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Monday 09:00 - 17:00 Tuesday 09:00 - 17:00 Wednesday 09:00 - 17:00 Thursday 09:00 - 17:00 Friday 09:00 - 17:00 Saturday 10:00 - 14:00

Onco-genomics

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Nigeria
Alimosho
Onco-genomics

Your future. Your family's future. We're here to illuminate the path.

We specialize in advanced genetic testing across various life stages, ensuring your family’s health and well-being are always at the forefront.

04/07/2025

Embarking on the journey of pregnancy brings so much joy and anticipation! Understanding your baby's health is a priority, and Non-Invasive Prenatal Testing (NIPT) offers valuable insights with a simple blood test from the mother. The main reason for NIPT is to assess the risk of common fetal chromosomal abnormalities like Trisomy 21 (Down Syndrome), Trisomy 18 (Edwards Syndrome), and Trisomy 13 (Patau Syndrome).

It can also screen for certain s*x chromosome aneuploidies. This non-invasive approach means no risk of miscarriage, unlike traditional diagnostic tests, and it can be performed as early as 10 weeks of pregnancy.

02/07/2025

We don’t just test—we interpret and empower. Our team of clinical genetics experts goes beyond delivering lab results by translating complex genetic data into clear, personalized, and actionable insights you can understand and use. Genetic information can be overwhelming, but with expert interpretation, it becomes a powerful tool for making informed health decisions—whether it’s understanding your risk for inherited conditions, optimizing medication through pharmacogenomics, or planning for a healthy pregnancy. We guide you every step of the way, turning raw data into meaningful answers, so you’re never left wondering what your results mean or what to do next. Because knowledge is powerful—when it’s made clear.

01/07/2025

May this radiant month infuse you with a boundless wellspring of energy, propelling you towards your aspirations with grace and determination. Expect beautiful moments to blossom, unexpected joys to unfurl, and every step to be a testament to your evolving strength and resilience.

Happy New Month Everyone.

30/06/2025

Our broad-scale genetic screening programs are designed to do more than help individuals—they empower entire populations. By identifying people who carry genetic risks for conditions such as cancer, heart disease, neurological disorders, and other inherited illnesses, these programs enable communities to move from reactive treatment to proactive prevention. Early identification of genetic risk factors means earlier interventions, targeted surveillance, and lifestyle changes that can significantly reduce the burden of disease. Whether implemented through public health initiatives, employee wellness programs, or community-based outreach, population-level genetic screening helps create a healthier, more informed society—one person, one family, one community at a time.

27/06/2025

If cancer runs in your family, don’t wait for symptoms to appear—genetic screening can help you stay one step ahead. Our hereditary cancer screening tests are designed to detect inherited genetic mutations—such as those in the BRCA1, BRCA2, and other high-risk genes—before cancer has a chance to develop. These mutations can significantly increase your lifetime risk of cancers like breast, ovarian, colorectal, prostate, pancreatic, and more. By identifying your risk early, you can take preventive steps such as enhanced monitoring, lifestyle changes, and risk-reducing strategies tailored specifically to you. Knowledge of your genetic risk doesn’t just help you—it can also protect your children, siblings, and other family members. When it comes to cancer, early awareness can lead to life-saving action.

25/06/2025

Why guess when it comes to your medications? Pharmacogenomic testing takes the uncertainty out of treatment by analyzing how your genes affect the way your body responds to specific drugs. Everyone’s genetic makeup is unique—and that means medications don’t work the same for everyone. This advanced test helps identify which medications are likely to be most effective for you, and which may cause side effects or be less beneficial. From pain management and mental health medications to cardiovascular and cancer treatments, pharmacogenomics empowers your doctor to prescribe the right drug at the right dose—personalized to your DNA. It’s precision medicine at its best, improving outcomes, reducing trial and error, and helping you feel better, faster.

23/06/2025

You could carry a serious genetic condition without ever showing symptoms—and without even knowing it. That’s why carrier screening is such an important part of responsible family planning. This simple genetic test checks whether you or your partner carry mutations linked to inherited conditions such as cystic fibrosis, sickle cell disease, Tay-Sachs disease, spinal muscular atrophy (SMA), and many others. If both parents are carriers of the same condition, there’s a higher chance of passing it on to their child. Carrier screening allows you to understand these risks early on—before or during pregnancy—so you can make informed choices about your reproductive options and prepare for your family’s future with confidence, clarity, and care.

20/06/2025

Early detection saves lives—and genetic testing makes it possible. Our specialized oncology genetic tests are designed to identify inherited mutations and genetic markers linked to various cancers before symptoms ever appear. Whether you have a family history of cancer or simply want to take a proactive approach to your health, these tests can reveal your personal risk for conditions such as breast, ovarian, colorectal, prostate, and other hereditary cancers. By detecting these markers early, you gain the power to take preventive action—through lifestyle changes, regular screenings, or personalized medical strategies—potentially reducing your risk and improving long-term outcomes. Because when it comes to cancer, knowledge truly is power—and the earlier you know, the more options you have.

18/06/2025

If there’s a pattern of illness in your family—such as cancer, neurological disorders, heart disease, or unexplained health conditions—clinical genetics could provide the answers you’ve been searching for. Through advanced genetic testing and expert evaluation, we can help identify inherited conditions, uncover the root causes of recurring illnesses, and give you and your family the knowledge needed to make proactive, personalized health decisions. Whether you're looking for clarity, early detection, or better management of hereditary risks, clinical genetics offers powerful insight into your family’s health story—and the tools to shape a healthier future.

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16/06/2025

Our certified genetic counselors are here to guide and support you at every step, helping you understand your results clearly, answering your questions with compassion, and empowering you to make informed decisions for yourself and your growing family—because you deserve expert care that truly walks beside you throughout your pregnancy journey.

15/06/2025

To every father, grandfather, stepfather, mentor, brother, uncle, guardian, and friend — today we see you, we celebrate you, and we thank you.

You are the quiet force behind dreams, the shoulders that carry generations, and the steady hands that hold families together.
You may not always wear a cape, but your sacrifices, your silent prayers, your guidance, and your love have changed lives in ways words can never fully express.

Whether you're a father by blood, by choice, or by role — your presence is powerful, your love is legacy, and your impact is immeasurable.
Thank you for standing strong, showing up, and leading with heart.

We celebrate you. We honor you. We cherish you.

Address

Plot 8, Unity Street, Coker Estate, Shasha, Akowonjo, Egbeda Lagos
Alimosho
100275

Opening Hours

Monday	09:00 - 17:00
Tuesday	09:00 - 17:00
Wednesday	09:00 - 17:00
Thursday	09:00 - 17:00
Friday	09:00 - 17:00
Saturday	10:00 - 14:00

Telephone

+2349039994550

Website

https://oncogenomics.com.ng/

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