Dr. DNA from ExpressGene offers comprehensive and affordable lab testing accessible to everyone, no prescription needed. Simply order a kit, collect a sample with an easy swab, and send it back. Your results will be securely delivered through a private digital portal, ensuring confidentiality and ease of access.
Express Gene Molecular Diagnostics Laboratory is a CLIA Certified Laboratory located in Miami, Florida. Our focus is genetic testing and we are offer a number of important genetic tests, including pharmacogenomics test. Pharmacogenetic (PGx) testing is a type of genetic test that assesses a patient’s risk of an adverse response or likelihood to respond to a given drug. This gives health care providers insight into what medications to use for a given condition. The PGx test allows physicians to make informed, science-based drug selection and to appropriately adjust the dosing.
Express Gene is also a biotechnology company focused on providing tools and services for clinical research applications of genomics. We provide to researchers around the world with services such as, microbiome sequencing, Exome-Seq, Methyl-Seq, ChIP-Seq, and 16s metagenomics. We offer whole genome sequencing to help you analyze a single cell or assemble and finish the genome of your organism of interest.
Unlock health insights with Express Gene’s genetic testing—your roadmap to personalized well-being awaits.
This panel investigates drug sensitivity and the way body react to various medications. This test determines which medications are most appropriate based on genetic build up of individuals.
Investigates the risk of early onset dementia and other neurological disorders in families
This panel identifies the risk of genetic factors for various cancers such as breast cancer, ovarian cancer, prostate cancer, and others that run in a family.
Maturity Onset Diabetic of the Young (MODY) is a group of disorders characterized by type I or type II diabetes that start at in the initial decades of life. This panel tests for genes involved in this disorder.
This panel investigates genetic variances related to autoimmune disorders, sarcoidosis, and inborn immunodeficiency.
DM is a group of metabolic disorders characterized by a high blood sugar level over a prolonged period of time . This panel tests for genes involved in this disorder.
The genes and mutations in this panel, investigate genetic susceptibility to COPD, Asthma, Interstitial Lung Disease, Cystic Fibrosis, Pneumonia, Sarcoidosis, and Mycobacterial Disease.
This panel checks for the likelihood of developing various retinopathies, leber congenital amaurosis, cataract, and glaucoma. Some patients with retinopathies may receive gene therapy based on the type of mutation identified.
This important prenatal test recommended for all pregnant ladies at 10 weeks of gestations. The NIPT test determining the risk that the fetus will be born with certain chromosomal abnormalities, such as Trisomy 21 (Down Syndrome), Trisomy 18, and Trisomy 13.
Tests all coding exons to identify causes of unidentified genetic conditions.
This panel investigates mutations as well as deletions and duplications in two genes related to breast cancer.
This panel investigates genes involved in hearing impairments. Hearing impairment can be deafness or partial hearing impairments.
Identifies if a healthy person is a carrier of genetic mutation and consequences such as disease later in life and the ability to pass to the next generation
This panel investigates the possibility and causes of metabolic diseases such as early infantile diabetes, liver enzyme processing problems, and maple syrup urine disorder (MSUD).
Used to determine the susceptibility of various cardiomyopathy and other cardiac related disorders.
This panel investigates the cause of various skin disorders such as atopy, psoriasis, butterfly disease, and eczema.
This panel investigates rare multi-systemic congenital or infantile disorders.
This panel investigates hereditary causes of intellectual disabilities in children and young adults.
Explores genetic causes of any hematological disorders such as Sickle-cell anemia and coagulopathies (bleeding disorders).
This panel investigates the cause of diseases related to mitochondrial chain reaction. Mitochondria are organelles that generate energy for all cellular activities.
This panel investigates disorders related to muscle and the neuromuscular system such as limb-girdle muscular dystrophy.
Examines 110 genes related to Autism
Used to determine the genetic/blood relationship between 2 or 3 people
Access gene lists, requisitions, and consent forms for a detailed understanding of our genetic tests. Download now.
9000 SW 152nd St Ste 209 Miami, FL 33157
info@expressgene.us
+1 (786) 250-3419