dr. Donald Rucknagel is a specialist in genetics. He graduated from Washington University in St. Louis School of Medicine. Dr. Rucknagel honors several insurance carriers, including Humana HMO, Humana Bronze, and Humana Catastrophic.
Dr. Thomas Burrow is a physician who specializes in genetics. He is an in-network provider for several insurance carriers, including Humana HMO, Humana Bronze, and Humana Catastrophic. He studied medicine at the University of Arkansas for Medical Sciences College of Medicine.
Dr. Bradley Tinkle's area of specialization is genetics. He studied medicine at Indiana University School of Medicine. He accepts Humana HMO, Humana Bronze, and Humana Catastrophic, in addition to other insurance carriers.
Dr. Elizabeth Schorry is a genetics specialist in Cincinnati, OH. Humana HMO, Humana Bronze, and Humana Catastrophic are among the insurance carriers that Dr. Schorry honors. She attended medical school at the University of Michigan Medical School.
Dr. Derek Neilson is a genetics specialist in Cincinnati, OH. He accepts Humana HMO, Humana Bronze, Humana Catastrophic, and more. 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.