At Scientia Genetics, our name reflects what we value most: knowledge you can trust. Scientia means knowledge, and it represents our commitment to evidence-based care, thoughtful interpretation, and clear communication, grounded in science, not guesswork.
Discover the Science of You
Your genetics are more than test results—they’re part of your story. At Scientia Genetics, we help you understand your DNA and family history in a way that feels personal, empowering, and relevant to your life. Our goal is clarity you can use, not information overload.
Knowledge You Can Trust
Scientia means knowledge. Our care is grounded in evidence-based science, thoughtful interpretation, and clear communication. You’ll work with a board-certified genetic counselor who explains complex information in plain language—so you can feel confident in what you’re learning and why it matters.
Personalized, Judgment-Free Care
Every session is centered on you. We help you explore inherited risk, review genetic test results, and ask questions about your health or family history in a supportive, judgment-free space. You’re an active participant, guided with care and respect at every step.
Clarity Without Overwhelm
Genetic counseling doesn’t have to feel overwhelming. We focus on understanding—not predictions or labels. By providing context and explanation, we help replace confusion with clarity, so genetic information becomes a tool for insight, reassurance, and informed decision-making.
Care That Meets You Where You Are
With convenient telehealth appointments and flexible visit types, our services are designed to meet you where you are. Whether you’re planning ahead, navigating a diagnosis, or seeking answers, we help you understand your genetic story and use that knowledge with confidence.
At Scientia Genetics, we offer personalized genetic counseling designed to meet you where you are.
You can work with us based on your life stage or situation, and choose from a range of appointment types that fit your needs.
Care Across Life Stages and Situations
Before & During Pregnancy
Planning a pregnancy or already expecting can raise important questions. Genetic counseling helps you understand genetic risks, testing options, and results so you can make informed decisions with confidence.
We support individuals and couples before and throughout pregnancy with clear, compassionate guidance.
Before Pregnancy
- Carrier screening for inherited conditions
- Family history of genetic or inherited conditions
- Planning pregnancy later in life
- Desire for proactive genetic information
During Pregnancy
- Advanced maternal age
- Abnormal or uncertain screening results
- Ultrasound findings
- Personal or family history concerns
Pregnancy Genetics FAQ
Do I need genetic counseling before getting pregnant?
Not always, but counseling can help identify inherited risks, review carrier screening options, and support informed planning before conception.
What is carrier screening?
Carrier screening looks for inherited conditions you could pass on to a child, even if you have no symptoms.
Should I meet with a genetic counselor after an abnormal NIPT result?
Yes. Genetic counseling helps explain what results mean, discusses follow-up options, and provides emotional support during decision-making.
Does genetic counseling replace my OB or prenatal care?
No. Genetic counseling complements your prenatal care and supports informed conversations with your healthcare providers.
Is genetic testing required?
No. Testing is optional and only pursued if it aligns with your goals and medical situation.
Children & Adolescent
When a child or teen has a health concern, genetic counseling helps families understand possible genetic causes, testing options, and next steps in a supportive, clear way.
We work with parents, caregivers, and adolescents to review family history, explain results, and support informed decisions about care and follow-up.
Common Concerns
- Developmental delays or learning differences
- Congenital differences or birth conditions
- Autism spectrum concerns
- Epilepsy or unexplained neurological symptoms
- Suspected or confirmed genetic conditions
- Abnormal genetic test results
- Family history of inherited childhood conditions
Pediatric Care Disclaimer
Genetic counseling supports understanding and informed decision-making. Testing decisions for children are made thoughtfully, with consideration for medical benefit, family values, and the child’s best interest.
Pediatric Genetics FAQs
Do children need genetic testing to meet with a genetic counselor?
No. Many families meet with a genetic counselor to review history, understand concerns, or decide whether testing may be helpful.
Can adolescents participate in the session?
Yes. When appropriate, adolescents are welcome to join sessions, and discussions are tailored to their age and comfort level.
What if testing was already done elsewhere?
We can review prior genetic testing, explain results, and discuss what they may mean for your child and family.
Is genetic counseling only for rare conditions?
No. Families seek genetic counseling for a wide range of concerns, from common conditions to rare or unexplained diagnoses.
Adults
Adult genetic counseling is designed for individuals who have a personal diagnosis, symptoms and/or a family history that raises questions about genetic conditions, or genetic test results and want to better understand how genetics may play a role in health.
We help adults make sense of genetic information in the context of their own medical history, current concerns, and future planning, providing clarity, support, and informed guidance.
Common Concerns
- Personal or family history of cancer, heart disease, or other inherited conditions
- Reviewing genetic test results from direct-to-consumer or clinical testing
- Planning preventive screening or health management
- Clarifying inherited risk for yourself or family members
- Seeking a second opinion or additional context for prior testing
Adult Genetics FAQs
Is genetic counseling only for people with a diagnosis?
