Comprehensive Genetic Testing — The Catalyst Clinic

London · New York · Zürich

Comprehensive
Genetic & Genomic
Testing
Preventative-First.

Physician-Reviewed  ·  Counselling-Supported  ·  Fully Integrated

Your bloodwork shows how your biology is performing today. Your genome reveals the lifelong predispositions and metabolic tendencies that make genuinely preventative care possible. The Catalyst Clinic is the only clinic in Europe to offer anywhere integrated accredited genetic testing directly into a physician-led peptide and supplementation programme — from a single blood draw, reviewed personally by Dr. Ethan Hausman-Marquis.

Genetic and genomic testing is provided as accredited clinical diagnostic testing, distinct from the peptide research compounds discussed elsewhere. A result indicating elevated risk is not a diagnosis. Predisposition testing is accompanied by a registered genetic counselling service.

Testing Overview

Sample

Single Blood DrawOne vacutainer · in-clinic or mobile

Laboratories

AccreditedClinical-grade sequencing & PCR

Genetic Counselling

IncludedPre- and post-test, on predisposition panels

Turnaround

7 days–6 weeksDepending on panel complexity

Physician Review

PersonalEvery result read by Dr. Ethan

Integration

AURION™Feeds supplementation & monitoring

Who It's For

Preventative-Minded PatientsAdd-on to any advisory programme · remote worldwide

Testing is optional and additive to your programme. Nothing on this page constitutes medical advice or a treatment recommendation.

The Catalyst Clinic provides physician-led advisory consultations within a fully regulated private medical framework by GMC, European and US-registered physicians. Genetic testing is offered as accredited clinical diagnostic testing. A genetic result is not, in itself, a diagnosis. Read our full compliance statement →
Single Blood Draw Accredited Laboratories Genetic Counselling Included PhD-Level Physician Review Integrated With Your Programme Remote Worldwide

Why Test Your DNA

Preventative Health, Written In Your Genome.

Most health data is a snapshot. Bloodwork tells you how your body is functioning on the day it was drawn — invaluable, but temporary. Your genome is different: it does not change, and it carries the deeper context of the predispositions and metabolic tendencies you have held since birth.

Reading that context lets us move from reactive to genuinely preventative. Rather than waiting for a marker to drift out of range, we can anticipate where your biology is most likely to need support and build your programme around it from the outset — the right form of a nutrient, the systems worth watching most closely, the areas where early attention pays off.

At The Catalyst Clinic your results are never a report filed away. Every panel is reviewed personally by Dr. Ethan Hausman-Marquis — PhD, Cell and Genomic Biology, Karolinska Institute — and integrated directly into your AURION™ supplementation plan and your monitoring schedule.

What Your Genome Informs

  • How you absorb and use key vitamins — feeding your AURION™ plan
  • The right form of a nutrient for your biology (e.g. methylfolate vs. folic acid)
  • Your genetic baseline Omega 3:6 ratio and inflammatory tendency
  • Caffeine metabolism and fasting response
  • Inherited cardiac, cholesterol and iron-handling predispositions
  • Cancer predisposition — informing screening and monitoring cadence
  • Gut microbiome composition and diversity
  • Which biomarkers to track most closely over the life of your programme

The Panels

Tests Available & What Each One Does

Every panel below can be added to your programme. Which panels are appropriate is a decision Dr. Ethan makes with you, guided by your history, family history and goals — never a blanket recommendation.

Nutrigenomic — Directly Feeds Your Supplementation

The genomic layer that most directly shapes your AURION™ plan, translating your DNA into precise, personalised supplementation.

Nutrition & Lifestyle DNA

Nutrigenomic Profile

Personalised insight into how your biology handles key nutrients — vitamin absorption, folate and vitamin D deficiency risk, your baseline Omega 3:6 ratio and inflammatory tendency, fasting response, and caffeine metabolism. The panel that most directly translates into your AURION™ morning and evening formulations.

MTHFRVDROmega 3:6CaffeineFasting

NGS · Single blood draw

Genetic Lactose Intolerance

Nutrigenomic Profile

Genotyping of the lactase-persistence variants that determine whether your body continues to produce lactase into adulthood — clarifying whether dairy is a genuine trigger and informing dietary and supplementation guidance.

MCM6LCT

RT-PCR · Single blood draw

Microbiome Testing

Metagenomic Sequencing

In-depth shotgun sequencing of the gut microbiome, identifying 30+ biomarkers — overall diversity, the Firmicutes/Bacteroidetes ratio, probiotic and potentially harmful species, fibre-degrading and butyrate-producing bacteria, plus fungi, archaea and viruses. Informs targeted dietary and gut-support recommendations.

F/B ratio15 probiotic markersDiversity

Shotgun sequencing · Home collection

Cardiometabolic & Metabolic Predisposition

Inherited tendencies that shape which systems your programme monitors most closely and how often we repeat your bloodwork.

Genetic Full Cardiac Risk

Inherited Cardiac Conditions

A next-generation sequencing screen covering over 100 genes associated with inherited cardiac conditions — cardiomyopathies, channelopathies and aortopathies. Particularly relevant where there is a family history of cardiac disease or unexplained cardiac symptoms.

