We found 8 genetics specialists who accept Humana Simplicity HMO Open Access Silver 04/100 near Cincinnati, OH.
Dr. Taosheng Huang specializes in genetics and practices in Cincinnati, OH. Dr. Huang accepts Health Net, Humana HMO, and Humana Bronze, as well as other insurance carriers. He is a graduate of Fujian Medical University. He is conversant in Mandarin.
Dr. Robert Hopkin is a Cincinnati, OH physician who specializes in genetics. Dr. Hopkin takes Humana HMO, Humana Bronze, and Humana Catastrophic, in addition to other insurance carriers. He graduated from the University of Nevada School of Medicine. For his residency, Dr. Hopkin trained at Phoenix Hospitals Affiliated Pediatric Program.
Dr. Donald Rucknagel's area of specialization is genetics. Dr. Rucknagel takes Humana HMO, Humana Bronze, Humana Catastrophic, and more. He attended medical school at Washington University in St. Louis School of Medicine.
Dr. Thomas Burrow is a specialist in genetics. Dr. Burrow 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's area of specialization is genetics. He honors Humana HMO, Humana Bronze, Humana Catastrophic, and more. Dr. Tinkle attended medical school at Indiana University School of Medicine.
Dr. Elizabeth Schorry's area of specialization is genetics. She is an in-network provider for Humana HMO, Humana Bronze, Humana Catastrophic, and more. She is a graduate of the University of Michigan Medical School.
Dr. Derek Neilson is a medical specialist in genetics. He is an in-network provider for Humana HMO, Humana Bronze, and Humana Catastrophic, in addition to other insurance carriers. 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.