No. Many adults seek counseling to understand risk, review family history, or explore testing before any diagnosis
Do I have to get genetic testing?
No. Testing is optional. Counseling can help you decide whether testing is appropriate or helpful for you.
Can genetic counseling help with family planning or future health decisions?
Yes. Many adults use genetic counseling to better understand inherited risks and plan proactively.
Can genetic counseling help if I already had genetic testing?
Yes. Many adults seek genetic counseling to better understand prior test results, clarify what they mean for their health, or decide whether additional testing or follow-up may be helpful.
Can genetic counseling still help if I have little or no family information?
You don’t need a complete family history to benefit from genetic counseling. We focus on what is known, your personal health history, available records, and your questions, we discuss population-based risk and whether genetic testing can be helpful.
Can genetic counseling help if my symptoms are unexplained?
Yes. Counseling can help assess whether genetics may be relevant and discuss appropriate options.
Family History & Inherited Risk
Family History & Inherited Risk counseling is for individuals without symptoms or diagnoses, but who have concerns based on family history of genetic conditions or inherited health risks.
We help you understand patterns across generations, clarify your personal risk, and explore whether genetic testing or screening may be appropriate.
Common Concerns
- Relatives with cancer, heart disease, or genetic conditions
- Multiple family members with similar health concerns
- Early-onset conditions in the family
- Known genetic variants in relatives
- Limited or unclear family medical history
Family History & Inherited Risk FAQs
What if I don’t know much about my family history?
That’s common. We work with whatever information is available and can still provide guidance.
Does a family history mean I will develop the same condition?
Not necessarily. Genetic counseling helps clarify risk, not predict outcomes.
What if I have a family history of symptoms or a genetic condition, but no diagnosis myself?
Genetic counseling can still be helpful. We can review your family history, discuss possible inherited risks, and explore whether genetic testing or screening may be appropriate for you.
Can this help my family members too?
Yes. Understanding inherited risk can support shared awareness and informed conversations within families.
Can I schedule an appointment for multiple family members with the same concern?
Yes. We offer family sessions that allow multiple relatives to meet together to review shared family history, genetic risks, and next steps in a coordinated, supportive way.
Medication Response
Medications don’t work the same way for everyone. Genetic counseling can help you understand how your genes may influence how your body processes certain medications providing insight that supports safer, more informed conversations with your healthcare providers.
We work with individuals who have questions about medication effectiveness, side effects, or prior pharmacogenetic (PGx) testing. Sessions focus on explaining results, reviewing relevant genetic factors, and helping you understand what information may be helpful to share with your prescribing provider.
Common Concerns
- Prior pharmacogenetic (PGx) testing results
- Unexpected side effects or limited response to medications
- Questions about how genetics may affect medication metabolism
- Preparing for a conversation with a prescribing provider
- Reviewing medication-related genetic information already obtained
Medication Response FAQ
Does genetic counseling tell me which medication I should take?
No. Genetic counseling explains how your genetic results may relate to medication response and helps you prepare for informed discussions with your prescribing provider.
Do I need genetic testing before this appointment?
Not necessarily. We can review existing results or discuss whether pharmacogenetic testing may be appropriate to consider.
Can you review PGx results from another lab or provider?
Yes. We can help explain prior pharmacogenetic test results and place them in context for your health and medications.
Will you communicate directly with my doctor or pharmacist?
With your permission, we can participate in joint provider sessions or help you understand how to share your results effectively with your care team.
Is this service a replacement for medical advice?
No. Genetic counseling provides education and context around genetic information but does not offer medical, prescribing, or treatment recommendations.
Rare & Undiagnosed Conditions
Living with unexplained symptoms or a rare condition can be frustrating and isolating. Genetic counseling offers a supportive space to review your health history, prior testing, and possible genetic explanations—at a pace that respects uncertainty.
We work with individuals and families to interpret existing results, review complex histories, and discuss whether additional testing or next steps may be helpful, offering clarity and guidance along the way.
Common Concerns
- Long-standing or unexplained symptoms
- Suspected genetic or rare conditions
- Multiple specialists with no unifying diagnosis
- Atypical presentation of a known condition
- Prior genetic testing with uncertain or negative results
- Concerns about recurrence risk for family members
Rare & Undiagnosed Conditions FAQs
Can genetic counseling help even if I don’t have a diagnosis?
Yes. Genetic counseling can help organize your medical history, review prior testing, and explore whether a genetic cause may be worth considering—even when answers are not yet clear.
Do I need to have genetic testing done before this visit?
No. Many patients come with prior testing or none at all. We’ll review what’s already been done and discuss whether additional testing might be helpful.