MYH7MYBPC3KCNQ1SCN5A+100 more

NGS · Single blood draw

Familial Hypercholesterolaemia

Inherited Cholesterol Risk

Screens five genes for variants that drive genetically elevated cholesterol and premature cardiovascular risk. Relevant for adults with unexplained high total or LDL cholesterol, or a family history of early heart disease.

APOBAPOELDLRLDLRAP1PCSK9

NGS · Single blood draw

Genetic Haemochromatosis

Iron Overload Risk

Genotyping of three HFE variants commonly associated with hereditary iron overload. Especially relevant for those of Northern European ancestry with unexplained raised ferritin or transferrin saturation — guiding iron-related monitoring and supplementation decisions.

HFE C282YHFE H63DHFE S65C

RT-PCR · Single blood draw

Digestive & Autoimmune Predisposition

Clarifying genetic drivers behind digestive symptoms so guidance is targeted rather than trial-and-error.

Genetic Coeliac Disease

Autoimmune Predisposition

Genotyping for the HLA-DQ2 and HLA-DQ8 haplotypes, which are present in up to 99.7% of coeliac patients. A negative result effectively rules out coeliac disease — useful for anyone with chronic digestive symptoms, fatigue, or a family history.

HLA-DQ2.2HLA-DQ2.5HLA-DQ8

Genotyping · Single blood draw

Specialist Oncology — Cancer Predisposition

Hereditary cancer-risk panels. These carry meaningful personal and family implications and are always accompanied by our complimentary genetic counselling service, before and after testing.

Breast & Ovarian Cancer Risk

Hereditary Cancer Panel

Screens eight genes for variants that may increase risk of breast and ovarian cancer — relevant where there is a personal or family history, or Ashkenazi Jewish ancestry.

BRCA1BRCA2ATMCHEK2PALB2TP53PTENCDH1

NGS · 8 genes · With counselling

Bowel Cancer Risk

Hereditary Cancer Panel

Screens 11 genes linked to hereditary bowel cancer and Lynch Syndrome — relevant where there is a personal or family history of bowel or Lynch-related cancers.

MLH1MSH2MSH6PMS2APCMUTYHEPCAM+4 more

NGS · 11 genes · With counselling

Prostate Cancer Risk

Hereditary Cancer Panel

Screens 14 genes for variants that may increase prostate cancer risk — relevant where there is a personal or family history of prostate cancer, or Ashkenazi Jewish ancestry.

BRCA1BRCA2ATMCHEK2HOXB13+9 more

NGS · 14 genes · With counselling

Core Cancer Genetic Risk

Comprehensive Panel

A broader screen of 29 genes covering variants associated with common cancers — including breast, bowel, prostate and ovarian. Suited to those with a wider family history or where a smaller panel returned no variant.

29 genesBRCA1/2Lynch genesTP53

NGS · 29 genes · With counselling

Genetic Full Cancer Risk

Most Comprehensive Panel

Our most comprehensive hereditary screen — 94 genes covering variants linked to both common and rare cancers. The deepest predisposition picture available, for those who want the fullest genomic context.

94 genesCommon + rareDeep NGS

NGS · 94 genes · With counselling

A note on the oncology panels: hereditary cancer-risk testing has significant personal and family implications and is never entered into lightly. Every predisposition panel at The Catalyst Clinic includes access to a registered genetic counsellor for both pre-test and post-test discussion. A result indicating elevated risk is not a diagnosis — it is information that guides screening, monitoring and, where appropriate, onward specialist referral.

Integration

How Your Genome Shapes Your Programme.

Genetic data is only valuable when it changes what we actually do. At The Catalyst Clinic your results are integrated into three parts of the Catalyst Method — reviewed personally by Dr. Ethan, never by algorithm.

01

Precision Supplementation

Your Nutrition & Lifestyle DNA results flow directly into your AURION™ plan. A folate-processing variant may mean methylfolate rather than folic acid; a vitamin D absorption tendency informs dosing; your genetic Omega 3:6 baseline guides EPA/DHA. Supplementation matched to your biology, not a generic stack.

02

Targeted Monitoring

Predisposition data tells us which systems to watch most closely. A cardiac or cholesterol predisposition means tighter lipid and cardiovascular monitoring and, where indicated, more frequent bloodwork — so your programme is genuinely preventative rather than reactive.

03

A Life-Long Baseline

Unlike bloodwork, your genome does not change. Established once, it becomes a permanent layer of context beneath every future review — informing how your advisory programme evolves and where preventative attention is best directed over the years ahead.

The Process

Simple To Begin. Fully Supported.

From a single blood draw to a report you can actually understand — with a registered genetic counsellor available at every stage of the predisposition panels.

Step 01

Consultation & Panel Selection

Dr. Ethan discusses your history, family history and goals, and helps you decide which panels are genuinely worthwhile for you. Optional pre-test genetic counselling is available for the predisposition panels.

Step 02

A Single Blood Draw

Most panels require only one blood sample, taken in clinic or by arrangement. The microbiome panel uses a simple home-collection kit. No repeat visits to begin.

Step 03

Accredited Laboratory Analysis

Your sample is processed through accredited laboratories using clinical-grade sequencing and PCR. Turnaround ranges from seven days to six weeks depending on the complexity of the panel.

Step 04

Physician Review & Counselling

Dr. Ethan reviews your results personally and you receive a clinical report written to be understood. Predisposition results are accompanied by complimentary post-test genetic counselling.

Step 05

Integration Into Your Programme

Your genomic data is folded into your AURION™ supplementation plan and your monitoring schedule — becoming a permanent layer of context beneath every future review.

Step 06

Ongoing Preventative Care

Because your genome does not change, it continues to inform your care indefinitely — guiding where preventative attention is best directed as your programme evolves over the years ahead.

Why The Catalyst Clinic

Genomics, Integrated — Not Isolated.

Many providers will sell you a genetic test and a PDF. Very few anywhere fold that data into a physician-led peptide and supplementation programme, reviewed personally and revisited at every appointment. That integration is the difference between an interesting report and genuinely preventative care.

01

Physician-Reviewed, Not Automated

Every result is read personally by Dr. Ethan Hausman-Marquis — PhD, Cell & Genomic Biology, Karolinska Institute. No algorithm-only interpretation, no delegation.

02

Integrated With AURION™

Your nutrigenomic data flows directly into your supplementation plan — the right form and dose of each nutrient for your biology, not a generic stack.

03

Counselling-Supported

Predisposition panels include a registered genetic counsellor for pre- and post-test discussion — so results are understood and handled responsibly.

04

Accredited Laboratories

Clinical-grade sequencing and PCR through accredited laboratories, with reports written in plain language alongside the science.

05

A Lifelong Baseline

Tested once, your genome informs your care indefinitely — a permanent layer of context beneath every future review and adjustment.

06

Remote Worldwide

The same standard applies whether you attend in London, New York or Zürich, or consult remotely from anywhere in the world.

Common Questions

Frequently Asked

No. Comprehensive bloodwork is mandatory before any advisory consultation, but genetic testing is entirely optional and additive. It is offered for patients who want the deepest, most preventative picture of their biology, and can be added at any stage of your programme.
Most panels require only a single blood draw, taken in clinic or by arrangement — often alongside your standard programme bloodwork, so there is no additional visit. The microbiome panel is the exception and uses a simple home-collection kit.
It depends on the panel. Nutrigenomic testing shows how your biology handles key nutrients — informing your supplementation. Predisposition panels indicate inherited tendencies for cardiac, metabolic, digestive or cancer-related conditions — informing screening and monitoring. Importantly, a predisposition result describes elevated or reduced risk; it is not a diagnosis and does not mean a condition is present or certain to develop.
Yes. For the predisposition panels — particularly the hereditary cancer screens — a registered genetic counsellor is available for both pre-test and post-test discussion at no additional cost. Genetic counsellors are trained to explain inheritance patterns, interpret results, and support the personal and family implications a result can raise.
Your Nutrition & Lifestyle DNA results feed directly into the AURION™ system. A folate-processing variant may mean we recommend methylfolate rather than folic acid; a vitamin D absorption tendency informs dosing; your genetic Omega 3:6 baseline guides EPA/DHA. The result is supplementation matched to your biology rather than a one-size-fits-all stack.
Turnaround depends on the panel — simple genotyping panels return in around seven days, while comprehensive next-generation sequencing panels can take up to six weeks. Dr. Ethan reviews every result personally before it is shared with you.
Yes. Remote patients across the UK, Europe, the UAE, Australia, Canada and the United States can access genetic testing with the same standard of physician review and genetic counselling. Sample collection is arranged conveniently, and results are reviewed and discussed with you remotely.

Begin

Understand your
biology at its
deepest level.

Add comprehensive genetic testing to your Catalyst Clinic programme, or begin with a discovery consultation to discuss which panels are right for you — in person in London, New York or Zürich, or remotely, anywhere in the world.

What's Included

  • Single blood draw — often alongside programme bloodwork
  • Accredited laboratory sequencing & PCR
  • Personal review by Dr. Ethan Hausman-Marquis
  • Clinical report written to be understood
  • Registered genetic counselling on predisposition panels
  • Integration into your AURION™ supplementation plan
  • A lifelong genetic baseline for future reviews

London · 96 Kensington High Street, W8 4SG
New York · 154 Grand St, 5th Floor, NY 10013
Zürich · Bahnhofstrasse 10, 8001
Remote consultations available worldwide
hello@thecatalystclinic.com

Regulatory Notice

Genetic and genomic testing at The Catalyst Clinic is provided as accredited clinical diagnostic testing and is distinct from the peptide research compounds discussed elsewhere on this website. A genetic result indicating elevated risk is not a diagnosis; predisposition testing is accompanied by a registered genetic counselling service and, where appropriate, onward specialist referral. Genetic testing is optional and additive to a physician-led advisory programme. Nothing on this page constitutes a treatment recommendation, prescribing guide, or medical advice. For our full compliance statement please visit thecatalystclinic.com/compliance-uk.