What if my previous genetic testing was “negative” or uncertain?
We can help interpret prior results, explain limitations of past testing, and discuss whether newer or different approaches may be appropriate.
Do you offer second opinions or review prior genetic test results?
Yes. We offer second-opinion genetic counseling, including a careful review of prior genetic testing, medical records, and previous counseling. We help explain what’s already been done, clarify results, and discuss whether additional steps or updated testing may be worth considering.
Explore Appointment Menu:
Begin with an appointment tailored to your needs, informed by expertise and delivered with precision and care.
A simple place to start. Talk through your questions about genetics, testing, family history, or health. We’ll help you understand how genetic counseling may help and what next steps make sense. No testing required.
Not sure where to start? A Discovery Call can help you decide.
Counseling Sessions
A comprehensive starting visit. We review your personal and family history, assess possible genetic or hereditary risks, and discuss whether genetic testing may be helpful.
For Individuals who:
- Are seeking their first & general genetic counseling appointment
- Have not previously undergone genetic testing
- Want a thorough review of personal and family history
- Looking for a comprehensive & personalized risk assessment
- Need expert guidance on testing options
For a specific concern or question. This session focuses on one main issue (family planning, cancer risk, or heart disease, etc.) while still reviewing relevant history. We assess risk, discuss testing if appropriate, and create a clear plan forward.
For Individuals who:
- Want expert guidance around one targeted health issue
- Have a specific concern (such as cancer risk, heart disease, or family planning)
- Have received an abnormal screening result
- Have had prior genetic testing and want focused guidance
- Have a known genetic condition or familial mutation in the family
A comprehensive starting visit for broad questions or first-time genetics care.
A targeted visit for one defined concern, prior testing, or known family risk.
Shared guidance for families. A joint session for multiple family members navigating inherited conditions or shared genetic results. We provide education, alignment, and support for next steps, together.
For Individuals who:
- Have multiple relatives affected by the same genetic condition
- Share a known familial mutation
- Are considering or coordinating cascade testing
- Want to learn and plan together as siblings, parents and adult children, or extended family
- Want everyone to hear the same information at the same time
Collaborative & aligned care. A joint appointment with your healthcare provider or on your behalf to review genetic findings, coordinate care, and ensure everyone is aligned on screening, treatment, or follow-up plans.
For Individuals who:
- Want support explaining genetic results to their doctor or healthcare provider
- Need help coordinating care after genetic testing
- Have complex results that involve multiple medical providers (ex, cardiology, neurology)
- Want everyone aligned on screening, prevention, or follow-up plans
- Prefer shared conversations rather than relaying information themselves
Clarity and reassurance. We offer a thorough review of prior genetic testing and medical records. We take a deep dive into your results and place them in the context of your personal and family history. You’ll have space to ask questions, address lingering uncertainty, and gain clear insight into what your results truly mean.
For Individuals who:
- Have had genetic testing in the past and want a clearer explanation
- Feel uncertain or unsettled about previous results
- Want a fresh, independent review of their genetic test results
- Want results reviewed in the context of personal and family history
- Are seeking reassurance before making health or screening decisions
A visit for multiple family members navigating inherited condition or results together.
A collaborative visit to align genetic findings with your doctor or healthcare team.
A focused review of prior genetic testing for clarity, reassurance, and insight.
Genetic Testing Sessions
Support before testing. Helps you decide whether genetic testing is right for you. We review options, benefits, limits, and possible outcomes. This session may be included as part of or scheduled separately after any full session.
For Individuals who:
- Decided to pursue testing
- Are considering genetic testing and want to understand their testing options
- Want to review benefits, limitations, and possible outcomes before testing
- Need more information to feel confident before moving forward
Clear understanding, thoughtful next steps. We explain your results in plain language, discuss health and family implications, and outline next steps such as screening, prevention, or follow-up care.
For Individuals who:
This visit is typically scheduled as a follow-up for patients who pursued genetic testing with Scientia Genetics and are ready for results disclosure, interpretation, and support with next steps or follow-up care.
Guided support before testing, so you have clarity before you decide.
We help you clearly understand your results and create a personalized plan to support your health.
How Telehealth Works at Scientia Genetics?
Step 1: Request a session online
Submit a short, secure appointment request.
Step 2: Confirm your appointment
We’ll contact you through secure email with next steps.
Step 3: Complete intake forms
Fill out secure forms before your visit.
Step 4: Join your video session
Meet with a licensed genetic counselor by secure video.
Step 5: Receive follow-up support
Ongoing communication is handled securely.
Your Privacy Is Important
Patient privacy is central to our practice. We use HIPAA-compliant systems and appropriate safeguards to protect health information across referrals, counseling, telehealth, and follow-up care. We are happy to discuss privacy practices or secure communication preferences as needed.